An exciting opportunity to join a large pharmaceutical company.

You will be responsible for all procedures and processes associated with the Manufacture of Commercial Large-Scale Drug Substance at the manufacturing facility.

You will be responsible for the preparation, operation and monitoring of equipment, use of business systems and carrying out tasks including but not limited to the cleaning, validation, in-process testing and basic maintenance of equipment in accordance with current Good Manufacturing Practices (cGMPs).

Job Description:

You will be responsible for the preparation, operation and monitoring of equipment.
Use of business systems and carrying out tasks including but not limited to the cleaning.
In-process testing and basic maintenance of equipment in accordance with current Good Manufacturing Practices (cGMPs).
Bring energy, knowledge, innovation to carry out the following:
Work with the manufacturing operations group, project design team, the CQV team, the Automation/CSV reps to facilitate the development and validation of the manufacturing facility.
Support Equipment Design/ HAZOP and Room programming reviews.
Support Operations team to consistently deliver on specific area Key Performance Indicators (KPIs), e.g. EHS metrics, Production Plan, OEE, compliance and team training.
Execute commercial manufacturing processes according to established work instructions and Standard Operating Procedures.
Generate SOPS/Electronic Batch Records.
Adhere to Right First-Time principals
Provide assistance and/or support maintenance, engineering, quality or other colleagues as requested.
Escalate issues as appropriate to Process Lead
Liaise with other groups and individuals to ensure planning of tasks is effective and linked into the manufacturing process plan.Skills/Knowledge/Experience:
Minimum of a Level 7 qualification in a science or engineering discipline.
Team worker.
Ability to work cross functionally and with multiple stakeholders.
Trouble shooting capabilities.
Understanding of Drug Substance Manufacturing Operations.
Understanding of GMP requirements in a Bio-pharmaceutical Facility.
Excellent communication skills.
Ability to multi task.

This role is based on shift pattern of 24/7. This involves 12 hour shifts on days and nights, with a 33.33% shift allowance.