
Career Advancement Opportunities for Quality Professionals
4 days ago
Job Overview
Quality Assurance Specialist - Career Progression ProgramWe are seeking a Quality Assurance Specialist to join our team in Singapore. This is a 15-month training program that will provide participants with the requisite skills and experience to meet the anticipated hiring demand within the biopharmaceutical manufacturing sector.
The incumbent will be responsible for driving quality culture and promoting GMP compliant behaviors at the site. They will ensure site compliance to Pfizer Quality Standards (PQS) and ICH guidelines, and provide quality oversight to vendor management to ensure production materials used meet Pfizer Quality Standards (PQS).
Key Responsibilities:
- Review and approve GMP documentation to ensure their compliance with PQS.
- Qualify and manage vendors according to PQS and maintain accurate records of vendor status.
- Conduct internal audits to ensure internal controls are effective.
- Manage logistics for internal and external GMP inspections, including site communications and training.
- Maintain inspection readiness and support inspections from regulatory agencies and customers.
Requirements:
- Degree in Chemistry, Microbiology, Engineering or other Science related discipline.
- Minimum 1 year experience within the pharmaceutical industry.
- Strong written and oral communication skills.
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.
BenefitsThis comprehensive program is meticulously designed to provide participants with the requisite skills and experience to meet the anticipated hiring demand within the biopharmaceutical manufacturing sector. We invite eligible candidates to apply for this exceptional opportunity to advance their careers with one of the industry's leading organizations.
Program OverviewThis Career Progression Program (CCP) is aimed at cultivating the next generation of skilled professionals for Singapore's biopharmaceutical manufacturing industry. The program is open to Singapore Citizens or Singapore Permanent Residents who have no prior working experience in the biopharmaceutical sector and have graduated for at least 2 years prior to point of application.
Organizational RelationshipsThe incumbent will interact with all site departments for GMP related operations and activities e.g. Manufacturing Operations Process Teams, Quality Control, Supply Chain, Engineering, New Production Introduction and Technical Services teams as well as above site teams (e.g. PQS SMEs). For vendor management, inspection / regulatory related issues, this position will interact with quality or regulatory representatives from drug product sites, corporate groups or Global Chemistry Manufacturing & Compliance (GCMC) teams and material / GMP service vendors.
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