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PHARMA JOBS POST > announcement > Tagoor Laboratories Hiring for Head – Quality Control (Unit-III) | Apply Now
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Tagoor Laboratories Hiring for Head – Quality Control (Unit-III) | Apply Now

RAJLAXMI
Last updated: November 20, 2025 9:00 am
RAJLAXMI 11 months ago
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Tagoor Laboratories, a rapidly expanding pharmaceutical company specializing in APIs, Intermediates, and KSMs, has announced a major job opening for the position of Head – Quality Control (Unit-III). This role is based at their Unit-III facility in Visakhapatnam and is an excellent opportunity for an experienced QC professional to lead critical lab operations and ensure high standards of product quality and regulatory compliance.

Contents
About the OpportunityKey ResponsibilitiesWho Can Apply?How to Apply

About the Opportunity

The selected candidate will be responsible for overseeing all Quality Control functions across Raw Materials, Intermediates, APIs, and Finished Products. Tagoor Laboratories is looking for a dynamic leader who can drive excellence, maintain compliance, and strengthen the QC team through effective guidance and supervision.

Key Responsibilities

•The Head – QC (Unit-III) will handle a wide range of responsibilities, including:
•Managing QC operations for RM, Intermediates, APIs, and Finished Products.
•Ensuring timely sample testing and batch release.
•Supervising Wet Lab, Microbiology Lab, and Instrumentation Lab.
•Approving SOPs, STPs, COAs, and various product specifications.
•Maintaining and calibrating instruments like HPLC, GC, UV, IR, KF.
•Handling OOS, OOT, deviations, and implementing CAPA.
•Ensuring adherence to cGMP, GLP, and Data Integrity standards.
•Supporting regulatory audits and customer audits.
•Guiding and training the QC team to achieve exceptional performance.
•Coordinating with QA, R&D, Production, and Plant teams for smooth operations.

Who Can Apply?

•Tagoor Laboratories is seeking candidates who meet the following criteria:

•Educational Qualification: M.Sc Chemistry / M.Pharm / B.Tech Chemical Engineering.

•Experience: 12–20 years in Pharmaceutical API or Bulk Drug Quality Control.

•Strong hands-on expertise in HPLC, GC, UV, IR, KF, and other analytical instruments.

•Proven experience managing regulatory and customer audits (cGMP, GLP, Data Integrity).

•Strong analytical skills in OOS/OOT investigations and compliance documentation.

•Excellent communication, leadership, and team management capabilities.

How to Apply

Interested and eligible candidates can send their updated resume to:

📧 Email: career@tagoor.com
📌 Subject Line: Application – Head Quality Control

For more details, visit: www.tagoorlabs.com

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