Compounding Unit Operator

Pertemps Derby; Burton upon Trent; On-site; GBP 60,000 - 80,000; Full time

Job summary

A clinical logistics company in Burton upon Trent is seeking a Compounding Unit Operator for full-time work. You will join the clinical manufacturing team to aseptically prepare and quality check medicinal products. Ideal candidates should have experience in controlled environments, strong attention to detail, and fluent English. This initially temporary position offers potential for a permanent contract in the future.

Qualifications

• Experience working in controlled environments is ESSENTIAL.
• Meticulous attention to detail and ability to follow instructions.
• Fluent in English both verbal and written.

Responsibilities

• Prepare and record starting materials as listed in batch documents.
• Aseptically manufacture products following department procedures.
• Perform visual quality checks, label and pack products for dispatch.

Skills

Attention to detail

Ability to follow instructions

Experience in controlled environments

Job description

Compounding Unit Operator

Burton on Trent | £12.76p/h | Full Time, Temp to Perm
Start Date Monday 1st December

We are currently recruiting for skilled operatives to join the team at a clinical logistics company in Burton on Trent. In this role you will be working with the clinical manufacturing team in an aseptic environment to prepare, assemble and quality check medicinal products ready for delivery to patients.

Hours of Work

Week 1: Monday to Friday: 6am-2pm
Week 2: Monday to Thursday 1pm-9pm and Friday 11am-7pm

Duties

• Prepare and record starting materials as listed in batch documents.
• Aseptically manufacture products following department procedures and GMP.
• Perform visual quality checks, label and pack the finished product ready for dispatch.
• Work in a controlled clean room and wear the required clean room clothing.
• Support supervisors and managers by keeping stock levels maintained and ordering supplies when needed.
• Order and receive stock, and report or resolve any differences quickly.
• Help maintain and monitor environmental conditions as required, and support other monitoring or validation tasks.
• Make sure all GMP documents are filled in clearly and at the time of each activity.
• Carry out ADHOC tasks as requested by the senior team.

About you

Experience working within a controlled environment is ESSENTIAL, pharmaceutical, laboratory or food manufacturing environments would be ideal.
Meticulous attention to detail and ability to follow instructions.
Able to manage and prioritize daily workload as there will time times when working alone.
Due to the nature of the sterile working environment, any pre existing skin conditions must be disclosed at point of application.
Fluent in English both verbal and written.
This role is based completely on site, so you must be able to commute to DE14 2WS for the required shift times.
This role is offered initially on a temporary basis however opportunity to transfer to permanent contract available in 2026.