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 Rasayanika.com.
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
- Working experience in TS equipment train i.e Formulation process equipment, automation, Filling, and Terminal sterilization.
- Good knowledge of pharma equipment and its engineering aspects.
- Problem-solving skills
- Process analytical skills
- Hands-on experience leading the investigations independently.
- 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
Responsibilities:
- 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
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