Associate Suite-3

3 - 7 years

0 Lacs

Posted:4 weeks ago| Platform: Shine logo

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Work Mode

On-site

Job Type

Full Time

Job Description

Role Overview: You will be responsible for ensuring the manufacturing of pharmaceutical dosage forms in compliance with cGMP and quality management systems. Your role will involve technical writing, document review, and revision of standard operation procedures (SOP) and manufacturing documents. Additionally, you will be required to make decisions on activities according to GMP procedures and Pfizer global policies while effectively communicating with cross-functional teams. Key Responsibilities: - Possess a Diploma in Pharmaceutical Science Discipline/Engineering - Demonstrate knowledge of manufacturing pharmaceutical dosage forms - Understand and apply cGMP and quality management systems - Exhibit good documentation practices - Utilize technical writing and document review skills - Write and revise standard operation procedures (SOP) and related manufacturing documents - Demonstrate strong interpersonal skills - Apply analytical thinking to provide solutions for complex technical issues - Make decisions on activities according to GMP procedures and Pfizer global policies - Communicate effectively with all cross-functional teams within the organization - Possess technical knowledge of manufacturing operations and operation process flow Qualifications Required: Must-Have: - Diploma in Pharmaceutical Science Discipline/Engineering - Knowledge on manufacturing of pharmaceutical dosage forms - Preferably experiences in good understanding of manufacturing and quality systems - cGMP and application of quality management systems - Good documentation practices - Technical writing and document review skills - Ability to write and revise standard operation procedures (SOP) and related manufacturing documents - Strong interpersonal skills - Analytical thinking to grasp complex technical issues and provide feasible solutions by discussing with superior - Decision making on activities in the area according to GMP procedures and Pfizer global policies - Ability to communicate effectively with all cross functional teams (CFTs) within the organization - Technical knowledge of manufacturing operations and operation process flow Nice-to-Have: - 3-6 Years of experience in Pharmaceuticals industry - MES (AMPS, SAP or similar electronic system/software) experience Note: No additional details about the company were provided in the job description.,

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Pfizer logo
Pfizer

Pharmaceutical Manufacturing

New York New York

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