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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

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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