Life Science Jobs at Zentiva | Candidates Apply Now
Are you looking for Life Science Jobs in the pharmaceutical industry? Zentiva Careers has announced an excellent opportunity for professionals seeking QA Jobs. The company is hiring an Executive – Quality Assurance, Pharma for its Ankleshwar location. Candidates with a Bachelor’s or Master’s degree in Pharmacy, Pharmaceutical Sciences, Life Sciences, or a related discipline and 1–5 years of Quality Assurance experience are encouraged to apply. Explore the complete eligibility, responsibilities, qualifications, and application details below.
About Zentiva
Zentiva is a leading pharmaceutical company committed to providing high-quality, affordable medicines to improve healthcare worldwide. With a strong focus on quality, compliance, innovation, and patient care, Zentiva offers rewarding career opportunities for professionals looking to grow in pharmaceutical manufacturing, quality assurance, regulatory compliance, and life sciences. The company fosters a collaborative work environment while maintaining the highest standards of quality and regulatory excellence.
Job Overview
- Job Role: Executive I – Quality Assurance, Pharma
- Company: Zentiva
- Location: Ankleshwar, India
- Job Type: Full-Time
- Experience: 1–5 Years
Key Responsibilities
Quality Management & Continuous Improvement
- Perform line clearance and ensure shop floor compliance.
- Carry out in-process checks and calibration of IPQC instruments.
- Handle e-tools such as SAP Hana, LIMS, eDMS, and the Track Wise system.
- Assist in the complaint investigation system at the site.
- Assist in the qualification and validation system, the change control system, and deviations.
- Prepare and review the Annual Product Quality Review (APQR).
- Review Batch Manufacturing Records (BMR) and Batch Packing Records (BPR).
- Coordinate cGMP training activities.
Compliance
- Ensure adherence to company Quality Standards and Local FDA/MHRA regulations by:
- Understanding regulatory requirements.
- Performing gap analysis to identify gaps in the existing system.
- Preparing compliance plans for gap closure.
- Executing compliance plans.
- Reviewing completion of compliance activities.
Validations & Qualifications
- Ensure validated status of equipment, manufacturing processes, and cleaning processes.
- Review qualification and validation protocols for facilities, equipment, products, and processes.
- Review validation reports after execution of facility, equipment, product, and process validation.
Documentation Control
- Prepare and review Standard Operating Procedures (SOPs).
- Manage controlled distribution and archival of documents and records.
- Maintain control of master documents.
Product Quality Assurance
- Ensure compliance with SOPs.
- Review Batch Manufacturing and Packing Records.
- Ensure implementation of Corrective and Preventive Actions (CAPA) arising from deviations and customer complaints.
- Review the effectiveness of the implemented CAPA.
cGMP Training
- Prepare GMP training modules.
- Organise and execute GMP training programs in coordination with concerned departments.
Other Responsibilities
- Review maintenance and calibration programs.
Qualifications
- Bachelor’s or Master’s degree in Pharmacy, Pharmaceutical Sciences, Life Sciences, or a related discipline.
Experience
- 1–5 years of relevant experience in Pharma Quality Assurance or Documentation.
Skills Needed
- Strong knowledge of cGMP, GDP, and Quality Systems.
- Hands-on experience with batch documentation and document control systems.
- Good understanding of APQR preparation and regulatory expectations.
- Strong analytical, organisational, and coordination skills.
- Effective communication and cross-functional collaboration abilities.
- Attention to detail and commitment to data integrity.
If you are looking for Life Science Jobs in the pharmaceutical industry, this opportunity through Zentiva Careers is an excellent choice for professionals interested in QA Jobs. Candidates with relevant qualifications and experience in Quality Assurance, documentation, cGMP, and compliance are encouraged to apply and build a rewarding career with Zentiva.
