Job Description
GMP Pharmaceutical Production Supervisor
Night Shift – Sunday to Thursday - 10pm – 6.30am (G20 0XA) Salary plus shift allowance
This is a new position created due to the growth of our Curia Glasgow site. We are looking for a Supervisor who has GMP experience as well as knowledge of working in a clean room environment to join and help us grow our established team. Curia (Scotland) Limited is a leading global provider of advanced drug development, contract research and manufacturing solutions to the pharmaceutical and biotechnology industries. We have an opportunity for a Pharmaceutical Production Supervisor to join our Manufacturing team supporting the development of new medicines, primarily sterile injectable products. This role is for a night shift working position Sunday to Thursday 10pm to 6.30am. This is a great opportunity for someone who has experience growing and developing a team to join us at the start of our next phase of growth.
Curia work to a high standard of GMP (Good Manufacturing Practices) and within a sterile environment. Curia provides the Gold Standard of pharma training and development in our niche area of expertise. This training starts with a commitment to reading and understanding standard operating procedures before applying this knowledge to cleanroom manufacturing activities. Full training will be provided for bespoke Curia processes however he individual will be expected to have industry experience in a similar environment. Upon completion of training, you will receive ongoing support and work with a friendly team. Please note this position requires you to work for long periods fully gowned/masked in a class A cleanroom environment.
Training is ongoing and includes learning the flow of work to progress our team members through different job levels. This will cover a variety of tasks, from being responsible for carrying out routine activities required for the cleaning and maintenance of the clean rooms to participating in varied tasks supporting the manufacture of sterile medicinal products. Overall we pride ourselves on the career and training we offer at Curia to be the gold standard in Pharmaceutical Industry. Curia pursues excellence because our work has the power to improve patients’ lives within our collaborative environment, we develop and manufacture life changing products. If you are looking for a career where your work makes a difference in the world and want to be part of a great company, read on and apply today.
An indication of the duties and responsibilities in the role include:
Direct line supervisor for nightshift team of up to 7 people.
· Responsible for scheduling work allocation to team members considering realistic timeframe, equipment and support needed, knowledge and competency levels of individuals.
· Accountability for ensuring tasks are completed as scheduled or offering support/solutions to drive completion for nightshift workload.
· Lead by example to ensure operators adopt safe working practices and high standards at all times. Drive adherence to SOP’S and regulations, encouraging a safe environment for team members to speak up and escalate any deviation to you and the production manager.
· Preparation and sterilisation (as required) of equipment for use in clean rooms including components, raw materials, equipment, peripherals and cleaning equipment
· Manufacturing of products in compliance with all relevant internal procedures, cGMP and customer specific documentation
· Accurate and timely completion of batch manufacturing records, worksheets and logbooks to the required standard in support of the above activities
· Participation in training sessions in support of manufacturing activities
· Ensuring own and team Training Records are suitably maintained with appropriate documentation to show competency for each activity performed including but not limited to reading SOP’s, attending overview sessions and practical session.
· Ensure a team player culture throughout Production, assisting in other areas when required.
· Participate in maintaining housekeeping standards and audit readiness of facility adhering to high standards with a safety-first mindset at all times.
Previous experience and qualifications:
· Previous experience in a similar pharmaceutical production environment is preferred.
· The ideal person will already have a good understanding of GMP requirements and quality systems, gained through working in a regulated GMP environment.
· A science-related academic qualification or alternative industry work experience.
· A fair and motivated demonstrated leader who is a strong team player.
· A high level of planning & organisational skills are essential for this role
· A high level of communication skills both verbal and written
· A safety first, Quality focussed mindset with strong attention to detail.
· A can-do attitude with critical thinking and problem-solving skills
· Focussed on delivery output - flexible approach to ensure the work is complete
· Flexibility and paid overtime when required
· At Curia learning is infinite and the ideal person will want to continuously develop and improve themselves and their team.
Excellent Benefits including: up to 9% contributed to pension, private healthcare, dental scheme, 4 x salary death in service, 34 rising to 39 holidays, holiday purchase scheme, gym contribution, cycle to work and much more
Salary based on skillset plus shift allowance
You must hold right to work in UK as sponsorship is unavailable at this time.
Job: Manufacturing permanent contract
Primary Location: Glasgow, United Kingdom
Schedule: Full-time perm
Job Types: Full-time, Permanent
Pay: From £32,000.00 per year
Benefits:
- Additional leave
- Bereavement leave
- Company pension
- Cycle to work scheme
- Employee mentoring programme
- Free parking
- Gym membership
- Life insurance
- On-site parking
- Private dental insurance
- Private medical insurance
- Referral programme
- Sick pay
- Wellness programme
Schedule:
- 8 hour shift
- Night shift
- Overtime
- Weekend availability
Experience:
Licence/Certification:
- Right to work in the UK (required)
Work Location: In person
Reference ID: SW/BK2704
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