QC Chemical Compliance Supervisor

Pfizer (Indonesia)

Pfizer (Indonesia) (Jakarta)

Jakarta

DKI Jakarta, อินโดนีเซีย

Pfizer is a leading research-based biopharmaceutical company. We apply science and our global resources to deliver innovative therapies that extend and significantly improve lives. We make medicines and vaccines that help people when they are sick and prevent them from getting sick in the first place, as well as some of the world’s best-known consumer healthcare brands. For more than 150 years, Pfizer has worked to make a difference for all who rely on us. Every day, our colleagues work in developed and emerging markets to treat, cure and eradicate life-threatening conditions and challenge some of the most feared diseases of our time.

คลิกเพื่อดูงานที่คล้านกันในประเทศ อินโดนีเซีย:

ฝ่าย: การจัดการคุณภาพ

อุตสาหกรรม: การดูแลสุขภาพและการแพทย์ เภสัชกรรม

เกี่ยวกับตำแหน่งนี้

The QC Chemical Compliance Supervisor at Pfizer will be responsible for managing compendia compliance, laboratory documentation, and method validation/verification activities to ensure the quality of test results. This role involves overseeing daily activities, leading work teams, and driving team engagement within the Chemical Compliance Team.

หน้าที่รับผิดชอบ

• Manage multiple projects and ongoing work activities of within a work team and ensure agreed upon timelines are met.
• Coordinate and supervise daily activities of compendia compliance, laboratory documentation, 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.

คุณสมบัติ

• 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

• Master's degree (Nice-to-Have)
• Relevant pharmaceutical experience (Nice-to-Have)
• Knowledge of Laboratory Information Management System, Empower and Microsoft Office (Nice-to-Have)
• Working knowledge and understanding of requirements as it relates to method qualification and testing of components and finished products (Nice-to-Have)

สิทธิประโยชน์

Huneety A.I Salary Estimate

10,000,000 - 28,000,000 IDR per month