Founded in 1849, Pfizer is the world's premier biopharmaceutical company taking new approaches to better health. We discover, develop, manufacture and deliver quality, safe and effective prescription medicines to treat and help prevent disease for both people and animals. We also partner with healthcare providers, governments and local communities around the world to expand access to our medicines and to provide better quality health care and health system support.
Post : Senior Research Associate
Job Description
- Contribute to achievement of goals and influences at the work group/project team level.
- Assist in the establishment of analytical procedures and interpret results/technical data.
- Communicate progress, plans, requirements and risks to the senior analyst, manager, stakeholders in partner groups and higher management informally and, if required, formally through written reports and presentations.
- Actively participate and report progress into cross-functional project teams to meet customer expectations, project milestones and Good Manufacturing Practices {also cGMP} standards.
- Prepare and review technical documents, including validation protocols and reports, analytical test procedures, investigation reports, and change controls.
- Develop analytical methodologies and strategies needed to progress biotherapeutic products in the pipeline.
- Support development, qualification, validation, and transfer of cell-based and immunoassays in support of diverse portfolio in varying stages of clinical development.
- Analyze and communicate experimental results both orally and in written reports to colleagues and management.
- Provide the necessary documentation for regulatory submissions as required and writes deficiency responses.
Candidate Proflie
• Masters degree in Chemistry/M pharm
• 8+ years of experience
• Experience with interdisciplinary drug development teams and industrial experience developing analytical strategies and methods in support of product and process development and to assess the quality and characteristics of biotherapeutics
• Experience working in a regulated environment, such as Good Laboratory Practices {part of GxP}
• Demonstrated technical expertise in functional verification of design
• Working knowledge of applicable industry test standards, relevant regulatory guidance, Design Controls and Product Development Process
• Able to interact effectively with peers and leaders as part of a multi-disciplinary team
• Effective verbal and written communication skills
Additional Information
Experience : 8+ years
Qualification : M.Pharm, MSc
Location : Sholinganallur
Industry Type : Pharma/ Healthcare/ Clinical research
Functional Area : R&D
End Date : 30th December, 2020
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