Job description
Catalent’s Nottingham facility focuses on early stage development of small molecule drug candidates from the bench to clinic. We are currently recruiting for an Operator to join the team. The Operator will perform manufacturing operations in accordance with cGMP standards. Record critical manufacturing data. Complete and follow batch records. Comply with standard operating procedures.
This is an exciting opportunity to be part of our Patient First mindset and continue to develop your career in pharma.
Shift Pattern:
Week 1 – 06.00 – 14.00
Week 2 – 14.00 – 22.00
The Role;
To conduct manufacturing and supportive operations to manufacturing in compliance with cGMP standards and the Quality Management System.
To record experimental and manufacturing data and processing details in laboratory notebooks and manufacturing records to the required standard.
Prepare, setup and clean experimental and manufacturing equipment.
Assist with the cleaning and maintenance of the GMP and development facilities.
Comply with assigned SOP’s.
Complete batch records and cGMP documentation in line with expected standards.
Perform all work in a responsible and safe manner in accordance with Health and Safety policies and ensure that all Health and Safety considerations are appropriately documented prior to commencement of work.
Maintain personnel training record at all times and proactively identify any training requirements for the job role.
Demonstrate a high level of flexibility to support the business needs and our client’s requirements.
The Candidate;
Degree in a scientific subject or equivalent experience
Experience in pharma production desirable
Knowledge of GMP standards
High attention to detail
Ability to follow instructions and written to procedures.
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 exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.
Catalent is committed to the health and safety of its employees, visitors and the customers and patients we serve. As a result of the global pandemic, we have modified many of our recruitment and on-boarding processes to maintain everyone’s safety. The Human Resources teams will communicate all necessary safety processes and procedures throughout each stage.
personal initiative. dynamic pace. meaningful work.
Visit Catalent Careers to explore career opportunities.
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, and confirming your request for an accommodation and include the job number, title and location to [email protected]. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.
Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.