Posts Tagged ‘quality assurance’

Qualified Person Job – Hertfordshire, UK

Tuesday, April 5th, 2011

CK Science are working exclusively on an assignment for a Qualified Person to join a global Pharma company based in Hertfordshire.

The company work on discovery of new molecules both NCEs and NBEs, in the branded generics markets and they also market APIs. They employ 6000 people in over 80 countries and have twelve manufacturing facilities and five R&D centres across Europe, Asia, Africa and South America. They are currently selling products in over 70 countries and are one of the most exciting and expanding pharma companies in the world today.

Responsibilities:

This role is based in the Generics  arm of the business and you will act as a Qualified Person in accordance with EU GMP to provide final certification/release along with Quality Assurance a Regulatory support. You will perform audits of third party providers in order to ensure EU GMP standards have been achieved and will support the internal audit programme to enable permanent inspection readiness. You will also provide QP GMP declarations in support of importation activities and will be expected to maintain an up to date awareness of regulatory issues.

 

Qualifications and experience:

It is essential that you are a fully qualified QP and that you are experienced with final certification/release within the EU. Quality systems management, audit experience (internal and external) and a strong EU regulatory understanding are also essential for this role. A good knowledge of Quality Systems (compliance, CAPA, continuous improvement) and importation would be advantageous.

The ideal person will have the experience and the confidence to interact with QA and Regulatory teams and will have the strength of character to guide teams of professionals. Generics QP experience would be adistinct advantage but applications from QPs that have had exposure to a broad range of activities are welcome. 

This is a key role for the company and is a sign of their ambition for the future. The position is full time, permanent and it is envisaged that the role will be based on site. 

This role is being handled exclusively by CK Science and we would be happy to discuss details further at your convenience.

 

Apply now

For more information or to apply for this Qualified Person role, please contact Jason Johal at CK Science on 01438 723 500 or email jjohal@ckscience.co.uk. Please quote reference ST21673 in all correspondence.

Apply online now!

Regulatory Conformance Officer Job – County Durham, UK

Thursday, February 3rd, 2011

Our client, a major pharmaceutical company located in County Durham, seek a Regulatory Conformance Officer to join their company based in County Durham on a temporary basis.

Responsibilities:

The main responsibilities of this Regulatory Conformance Office  role are to minimise risk to the supply chain as a result of non-compliance activities, provide compliance solutions, help meet the training needs for the site and represent regulatory conformance in tech-transfer project teams for new product introduction.

Person Specification:

The ideal candidate will have knowledge of GMP, CFR, FDA, MHRA and other regulatory authority requirements, have excellent communication skills, demonstrate understanding of OE tools and techniques, new business introductions, new business applications and supply chain operations.

Apply Now

For more information or to apply for this Regulatory Conformance Officer position, please contact Graeme Pallas at CK Science on 0191 3848905 or email gpallas@ckscience.co.uk.

Alternatively, click here to apply for this Regulatory Conformance Officer position online now.

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Quality Assurance (QA) Specialist Job – Berkshire, UK

Tuesday, January 11th, 2011

We are currently recruiting for a QA Specialist to join a Global Pharma company based in Berkshire in a brand new role to provide QA Support for Pharmaceutical products within their Medical Division.

We are looking for someone that is experienced in the following:

  • Developing and managing QMS
  • The management of complaint handling of both imported and UK manufactured products for UK markets
  • The development and implementation of Change Control systems
  • The management of non-conformance management processes (including ER, CAPA & SCARs)
  • The ability to conduct supplier audits and create / review technical agreements.

The ideal candidate for this QA Specialist position will have gained experience of QA within the Pharmaceutical or Medical Device industry and will be experienced with GDP and GMP. An understanding and preferably training in ISO and FDA/MHRA regulatory requirements is also required.

This QA Specialist role will involve travel to suppliers and occasional trips to European sites.

 

Apply Now

For more information or to apply for this QA Specialist position, please contact Jason Johal at CK Science on 01438 723 500 or email jjohal@ckscience.co.uk. Please quote reference ST21098 in all correspondence.

 

Alternatively, click here to apply for this QA Specialist position online now.

 

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Quality Assurance Officer Job (Pharmaceutical) – Angus

Friday, December 17th, 2010

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.

 

Apply Now

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.

Alternatively, click here to apply for this Quality Assurance Office position online now. 

Senior QA Officer Job – Suffolk, UK

Tuesday, October 12th, 2010

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.

Apply Now:

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.

Alternatively, click here to apply for this Senior QA Officer position online now.


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QA Manager Job – London, UK

Thursday, October 7th, 2010

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.

Apply Now

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.

Alternatively, click here to apply for this QA Manager role online now.


 

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Senior QA Officer Job – Cambridgeshire, UK

Tuesday, August 31st, 2010

Our client, is a leading global biotechnology company based in the Cambridgeshire/Suffolk area, looking for a Senior Quality Assurance Officer to join their QA team.

As Senior QA Officer, you will be responsible for reviewing documentation in accordance to in-house specifications as well as cGMP. You will also provide QA advice for deviation investigation, root causing and change management. Part of the role will include internal auditing and supervision of less experienced staff.

To be successful for this Senior QA Officer role you will have a BSc in a scientific discipline (or equivalent). Previous experience with deviation investigation, batch release of API and dealing with customer complaints is essential. Experience in auditing or documentation review within a Quality Management System is also essential.

This is a fantastic opportunity to join a biopharmaceutical company within an easy commuting distance from Cambridge.

Apply Now

For more information, or to apply for this Senior QA Officer position, please contact Reena at CK Science on 01438 723 500 or email rdhana@ckscience.co.uk. Please quote reference ST20411 in all correspondence.

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QA Officer (Medical Devices) – North East, UK

Thursday, August 19th, 2010

Our client is urgently seeking two experienced QA (Quality Assurance) Officers to join their team on a short term contract basis to assist with the company’s preparations for an FDA audit.

Duties of these QA Officer roles will include checking batch records for compliance with cGMP and dealing with non-conformances.

The ideal candidate for these QA Officer positions will have some previous experience in a QA role in medical devices, diagnostics or pharmaceuticals, together with some experience of FDA audits.

Apply Now

For more information, or to apply for these QA Officer roles, please contact Graeme Pallas on 0191 384 8906 or email gpallas@ckscience.co.uk. Please quote reference DH20357 in all correspondence.

Alternatively, click here to apply for this QA Officer position online now.

QP (Pharmaceuticals) – Nottingham, UK

Thursday, July 22nd, 2010

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.

 

Apply now

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.

Alternatively, click here to apply for this QP role online now.

Quality Manager (Polymers) – North West, UK

Thursday, July 8th, 2010

A high performance polymer manufacturer based in the North West of England is currently recruiting for a Quality Manager to lead their QC, QA and Specifications departments.

The key roles and responsibilities of this Quality Manager will include:

  • Implementation of QC and QA systems
  • Implementing analytical and statistical techniques
  • Polymer manufacture
  • Extrusion and compounding processes
  • Supporting internal customers and successfully managing quality relationships with external
  • Customers. This will include performing audits and carrying out questionnaires.

As an experienced leader, you will enthusiastically lead, develop and coach the quality team to successfully meet objectives and to drive continuous improvement.

The requirements for this Quality Manager role are as follows:

  • You must have a proven track record of successful implementation of QC and QA systems.
  • An excellent understanding of analytical and statistical techniques and proven experience and understanding of polymer manufacture, extrusion and compounding processes is essential.
  • You will have strong analytical, statistical and problem solving skills and also well developed communication and negotiation skills.
  • You will be educated to degree level (or equivalent) in a relevant discipline and qualified in advanced statistical techniques with excellent IT skills.
  • You will be a quality assurance professional certified as an ISO9001 and ISO13485 auditor.

 

Apply now

For more information, or to apply for this Quality Manager job, please contact Victoria Walker at CK Science on 0114 283 9956 or email vwalker@ckscience.co.uk.

Alternatively, click here to apply for this Quality Manager job online now.

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