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Process/Equipment Validation Lead

Adexen

Lagos, Nigeria

Job description

Job Introduction

    Adexen is mandated by one of its clients in the FMCG/Pharmaceuticals industry to recruit a Process/Equipment Validation Lead. The position is based in Lagos, Nigeria.

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
We thank all applicants however only those selected will be contacted.

Industry

FMCG

Job Seniority

Mid-Senior level

Job Category

Operations and Production

Employment Type

Full time

Experience

3 - 5 years

Skills

Project Coordination, Innovation, Project Management

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