Quality Control Analyst Placement

by Bard Pharmaceuticals

Job Details

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Deadline: 29th January 2018
Length: Placement (10 Months+)
Roles: Manufacturing, Pharmaceutical
Location: East of England
City: Cambridge

About Bard Pharmaceuticals

Bard Pharmaceuticals Limited is the Production and Supply Chain business of the Napp Pharmaceutical Group. We have a collaborative approach to business and a strong track record in manufacturing innovative treatments that make a difference to patients’ lives.

We have great products, modern technology, outstanding facilities and, more importantly, highly talented people who make our company one of the best employers and places to work. We are committed to providing our employees with excellent training and development opportunities and we are currently looking for an exceptional individual to come and join us.

Quality Control Analyst Placement

Broad purpose of role:

To provide practical, analytical support within the Analytical systems section and Quality Control sections, assisting in the routine maintenance and daily upkeep of the laboratory and instrumentation. Assist in the analysis of product and raw materials where required.
To gain practical, laboratory experience, to support theoretical knowledge and technical skills.

Specific Duties & Responsibilities

  • To assist method re-qualification and product validation.
  • Assist in the routine maintenance and performance testing of analytical equipment.
  • Carry out the analysis and testing of pharmaceutical ingredients and appropriate product batches for affiliated companies within the Purdue, Mundipharma, Napp and Bard group.
  • Assist in solving supply chain/manufacturing process investigations and projects.
  • Ensure the maintenance and checking of accurate and comprehensive records of the work undertaken within projects. As appropriate, ensure reports and presentations are prepared to the highest standard and review their content and accuracy.

  • Ensure that all activities are undertaken in compliance with company standard operating procedures (SOP’s), relating to documentation and record keeping, Good Laboratory and Manufacturing Practice (GxP) and Health and Safety in the workplace.

  • Undertakes any other reasonable tasks as requested by the Department Manager, Head of Section and Section Leaders.
  • Leadership Attributes and Core values. Must be able to demonstrate and perform in accordance with the leadership attributes and core values of the Company.

How to apply

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