Associate - MSAT

Use Your Power for Purpose

Whether you are involved in the design and development of manufacturing processes for products or supporting maintenance and reliability, engineering is crucial to ensuring customers and patients receive the medicines they need, precisely when they need them. By collaborating with our forward-thinking engineering team, you'll play a key role in accelerating the delivery of medicines to the world. Your innovative ideas and proactive actions will help us imagine new possibilities and bring them to life, making a significant impact on global health.

What You Will Achieve

• Contribute to project tasks and milestones, ensuring work is organized to meet deadlines.
• Learn and apply basic team effectiveness skills within the immediate work team.
• Make decisions within limited options to resolve basic problems, under the supervisor's direction.
• Work in a structured environment using established procedures, seeking guidance from colleagues as needed.
• Have your work regularly reviewed for technical judgment, completeness, and accuracy, relying on your supervisor's judgment.
• Play a pivotal role in transitioning products from research to manufacturing, leveraging technical skills to address challenges.
• Collaborate closely with pilot-plant and production departments to ensure smooth technology transfer.
• Conduct tests and measurements throughout production stages, troubleshooting process or equipment issues.
• Prepare and review scale-up protocols, technology transfer protocols, batch manufacturing records, batch packaging records, and bill of materials.
• Establish small-scale production processes, use scaled-down lab processes for troubleshooting and share knowledge through existing systems while following effective safety protocols.

Here Is What You Need (Minimum Requirements)

• Applicant must have a bachelor's degree with any years of experience, or an Associate's degree with 4 years of relevant experience, or a high school diploma (or equivalent) and 6 years of relevant experience
• Demonstrated knowledge and experience with Good Manufacturing Practices and analytical techniques.
• Strong communication skills
• Self-motivated attitude with the ability to work with minimal direction
• Flexibility and adaptability to changing priorities
• Ability to meet deadlines and perform well under pressure
• Proficiency in troubleshooting and problem-solving

Bonus Points If You Have (Preferred Requirements)

• Prior experience in the pharmaceutical industry
• Experience with technology transfer and Method development and Validation
• Strong attention to detail
• Ability to navigate complex challenges and opportunities
• Experience in a structured, Analytical-driven environment
• Experience using common AI tools, including generative technologies such as ChatGPT or Microsoft Copilot, to support problem solving and enhance productivity. Demonstrated curiosity for exploring how these tools can improve outcomes and understanding of responsible AI practices, including risk management and ethical use

Roles and Responsibilities:

• Analysis of Raw materials and Packing materials
• Analysis of in-process, finished, stability samples, MOC studies, Filter compatibility studies etc
• Calibration of various analytical instruments
• Execution of various documentation related to Analytical Development functions
• Execution of Analytical method development and Method validation/ Method transfer     
• Responsible for other functions related to Analytical Development assigned by the Group Leader
• Follow all the safety rules and regulations in the premises adhere to cGLP practices and   procedures
• Download, review and compilation of analytical method & reports, procedures for Raw materials, finished product, stability, packaging materials from originating sites          .
  • Feasibility studies for raw materials and finished products.
  • Maintaining/Coordinating amongst all internal & external customers. Ensure the personnel safety in the work area.
  • Generation of Working standards/Reference standards
• Preparation & Execution of Method validation/Method development, Method transfer, Material of contact study protocols, Feasibility study Protocols
• Ensure Method transfer activities in adherence to cGMP/ cGLP systems and procedure
• Support for investigation of OOS/OOT
• Skills in handling, evaluation and identification of Particles to support particulate investigations.

• Technical report writing skills

  
 

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

To learn more about acceptable and prohibited uses of AI during the recruitment process, please review our candidate AI-use guidelines available on Pfizer Careers.


Engineering