Time left to apply End Date: February 28, 2025 (15 days left to apply)
Job requisition ID: 0087238
Catalent is currently recruiting for a Quality Specialist II to join the Bathgate site. The Quality Specialist will carry out functions relevant to the Quality (GMP) objectives and policies of Catalent.
This role will see you join the dedicated Quality function that is an integral part of our success here at Catalent. In this role, you will be responsible for the movement, control, and tracking of documentation to adhere to the production schedule.
Working hours:
Early shift: 7am – 3pm
Late shift: 2pm – 10pm
The Role:
* To be responsible for the movement, control, and tracking of documentation, ensuring a timely flow to adhere to the production schedule.
* Review and approve Material Specifications to ensure compliance with pharmacopoeia and client requirements.
* To review and approve Incoming Bulk, Intermediate, and Finished Materials to ensure compliance with pharmacopoeia and client requirements.
* Review and approve Randomisations to ensure compliance with GMP and client requirements.
* Review and approve GMP information to ensure accuracy and compliance with company procedures.
* Review and approve production (Pre and Post Packaging Batch) Records to ensure compliance with GMP and company procedures.
* Liaise with relevant department staff and management on quality issues and timelines.
* Review and approve observation and deviation reports to ensure compliance with GMP.
* Perform internal audits as scheduled and monitor/trend findings.
The Candidate:
* Educated to HNC level in a relevant scientific topic or equivalent in a pharmaceutical environment.
* Experience of Pharmaceutical/Clinical Trials Packaging and GMP Processes.
* A high level of concentration and a good eye for detail is essential.
* The ability to be decisive when required on material/product quality issues to ensure compliance.
Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world.
Catalent is an Equal Opportunity Employer and does not discriminate based on any characteristic protected by local law.
If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email to DisabilityAccommodations@catalent.com.
About Us
Catalent = Catalyst + Talent
Your talents, ideas, and passion are essential to our mission: to develop, manufacture, and supply products that help people live better, healthier lives. Join us!
Catalent is the perfect place to grow your career if…
* You enjoy the fast pace of a start-up, but want the opportunities and stability of a growing, publicly traded company (Listed on NYSE: CTLT).
* You want meaningful work. From cough treatments to cancer-fighting drugs, biologics, and vitamins, we help develop, launch, and supply over 200 new products each year.
* You want to plant your career in a growing company. Over the last five years, Catalent has re-invested more than $2 billion back into the company and its people.
* You are excited about learning, collaborating, and growing alongside a global diverse team.
* You want to make a global impact!
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