Zentiva
Executive QA Documentation
India · Work style not stated · Full time
Apply on the employer’s site ↗See how well you match this job
You apply directly with the employer. ROLIVA does not submit applications from this page and is not the employer.
About the role
Description from the employer’s posting. Check the employer’s page for the current version.
- EmployerZentiva
- LocationIndia
- Work styleWork style not stated
- Employment typeFull time
- Employer posted
Position Title: Executive QA Documentation
Qualifications & Experience
Educational Qualification
- 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 / Documentation
Skills & Competencies
- 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, organizational, and coordination skills
- Effective communication and cross-functional collaboration abilities
- Attention to detail and commitment to data integrity
Key Responsibilities
Review of Master Documents
- Review and maintain Master Batch Manufacturing Records and Master Batch Packing Records to ensure accuracy, regulatory compliance, and alignment with approved specifications and process related changes.
- Coordinate with Production, QC, and Regulatory Affairs for timely updates and approvals.
Show full description
Annual Product Quality Review (APQR)
- Prepare, compile, and review Annual Product Quality Reviews (APQRs) in line with regulatory expectations.
- Support identification of improvement opportunities and follow-up of CAPAs arising from APQR findings.
cGMP Training Coordination
- Coordinate and monitor cGMP and quality-related training programs for site personnel.
- Maintain trainingschedules, records, and effectiveness assessments.
Archival & Records Retention
- Manage the archival room and document storage systems for controlled and historical GMP documents.
- Ensure secure storage, easy retrieval, retention compliance, and protection against unauthorized access or damage.
- Support audits and inspections by ensuring availability of archived records.
Check your resume against this job Free, no sign-up. Nothing you paste is stored.
Staying safe while you apply
- Never pay to apply, interview or accept an offer. ROLIVA never asks you for payment to apply to a job.
- Apply only through the official “Apply on the employer’s site” button, on the employer’s own site, and check that a recruiter’s email uses that employer’s own domain rather than a free email address.
- Be cautious of an offer made with no real interview, or pressure to decide quickly or share financial details early.
Does something look wrong with this listing? Use “Report broken link” in the role details, or read ROLIVA’s full job-safety guidance ↗.
Preparing for this role with ROLIVA
- Check the fit.
Compare the requirements with the experience you have confirmed, including gaps.
- Prepare honestly.
Build interview stories and application drafts from your own evidence.
- Keep track.
Save the role and record your own application status and follow-ups.
At a glance
- Employment typeFull time
- Employer posted
- Added to ROLIVA
- Last checked