Why Patients Need You
Pfizer\xe2\x80\x99s purpose is to deliver breakthroughs that change patients\xe2\x80\x99 lives. Research and Development is at the heart of fulfilling Pfizer\xe2\x80\x99s purpose as we work to translate advanced science and technologies into the therapies and vaccines that matter most. Whether you are in the discovery sciences, ensuring drug safety and efficacy or supporting clinical trials, you will apply cutting edge design and process development capabilities to accelerate and bring the best in class medicines to patients around the world.

What You Will Achieve
As a Senior Associate Scientist, you will be at the center of our operations and you\xe2\x80\x99ll find that everything we do, every day, is in line with an unwavering commitment to quality. Your significant experience of applying knowledge of principles, concepts, and practices of the discipline will make you a critical member of the team.
You will perform qualitative and quantitative analyses of organic, inorganic compounds, or biologics to determine chemical and physical properties during chemical syntheses, fermentation or drug product development process. Your skill and knowledge will help in making decisions that require choosing among limited options. You are proactive in contributing to all team discussions and creating an environment of collaboration.
It is your innovative scientific temperament that will help in making Pfizer ready to achieve new milestones and help patients across the globe.

How You Will Achieve It

• Hands on experience in Visual inspection & packing automation technologies. (SD, Camera Vision, HVLD, Pressure/Vacuum, line master etc.,)
• Provides support for site-to-site parenteral product/process transfer by interfacing with cross functional departments across sites.
• Prepare study protocols, Gap assessment, Risk assessment reports, recipe parameter recommendations and CPP requirements in the developed recipe parameters.
• Evaluate Visual Inspection & Packing Process Parameters/ CPPs for Scale up and Exhibit batches manufacturing.
• Actively support in execution of Process Validation batches, Equipment Qualifications, validations/recipe establishment.
• Familiar with US FDA Guidelines, PDA & industry practices there by implementing Continuous Improvement Projects.
• Trouble shooting, ongoing technical support to Manufacturing team for Process validation, Continuous Process Verification and Process improvement
• Actively involve and drive Investigations related to Process engineering and Equipment to evolve CAPAs and monitor the effectiveness of CAPAs. Be able to apply DMAIC tool to drive investigation studies.
• Independently carry out all aspects of practical work necessary to provide right first-time results.
• Responsible for performing Engineering batches, scaleup batches, and Exhibit batches as part of technology transfer activities.
• Attend project team and brainstorming meetings and present data.
• Hands on experience in Visual inspection & packing automation technologies. (SD, Camera Vision, HVLD, Pressure/Vacuum, line master etc.,)
• Provides support for site-to-site parenteral product/process transfer by interfacing with cross functional departments across sites.
• Prepare study protocols, Gap assessment, Risk assessment reports, recipe parameter recommendations and CPP requirements in the developed recipe parameters.
• Evaluate Visual Inspection & Packing Process Parameters/ CPPs for Scale up and Exhibit batches manufacturing.
• Actively support in execution of Process Validation batches, Equipment Qualifications, validations/recipe establishment.
• Familiar with US FDA Guidelines, PDA & industry practices there by implementing Continuous Improvement Projects.
• Trouble shooting, ongoing technical support to Manufacturing team for Process validation, Continuous Process Verification and Process improvement
• Actively involve and drive Investigations related to Process engineering and Equipment to evolve CAPAs and monitor the effectiveness of CAPAs. Be able to apply DMAIC tool to drive investigation studies.
• Independently carry out all aspects of practical work necessary to provide right first-time results.
• Responsible for performing Engineering batches, scaleup batches, and Exhibit batches as part of technology transfer activities.
• Attend project team and brainstorming meetings and present data.

Qualifications

Must-Have

• Bachelor\'s Degree or any equivalent degree
• 6+ years of experience
• Experience with Visual inspection & packing automation technologies. (SD, Camera Vision, HVLD, Pressure/Vacuum, line master etc.,) .
• Ability to extract relevant information from scientific literature, accurately record observations, facts, data and conclusions during studies or Good Manufacturing Practices {also cGMP} investigations
• Interact effectively with peers and leaders as part of a multi-disciplinary team
• Effective verbal and written communication skills

Nice-to-Have

• Masters degree
• Certified in Problem solving skills - Yellow belt / Green belt.
• Experience in a {Current} Good Manufacturing Practices {part of GxP} laboratory
• Understanding of various scientific software or software used in pharmaceutical or production environment
• Desire to develop their own technical skill set is essential.

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