Do you have a keen eye for detail and a passion for ensuring 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 life-cycle of all GMP equipment by performing re-qualification 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.