Saturday, February 2, 2019

Process/Equipment Validation Lead at Adexen Recruitment Agency


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Adexen Recruitment Agency - Our client in the FMCG/Pharmaceuticals industry is recruiting suitably qualified candidates to fill the position below:
Job Title: Process/Equipment Validation Lead

Location: Lagos

Responsibilities

  • Execute Validation activities (from planning stage to execution)
  • Maintain systems in a validated state
  • Partake in relevant project meetings/coordination of validation meetings
  • Generate validation protocols (DQ/FAT/IQ/OQ/PQ/PV)
  • Execute validation protocols (IQ/OQ/PQ/PV)
  • Write validation reports (DQ/FAT/IQ/OQ/PQ/PV)
  • Write Validation Summary report
  • Ensure deviations from pre-approved protocol are managed accordingly
  • Equipment decommissioning
  • Conduct validation reviews/equipment requalification in line with periodic validation review
  • Contact person to interface with process owners/other departments on site to ensure systems are in line with the Validation Life Cycle Approach
  • Support in the development of User Requirement
  • Lead and execute the Commissioning and Qualification (C&Q) of validation projects to ensure the C&Q is in line with the pre-approved URS and relevant Company/regulatory policies.
  • Execute temperature mapping for controlled chambers such as cold rooms, freezers, warehouse, etc.
  • Work with the project group/teams during the C&Q to ensure compliance with Company policies and appropriate regulatory bodies (NAFDAC)
  • Work with the New Product Development Manager to coordinate with other cross functional resources (manufacturing operations, engineering, etc.) in identifying prerequisite documents needed pre- and post-qualification
  • Work with the Product Development Manager in the preparation of Validation Documents for Audit readiness
  • Review change controls documents relating to technical and process changes during the execution of the validation activities.
Desired Skills and Experience
  • B.Sc./HND in Industrial Chemistry, Biochemistry, Biological and Physical Sciences and other related disciplines/Computer literacy is an added advantage.
  • Minimum of 3 years practical experience in Pharmaceuticals/Food and Beverages with knowledge of GMP and Validation.
  • Listening Skill; Project Management; Quality Management Standards; Validation and Report Writing
  • Knowledgeable in Good Manufacturing Practice (GMP). The holder should be familiar with the operations of a Drinks industry.
  • Ability to prioritize and act appropriately is essential.
  • Ability to provide comprehensive situation reports and hold secret of all confidential information relating to the company’s business.
  • Display of innovation and improvement in systems are necessary for career development.
  • Able to carry out work with agreed/approved specifications and limits in line with Quality Standards requirements

Application Closing Date
Not Specified.

How to Apply
Interested and qualified candidates should:

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