QC Chemical Compliance Supervisor Apply locations Indonesia - Jakarta Time type: Full time Posted on: Posted 5 Days Ago Job requisition id: 4916941 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, your contribution will directly impact patients. What You Will Achieve You will be a member of Pfizer's dedicated and highly effective quality control team. You will be responsible for managing compendia compliance, laboratory documentation (including registration dossier related to laboratory document) and method validation/verification activities, which will help Pfizer provide safe drugs to patients. Your understanding of testing methods and instruments will help us meet specifications against established standards. You will also be relied on for setting requirements for the transfer of methodology to routine operation. As a Team lead, you will be involved in leading work teams within your division, including the technical and financial resources of the team. Thanks to your technical skills, you will coach your direct reports on day-to-day activities. You will be relied on to solve complex problems within your area of expertise. It is your hard work and commitment that will make Pfizer ready to achieve new milestones and help patients across the globe. How You Will Achieve It Manage multiple projects and ongoing work activities within a work team and ensure agreed upon timelines are met. Coordinate and supervise daily activities of compendia compliance, laboratory documentation (including registration dossier related to laboratory document) and method validation/verification in Chemical Laboratory to ensure quality of the test results. Oversee and review/approve investigations, CAPA (Corrective Action and Preventive Action) and change controls. Manage review and approval of Good Manufacturing Practices (also cGMP) documentation, such as procedures, data and reports. Drive team engagement, effective communication, and the development of direct reports within the Chemical Compliance Team. Qualifications Must-Have Bachelor's Degree 3+ years' experience Laboratory supervisory experience Knowledge of Good Manufacturing Practices (also cGMP) compliance requirements for Quality Control Laboratories, including pharmacopeia requirement Experience with leading colleagues and/or projects Strong people management experience Demonstrated skills in collaboration, attention to detail, and communication skills Ability to handle complex and detailed situations with a focus on quality Nice-to-Have Master's degree Relevant pharmaceutical experience Knowledge of Laboratory Information Management System, Empower and Microsoft Office Working knowledge and understanding of requirements as it relates to method qualification and testing of components and finished products 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. Quality Assurance and Control #LI-PFE
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