Associate Manager - MSAT Tech Transfer

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
  
  

• 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.
• Knowledge of validation and practices related to the manufacturing process
• 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
  
  

• 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