Do you have a keen eye for detail and a passion for ensuring top-notch equipment performance?

We are seeking a highly motivated Equipment Validation Specialist to play a vital role in maintaining the integrity and efficiency of pharma manufacturing processes.

In this role, you will be responsible for:

• Defining and executing equipment validation activities, ensuring all equipment meets the required standards.
• Coordinating and managing the procurement and qualification process, from selecting and acquiring equipment to ensuring its proper validation.
• Providing technical support to Manufacturing Operations during troubleshooting and investigations.
• Conducting data integrity assessments for GMP equipment, safeguarding the accuracy and reliability of collected data.
• Maintaining the qualification lifecycle of all GMP equipment by performing requalification activities as necessary.

We are looking for someone who possesses the following qualifications:

• Bachelor's degree (BSc) or a Doctorate (PhD) in a Life Science or Engineering field.
• Proven experience in validating manufacturing equipment and processes.
• Solid understanding of Good Manufacturing Practices (GMP) regulations.
• Experience in collaborating effectively with internal and external stakeholders.
• Adept at multitasking and thriving in a busy environment.
• Strong relationship builder with excellent communication skills.
• Exceptional attention to detail and a knack for problem-solving.
• Demonstrated leadership abilities.
• Proficiency in using essential IT applications (Word, Excel, Outlook).

Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy.