PHARMA STUFF

Category: Featured

Featured posts

  • Aurore Pharmaceuticals Recruitment for QC Staff

    Aurore Pharmaceuticals Private Limited is conducting a walk-in drive for Quality Control (QC) positions at its pharmaceutical manufacturing facility in Quthbullapur, Telangana.
    The company is inviting candidates with B.Sc. or M.Sc. qualifications in Chemistry, Microbiology, or Biotechnology.
    Applicants with 1–5 years of experience in pharmaceutical Quality Control are eligible to apply for this recruitment drive.
    The walk-in interview is scheduled for 30 October 2026, and interested candidates can share their updated CV with the recruitment team by email.

    Aurore Pharmaceuticals Recruitment: Quality Control Department

    Aurore Pharmaceuticals Private Limited is inviting applications from eligible candidates for its Quality Control department. This opportunity is suitable for science graduates and postgraduates with relevant pharmaceutical QC experience who are looking to develop their careers in pharmaceutical manufacturing.

    Company Overview

    Aurore Pharmaceuticals Private Limited operates in the pharmaceutical industry. The company is recruiting QC professionals to support its quality operations and pharmaceutical manufacturing activities.

    Job Role & Responsibilities

    Department: Quality Control (QC)

    The recruitment poster announces openings for Quality Control staff. Detailed job responsibilities and individual designations have not been specified.

    Candidates applying for these positions should have relevant Quality Control experience in the pharmaceutical industry.

    Eligibility & Qualifications

    Educational Qualifications

    Candidates with the following qualifications are eligible to apply:

    • B.Sc. in Chemistry

    • M.Sc. in Chemistry

    • B.Sc. in Microbiology

    • M.Sc. in Microbiology

    • B.Sc. in Biotechnology

    • M.Sc. in Biotechnology

    Experience Requirements

    • Required experience: 1–5 years.

    • Relevant experience in pharmaceutical Quality Control is required.

    Location & Salary

    Work Location: Aurore Pharmaceuticals Private Limited, Unit-1, 49/13, IDA Jeedimetla Road No. 51, Quthbullapur, Telangana – 500055.

    The recruitment poster does not specify the salary package. Candidates can contact the recruitment team for information about compensation and other employment benefits.

    Walk-In Interview Details

    Particulars Details
    Company Aurore Pharmaceuticals Private Limited
    Department Quality Control (QC)
    Position Quality Control Staff
    Qualification B.Sc. / M.Sc. in Chemistry, Microbiology, or Biotechnology
    Experience 1–5 years
    Interview Date 30 October 2026
    Work Location Quthbullapur, Telangana
    Interview Time Not specified in the poster

    How to Apply

    Interested candidates can send their updated CV to the recruitment email address provided in the poster.

    Email: APL.Recruitments@aurorels.com

    Candidates should include their educational qualifications, relevant Quality Control experience, and contact information in their CV. Applicants are advised to confirm the interview timing and any additional requirements with the recruitment team before attending.

    Documents Required

    Candidates should keep the following documents ready:

    • Updated CV or resume

    • Educational certificates and mark sheets

    • Relevant experience certificates

    • Government-issued photo identification

    The poster does not provide an official document checklist, so candidates should confirm the requirements with the recruitment team.

    Important Instructions

    • The walk-in drive is for the Quality Control department.

    • Candidates should have 1–5 years of relevant QC experience.

    • The listed educational backgrounds are Chemistry, Microbiology, and Biotechnology.

    • The interview date is 30 October 2026.

    • The interview time is not mentioned in the poster.

    Frequently Asked Questions

    1. Which company is hiring for Quality Control positions?

    Aurore Pharmaceuticals Private Limited is recruiting candidates for its Quality Control department.

    2. What qualifications are required for these QC positions?

    Candidates with B.Sc. or M.Sc. qualifications in Chemistry, Microbiology, or Biotechnology can apply.

    3. How much experience is required?

    Applicants should have 1–5 years of experience in pharmaceutical Quality Control.

    4. When is the Aurore Pharmaceuticals walk-in drive?

    The recruitment poster lists the walk-in date as 30 October 2026.

    5. Where is the job located?

    The position is based at Aurore Pharmaceuticals Private Limited, Quthbullapur, Telangana – 500055.

    6. How can candidates apply?

    Candidates can email their updated CV to APL.Recruitments@aurorels.com.

    Job Summary

    Category Details
    Company Aurore Pharmaceuticals Private Limited
    Vacancies Quality Control (QC) Staff
    Required Education B.Sc. / M.Sc. in Chemistry, Microbiology, or Biotechnology
    Experience 1–5 years in pharmaceutical Quality Control

  • SynSmart Recruitment for Junior Chemist / Intern

    SynSmart is conducting a walk-in interview drive for the position of Junior Chemist / Intern for candidates with a B.Sc. in Chemistry.
    Freshers with 0–1 year of experience and a strong understanding of compound polarity, adsorption and partition principles, and solvent properties are eligible to apply.
    The opportunity is based at SynSmart’s facility on Rabale MIDC Road, MIDC Industrial Area, Rabale, Navi Mumbai, Maharashtra.
    Interested candidates can attend the recruitment drive on 30 October 2026 and contact the recruitment team by email for further information.

    SynSmart Recruitment: Junior Chemist / Intern

    SynSmart is inviting applications for the Junior Chemist / Intern position. This opportunity is suitable for Chemistry graduates seeking an entry-level role and practical exposure to chemistry-related work.

    Company Overview

    SynSmart operates in the discovery solutions sector. The company is inviting fresh graduates to explore an entry-level opportunity in its team.

    Job Role & Responsibilities

    Position: Junior Chemist / Intern

    • Position: Junior Chemist / Intern

    • Department: Not specified in the recruitment poster.

    • Experience: Freshers with 0–1 year of experience.

    • Qualification: B.Sc. Chemistry.

    • Work Location: Rabale, Navi Mumbai, Maharashtra.

    The recruitment poster does not provide a detailed list of job responsibilities. Candidates should confirm the day-to-day duties and training arrangements with the company during the recruitment process.

    Eligibility & Qualifications

    Educational Qualification

    Candidates must have a B.Sc. in Chemistry.

    Experience

    • Freshers can apply.

    • Candidates with 0–1 year of experience are eligible.

    Required Skills

    Applicants should have a strong fundamental understanding of:

    • Compound polarity

    • Adsorption and partition principles

    • Solvent properties

    Candidates should be prepared to discuss their Chemistry fundamentals during the selection process.

    Location & Salary

    Work Location: SynSmart, R-463, Rabale MIDC Road, MIDC Industrial Area, Rabale, Navi Mumbai, Maharashtra – 400701.

    The salary package has not been mentioned in the recruitment poster. Candidates can contact the recruitment team to enquire about compensation, internship terms, and other employment conditions.

    Walk-In Interview Details

    Particulars Details
    Company SynSmart
    Position Junior Chemist / Intern
    Interview Date 30 October 2026
    Interview Time Not specified in the poster
    Location Rabale MIDC Road, Rabale, Navi Mumbai, Maharashtra – 400701
    Experience Freshers (0–1 year)
    Qualification B.Sc. Chemistry

    How to Apply

    Interested candidates can contact SynSmart through the following official contact details provided in the recruitment poster:

    The poster also includes a QR code labelled “Scan to Register.” Candidates can scan the code on the original recruitment poster to access the registration process.

    Applicants should keep their updated resume and educational details ready. Confirm the interview timing and registration requirements with the recruitment team before attending.

    Documents Required

    The recruitment poster does not specify a mandatory document checklist. Candidates should keep the following documents ready as a practical precaution:

    • Updated resume or CV

    • B.Sc. Chemistry certificate or provisional certificate

    • Academic mark sheets

    • Government-issued photo identification

    Confirm the exact requirements with the company before the interview.

    Important Instructions

    • The opportunity is intended for candidates with a B.Sc. in Chemistry.

    • Freshers and candidates with up to one year of experience can apply.

    • The interview date is 30 October 2026.

    • The interview time is not stated in the poster, so contact the recruitment team for confirmation.

    • Salary and detailed job responsibilities have not been disclosed.

    Frequently Asked Questions

    1. Who can apply for the SynSmart Junior Chemist / Intern position?

    Candidates with a B.Sc. in Chemistry can apply.

    2. Can freshers apply?

    Yes. Freshers with 0–1 year of experience are eligible.

    3. What skills are required for this position?

    Candidates should understand compound polarity, adsorption and partition principles, and solvent properties.

    4. Where is the job located?

    The position is based at R-463, Rabale MIDC Road, MIDC Industrial Area, Rabale, Navi Mumbai, Maharashtra – 400701.

    5. When is the walk-in interview?

    The recruitment poster lists the date as 30 October 2026. The interview time is not specified.

    6. How can candidates apply?

    Candidates can email their resume to hr@synsmart.in or use the QR code labelled “Scan to Register” on the recruitment poster.

    Job Summary

    Category Details
    Company SynSmart
    Vacancies Junior Chemist / Intern
    Required Education B.Sc. Chemistry
    Experience Freshers (0–1 year)

  • Aculife Healthcare Walk-In Interview for QA, QC and ADL

    Aculife Healthcare Private Limited is conducting a walk-in interview for multiple positions in its Quality Assurance (QA), Quality Control (QC), and Analytical Development Laboratory (ADL) departments.
    The recruitment drive is for the company’s sterile and injectable manufacturing plant, with opportunities for candidates holding B.Sc., M.Sc., B.Pharm, M.Pharm, and relevant analytical chemistry qualifications.
    Candidates with 0–5 years of experience can apply for QA and QC positions, while ADL opportunities require 2–5 years of relevant experience.
    The walk-in interview is scheduled for 30 October 2026, from 8:30 AM to 1:00 PM, at Aculife Healthcare Private Limited, Sachana, Ahmedabad, Gujarat.

    Company Overview

    Aculife Healthcare Private Limited operates in the pharmaceutical manufacturing sector, with a focus on sterile and injectable products. The company is inviting qualified candidates to join its Quality Assurance, Quality Control, and Analytical Development Laboratory teams.

    Aculife Healthcare Walk-In Interview Details

    Departments and Positions

    • Quality Assurance (QA)

    • Quality Control (QC)

    • Analytical Development Laboratory (ADL)

    Interview Date: 30 October 2026
    Interview Time: 8:30 AM to 1:00 PM
    Job Location: Sachana, Ahmedabad, Gujarat
    Manufacturing Unit: Sterile / Injectable Plant

    Job Role & Responsibilities

    1. Quality Assurance (QA)

    Key Areas: IPQA, QMS, Laboratory Quality Assurance, Validation, QA Documentation, Compliance, Vendor and Audit Support.

    Key Responsibilities:

    • Perform in-process quality assurance activities in sterile manufacturing.

    • Implement and maintain the Quality Management System (QMS).

    • Review and approve documents, including SOPs, BMRs, and BPRs.

    • Review batch records and manage change control.

    • Conduct validation activities involving processes, equipment, and cleaning.

    • Handle deviations, out-of-specification (OOS) results, and CAPA.

    • Support regulatory and customer audits, including USFDA and EU audits.

    • Maintain GMP compliance and promote a strong quality culture.

    2. Quality Control (QC)

    Key Areas: Raw Material Testing, In-Process Testing, Finished Product Testing, Stability, Microbiology, and Instrumental Analysis.

    Key Responsibilities:

    • Analyse raw materials, packaging materials, in-process samples, and finished sterile products.

    • Operate and analyse samples using HPLC, GC, UV, dissolution, and other analytical instruments.

    • Perform method validation, method transfer, and routine testing.

    • Conduct microbial testing and environmental monitoring, where applicable.

    • Ensure compliance with pharmacopoeial and regulatory requirements, including IP, USP, and BP.

    • Maintain documentation, data integrity, and laboratory compliance.

    • Perform stability sample analysis and trend reviews.

    3. Analytical Development Laboratory (ADL)

    Key Areas: Analytical Method Development, Method Validation, Method Transfer, Instrument Handling, Troubleshooting, and Technical Support.

    Key Responsibilities:

    • Develop and optimise analytical methods for injectable products.

    • Develop and validate analytical methods using HPLC, UPLC, GC, UV-Visible spectroscopy, and dissolution testing.

    • Transfer analytical methods and technology to the Quality Control department.

    • Troubleshoot analytical instruments.

    • Prepare documentation in accordance with regulatory requirements.

    • Handle stability studies, forced degradation studies, and method robustness studies.

    • Prepare analytical reports and interpret data.

    Eligibility & Qualifications

    Quality Assurance (QA)

    Eligible qualifications:

    • B.Sc.

    • M.Sc.

    • B.Pharm

    • M.Pharm

    Experience: 0–5 years in a sterile or injectable manufacturing plant.

    Quality Control (QC)

    Eligible qualifications:

    • B.Sc.

    • M.Sc.

    • B.Pharm

    • M.Pharm

    Experience: 0–5 years in a sterile or injectable manufacturing plant.

    Analytical Development Laboratory (ADL)

    Eligible qualifications:

    • M.Sc. in Analytical Chemistry

    • B.Pharm

    • M.Pharm

    Experience: 2–5 years in a sterile or injectable manufacturing plant.

    Location & Salary

    Work Location: Aculife Healthcare Private Limited, near Railway Crossing, Sachana, Taluka Viramgam, Ahmedabad District, Gujarat – 382150.

    The recruitment poster does not specify salary details. Compensation will need to be confirmed with the recruitment team.

    How to Apply

    Interested candidates should send their updated CV to either of the following recruitment email addresses:

    Candidates should mention the relevant department or position in the email subject line and include their qualifications, work experience, and contact details.

    Eligible applicants can also attend the walk-in interview directly at the company’s venue on 30 October 2026, between 8:30 AM and 1:00 PM.

    Documents Required

    Candidates should carry an updated resume and relevant supporting documents. The recruitment poster does not provide a detailed document checklist, so applicants should confirm any additional requirements with the recruitment team.

    Important Interview Details

    • Date: 30 October 2026

    • Time: 8:30 AM to 1:00 PM

    • Venue: Aculife Healthcare Private Limited

    • Location: Near Railway Crossing, Sachana, Taluka Viramgam, Ahmedabad District, Gujarat – 382150

    • Departments: QA, QC, and ADL

    • Facility: Sterile / Injectable Plant

    • Preference: Male candidates are preferred, as stated in the recruitment poster.

    Frequently Asked Questions

    1. Which departments are hiring at Aculife Healthcare?

    The company is hiring for Quality Assurance (QA), Quality Control (QC), and Analytical Development Laboratory (ADL).

    2. What qualifications are required for QA and QC positions?

    Candidates with B.Sc., M.Sc., B.Pharm, or M.Pharm qualifications are eligible to consider QA and QC opportunities.

    3. What qualifications are required for ADL positions?

    The ADL department lists M.Sc. in Analytical Chemistry, B.Pharm, and M.Pharm qualifications.

    4. How much experience is required?

    QA and QC positions require 0–5 years of experience, while ADL positions require 2–5 years in a sterile or injectable manufacturing plant.

    5. When is the Aculife Healthcare walk-in interview?

    The interview is scheduled for 30 October 2026, from 8:30 AM to 1:00 PM.

    6. How can candidates apply?

    Candidates can send their CV to recruitment@aculife.co.in or rajeshthakor@aculife.co.in, or attend the walk-in interview at the specified venue.

    Job Summary

    Category Details
    Company Aculife Healthcare Private Limited
    Vacancies QA, QC, and ADL positions; exact vacancy count not specified
    Required Education B.Sc., M.Sc., B.Pharm, M.Pharm, M.Sc. in Analytical Chemistry
    Experience QA: 0–5 years; QC: 0–5 years; ADL: 2–5 years

  • Anthem BioSciences Chemical Synthesis Walk-In Interview

    Anthem BioSciences is conducting a walk-in interview for its Chemical Synthesis Plant at Unit-3, Harohalli, Bengaluru.
    The recruitment drive is open to candidates with qualifications in Chemical Engineering and Chemistry for opportunities in pharmaceutical manufacturing.
    Applicants with 0–5 years of hands-on experience in high-potency active pharmaceutical ingredients (HPAPI), API manufacturing, and intermediate manufacturing can apply.
    The interview is scheduled for 21 November 2026, from 9:00 AM to 1:00 PM, at NeoAnthem Lifesciences Pvt. Ltd., Harohalli, Bengaluru.

    Company Overview

    Anthem BioSciences is a biotechnology and pharmaceutical research company involved in drug development and manufacturing services. This recruitment drive focuses on the Chemical Synthesis Plant, with opportunities for candidates interested in API production, peptide synthesis, and related pharmaceutical manufacturing activities.

    Anthem BioSciences Walk-In Interview Details

    Department: Chemical Synthesis Plant

    Job Location: Unit-3, Harohalli, Bengaluru

    Interview Date: Saturday, 21 November 2026
    Interview Time: 9:00 AM to 1:00 PM

    Interview Venue:

    NeoAnthem Lifesciences Pvt. Ltd.
    Plot No. 313-P, 314-P & 318-P, Survey No. 20,
    Harohalli Industrial Area, Phase 2, Bannikupe Road,
    Harohalli, Bengaluru South District – 562112.

    Job Role & Responsibilities

    Candidates applying for the Chemical Synthesis Plant should have relevant knowledge or experience in pharmaceutical manufacturing operations.

    Key areas of experience mentioned in the recruitment notice include:

    • High-potency active pharmaceutical ingredients (HPAPI) manufacturing.

    • Active pharmaceutical ingredient (API) manufacturing.

    • Pharmaceutical intermediate manufacturing.

    • Peptide synthesis.

    • HPLC (DAC).

    • Lyophilization.

    The exact designation and number of vacancies have not been specified in the recruitment notice.

    Eligibility & Qualifications

    Candidates with the following educational qualifications are eligible to consider the opportunity:

    • Diploma in Chemical Engineering

    • B.Sc. in Chemistry

    • M.Sc. in Chemistry

    • B.Tech. in Chemical Engineering

    • B.E. in Chemical Engineering

    Experience Requirements

    • 0–5 years of hands-on experience in HPAPI, API, and intermediate manufacturing.

    • Experience in peptide synthesis, HPLC (DAC), and lyophilization is also mentioned.

    Candidates should review the listed experience requirements and ensure their qualifications and practical skills are relevant to the Chemical Synthesis Plant.

    Location & Interview Details

    Particulars Details
    Company Anthem BioSciences
    Department Chemical Synthesis Plant
    Job Location Unit-3, Harohalli, Bengaluru
    Interview Venue NeoAnthem Lifesciences Pvt. Ltd., Harohalli Industrial Area, Bengaluru South District – 562112
    Interview Date 21 November 2026
    Interview Time 9:00 AM to 1:00 PM
    Experience 0–5 years

    How to Apply

    Interested candidates should attend the walk-in interview at the specified venue on 21 November 2026 between 9:00 AM and 1:00 PM.

    Candidates should carry an updated resume and relevant educational and experience documents. The recruitment poster does not specify an application email address, contact number, or online application link.

    For additional information, candidates can refer to the company’s official website: www.anthembio.com.

    Documents Required

    The recruitment poster does not provide a specific list of documents to carry. Candidates should prepare the following standard documents for a walk-in interview:

    • Updated resume or CV

    • Educational certificates and mark sheets

    • Experience certificates, if applicable

    • Government-issued photo identification

    Frequently Asked Questions

    1. Which company is conducting the walk-in interview?

    Anthem BioSciences is advertising the recruitment drive for its Chemical Synthesis Plant.

    2. What qualifications are required?

    Candidates with a Diploma in Chemical Engineering, B.Sc. or M.Sc. in Chemistry, or B.Tech. or B.E. in Chemical Engineering are listed.

    3. How much experience is required?

    The recruitment notice specifies 0–5 years of hands-on experience in HPAPI, API, and intermediate manufacturing.

    4. When is the walk-in interview?

    The interview is scheduled for Saturday, 21 November 2026, from 9:00 AM to 1:00 PM.

    5. Where will the interview take place?

    The interview venue is NeoAnthem Lifesciences Pvt. Ltd., Harohalli Industrial Area, Bengaluru South District, Karnataka – 562112.

    6. How can candidates apply?

    Candidates can attend the walk-in interview at the specified venue and time. An email address and online application link are not provided in the recruitment poster.

    Job Summary

    Category Details
    Company Anthem BioSciences
    Vacancies Chemical Synthesis Plant opportunities; specific designations and vacancy count not specified
    Required Education Diploma in Chemical Engineering, B.Sc. Chemistry, M.Sc. Chemistry, B.Tech. Chemical Engineering, B.E. Chemical Engineering
    Experience 0–5 years

  • Alkem Laboratories Walk-In Interview for Pharma Jobs

    Alkem Laboratories is organizing a walk-in interview drive for its Daman manufacturing facility, with openings in Quality Control (QC) Formulation, Production Formulation, and Production Packing.
    The recruitment drive offers opportunities for Senior Officers, Executives, Technical Associates, and other eligible manufacturing professionals with relevant pharmaceutical industry experience.
    Candidates with qualifications such as M.Sc., B.Pharm, B.Sc., Diploma, and ITI can apply for suitable positions, depending on the department and role.
    The walk-in interview will be held on 1 November 2026, from 9:00 AM to 3:00 PM, at Pride Plaza Hotel, Ahmedabad, Gujarat.

    Company Overview

    Alkem Laboratories Ltd. is conducting a walk-in recruitment drive to fill positions supporting its pharmaceutical manufacturing operations. The openings cover formulation quality control, formulation production, and packing operations, with specific experience in analytical instruments, manufacturing equipment, and packaging processes.

    Alkem Laboratories Walk-In Interview: Department-Wise Vacancies

    1. Quality Control (QC) – Formulation

    Designation: Senior Officer / Executive
    Qualification: M.Sc. / B.Pharm
    Experience: 2–7 years

    Required skills and responsibilities:

    • Experience in finished product (FP), stability, and analytical instrumentation.

    • Knowledge of HPLC, UV, and dissolution testing.

    • Experience handling LIMS and Empower software.

    • Familiarity with HPLC Waters systems.

    2. Production – Formulation

    Designation: Technical Associate
    Qualification: Diploma / B.Sc. / ITI
    Experience: 2–6 years

    Required skills and responsibilities:

    Manufacturing core area:

    • Wurster coating, including Glatt and 21 CFR SCADA systems.

    • Pellet coating and bottom spray using Glatt equipment.

    • Granulation using integrated lines, GEA, Glatt, and flow coaters.

    • Compression using KORSCH, SEJONG, GEA, and CADMACH equipment.

    • Coating using Glatt coaters.

    • Liquid manufacturing and filling.

    • Sachet filling machines, including Wraptech and Bossar.

    3. Production – Packing

    Designations: Senior Officer / Executive / Technical Associate
    Qualifications: B.Pharm / Diploma / B.Sc. / ITI
    Experience: 2–6 years

    Required skills and responsibilities:

    Packing primary area:

    • Blister packing using Uhlmann, Elm ach, and BQS equipment.

    • Bulk packing, bottle packing, and CVC systems.

    • Liquid packing operations.

    Eligibility & Qualifications

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

    • M.Sc. / B.Pharm: Quality Control – Formulation.

    • Diploma / B.Sc. / ITI: Production – Formulation.

    • B.Pharm / Diploma / B.Sc. / ITI: Production – Packing.

    Experience requirements range from 2 to 7 years, depending on the position.

    Location & Walk-In Interview Details

    • Company: Alkem Laboratories Ltd.

    • Recruitment Location: Daman manufacturing facility

    • Interview Date: Sunday, 1 November 2026

    • Interview Time: 9:00 AM to 3:00 PM

    • Interview Venue: Pride Plaza Hotel, Judges Bungalow Road, off S.G. Highway, Bodakdev, Ahmedabad, Gujarat – 380054

    Important: The manufacturing facility is in Daman, while the walk-in interview venue is in Ahmedabad, Gujarat.

    How to Apply

    Eligible candidates should attend the walk-in interview at the specified venue and time.

    Applicants should bring the following documents:

    • Updated resume

    • Salary breakup or latest increment letter

    • Recent passport-size photograph

    • Copy of Aadhaar card

    • Copy of PAN card

    Candidates should ensure that their resumes include accurate educational qualifications, relevant experience, and contact information.

    Frequently Asked Questions

    1. Which company is conducting the walk-in interview?

    Alkem Laboratories Ltd. is conducting the recruitment drive.

    2. Which departments have vacancies?

    The openings are in Quality Control (QC) Formulation, Production Formulation, and Production Packing.

    3. What qualifications are required?

    The recruitment poster lists M.Sc., B.Pharm, B.Sc., Diploma, and ITI, depending on the position.

    4. How much experience is required?

    Candidates need 2–7 years of experience, depending on the role.

    5. When is the walk-in interview?

    The interview is scheduled for 1 November 2026, from 9:00 AM to 3:00 PM.

    6. What documents should candidates bring?

    Candidates should carry an updated resume, salary breakup or increment letter, passport-size photograph, Aadhaar card copy, and PAN card copy.

    Job Summary

    Category Details
    Company Alkem Laboratories Ltd.
    Vacancies Senior Officer / Executive – QC Formulation; Technical Associate – Production Formulation; Senior Officer / Executive / Technical Associate – Production Packing
    Required Education M.Sc., B.Pharm, B.Sc., Diploma, ITI
    Experience 2–7 years, depending on the position

  • Amneal Pharmaceuticals Walk-In Drive for Pharma Jobs

    Amneal Pharmaceuticals is conducting a walk-in drive for multiple pharmaceutical manufacturing and quality assurance positions at its Baroda Productivity Council (BPC) venue in Vadodara.
    The recruitment drive includes openings in Injectable Production, Packing, Environmental Monitoring (EM), and IPQA & Validation for candidates with relevant pharmaceutical manufacturing experience.
    Candidates with qualifications such as ITI, Diploma, D.Pharm, B.Sc., B.Pharm, M.Pharm, and M.Sc. can apply for suitable positions, depending on the department.
    The walk-in interview is scheduled for 1 November 2026, from 9:00 AM to 4:00 PM, and eligible candidates who cannot attend may submit their CVs through email or the online application process.

    Company Overview

    Amneal Pharmaceuticals is a global pharmaceutical company involved in the development, manufacturing, and distribution of medicines. The company is inviting experienced candidates to join its pharmaceutical manufacturing operations across Production, Packing, Environmental Monitoring, and In-Process Quality Assurance (IPQA) and Validation.

    Amneal Pharmaceuticals Walk-In Drive: Department-Wise Vacancies

    1. Manufacturing – Production

    Designations: Assistant, Associate, Officer, Executive
    Location: Ahmedabad
    Experience: 1–7 years

    Required qualifications:

    • ITI

    • Diploma

    • D.Pharm

    • B.Sc.

    • B.Sc. (M.Sc. as listed in the recruitment poster)

    • B.Pharm

    • M.Pharm

    Required skills and responsibilities:

    • Hands-on experience in complex manufacturing processes, such as emulsion and suspension manufacturing.

    • Experience in vial and bag filling machines, including SHINVA bag filling and PLUMAT.

    • Knowledge of emulsion and suspension lines, bag lines, inhalation lines, PFS, LYO, cartridges, and filling machines with isolators.

    2. Manufacturing – Packing

    Designations: Assistant, Associate, Officer, Executive
    Location: Ahmedabad
    Experience: 2–7 years

    Required qualifications:

    • ITI

    • Diploma

    • D.Pharm

    • B.Sc.

    • M.Sc.

    • B.Pharm

    • M.Pharm

    Required skills and responsibilities:

    • Experience in packing and visual inspection using MVI and AVI.

    • Knowledge of pouching machines, Brevetti machines, labelling machines, cartoning, and track-and-trace systems.

    • Experience with packing QMS and related documentation.

    • Understanding of change control, deviations, and machine qualification or requalification.

    3. Quality Assurance – Environmental Monitoring (QA-EM)

    Designations: Officer, Executive
    Location: Ahmedabad
    Experience: 1–7 years

    Required qualifications:

    • B.Sc. in Microbiology

    • M.Sc. in Microbiology

    Required skills and responsibilities:

    • Experience in environmental monitoring.

    • Knowledge of non-viable particle monitoring.

    • Understanding of sterile and aseptic manufacturing environments.

    4. Quality Assurance – IPQA & Validation

    Designations: Officer, Executive
    Location: Ahmedabad
    Experience: 2–7 years

    Required qualifications:

    • B.Pharm

    • M.Pharm

    • M.Sc.

    Required skills and responsibilities:

    • Experience in line clearance and validation activities for manufacturing and packing areas.

    • Knowledge of BMR and BPR review.

    • Experience in shop-floor compliance and visual inspection qualification.

    • Media-fill experience is preferred.

    Eligibility & Qualifications

    Candidates must possess the educational qualification relevant to the department and position they wish to apply for.

    Eligible qualifications include:

    ITI | Diploma | D.Pharm | B.Sc. | M.Sc. | B.Pharm | M.Pharm

    Candidates should have relevant experience in pharmaceutical manufacturing, injectable production, packing operations, environmental monitoring, or IPQA and validation. Experience requirements range from 1 to 7 years, depending on the role.

    Location & Walk-In Interview Details

    • Company: Amneal Pharmaceuticals

    • Walk-In Drive: BPC, Vadodara

    • Date: Sunday, 1 November 2026

    • Time: 9:00 AM to 4:00 PM

    • Venue: Baroda Productivity Council, 2nd Floor, Productivity House, Productivity Road, Alkapuri, Vadodara – 390007

    Note: The recruitment poster lists Ahmedabad in the department-wise job table, while the walk-in venue is in Vadodara. Candidates should confirm the work location for their selected role before attending.

    How to Apply

    Eligible candidates can attend the walk-in interview at the venue mentioned above.

    Candidates who cannot attend the interview may send their CV by email or apply online by scanning the QR code provided in the recruitment notice.

    Email contacts:

    Email subject line: Application for INJ Mfg./ Packing/ IPQA/ EM

    Applicants should mention the relevant department in their application and provide accurate contact details.

    Documents Required

    Candidates should keep the following documents ready:

    • Updated CV or resume

    • Educational certificates

    • Relevant experience documents, if applicable

    Frequently Asked Questions

    1. Which company is conducting this walk-in drive?

    Amneal Pharmaceuticals is conducting the recruitment drive.

    2. Which departments have vacancies?

    The openings are in Manufacturing – Production, Manufacturing – Packing, Quality Assurance – Environmental Monitoring, and Quality Assurance – IPQA & Validation.

    3. What qualifications are accepted?

    The recruitment poster lists ITI, Diploma, D.Pharm, B.Sc., M.Sc., B.Pharm, and M.Pharm, depending on the position.

    4. How much experience is required?

    The experience requirement ranges from 1 to 7 years, depending on the role.

    5. When is the walk-in interview?

    The interview is scheduled for 1 November 2026, from 9:00 AM to 4:00 PM.

    6. How can candidates apply if they cannot attend?

    Candidates who cannot attend can send their CV to one of the listed recruitment email addresses or use the online application option shown in the recruitment poster.

    Job Summary

    Category Details
    Company Amneal Pharmaceuticals
    Vacancies Assistant, Associate, Officer, Executive – Production; Assistant, Associate, Officer, Executive – Packing; Officer, Executive – Environmental Monitoring; Officer, Executive – IPQA & Validation
    Required Education ITI, Diploma, D.Pharm, B.Sc., M.Sc., B.Pharm, M.Pharm
    Experience 1–7 years, depending on the position

  • Centaur Pharmaceuticals Walk-In Interview for QA and QC

    Centaur Pharmaceuticals Pvt. Ltd. is conducting a walk-in interview for multiple positions in Quality Assurance (QA) and Quality Control (QC) at its Hinjewadi, Pune facility.
    The recruitment drive includes openings for Executives, Senior Executives, Officers, Assistant Managers, Deputy Managers, and Junior Executives across various quality functions.
    Candidates with qualifications including B.Pharm, M.Pharm, and M.Sc., along with relevant pharmaceutical manufacturing experience, can apply for suitable positions.
    The walk-in interview is scheduled for 1 November 2026, starting at 8:30 AM, and eligible candidates who cannot attend may send their updated resumes by email.

    Centaur Pharmaceuticals Walk-In Interview: Company Overview

    Centaur Pharmaceuticals Pvt. Ltd. is inviting experienced pharmaceutical professionals to join its Quality Assurance and Quality Control teams. The recruitment drive covers quality systems, investigations, analytical quality assurance, qualification, validation, raw materials, stability, analytical instruments, and laboratory information management systems.

    Centaur Pharmaceuticals Job Vacancies: Department-Wise Details

    1. Quality Assurance (QA)

    Designation Role Qualification Experience
    Executive / Senior Executive ITQA B.Pharm / M.Pharm / M.Sc. 6–10 years
    Assistant Manager / Deputy Manager QMS – Investigations B.Pharm / M.Pharm / M.Sc. 12–16 years
    Assistant Manager / Deputy Manager Analytical QA B.Pharm / M.Pharm / M.Sc. 12–16 years
    Senior Officer / Executive Qualification / Validation B.Pharm / M.Pharm 5–10 years

    2. Quality Control (QC)

    Designation Role Qualification Experience
    Assistant Manager / Deputy Manager RM – Section Head M.Sc. 12–16 years
    Assistant Manager / Deputy Manager Stability – Section Head M.Sc. 12–16 years
    Assistant Manager / Deputy Manager AMV/AMT – Section Head M.Sc. 12–16 years
    Assistant Manager / Deputy Manager GLP – Section Head M.Sc. 12–16 years
    Executive / Senior Executive QMS M.Sc. 10–15 years
    Officer / Senior Officer HPLC, GC, UV, dissolution and other sophisticated instruments M.Sc. 3–5 years
    Junior Executive / Executive HPLC, GC, UV, dissolution and other sophisticated instruments M.Sc. 6–10 years
    Officer / Senior Officer LIMS Master and Specification Preparation M.Sc. 3–5 years
    Junior Executive / Executive LIMS Master and Specification Reviewer M.Sc. 8–12 years

    Eligibility & Qualifications

    Candidates must have qualifications relevant to the position they are applying for. The recruitment poster lists the following educational qualifications:

    • B.Pharm

    • M.Pharm

    • M.Sc.

    Experience: The required experience ranges from 3 to 16 years, depending on the position.

    Additional Requirements

    • Candidates should have experience in pharmaceutical formulation manufacturing, particularly in OSD (oral solid dosage) facilities.

    • Experience with regulatory audits involving USFDA, MHRA, and EU requirements is mandatory.

    Location & Walk-In Interview Details

    • Company: Centaur Pharmaceuticals Pvt. Ltd.

    • Department: Quality Assurance and Quality Control

    • Location: Hinjewadi, Pune, Maharashtra

    • Walk-In Date: 1 November 2026

    • Interview Time: 8:30 AM onwards

    • Venue: Plot No. 4, International Biotech Park, Hinjewadi Phase II, Pune, Maharashtra – 411057

    How to Apply

    Eligible candidates can attend the walk-in interview at the specified venue and time.

    Candidates who cannot attend the interview may email their updated resume and a recent passport-size photograph to the recruitment team.

    Email: hrpune@centaur.co.in

    For further information, candidates can contact Centaur Pharmaceuticals at +91-20-66739510.

    Documents Required

    Candidates should keep the following documents ready for the recruitment process:

    • Updated resume

    • Recent passport-size photograph

    • Educational certificates

    • Relevant experience documents, if applicable

    Frequently Asked Questions

    1. Which company is conducting this walk-in interview?

    Centaur Pharmaceuticals Pvt. Ltd. is conducting the recruitment drive.

    2. Which departments have vacancies?

    The openings are in Quality Assurance and Quality Control.

    3. What qualifications are required?

    The poster lists B.Pharm, M.Pharm, and M.Sc. for different positions.

    4. How much experience is required?

    Experience requirements vary by role, ranging from 3 to 16 years.

    5. When is the walk-in interview?

    The interview is scheduled for 1 November 2026, starting at 8:30 AM.

    6. Can candidates apply if they cannot attend in person?

    Yes. Candidates who cannot attend can send their resume and a recent passport-size photograph to hrpune@centaur.co.in.

    Job Summary

    Category Details
    Company Centaur Pharmaceuticals Pvt. Ltd.
    Vacancies Executive / Senior Executive – ITQA; Assistant Manager / Deputy Manager – QMS Investigations; Assistant Manager / Deputy Manager – Analytical QA; Senior Officer / Executive – Qualification / Validation; Assistant Manager / Deputy Manager – QC Section Heads; Executive / Senior Executive – QMS; Officer / Senior Officer – Analytical Instruments; Junior Executive / Executive – Analytical Instruments; Officer / Senior Officer – LIMS Master and Specification Preparation; Junior Executive / Executive – LIMS Master and Specification Reviewer
    Required Education B.Pharm, M.Pharm, M.Sc.
    Experience 3–16 years, depending on the position

  • Zenotech Laboratories Walk-In Drive for Pharma Jobs

    Zenotech Laboratories, associated with Sun Pharma, is conducting a walk-in drive for multiple pharmaceutical manufacturing and quality roles at its facility in Shameerpet, Genome Valley, Thurkappally.
    The recruitment drive includes openings in Quality Control, Quality Assurance, and Production for candidates with qualifications such as B.Pharm, M.Pharm, M.Sc., ITI, and Diploma.
    Candidates with 2–8 years of experience, depending on the position, can apply for suitable roles in injectable manufacturing.
    Interested applicants should attend the walk-in interview on 30 and 31 October 2026, from 9:00 AM to 2:00 PM, with an updated CV and relevant documents.

    Company Overview

    Zenotech Laboratories, associated with Sun Pharma, is inviting experienced pharmaceutical professionals to join its Quality Control, Quality Assurance, and Production teams. The openings cover general injectable manufacturing, analytical testing, quality management systems, validation, and production operations.

    Zenotech Laboratories Walk-In Drive: Departments, Designations and Responsibilities

    1. Quality Control

    Designation: Senior Officer
    Sub-department: Analysis – OSD & General Injectable
    Experience: 2–4 years

    Responsibilities:

    • Operate, calibrate, and maintain GC, HPLC, and other analytical instruments.

    • Analyse raw materials, finished products, cleaning samples, and stability samples.

    2. Quality Assurance

    Senior Officer / Executive – QMS

    Sub-department: QMS – General Injectable
    Experience: 2–8 years

    Responsibilities:

    • Manage and monitor the Quality Management System (QMS).

    • Handle change controls, deviations, CAPA, OOS, and product quality complaints.

    • Review, track, and ensure timely closure and effectiveness of CAPA and quality systems.

    • Maintain SOPs, protocols, training records, and EDMS documentation.

    • Support regulatory compliance, product recalls, audits, and continuous quality improvement.

    Executive – AQA

    Sub-department: AQA – General Injectable
    Experience: 5–8 years

    Responsibilities:

    • Handle QMS activities, including change controls, deviations, CAPA, and OOS.

    • Manage SOPs, training, and quality documentation.

    • Ensure CAPA effectiveness, compliance, and regulatory readiness.

    • Support product recalls, audits, and continuous quality improvement.

    Senior Officer / Executive – Validation

    Sub-department: Validation – General Injectable
    Experience: 2–7 years

    Responsibilities:

    • Perform process validation.

    • Conduct cleaning validation.

    • Handle equipment validation.

    3. Production

    Officer – General Injectable

    Qualification: B.Pharm / M.Pharm / M.Sc.
    Experience: 2–4 years

    Responsibilities:

    • Perform filling operations.

    • Handle vial washing.

    • Carry out manufacturing activities.

    • Operate autoclaves.

    Operator – General Injectable

    Qualification: ITI / Diploma
    Experience: 2–4 years

    Responsibilities:

    • Perform filling operations.

    • Handle vial washing.

    • Carry out manufacturing activities.

    • Work with lyophilizers and autoclaves.

    Eligibility & Qualifications

    Candidates should hold the qualification relevant to their chosen department and designation.

    • B.Pharm

    • M.Pharm

    • M.Sc.

    • ITI

    • Diploma

    Experience requirements vary by position, from 2 to 8 years. Candidates should review the designation-specific requirements before attending the interview.

    Location & Walk-In Interview Details

    • Company: Zenotech Laboratories / Sun Pharma

    • Departments: Quality Control, Quality Assurance, Production

    • Location: Shameerpet, Genome Valley, Thurkappally

    • Walk-in Dates: 30 and 31 October 2026

    • Interview Time: 9:00 AM to 2:00 PM

    How to Apply

    Eligible candidates should attend the walk-in interview at the specified location during the announced dates and timings.

    Documents to carry:

    • Updated CV

    • Relevant educational certificates and supporting documents

    Candidates should carry their updated resumes and documents for the interview and be prepared to discuss their relevant pharmaceutical manufacturing, quality control, quality assurance, or validation experience.

    Frequently Asked Questions

    1. Which company is conducting the walk-in drive?

    Zenotech Laboratories, associated with Sun Pharma, is conducting the recruitment drive.

    2. Which departments have vacancies?

    The openings are in Quality Control, Quality Assurance, and Production.

    3. What qualifications are accepted?

    The poster lists B.Pharm, M.Pharm, M.Sc., ITI, and Diploma, depending on the position.

    4. How much experience is required?

    Experience requirements range from 2 to 8 years, depending on the role.

    5. When is the walk-in interview?

    The interview is scheduled for 30 and 31 October 2026, from 9:00 AM to 2:00 PM.

    6. What documents should candidates bring?

    Candidates should bring an updated CV and relevant supporting documents.

    Job Summary

    Category Details
    Company Zenotech Laboratories / Sun Pharma
    Vacancies Senior Officer – QC; Senior Officer / Executive – QMS; Executive – AQA; Officer – Production; Operator – Production; Senior Officer / Executive – Validation
    Required Education B.Pharm, M.Pharm, M.Sc., ITI, Diploma
    Experience 2–8 years, depending on the position

  • Avencia Molecules QC Officer Recruitment

    Avencia Molecules Pvt. Ltd. is inviting applications for the position of QC Officer at its manufacturing facility in Panoli, Ankleshwar, Gujarat.
    The company has announced four vacancies for male candidates with 1–2 years of experience, preferably in the pharmaceutical industry.
    Candidates with hands-on knowledge of HPLC, GC, UV, FTIR, GMP/GLP, and laboratory documentation are encouraged to apply.
    Interested applicants can submit their updated CV by email and contact the company for further details about the recruitment process.

    Company Overview

    Avencia Molecules Pvt. Ltd. is a pharmaceutical industry employer located at GIDC Estate, Panoli, Ankleshwar, Gujarat. The company is inviting applications for its Quality Control (QC) department and highlights career growth, skill development, workplace safety, and competitive compensation as employee benefits.

    Avencia Molecules Recruitment: Job Role & Responsibilities

    QC Officer

    • Vacancies: 4

    • Experience: 1–2 years

    • Preferred Background: Pharmaceutical industry

    The recruitment announcement does not provide a detailed list of daily responsibilities for this position. Candidates should have relevant QC laboratory skills and familiarity with pharmaceutical quality requirements.

    Technical Skills Required

    • High-Performance Liquid Chromatography (HPLC)

    • Gas Chromatography (GC)

    • UV analysis

    • Fourier Transform Infrared Spectroscopy (FTIR)

    • Good Manufacturing Practices (GMP)

    • Good Laboratory Practices (GLP)

    • Laboratory documentation

    Eligibility & Qualifications

    Educational Qualification

    The recruitment poster does not specify a mandatory educational qualification. Candidates with relevant pharmaceutical QC experience and the technical skills listed in the announcement can contact the company to confirm their eligibility.

    Experience Required

    • 1–2 years of experience.

    • Preference for candidates with experience in the pharmaceutical industry.

    • Familiarity with analytical instruments and laboratory documentation.

    Additional Requirements

    • The recruitment poster specifies four vacancies for male candidates.

    • Candidates should have relevant technical knowledge for pharmaceutical quality control activities.

    Location & Salary

    • Company: Avencia Molecules Pvt. Ltd.

    • Department: Quality Control (QC)

    • Designation: QC Officer

    • Work Location: Plot No. 3505, GIDC Estate, Panoli, Ankleshwar, Gujarat – 394115

    • Salary: Not specified in the recruitment announcement.

    Employee Benefits

    The company highlights the following benefits:

    • Canteen facility.

    • Travelling facility from Ankleshwar.

    • Career growth opportunities.

    • Safe and healthy work environment.

    • Skill development opportunities.

    • Competitive compensation.

    How to Apply

    Interested candidates can send their updated CV to the recruitment email address below.

    Applicants should mention their QC experience, analytical instrument knowledge, and familiarity with GMP/GLP practices in their resumes.

    Frequently Asked Questions

    1. Which company is hiring QC Officers?

    Avencia Molecules Pvt. Ltd. is recruiting QC Officers for its facility in Panoli, Ankleshwar, Gujarat.

    2. How many vacancies are available?

    The recruitment poster lists four vacancies for QC Officers.

    3. What experience is required?

    Candidates should have 1–2 years of experience, preferably in the pharmaceutical industry.

    4. Which technical skills are required?

    The listed skills include HPLC, GC, UV, FTIR, GMP/GLP, and documentation.

    5. What is the job location?

    The position is based at GIDC Estate, Panoli, Ankleshwar, Gujarat.

    6. How can candidates apply?

    Candidates can email their updated CV to hr@avenciamolecules.com or contact the company at 02646 299 411.

    Job Summary

    Category Details
    Company Avencia Molecules Pvt. Ltd.
    Vacancies QC Officer – 4 positions
    Required Education Not specified in the recruitment poster
    Experience 1–2 years; pharmaceutical industry experience preferred

  • Veedo Lifesciences Auditor – Analytical QA Jobs

    Veedo Lifesciences is hiring an experienced professional for the position of Auditor – Analytical QA at its facility in Peenya, Bangalore.
    Candidates with 5–8 years of experience in analytical quality assurance, analytical characterization, and pharmaceutical or biosimilar development can apply.
    The role involves reviewing analytical studies, auditing technical documentation, ensuring data integrity, and maintaining compliance with applicable regulatory requirements.
    Interested candidates with relevant experience in analytical characterization techniques and quality assurance can submit their updated CV by email.

    Company Overview

    Veedo Lifesciences is recruiting for an Auditor – Analytical QA position focused on analytical quality assurance and biosimilar development activities. The role requires experience in reviewing analytical characterization studies, technical reports, and supporting documentation.

    Veedo Lifesciences Recruitment: Job Role & Responsibilities

    Auditor – Analytical QA

    The selected candidate will support analytical quality assurance activities related to analytical characterization studies and biosimilar development.

    Key responsibilities include:

    • Performing QA reviews and audits of analytical characterization studies supporting biosimilar development.

    • Reviewing study protocols, reports, raw data, and supporting documentation for compliance with GLP principles where applicable, ALCOA+ principles, internal procedures, and data integrity requirements.

    • Ensuring compliance with applicable regulatory requirements, including FDA, EMA, and relevant ICH guidelines such as Q5E, Q6B, Q2(R2), Q9, and Q14.

    • Reviewing complex analytical characterization data, including HOS, SPR, NMR, FTIR, CD, DSC, DLS, peptide mapping, glycan profiling, and comparability assessments.

    • Conducting internal audits of CMC R&D functions and participating in sponsor audits, regulatory inspections, and due diligence audits.

    • Reviewing analytical comparability assessments and associated statistical evaluations to support scientific validity and appropriate biosimilarity conclusions.

    • Providing QA guidance and support during biosimilar development activities and regulatory filing programs.

    • Reviewing and approving analytical study protocols, validation protocols and reports, characterization reports, technical reports, change controls, deviations, OOS/OOT investigations, CAPAs, and risk assessments.

    Eligibility & Qualifications

    Educational Qualification

    The recruitment announcement does not specify a mandatory degree or particular educational qualification. Candidates should have relevant experience in analytical QA and pharmaceutical or biosimilar development.

    Experience Required

    • 5–8 years of professional experience.

    • Experience in analytical characterization studies and quality assurance audits.

    • Familiarity with regulatory compliance and data integrity requirements.

    Required Technical Skills

    • Analytical characterization techniques, including HOS, SPR, NMR, FTIR, CD, DSC, and DLS.

    • Peptide mapping and glycan profiling.

    • Analytical comparability assessments.

    • Knowledge of ALCOA+ principles and GLP, where applicable.

    • Familiarity with FDA, EMA, and relevant ICH guidelines.

    • Documentation review, audit execution, deviation management, and CAPA review.

    Location & Salary

    • Designation: Auditor – Analytical QA

    • Location: Peenya, Bangalore

    • Experience: 5–8 years

    • Salary: Not specified in the recruitment announcement.

    How to Apply

    Interested candidates can send their updated CV to the recruitment email address provided below.

    Email: Mahendra.t3705@veedolifesciences.com

    Candidates should highlight their analytical QA experience, audit exposure, regulatory knowledge, and analytical characterization expertise in their CV.

    Frequently Asked Questions

    1. Which company is hiring for the Auditor – Analytical QA position?

    Veedo Lifesciences is hiring for the Auditor – Analytical QA role.

    2. How much experience is required?

    Candidates with 5–8 years of experience are sought for this position.

    3. Where is the job located?

    The position is based in Peenya, Bangalore.

    4. What are the main responsibilities?

    The role includes analytical QA audits, documentation review, regulatory compliance, analytical characterization review, and support for biosimilar development.

    5. Which analytical techniques are mentioned?

    The recruitment announcement lists HOS, SPR, NMR, FTIR, CD, DSC, DLS, peptide mapping, and glycan profiling.

    6. How can candidates apply?

    Candidates can email their CV to Mahendra.t3705@veedolifesciences.com.

    Job Summary

    Category Details
    Company Veedo Lifesciences
    Vacancies Auditor – Analytical QA
    Required Education Not specified in the recruitment announcement
    Experience 5–8 years