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 assurance and control team. You will be responsible for analyzing chemical, biological or microbiological products to support our quality programs. Your contribution to environmental testing, utility monitoring, analytical testing, microbial identification and sterility 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. You will also be relied on for setting requirements for the transfer of methodology from R&D.

As a Scientist, your deep knowledge in the discipline, will make you an active team member who influences at the project team level. You will be using your scientific judgment to adapt standard methods and techniques by applying prior work experience and consulting others. Your ability to plan will help in preparing short-term work activities on projects. Your creativity in developing novel processes and new ideas will be used frequently. You will undertake mentoring activities to guide your team members.

It is your knowledge and skills that will help in making Pfizer ready to achieve new milestones and help patients across the globe.

How You Will Achieve It

• Contribute to achievement of goals at the work group/ project team level as a full team participant.
• Perform tasks associated with maintaining {Current} Good Manufacturing Practices {part of GxP} compliant Quality Control and Stability laboratories.
• Represent Quality Control in cross functional and site product meetings.
• Interpret data and make recommendations and reach decisions based on data and management input.
• Apply existing techniques and procedures, with recommendations, and implementation of modifications for improved efficiency, or devise and develop new microbiological Reporting issues to management and participating in issue resolution.
• Provide subject matter expertise for standard operating procedures and quality standards content, as well as providing gap analysis to ensure that the environmental monitoring program is compliant with all regulatory requirements.
• Support change controls, investigations and other technical documents.
• Participate in regulatory filing writing in sections related to analytical method and stability testing.
• Conduct and review non-conformance investigations related to aseptic manufacturing.

Qualifications

Must-Have

• Bachelor's Degree
•  3+ years' experience
• Demonstrated experience in industrial and/or aseptic pharmaceutical production environment, technical knowledge of aseptic processing and sanitization
• Demonstrated independent accomplishment of complex analytical method development and validation
• Ability to receive feedback and takes accountability for actions and personal development
• Excellent effective written and verbal communication and interpersonal skills
• Basic computer skills, such as data entry, with a high level of attention to detail, are also required

Nice-to-Have

• Master's degree and 2+ years of relevant experience
• Experience leading continuous improvement projects
• Experience defending laboratory practices in regulatory audit.

• Working knowledge of organic chemistry, including degradation mechanisms of pharmaceutical active ingredients and pharmaceutical products

Relocation assistance may be available based on business needs and/or eligibility.