About this role
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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About Pfizer
We’re celebrating over 175 years of daring scientific innovation—and we’re not done yet. Let’s outdo yesterday. Protect your health at PfizerForAll.com
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What you'll do
- The Associate Manager - MES will oversee manufacturing operations and ensure compliance with regulatory standards. They will also be involved in the design of electronic batch records and collaborate with cross-functional teams.
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