Process Operator Job Edinburgh area,City of Edinburgh Scotland UK,Manufacturing / Production

Location: City of Edinburgh

Role Overview

To operate pharmaceutical plant to manufacture bulk pharmaceuticals, intermediates and other chemical products in accordance with current good manufacturing practice (cGMP) and Health and safety practices.

Core Responsibilities

To perform chemical reactions according to batch sheet and process instructions as requested.
To recognise key reaction criteria and notify a Supervisor or Shift Manager of any unusual signs.
To record process changes and notify a Supervisor or Shift Manager where appropriate.
To operate equipment and conduct all plant operation and activities according to good manufacturing practice (cGMP), complying with current SOP's and appropriate health and safety precautions and Controlled Drug regulations.
To carry out material handling duties as necessary for the operation of the Production plant.
To operate mechanical and electro‑mechanical material handling equipment as required.
To weigh and check weigh materials and containers and record the weight as appropriate.
To dispense liquids to and from drum stocks and bulk supplies and to record the quantities dispensed.
To perform and record cleaning procedures for vessels and plant as appropriate in accordance with cGMP.
To clean drums, tanks and other containers for disposal or reuse.
To wear appropriate protective clothing for personal protection and protection of the product from contamination.
To exercise an appropriate degree of care in the handling of hazardous materials.
To record and maintain full and accurate process records as required.
To ensure that waste materials, or waste streams for analysis or otherwise are appropriately handled and labelled.
To carry out in‑process sampling and in‑process testing as required.
To assist with the operation of plant and equipment in the introduction of new products and the development of existing processes.
To carry out on‑plant/process training of operating staff where directed by supervisory staff.
Participate in Continuous Improvement and Lean Manufacturing activities on site.
To conduct any other reasonable tasks as required by Supervisor Staff.
To carry out any other duties which are within the employee’s skills and abilities whenever reasonably instructed.

Special Factors

This role involves day/night shift working.

Qualifications

A Diploma in Process Technology is desirable.
Experience in a fine chemical or related processing industry would be desirable, but not essential, as training will be given.
Experience of working within a cGMP environment preferred.

Additional Information

Under UK legislation, we are required to ensure that all employees have the legal right to work in the UK, both at the time of offer and throughout their employment. Please note that we are not able to provide sponsorship for this role, so applicants must have the necessary right to work in place independently.

Veranova is an equal opportunities employer and positively encourages applications from suitably qualified and eligible candidates regardless of sex, race, disability, age, sexual orientation, marriage or civil partnership, pregnancy or maternity, religion or belief.

All applications are carefully considered, and your details will be stored on our secure Application Management System. This is used throughout Veranova for the selection of suitable candidates for our vacancies as they arise. Veranova respects your privacy and is committed to protecting your personal information. For more information about how your personal data is used please view our privacy notice.

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