Job Reference: R111628
Life changing therapies. Global impact. Bridge to thousands of biopharma companies and their patients.
We Are PCI:
Our investment is in People who make an impact, drive progress and create a better tomorrow. Our strategy includes building teams across our global network to pioneer and shape the future of PCI.
The Role:
This role will be responsible for the sampling, inspection, and compliance tasks in pharmaceutical quality assurance, including liaising with QC and QA, maintaining documentation, ensuring SOP compliance, and managing projects as needed.
Main Responsibilities:
Qualifications:
Benefits:
At PCI, we believe that our employees are our most valuable asset. That's why we are committed to providing a benefits package designed to support your well-being and enhance your overall quality of life. Here's what we offer:
PCI is your world leading CDMO, providing integrated end-to-end drug development, manufacturing, and packaging solutions to increase product speed to market and opportunities for commercial success.
PCI brings the proven experience that comes with more than 90 successful product launches each year and over five decades in the delivery of CDMO services. With 30 sites across Australia, Canada, North America, the UK, and Europe and over 6000+ dedicated employees, together, delivering life changing therapies.
PCI Pharma Services has grown by continually investing in high caliber, motivated people – and then supporting their continued development through training and mentoring.
Western Avenue
Bridgend Industrial Est
Bridgend
CF31 3RT
Bridgend Train Station 0.6 miles / 15mins walk
Bridgend, South Wales Police HQ 0.2 miles / 5mins walk