We have a great opportunity for Pharmaceutical Operator Specialist's working in the Pilot Plant here in Abingdon, Oxfordshire.
Our pilot plant has the capability to produce a range of different products (both developmental and commercial) at large scale, making this role an exciting opportunity for you to develop your skills and knowledge. Successful candidates will have the opportunity to use a variety of equipment, running multiple chemical syntheses on plant, many of which haven’t been done at scale before.
Aptuit is a member company of Evotec, a global Pharmaceutical business. Evotec covers all activities from target-to-clinic to meet the industry’s need for innovation and efficiency in drug discovery and development. The Company has established a unique position by assembling top-class scientific experts and integrating state-of-the-art technologies as well as substantial experience and expertise in key therapeutic areas including neuronal diseases, diabetes and complications of diabetes, pain and inflammation, oncology, infectious diseases, respiratory diseases and fibrosis.
Role: Pharmaceutical Operator Specialist I
Job Type: Permanent
Location: Milton Park, Abingdon, Oxfordshire, UK
Hours: 12-hour shifts (days and nights) including paid breaks (90 minutes).
Shift Pattern: 42 hours per week on average, 28-day shift pattern cycle:
Week 1: 2 x Day shifts, 2 x Night shifts, 3 days off
Week 2: 2 x Days off, 2 x Day shifts, 3 x Night shifts
Week 2: 4 x Days off, 3 x Day shifts
Week 4: 2 x Night shifts, 5 x Days off
(then repeats)
Role & Responsibilities:
Operate the pilot plant reactors and ancillary equipment following all current procedures (IOPs, BPGs, etc.) to maintain high standards of safety, housekeeping, hygiene and quality.
Ensure written instruction/directions are followed correctly.
Notify your supervisor or Manager immediately of any irregularities so that corrective actions can be planned and implemented.
Promptly and accurately complete documents as directed and record all irregularities.
Support environmental monitoring and report/record information.
Carry out routine maintenance and re-configuration of reaction vessels and ancillary equipment to ensure production is carried out in a timely and safe manner, complying with Health and Safety obligations.
Participate fully and diligently in all training schemes.
Participate fully and diligently in project schemes to support continuous improvement in working practices.
Skills & Qualifications:
Qualification in Chemistry, or other related discipline, advantageous.
Awareness of cGMP, regulatory aspects and pharmaceutical regulations desirable.
Good planning and organisational skills.
Able to communicate effectively at all levels within the organisation.
Able to interact effectively and positively with internal customers.
Able to work on your own and as part of a team.
Good time management and prioritisation capabilities.
Ability to successfully manage multiple tasks simultaneously.
Flexible and adaptable with an open-minded view and creative problem-solving skills.
Strong sense of accountability for the outcome.
Contribute to shift handovers.
Liaise between production management, chemists and other departments.
IT literate with strong Microsoft Office skills.
Essential Requirements & Working Environment
To ensure safety, compliance, and effectiveness in this GMP-regulated role, applicants should be aware of the following key job demands
Manual Handling: The role involves regular movement of heavy materials, including manoeuvring pallets of 200L drums. The safe use of handling aids (e.g., pallet trucks, drum trollies, hoists etc.).
Cluttered & Confined Spaces: Work is carried out in an operational plant setting where space may be restricted and cluttered at times, requiring constant awareness of surroundings and safe navigation.
GMP Documentation: A strong level of written literacy and attention to detail is essential to follow instructions, complete…