Author: Sudheer vanguri

Graviti Pharmaceuticals is conducting walk-in interviews for experienced candidates in its Oral Solid Dosage (OSD) formulation facility. The company is hiring Operators and Senior Operators for Production and Packing, along with Officers and Executives for Production / QMS.
Candidates with 2–8 years of relevant experience can apply for these pharmaceutical manufacturing jobs.
Immediate joiners are preferred for the available positions.
The walk-in interviews will be held from 22 October to 24 October 2026, between 10:00 AM and 1:00 PM, at Graviti Pharmaceuticals, Patancheru Mandal, Telangana.

Graviti Pharmaceuticals Walk-In Interview: Production, Packing and QMS

Company Overview

Graviti Pharmaceuticals is inviting applications for multiple positions at its OSD formulation facility. The recruitment drive is suitable for professionals with experience in pharmaceutical production, secondary packing and Quality Management System (QMS) activities.

Job Openings at Graviti Pharmaceuticals

1. Production Department

Area of Work: Compression

Designation: Operator / Senior Operator

Experience: 4–8 years

Candidates with relevant experience in pharmaceutical compression operations can apply for these positions.

2. Packing Department

Area of Work: Secondary Packing

Designation: Operator / Senior Operator

Experience: 4–8 years

Candidates with experience in secondary packing operations in pharmaceutical manufacturing facilities are eligible to attend.

3. Production / QMS Department

Area of Work: Not specified

Designation: Officer / Executive

Experience: 2–4 years

Professionals with relevant experience in pharmaceutical production or Quality Management System activities can consider this opportunity.

Job Role & Responsibilities

Production and Compression

• Support compression operations in the OSD manufacturing facility.
• Follow applicable manufacturing procedures and production requirements.
• Maintain proper documentation and comply with established quality standards.

Packing and Secondary Packing

• Support secondary packing operations.
• Follow packaging procedures and applicable documentation requirements.
• Maintain compliance with pharmaceutical manufacturing practices.

Production / QMS

• Support production-related activities and QMS procedures, as applicable to the assigned role.
• Maintain documentation and follow relevant quality requirements.

The responsibilities above describe typical activities associated with these roles. The recruitment announcement does not provide a detailed, position-wise responsibility list.

Eligibility & Qualifications

• Production: Operator / Senior Operator, Compression | 4–8 years of experience.
• Packing: Operator / Senior Operator, Secondary Packing | 4–8 years of experience.
• Production / QMS: Officer / Executive | 2–4 years of experience.

Candidates should have relevant pharmaceutical industry experience for the position they are applying for. The recruitment announcement does not specify the required educational qualifications.

Location & Salary

Work Location: Graviti Pharmaceuticals, Pennar Lane, Survey No. 621, Isnapur Village, Patancheru Mandal, Sangareddy District, Telangana – 502307.

Salary details have not been provided in the recruitment announcement.

Walk-In Interview Details

• Company: Graviti Pharmaceuticals
• Interview Dates: 22–24 October 2026
• Days: Thursday to Saturday
• Time: 10:00 AM to 1:00 PM
• Venue: Pennar Lane, Survey No. 621, Isnapur Village, Patancheru Mandal, Sangareddy District, Telangana – 502307
• Hiring Preference: Immediate joiners preferred

How to Apply

Interested candidates can attend the walk-in interview at the specified venue during the announced dates and timings.

Applicants should carry an updated resume and the relevant supporting documents for the interview.

Documents Required

Candidates should bring the following documents:

• Updated resume
• Salary slips for the last three months, if applicable
• Cost to Company (CTC) annexure, if applicable
• Educational documents
• Aadhaar card
• PAN card

Important Instructions

• Candidates should attend the interview between 10:00 AM and 1:00 PM on one of the scheduled dates.
• Immediate joiners are preferred.
• Carry the required documents for verification.

Frequently Asked Questions

1. Which positions are available at Graviti Pharmaceuticals?

The openings are for Operators and Senior Operators in Production and Packing, and Officers / Executives in Production / QMS.

2. How much experience is required?

Production and Packing positions require 4–8 years of experience. Production / QMS positions require 2–4 years.

3. Are immediate joiners preferred?

Yes. The recruitment poster states that immediate joiners are preferred.

4. When is the Graviti Pharmaceuticals walk-in interview?

The walk-in interview is scheduled from 22 October to 24 October 2026, between 10:00 AM and 1:00 PM.

5. Where is the interview venue?

The interview will take place at Graviti Pharmaceuticals, Pennar Lane, Survey No. 621, Isnapur Village, Patancheru Mandal, Sangareddy District, Telangana – 502307.

6. What documents should candidates bring?

Candidates should bring an updated resume, the last three months’ salary slips if applicable, a CTC annexure if applicable, educational documents, an Aadhaar card and a PAN card.

Job Summary

Category	Details
Company	Graviti Pharmaceuticals
Vacancies	Operator / Senior Operator – Production (Compression); Operator / Senior Operator – Packing (Secondary Packing); Officer / Executive – Production / QMS
Required Education	Not specified in the recruitment announcement
Experience	Production / Packing: 4–8 years; Production / QMS: 2–4 years

Aculife Healthcare Private Limited is conducting a walk-in interview for the position of Production Chemist at its sterile manufacturing facility in Sachana Village, Viramgam, Ahmedabad, Gujarat. Candidates with B.Sc., M.Sc., B.Pharm or M.Pharm qualifications and 0–5 years of experience are eligible to attend.
The opening covers production activities in infusion, small-volume parenteral (SVP) and injectable manufacturing areas.
Applicants should have an understanding of GMP, safety standards, line clearance, batch documentation and in-process checks.
The walk-in interview is scheduled for 28 October 2026, from 8:00 AM to 11:00 AM, at Aculife Healthcare Private Limited, Gujarat.

Aculife Healthcare Recruitment: Production Chemist

Company Overview

Aculife Healthcare Private Limited is inviting applications for a Production Chemist position at its pharmaceutical manufacturing facility in Gujarat. The opportunity is suitable for freshers and experienced candidates interested in sterile pharmaceutical production.

Job Role & Responsibilities

Production Chemist: Key Responsibilities

Selected candidates will support production operations across infusion, small-volume parenteral (SVP) and injectable manufacturing areas.

Key responsibilities include:

• Operate and monitor production activities in sterile manufacturing areas.
• Maintain GMP compliance and follow safety standards.
• Perform line clearance and maintain batch records and production documentation.
• Conduct in-process checks and troubleshoot production-related issues.
• Maintain cleanliness and hygiene in the work area.
• Follow Quality Management System (QMS) procedures and regulatory requirements.

Eligibility & Qualifications

• Educational Qualifications: B.Sc. / M.Sc. / B.Pharm / M.Pharm.
• Experience: 0–5 years.
• Eligible Candidates: Freshers and experienced candidates.
• Department: Production.
• Work Areas: Infusion, SVP and injectable manufacturing.

Location & Salary

Job Location: Aculife Healthcare Private Limited, Sachana Village, Viramgam, Ahmedabad – 382150, Gujarat.

Salary details have not been specified in the recruitment announcement.

Walk-In Interview Details

• Company: Aculife Healthcare Private Limited
• Designation: Production Chemist
• Interview Date: 28 October 2026
• Interview Time: 8:00 AM to 11:00 AM
• Interview Type: Walk-in interview
• Venue: Sachana Village, Viramgam, Ahmedabad – 382150, Gujarat

How to Apply

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

Candidates should carry an updated resume and the required supporting documents for verification during the interview.

Documents Required

Candidates should bring the following documents:

• Updated resume
• Educational certificates
• Experience certificates, if applicable
• Latest increment letter, if applicable
• Passport-size photograph
• Aadhaar card and PAN card

Important Instructions

• Candidates with 0–5 years of experience can attend the interview.
• Applicants should be prepared to discuss their knowledge of sterile manufacturing operations and GMP practices.
• Carry all applicable educational and employment documents to the interview.

Frequently Asked Questions

1. What is the qualification required for the Aculife Production Chemist position?

Candidates with B.Sc., M.Sc., B.Pharm or M.Pharm qualifications can apply.

2. Can freshers apply for this job?

Yes. The stated experience requirement is 0–5 years, so freshers are eligible.

3. When is the walk-in interview scheduled?

The interview is scheduled for 28 October 2026, from 8:00 AM to 11:00 AM.

4. Where is the job located?

The position is based at Aculife Healthcare Private Limited, Sachana Village, Viramgam, Ahmedabad, Gujarat.

5. What are the main responsibilities of a Production Chemist?

The role includes monitoring sterile production activities, maintaining GMP and safety compliance, performing line clearance, maintaining batch records and conducting in-process checks.

6. Which documents should candidates carry?

Candidates should bring an updated resume, educational certificates, applicable experience certificates, an increment letter if applicable, a passport-size photograph, Aadhaar card and PAN card.

Job Summary

Category	Details
Company	Aculife Healthcare Private Limited
Vacancies	Production Chemist
Required Education	B.Sc. / M.Sc. / B.Pharm / M.Pharm
Experienceyears	0–5

Caidya is inviting applications for the position of Clinical SAS Programmer in India, with the option to work remotely or from an office. Candidates with a bachelor’s degree in Mathematics, Biostatistics, Statistics, or Computer Science, or equivalent relevant work experience, can apply. The role requires 2–3 years of experience in statistical programming, with knowledge of SAS programming procedures, clinical trial data, and data reconciliation. This opportunity is suitable for professionals interested in clinical data management, statistical programming, and clinical research reporting.

Caidya Clinical SAS Programmer Recruitment

Company Overview

Caidya provides clinical research and development services to support clinical trials and pharmaceutical research. The company’s data operations teams work on programming, reporting, and data management activities that support clinical research projects.

Job Details

• Company: Caidya
• Designation: Clinical SAS Programmer
• Department: Clinical Data Management / Data Operations
• Job Location: India
• Work Arrangement: Remote or office-based
• Experience: 2–3 years in statistical programming
• Requisition ID: 8588

Job Role & Responsibilities

The Clinical SAS Programmer will support Caidya’s data operations by providing programming services to the Data Management department. The position works under the supervision of a Senior Clinical SAS Programmer and/or management and involves assigned programming, data checking, and reporting activities.

Key Responsibilities

• Develop complex data checks and data reconciliation reports.
• Create customized reports using SAS and other tools as requested by the Data Management department.
• Merge external data with Electronic Data Capture (EDC) data and check for consistency.
• Convert SAS datasets, delimited data files, and other file formats into Excel for data review.
• Automate reports to improve efficiency for team members.
• Collaborate and communicate with colleagues across local and international teams.
• Perform other duties as assigned.

Supervisory Responsibilities

This position does not include supervisory responsibilities.

Eligibility & Qualifications

Educational Qualifications

Candidates should have one of the following:

• Bachelor’s degree in Mathematics.
• Bachelor’s degree in Biostatistics.
• Bachelor’s degree in Statistics.
• Bachelor’s degree in Computer Science.
• Equivalent work experience demonstrating the required knowledge and skills.

Experience Required

• 2–3 years of experience providing statistical programming services.
• Knowledge of SAS DATA step programming.
• Familiarity with PROC IMPORT, PROC SQL, and ODS programming in SAS.
• Basic understanding of clinical trial databases and clinical trial data reports is preferred.

Required Skills

• Data merging, transposing, sorting, and other data manipulation techniques.
• Working knowledge of Microsoft Excel.
• Ability to understand reporting requests and select appropriate approaches for creating useful reports and listings.
• Problem-solving skills and the ability to work with limited supervision.
• Strong interpersonal and communication skills.
• Effective time management and organizational abilities.
• Ability to manage multiple projects simultaneously.
• Basic knowledge of UNIX, Windows, and PowerShell commands is preferred.
• Ability to work remotely when required.

Location & Salary

• Job Location: India.
• Work Arrangement: Remote or office-based.

Candidates should confirm compensation and other employment terms during the recruitment process.

How to Apply

Interested candidates can apply through Caidya’s official recruitment portal.

Application Process

1. Visit the official job listing using the link below.
2. Review the job requirements and responsibilities.
3. Prepare an updated resume highlighting SAS programming experience, data manipulation skills, and relevant clinical research exposure.
4. Complete the online application with accurate educational and professional details.
5. Submit the application through the recruitment portal.

Official Apply Link: Apply for Clinical SAS Programmer at Caidya

Recruitment Contact: careers@caidya.com

Important Recruitment Note

The company states that it does not accept unsolicited resumes from third-party vendors.

Important Dates

Candidates should check the official recruitment portal for the latest vacancy status and application availability.

Documents Required

Keep the following documents ready, as applicable:

• Updated resume or CV.
• Educational certificates and mark sheets.
• Details of relevant statistical programming experience.
• Information about SAS programming skills and clinical data management experience.
• Valid contact information.

Additional Requirements

• Candidates should be able to work collaboratively with local and international teams.
• Strong attention to detail is important when checking data consistency and preparing reports.
• Applicants should be comfortable handling multiple assignments and deadlines.
• The role requires the ability to work remotely when needed.
• Caidya is an equal opportunity employer and provides reasonable accommodation during the recruitment process for eligible individuals who require it.

Frequently Asked Questions

1. What qualification is required for the Caidya Clinical SAS Programmer position?

Candidates need a bachelor’s degree in Mathematics, Biostatistics, Statistics, or Computer Science. Equivalent work experience demonstrating the required skills may also be accepted.

2. How much experience is required?

The position requires 2–3 years of experience providing statistical programming services.

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

The job listing allows candidates to work remotely or from an office in India.

4. Which SAS skills are required?

Candidates should know DATA step programming, PROC IMPORT, PROC SQL, and ODS programming. Familiarity with data manipulation and clinical trial databases is also relevant.

5. What is the salary offered by Caidya?

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

6. How can candidates apply?

Candidates can submit their applications through the official Caidya recruitment portal using the link provided above.

Job Summary Table

Category	Details
Company	Caidya
Vacancies	Clinical SAS Programmer
Required Education	Bachelor’s degree in Mathematics, Biostatistics, Statistics, or Computer Science, or equivalent relevant work experience
Experience	2–3 years in statistical programming
Location	India, remote or office-based

Sun Pharmaceutical Industries Ltd. is conducting a walk-in interview drive at its Panoli facility in Gujarat on October 24, 2026, for Apprentice, Quality Assurance (QA), and Quality Control (QC) positions. The recruitment drive includes opportunities for freshers in Production Engineering, EHS, and Stores apprenticeships, along with experienced openings in Quality Assurance and Quality Control. Candidates with Diploma, B.E., B.Sc., M.Sc., B.Com, B.Pharm, or M.Pharm qualifications may be eligible depending on the position. Interested candidates should attend the walk-in interview with the required documents at the specified venue.

Sun Pharma Panoli Walk-In Interview 2026

Company Overview

Sun Pharmaceutical Industries Ltd. is a pharmaceutical company involved in the development and manufacturing of medicines for healthcare markets worldwide. The company is inviting candidates to attend its walk-in recruitment drive at the Panoli facility in Gujarat.

Job Details

• Company: Sun Pharmaceutical Industries Ltd.
• Recruitment Type: Walk-In Interview
• Job Location: Panoli, Bharuch, Gujarat
• Interview Date: October 24, 2026 (Saturday)
• Interview Time: 10:00 AM to 3:00 PM
• Departments: Production Engineering, EHS, Stores, Quality Assurance, Quality Control

Job Openings at Sun Pharma Panoli

1. Apprentice

Departments: Production Engineering, EHS, Stores

Eligible Qualifications:

• Diploma in Chemical Engineering
• B.E. in Chemical Engineering
• B.E. in Mechanical Engineering
• B.Sc.
• M.Sc.
• B.Com.

Experience: Freshers

Desired Work Profile:

• Operator activities
• Documentation

2. Senior Officer / Executive

Department: Quality Assurance (QA)

Eligible Qualifications:

• M.Sc.
• B.Pharm
• M.Pharm

Experience: 4–8 years of pharmaceutical experience

Desired Work Profile:

• Quality Management Systems (QMS)
• Quality Assurance
• Quality Control
• Microbiology QA

3. Officer / Senior Officer

Department: Quality Control (QC)

Eligible Qualifications:

• M.Sc.
• B.Pharm
• M.Pharm

Experience: 4–6 years of pharmaceutical experience

Desired Work Profile:

• Handling HPLC
• Gas Chromatography (GC)
• Chemical laboratory activities

Eligibility & Qualifications

Candidates should hold the relevant educational qualification and experience required for their preferred position.

• Apprentice: Diploma, B.E., B.Sc., M.Sc., or B.Com. Freshers are eligible.
• Quality Assurance: M.Sc., B.Pharm, or M.Pharm with 4–8 years of pharmaceutical experience.
• Quality Control: M.Sc., B.Pharm, or M.Pharm with 4–6 years of pharmaceutical experience.

Applicants should review the position-specific requirements before attending the interview.

Location & Salary

• Work Location: Sun Pharmaceutical Industries Ltd., 24/2, 25, Phase IV, G.I.D.C., Panoli, Bharuch, Gujarat 394116, India.
• Interview Venue: Sun Pharmaceutical Industries Ltd., 24/2, 25, Phase IV, G.I.D.C., Panoli, Bharuch, Gujarat 394116.

How to Apply

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

Walk-In Interview Details

• Date: October 24, 2026 (Saturday)
• Time: 10:00 AM to 3:00 PM
• Venue: Sun Pharmaceutical Industries Ltd., 24/2, 25, Phase IV, G.I.D.C., Panoli, Bharuch, Gujarat 394116.

Documents Required

Candidates must bring the following documents:

• One recent clean-shaven photograph.
• PAN card copy.
• Aadhaar card copy.
• Educational certificates and mark sheets.
• Previous organization’s experience letters, where applicable.
• Current organization’s appointment letter.
• Salary slips for the last three months.
• Current Cost to Company (CTC) details.

Important Instructions

• Carry all required documents to the interview venue.
• Candidates should ensure their educational and experience details are accurate.
• Sun Pharma does not ask prospective candidates to pay money for employment or authorize agencies or individuals to collect recruitment fees. Be cautious of fraudulent recruitment requests.

Frequently Asked Questions

1. When is the Sun Pharma Panoli walk-in interview?

The walk-in interview is scheduled for October 24, 2026, from 10:00 AM to 3:00 PM.

2. Which positions are available?

The openings include Apprentice positions in Production Engineering, EHS, and Stores, along with Senior Officer/Executive roles in QA and Officer/Senior Officer roles in QC.

3. Can freshers apply?

Yes. Freshers can apply for the Apprentice positions if they meet the specified educational requirements.

4. What qualifications are accepted?

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

5. What experience is required for QA and QC positions?

QA positions require 4–8 years of pharmaceutical experience, while QC positions require 4–6 years.

6. What documents should candidates carry?

Candidates should bring a clean-shaven photograph, PAN card copy, Aadhaar card copy, educational certificates, relevant experience documents, the current appointment letter, three months of salary slips, and current CTC details.

Job Summary Table

Category	Details
Company	Sun Pharmaceutical Industries Ltd.
Vacancies	Apprentice, Senior Officer/Executive – QA, Officer/Senior Officer – QC
Required Education	Diploma, B.E., B.Sc., M.Sc., B.Com., B.Pharm, M.Pharm
Experience	Freshers for Apprentice; 4–8 years for QA; 4–6 years for QC
Location	Panoli, Bharuch, Gujarat, India

Sanofi is hiring for the position of Medical Information Writer in Hyderabad, India. Candidates with an advanced degree in Life Sciences, Pharmacy, or a related discipline and 2–3 years of relevant experience in medical writing or a clinical setting are eligible to apply. The role requires at least 1–2 years of direct medical information experience in a pharmaceutical company, along with strong scientific writing, literature evaluation, and medical editing skills. Interested professionals can apply through Sanofi’s official careers portal before October 31, 2026.

Sanofi Medical Information Writer Recruitment

Company Overview

Sanofi is a global healthcare and pharmaceutical company with operations spanning specialty care, vaccines, general medicines, consumer healthcare, and research and development.

Sanofi Business Operations, based in India, supports global business functions by centralizing processes and activities for medical, health economics and value assessment (HEVA), commercial, research and development, data, and digital teams.

Job Details

• Company: Sanofi
• Designation: Medical Information Writer
• Department: Sanofi Business Operations / Global Medical Information
• Job Location: Hyderabad, India
• Experience: 2–3 years in medical writing or a clinical setting
• Relevant Experience: 1–2 years of direct medical information experience in a pharmaceutical company
• Employment Type: Regular
• Job Posted: September 30, 2026
• Application Deadline: October 31, 2026

Job Role & Responsibilities

The Medical Information Writer will research and prepare scientific response documents under the direction of the Global Medical Information (GMI) team. The role involves scientific literature evaluation, evidence-based content development, document management, and collaboration with global and local medical information teams.

Key Responsibilities

Scientific Research and Medical Writing

• Conduct scientific literature searches and reviews.
• Extract, analyze, and summarize complex information from scientific publications.
• Prepare accurate, current, evidence-based, and fair-balanced scientific response documents.
• Develop and maintain medical information content for products in assigned therapeutic areas.
• Adapt global scientific response documents for specific countries.
• Prepare responses to escalated medical information inquiries for assigned countries.
• Contribute to US New Drug Application (NDA) Annual Reports.
• Participate in US compendia reviews.
• Develop expertise in assigned therapeutic areas.

Quality Review and Project Management

• Execute medical information projects with guidance from experienced team members or managers.
• Conduct quality checks on colleagues’ work when required.
• Ensure assigned deliverables meet agreed timelines and quality standards.
• Maintain accurate documentation and perform data quality checks.
• Participate in cross-functional project teams as needed.
• Collaborate with Global Medical Information teams to implement content plans.

Stakeholder Management

• Maintain effective relationships with medical and scientific stakeholders.
• Coordinate with medical and pharmacovigilance departments.
• Work with regional medical teams to identify medical writing requirements.
• Prepare customized scientific deliverables in collaboration with medical departments.
• Support knowledge sharing and help other medical information writers develop their expertise.

Process and Performance Responsibilities

• Conduct data checks and deliver accurate outputs with minimal supervision.
• Support medical information needs assessments.
• Implement assigned country-level content plans and related activities.
• Coordinate with selected regional vendors to complete deliverables according to established processes.
• Contribute to improvements in content planning and delivery based on stakeholder feedback.

Eligibility & Qualifications

Educational Qualifications

Candidates should possess an advanced degree in one of the following areas:

• Pharmacy.
• Life Sciences.
• Master of Science (M.Sc.).
• A similar or related discipline.
• MBA or equivalent qualification.

Experience Required

• 2–3 years of experience in medical writing within the pharmaceutical or healthcare industry, or equivalent experience in a clinical setting.
• At least 1–2 years of direct medical information experience in a pharmaceutical company.

Required Skills

• Excellent scientific and medical writing skills.
• Strong technical editing and proofreading abilities.
• Knowledge of scientific literature searches and evaluation.
• Ability to develop multilevel responses to medical information inquiries.
• Stakeholder management and communication skills.
• Ability to work independently and collaboratively.
• Time management and risk management skills.
• Ability to manage multiple deliverables and meet deadlines.
• Excellent written and spoken English proficiency.

Location & Salary

• Job Location: Hyderabad, Telangana, India.
• Employment Type: Regular.

How to Apply

Eligible candidates can submit their applications through Sanofi’s official careers portal.

Application Process

1. Visit the official job listing using the application link below.
2. Review the job responsibilities and eligibility requirements.
3. Prepare an updated resume highlighting medical writing, scientific literature evaluation, and medical information experience.
4. Complete the online application with accurate details.
5. Submit the application before the closing date.

Official Apply Link: Apply for Medical Information Writer at Sanofi

Official Job Listing: View Medical Information Writer Vacancy

Important Dates

• Job Posted: September 30, 2026.
• Application Deadline: October 31, 2026.

Candidates should submit their applications before the closing date.

Documents Required

Keep the following documents ready for the application process:

• Updated resume or CV.
• Educational certificates and postgraduate qualification documents.
• Details of relevant medical writing experience.
• Information about medical information projects and scientific writing experience.
• Valid contact information.

Additional Requirements

• Strong understanding of scientific literature and evidence-based content development.
• Ability to prepare accurate and fair-balanced medical information documents.
• Willingness to coordinate with global and regional medical teams.
• Ability to follow established documentation processes and quality standards.
• Commitment to completing assigned projects within agreed timelines.
• Ability to manage stakeholder feedback and incorporate review comments.

Frequently Asked Questions

1. What qualification is required for the Sanofi Medical Information Writer position?

Candidates should have an advanced degree in Pharmacy, Life Sciences, a related discipline, M.Sc., MBA, or an equivalent qualification.

2. How much experience is required?

The position requires 2–3 years of medical writing or equivalent clinical experience, including at least 1–2 years of direct medical information experience in a pharmaceutical company.

3. Where is the job located?

The position is based in Hyderabad, Telangana, India.

4. What are the main responsibilities of a Medical Information Writer?

The role includes scientific literature research, medical information response writing, document adaptation, US NDA Annual Report contributions, compendia reviews, quality checks, and collaboration with global medical teams.

5. What is the salary offered by Sanofi?

The salary is not disclosed in the supplied job announcement. Candidates should confirm compensation with the recruitment team.

6. What is the last date to apply?

The application deadline is October 31, 2026.

Job Summary Table

Category	Details
Company	Sanofi
Vacancies	Medical Information Writer
Required Education	Advanced degree in Pharmacy, Life Sciences, a related discipline, M.Sc., MBA, or equivalent
Experience	2–3 years in medical writing or a clinical setting, including 1–2 years of direct medical information experience
Location	Hyderabad, Telangana, India

Amgen Technology is inviting applications for the position of Senior Associate, Pharmacovigilance Operations in Hyderabad, Telangana. Candidates with 2–5 years of experience and a graduate or postgraduate qualification can explore this opportunity in pharmacovigilance and drug safety reporting. The role focuses on preparing, compiling, reviewing, and managing Periodic Aggregate Safety Reports (PASRs) in accordance with applicable regulatory requirements. Professionals with experience in safety report authoring, clinical research documentation, quality review, and regulatory compliance are encouraged to apply.

Amgen Senior Associate Pharmacovigilance Operations Recruitment

Company Overview

Amgen is a biotechnology company focused on developing medicines for serious diseases. Its operations include activities supporting drug development, patient safety, and regulatory compliance.

Job Details

• Company: Amgen Technology
• Designation: Senior Associate, Pharmacovigilance Operations
• Department: Pharmacovigilance Operations
• Job Location: Hyderabad, Telangana, India
• Experience: 2–5 years
• Employment Type: Full-time, Permanent
• Industry: Pharmaceutical and Life Sciences
• Salary: Not disclosed

Job Role & Responsibilities

The selected candidate will support the end-to-end preparation and management of Periodic Aggregate Safety Reports (PASRs). The role involves coordinating report contributions, authoring safety content, conducting quality reviews, managing approvals, and ensuring reports are completed within regulatory timelines.

Key Responsibilities

PASR Compilation and Authoring

• Compile and author periodic aggregate safety reports in accordance with global regulatory requirements.
• Support the preparation of Development Safety Update Reports (DSURs).
• Work on Periodic Benefit-Risk Evaluation Reports (PBRERs) and Periodic Safety Update Reports (PSURs).
• Support preparation of Semi-Annual Safety Update Reports (SSURs), Periodic Adverse Drug Experience Reports (PADERs/PAERs), and Device PSURs.
• Assist with country-specific reports, including Korea PSURs, Brazil PSURs, and Colombia Clinical Research Annual Safety Report Submission and Evaluation forms.
• Collaborate with Therapeutic Area Safety Scientists to prepare safety content.

Stakeholder Coordination and Timeline Management

• Schedule and coordinate meetings with cross-functional stakeholders.
• Collect report contributions from internal teams and external business partners.
• Compile submitted content into the appropriate PASR templates.
• Monitor report timelines and escalate risks or delays to team leads and management.
• Coordinate report reviews and resolve comments before final approval.

Quality Review and Documentation

• Conduct peer quality control reviews of authored safety sections.
• Coordinate internal reviews and initiate approval workflows.
• Review and approve published report versions, including blinded, unblinded, EU/FDA, and Rest of World versions, as applicable.
• Maintain and archive accurate report documentation.
• Distribute reports to Contract Research Organizations (CROs) and business partners.
• Perform peer and quality reviews within established timelines using applicable checklists.

Regulatory Compliance and Reporting Metrics

• Ensure compliance with regulatory guidelines, internal processes, report styles, and applicable standards.
• Maintain current knowledge of regulatory requirements, technological developments, and industry practices.
• Generate Periodic Aggregate Safety Report metrics, including Key Compliance Indicators (KCIs) and Key Performance Indicators (KPIs).

Literature Management

• Assist with literature management activities when required.

Eligibility & Qualifications

Educational Qualifications

The recruitment listing specifies the following educational requirements:

• Any graduate.
• Any postgraduate.

Experience Required

• 2–5 years of professional experience.
• Relevant experience in pharmacovigilance operations, periodic safety reporting, safety report authoring, or regulatory documentation would be applicable to the responsibilities of this position.

Relevant Skills

• Pharmacovigilance operations.
• Periodic Aggregate Safety Report (PASR) compilation.
• Safety report authoring and quality control.
• Development Safety Update Report (DSUR).
• Periodic Benefit-Risk Evaluation Report (PBRER).
• Periodic Safety Update Report (PSUR).
• PADER and related regulatory reports.
• Clinical research documentation.
• Regulatory compliance.
• Stakeholder coordination and workflow management.
• Literature management.
• Reporting metrics and quality review.

Location & Salary

• Job Location: Hyderabad, Telangana, India.
• Salary: Not disclosed in the recruitment listing.
• Employment Type: Full-time, permanent.

Candidates should confirm compensation and other employment terms during the recruitment process.

How to Apply

Interested candidates can apply through the job listing on Naukri.

Application Process

1. Open the job listing using the link below.
2. Review the job responsibilities and eligibility requirements.
3. Update your resume to include relevant pharmacovigilance, safety reporting, and regulatory documentation experience.
4. Complete the application process through the recruitment portal.
5. Monitor your registered email and phone for further communication.

Apply Here: Amgen Senior Associate Pharmacovigilance Operations

Selection Process

The supplied recruitment listing does not specify the interview rounds or selection stages. Applicants should follow the instructions provided through the recruitment portal.

Important Dates

Candidates should refer to the official recruitment listing for the latest application status and availability.

Documents Required

Keep the following documents ready, as applicable:

• Updated resume or CV.
• Educational certificates and mark sheets.
• Relevant work experience details.
• Information about pharmacovigilance and safety reporting experience.
• Valid contact information.

Additional Requirements

• Ability to manage multiple reports and deadlines.
• Strong attention to detail during report preparation and quality review.
• Effective communication with cross-functional teams and external partners.
• Understanding of regulatory reporting processes and applicable guidelines.
• Ability to maintain accurate documentation and follow established workflows.
• Willingness to support literature management activities when required.

Frequently Asked Questions

1. What qualification is required for the Amgen Senior Associate Pharmacovigilance Operations position?

The recruitment listing specifies any graduate or any postgraduate qualification.

2. How much experience is required?

Candidates should have 2–5 years of experience.

3. Where is the job located?

The position is listed in Hyderabad, Telangana, India.

4. What are the main responsibilities?

The role involves PASR compilation and authoring, safety report quality review, stakeholder coordination, regulatory compliance, report distribution, and documentation management.

5. What is the salary offered by Amgen?

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

6. How can candidates apply?

Candidates can submit their applications through the Naukri job listing linked above.

Job Summary Table

Category	Details
Company	Amgen Technology
Vacancies	Senior Associate, Pharmacovigilance Operations
Required Education	Any Graduate or Any Postgraduate
Experience	2–5 years
Location	Hyderabad, Telangana, India

MacLeods Pharmaceuticals is inviting applications for a position in its Medical Services Department for candidates with 2–3 years of relevant experience. The opening is suitable for M.Pharm graduates, including candidates with an M.Pharm in Pharmacology.
The selected candidate will be responsible for preparing clinical and non-clinical regulatory documents, product information leaflets, product monographs and supporting documentation.
The role also involves literature searches, artwork approvals, preparation of clinical and non-clinical study matrices, and monitoring in-house bioavailability and bioequivalence (BA/BE) studies.
Freshers are not eligible for this opportunity. Experienced candidates can apply by emailing their updated resume and mentioning “Medical Services” in the email subject line.

MacLeods Pharmaceuticals Recruitment: Medical Services Department

Company Overview

MacLeods Pharmaceuticals is recruiting an experienced professional for its Medical Services Department. The position focuses on clinical and non-clinical regulatory documentation, product information preparation and related medical services activities.

Job Role & Responsibilities

Medical Services Department

The selected candidate will handle the following responsibilities:

• Prepare Module 2.4 Non-Clinical Overview documents and non-clinical study matrices.
• Prepare Module 2.5 Clinical Overview documents and clinical study matrices.
• Prepare Package Inserts (PI), Patient Information Leaflets (PIL) and Summary of Product Characteristics (SmPC/SPC).
• Review and approve product artworks.
• Conduct literature searches covering non-clinical, clinical and formulation-related topics.
• Prepare product monographs.
• Prepare different types of scientific rationales, including those related to fixed-dose combinations (FDCs), efficacy and dosing.
• Monitor in-house bioavailability and bioequivalence (BA/BE) studies.

Eligibility & Qualifications

Educational Qualifications:

• M.Pharm
• M.Pharm in Pharmacology

Experience Required: 2–3 years of relevant experience.

Freshers: Freshers are not eligible. Only experienced candidates should apply.

Location & Salary

The job location and salary details have not been specified in the recruitment announcement.

How to Apply

Interested and eligible candidates can send their updated resume to the recruitment contact below.

Email: adityab@macleodspharma.com

Important instruction: Mention Medical Services in the email subject line. Applications from freshers are not being considered for this position.

Important Recruitment Details

• Company: MacLeods Pharmaceuticals
• Department: Medical Services
• Vacancies: 1 position
• Qualification: M.Pharm / M.Pharm (Pharmacology)
• Experience: 2–3 years
• Eligibility: Experienced candidates only

Frequently Asked Questions

1. What qualification is required for this Medical Services position?

Candidates with an M.Pharm qualification, including M.Pharm in Pharmacology, are eligible.

2. Can freshers apply for this opening?

No. The recruitment notice specifically states that freshers should not apply.

3. How much experience is required?

Candidates should have 2–3 years of relevant experience.

4. What are the main responsibilities?

The role involves preparing clinical and non-clinical overviews, study matrices, product information documents, product monographs and scientific rationales, along with literature searches, artwork approvals and monitoring in-house BA/BE studies.

5. How can candidates apply?

Candidates can email their updated resume to adityab@macleodspharma.com and mention “Medical Services” in the subject line.

6. How many vacancies are available?

There is one position available in the Medical Services Department.

Job Summary

Category	Details
Company	MacLeods Pharmaceuticals
Vacancies	Medical Services Department, 1 position
Required Education	M.Pharm / M.Pharm (Pharmacology)
Experience	2–3 years

Asence Pharma Pvt. Ltd. is inviting applications for the position of Regulatory Affairs Executive at its facility in Ranoli, Vadodara, Gujarat. Candidates with M.Pharm, B.Pharm or M.Sc. qualifications in Pharmaceutical Regulatory Affairs, Organic Chemistry or a relevant discipline are eligible to apply.
The company is looking for professionals with 3–5 years of relevant experience in API manufacturing units. Candidates with a background in Quality Control (QC) will be preferred.
The selected candidate will support regulatory documentation, international submissions, regulatory database maintenance and post-approval change management.
Interested candidates can share their updated CV with the recruitment team by email.

Asence Pharma Regulatory Affairs Executive Recruitment

Company Overview

Asence Pharma Pvt. Ltd. is hiring a Regulatory Affairs Executive for its facility in Ranoli, Vadodara, Gujarat. The position focuses on regulatory documentation and submissions for active pharmaceutical ingredient (API) manufacturing operations.

Job Role & Responsibilities

Regulatory Affairs Executive

The selected candidate will support regulatory documentation, submission activities and coordination with internal departments.

Key responsibilities include:

• Assist in preparing regulatory documents, including Drug Master File (DMF) sections, Certificate of Pharmaceutical Product (CoPP), GMP and Certificate of Suitability (CEP) documentation.
• Collect and review technical and quality data from Research and Development (R&D), Quality Control (QC), Quality Assurance (QA) and Production departments.
• Assist with regulatory submissions across international markets and track approval status.
• Maintain regulatory databases, filing records and regulatory documentation.
• Coordinate responses to regulatory deficiencies and manage post-approval changes.

Eligibility & Qualifications

Candidates must meet the educational and experience requirements for the Regulatory Affairs Executive position.

Educational Qualifications:

• M.Pharm
• B.Pharm
• M.Sc. in Pharmaceutical Regulatory Affairs, Organic Chemistry or a relevant discipline

Experience Required: 3–5 years of relevant experience in API manufacturing units.

Preferred Background: Candidates with Quality Control (QC) experience will be preferred.

Location & Salary

Job Location: Ranoli, Vadodara, Gujarat.

Salary details have not been specified in the recruitment announcement.

How to Apply

Interested and eligible candidates can apply by sending their updated CV to the recruitment team.

Email: hr@asence.com

Candidates should include their educational qualifications, relevant API industry experience and current contact details in their CV.

Important Recruitment Details

• Company: Asence Pharma Pvt. Ltd.
• Designation: Regulatory Affairs Executive
• Department: Regulatory Affairs
• Location: Ranoli, Vadodara, Gujarat
• Experience: 3–5 years
• Preferred Candidates: Professionals with a Quality Control background

Frequently Asked Questions

1. What is the qualification required for the Asence Pharma Regulatory Affairs Executive position?

Candidates with M.Pharm, B.Pharm or M.Sc. in Pharmaceutical Regulatory Affairs, Organic Chemistry or a relevant discipline can apply.

2. How much experience is required?

Applicants should have 3–5 years of relevant experience in API manufacturing units.

3. Are QC professionals eligible to apply?

Yes. Candidates with a Quality Control background will be preferred.

4. Where is the job located?

The position is based in Ranoli, Vadodara, Gujarat.

5. How can candidates apply?

Candidates can email their updated CV to hr@asence.com.

6. What are the main responsibilities of this role?

The role involves regulatory documentation, international submissions, regulatory database maintenance, deficiency responses and post-approval changes.

Job Summary

Category	Details
Company	Asence Pharma Pvt. Ltd.
Vacancies	Regulatory Affairs Executive
Required Education	M.Pharm / B.Pharm / M.Sc. in Pharmaceutical Regulatory Affairs, Organic Chemistry or a relevant discipline
Experience	3–5 years in API manufacturing units

Zenvision Pharma is hiring a Research Associate for its Formulation Research & Development department at Mahape MIDC. The opening is suitable for M.Pharm (Pharmaceutics) candidates with 0–5 years of experience, including freshers.
The selected candidate will work on formulation development, pre-formulation studies, literature research, product characterization and technology transfer documentation.
Applicants should have knowledge of QbD-based formulation development, QTPP, CQA, stability studies, laboratory instruments and GMP/GLP documentation practices.
Eligible male and female candidates can apply for this opportunity, with one position available at the Mahape MIDC location.

Zenvision Pharma Recruitment: Company Overview

Zenvision Pharma is recruiting a Research Associate for its Formulation Research & Development (FR&D) department. The role focuses on pharmaceutical formulation development, research activities, product characterization and technical documentation.

Zenvision Pharma Research Associate: Job Responsibilities

Formulation Research & Development

The selected candidate will be responsible for the following activities:

1. Formulation Development: Develop formulations using a Quality by Design (QbD) approach for ophthalmic, solid, semisolid and liquid dosage forms.
2. Literature Research: Conduct literature searches on APIs, patent excipients and formulation development technologies. Review patent searches, patent landscapes, API searches, innovator specifications and literature reports.
3. Product Characterization: Perform innovator product characterization and plan formulation strategies by assessing QTPP and CQA.
4. Documentation: Maintain laboratory notebooks (LNBs), raw data sheets, analytical reports and data compilations. Interpret results and prepare technical documentation and review reports.
5. Laboratory Instrument Calibration: Perform daily, monthly and yearly calibration activities for laboratory instruments.
6. Pre-formulation Studies: Plan and execute pre-formulation studies, develop trial batches and conduct stability batches to optimize formulation and manufacturing processes through QbD/DoE-based trials.
7. Laboratory Notebook Maintenance: Write and maintain laboratory notebooks according to SOPs and follow GDP and GLP practices.
8. Technical Documentation: Prepare product development, technology transfer and Drug Control General of India (DCGI) documents.

Eligibility & Qualifications

• Educational Qualification: M.Pharm in Pharmaceutics.
• Experience: 0–5 years.
• Eligible Candidates: Freshers and experienced candidates.
• Gender: Male / Female.
• Department: Formulation Research & Development.
• Required Knowledge: Formulation development, QbD, QTPP, CQA, literature research, stability studies, laboratory instrument calibration, documentation, GDP and GLP practices.

Location & Salary

Job Location: Mahape MIDC, Maharashtra.

Salary details have not been provided in the recruitment announcement.

How to Apply

Interested and eligible candidates can share their updated CV with Zenvision Pharma through the email address provided below.

Email: hr@zenvisionpharma.com

Applicants should ensure that their CV includes their educational qualifications, relevant formulation R&D experience, technical skills and contact details.

Important Recruitment Details

• Company: Zenvision Pharma
• Department: Formulation Research & Development
• Designation: Research Associate
• Number of Positions: 1
• Qualification: M.Pharm (Pharmaceutics)
• Experience: 0–5 years
• Location: Mahape MIDC
• Application Email: hr@zenvisionpharma.com

Frequently Asked Questions

1. What is the qualification required for the Zenvision Pharma Research Associate position?

Candidates must have an M.Pharm qualification in Pharmaceutics.

2. Can freshers apply for this Research Associate job?

Yes. The stated experience requirement is 0–5 years, making the opportunity suitable for freshers as well as experienced candidates.

3. Where is the Research Associate vacancy located?

The position is based at Mahape MIDC, Maharashtra.

4. What department is hiring?

The vacancy is in Formulation Research & Development (FR&D).

5. How many vacancies are available?

One Research Associate position is available.

6. How can candidates apply?

Interested candidates can email their CV to hr@zenvisionpharma.com.

Job Summary

Category	Details
Company	Zenvision Pharma
Vacancies	Research Associate
Required Education	M.Pharm (Pharmaceutics)
Experience	0–5 years

Amneal Pharmaceuticals is conducting a walk-in interview for experienced pharmaceutical professionals at its Raks Pharma facility in Dahej, Bharuch, Gujarat. The recruitment drive offers opportunities in QC Microbiology, QC Analytical, QA IPQA and QA QMS / Documentation Management.
Candidates with M.Sc. Microbiology, B.Sc. / M.Sc. Chemistry, B.Pharm, M.Pharm and M.Sc. qualifications can apply for relevant positions based on their experience.
Professionals with experience in pharmaceutical manufacturing, laboratory testing, GMP compliance, quality assurance and quality management systems are encouraged to attend the interview.
The walk-in interview is scheduled for 1 November 2026, from 9:00 AM to 4:00 PM, at Raks Pharma Pvt. Ltd., Dahej SEZ, Bharuch, Gujarat.

Amneal Pharmaceuticals Walk-In Interview: Company Overview

Amneal Pharmaceuticals is a global pharmaceutical company involved in the development, manufacturing and distribution of medicines. The recruitment drive is being conducted at Raks Pharma Pvt. Ltd., a division of Amneal Pharmaceuticals, at its Dahej facility.

The company is looking for qualified professionals for quality control, quality assurance and quality management roles. Candidates with experience in peptide manufacturing and USFDA-approved sites are preferred.

Amneal Pharmaceuticals Job Vacancies and Responsibilities

1. QC Microbiology Executive

Position: QC Microbiology Executive
Grade: Officer / Executive
Qualification: M.Sc. Microbiology
Experience: 3–8 years

Key Skills:

• Environmental monitoring
• Water testing and utility qualification
• Sterility testing
• GLP and GMP practices

Job Responsibilities:

• Perform microbiological testing.
• Conduct environmental monitoring and purified water testing.
• Support utility qualification and qualification-related activities.

2. QC Analyst

Position: QC Analyst
Grade: Officer / Executive
Qualification: B.Sc. / M.Sc. Chemistry
Experience: 2–8 years

Key Skills:

• HPLC and GC
• UPLC
• Wet analysis
• Method transfer
• Stability testing
• Documentation

Job Responsibilities:

• Perform raw material, in-process and finished product testing.
• Conduct stability testing.
• Support analytical method transfer, validation and routine laboratory activities.

3. QA IPQA Executive

Position: QA IPQA Executive
Grade: Officer / Executive
Qualification: B.Pharm / M.Pharm / M.Sc.
Experience: 3–8 years

Key Skills:

• GMP and IPQA
• Batch review
• Shop-floor compliance
• Investigations
• Documentation

Job Responsibilities:

• Monitor pharmaceutical manufacturing activities.
• Ensure GMP compliance on the shop floor.
• Perform line clearance and batch record reviews.
• Support in-process quality assurance activities.

4. QA QMS / Documentation Manager

Position: QA QMS / Documentation Manager
Grade: Manager / Senior Manager
Qualification: B.Pharm / M.Pharm / M.Sc.
Experience: 10–15 years

Key Skills:

• Quality Management Systems (QMS)
• Change control
• Deviations and CAPA
• Audit management
• Regulatory compliance

Job Responsibilities:

• Manage quality management systems and documentation control.
• Oversee SOP lifecycle management.
• Handle investigations, CAPA and change control activities.
• Support audit readiness and regulatory compliance.

Eligibility & Qualifications

Candidates should have the educational qualifications and relevant experience required for their preferred position.

• QC Microbiology Executive: M.Sc. Microbiology with 3–8 years of experience.
• QC Analyst: B.Sc. / M.Sc. Chemistry with 2–8 years of experience.
• QA IPQA Executive: B.Pharm / M.Pharm / M.Sc. with 3–8 years of experience.
• QA QMS / Documentation Manager: B.Pharm / M.Pharm / M.Sc. with 10–15 years of experience.

Candidates from peptide manufacturing facilities and USFDA-approved manufacturing sites are preferred.

Location & Salary

Job Location: Raks Pharma Pvt. Ltd. (A division of Amneal Pharmaceuticals), Plot No. Z/111/A, Dahej SEZ, Part II, Dahej, Bharuch, Gujarat – 392130.

Salary details have not been provided in the recruitment announcement.

Walk-In Interview Details

• Company: Amneal Pharmaceuticals / Raks Pharma Pvt. Ltd.
• Interview Date: Sunday, 1 November 2026
• Interview Time: 9:00 AM to 4:00 PM
• Interview Type: Walk-in interview
• Location: Dahej SEZ, Bharuch, Gujarat

Bus Transportation Facility

Bus transportation has been arranged for candidates attending the interview.

Bus Number	Timing	Pickup Location
GJ-16-AW-3056	06:10 AM	BAPS Swaminarayan Temple, near Zadeshwar Chowk, Bharuch
GJ-16-AW-3185	09:00 AM	BAPS Swaminarayan Temple, near Zadeshwar Chowk, Bharuch
GJ-16-AW-3056	11:00 AM	BAPS Swaminarayan Temple, near Zadeshwar Chowk, Bharuch
GJ-16-AW-2383	13:05 PM	BAPS Swaminarayan Temple, near Zadeshwar Chowk, Bharuch

Bus Coordinator: Mr. Bhavin Vaidya
Contact Number: 8460647678

How to Apply

Eligible candidates can attend the walk-in interview directly at the venue on the scheduled date and time.

Candidates who cannot attend the interview may send their updated CV to the recruitment contact below.

Email: harshad.d.bhavsar@amneal.com

Candidates should ensure that their CV includes their qualifications, relevant pharmaceutical industry experience and current contact details.

Important Instructions

• Candidates with experience in peptide manufacturing and USFDA-approved facilities are preferred.
• A bus facility is available for candidates attending the interview from the specified pickup location.
• Candidates who cannot attend the walk-in interview can share their CV by email.
• Amneal Pharmaceuticals states that it provides equal employment opportunities and does not charge recruitment fees.

Frequently Asked Questions

1. Which positions are available at Amneal Pharmaceuticals?

The openings include QC Microbiology Executive, QC Analyst, QA IPQA Executive and QA QMS / Documentation Manager.

2. What qualifications are required?

The listed qualifications include M.Sc. Microbiology, B.Sc. / M.Sc. Chemistry, B.Pharm, M.Pharm and M.Sc., depending on the role.

3. How much experience is required?

Experience requirements range from 2 to 15 years, depending on the position.

4. When is the Amneal Pharmaceuticals walk-in interview?

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

5. Where is the interview venue?

The interview will be held at Raks Pharma Pvt. Ltd., Plot No. Z/111/A, Dahej SEZ, Part II, Dahej, Bharuch, Gujarat – 392130.

6. How can candidates apply if they cannot attend?

Candidates who cannot attend can email their CV to harshad.d.bhavsar@amneal.com.

Job Summary

Category	Details
Company	Amneal Pharmaceuticals / Raks Pharma Pvt. Ltd.
Vacancies	QC Microbiology Executive, QC Analyst, QA IPQA Executive, QA QMS / Documentation Manager
Required Education	M.Sc. Microbiology, B.Sc. / M.Sc. Chemistry, B.Pharm, M.Pharm, M.Sc.
Experience	2–15 years, depending on the position