Formulation Technician - 12h GMP Production (Swindon)

Manpower UK; Swindon; On-site; GBP 21,000 - 29,000; Full time

Benefits offered by this job

Shift allowance

Training provided

Job summary

Manpower UK in Swindon is seeking a Senior Formulation Technician for a temporary role at a pharmaceutical manufacturing site. You will handle formulation and production duties in a highly regulated GMP environment, with a 12-hour day/night shift pattern and 40% shift allowance.

The role requires meticulous attention to detail, strong teamwork, and adherence to compliance protocols, contributing to patient safety and product quality within a global pharmaceutical manufacturer.

Qualifications

• GCSE Maths (Grade C/4 or above) or equivalent numeracy skills.
• GCSE English (Grade C/4 or above) or equivalent literacy skills.
• Basic IT skills, including Microsoft Office.
• Ability to follow detailed written and verbal instructions.
• Strong attention to detail and commitment to quality.

Responsibilities

• Operating bulk manufacturing and compounding equipment.
• Preparing and setting up equipment for production, including CIP, SIP, filter integrity testing and pressure testing.
• Performing pharmaceutical formulation activities in line with manufacturing records.
• Completing batch documentation accurately and in compliance with cGMP standards.
• Operating cleanroom equipment, airlocks and autoclaves.
• Carrying out cleaning and sterilisation activities to pharmaceutical industry standards.
• Monitoring equipment performance and reporting faults or issues.
• Supporting validation projects and new product introductions.
• Assisting with basic equipment maintenance where required.
• Ensuring any non-conformances are escalated and investigated appropriately.

Skills

Maths

English

IT skills

Follow instructions

Attention to detail

Job description

Manpower UK in Swindon is seeking a Senior Formulation Technician for a temporary role at a pharmaceutical manufacturing site. You will handle formulation and production duties in a highly regulated GMP environment, with a 12-hour day/night shift pattern and 40% shift allowance.

The role requires meticulous attention to detail, strong teamwork, and adherence to compliance protocols, contributing to patient safety and product quality within a global pharmaceutical manufacturer.