Job Details

GMP Production Manufacturing Technician

Job Description

GMP Production Manufacturing Technician Opportunity andndash; Swindonandnbsp; andnbsp; andnbsp; andnbsp; andnbsp; andnbsp; andnbsp; andnbsp; andnbsp; andnbsp; andnbsp;andnbsp;

Opportunity:

An exciting opportunity has been created due to company growth.andnbsp; My client a global pharmaceutical manufacturing company are looking to recruit a Production Manufacturing Technician based in Swindon where you will be working in a GMP clean room manufacturing environment making drug products / compounding as allocated on the production planning system to cGMP, current pharmaceutical regulations, whilst adhering to EHandamp;S requirements.

The hours of work are:

7:00 am to 7:00 pm / 7:00 pm to 7:00 am / 2 days / 2 nights then 4 days off.

Day to day duties include:

  • Accurately complete documentation related to the Encapsulation process.
  • Operate and maintain up to two Encapsulation Machines (and covers up to as many as four during breaks).
  • Maintaining a clean work area.
  • Performing in-process checks and evaluating in detail, product quality.
  • Monitoring material and gel usage at the machine and change receivers as needed ensuring that components are not used past expiration date and time.
  • Monitoring encapsulation process to minimize rejected product at the machine.
  • Tearing down machine at changeover.
  • Setting-up/assembling Encapsulation Machine for operation per batch record instructions.
  • Troubleshooting equipment to maintain a quality product.
  • Monitoring and replenishing solvents and lubricants as required.
  • Stock control and replenishment. andnbsp;
  • Packaging and labelling.

This is a 3 months contract based in Swindon which will be reviewed for a possible extension or go permanent but this is all dependent on the candidate and business performance.andnbsp;

The PAYE rate andpound;13.90 per hour.

Skills:

To apply for the role of GMP Production Manufacturing Technician you will have the following:

  • Ideally Pharmaceutical / medical device GMP production / manufacturing / operator experience.
  • High attention to detail and strong documentation skills.
  • Familiarity with ERP systems (JDE preferred), MS Office, and inventory control processes.

How to Apply:

To apply for this one off opportunity, please send a word copy of your CV to me now by clicking on the Apply button or call me for a confidential chat.andnbsp; Please ensure you have read and agree to our Privacy Policy which can be found on the Quality Startandnbsp;website.andnbsp;andnbsp;

If this sounds like the role for you or a colleague then please donandrsquo;t hesitate to contact us. If we manage to successfully fill a permanent placement from your recommendation then we will send you a cheque of andpound;300. We also have many incentive schemes for referring contractors/temp staff so please contact us with the referral and we can provide you with more information.

For a list of our current vacancies, please visit the Quality Start website.andnbsp;

If you do not hear from Quality Start within 2 weeks your CV has not been short listed for this role.andnbsp;

Quality Start are acting as a specialist recruitment consultancy for this role.