Deputy Manager - Quality Assurance Operations

Centrient Pharmaceuticals; Balachaur; On-site; INR 2,500,000 - 4,000,000; Full time

Job summary

Centrient Pharmaceuticals is seeking a seasoned QA Operations professional to oversee batch records reviews, product release decisions, and CAPA management in a high‑volume API environment.

You will supervise QMS activities, investigate deviations, and ensure QC test results align with specifications while maintaining strict safety, health, and environmental standards. This role reports to the Manager - QA Operations.

Qualifications

• Education: M.Sc. in Chemistry or M.Pharma.
• Experience: 10–15 years in QA Operations with API exposure.
• Candidate should have API experience.

Responsibilities

• Handing & tracking of QMS related activities CAPA, Deviations, Customer Complaints. OOS/OOT, Investigations
• Ensure timely review of Batch Production record, Review & approval of investigation, verification of CAPAs, review of QC test results, batch disposition quarantine, rejections approval
• Release/Rejection of finished products as per approved specifications
• Calibration & Maintenance QA oversight
• To perform cleaning verification during product change over and dispatch verification of finished as per established procedures
• Verification of reprocessing activities in the site
• Handling of Sale Returns
• Complying to the laid down norms of Safety Health & Enviroment
• Any job assigned time to time by superior based upon training on the procedure

Skills

Working with People

Relating & New working

Adhering to principles & Values

Adapting & responding to changes

Coping with Pressure & Setbacks

Achieving Personal work Goals & Obectv

Audits exposure

Education

M.Sc. in Chemistry/M.Pharma

Job description

• The Role is responsible for reviewing the Batch Production Record, Issuance and Reviewing the Product Labels

• The Role is responsible for reviewing the Batch Production Record, Issuance and Reviewing the Product Labels

Release of finished products, Verification activities of finished goods at the sites.

Key Individual Accountabilities

• Handing & tracking of QMS related activities CAPA, Deviations, Customer Complaints. OOS/OOT, Investigations
• Ensure timely review of Batch Production record, Review & approval of investigation, verification of CAPAs, review of QC test results, batch disposition quarantine, rejections approval
• Release/Rejection of finished products as per approved specifications
• Calibration & Maintenance QA oversight
• To perform cleaning verification during product change over and dispatch verification of finished as per established procedures
• Verification of reprocessing activities in the site
• Handling of Sale Returns
• Complying to the laid down norms of Safety Health & Enviroment
• Any job assigned time to time by superior based upon training on the procedure

Requirements

Required Competencies:

• Working with People
• Relating & New working
• Adhering to principles & Values
• Adapting & responding to changes
• Coping with Pressure & Setbacks
• Achieving Personal work Goals & Objectives
• Have the Exposure of Audits.

Education :

M.Sc. in Chemistry/ M.Pharma

Experience: 10 to 15 years. (Candidate should have API Experience)

Reporting: Manager - QA Operations