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Visual Inspection Supervisor

5.00 to 7.00 Years   Delhi   09 Sep, 2021
PFIZER LIMITED
Job LocationDelhi
EducationNot Mentioned
SalaryNot Disclosed
IndustryPharma / Biotech
Functional AreaEngineering Design / Construction,Testing
EmploymentTypeFull-time

Job Description

Your expertise in the manufacturing domain will help to ensure that the process area operates in safe and GMP compliant manner at all times. You will help in developing and managing performance of a team of process technicians. Your role will be to build upon and improve existing process design to optimize process, facility and equipment used while conforming to SOPs and cGMP requirements. You will maintain regulatory compliance through established programs for testing, maintenance, training, SOPs, validation, and cleaning in your area of responsibility.As a Team leader, you will be involved in leading work teams within a division. You will lead the people, technical and financial resources of the team. Thanks to your technical skills, you will coach your direct reports on day to day activities. You will be relied on to solve complex problems within your area of expertise. It is your dedication that will make it possible for Pfizer s customers and patients to receive the medicines they need, when they need them.How You Will Achieve It

  • Manage multiple projects and work activities (timelines, work plans, deliverables) within the team.
  • Support development of SMART Objectives for the full team.
  • Participate in Pfizer Network programs, to ensure best practice sharing.
  • Assist with the development of your unit from commissioning, through to start-up, validation, and {Current} Good Manufacturing Practices {part of GxP} operations.
  • Lead System Application & Products Materials process for Shift.
  • Perform quality check on processing activities and process confirmations of Integrated Manufacturing Excellence (IMex) elements.
  • Drive implementation and embedding of Lean Tools in the area.
  • Act as interface between management team and functional team.
  • Support Shift Colleagues Individual Development Plan.
  • Ensure contingent staff are managed appropriately in terms of performance and training
QualificationsPreferred Education/ Qualification
  • Graduate/ Post- Graduate in Pharmaceutical Science or any science discipline
Experience:
  • 5 years of Experience in Manufacturing of parenteral dosage forms / Visual Inspection
Core Competencies:
  • Should have Knowledge regarding the risks associated in Visual Inspection Process
  • Should be M1 certified/ trained
  • Strong Technical Knowledge on Visual Inspection Process
Standards, Processes and Policies:
  • cGMP and application of Quality Management Systems
  • Good documentation practices and Data Integrity
  • Technical writing and document review skills
  • Ability to write and revise standard operation procedures and related manufacturing documents
  • Good Understanding of Manufacturing and Quality Systems
Behavioral/ Any Other Skills
  • Strong Interpersonal Skills
  • Ability to supervise a team with effective teamwork and coordination
  • Analytical thinking to grasp complex technical issues and provide feasible solutions
  • Decision making on activities in the area according to GMP procedures and Pfizer global policies
  • Ability to communicate effectively with all levels within the organization
Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.Manufacturing #LI-PFE,

Keyskills :
inspectiondocumentationhousekeepingsiteequal employment opportunitycontinuous improvement facilitationlean toolsquality checkprocess designdocument reviewtechnical skillsvisual inspection

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