Author: Sudheer vanguri

  • Ajanta Pharma Recruitment for Production, QC and QA

    Ajanta Pharma Ltd. is conducting a walk-in interview for experienced pharmaceutical professionals at its US FDA-approved Oral Solid Dosage (OSD) formulation facility in Paithan, Chhatrapati Sambhajinagar, Maharashtra. The recruitment drive includes vacancies in Production, Quality Control (QC) and Quality Assurance (QA).
    Candidates with B.Pharm, M.Pharm, B.Sc. or M.Sc. qualifications and relevant pharmaceutical industry experience can apply for suitable positions.
    Applicants with experience in OSD manufacturing, packing operations, analytical testing, method validation, IPQA and GMP documentation will be preferred for relevant roles.
    The walk-in interview is scheduled for 25 October 2026 at Ajanta Pharma Ltd., Chhatrapati Sambhajinagar.

    Ajanta Pharma Recruitment 2026: Company Overview

    Ajanta Pharma Ltd. is a specialty pharmaceutical company involved in the development, manufacture and marketing of quality finished dosage products for domestic and international markets. The company operates seven state-of-the-art manufacturing facilities in India.

    The current recruitment is for its US FDA-approved OSD formulation facility at Paithan, Maharashtra.

    Ajanta Pharma Job Vacancies and Responsibilities

    1. Production Officer / Senior Officer

    Qualification: B.Pharm / M.Pharm
    Experience: 3–6 years

    Job Responsibilities:

    • Handle OSD manufacturing operations, including granulation, compression, coating, pellet coating and capsule filling.
    • Work with process systems such as PAS-X, SCADA and electronic logbooks.
    • Support primary and secondary packing operations.
    • Understand PAS-X, electronic logbooks, track-and-trace systems and e-BMR documentation.

    2. Quality Control Officer / Senior Officer

    Qualification: B.Pharm / B.Sc. / M.Sc.
    Experience: 3–5 years

    Job Responsibilities:

    • Perform analysis of finished product (FP), in-process (IP), process validation (PV) and stability samples.
    • Support method validation, method transfer and investigation activities under the Quality Management System (QMS).
    • Operate laboratory instruments, including HPLC and LIMS systems.

    3. Quality Assurance Officer

    Qualification: B.Pharm / M.Pharm
    Experience: 2–3 years

    Job Responsibilities:

    • Handle in-process quality assurance (IPQA) activities in manufacturing and packing sections.
    • Work with SCADA equipment and PAS-X batch records.
    • Support equipment qualification, facility qualification, utility qualification and validation activities.

    4. Quality Assurance Officer / Senior Officer

    Qualification: B.Pharm / M.Pharm / M.Sc.
    Experience: 3–5 years

    Job Responsibilities:

    • Perform analytical QA activities and review analytical reports.
    • Review chemical and microbiological testing, GLP functions and QC instrument software qualifications.
    • Support laboratory investigations.
    • Work with LIMS software, OpenLab and LC solutions.
    • Maintain working knowledge of QMS, change control, CAPA, incidents, deviations and market complaints.

    Eligibility & Qualifications

    Candidates must possess the qualification and experience relevant to the position they are applying for.

    • Production: B.Pharm / M.Pharm with 3–6 years of experience.
    • Quality Control: B.Pharm / B.Sc. / M.Sc. with 3–5 years of experience.
    • Quality Assurance Officer: B.Pharm / M.Pharm with 2–3 years of experience.
    • Quality Assurance Officer / Senior Officer: B.Pharm / M.Pharm / M.Sc. with 3–5 years of experience.

    Candidates with exposure to regulatory requirements, documentation under cGMP/GDP and experience working in regulated pharmaceutical manufacturing plants will be preferred.

    Location & Salary

    Job Location: Ajanta Pharma Ltd., Plot No. 3 & 4, Gangotri Apartment, Opposite Deogiri Bank, N-5, CIDCO, Chhatrapati Sambhajinagar, Maharashtra – 431005.

    Salary details have not been specified in the recruitment announcement.

    Walk-In Interview Details

    • Company: Ajanta Pharma Ltd.
    • Interview Date: Sunday, 25 October 2026
    • Interview Time: 10:00 AM to 4:00 PM
    • Interview Type: Walk-in interview
    • Facility: US FDA-approved OSD formulation facility

    How to Apply

    Eligible candidates should attend the walk-in interview with their updated CV and relevant documents.

    Candidates who cannot attend the interview can forward their updated CV to the recruitment email address below.

    Email: cv.ptn@ajantapharma.com

    Applicants should mention their relevant experience and the position they are applying for in their CV.

    Documents Required

    Candidates attending the interview should carry:

    • Updated CV or resume
    • Current CTC structure details
    • Recent salary slips
    • Educational certificates and relevant experience documents

    The recruitment notice specifically mentions an updated CV, current CTC structure and recent salary slips.

    Important Instructions

    • Candidates with relevant experience in pharmaceutical manufacturing and regulated plants will be preferred.
    • Applicants should have experience aligned with the responsibilities of the selected position.
    • Candidates unable to attend the walk-in interview may email their updated CV to the recruitment team.

    Frequently Asked Questions

    1. Which positions are available at Ajanta Pharma?

    The vacancies are for Production Officer / Senior Officer, Quality Control Officer / Senior Officer, Quality Assurance Officer and Quality Assurance Officer / Senior Officer.

    2. What qualifications are required?

    Eligible qualifications include B.Pharm, M.Pharm, B.Sc. and M.Sc., depending on the position.

    3. How much experience is required?

    The required experience ranges from 2 to 6 years across the advertised positions.

    4. When is the Ajanta Pharma walk-in interview?

    The interview is scheduled for 25 October 2026, from 10:00 AM to 4:00 PM.

    5. Where will the interview take place?

    The interview will take place at Ajanta Pharma Ltd., Plot No. 3 & 4, Gangotri Apartment, Opposite Deogiri Bank, N-5, CIDCO, Chhatrapati Sambhajinagar, Maharashtra – 431005.

    6. How can candidates apply if they cannot attend?

    Candidates who cannot attend the interview can email their updated CV to cv.ptn@ajantapharma.com.

    Job Summary

    Category Details
    Company Ajanta Pharma Ltd.
    Vacancies Production Officer / Senior Officer; Quality Control Officer / Senior Officer; Quality Assurance Officer; Quality Assurance Officer / Senior Officer
    Required Education B.Pharm / M.Pharm / B.Sc. / M.Sc., depending on the position
    Experience 2–6 years, depending on the position

     

  • Cliniqon Home Health Medical Coder Jobs

    Cliniqon is hiring Home Health Medical Coders with 1–2 years of professional experience in home health coding. Candidates with experience in Plan of Care (POC) and OASIS review, along with an HCS-O or HCS-D certification, are encouraged to apply. This opportunity offers 100% permanent work from home for eligible certified coders across the Philippines. Applicants should have working knowledge of ICD-10-CM, CPT, and HCPCS coding systems and be available to commence employment as soon as possible.

    Cliniqon Home Health Medical Coder Recruitment

    Company Overview

    Cliniqon provides healthcare-related services and is recruiting certified professionals for its Home Health Medical Coding team. The company highlights remote working opportunities, employee benefits, professional development, and support for home health coding certification renewals.

    Job Details

    • Company: Cliniqon
    • Designation: Home Health Medical Coder
    • Department: Medical Coding
    • Job Location: Philippines
    • Work Arrangement: 100% Permanent Work From Home
    • Experience: 1–2 years of professional experience in home health coding
    • Employment Type: Permanent
    • Joining: Immediate availability required

    Job Role & Responsibilities

    The selected candidates will support home health medical coding activities and review clinical documentation according to applicable coding requirements.

    Key Responsibilities

    • Perform home health medical coding activities.
    • Review Plan of Care (POC) documentation.
    • Support OASIS review activities.
    • Apply knowledge of ICD-10-CM, CPT, and HCPCS coding systems.
    • Maintain accuracy and quality in coding-related work.
    • Collaborate effectively with team members while managing assigned responsibilities independently.

    Eligibility & Qualifications

    Required Qualifications

    • Candidates with 1–2 years of professional experience in home health coding.
    • Demonstrated experience in Plan of Care (POC) and OASIS review.
    • HCS-O or HCS-D certification is mandatory.
    • Working knowledge of ICD-10-CM, CPT, and HCPCS coding systems.
    • Excellent communication and interpersonal skills.
    • Ability to collaborate effectively with a team.
    • Ability to work independently.
    • Availability to join as soon as possible.

    Eligible Background

    Home Health Medical Coding | Medical Coding | POC Review | OASIS Review | ICD-10-CM | CPT | HCPCS

    Location & Salary

    • Location: Philippines
    • Work Mode: 100% permanent work from home.
    • Salary: Not disclosed in the recruitment announcement.

    Employee Benefits

    Cliniqon highlights the following benefits for this opportunity:

    • 100% permanent work-from-home arrangement.
    • Company-provided equipment.
    • Retention bonuses.
    • Merit-based performance reviews.
    • Comprehensive HMO coverage.
    • Career growth opportunities.
    • Home health coding certification renewals.

     

    How to Apply

    Interested candidates can apply by sending their updated resume directly to the recruitment team.

    Application Process

    1. Update your resume with relevant home health coding experience and certifications.
    2. Send your resume to the recruitment email address below or contact the company through LinkedIn.
    3. Include your experience with POC, OASIS, and medical coding systems in your application.

    Apply via Email: phcareers@cliniqon.com

     

    Important Dates

    Candidates should apply as soon as possible, as immediate availability is required.

    Documents Required

    • Updated resume or CV.
    • HCS-O or HCS-D certification details.
    • Relevant home health coding experience details.
    • Other supporting documents requested by the recruitment team.

    Additional Requirements

    • Applicants must meet the required home health coding experience criteria.
    • HCS-O or HCS-D certification is mandatory.
    • Candidates should be comfortable working remotely.
    • Applicants must have strong communication and collaboration skills.
    • Candidates should be ready to commence employment as soon as possible.

    Frequently Asked Questions

    1. What is the qualification required for Cliniqon Home Health Medical Coder jobs?

    Candidates need relevant home health coding experience, POC and OASIS review experience, and an HCS-O or HCS-D certification.

    2. How much experience is required?

    The recruitment announcement specifies 1–2 years of professional experience in home health coding.

    3. Is this a work-from-home job?

    Yes. The position offers a 100% permanent work-from-home arrangement for eligible candidates across the Philippines.

    4. What coding knowledge is required?

    Candidates should have working knowledge of ICD-10-CM, CPT, and HCPCS coding systems.

    5. What benefits does Cliniqon offer?

    The listed benefits include company-provided equipment, retention bonuses, merit-based performance reviews, HMO coverage, career growth opportunities, and home health coding certification renewals.

    6. How can candidates apply?

    Candidates can email their updated resume to phcareers@cliniqon.com or contact Cliniqon through LinkedIn.

    Job Summary Table

    Category Details
    Company Cliniqon
    Vacancies Home Health Medical Coder
    Required Education Relevant qualifications with mandatory HCS-O or HCS-D certification
    Experience 1–2 years in home health coding
    Location Philippines, 100% Work From Home
  • Fedora Recruitment for Accounts, Authorization and Billing

    Fedora is conducting daily walk-in interviews for Accounts Receivable (A/R) Executives, Authorization Executives and Billing Executives at its corporate office in Ahmedabad, Gujarat.
    The recruitment drive offers opportunities for candidates with 0–1 year of experience in the relevant field.
    Applicants should have strong English communication skills and the ability to resolve problems quickly and effectively.
    Candidates applying for the Authorization Executive role must have a science background, as specified in the recruitment announcement.

    Fedora Recruitment: Company Overview

    Fedora is hiring candidates for multiple executive-level positions in accounts receivable, authorization and billing operations. The walk-in interviews are conducted daily at Magnet Corporate Park, near Sola Overbridge, Thaltej, Ahmedabad.

    Fedora Job Vacancies and Position Details

    1. Accounts Receivable (A/R) Executive

    • Department: Accounts Receivable
    • Designation: Accounts Receivable Executive
    • Experience: 0–1 year in the same field

    Candidates with relevant experience and strong communication skills can apply for this position.

    2. Authorization Executive

    • Department: Authorization
    • Designation: Authorization Executive
    • Experience: 0–1 year in the same field
    • Additional Requirement: A science background is mandatory.

    Applicants should be able to communicate effectively and resolve work-related issues efficiently.

    3. Billing Executive

    • Department: Billing
    • Designation: Billing Executive
    • Experience: 0–1 year in the same field

    Candidates with relevant experience, problem-solving ability and strong English communication skills can attend the walk-in interview.

    Eligibility & Qualifications

    Candidates interested in Fedora’s executive vacancies should meet the following requirements:

    • Experience: 0–1 year of work experience in the same field.
    • Communication Skills: Strong English communication skills are mandatory.
    • Problem-Solving Skills: Ability to resolve problems quickly and effectively.
    • Authorization Executive: A science background is compulsory.

    The recruitment announcement does not specify a particular degree for the Accounts Receivable and Billing Executive positions.

    Location & Interview Timings

    • Company: Fedora
    • Interview Type: Walk-in interview
    • Interview Schedule: Daily
    • Interview Time: 10:30 AM to 4:30 PM
    • Interview Address: 21, Fedora, Magnet Corporate Park, near Sola Overbridge, Thaltej, Ahmedabad, Gujarat.

    Candidates should visit the interview venue during the stated hours.

    How to Apply for Fedora Recruitment

    Interested candidates can attend the walk-in interview directly at the company’s Ahmedabad office.

    Application steps:

    1. Review the eligibility requirements for the preferred executive position.
    2. Ensure that you have 0–1 year of relevant experience.
    3. Candidates applying for Authorization Executive should have a science background.
    4. Visit the interview venue between 10:30 AM and 4:30 PM.

    Candidates should be prepared to discuss their relevant experience, communication skills and suitability for the selected position.

    Frequently Asked Questions

    1. Which positions are available at Fedora?

    The openings are for Accounts Receivable (A/R) Executives, Authorization Executives and Billing Executives.

    2. Can freshers apply for Fedora executive jobs?

    Candidates with 0–1 year of experience are eligible. Freshers with no prior experience may apply if they meet the role requirements.

    3. Is a science background mandatory for all positions?

    No. A science background is specifically mandatory for the Authorization Executive position.

    4. What communication skills are required?

    Strong English communication skills are mandatory for the advertised positions.

    5. When are the walk-in interviews conducted?

    The interviews are conducted daily from 10:30 AM to 4:30 PM.

    6. Where is the interview venue?

    The venue is 21, Fedora, Magnet Corporate Park, near Sola Overbridge, Thaltej, Ahmedabad, Gujarat.

    Job Summary

    Category Details
    Company Fedora
    Vacancies Accounts Receivable (A/R) Executive; Authorization Executive; Billing Executive
    Required Education Science background mandatory for Authorization Executive; specific degree requirements are not stated for the other roles
    Experience 0–1 year in the same field
  • Concord Biotech Recruitment for ADL, QA and Accounts

    Concord Biotech Limited, Unit II, Valthera, is conducting walk-in interviews for experienced professionals in Analytical Development Laboratory (ADL), Quality Assurance (QA), and Accounts.
    The recruitment drive includes positions for IPQA, Stability Officer, Sr. Officer, Chemist, Executive, Sr. Executive, and Accounts Officer.
    Candidates with B.Pharm, M.Pharm, B.Sc, M.Sc, B.Com, or M.Com qualifications can apply for the relevant positions.
    The walk-in interview is scheduled for 24 October 2026, from 10:00 AM to 2:00 PM, at the company’s Valthera unit in Gujarat.

    Concord Biotech Recruitment: Company Overview

    Concord Biotech Limited is inviting applications for multiple roles at its Unit II facility in Valthera, Gujarat. The current hiring drive covers Analytical Development Laboratory (ADL), Quality Assurance, Accounts, and ADL Semi-Solid operations for the US market.

    Concord Biotech Job Vacancies and Department Details

    1. Quality Assurance (QA)

    Position: IPQA

    • Qualification: B.Pharm / M.Pharm
    • Experience: 3–10 years
    • Job Responsibilities: Experience in IPQA activities for oral solid dosage forms, including tablets, capsules and dry syrups.

    Position: Stability Officer / Sr. Officer

    • Qualification: B.Pharm / M.Pharm
    • Experience: 3–8 years
    • Job Responsibilities:

      • Stability sample charging and stability sample withdrawal.
      • Additional sample-related activities.
      • Destruction of stability samples.
      • Preparation of stability master schedule.
      • Preparation of stability protocols.
      • Preparation of monthly plans.
      • Maintaining stability sample quantities in the stability chambers and retaining samples.
      • Handling raw material and packing material, and drug product samples.
      • Maintaining retain/control samples.

    2. Accounts Department

    Position: Officer

    • Qualification: B.Com / M.Com
    • Experience: 2–3 years

    Candidates with commerce qualifications and relevant accounts experience can apply for this position.

    3. ADL Semi-Solid for the US Market

    Position: Chemist / Officer

    • Qualification: B.Pharm / B.Sc / M.Sc
    • Experience: 1–3 years
    • Job Responsibilities:

      • Experience in chemical analysis.
      • Handling raw materials and finished products.
      • Analysis of semi-solid finished products using pharmacopoeial methods.
      • Handling instruments such as IR, SOR, Muffle Furnace, Vacuum Oven, Rheology Viscometer, KF, Particle Size/Globule Size equipment and other laboratory instruments.
      • Knowledge of GDP/GLP in the laboratory.

    Position: Executive

    • Qualification: M.Pharm / M.Sc
    • Experience: 5–8 years
    • Job Responsibilities:

      • Experience in handling semi-solid products such as creams, ointments and gels.
      • Having experience in formulation development of semi-solid dosage forms.
      • Handling instruments such as HPLC, GC and PSD.
      • Routine stability and FND support for the semi-solid product laboratory.
      • Knowledge of GDP/GLP in the laboratory.

    Position: Sr. Executive

    • Qualification: M.Pharm / M.Sc
    • Experience: Around 10 years
    • Job Responsibilities:

      • Experience in handling semi-solid products such as creams, ointments and gels.
      • Having experience in stability indicating method development and method validation for semi-solid dosage forms.
      • Handling instruments such as HPLC, GC and PSD.
      • Experience in handling the instrument printer and vertical diffusion cell (Franz Cell) and method development study and validation study.
      • Knowledge of assessment studies for Q1/Q2 and characterization for Q3 comparison.
      • Exposure to handling US, EU and Brazil markets.

    Eligibility & Qualifications

    Candidates should meet the education and experience requirements for their preferred department.

    • Quality Assurance (IPQA): B.Pharm / M.Pharm | 3–10 years
    • Quality Assurance (Stability): B.Pharm / M.Pharm | 3–8 years
    • Accounts Officer: B.Com / M.Com | 2–3 years
    • ADL Chemist / Officer: B.Pharm / B.Sc / M.Sc | 1–3 years
    • ADL Executive: M.Pharm / M.Sc | 5–8 years
    • ADL Sr. Executive: M.Pharm / M.Sc | Around 10 years

    Important eligibility condition: Only applicants residing in the Ahmedabad area are eligible to apply.

    Location & Walk-In Interview Details

    • Company: Concord Biotech Limited
    • Unit: Unit II, Valthera
    • Walk-In Date: 24 October 2026
    • Interview Time: 10:00 AM to 2:00 PM
    • Address: 297–298/2P, At Valthera, Taluka Dholka, District Ahmedabad, Gujarat – 382225, India.

    Documents Required

    Candidates attending the interview should bring:

    • Updated CV
    • Current salary proof
    • Passport-size photograph

    Candidates who cannot attend the walk-in interview can apply by emailing their CV to careerfd@concordbiotech.com. The email should clearly mention the position applied for in the subject line.

    How to Apply for Concord Biotech Recruitment

    Interested and eligible candidates can attend the walk-in interview on 24 October 2026, between 10:00 AM and 2:00 PM.

    Application steps:

    1. Check the eligibility requirements for your preferred position.
    2. Prepare an updated CV, current salary proof and passport-size photograph.
    3. Attend the walk-in interview at the Valthera unit on the scheduled date.
    4. If unable to attend, email your CV to careerfd@concordbiotech.com.
    5. Clearly mention the position applied for in the email subject line.

    Frequently Asked Questions

    1. Which positions are available at Concord Biotech?

    The openings include IPQA, Stability Officer / Sr. Officer, Accounts Officer, and Chemist / Officer, Executive and Sr. Executive positions in ADL Semi-Solid for the US market.

    2. Which qualifications are required?

    Depending on the position, eligible qualifications include B.Pharm, M.Pharm, B.Sc, M.Sc, B.Com and M.Com.

    3. Can freshers apply for these vacancies?

    The recruitment poster specifies experience requirements for all listed positions. Candidates should match the experience criteria for their chosen role.

    4. When is the Concord Biotech walk-in interview?

    The walk-in interview is scheduled for 24 October 2026, from 10:00 AM to 2:00 PM.

    5. Where is the interview venue?

    The interview will take place at Concord Biotech Limited, Unit II, Valthera, Gujarat.

    6. How can candidates apply if they cannot attend?

    Candidates can email their CV to careerfd@concordbiotech.com and mention the position applied for in the subject line.

    Job Summary

    Category Details
    Company Concord Biotech Limited
    Vacancies IPQA; Stability Officer / Sr. Officer; Accounts Officer; Chemist / Officer; Executive; Sr. Executive
    Required Education B.Pharm / M.Pharm / B.Sc / M.Sc / B.Com / M.Com, depending on the position
    Experience 1–3 years, 2–3 years, 3–8 years, 3–10 years, 5–8 years and around 10 years, depending on the position

     

  • Higgs Healthcare Recruitment for QA, QC and Microbiology

    Higgs Healthcare Ltd. is inviting applications from qualified professionals for multiple positions at its Liquid Injectable Manufacturing Plant in Bhatoli Kalan, Baddi, Himachal Pradesh.
    The current vacancies include QA Officer / Executive, QC Officer / Executive, and Microbiology Officer / Executive / Senior Executive.
    Candidates with B.Pharm, B.Sc, M.Sc, B.Tech or Biotechnology qualifications can apply for the relevant positions.
    Professionals with 1 to 5 years of experience, depending on the role, are encouraged to apply for these pharmaceutical manufacturing jobs.

    Higgs Healthcare Ltd. Recruitment: Company Overview

    Higgs Healthcare Ltd. is hiring professionals for its liquid injectable manufacturing facility in Baddi, Himachal Pradesh. The recruitment drive covers Quality Assurance, Quality Control and Microbiology departments.

    Higgs Healthcare Ltd. Job Vacancies

    1. QA Officer / Executive

    • Department: Quality Assurance (QA)
    • Number of Vacancies: 2
    • Qualification: B.Pharm
    • Experience: 2–5 years

    Candidates with a B.Pharm qualification and relevant experience in pharmaceutical Quality Assurance can apply.

    2. QC Officer / Executive

    • Department: Quality Control (QC)
    • Number of Vacancies: 2
    • Qualification: B.Sc / M.Sc / B.Pharm
    • Experience: 1–4 years

    Candidates with the specified qualifications and experience in pharmaceutical Quality Control are eligible for this position.

    3. Microbiology Officer / Executive / Senior Executive

    • Department: Microbiology
    • Number of Vacancies: 3
    • Qualification: B.Tech / Biotechnology
    • Experience: 1–5 years

    Candidates with relevant educational qualifications and experience in pharmaceutical microbiology can apply.

    Eligibility & Qualifications

    Candidates must meet the educational and experience requirements for their preferred position.

    • QA Officer / Executive: B.Pharm | 2–5 years of experience
    • QC Officer / Executive: B.Sc | M.Sc | B.Pharm | 1–4 years of experience
    • Microbiology Officer / Executive / Senior Executive: B.Tech | Biotechnology | 1–5 years of experience

    Applicants should select the position that matches their qualifications and professional experience.

    Location & Salary

    • Company: Higgs Healthcare Ltd.
    • Manufacturing Facility: Liquid Injectable Plant
    • Location: Bhatoli Kalan, Baddi, Himachal Pradesh
    • Salary: Hike on current salary; the recruitment announcement describes the package as best in the industry.

    The final salary and increment will depend on the candidate’s current salary and the company’s offer.

    How to Apply for Higgs Healthcare Ltd. Recruitment

    Interested candidates can share their updated resumes using the contact details provided below.

    Candidates should mention their preferred designation and relevant experience when contacting the recruitment team.

    Documents Required

    Candidates should keep the following documents ready when applying:

    • Updated resume or CV
    • Educational qualification details
    • Relevant work experience details
    • Current salary information for salary discussions

    Frequently Asked Questions

    1. Which positions are available at Higgs Healthcare Ltd.?

    The company is recruiting for QA Officer / Executive, QC Officer / Executive, and Microbiology Officer / Executive / Senior Executive positions.

    2. What qualifications are required for QA jobs?

    Candidates must have a B.Pharm qualification for the QA Officer / Executive vacancies.

    3. Can B.Sc and M.Sc candidates apply for QC jobs?

    Yes. B.Sc, M.Sc and B.Pharm candidates are eligible for the QC Officer / Executive positions.

    4. What is the experience requirement?

    The experience requirements are 2–5 years for QA, 1–4 years for QC, and 1–5 years for Microbiology.

    5. What salary does Higgs Healthcare Ltd. offer?

    The recruitment announcement mentions a hike on the candidate’s current salary but does not specify a fixed salary amount.

    6. How can candidates apply?

    Candidates can email their updated resume to hr@higgs.co.in or contact the recruitment team at 9817728770.

    Job Summary

    Category Details
    Company Higgs Healthcare Ltd.
    Vacancies QA Officer / Executive (2); QC Officer / Executive (2); Microbiology Officer / Executive / Senior Executive (3)
    Required Education B.Pharm; B.Sc; M.Sc; B.Tech; Biotechnology, depending on the position
    Experience QA: 2–5 years; QC: 1–4 years; Microbiology: 1–5 years
  • Novo Nordisk India Hiring Product Specialist I/II/III Cardiometabolic Sales (Insulin) 

    Novo Nordisk India Pvt. Ltd. is inviting applications for Product Specialist I/II/III in the Cardiometabolic Sales (Insulin) department in Madurai, Tamil Nadu. Candidates with a full-time bachelor’s degree in Pharmacy or Life Sciences and 3–7 years of pharmaceutical sales experience are eligible to apply, subject to the company’s additional experience and sales performance criteria. Applicants must have at least three years of experience with Novo Nordisk India Pvt. Ltd. and meet the specified sales achievement targets. This opportunity is suitable for experienced pharmaceutical sales professionals with strong territory management, doctor engagement, and business development skills.

    Novo Nordisk Product Specialist I/II/III Recruitment

    Company Overview

    Novo Nordisk is a global healthcare company focused on developing treatments for serious chronic diseases, including diabetes. Novo Nordisk India Pvt. Ltd. operates in the pharmaceutical sector, supporting healthcare professionals with products and services in areas such as diabetes care.

    Job Details

    • Company: Novo Nordisk India Pvt. Ltd.
    • Designation: Product Specialist I/II/III
    • Department: Cardiometabolic Sales (Insulin)
    • Job Location: Madurai, Tamil Nadu
    • Job Function: Sales
    • Experience: 3–7 years in pharmaceutical sales
    • Additional Experience Requirement: Minimum 3 years of experience with Novo Nordisk India Pvt. Ltd.
    • Application Deadline: October 28, 2026

    Job Role & Responsibilities

    The selected candidate will manage pharmaceutical sales activities in the assigned territory, promote insulin products to healthcare professionals, maintain product availability, and work with the Area Sales Manager to achieve business objectives.

    Key Responsibilities

    • Identify and map important stakeholders in the assigned territory.
    • Implement marketing initiatives in coordination with the Area Sales Manager.
    • Engage doctors regularly to promote insulin products, answer questions, address objections, and support prescribing decisions.
    • Meet sales effectiveness key performance indicators, including call averages, call frequency, customer coverage, and personal order bookings.
    • Coordinate with C&FA agents and stockists to maintain product availability.
    • Place orders on time to support a reliable product supply.
    • Conduct prescription audits and competitor analysis to evaluate doctor engagement and market activity.
    • Support doctor segmentation and provide market feedback to sales leadership.
    • Coordinate approved educational activities with internal teams.
    • Maintain timely and accurate reporting and administrative records.
    • Use prescription trends and competitor information to support territory-level business decisions.

    Eligibility & Qualifications

    Educational Qualifications

    • Full-time bachelor’s degree in Pharmacy.
    • Full-time bachelor’s degree in Life Sciences.

    Experience Requirements

    • 3–7 years of pharmaceutical sales experience.
    • Minimum 3 years of experience with Novo Nordisk India Pvt. Ltd. (NNIPL).
    • Strong knowledge of the assigned territory, local pharmaceutical market, and stockists.

    Sales Performance Criteria

    Candidates must meet the sales achievement criteria specified in the recruitment announcement:

    • At least 100% sales achievement in one of the three specified years: YTD 2025, 2024, and 2023.
    • Sales achievement of 90% or above in two of those years.

    Required Skills

    • Pharmaceutical sales and territory management.
    • Doctor engagement and product promotion.
    • Communication, negotiation, and collaboration.
    • Ability to address doctors’ questions and objections.
    • Business understanding and analytical skills.
    • Ability to interpret prescription and competitor data.
    • Stakeholder management and market development.
    • Sales reporting and administrative discipline.

    Location & Salary

    • Job Location: Madurai, Tamil Nadu, India.
    • Salary: Not disclosed in the supplied recruitment details. Compensation should be confirmed with Novo Nordisk during the recruitment process.

    How to Apply

    Eligible candidates can apply through the official Novo Nordisk careers portal.

    Application Process

    1. Visit the official job listing using the link below.
    2. Review the educational, experience, and sales achievement requirements.
    3. Prepare your updated CV, motivation letter, and relevant supporting documents.
    4. Complete the online application and submit the required information before the deadline.
    5. Internal candidates should inform their line manager before applying.

    Official Apply Link: Apply for Product Specialist I/II/III at Novo Nordisk

    Important Dates

    • Application Deadline: October 28, 2026.

    Candidates should submit their applications before the stated deadline.

    Documents Required

    Prepare the following documents for the application:

    • Updated CV or resume.
    • Motivation letter.
    • Educational certificates or relevant documentation.
    • Employment and experience details.
    • Sales performance records, where applicable.

    Additional Requirements

    • Candidates must satisfy the minimum Novo Nordisk India Pvt. Ltd. experience requirement.
    • Sales achievement must meet the stated performance criteria.
    • Applicants should understand local market dynamics and stockist networks.
    • Candidates must be comfortable engaging healthcare professionals and coordinating with internal and external stakeholders.
    • Internal applicants should notify their line manager before submitting an application.

    Frequently Asked Questions

    1. What qualification is required for the Novo Nordisk Product Specialist position?

    Candidates must hold a full-time bachelor’s degree in Pharmacy or Life Sciences.

    2. How much experience is required?

    The position requires 3–7 years of pharmaceutical sales experience, including a minimum of three years with Novo Nordisk India Pvt. Ltd.

    3. What are the sales performance requirements?

    Candidates must have achieved 100% sales achievement in at least one of the specified years and 90% or above sales achievement in two years, based on the stated criteria for YTD 2025, 2024, and 2023.

    4. Where is the job located?

    The position is based in Madurai, Tamil Nadu, India.

    5. What is the salary for this position?

    The salary is not disclosed in the supplied recruitment announcement. Candidates should confirm compensation during the recruitment process.

    6. What is the last date to apply?

    The application deadline is October 28, 2026.

    Job Summary Table

    Category Details
    Company Novo Nordisk India Pvt. Ltd.
    Vacancies Product Specialist I/II/III
    Required Education Full-time bachelor’s degree in Pharmacy or Life Sciences
    Experience 3–7 years in pharmaceutical sales, including at least 3 years with NNIPL
    Location Madurai, Tamil Nadu, India
  • Remote Hiring Indero Clinical Data Coder

    Indero is hiring for the position of Clinical Data Coder for a permanent, full-time, home-based opportunity in India. Candidates with a degree in Pharmacy, Life Sciences, or a related field can apply, while candidates with medical or nursing qualifications may also be eligible with two years of relevant experience or an equivalent combination of education, training, and experience. The role involves clinical data coding, medical terminology coding using MedDRA and WHO Drug, and supporting clinical data management activities for ongoing clinical trials. Professionals with knowledge of clinical research, query management, medical dictionaries, and Good Clinical Practice (GCP) can explore this opportunity through Indero’s official careers portal.

    Indero Clinical Data Coder Recruitment

    Company Overview

    Indero, formerly known as Innovaderm, is a contract research organization (CRO) specializing in dermatology and rheumatology clinical research. The company supports pharmaceutical and biotechnology sponsors with clinical trial services, including protocol design, patient recruitment, trial monitoring, and biometrics.

    With more than 25 years of clinical research and trial delivery experience, Indero operates across North America, Europe, Asia Pacific, and Latin America.

    Job Details

    • Company: Indero
    • Designation: Clinical Data Coder
    • Department: Clinical Data Management
    • Job Location: Home-based, India
    • Employment Type: Permanent, Full-time
    • Experience: Relevant experience requirements depend on the candidate’s qualification and background.
    • Work Arrangement: Remote / Home-based

    Job Role & Responsibilities

    The Clinical Data Coder will support medical and medication coding for ongoing clinical studies and contribute to clinical data management activities. The role requires accurate coding, consistent application of medical dictionaries, and compliance with regulatory requirements, industry guidelines, company SOPs, sponsor requirements, and study timelines.

    Key Responsibilities

    • Perform and oversee accurate coding of medical terms and medications using MedDRA, WHO Drug, and internal coding conventions.
    • Set up coding modules for assigned clinical studies and ensure that configurations and workflows are appropriate.
    • Develop, document, and maintain coding conventions and synonym lists to ensure consistency across studies.
    • Validate sponsor coding licenses.
    • Coordinate coding activities across multiple studies while acting as the Lead Coder.
    • Prioritize coding activities and manage workloads to meet study timelines.
    • Contribute to the coding section of Data Management Plans.
    • Perform and oversee medical dictionary version upgrades and related activities.
    • Validate and test coding configurations, coding report programming, and associated database checks.
    • Support clinical data review and resolve data clarifications within the required timelines.
    • Maintain effective communication with Data Management Leads, Clinical Research Associates (CRAs), and other stakeholders.

    Eligibility & Qualifications

    Educational Qualifications

    Candidates with the following qualifications or equivalent educational backgrounds may be eligible:

    • Bachelor’s degree in Pharmacy.
    • Bachelor’s degree in Life Sciences.
    • Bachelor’s degree in a related field.
    • Medical qualification with two years of relevant experience.
    • Nursing qualification with two years of relevant experience.
    • An equivalent combination of education, training, and experience.

    Experience & Technical Requirements

    • Thorough knowledge of medical terminology and medical dictionaries used for coding, including MedDRA and WHO Drug Dictionary (WHODD).
    • Experience in clinical trials or the pharmaceutical industry is preferred.
    • Understanding and practical experience of query management processes.
    • Ability to manage multiple projects and prioritize work to meet deadlines.
    • Strong written and verbal English communication skills.
    • Ability to work effectively in a global team environment.
    • Good organizational and analytical skills.
    • Strong attention to detail.
    • Knowledge of Good Clinical Practice (GCP) and applicable Health Canada and US Food and Drug Administration (FDA) regulations and guidelines.

    Eligible Qualifications

    B.Pharm | M.Pharm | Pharm.D | BSc Life Sciences | MSc Life Sciences | Related Life Sciences Degrees | Medical Qualifications | Nursing Qualifications

    Eligibility depends on the applicable education, training, and experience requirements specified by Indero.

    Location & Salary

    • Job Location: Home-based, India.
    • Work Schedule: Flexible work schedule.
    • Employment Type: Permanent, full-time.
    • Salary: Not disclosed in the supplied recruitment details. Compensation should be confirmed during the hiring process.

    Candidates should be prepared to attend some meetings outside regular business hours, primarily during the evening.

    How to Apply

    Eligible candidates can submit their applications through Indero’s official careers website.

    Application Process

    1. Visit the official Indero careers page using the link below.
    2. Review the Clinical Data Coder job description and eligibility requirements.
    3. Complete the application form with accurate personal, educational, and professional details.
    4. Submit your updated resume and any other information requested by the employer.
    5. Monitor your email for recruitment-related communication.

    Official Apply Link: Apply for Clinical Data Coder at Indero

    Selection Process

    The recruitment announcement does not specify the interview rounds or selection stages. Applicants should follow the instructions provided by Indero during the recruitment process.

    Important Dates

    Candidates should visit the official careers page to check the current vacancy status and application availability.

    Documents Required

    Keep the following documents ready, as applicable:

    • Updated resume or CV.
    • Educational certificates and academic mark sheets.
    • Relevant medical or nursing qualification certificates, where applicable.
    • Proof of relevant work experience.
    • Details of clinical research and clinical data coding experience.
    • Valid contact information.

    Additional Requirements

    • Candidates must be legally authorized to work in India.
    • Applicants should be comfortable working remotely with international teams.
    • Flexibility to attend evening meetings when required is necessary.
    • Candidates should be capable of managing coding activities across multiple clinical studies.
    • Strong knowledge of medical terminology, coding dictionaries, and data review procedures is important.

    Employee Benefits

    Indero highlights the following benefits for this position:

    • Flexible work schedule.
    • Permanent, full-time employment.
    • Ongoing learning and development opportunities.
    • Opportunities for professional advancement.

    Indero also provides accommodations during the recruitment and selection process for applicants with disabilities upon request.

    Frequently Asked Questions

    1. What qualification is required for the Indero Clinical Data Coder position?

    Candidates with a bachelor’s degree in Pharmacy, Life Sciences, or a related field may be eligible. Medical or nursing qualifications may also be accepted with two years of relevant experience or an equivalent combination of education, training, and experience.

    2. Is the Clinical Data Coder position work from home?

    Yes. The vacancy is listed as a home-based position in India. Some meetings may take place outside regular business

  • Abbott Hiring Fresher Trainee Territory Business Manager

    Abbott is inviting applications for the position of Trainee Territory Business Manager in Mumbai, Maharashtra. This opportunity is open to freshers who have completed a degree in Science and possess good communication and analytical skills. The role focuses on pharmaceutical sales, territory management, healthcare professional engagement, and product promotion. Candidates interested in starting their careers in pharmaceutical sales and medical representative roles can apply through Abbott’s official careers portal.

    Abbott Trainee Territory Business Manager Recruitment

    Company Overview

    Abbott is a global healthcare company operating across pharmaceuticals, medical devices, diagnostics, and nutrition. The company offers career opportunities in sales and healthcare professional engagement.

    Job Details

    • Company: Abbott
    • Designation: Trainee Territory Business Manager
    • Department: Sales
    • Job Location: Mumbai, Maharashtra, India
    • Experience: Fresher
    • Qualification: Any Science Graduate
    • Employment Type: Business partner payroll

    Job Role & Responsibilities

    The selected candidate will support territory sales activities, implement sales strategies, engage healthcare stakeholders, and promote products among doctors and chemists.

    Key Responsibilities

    • Monitor and follow up on sales performance within the assigned territory.
    • Implement and execute sales strategies.
    • Engage with doctors, stockists, retailers, chemists, and institutional pharmacies.
    • Maintain discipline and meet deadlines for internal processes.
    • Use basic computer applications, including Microsoft Excel, Word, and email.
    • Learn quickly and adapt to changes in the market.
    • Communicate effectively in English and the local language.
    • Maintain effective performance during in-clinic visits.
    • Understand basic anatomy and physiology and explain the relevant product portfolio.
    • Conduct science-based discussions with doctors and chemists to promote products in clinics and pharmacies.
    • Execute the customer management plan and ensure customer coverage according to the assigned plan.

    Eligibility & Qualifications

    Educational Qualification

    • Any graduate with a degree in Science.

    Experience Required

    • Freshers are eligible to apply.
    • Candidates should have good communication and analytical skills.

    Required Skills

    • Strong verbal communication skills.
    • Proficiency in English and the local language.
    • Basic computer knowledge, including Excel, Word, and email.
    • Ability to understand anatomy, physiology, and product information.
    • Sales monitoring and territory management skills.
    • Customer engagement and relationship-building abilities.
    • Adaptability and willingness to learn.
    • Ability to follow schedules and meet deadlines.

    Location & Salary

    • Job Location: Mumbai, Maharashtra, India.
    • Salary: Not disclosed in the supplied recruitment details. Compensation should be confirmed during the recruitment process.
    • Payroll: The position is offered on a business partner’s payroll.

    How to Apply

    Eligible candidates can apply online through Abbott’s official careers website.

    Application Process

    1. Visit Abbott’s official job listing.
    2. Review the job responsibilities and eligibility criteria.
    3. Complete the online application with accurate details.
    4. Submit the application as instructed on the careers portal.

    Official Apply Link: Apply for Trainee Territory Business Manager at Abbott

    Important Dates

    Candidates should refer to the official careers page for the latest application status and recruitment updates.

    Documents Required

    Keep the following documents ready, as applicable:

    • Updated resume or CV.
    • Science degree certificate or provisional certificate.
    • Academic mark sheets.
    • Valid contact details.
    • Other documents requested during the application process.

    Additional Requirements

    • Willingness to work in pharmaceutical sales and territory management.
    • Ability to interact professionally with doctors and pharmacy stakeholders.
    • Basic understanding of scientific concepts related to anatomy and physiology.
    • Readiness to execute customer coverage plans and sales strategies.
    • Ability to work according to internal processes and timelines.

    Frequently Asked Questions

    1. Can freshers apply for the Abbott Trainee Territory Business Manager position?

    Yes. The vacancy is specifically listed for freshers.

    2. What is the required qualification?

    Candidates must have a degree in Science. The recruitment details specify that any Science Graduate can apply.

    3. Where is this job located?

    The position is based in Mumbai, Maharashtra, India.

    4. What are the main responsibilities?

    The role involves territory sales monitoring, product promotion, customer engagement, implementation of sales strategies, and interactions with doctors, chemists, and other healthcare stakeholders.

    5. What is the salary for this position?

    The salary has not been disclosed in the supplied recruitment details. Candidates should confirm compensation during the hiring process.

    6. Is the position on Abbott’s direct payroll?

    The supplied job description states that the position is on a business partner’s payroll.

    Job Summary Table

    Category Details
    Company Abbott
    Vacancies Trainee Territory Business Manager
    Required Education Any Science Graduate
    Experience Fresher
    Location Mumbai, Maharashtra, India
  • Fortrea Hiring Freshers Assistant Clinical Data Analyst 

    Fortrea is hiring for the position of Assistant Clinical Data Analyst in Bangalore, Karnataka. Candidates with a degree in Life Sciences, Health Sciences, Information Technology, or a related subject, as well as relevant allied health certifications, are eligible to apply. This is a full-time opportunity for candidates with 0–1 year of clinical research experience who are interested in clinical data management and electronic data capture (EDC) operations. Eligible candidates should review the responsibilities and submit their applications through Fortrea’s official careers portal before the application deadline.

    Fortrea Assistant Clinical Data Analyst Recruitment

    Company Overview

    Fortrea is a global contract research organization (CRO) supporting clinical development and research services for the pharmaceutical, biotechnology, and healthcare industries.

    Job Details

    • Company: Fortrea
    • Designation: Assistant Clinical Data Analyst
    • Department: Clinical Data Management
    • Job Location: Bangalore, Karnataka
    • Job Type: Full-time
    • Experience: 0–1 year in clinical research
    • Requisition ID: 266230
    • Application Deadline: October 22, 2026

    Job Role & Responsibilities

    The selected candidate will support clinical data management activities, electronic data capture (EDC) user access, database review, and compliance with applicable procedures and regulatory requirements.

    Key Responsibilities

    • Follow departmental Standard Operating Procedures (SOPs) and Work Instructions.
    • Complete assigned training within the required timelines.
    • Review and resolve data queries within specified timelines while maintaining quality standards.
    • Perform assigned operational activities according to established Data Management workflows.
    • Review reports and take appropriate action as defined in the Data Management Plan (DMP) or eCRF Review Manual.
    • Conduct ongoing and final consistency checks and review data listings as specified in the DMP and eCRF Review Manual.
    • Ensure clinical data management activities comply with applicable regulatory requirements and Good Clinical Practice (GCP).
    • Set up and maintain Electronic Data Capture (EDC) user access accounts for databases.
    • Process EDC database access requests accurately and efficiently.
    • Troubleshoot user access issues and coordinate with EDC vendors for technical support when required.
    • Prepare, format, and distribute User Access Reports to Project Managers and Lead Data Managers for access reconciliation.
    • Assist with decommissioning and archiving activities.
    • Generate and distribute reports and support other assigned tasks.

    Eligibility & Qualifications

    Required Educational Qualifications

    Candidates must meet at least one of the following requirements:

    • A university or college degree in Life Sciences.
    • A degree in Health Sciences.
    • A degree in Information Technology.
    • A degree in a related subject.
    • Certification in allied health professions from an appropriately accredited institution.

    Fortrea may consider relevant and equivalent work experience in place of the stated educational requirements.

    Experience Required

    • 0–1 year of experience in clinical research.
    • Ability to organize work and communicate effectively.
    • Strong attention to detail.
    • Ability to collaborate effectively with colleagues.
    • Ability to deliver consistent, high-quality work.
    • Proficiency in using computers and relevant departmental tools.

    Eligible Qualifications

    Life Sciences | Health Sciences | Information Technology | Related Subjects | Allied Health Professions Certification

    Location & Salary

    • Location: Bangalore, Karnataka, India
    • Work Arrangement: Office-based and/or home-based, as applicable.
    • Salary: The official job announcement does not provide a salary figure. Compensation will depend on Fortrea’s hiring terms and the candidate’s qualifications and experience.

    Work Environment

    • Candidates may be required to work overtime or on weekends according to business needs.
    • Flexibility to work in different shifts is required.
    • The role involves following established data management procedures and maintaining work quality.

    How to Apply

    Eligible candidates can apply online through Fortrea’s official careers portal.

    Application Process

    1. Open the official application link below.
    2. Review the job description and eligibility requirements.
    3. Complete the online application with accurate information.
    4. Submit the required details and updated resume through the portal.
    5. Monitor your registered email and phone for recruitment-related communication.

    Official Apply Link: Apply for Assistant Clinical Data Analyst at Fortrea

    Official Job Listing: View the complete vacancy details

    Interview and Selection Process

    The recruitment announcement does not specify the interview rounds or selection schedule. Candidates should check their application status and follow any instructions provided by Fortrea’s recruitment team.

    Important Dates

    • Application Deadline: October 22, 2026.
    • Apply as early as possible because the published deadline is approaching.

    Documents Required

    Keep the following documents ready when completing your application, as applicable:

    • Updated resume or CV.
    • Educational certificates and mark sheets.
    • Relevant allied health certification, if applicable.
    • Details of relevant clinical research experience, if applicable.
    • Valid contact information and other details requested in the application form.

    Additional Requirements

    • Follow applicable departmental SOPs and Work Instructions.
    • Complete mandatory training within the specified timelines.
    • Maintain accuracy and consistency when reviewing clinical data.
    • Follow applicable regulatory requirements and GCP principles.
    • Be prepared to work flexible shifts, overtime, or weekends when required by business needs.
    • Maintain effective communication and collaboration with the data management team.

    Frequently Asked Questions

    1. What is the qualification required for the Fortrea Assistant Clinical Data Analyst position?

    Candidates need a university or college degree in Life Sciences, Health Sciences, Information Technology, or a related subject. An appropriate accredited allied health certification may also be accepted.

    2. Can freshers apply for this Fortrea vacancy?

    The listed experience requirement is 0–1 year in clinical research. Candidates at the entry level may be eligible if they meet the educational requirements.

    3. What is the job location?

    The position is based in Bangalore, Karnataka, India. The listed work environment may include office-based and/or home-based work.

    4. What is the salary for the Assistant Clinical Data Analyst role?

    Fortrea has not disclosed the salary in the supplied recruitment details. Candidates should confirm compensation during the recruitment process.

    5. How can candidates apply?

    Candidates can submit their applications through the official Fortrea Workday careers portal using the application link provided above.

    6. What is the last date to apply?

    The published application deadline is October 22, 2026. Candidates should submit their applications before the deadline.

    Job Summary Table

    Category Details
    Company Fortrea
    Vacancies Assistant Clinical Data Analyst
    Required Education Life Sciences, Health Sciences, Information Technology, related subjects, or an appropriate allied health certification
    Experience 0–1 year in clinical research
    Location Bangalore, Karnataka, India
  • Fortrea RFI Apprentice

    Fortrea Recruitment 2026 – RFI Apprentice, Bengaluru

    Fortrea is inviting applications for the RFI Apprentice position in Bengaluru, India. The role focuses on maintaining and updating the company’s experience data repository, reconciling information from different sources, and supporting data quality improvements. Candidates should be proficient in Microsoft Excel and Word, able to work with trial data, and resourceful in locating and verifying information. The position is listed as full-time and remote, with the application deadline stated as 22 October 2026.

    Company Overview

    Fortrea is a global contract research organization (CRO) that supports pharmaceutical, biotechnology, medical device, and diagnostic companies with clinical development and related services.

    Job Details

    Particulars Details
    Company Fortrea
    Job Role RFI Apprentice
    Job Requisition ID 266217
    Job Location Bengaluru, Karnataka
    Work Mode Remote, as listed
    Employment Type Full-time
    Application Deadline 22 October 2026
    Application Mode Online

    Job Responsibilities

    The selected candidate will support the maintenance and improvement of company experience data and related information repositories.

    • Work with clinical trial data and reconcile information from different sources.
    • Use Microsoft Excel and Word to review, organize, and manage data.
    • Locate missing information using internal databases, external libraries, and other available resources.
    • Support the maintenance and improvement of the company’s experience data under supervision.
    • Correct or update existing information and complete missing data where required.
    • Upload new or revised information to the company’s experience data repository, including the SharePoint platform.
    • Perform additional duties assigned by the manager in line with business requirements.

    Eligibility & Qualifications

    The supplied job listing highlights the following skills and capabilities:

    • Experience working with trial data and reconciling information from multiple sources.
    • Strong proficiency in Microsoft Excel and Word.
    • Ability to research information, identify gaps, and suggest improvements.
    • Attention to detail when reviewing and updating records.
    • Ability to work under supervision and complete assigned tasks accurately.

    The supplied listing excerpt does not specify the required educational qualification or minimum years of experience. Candidates should review the official job posting for the complete eligibility criteria.

    How to Apply

    Interested candidates can apply through Fortrea’s official careers portal.

    Apply Online – RFI Apprentice at Fortrea

    • Job ID: 266217
    • Application Deadline: 22 October 2026

    The listing indicates that the application deadline is approaching. Check the official portal immediately to confirm whether applications are still being accepted.

    Job Summary

    Category Details
    Company Fortrea
    Vacancies (position titles) RFI Apprentice
    Required Education Not specified in the supplied listing excerpt
    Experience Experience with trial data and data reconciliation is highlighted; minimum years are not specified