This job is with Pfizer, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community. Please do not contact the recruiter directly.
Use Your Power for Purpose
As a Senior Associate, you will play a crucial role in improving patients' lives while working at Pfizer. Your contributions will directly impact the development and delivery of innovative solutions that enhance the quality of life for patients worldwide. Join us in our mission to bring breakthroughs that change patients' lives.
What You Will Achieve
In this role, you will :
Handle Technology Transfer activities & New Product Introduction process
Knowledge of validation and practices related to the manufacturing process, analytical method, cleaning methods, facility, equipment, instrument, utility system, and CSV systems.
Conversant with design & working principles of upstream equipment used in sterile manufacturing -solution preparation, vial washing, heat tunnel, homogenizers, filling machines, filter integrity testing devices autoclave and cleaning validations.
Well versed with Manufacturing process - design, execution, and review.
Understanding of pharmaceutical manufacturing, quality assurance, and quality control operations.
Knowledge in parenteral formulation development like liquid / dry powder and lyophilized formulations
Experience in plant and TS operations
Good document written skills, with ability to identify issues and recommend actions.
Good grasping power of technical matters
Here Is What You Need
(Minimum Requirements)
6+ years of experience in tech transfer activities and / or validation function with any degree of
B.Pharm / M.Pharm / M.S (Pharmacy) / M.Sc / BE.
Must have an experience
of sterile dosage form facility / Formulation Development / Product Development / Process Development / manufacturing of Injectable formulations to cater regulated market, essentially experience in Plant Technology Transfer support in Injections.
Strong technical skills in process development and optimization
Proficiency in data analysis and interpretation
Experience with project management tools and methodologies
Knowledge of regulatory requirements and compliance standards
Ability to work collaboratively in a team environment
Strong communication skills, both written and verbal
Proficiency in Microsoft Office Suite
Bonus Points If You Have
(Preferred Requirements)
Experience in the pharmaceutical or biotechnology industry
Familiarity with Good Manufacturing Practices (GMP)
Experience with statistical software (e.g., Minitab, JMP)
Ability to lead cross-functional teams
Strong organizational skills
Adaptability and flexibility in a dynamic work environment
Ability to mentor and develop junior team members
Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.
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