Are you looking for an exciting opportunity, a rewarding, enriching, and fulfilling career, and the opportunity to grow to greater levels of success with a company that values you? Then look no further! Join Eurofins PSS: a world class company that is growing by leaps and bounds while making a difference to humanity.
At Eurofins PSS, you will gain experience working in state-of-the-art laboratories, and be a part of a team that is dedicated to testing, development, and advancement of life-saving drug products to make the world a healthier and happier place to live in. Our people are our chemistry and we need talented people like you now more than ever.
Eurofins PSS is an international life sciences company, providing a unique range of analytical testing services to clients making life and our environment safer, healthier and more sustainable. Eurofins PSS works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic, and labelling is accurate.
Why Eurofins?
A focus on your professional development because your growth is our growth
A chance to step in to the pharmaceutical/biopharmaceutical industry and move up the ladder of success to help you achieve your career goals
Healthy work/life balance, an essential need for employee satisfaction
Excellent benefits such as tuition reimbursement, mentoring and leadership programs, 401k, medical/vision/dental insurance, PTO, and much more!
Opportunity for involvement in several innovative committees surrounding sustainability, equality, development, and much more!
So, what are you waiting for? Join Eurofins, PSS today!
Job Description
Coordination of lab equipment installation process including procurement approvals.
Coordination of activities relating to the qualification, calibration, and maintenance of laboratory equipment and related systems.
Review qualification and validation documents as needed.
Scheduling and coordinating qualification work performed by outside contractors (includes ensuring vendors are in compliance with site requirements prior to performing equipment-related services).
Ensure qualification activities are communicated to and scheduled with the affected QC functional area and that area management is informed.
Review of vendor documentation in support of qualification.
Understand vendor specifications and track updates and critical bugs affecting hardware and software.
Review and track, work records in BMRAM equipment database as needed.
Support change control activities impacting QC equipment; provide impact assessments when required.
Support investigations of equipment-related deviations as needed.
Complies with all pertinent regulatory agency requirements.
Writes and revises Equipment related SOPs as necessary.
Working with Cross-function teams that will be supporting a long-term project.
Leadership Responsibilities
Supports and monitors team of analysts.
Monitors and reports all productivity and quality metrics.
