Quality Control Executive Job – at Zentiva, Apply Now!
Are you looking to elevate your career in the pharmaceutical industry? Join Sanofi as an Executive – Quality Control (QC) at our Ankleshwar site in Gujarat, a position that offers hands-on experience with GMP, GLP, stability studies, and method validation. This opportunity is ideal for candidates with a strong background in organic/analytical chemistry or pharmacy, seeking a collaborative, regulated, and innovation-driven work environment in pharmaceutical quality control.
- Job Opportunity: Executive – Quality Control, Pharmaceuticals
- Location: Ankleshwar, Gujarat, India
- Job Requisition ID: R2468223
- Department: Quality Control
About The Company
Zentiva is a leading pharmaceutical company headquartered in Prague, delivering high-quality, affordable generic and OTC medicines across Europe and India. With manufacturing and R&D sites in Prague, Bucharest, and Ankleshwar, Zentiva serves over 100 million patients annually. Backed by Advent International, it is known for its scientific excellence, sustainability efforts, and a strong presence in the Indian pharma sector through its Ankleshwar facility.
Job Summary
As an Executive – Quality Control, you will play a critical role in maintaining the quality of pharmaceutical products by conducting analytical testing, calibrating equipment, documenting processes, and ensuring compliance with global quality directives. This role ensures that
all raw materials, in-process samples, and finished goods meet the required regulatory standards, contributing to continuous improvement initiatives in the QC laboratory.Quality Control Executive Job – Key Responsibilities
- Analytical Activities:
- Perform timely sampling and analysis of raw materials, intermediates, bulk, and finished products.
- Conduct testing for stability studies, process validation, and cleaning validation samples.
- Review and maintain laboratory raw data and analytical test records.
- Equipment & Lab Operations:
- Calibrate, maintain, and assist in the qualification of laboratory equipment.
- Manage reference standards, chemicals, reagents, and lab consumables.
- Prepare SOPs, protocols, and control documents as per GLP/GMP requirements.
- Validation & Documentation:
- Draft protocols for analytical method validation and cleaning validation.
- Execute validation exercises by documented procedures.
- Monitor and ensure the integrity and compliance of documentation.
- Coordination & Compliance:
- Coordinate with production and warehouse teams for sampling and analytical needs.
- Ensure compliance with HSE and regulatory standards for lab safety.
- Report unsafe conditions and proactively implement corrective actions.
Quality Control Executive Job – Requirements & Qualifications
- Education: M.Sc. in Organic / Analytical Chemistry or B. Pharm
- Experience: 2–5 years in a pharmaceutical QC environment
- Skills:
- Strong knowledge of GMP/GLP principles
- Hands-on experience with HPLC/GC (preferred)
- Good coordination, problem-solving, and communication skills
What Makes This Role Unique?
- Direct involvement in regulatory-quality testing for domestic and international markets.
- Opportunity to work in a globally compliant GMP/GLP facility.
- Exposure to method validation and regulatory documentation best practices.
- Work with a multidisciplinary team at one of India’s leading pharma manufacturing hubs—Ankleshwar GIDC.
Keywords: Job Posting, Executive, Quality Control, Pharmaceuticals, Job Opportunity, Ankleshwar, GMP, GLP, Analysis, Validation, Laboratory Consumables, HSE Requirements
