Job Description

Competitive salary and bonus + excellent benefits

Days shift

Holmes Chapel, UK based



This role provides testing, reporting and investigation laboratory activities to enable compliant, on time delivery of product to market. This is a key position within a QC team ensuring that the exacting standards of GMP, Site procedures, HSE and LEAN are delivered at all times



\xc2\xa7 Good technical knowledge and expertise of quality control principles and systems in a GMP environment.

\xc2\xa7 Computer-literate with experience in the use of Laboratory (LIMS, Data capture) systems as well as MS Word, Excel and PowerPoint

\xc2\xa7 Demonstrated ability to actively participate in projects and investigation

\xc2\xa7 Knowledge and understanding of global pharmaceutical regulations and guidelines.

\xc2\xa7 Demonstrates competence and clarity in both written and oral communication e.g. presentations at team meetings, ability to write ILIs and demonstrates understanding to execute FSIs as well as non-complex technical and investigational reports, communication at team meeting

\xc2\xa7 Good interpersonal skills with an ability to communicate procedures and concepts within the team and on occasions to the department. Ability to train instructional techniques

\xc2\xa7 Self-motivated with ability to plan and manage own workload with some supervision during the working day.

\xc2\xa7 Challenges and questions locally and across team ways of working to seek improved processes and performance

\xc2\xa7 Takes responsibility for supporting change, is prepared to take or support action, and/or escalate to ensure implementation of appropriate actions

\xc2\xa7 Ability to respond to auditor questions and describing local systems on external audit tours with positive outcomes

\xc2\xa7 The individual should have good knowledge and understanding of the principles and concepts of compliance management and GMP/GLP

\xc2\xa7 The individual should have a good understanding of analytical chemistry or microbiology, laboratory instrumentation and/or related information systems.

\xc2\xa7 The individual should have a basic understanding of the industry and be responsive to of regulatory changes, new technologies, Pharmacopoeial requirements and their impact on the function.

\xc2\xa7 An understanding of own quality assurance function, as well as a basic understanding of other functions and how they contribute to achieving the objectives of the business.

\xc2\xa7 The individual has some understanding of business functions and supports reacting to issues on how QC performance impacts functional customer service.



\xc2\xa7 A science degree / HND/ NVQ 4 or equivalent with at least 1 years working experience in a GMP environment

About Recipharm
Recipharm is a leading Contract Development and Manufacturing Organisation (CDMO) in the pharmaceutical industry employing almost 9,000 employees. Recipharm offers manufacturing services of pharmaceuticals in various dosage forms, production of clinical trial material and APIs, pharmaceutical product development and development and manufacturing of medical devices. Recipharm manufactures several hundred different products to customers ranging from big pharma to smaller research and development companies. Recipharm\'s annual turnover is approximately SEK 11 billion. The company operates development and manufacturing facilities in France, Germany, India, Israel, Italy, Portugal, Spain, Sweden, the UK and the US and is headquartered in Stockholm, Sweden.

For more information on Recipharm and our services, please visit www.recipharm.com

Recipharm