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Validation Specialist

Kinetica

England

On-site

GBP 30,000 - 50,000

Full time

9 days ago

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An established industry player is seeking a skilled Validation Specialist to enhance their operations at a state-of-the-art GMP manufacturing facility in Kent. This role offers the chance to work on critical validation projects, ensuring compliance and quality in the pharmaceutical sector. You will be responsible for executing validation activities, maintaining documentation, and providing technical expertise. If you have a passion for quality assurance and a strong background in validation processes, this is an exciting opportunity to contribute to a dynamic team and make a significant impact in the industry.

Experience in validation activities for equipment and processes.
Understanding of IQ, OQ, PQ, and PV methodologies.

Complete validation activities and maintain relevant documentation.
Prepare and execute validation procedures and protocols.
Gather and analyze validation data, preparing reports.

Validation Procedures

Temperature Mapping

Cleaning Validation

Communication Skills

GMP Knowledge

Validation Specialist – Kent – Pharmaceuticals

About the Company:

We are looking for an experienced Validation Specialist to join a pharmaceutical manufacturing site in Kent (commutable from SE London). You will have the opportunity to work in a newly built GMP manufacturing facility.

This is a 1-year parental cover contract on a FTC.

Responsibilities:

• Completion of validation activities and projects for equipment and processes.

• Maintenance of relevant documentation.

• Preparation and execution of validation procedures and protocols for re-qualification, cleaning validation, and temperature mapping.

• Maintenance of the re-qualification schedule for validated equipment.

• Gathering and analysing validation data and prepare reports.

• Assisting with the compilation of and maintain the validation master plan (VMP).

• Providing advice and suggestions concerning changes and improvements.

• Providing technical expertise in terms of investigation, trouble shooting and finding solutions.

• Maintaining documentation and files.

Requirements:

• An understanding of and experience in IQ, OQ, PQ and PV.

• Experience of temperature mapping and cleaning validations.

• Experience working in a process and equipment validation position in the pharmaceutical, biopharmaceutical or biotechnology manufacturing industry.

• Ability to write and carry out validation procedures.

• An understanding of the principes of calibration.

• Excellent communication skills.

• An understanding of the requirements of GMP.

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Validation Specialist

Kinetica

England

On-site

GBP 30,000 - 50,000

Full time

Job summary

Qualifications

Responsibilities

Skills

Job description