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+ Excellent written and verbal skills

+ Impeccable attention to detail and accuracy.

+ Strong internet research skills

+ Good Organizational, time management and priority setting skills, and the flexibility to multi - task in a fast -paced environment.

+ Ability to think critically, work independently and follow instructions.

+ Working knowledge of Microsoft Excel and Word.

+ Familiarity with drug development process **especially Sterile Injectables.**

+ Support in the preparation and review of technical data, identifying and evaluating CPPs, stability data, annual product quality reports, technical documents.

+ Coordinate with internal departments like Analytical R&D, Production, Quality Control, Regulatory Affairs, Quality Assurance, Project Management, Engineering etc., for seamless technology transfer.

+ Finalize manufacturing process and parameters/ CPPs for scale up, pre exhibit, exhibit, process validation batches and commercial batches.

+ Trouble shooting, ongoing technical support to Manufacturing team for process validation, continuous process verification and process improvement.

+ Follow effective safety systems that are implemented in the premises.

+ Serving as a key scientific and technical representative for process-related issues for commercial products.

+ Conducting Literature search and preparation of Literature Report

+ Formula and Process Optimization studies

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

Posted: 2020-05-07 Expires: 2020-06-07
Sponsored by:
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