Clinical Quality Assurance Careers and Pharmaceutical Operations Consultant Openings
Zentiva, a leading European pharmaceutical company and Great Place to Work Certified employer, is conducting a walk-in interview for multiple openings in Quality Assurance and Quality Operations. The hiring drive is for professionals seeking pharma compliance and operational excellence roles, with work opportunities connected to Zentiva’s global affiliates. The walk-in interview will be held in Vadodara, Gujarat, offering excellent long-term career growth in the pharmaceutical quality domain.
Zentiva Hiring for below positions
1) Department: Quality Assurance / Operations
Designation: Quality Complaints Specialist
Experience: Quality Assurance/Operations Jr level: 2 to 5 years
Qualification: Bachelors or Masters in Pharmacy / Life Sciences or MSc. Pharmaceutical Chemistry
Key skill or job description: GMP/GDP & GxP expertise, QMS, Document Validation, Deviation, Investigations, Complaint & CAPA Mgmt., Quality System Mgmt & SOP creation (eDMS), Dossier Writing & Review, Batch release & product quality Mgmt, CoA/CoC review, temperature data checks, APQR handling, Transport Validation, Digital Quality Systems: Quality Forward, eDMS, SAP/Fiori, Audit & inspection readiness, Cross functional collaboration (RA, Supply Chain, CMOs), Excellent Communication & MS Excel
2) Department: Quality Assurance / Operations
Designation: Junior Quality Manager – Operations
Experience: Quality Assurance/Operations Jr level: 2 to 5 years
Qualification: Bachelors or Masters in Pharmacy / Life Sciences or MSc. Pharmaceutical Chemistry
Key skill or job description: GMP/GDP & GxP expertise, QMS, Document Validation, Deviation, Investigations, Complaint & CAPA Mgmt., Quality System Mgmt & SOP creation (eDMS), Dossier Writing & Review, Batch release & product quality Mgmt, CoA/CoC review, temperature data checks, APQR handling, Transport Validation, Digital Quality Systems: Quality Forward, eDMS, SAP/Fiori, Audit & inspection readiness, Cross functional collaboration (RA, Supply Chain, CMOs), Excellent Communication & MS Excel
3) Department: Quality Assurance / Operations
Designation: Transport Validation Specialist
Experience: Quality Assurance/Operations Jr level: 2 to 5 years
Qualification: Bachelors or Masters in Pharmacy / Life Sciences or MSc. Pharmaceutical Chemistry
Key skill or job description: GMP/GDP & GxP expertise, QMS, Document Validation, Deviation, Investigations, Complaint & CAPA Mgmt., Quality System Mgmt & SOP creation (eDMS), Dossier Writing & Review, Batch release & product quality Mgmt, CoA/CoC review, temperature data checks, APQR handling, Transport Validation, Digital Quality Systems: Quality Forward, eDMS, SAP/Fiori, Audit & inspection readiness, Cross functional collaboration (RA, Supply Chain, CMOs), Excellent Communication & MS Excel
4) Department: Quality Assurance / Operations
Designation: Commercial Operations Specialist
Experience: Quality Assurance/Operations Jr level: 2 to 5 years
Qualification: Bachelors or Masters in Pharmacy / Life Sciences or MSc. Pharmaceutical Chemistry
Key skill or job description: GMP/GDP & GxP expertise, QMS, Document Validation, Deviation, Investigations, Complaint & CAPA Mgmt., Quality System Mgmt & SOP creation (eDMS), Dossier Writing & Review, Batch release & product quality Mgmt, CoA/CoC review, temperature data checks, APQR handling, Transport Validation, Digital Quality Systems: Quality Forward, eDMS, SAP/Fiori, Audit & inspection readiness, Cross functional collaboration (RA, Supply Chain, CMOs), Excellent Communication & MS Excel
5) Department: Quality Assurance / Operations
Designation: QMS Expert
Experience: Quality Assurance/Operations Jr level: 2 to 5 years
Qualification: Bachelors or Masters in Pharmacy / Life Sciences or MSc. Pharmaceutical Chemistry
Key skill or job description: GMP/GDP & GxP expertise, QMS, Document Validation, Deviation, Investigations, Complaint & CAPA Mgmt., Quality System Mgmt & SOP creation (eDMS), Dossier Writing & Review, Batch release & product quality Mgmt, CoA/CoC review, temperature data checks, APQR handling, Transport Validation, Digital Quality Systems: Quality Forward, eDMS, SAP/Fiori, Audit & inspection readiness, Cross functional collaboration (RA, Supply Chain, CMOs), Excellent Communication & MS Excel
6) Department: Quality Assurance / Operations
Designation: PQR – Quality Operations Specialist (A. Quality Operations Specialist, B. Sr. Quality Operations Specialist, C. Manager Quality Operations)
Experience: Junior level: 2 to 5 years | Mid-level: 5 to 8 years | Managerial/Senior level: 12+ years
Qualification: Bachelors or Masters in Pharmacy / Life Sciences or MSc. Pharmaceutical Chemistry
Key skill or job description: GMP/GDP & GxP expertise, QMS, Document Validation, Deviation, Investigations, Complaint & CAPA Mgmt., Quality System Mgmt & SOP creation (eDMS), Dossier Writing & Review, Batch release & product quality Mgmt, CoA/CoC review, temperature data checks, APQR handling, Transport Validation, Digital Quality Systems: Quality Forward, eDMS, SAP/Fiori, Audit & inspection readiness, Cross functional collaboration (RA, Supply Chain, CMOs), Excellent Communication & MS Excel
Who Can Apply
- Candidates holding a Bachelor’s or Master’s degree in Pharmacy, Life Sciences, or M.Sc. Pharmaceutical Chemistry can apply.
- Applicants must have relevant pharmaceutical Quality Assurance or Quality Operations experience in regulated environments.
- Professionals with expertise in GMP, GDP, GxP compliance, QMS, CAPA, audit readiness, and digital quality systems are strongly encouraged to apply.
Career Growth at Zentiva
- Zentiva offers exceptional career opportunities for pharmaceutical professionals seeking global exposure in quality systems and operational excellence.
- Employees benefit from hybrid working models, international collaboration with global affiliates, and advanced digital platforms such as SAP, eDMS, and Quality Forward.
- The company supports continuous professional development, regulatory compliance training, and structured career progression in a certified high-performance workplace.
Walk-In Interview Details:
Date: 24th May 2026, Sunday
Time: 10:00 AM Onwards
Work Location / Interview Venue: The Fern, Behind Dinesh Mill Pvt. Ltd., Akota, Vadodara, Gujarat – 390020
Mention your target designation and experience bracket in the email subject line.
Send your CV to the official recruitment email ID: ank_recruitment@zentiva.com
Frequently Asked Questions
1. What is the work model offered for these positions?
These roles operate in a hybrid working model with collaboration across Zentiva’s global affiliate network.
2. Where is the walk-in interview being conducted?
The walk-in interview will take place at The Fern, Behind Dinesh Mill Pvt. Ltd., Akota, Vadodara, Gujarat.
3. What experience levels are eligible for these openings?
Junior-level candidates with 2–5 years, mid-level professionals with 5–8 years, and senior managers with 12+ years can apply depending on the role.
4. Can candidates apply online if unable to attend the walk-in interview?
Yes, applicants can send their updated CV to the official recruitment email provided.
5. What technical skills are preferred for these positions?
Experience in GMP/GDP/GxP, QMS, CAPA, validation, audits, SAP, eDMS, and pharmaceutical compliance systems is highly preferred.
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| Zentiva Walk-In Interview for Quality Assurance and Operations Jobs in Vadodara |
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