Pfizer Pharma Assistant Manager Vacancy – Apply Online

Pfizer Pharma Assistant Manager Vacancy - Apply Online

Pfizer Pharma Assistant Manager Vacancy – Apply Online

Pfizer Vacancies – Pharma Vacancy. MPharma candidates are eligible to apply online for an Assistant Manager – MSAT Process Engineering vacancy at Pfizer. Pharma job opening 2020. Check out all the details on our website

Job Title: Assistant Manager – MSAT Process Engineering

Location: India – Vizag

Preferred Qualification: Bachelors or Master’s in Pharmacy

Target years of experience: 6 to 10 years

Knowledge & Skills:

Expertise in Process Engineering aspects related to sterile drug product/injectables manufacturing

  1. Working experience in TS equipment train i.e Formulation process equipment, automation, Filling, and Terminal sterilization.
  2. Good knowledge of pharma equipment and its engineering aspects.
  3. Problem-solving skills
  4. Process analytical skills
  5. Hands-on experience leading the investigations independently.
  6. Yellow belt certification is a must. Candidates who were trained and working for the M2 project will be preferred.

Soft skills:

  • Good Communication & Presentation Skills
  • Effective negotiation and Interpersonal Skills
  • Leadership skills


  • To Provide technical support for the equipment technologies during technology transfer.
    Technical support for Investigations and CAPAs for Process equipment.
  • To ensure and adhere to the Pfizer EHS requirements for safety at the work.
  • To lead and Coordination with internal teams of mechanical, Instrumentation and Automations as per functional requirements.
  • Engineering support for Equipment Qualification activities DQ, FAT, recipient of equipment, SAT, Commissioning, IQ, OQ, PQ-qualification of equipment as per the
  • Qualification protocols and Technical Support to the user for various deliverables.
  • Responsible for preparation of various regulatory inspections, audits and need-based active participation during audits.
  • Provides process engineering support for site-to-site parenteral product transfers by interfacing with cross-functional departments across sites.
  • Conducts equipment and process-related technical investigations and makes recommendations on corrective Prepares, reviews, and provides input on user requirements specification (URS) documents and P&IDs
    Will lead activities to implement novel technologies for process improvements to increase yield and reduce process variability
  • Ensure the compliance to cGMP/cGLP, organizational procedures and practices.
  • Involve in manufacturing, Validations/engineering related CAPAs and monitor the effectiveness of CAPAs
  • Seek training from technology vendors and train the end-users

Apply Online

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