Force Recruitment is partnering with our client, a leading pharmaceutical manufacturer, to hire a Validation Specialist.
This role is responsible for executing validation projects across various production areas, including process, cleaning, software, utilities, and facilities. The Validation Specialist will ensure compliance with cGMP requirements and support both existing and new product introductions.
Responsibilities:

• Lead process validation and qualification activities in accordance with regulatory standards.

• Draft, execute, and close out validation protocols and reports.

• Support ongoing process validation by assessing process stability and capability.

• Conduct and document risk assessments (FMEA) related to validation activities.

• Perform validation functional testing and track deviations during qualification.

• Collaborate cross-functionally to support technical transfers and ensure compliance with Annex 11 and Annex 15 regulations.

Qualifications:

• A BSc in Science, Engineering, Technology, or a related discipline.

• A minimum of 2 years’ experience in a validation role within a cGMP-regulated environment, preferably in oral solid dose manufacturing.

• Strong technical writing skills and familiarity with validation documentation.

• Knowledge of Minitab software is advantageous.

• Excellent problem-solving, time management, and communication skills.

• Ability to work independently and manage multiple priorities effectively.

This role offers a competitive salary, excellent career development opportunities, and a comprehensive benefits package.
If you are interested in this opportunity, please apply today or reach out for more information.