Qualifications
Must-Have

·       Graduate or Postgraduate in Pharmaceutical Science Discipline/Engineering.

·       Minimum 8+ years of experience.

·       Experience in manufacturing of pharmaceutical dosage forms (Sterile facility)

·       Strong background and knowledge in manufacturing operations, compliance processes and systems.

·       Experience and hand on electronic batch record design along with any associated software (i.e. FTPS (AMPS), SAP, MLM etc.) working exposure.

·       Technical knowledge of manufacturing and packaging operations and operation process flow.

·       Experience in defending process in regulatory audits /inspection.

·       Preferably experiences in good understanding of manufacturing and quality systems.

·       Effective communication skills are required, both written and verbal.

·       Must be comfortable working both independently and collaboratively.

·       Ability to communicate effectively with all cross functional teams (CFTs) within the organization.

Nice-to-Have
•Master's degree
•Previous experience on SAP and Electronic batch record designing. (FTPS, PAS|X)

 
Work Location Assignment: On Premise

  
Work Location Assignment: On Premise

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

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