Zydus Takeda Healthcare Private Limited, a 50:50 joint venture between Zydus Lifesciences Limited and Takeda Pharmaceutical Company Limited, is hosting a walk-in interview for Quality Assurance (QA) roles at its state-of-the-art API manufacturing facility in Navi Mumbai.
Established in 1999, Zydus Takeda is a 100% export-oriented unit with USFDA and EDQM approvals, specializing in APIs and intermediates for global markets (Europe, Japan, Brazil, Korea). The company, rated 4.1/5 for work culture on AmbitionBox (46+ reviews), employs 200+ professionals and is celebrated for its 25-year legacy of quality and innovation.
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Event Details
- Date: 17th May 2025 (Saturday)
- Time: 9:00 AM – 3:00 PM
- Venue: Zydus Takeda Healthcare Pvt. Ltd., C-4, MIDC, TTC Industrial Area, Village Pawne, Thane-Belapur Road, Vashi, Navi Mumbai – 400703, Maharashtra, India
- Job Location: Navi Mumbai, Maharashtra
- Contact: Not provided; email hr.zydustakeda@zyduslife.com for queries or to share resumes (outstation candidates).
- Note: Candidates with API/Bulk Drug experience preferred. Male candidates may be prioritized due to shift-based roles.
Job Opportunity: Quality Assurance (Sr. Executive & Executive)
- Designation: Senior Executive / Executive – Quality Assurance
- Experience: 3–7 years in Quality Assurance (API/Bulk Drug manufacturing preferred)
- Qualification: B.Pharm, M.Pharm, M.Sc. (Chemistry, Biotechnology, Microbiology)
- Salary: ₹5.0–9.0 Lakhs/year (estimated, Navi Mumbai, based on AmbitionBox and Glassdoor data for similar roles)
Required Skills:
- Hands-on experience in IPQA (In-Process Quality Assurance) for API manufacturing.
- Expertise in QMS (Quality Management Systems): Change control, deviations, CAPA, OOS, investigations.
- Knowledge of validation/qualification: Equipment, process, and cleaning validation.
- Familiarity with cGMP , 21 CFR Part 11, and GDP.
- Proficiency in reviewing BMR/BPR and audit documentation.
- Experience with regulatory audits (USFDA, EDQM) and tools like Trackwise, LIMS, or SAP.
Responsibilities:
- Conduct IPQA checks during API production to ensure compliance with cGMP.
- Manage QMS activities: Handle deviations, CAPA, change controls, and OOS investigations.
- Perform validation/qualification of equipment, processes, and cleaning procedures.
- Review batch records (BMR/BPR) and ensure data integrity.
- Support USFDA/EDQM audits and prepare audit responses.
- Coordinate with production, QC, and regulatory teams for compliance.
Preferences:
- Experience in API/Bulk Drug plants with USFDA/EDQM approvals.
- Knowledge of SAP SuccessFactors or Bloom (Zydus Takeda’s learning platforms).
- Familiarity with digital automation tools and audit trails.
Why Join Zydus Takeda Healthcare?
- Work in a USFDA/EDQM-approved, 25,000 sq.m. API facility with a 25-year legacy.
- Contribute to a 100% export-oriented unit supplying APIs to Europe, Japan, Brazil, and Korea.
- Rated 4.0/5 for work-life balance and 3.9/5 for job security (AmbitionBox, 70+ reviews).
- Access skill enhancement programs (Quality Culture Lab, safety campaigns) and global systems like SAP SuccessFactors.
- Join a team of 200+ professionals with awards like the National Award for Excellence in Cost Management (2018, 2019).
- Career growth in a patient-centric, innovation-driven JV between Zydus and Takeda.
How to Prepare and Attend
- Documents to Carry:
- Updated CV (highlighting API QA experience, QMS, and audit exposure).
- Academic mark sheets (B.Pharm, M.Pharm, M.Sc.).
- Experience certificates (mandatory for 3+ years).
- Last 3 months’ payslips and bank statement.
- Aadhaar, PAN copies.
- 2 passport-size photographs.
- Outstation Candidates: Email CV to hr.zydustakeda@zyduslife.com with subject “QA Executive/Sr. Executive – Navi Mumbai Walk-In 17 May 2025.”
- Preparation Tips:
- Technical Knowledge: Study ICH Q7, cGMP, and 21 CFR Part 11. Be ready for questions like: “How do you handle an OOS investigation?” or “Explain the CAPA process for a deviation.”
- Audit Readiness: Prepare for scenarios on USFDA/EDQM audit observations. Example: “How do you ensure data integrity in BMR?”
- QMS Tools: Highlight experience with Trackwise, LIMS, or SAP. Review change control and deviation workflows.
- General: Brush up on validation protocols (DQ, IQ, OQ, PQ) and GDP. Marathi or Hindi proficiency is a plus.
- Interview Process:
- Venue Access: The facility is 3 km from Vashi Railway Station (10 min by cab). Arrive by 8:30 AM to avoid queues. Parking is limited; use public transport if possible.

Important Notes
- Eligibility: Candidates with 3–7 years of API QA experience preferred. Freshers are unlikely to qualify unless specified.
- Fraud Alert: Zydus Takeda does not charge fees for recruitment. Verify communications via @zyduslife.com or @takeda.com emails. Report suspicious activity to hr.zydustakeda@zyduslife.com or Bhagyesh.r@zyduslife.com. All offer letters include a QR code for authenticity.
- Previous Applicants: Candidates interviewed in the last 6 months at Zydus Takeda should not reapply.
- Work Environment: Roles involve desk-based work with occasional international travel for audits or training. Expect rotational shifts in a cGMP-compliant facility.
About Zydus Takeda Healthcare
Founded in 1999, Zydus Takeda Healthcare Pvt. Ltd. is a Navi Mumbai-based joint venture between Zydus Lifesciences (India) and Takeda Pharmaceuticals (Japan). Spanning 25,000 sq.m., its Vashi plant is a 100% export-oriented unit producing APIs and intermediates for Takeda’s global markets.
With a workforce of 200+, the company has won the National Award for Excellence in Cost Management (2018, 2019) and is committed to sustainability (renewable energy, net-zero goals) and digital automation. Zydus Takeda’s focus on patient-centricity, quality, and innovation makes it a strategic site within Takeda’s network.
Join Zydus Takeda’s Mission
Join Zydus Takeda Healthcare’s mission to deliver “Better Health for People, Brighter Future for the World” through high-quality APIs! Attend the walk-in interview on 17th May 2025 in Navi Mumbai and grow with a global leader in pharmaceutical manufacturing!
Dear sir,
I am shubham kate,
Sir I have upto 3 year experience in QA department.
Sir recently I see ad about QA department opening but I can’t come to walk in because I am currently working in marksans pharma.
And goa to Navi Mumbai is a long distance so can you arrange my interview shedule offline or as possible online/telephonic.
Pls check once my CV.
Please whatsapp me