Technical Specialist

5 days ago


Loughborough, United Kingdom Almac Group Full time

**12 Months Fixed Term Contract**

**Hours**: 37.5 hours per week

**Salary**: Competitive

**Ref No**: HRJOB9462

**Business Unit**: Pharma Services

**Location**: Loughborough, Leicestershire

**About The Role**

To work as part of the Manufacturing Process Development team at Almac Pharma Service’s Charnwood facility in Loughborough, UK

The Technical Specialist (Manufacturing Process Development) will be responsible for delivery and implementation of lean manufacturing principles in Manufacturing Operations (e.g. 5S, housekeeping, poke yoke, standard work instructions), training support, supporting technical investigations, and monitoring of the EMS and PW system.

In addition, the individual will be responsible for co-ordinating and executing procurement and qualification activity during validation and continued lifecycle support for equipment (e.g. parts and modifications) or introduction of new commercial manufacturing processes. The individual will be responsible for supporting technical transfer and validation of commercial manufacturing processes.

**About You**

To be successful in this role, we’re looking for you to have:

- Bachelor’s degree (or above) in a scientific (Chemistry, Biology or Pharmacy) or technical (Engineering) or significant relevant experience working within the Pharmaceutical Manufacturing Industry in an Operations environment
- Experience within a pharmaceutical/GxP environment in technical operations.
- Experience in the technical transfer, scale-up and process validation of equipment and processes
- Proven ability to work effectively on own initiative as well as effectively contributing to the team environment
- Excellent attention to detail
- Effective communication skills (written and verbal)
- Master’s degree (or equivalent) in a related Scientific/Technical Discipline
- Significant experience in OSD (compression, capsule filling, stick pack)
- Knowledge of cGMP and manufacturing processes of pharmaceutical products
- Experience in technical work and/or significant hands on experience in pharmaceutical development and GMP manufacture
- Experience of working to aggressive timelines

**Reward**

**Closing Date**: 19 April 2024 at 1700 hours

LI-CT1


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