We are seeking a detail-oriented and experienced Manufacturing Technician to join our client's pharmaceutical production team. The successful candidate will be responsible for supporting manufacturing and quality control processes within a regulated laboratory environment. This role offers an excellent opportunity for someone who wants to expand experience within highly advanced pharmaceutical operation and is prepared to work in a cleanroom environment and ensure compliance with cGMP regulations at all times.
The ideal candidate will therefore have a pharmaceutical background and have ideally gained experience within a cGMP, FDA and MHRA regulated environment.
The shift pattern is weekly rotating day shift and afternoon shift, Monday to Friday. You will be expected to work 37.5 hours per week.
Responsibilities
- Manufacture of high end consumable products for commercial and clinical trial applications. Ensuring all activities are undertaken in accordance with cGMP, Health and Safety standards, and current SOPs
- Recording data appropriately in batch records and supporting documentation
- Maintaining hygiene standards in all production areas
- Supporting production activities through each stage of the manufacturing process (cleaning, mix preparation, capsule filling and sorting, blister and bottle packing)
- Set-up, operation and strip down of modern high speed production equipment
- Working flexibly within a team to ensure adherence to the production schedule
- Maintaining personal training records
Qualifications
- Previous experience of pharmaceutical manufacturing or working in a cleanroom environment
- Be conscientious and have a good eye for detail - to conduct quality checks and ensure data is accurately recorded
- Be flexibile - to ensure production output and client demands
- Have a high degree of integrity - to maintain compliance with GMP regulations
- Be reliable, and able to make a positive contribution to the production team
- Previous cGMP (current Good Manufacturing Practice) experience
- Good practical skills
- Demonstrates good literacy and numeracy skills
Required:
- Able to communicate well via written media with specific emphasis on report writing
- Able to work with minimal supervision
- High attention to detail
- Must have a keen interest in Life Sciences/Pharma industries
Computer skills:
Must be competent in the use of MS Office, particularly Excel and Word.
Literacy and Numeracy:
Must have excellent communication skills particularly, written English and interpretation and Maths.
Please note: Only candidates with permanent Right to Work in the UK will be considered.
Benefits
- Private Medical Insurance and Health Cash Plan with Bupa
- Group Personal Pension Plan
- Life Assurance
- Generous leave entitlement of 33 days per annum
- A friendly and focused working environment
- Career development opportunities
- Potential job share
- Cycle to work scheme
- Free parking
- Health & wellbeing programme
- On-site parking
This role provides an engaging environment for individuals committed to scientific excellence and quality assurance. Candidates should demonstrate a strong work ethic, analytical mindset, and the ability to follow detailed procedures meticulously.
Please email your CV or apply through this website.
