Deputy Manager - Quality Assurance Operations

Centrient Pharmaceuticals Netherlands; Dera Ghazi Khan Division; On-site; PKR 1,800,000 - 2,600,000; Full time

Job summary

Centrient Pharmaceuticals Netherlands is seeking an experienced QA Operations professional to review Batch Production Records, issue and review product labels, and oversee release of finished products. The role requires API experience and strong CAPA/Investigations capabilities.

The candidate will report to the Manager - QA Operations and will participate in audits, calibration activities, and site verification processes to ensure compliance with GMP and safety standards.

Qualifications

• MSc in Chemistry or M.Pharma required.
• Experience: 10–15 years with API exposure.
• Review and approval of Batch Production Records and investigations.

Responsibilities

• Review Batch Production Records and approve investigations.
• Release or reject finished products per approved specs.
• Verify QC test results and batch disposition, quarantine as needed.
• Release/Reject finished products as per specifications.
• Calibration & maintenance QA oversight.
• Perform cleaning verification during product changeovers.
• Verify reprocessing activities at the site.
• Handle sale returns.
• Comply with Safety, Health & Environment norms.
• Assign tasks as directed by supervisor.

Skills

QA Oversight

CAPA & Deviations

OOS/OOT Investigations

Batch Review & Release

QC Test Results Review

Calibration & Maintenance

GMP & Compliance

Safety & Environment

Education

MSc in Chemistry or M.Pharma

Job description

• 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.

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