22 Feb

Senior Production Scientist Jobs Vacancy at Scantec Woking

Position
Senior Production Scientist
Company
Scantec
Location
Woking ENG
Opening
22 Feb, 2018 30+ days ago

Scantec Woking urgently required following position for Senior Production Scientist. Please read this job advertisement carefully before apply. There are some qualifications, experience and skills requirement that the employers require. Does your career history fit these requirements? Ensure you understand the role you are applying for and that it is suited to your skills and qualifications.

Follow the online directions, complete all the necessary fields, and provide all relevant information so your application is submitted correctly. When you click the 'Apply this Job' button (open in new window) you will be taken to the online application form. Here you will be asked to provide personal and contact details, respond to employment-related questions, and show how you meet the key selection criteria.

Senior Production Scientist Jobs Vacancy at Scantec Woking Jobs Details:

Senior Production and Process Development Scientist, £40,000 -£45,000, Woking.

My client is an established Pharmaceutical business. Following a period of growth they are looking to recruit a Senior Production and Process development Scientist into the business on a permanent basis.

The primary remit of the role will be to provide management to the manufacturing function and to manage GMP compliance across the site, implementing continuous improvement activities across formulating, QA, QC and Production.

Duties will include; –

Coordinate manufacturing, distribution and labelling of pharmaceutical products in line with customer requirements, SOP’s and GMP guidelines. –
Project manage continuous improvement initiatives across the site. –
Be accountable for all production operations. –
Develop and train members of the team in the generation of technical documents, such as Batch Manufacturing Records, SOP’s, User requirements and validation change control. –
Coordinate both QC and QA teams to ensure appropriate testing of raw materials and finished products. –
To lead Quality investigations. –
Ad hoc duties as required.

To be considered for the role, candidates should have; –

A number of years GMP experience and pharma experience –
CRO experience desirable but not essential –
Experience supervising teams –
Implement continuous improvement activities –
Strong interpersonal skills –
Excellent communicator

To apply, please forward your CV for immediate consideration.


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