Baru Chemical Laboratory Spv

Job Description

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 You will be a member of Pfizer’s dedicated and highly effective quality control team. You will be responsible for analyzing chemical products to support our quality programs. Your contribution to analytical testing will help Pfizer provide safe drugs to patients. Your understanding of Quality Control instruments will help us meet their accuracy specifications against established standards. 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

• Coordinate and supervise daily activities of stability and finished goods testing in Chemical Laboratory to ensure quality of the test results.
• Organize and ensure that testing of bulk blends, finished goods, validation samples, and stability samples are performed in accordance with approved test method and ensure on time testing completion.
• Prepare Laboratory investigation in case of out of specification/questionable result.
• Maintain and ensure compliance in Quality and Safety.
• Ensure that all required equipment, reagents, reference standard are always available in adequate quantity, correct storage, correctly utilized, and its validity

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
• 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

• Pharmacist or 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

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