🚀 Role Highlight: Team Leader – Quality Control (CQA) at Cipla Ltd., Goa

If you're an experienced QC professional looking to lead analytical excellence at a global pharmaceutical company, this is one for you.

🏢 Why This Role Stands Out

• Industry Leader: Cipla is among India's premier pharma giants, posting strong demand across Quality Assurance, Production, Engineering, and Data Science roles nationwide (e.g., 2025 global hiring story at Naukri) (careers.cipla.com, recruitind.com).

• Strategic Location: Based in Cipla’s Verna, Goa site, a flagship hub for tablets and respiratory products.

🔍 Job Summary

Aspect	Description
Job Title	Team Leader – Quality Control (CQA Division)
Location	Goa (Cipla Verna site)
Req. ID	94172
Posting Date	July 16, 2025
Mode	Permanent, Full-Time

Primary Purpose: Lead the QC & CQA team in interpreting pharmacopoeial updates, validating analytical methods, and coordinating with suppliers and site functions to enforce cipla's global quality systems (recruitind.com, careers.cipla.com).

Key Responsibilities:

• Pioneer implementation of updated pharmacopoeial standards across Indian and export markets.

• Oversee method improvement, verification, and molecule retention discussions.

• Manage CAPA systems, handle deviations, and interface with purchase, regulatory affairs, and vendor engineering teams.

• Act as the Cochair for internal competence groups such as Pharmacopeia Forum (careers.cipla.com).

Ideal Candidate Profile:

• Education: B.Sc. or M.Sc. in Chemistry or allied field (GPAT/NET advantage).

• Experience: 8–10 years in pharma QC/CQA area with exposure to multiple regulatory environments (e.g., US FDA, WHO, UK-MHRA).

• Skillset: Proficiency in method validation/transfer, deviation & CAPA governance, managing audits, and familiarity with SAP‑based QC workflows (careers.cipla.com, careers.cipla.com).

✒️ Sample Blog Intro

“Leading Quality Control at the forefront of pharmaceutical innovation can define product success. As a QC team leader at Cipla, you’ll influence quality systems not just for Goa but for global exports.”

🎯 Why Apply for This Job?

Feature	Benefit
High-impact Quality Leadership	Strategize and influence QC systems across functions and markets.
Regulatory Exposure	Engage with US/EU/Indian pharmacopoeia and manage cross-site compliance.
Cross-functional Leadership	Work closely with Manufacturing, Regulatory Affairs, and Facilities to deliver analytical excellence.
Scope for Innovation	Champion continuous improvements through data-driven quality decisions.

📝 How to Apply

🔗 Click here to apply on Cipla’s official career portal

To access the role:

1. Visit the URL above, or open [Cipla Careers → Search Job ID 94172].

2. Use either “Apply with LinkedIn” or manual resume upload.

3. Recommended: also bring supporting documents when a call is triggered.

🛠️ Preparation Tips

1. Highlight your analytical mastery: Showcase successful method validations or CAPA closures with impact metrics (e.g., audit findings mitigated).

2. Key pharmacopeia familiarity: Be comfortable discussing updates like Gen III USP/Chemical methods or British Pharm tables and how you’ve implemented them.

3. Demonstrate leadership: Show evidence where you led QC/Micro/AQ teams during regulatory inspections or streamlined reporting systems.

4. Soft skills matter: The ability to communicate deftly with technical and commercial stakeholders is a big win at this level.

🧾 In Summary

This Team Leader – QC (CQA) role at Cipla, Goa is a rare opportunity to step into a strategic quality leadership position within a globally respected, regulated pharmaceutical environment. With ample cross-functional interaction, real exposure to pharmacopoeial strategy, and a need for strong technical leadership, it’s a great fit for mid‑senior QC professionals aiming to take the next big leap in their pharma career.

🔹 Interested in interview or resume support for this QC leadership role? I’d be happy to help!