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 recognized as a subject matter expert with specialized knowledge and skills in procedures, techniques, tools, materials and equipment. You will be entrusted with adapting standard methods and procedures by applying your knowledge, prior work experience and requirements. Your business awareness of cross-organizational impact on project delivery will elevate the quality of project deliverables. You will arrive at decisions on which methods and procedures are the best fit for different work situations.

You will train others and reinforce behaviors that will help us achieve our goal of providing the best healthcare to our patients.

How You Will Achieve It

• Perform Microbiological testing of raw material, products, stability samples, in accordance with approved procedures and test methods, and record the test results in timely manner.
• Assist QC Microbiology Lab and Packaging Material Supervisor or QC Manager in laboratory investigation in case of out of specification.
• Participating in media fill, validation, and qualification program
• Perform instrument verification or calibration according to approved procedures and schedule
• Monitor that all required equipment, reagents, reference standard are always available in adequate quantity and utilized in accordance with procedures.
• Ensure all reagents, media, reference cultures, reference standards, bio-indicator are valid and stored according to requirement
• Perform microbiological method validation/ verification in accordance with the approved protocol and provide report.
• Develop or revise SOP or test procedures in Microbiology Lab.
• Perform maintenance of reference working culture in accordance to the approved procedures.
• Maintain Microbiology lab area and facilities in a clean, orderly and operational state
• Support QC Microbiology Lab and Packaging Material Supervisor or QC Manager for developing method validation/ verification protocol, study protocol, and equipment/ instrument qualification protocol.
• Ensure compliant and timely documentation and resolution of events.
• Develop working process to enhance Good Manufacturing Practices {also cGMP} standards for the team.
• Maintain a high level of personal safety and housekeeping considerations.
• Identify Continuous Improvement opportunities and participates in Continuous Improvement projects.
• Author /review QC (Quality Control) documentation and document all results in accordance to Good Manufacturing Practices and Good Laboratory Practices requirements.
• Provide training for team members and perform peer reviews of data and logbooks.

Qualifications

Must-Have

• High School Diploma or GED
• 6+ years’ experience
• Certification in assigned area, if applicable
• Ability to write clear technical document.
• Good organizational and time management skills
• Good oral and written communication skills
• Good Microsoft Office skills

Nice-to-Have

• Bachelor's Degree
• Pharmaceutical, quality control, and stability experience
• Effective problem solving skills

Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.