Technical Manager – Lancashire

Victoria Walker is recruiting for a Technical Manager to join an cleaning chemicals manufacturing company based in Lancashire on a permanent basis.

Responsibilities include acting as a strategic interface between key stakeholders on product related matters, creation and maintenance of all QA Systems and be a driver of NPD for the business.

Our client is looking for a professional with a background in the soap/detergent industry and with experience in QA, Regulatory, FMCG, the NPD process and management.

Click here for more information or to apply

 

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Regulatory Section Head – West Midlands

Naynesh Mistry at CK Science is currently recruiting for a Regulatory & Intellectual Property Section Head to join a leading protein specialist company based in West Midlands on a permanent basis.

Responsibilities:

As a Regulatory Section Head you will:

  • Have management responsibility for the successful operation of the Regulatory affairs, FDA submission.
  • Management of FDA submissions, including keeping up to date with FDA directives which are pertinent to the company’s submissions and future targets.
  • To co-ordinate workload and set objectives for direct reports to ensure that operational objectives of the department are met and delivered within agreed timescales.
  • To agree personal development plans and be responsible for the annual appraisal process (including training planning and review) with direct reports and provide assistance and guidance in the management of indirect reports.
  • Assessment and management of staff.
  • Management of the departmental budgets.
  • To understand and plan the capacity of the departments.
  • To recruit staff as appropriate, in line with business needs.

Qualifications:

The successful Regulatory Section Head will have the following qualifications, skills and experiences:

  • BSc Hons biological sciences or related discipline
  • PhD or a Post graduate qualification in RA, patent law, ethical submissions
  • Successful FDA, regulatory body or IP submissions
  • Experience in RA, Intellectual Property or Ethical submissions
  • Experience in either  regulatory submissions (including 510K) , Pre-IDE, Ethics, IP submission
  • Willingness to travel and work weekends (both whilst abroad and at home) to meet the companies needs.

If successful you will be joining a leading Protein specialist company in the UK.

Naynesh Mistry - Recruiter at CK ScienceHow to apply:

Apply online:

To apply for this Regulatory Section Head position contact Naynesh Mistry via email: nmistry@ckscience.co.uk  or telephone 0114 283 9956.  Please quote reference SH25838 in all correspondence.

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Pharmaceutical Technical Executive – London

Jason Johal at CK Science is currently recruiting for a Pharmaceutical Technical Executive to join an international speciality Pharmaceutical company based in London on a 6 month contract initially.

Responsibilities:

As a Pharmaceutical Technical Executive you will:

  • Provide a technical support service to the Medical and Regulatory Affairs Unit
  • Advise on all relevant product issues
  • Approve technical documentation provided by third parties
  • Investigate and resolve technical issues from manufacturers
  • Be involved in site transfer projects
  • Be responsible for compliance documents
  • Be responsible for expert document writing
  • Apply for licences

Qualifications:

The successful Pharmaceutical Technical Executive will have the following qualifications, skills & experiences:

  • BSc in Pharmacy or Chemistry or equivalent
  • Relevant technical experience gained in the pharmaceutical industry
  • Regulatory experience of CMC documentation (essential)
  • Manufacturing experience (essential)
  • CMC sections experience
  • Document control experience (essential)
  • Regulatory knowledge needed including regulatory licensing
  • Product development experience
  • Technical knowledge across a range of dosage forms (tableting experience is essential)
  • Auditing experience
  • Problem solving experience (essential)
  • Experience dealing with 3rd party manufacturers (advantageous)
  • Technical Transfer knowledge
  • API & Finished product experience

Benefits:

If successful for this Pharmaceutical Technical Executive, you will be joining a rapidly growing pharma company with several new product realised already this year and several more in the pipeline.  In return you will gain excellent development experience an attractive salary and if successful career progression opportunities.

Jason Johal - Manager at CK ScienceHow to apply:

Apply online:

For more information or to apply for this Pharmaceutical Technical Executive position, please contact Jason Johal jjohal@ckscience.co.uk or 01438 723 500. Please quote reference ST24799 in all correspondence.

 

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Pharmaceutical Technical Executive – London, UK

Jason Johal at CK Science is recruiting for a Pharmaceutical Technical Executive to join an international speciality Pharmaceutical company based in London on a 6 month initial contract.

This is an excellent opportunity to join a growing pharmaceutical company with several new products launched this year and several more in the pipeline. As Pharmaceutical Technical Executive you will gain excellent development experience, and attractive salary and excellent personal development opportunities.

The Role:

As Pharmaceutical Technical Executive you will:

– Provide a technical support service to the Medical and Regulatory Affairs Unit

– Advise on all relevant product issues

– Approve technical documentation provided by third parties

– Investigate and resolve technical issues from manufacturers

– Be involved in site transfer projects

– Be responsible for compliance documents

– Be responsible for expert document writing

– Apply for licences

 

Qualifications, Skills and Experience:

The successful Pharmaceutical Technical Executive will have the following qualifications, skills & experiences:

– BSc in Pharmacy or Chemistry or equivalent

– Relevant technical experience gained in the pharmaceutical industry

– Regulatory experience of CMC documentation (essential)

– Manufacturing experience (essential)

– CMC sections experience

– Document control experience (essential)

– Regulatory knowledge needed including regulatory licensing

– Product development experience

– Technical knowledge across a range of dosage forms (tableting experience is essential)

– Auditing experience

– Problem solving experience (essential)

– Experience dealing with 3rd party manufacturers (advantageous)

– Technical Transfer knowledge

– API & Finished product experience

 

 

How to Apply:

 

Jason Johal at CK Science is recruiting for a Pharmaceutical Technical Executive – London

Please contact Jason for more details.

Click here to apply online now.

For more information regarding this Pharmaceutical Technical Executive position, contact Jason Johal via email: jjohal@ckscience.co.uk or telephone: 01438 723 500.Please quote reference ST24799 in all correspondence.

 

 

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Product Compliance Head Job in East Midlands

Naynesh Mistry at CK Science is currently recruiting for a Product Compliance Head to join a global pharmaceutical company at their site based in the East Midlands on a permanent basis.

Product Compliance Head Job Description

As Product Compliance Head, you will manage the compliance across the 3 production units, ensuring that all aspects of the handling, manufacturing and distribution of pharmaceutical products comply with the requirements of the Quality Manual and Policies and meet all relevant cGMP regulatory and legislative requirements

The purpose of this Product Compliance Head position is to provide technical leadership for the site in all product quality compliance related matters and ensure operational business comply with cGMP legal and regulatory requirements.

Key responsibilities of this Product Compliance Head job will include:

  • Ensure that all aspects of the handling, manufacturing and distribution of pharmaceutical products at the site comply with the requirements of the Pharma Corporate Quality Manual and Policies and meet all relevant cGMP regulatory and legislative requirements.
  • Ensure that the local Quality System and Standard Operating Procedures are in place and that compliance with cGMP
  • Ensure that a high quality of products is achieved through qualification and validation based upon quality risk analysis.
  • Ensure that the QA department maintains an innovative approach based on improvement, implementation of best practice.
  • Provide leadership, direction and support to the people within the QA Compliance area and ensure that they are qualified, achieve a high level of competence, are motivated and carry out their duties in a safe manner.
  • Maintain current knowledge of local and international regulatory and legislative requirements and trends to ensure that expert advice and appropriate technical support on product quality related matters is provided to the whole site.
  • Ensure that all components, drug product containers, closures, in process materials, packaging material, labelling and drug products are released in accordance with the registered specifications.
  • Manage complaints, recalls, counterfeits and product tampering according to the company Corporate Quality Manual.

To be considered for this Product Compliance Head position, you will have the following qualifications, skills and experience:

  • A degree in Sciences or equivalent
  • Experience in Quality Assurance and Quality Control and/or in manufacturing environment within the Pharmaceutical industry.
  • Previous experience in API manufacture and ICH guidelines are preferred, however experience within secondary pharmaceutical manufacture will also be considered if you show the technical and managerial skills required for this role.
  • Sound knowledge of pharmaceutical regulatory requirements and be familiar with international guidelines, including FDA and MHRA.

Naynesh Mistry - Scientific Recruitment Consultant at CK Science

Please contact Naynesh for more details.

How to apply:

Please click here to apply online now.

For more information regarding this Product Compliance Head position, please contact Naynesh Mistry at CK Science on 0114 283 9956 or email nmistry@ckscience.co.uk. Please quote reference SH24328 in all correspondence.

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Regulatory Manager – East Anglia

Jason Johal at CK Science is currently recruiting for a Regulatory Manager to join a global Biopharma company in East Anglia and close to Cambridge

The Job:

The role of this Regulatory Manager job is to provide effective regulatory and strategic input during product development and product life cycle management to support manufacturing activities on site and to ensure regulatory compliance for final product release. This is a dual reporting role to the Director of Quality Operations and to the Director of RA CMC Europe.

Responsibilities:

As a Regulatory Manager  you will have responsibility for 5 Quality Assurance and Regulatory Affairs professional staff and a budget up to $1MM key responsibilities include:

  • Partnering with Global RA CMC to deliver the strategy and execution for the preparation of CMC components for investigational medicinal products, new marketing applications, MAA variations and responses to agency questions.
  • Evaluation of post-approval CMC changes that affect EU MAA and International filings. Good working knowledge of EMA centralized variation system and variation application form. Scientific assessment of all relevant product related documents in compliance with EU regulatory requirements. Preparation of the EU quality components for CMC variations and maintenance of CMC sections in CTD format for EU MAA.
  • Collecting and developing responses to questions from regulatory authorities in close cooperation with project team members in US and EU.
  • Developing and maintaining a knowledge and understanding of current regulatory requirements for manufacture of API and testing, release and distribution of licensed medicinal products.
  • Maintaining regulatory compliance system for therapeutic products to support final product release and distribution to market.
  • Maintaining a high quality standards and a continuous improvement approach in responding to the evolving regulatory environment.
  • Maintaining CMC regulatory documents and liaison with appropriate Regulatory Authorities. This includes Site Master Files and manufacturing licenses and other regulatory approvals are maintained and available for regulatory agency and Customer Inspections.

Qualifications and Skills:

This Regulatory Manager role will require good working relationships with internal customers from QA/QC/Production/ Materials Management to improve regulatory compliance and awareness as well as collaboration with global regulatory personnel to ensure best practices and knowledge of global activities are communicated to site.

The company require someone capable of working independently to achieve goals and objective and with the ability to prioritise and organise daily work to meet overall deadlines. They must be able to influence others in a positive way and to identify and manage their own projects to completion. They will need the following:

  • A good knowledge of Pharmaceutical manufacturing processes and cGMP is essential as is knowledge and experience of international regulatory affairs environment for product life cycle management.
  • Practical experience of European regulatory procedures and the EU centralized procedure both pre and post approval are expected as is a good understanding of global change control management and regulatory compliance.
  • The ability to work on a number of projects with tight timelines, good scientific writing skills and the ability to work independently with minimal guidance are also required.

How to apply:

Apply online now

For more information or to apply for this Regulatory Manager role please contact Jason Johal on 01438 723 500 or email jjohal@ckscience.co.uk.  Please quote reference ST23896 in all correspondence.

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Quality Assurance Representative – North West

Hannah Milward is currently recruiting for a Quality Assurance Representative to join a global manufacturer of pharmaceutical and veterinary medicine products based in the Merseyside region. They require a Contract Quality Assurance Representative to join their team for an initial period of 12 months.

Job Purpose:

The successful candidate for this Quality Assurance Representative will provide the Quality Assurance Team the assurance that manufacturing is carried out in accordance with cGMP and Regulatory commitments and that production records provide full and accurate documentation of batch manufacture in accordance with SOP. The QAR is authorised, as appropriate, by the QA Team Leader to disposition materials with consideration being given to the Regulatory requirement for QP release of veterinary and medicinal products. The job holder also exercises control on the general cGMP activities for those teams he/she has QA responsibility for.

Responsibilities:

The responsibilities of this Quality Assurance Representative role will include:

• Disposition raw materials, including packaging items, water, intermediates and products according to the available data, including evaluation of any deviation reports, environmental monitoring (where appropriate), and advise on reprocessing or preventive actions in such cases.

• Monitor trends and identify problems in quality of purchased materials, packaging, intermediates, products, water and environmental data and promote action having regard to changes in processes, facilities, equipment and procedures.

• Write/revise/approve and give advise on quality documentation e.g. batch production records, specifications, procedures (Team and Site), PMISsheets, Stability protocols.

• Review and approve SOPs (Team and Site), change control documentation, validation protocols, completed validation packages, IQ/OQ/PQ protocols.

• Manage the Site stability programme to meet Corporate and Regulatory requirements.

• To advise on the investigation of customer complaints, approve customer complaint reports and promote corrective/preventive actions

• Participate in self-inspections and other audits of the manufacturing and relevant Support areas with particular reference to cGMP as defined by the various regulatory authorities.

• Provide training, support, advice and proactive assistance in the Site Quality systems to the product and support teams.

• Advise on and support appropriate validation of plant, processes and new projects, liaising with other disciplines appropriately to ensure that facilities are designed and commissioned to meet cGMP.

• Provide cover for other QARs in their absence.

• Prepare Quality Agreements as appropriate.

• Liaise with Contract Manufacturers, as appropriate, to ensure that the Quality systems at the Contract Manufacturers comply with Corporate/Regulatory requirements and that the Quality systems are being implemented appropriately.

Qualifications and skills:

To be considered for this Quality Assurance Representative position you will have experience working in a similar role reviewing and supplying batch record documentation to the QP for release. You will also have experience working in the Pharmaceutical industry.

How to apply:

For more information or to apply for this Quality Assurance Representative role please contact Hannah Milward on 0114 2839956 or email hmilward@ckscience.co.uk. Please quote reference SH23570 in all correspondence.

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Associate Director Job (Pharmaceuticals, Quality Auditing) – Suffolk, UK

We are currently looking for an Associate Director to join a global pharmaceutical company in the Suffolk region.

As Associate Director, you will be responsible for developing and managing audit programs for healthcare compliance and privacy at the company’s facilities to ensure they are meeting the relevant company and regulatory standards.

 

As Associate Director, you will also:

  • Develop and introduce a process for carrying out healthcare compliance audits. This will include the auditing procedure and the reporting of audit results and metrics to senior management.
  • Train company auditors in healthcare compliance auditing.
  • Auditing company facilities including country offices and relevant business units for healthcare compliance.
  • Develop and introduce a process for carrying out privacy audits. This will include the auditing procedure and the reporting of audit results and metrics to senior management.  The audits will check that the organization can both meet the requirements of the company and the relevant regulatory requirements.
  • Train auditors in privacy auditing.
  • Auditing facilities for privacy.

 

Person specification:

The ideal candidate for this Associate Director position will have the following qualifications, skills and experience:

  • Possess a Bachelors degree (or equivalent) with related industry experience.
  • Extensive experience in auditing
  • Expert knowledge of healthcare compliance and/or privacy requirements for the pharmaceutical and/or medical device industries
  • Strong written and oral communication skills.

 

How to apply

For more information or to apply for this Associate Director position, please contact Jason Johal at CK Science on 01438 723 500 or email jjohal@ckscience.co.uk. Please quote reference ST22200 in all correspondence.

 

Click here to apply online!

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Quality Engineer Job – (Medical Device) Hampshire

Our client is a world renowned Medical Device organisation who develop innovative & industry leading devices. They are currently looking for a Quality Engineer to join their QA & RA Division based from their site in Hampshire.

Responsibilities:

Working as a Quality Engineer, you will be responsible for working across the Production, Development & Quality internal teams as well   as external suppliers.

Your duties will include:

  • Developing, creating and maintaining regulatory & quality system (ISO 13485, ISO 9001, Medical Device Directives) documentation
  • Developing & carrying out equipment & process validation
  • Aiding with transfer of new products to manufacturing
  • Carrying out non-conformance & root cause analysis and implementing corrective actions as well as assisting with internal & external (customer & supplier) audits
  • In addition to your duties in the Medical Device side, you will also be involved in supporting a small pharmaceutical division as and when required.

This is an outstanding opportunity to join a blue chip Medical Device organisation, which in return offers an attractive salary, an excellent bonus scheme and benefits package.

Qualification and Experience:

To be considered for this role, you will have a demonstrated background in a Quality Engineer or related Regulatory Engineering  function gained within the Medical Device, Pharmaceutical, Biotechnology or a relevant industry.

Apply now:

For more information or to apply for this Quality Engineer position, please contact Andrew Bolton on 01438 723 500 or abolton@ckscience.co.uk. Please quote reference ST21952 in all correspondence.

Click here to apply online

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Qualified Person Job – Herts

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 Qualified Person role is based in the Generics arm of the business and you will act as a QP 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.

Person Specification:

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.

Apply now

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

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Qualified Person Job – Hertfordshire, UK

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!

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Regulatory Conformance Officer Job – County Durham

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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Preclinical Toxicology Scientist Job (ADME) – Surrey

Our client, a world leading Pharmaceutical organisation, are currently looking for a Preclinical Toxicology Scientist to join their Drug Development Group based from their state-of-the-art facilities in Surrey, UK.

This is an outstanding opportunity to join an early phase drug development group that manages a broad portfolio of new molecular entities from candidate selection through clinical Proof of Concept (PoC).

Working as a Preclinical Toxicology Scientist, you will be responsible for all phases of the toxicology and ADME plans for a product portfolio ranging from large biologics (antibodies, proteins and peptides) to small molecules.

 

Responsibilities:

Your duties will include creation and implementation of preclinical toxicology/ADME plans; development of safety assessment plans; approval of methodology, protocols and final study reports; project management activities related to preclinical work product (timeline, scope, budget, risk mitigation, contingency plans) as well as working closely with quality and regulatory to prepare nonclinical ADME safety pharmacology and toxicology sections of IB, INDs, CTD, IMPDs and other regulatory documentation.

As part of the role, you will also be required to build, establish and communicate a network of preclinical toxicology/ADME content experts as well as a network of external contract vendors to support activities.

 

Person Specification:

To be considered for this role, you will meet the following criteria:

Qualifications:

  • Degree / MSc / PhD in Toxicology
  • Veterinarian Medicine
  • Occupational Health
  • Health Sciences or a related discipline (or equivalent)

 

Experience:

  • Ability to identify structural/chemical class problems that will guide preclinical activities around specific identified issues with a compound.
  • Extensive experience working in Toxicology/ADME or equivalent.
  • Proven practical experience working across multiple phases of drug development.
  • Demonstrated experience preparing GLP regulatory documentation: ICH, FDA, and EMEA non clinical safety, toxicology and ADME guidance.

 

Apply Now

For more information, or to apply for this Preclinical Toxiciology Scientist position, please contact Jason Johal at CK Science on 01438 723 500 or email jjohal@ckscience.co.uk. Please quote reference ST20902 in all correspondence.

 

Alternatively, click here to apply for this Preclinical Toxicology Scientist position online now.

 

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Regulatory Affairs Officer (Chemical) London, UK

Our client, a world leading Chemical Distributor, are currently looking for a Regulatory Affairs Officer to join their UK flag ship facilities based in London, UK.

Working as a Regulatory Affairs Officer, you will be responsible for providing regulatory support to all departments on site including designing and outlining regulatory procedures as well as performing regulatory checks and auditing of all products (ISO 9001, ISO 14001, OHSAS 18001, GHP,REACH) and packaging (CLP) in line with industry quality standards. Your duties will also see you working closely with suppliers and customers to ensure completion and sending out Safety Data Sheets (SDS) and attending 3rd party audits.

This is an outstanding opportunity to join a leading Chemical Distributor who continues to have success across the UK and Europe. In return they offer an attractive salary and benefits package.

To be considered for this Regulatory Affairs Officer role, you will have a degree in Chemistry or a relevant discipline (or equivalent), demonstrated understanding & experience of working to chemical regulatory standards including ISO 9001, ISO 14001, OHSAS 18001 and REACH as well as knowledge of safety data sheets (SDS). Experience of auditing to ISO standards and/or within a supervisory or managerial function would be highly advantageous but it is not essential.

Apply Now

For more information, or to apply for this Regulatory Affairs Officer position, please contact Andrew Bolton at CK Science on 01438 870 013 or email abolton@ckscience.co.uk. Please quote reference ST20378 in all correspondence.

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


Meet Andrew – CK Science’s Specialist Chemical Industry Recruitment Consultant for the South, UK


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Medical Device Auditor – Hampshire, UK

Medical Device Auditor required for a world leading Medical Device Auditing Consultancy based in Hampshire, UK.

Our client, a world leading Medical Device Auditing Consultancy, are currently looking for an Auditor to join their busy and growing Auditing Team, based from their state-of-the-art facilities in Hampshire, UK.

Working as part of a multi-disciplinary team, as Medical Device Auditor, you will be involved in auditing medical device manufacturers and certifying their products against European standards (ISO 13485, MDD), as well as preparing and managing all relevant auditing documentation. As well as auditing and certification, you will also ensure that clients maximise the value and effectiveness of their quality systems. Due to the nature of this role some UK & Overseas travel is required.

This is an exciting opportunity to join a world leading Medical Device Auditing Consultancy, which in return offers an attractive salary and benefits package as well as a structured training program to develop the successful candidate in to a Lead Auditor.

The ideal candidate for this Medical Device Auditor job will have a degree in a relevant Scientific or Engineering discipline (or equivalent) and proven practical experience performing a Quality or Regulatory function within the Medical Device industry including demonstrated knowledge of the Medical Device Directives (MDD) and ISO 13485. Knowledge of a second European Language would be advantageous, but it is not essential.

How to Apply:

For more information, or to apply for this Medical Device Auditor job, please contact Andrew Bolton 01438 723 500 or email abolton@ckscience.co.uk. Please quote reference ST19606 in all correspondence.

Alternatively, click here to apply for this Medical Device Auditor job now.

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CK Exhibit at the DIA 22nd Annual EuroMeeting

CK Clinical at the DIAThis year, the DIA (Drug Information Association) chose Monaco and its state-of-the-art Grimaldi Forum to hold it’s 22nd Annual EuroMeeting, and CK Clinical, sister company of CK Science, had the pleasure of attending.

The DIA Annual EuroMeeting is the largest event of its kind in Europe.  From the 8-10th March 2010, 3,000 professionals from biopharmaceutical industry, contract service organisations, academic research centres, regulatory agencies, health ministries, patient organisations and trade associations, descended on Monaco.

CK Clinical’s first visit to the DIA Conference was a resounding success. Pharmaceutical jobs were brought in across all sectors, and the conference definitely acted as a brilliant springboard kick off our campaign to enter the European market.

We also ran a prize draw to win an Apple iPod Touch, the winner being a Departmental Manager from Novo Nordisk in Denmark. Thank you to everybody that entered.

056The Grimaldi Forum was an impressive waterfront venue, filled with daylight and a stunning glass entrance. A perfect venue to network with clients. Monaco was incredible with Ferrari’s, Mercedes Benz and Bentleys everywhere you looked. The hotel even had its own helipad!

We are very much looking forward to attending and exhibiting at next year’s DIA Conference in Geneva.

 

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