Our client is a specialist in implementing quality systems to businesses UK wide. They have a requirement for a QA Auditor specialising in ISO 27001 to work for their client base throughout Northern Ireland.
In your role as QA Auditor, you will conduct audits both desk based or on site, provide reports and support and provide advice in helping businesses to develop their quality systems. You must be qualified to auditor status in ISO 27001, preferably to lead auditor level and possess a proven track record in auditing to ISO standards.
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For more information, or to apply for this QA Auditor position, please contact Barney Smith at CK Science on 0191 384 8905 or email bsmith@ckscience.co.uk. Please quote reference DH21065 in all correspondence.
Our client, an innovative and industry leading Instrumentation and Medical Technology manufacturer, are currently looking for a Quality Manager to join their growing QA & RA Team based from their site in Hampshire, UK.
Working as a Quality Manager, you will be responsible for fostering, driving forward and embedding the organisation’s Quality Management Systems (QMS) in line with industry quality (ISO) and regulatory standards in terms of productdesign control, production, training of staff and customer support. Within these areas, you will also be required to initiate, facilitate and support process improvement; ensuring CE marked products meet EEA standards and directives as well as overseeing all product UL listings.
This is an outstanding opportunity to join a growing organisation that provides specialist Instruments and Technology to industries such as the Life Sciences, Biotechnology and Cell Science industries.
To be considered for this Quality Manager role, you will have a degree (or equivalent) in a relevant Scientific discipline and proven practical experience in a Quality Assurance (QA) or Regulatory Affairs (RA) function within the Instrumentation, Medical Device or a related industry. It is also essential to have knowledge of ISO quality standards (Incl. ISO 9001) and demonstrated supervisory or management experience.
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For more information or to apply for this Quality Manager position, please contact Andrew Bolton at CK Science on 01438 723 500 or email abolton@ckscience.co.uk. Please quote reference ST21022 in all correspondence.
Our client a blue chip pharmaceutical company located in Angus seeks a Quality Assurance Officer on a long-term temporary basis.
The main duties of this Quality Assurance Officer role will include:
To manage the batch release process
Participate in FDA, MHRA and internal audits
Investigate complaints
Continuous Improvement process
Deliver training on QA principles
Ensure activities are conducted to GMP and the site Quality Management System (QMS)
The successful candidate for this Quality Assurance Officer will have a degree in a science discipline or have demonstrable experience from a GMP regulated environment in a Quality Assurance function.
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For more information, or to apply for this Quality Assurance Officer position please contact Graeme Pallas at CK Science on 0191 384 8905 or email gpallas@ckscience.co.uk. Please quote reference DH21017 in all correspondence.
We are currently searching for a QA/QCTechnical Manager to join a new state of the art dairy processing facility on the South Coast.
The company are currently looking to double their output capacity and branch into Europe and as such they require a Technical Manager with the ability to change the company culture and drive them forwards.
You will oversee the QA and QC divisions as well as being heavily involved with product production, customer liasion and tackling commercial needs.
The ideal candidate will have the technical expertise to take on this senior role and will have knowledge and experience of the dairy industry and microbiology (aseptic).
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For more information, or to apply for this QA/QC Technical Manager position, please contact Barney Smith on 0191 384 8905 or email bsmith@ckscience.co.uk. Please quote reference ST20861 in all correspondence.
CK Science are currently searching for a QA/QC Technical Manager to join a new state of the art dairy processing facility on the South Coast.
The company are currently looking to double their output capacity and branch into Europe and as such they require a Technical Manager with the ability to change the company culture and drive them forwards.
As QA/QC Technical Manager you will oversee the QA and QC divisions as well as being heavily involved with product production, customer liasion and tackling commercial needs.
The ideal candidate for this QA/QC Technical Manager position will have the technical expertise to take on this senior role and will have knowledge and experience of the dairy industry and microbiology (aseptic).
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For more information, or to apply for this QA/QC Technical Manager role, please contact Jason Johal at CK Science on 01438 723 500 or jjohal@ckscience.co.uk. Please quote reference ST20861 in all correspondence.
Working within this busy Quality Assurance department based in Suffolk, as Senior QA Officer, you will be responsible for reviewing documentation in accordance with in-house specifications and cGMP.
Responsibilities:
As a Senior QA Officer, you will work to maintain and manage quality systems regarding cGMP for the site and support or perform audits and inspections to assure compliance with regulations. You will provide QA advice for deviation investigation and root causing, provide QA advice for change management and facilitate internal audits and inspections under direction and produces reports and action plans.
Qualifications and Experience:
The ideal candidate for this Senior QA Officer position will have demonstrated knowledge of working within a quality management system and cGMP and demonstrate the ability to successfully facilitate quality project work or audits.
This is a great opportunity to join a growing pharma company in the Suffolk region with excellent commuting links to Cambridge and the North.
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For more information, or to apply for this Senior QA Officer position, please contact Julie Marshall at CK Science on 01438 723 500 or email jmarshall@ckscience.co.uk. Please quote reference ST20551 in all correspondence.
We are currently looking for a QA Manager with extensive knowledge of GLP to join a Research company based in London, UK.
As QA Manager, you will be expected to develop a QA GLP & GCP laboratory audit strategy and implement an audit program in line with the overall QA strategy. You will also be expected to provide assurance that company GLP & GCP laboratory studies are performed in accordance with GLP regulatory requirements and local laws.
Day to day, responsibilities of this QA Manager will include:
The authoring of QA SOP’s and review of functional SOPs
The implementation of in-house GLP training programmes
The implementation and management of audit programs including audits of Study Reports, Facilities, In Process, Critical Phase, Protocols, Sub-Contractors and Suppliers and signing QA statement on GLP reports and protocols audited.
Project management responsibilities of this QA Manager position will involve providing support to pre-clinical staff and study directors on quality/regulatory issues, providing GLP& GCP laboratory advice and support to pre-Clinical personnel and ensuring project timelines are met.
The ideal candidate for this QA Manager role will hold a Degree, Masters or PhD in a Scientific Discipline (or equivalent) and will have industry GLP regulatory pharmaceutical/CRO experience. As you will be ensuring work is carried out according to GLP & GCP standards and you will be providing guidance and information on all aspects of Quality Assurance related to GLP activities, it is essential that you have experience of QA hands on auditing and Quality System experience including protocol, report, in process, critical phase and suppliers. A good knowledge of pre-clinical processes is also required.
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For more information, or to apply for this QA Manager position please contact Jason Johal at CK Science on 01438 723 500 or email jjohal@ckscience.co.uk. Please quote reference ST20673 in all correspondence.
You will act as Qualified Person (QP) for all products manufactured on the site and will be the key contact point for all QA/GMP issues on the site. This is a permanent position.
As a QP you will be responsible for the release of products to the market within the Directive 2001/83/EC and as named on the Manufacturer’s Licence. You will also release both Raw Materials and Bulk products and act as deputy Pharmacovigilance Qualified Person.
As part of this QP role you will be expected to develop appropriate QA systems for the site, approve master batch manufacturing and packing documents, review and QA approve SOPs, manage and implement the internal and external audit programmes and to review and approve change requests.
The ideal candidate for this QP role, you will hold a chemistry or pharmacy degree (or equivalent), will be on the register of eligible Qualified Persons and named in the appropriate Manufacturer’s Licence. You will also have experience gained within the pharmaceutical industry of working in a laboratory and an appreciation of other aspects of the business.
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For more details, or to apply for this Qualified Person position, please contact Jason Johal at CK Science on 01438 723 500 or email jjohal@ckscience.co.uk. Please quote reference ST20451 in all correspondence.
Our client is a food manufacturer based in the North East of England. Due to an internal promotion, they require a Senior Analyst to join their team.
Working closely with the Quality Manager and QA team, As Senior Analyst you will be responsible for maintenance and calibration of all laboratory equipment, manage the day to day running of the laboratory, train QA assistants to in house methods and system, provide laboratory support for new project work and co-ordinate external laboratory audits.
The ideal candidate for this Senior Analyst position will be qualified in a scientific subject or possess equivalent industrial experience. You must also have a proven track record in food chemistry analysis and supervisory roles.
Apply now For more information, or to apply this Senior Analyst position, please contact Barney Smith at CK Science on 0191 394 8905 or email bsmith@ckscience.co.uk
Our client, a leading provider of pharmaceutical dosage form development, is currently seeking to recruit a QP to work with them at their site in Nottingham on a permanent basis.
The QP will be responsible for the following:
Managing and implementing the quality policy and have quality management responsibility as defined in ISO17025:2005 and ensure compliance
Perform QP certification
Keep up to date with pharmaceutical regulation in the EU and USA
Monitor and correct any quality aspects in the facility
Authorise batch documentation prior to release
Manage staff in the QA function
Assist in GMP training
Perform audits and chair review meetings.
The ideal candidate for this QP role will be educated to degree level, or equivalent, in a scientific subject, and have commercial/IMP QP status. Experience within a similar position as well as an awareness of IMP development up to Phase 2 CT is also required.
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For more information, or to apply for this QP position online now, please contact Philippa Robertson on 0114 283 9956 or email probertson@ckscience.co.uk. Please quote reference SH20158 in all correspondence.
