Quality Assurance Specialist

Kent

Permanent

Competitive

SRG is delighted to be supporting a clinical trial manufacturer with their search for a quality assurance specialist. Due to their ongoing expansion of the business, they are now looking for 2 quality assurance specialists within steriles.

Key Responsibilities

• Collaborate with stakeholders to oversee the progression and timely execution of quality assurance activities.
• Manage deviations, investigations, and corrective actions.
• Oversee the documentation system, including reviewing and approving standard operating procedures, batch manufacturing records, and other controlled documentation.
• Ensure effective management of the document lifecycle, ensuring compliance with regulations and industry best practices
• Evaluating site compliance and implementing improvements through internal audits.

Requirements

• Experience in quality assurance within a pharmaceutical facility.
• Experience with process validation and cleaning validation and verification.
• Experience working on a sterile site would be advantageous
• Experience managing validation lifecycles from creation to retirement.
• Expert for equipment, facility, process change management.
• Excellent communication skills, both written and spoken English, and computer literacy.
• Ability to manage your own workload, meet deadlines & prioritise accordingly
• Good attention to detail and high standards in all work output.

For a dynamic, motivated professional, this role offers the chance to work at an ambitious and driven company while also building your professional profile with skills that'll accelerate your career.

Apply now by attaching your CV in Word, or contact Paige Keenan for further information about this new role: / 01223 978 504

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