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).