Job Description
The Manufacturing Science and Technologies team plays a critical role in Pfizer's product lifecycle. We oversee major process changes, provide technology and manufacturing support for products from R&D delivery to launch and throughout their lifecycle.
This includes assisting with new technologies, scale‑up, troubleshooting, and process and cleaning validation.
The MSAT – Analytical Manager has overall responsibility for the analytical chemistry aspects of technology transfer of PGS and Pfizer products from across all phases of development and through commercialization.
In this position, you will be both hands‑on in the laboratory and lead the Analytical team through all phases of projects including analytical method development and validation, formulation development, process development and validation, cleaning validation, regulatory submission, technology transfer and commercialization.
You will play a critical role optimizing the supply of world‑class, life‑saving medicines to our patients by leading cross‑functional collaborations to build a culture of understanding, belief and a commitment to excellence;
* Optimize Supply Chain by leading cross-functional teams to ensure timely decisions that are consistent with the site's goals, priorities and the Pfizer Blueprint;
* Cultivate Culture of Excellence by developing a strong culture of Recognition, Inclusivity, Equity and Diversity;
* Foster Continuous Improvement by simplifying processes, removing roadblocks and empowering continuous improvement;
* Lead Cross-Functional Teams to build trust, Joy, excitement and knowledge.
Required Skills and Qualifications
Bachelor's or higher degree in Chemistry, Pharmacy or related field combined with at least 5 years' experience within the pharmaceutical or allied industry.
Specialist technical skills and experience in pharmaceutical manufacturing, technology transfer, formulation development and process development.
Expertise in analytical method development and validation.
Knowledge and application of Good Manufacturing Practice and experience in dealing with Regulatory Authorities and Auditors.
Demonstrated Project Management skills with the ability to set, manage and deliver cross-functional milestones on time.
Demonstrated management experience with a track record of establishing and/or leading effective teams that have contributed to organizational outcomes.
Results-focused with demonstrated ability to meet business targets and objectives with strong customer focus.
Exceptional communication, negotiation, interpersonal & leadership skills (verbal and written).
Demonstrated ability to work under pressure and to agree on timelines with high attention to detail.
Experience within Manufacturing, Process Validation or Quality departments preferred.
Benefits
This role offers opportunities for professional growth and development.
You will work with a talented and dedicated team to make a meaningful impact on global health.
The successful candidate will have access to training and development programs to enhance their skills and career progression.
Others
The job requires the ability to work particular hours (shift, overtime) and adhere to safe work practices and procedures such as aseptic gowning.
Potential for early / late teleconferences outside of standard working hours.
Some travel may be required.