Sanofi Hiring Quality Assurance Specialist in Goa – B.Pharm/M.Pharm

Published on: October 18, 2026

Sanofi has listed a Quality Assurance Specialist position at its site in Verna Industrial Estate, Salcete, Goa. The opportunity is for candidates with 2–5 years of experience and a B.Pharm or M.Pharm qualification.

The role covers pharmaceutical quality systems, GMP documentation, validation activities, in-process quality assurance (IPQA) and shopfloor quality oversight. Candidates preparing for quality-related roles can also practice relevant questions through our Pharma Mock Tests.

1. Sanofi QA Specialist Job Overview

2. Key Responsibilities

The position combines quality systems management, documentation review, validation, production-floor quality checks and workplace safety responsibilities.

2.1 Quality Systems Management

The role involves maintaining and coordinating site quality systems to support pharmaceutical quality and compliance.

• Compiling, reviewing and managing Product Quality Reviews (PQRs).
• Coordinating change controls and managing the deviation system.
• Managing market complaint investigations and acting as the QA focal point for out-of-specification (OOS) and out-of-trend (OOT) management.
• Managing training and pest control systems.
• Performing nitrosamine assessments and reviews and managing ICH Q3D requirements.
• Coordinating the implementation of Sanofi Global Standards (STDs) and Global Operating Procedures (GOPs).
• Acting as the focal point for subcontractor and service provider management.
• Managing the Corrective and Preventive Action (CAPA) system.

2.2 Quality Documentation and Compliance

Responsibilities include reviewing controlled documents, maintaining records and supporting site-level quality compliance.

• Coordinating self-inspections according to the established planner.
• Reviewing and approving GxP documents, batch manufacturing records and batch packing records in the electronic document system.
• Implementing and controlling SOPs, master documents and other quality documents.
• Coordinating cGMP training and reviewing training modules.
• Supporting investigations and the closure of assigned CAPAs.
• Implementing assigned Efficiency Reviews (ERs).
• Acting as Primary Process Owner (PPO) for the Quality Maturity Index (QMI), as assigned.
• Supporting batch release activities and responding to Qualified Person (QP) queries.
• Managing data integrity activities, user access reviews and audit trail reviews.
• Handling the Site Master File (SMF), calibration document reviews, and document archiving and retrieval.
• Supporting analytical method creation and SMS initiatives.

For further information on pharmaceutical data integrity expectations, refer to the FDA’s Data Integrity and cGMP Guidance.

2.3 Validation and Qualification Activities

The Quality Assurance Specialist will act as a quality focal point for validation and qualification activities covering manufacturing processes, equipment and systems.

The role also includes managing the Site Qualification and Validation Master Plan.

Candidates can refer to the ICH Quality Guidelines for relevant international pharmaceutical quality guidance.

2.4 In-Process Quality Assurance (IPQA)

IPQA duties focus on quality oversight during manufacturing and validation activities.

• Reviewing and approving master and executed batch records.
• Reviewing and approving logbooks.
• Performing line clearance in production areas.
• Conducting in-process checks.
• Sampling products during routine production and validation activities.
• Providing quality oversight on the shopfloor.

2.5 Health, Safety and Environment (HSE)

The role includes supporting safe working conditions and implementing site HSE systems.

• Conducting daily training during +QDCI meetings and addressing unsafe conditions.
• Collecting suggestions from associates to improve workplace safety.
• Reviewing implemented procedures and evaluating their effectiveness.
• Training employees on safety practices and job responsibilities to help prevent workplace incidents.

3. Skills to Highlight in Your CV

Candidates can highlight relevant experience in the following areas, where applicable.

Use specific examples from your professional experience and list only skills you can demonstrate. Candidates exploring other quality-related opportunities can visit our QA/QC Jobs page or read our guide to a Career in Quality Assurance After B.Pharm.

4. How to Apply for the Sanofi QA Specialist Job

Interested candidates can review the full job description and submit their application through Sanofi’s official recruitment portal.

View Sanofi Quality Assurance Specialist Vacancy and Apply

Candidates should check the official listing for the latest vacancy status and application requirements before applying.

5. Frequently Asked Questions

5.1 Is the Sanofi QA Specialist position suitable for freshers?

The listed experience requirement is 2–5 years, so the position is intended for candidates with relevant professional experience.

5.2 What qualifications are required?

The stated qualifications are B.Pharm or M.Pharm.

5.3 What are the key technical skills required?

The main technical skills listed are IPQA, batch record review and shopfloor quality governance. Experience with quality systems, documentation and validation is also relevant to the responsibilities.

5.4 Does the job involve shift work?

Yes. The job details specify a three-shift work schedule.

5.5 Where can candidates apply?

Candidates can apply through the official Sanofi job listing linked in Section 4.

Disclaimer

PharmaCareerUpdates.com is an independent job-information website and is not affiliated with or endorsed by Sanofi. Job details may change. Candidates should verify the vacancy status, eligibility criteria and application instructions on Sanofi’s official recruitment website before applying.