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:
Click here to apply online