Why Patients Need You
Everything we do, every day, is in line with an unwavering commitment to the quality and the delivery of safe and effective products to patients. Our science and risk-based compliant quality culture is flexible, innovative, and customer oriented. Whether you are involved in development, maintenance, compliance or analysis through research programs, your contribution will directly impact patients.
What You Will Achieve
The incumbent is a member of the Quality Assurance team. Under the supervision of the Senior QA Manager / Lead QA Specialist, the incumbent will be responsible for the following:
- Drive quality culture and promote GMP compliance behaviours to the site.
- Provide QA oversight to the site GMP operations to ensure products produced in compliance with the Pfizer Quality Standards (PQS) and ICH guidelines
- Collaborate with cross functional teams to improve quality systems.
- Understand regulatory expectations and support site inspection readiness.
- Work with supply chain and drug product sites to ensure timely delivery of quality products.
- Work with GCMC to file products and address regulatory queries in an accurate and timely manner.
How You Will Achieve It
Responsibilities:
- Responsible to review and approve master batch records and subsequent batch records associated with the manufacturing, packaging and labeling of intermediates and active pharmaceutical ingredients (API) to ensure batches produced are in compliance with Pfizer quality standards and regulatory registered specifications.
- Review QC lab worksheets for intermediates, APIs and cleaning samples.
- Disposition of the intermediates and active pharmaceutical ingredients (API), including re-evaluation.
- Review and approve cleaning records and procedures and ensure compliance with the Pfizer Quality Standards (PQS) and guidelines.
- Support production startup activities including new product introduction (NPI), changeover activities, equipment releases, module clearance etc.
- Tank farm monitoring and QA oversight of the solvent recovery processes.
- Review and approve GMP documentation and ensure their compliance to Pfizer Quality Standards (PQS).
- Ensure adherence to quality procedures, regulatory requirements and cGMPs.
- Act as label administrator and manage Category 1 manual labels according to stipulated procedure.
- Write deviations according to the site procedures. Ensure issues are escalated according to the Pfizer Quality Standards (PQS).
- Coordinate with cross-functional team to prepare Annual Product Record Review, discuss trends and atypical observations and recommend improvement actions.
- Support and facilitate product return process.
- Support internal audits to ensure the internal controls are effective.
- Maintain inspection readiness and support inspections from regulatory agencies and customers. Actively participate in GMP walkdowns to ensure site operation and facility maintained in inspection ready state.
- Support the maintenance of validated stated of GMP systems and processes.
- Support regulatory queries in a timely manner, eg regulatory COA issuance.
- QA oversight of site processes and systems e.g. pest control program, warehouse and engineering (calibration and preventive maintenance).
- Continuous improvement on quality processes and practices on site .
- Any other tasks as assigned by manager.
Organizational Relationships:
The incumbent will interact with all site departments for GMP related operations and activities i.e. Manufacturing Operations Process Teams, Quality Control, Warehouse and Tank Farm teams and Engineering teams. In the event of quality or regulatory related issues, this position will interact with quality or regulatory representatives from drug product sites or Global Chemistry Manufacturing & Compliance (GCMC) teams.
Qualifications:
Bachelor Degree/Diploma in Science/Chemical Engineering or equivalent.
Experience:
A minimum of 1 year experience in pharmaceutical industry or related industry. Fresh graduate will still be considered.
Diploma in Pharmaceutical or Chemical Engineering with a minimum of 5 years experience in Quality Assurance role within the pharmaceutical industry
Work Location Assignment: On Premise
Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.
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What We Do
Our purpose ensures that patients remain at the center of all we do. We live our purpose by sourcing the best science in the world; partnering with others in the healthcare system to improve access to our medicines; using digital technologies to enhance our drug discovery and development, as well as patient outcomes; and leading the conversation to advocate for pro-innovation/pro-patient policies.
Why Work With Us
We are the inventors, the problem solvers, the big thinkers — those who surmount any hurdle to deliver breakthrough medicines to the people who are counting on them the most.
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