QA recruitment in the UK – research results

Over the past several years the CK Group has found the recruitment of Quality professionals more challenging than it has been historically. As a result we decided to undertake a UK wide survey of those currently working in the sector to build an accurate picture of the recruitment landscape within QA. This investigation has returned some unexpected results which has given us an accurate and focussed view of the sector as a whole and what those working in it require to change position.

Our investigation found that most people working within QA fall into either the 10 years+ experience or below 2 years of experience which has created a gulf of experience in the mid to senior level bracket. We have hypothesised that this is due to the market slump in 2008 – 2010 where those that were in mid to senior level roles have now progressed in to senior roles but as there were fewer candidates entering the industry we are now faced with this anomaly. This we believe, is why recruiting for people at this level has become such a challenge and from the rest of our findings is why companies have to seriously look at what they are offering to secure people in this part of the market

As expected, we found that most QA people are currently working within the pharmaceutical and manufacturing industries. However we also found a marked increase of positions within the Biotech sector. Biotech has grown substantially over the past few years and as it moves into more of a commercial phase the requirement for QA professionals will continue to grow. We believe there will be an increase of QA roles in this area in the coming years and it is a real area of interest for QA professionals..

In regards to the type of contract that QA people prefer there is an 80 / 20 split of permanent / temporary workers in the market currently. Interestingly, 80% of people stated that they will be looking for a new job within the next 2 years with most preferring a permanent contract. We found this proportion of people to be looking for a new role quite surprising considering the lack of movement at the moment. This could be a result of those in more junior positions currently, looking to move in to mid/senior level positions or a result of the economic growth in general. Either way this does mean that the permanent market will become stronger as we move forwards but as the rest of our findings will show, there are a number of key factors that the QA professional is looking at before they will consider making a move.

One of these key factors is location. Only 30% of people would definitely consider relocating for a role with 25% of people saying they may consider relocation. This means 45% of QA people are not willing to consider relocating under any circumstances. The good news is that there is a relatively even spread of QA people across the UK but with a noticeable higher number of people based in the South East, North West and  North East finding the very best candidate could be more difficult depending on location.

The other key factors are remuneration, status and security.

Nearly 50% of people said they would require a higher salary and a better benefits package to consider a move. This group also said they would only move to what they would perceive to be a “better company”.

Job security and progression/development opportunities scored very highly on key requirements which wasn’t surprising but what was a surprise was the large number of people that stated flexible hours to be a key factor when looking at a new position.

In summary, the market is currently made up of highly experienced and relatively inexperienced people leaving a gap of hard to find mid-level candidates.

Most people are only looking at positions based locally to them with a slight preference for roles based in London, the South East and the Midlands.

In order for our clients to secure the best QA people at any level but especially in the hard to find mid level sector, they are going to have to offer a stronger overall package than their competitors including  salary, benefits, progression/development opportunities, job security and working hours. We know that there will be more people in the market in the coming years but for now if you want the very best available it will come at a premium.

To view our results in more detail click here:

QA_infographic link

If you are a QA professional who is considering a career move click here to contact us for a confidential discussion

 

Or click here to search our QA jobs

 

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CK Science are exhibiting at the 2015 RQA Annual Conference

Taking place at the Queens Hotel in Leeds during the 11-13th November this year’s conference theme is: ‘Smart Quality a fresh perspective’.

The theme recognises the increasing demands made on QA professionals to work with greater effectiveness and efficiency using the tools and resources available to them. This year’s conference will provide attendees with the opportunity to obtain tips and techniques to enable more effective and efficient working through discussion topics such as:

  • Efficiency – need to work effectively and efficiently
  • Simplification – are we over thinking/applying regulations?
  • More with less – QA asked to achieve more with fewer tools/less resource/greater scope of responsibility/areas of work
  • Learning from each other – what is being used in one GxP can probably be applied to others easily

During the 3 day event QA professionals will be able to participate in plenary and parallel sessions, clinics, workshops as well as networking opportunities.

Recruiters Jason Johal from CK Science and Jim Gleeson from CK Clinical will also be there to provide you with advice and guidance on taking the next steps in your career.

If you would like contact Jason to arrange a confidential chat about your scientific QA career click here

If you would like to arrange a confidential chat with Jim Gleeson about your clinical QA career click here

 

Or search our current QA vacancies here

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Don’t forget our QA survey!

If you are a QA professional, we would love your feedback

We are currently undertaking some market research to get your view on the industry, your career and what you see as the most important element of your job hunting decision making.  If you have time, we would really appreciate you to complete our short survey – all you need to do is click on the link below.

Complete the QA survey here

Once you have completed the survey, you will have the chance to enter into a free prize draw for an Amazon Kindle.

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Quality Assurance survey

Calling all QA professionals!

Here at CK Science we are wanting to get your input into the industry, your career and what you see as the most important element of your job hunting decision making. To enter our short survey, all you need to do is click on the link below.

After you have completed the survey, you will also be given the opportunity to enter into a free prize draw for an Amazon Kindle.

Complete the QA survey here

 

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QA Manager/QP – North Wales

Naynesh Mistry is recruiting for a QA Manager/QP to join a leading manufacturer of veterinary pharmaceutical and animal health products in North Wales on a permanent basis.

Main responsibilities in this role include leading the quality function to ensure all processes are carried out in compliance with internal, regulatory and statutory requirements. You will also be required to act as the primary QP and be responsible for the review of batch manufacturing records, process deviations, LIRs and disposition.

To apply for this position you should have extensive experience in quality assurance, quality control, compliance and/or manufacturing. The ability to work as on-site QP in accordance with Directive 2001/83/EC and Annex 16 of the Rules and Guidance for Pharmaceutical manufacturers and Distributors 2002 is also required.

For more information on this position, or to apply, click here 

 

 

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QA Officer – Teesside

Sarah Farrow is recruiting for a QA Officer to join a global pharmaceutical company at their site in Teesside on a permanent basis.

In this position your responsibilities would include, reviewing all GMP documentation from a QA angle, carrying out audits and providing support to the manufacturing team.

To apply for this position you should have QA experience, ideally in a GMP manufacturing environment.

If you would like to join a global pharmaceutical company that provides excellent opportunities and benefits, click here

 

 

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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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QA/QC Co-ordinator – Aberdeen

Heather Deagle is recruiting for a QA/QC Coordinator to join a manufacturing company that produces products for the oil and gas industry in Aberdeen on a permanent basis.

Your main responsibilities will include ensuring all products (manufactured and off-the-shelf) and related documentation meet the required standard. You will also be required to coordinate the on-site equipment inspection and equipment at supplier locations.

If you have previous experience in a quality or engineering role and an understanding of quality plans, inspection techniques and documentation this could be a great opportunity for you.

Click here for more information or to apply

 

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Shift QA Technician – South Lincolnshire

Hannah Oakley is recruiting for a Shift QA Technician to join a well known, privately owned beverages company in South Lincolnshire on a full time, temp to perm basis.

Responsibilities in this role include carrying out routine product testing, completing all record keeping and paperwork associated with quality measurements and conducting GMP and Hygiene assessments across the entire manufacturing operation to ensure continued improvement of site and operation.

This role requires a QA Technician with Level 2 Food Hygiene Training, understanding of HACCP and a commitment to working a 2pm to 10pm shift.

For more information or to apply for this role click here

 

 

 

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Are you looking for a QA job?

If so contact CK Science today! We currently have a number of junior and senior level QA roles based in London, Hertfordshire and Bedfordshire, such as:

  • QA Officers
  • QA Execs
  • QA Managers
  • QA Auditors
  • QA Validation experts
  • Qualified Person (QP)

So if you have experience in QA area and some of the following skills:

  • Batch review
  • CAPA
  • Continuous improvement
  • Auditing
  • ISO: 9001
  • ISO: 13485
  • ISO 17025
  • RCA:
  • Medical Device Directive MDD
  • In Vitro diagnostics directive IVDD
  • MHRA
  • FDA
  • UKAS
  • IQ, OQ, PQ
  • GMP, GLP
  • CMC
  • IMP
  • Specials

WIth a background in either pharma, biotech, chemical or med devices/diagnostics then call us on 01438 723 500 or click here to search our QA jobs

 

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TrackWise Systems Associate – Hertfordshire

Reena Dhana at CK Science is currently recruiting for a TrackWise Systems Quality Associate to join one of the world’s leading research-based pharmaceutical companies based in Hertfordshire on a full time, 12 month fixed term contract.

Responsibilities:

We are searching for a candidate to ensure an Electronic TrackWise Quality Management System (QMS) and associated systems used for the manufacture, packaging, testing, storage and distribution of marketed drug products comply with current GMP and corporate expectations.  They will provide input to the review and writing of any associated quality policies, systems and procedures and support the generation of routine status and performance reports covering aspects of Electronic TrackWise  QMS.

As a TrackWise Systems Quality Associate you will:

  • Support the ongoing operation, maintenance and implementation of improvements to TrackWise processes and systems to meet company needs.
  • Support the company Training Management System.
  • Maintain copies of Corporate Policies, Guideline, Standards and Procedures.
  • Write and review all SOPs associated with the Electronic TrackWise QMS
  • Coordinate the Company SOP System.
  • Coordinate the internal and external audit process, audit schedules and the associated audit files.
  • Participate in Audits
  • Coordinate and support GMP Training.
  • Provide day to day support to other members of the TrackWise Systems team, as appropriate.
  • Support the reporting of Quality Operations and company Key Performance Indicators
  • Perform appropriate duties at the request of the Senior TrackWise Systems Associate
  • Identify and implement continuous improvement opportunities that result in cost savings and more efficient and compliant ways of working

Qualification:

The successful Track Wise Systems Quality Associate will have the following qualifications, skills & experiences:

  • Able to maintain working relationship and communication links within the company, affiliated organisations and third party contractors as appropriate.
  • Knowledge and experience of Quality Assurance, Quality Systems, GMP and a basic understanding of manufacture and packaging of pharmaceutical products.
  • Technical and scientific judgement.
  • Self motivating individual comfortable working with detailed information and data.
  • Good communication skills.
  • Developed presentation skills.
  • Computer literate e.g. Word, Excel and PowerPoint.
  • Able to follow defined processes and procedures.

Benefits:

If successful, you will join a company that truly values it’s employees and is completely focused on the patient. In return there is an attractive salary, coupled with excellent benefits and extensive training/career progression opportunities.

Reena Dhana - Scientific Recruitment ConsultantHow to apply:

Apply online:

To apply for this TrackWise Systems Quality Associate position please contact Reena Dhana via email: rdhana@ckscience.co.uk or telephone: 01438 723 500. Please quote reference ST26527 in all correspondence.

 

Are you looking for a new science job? Click here to see our latest science jobs

 

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QA Service Provider Strategy – Hertfordshire

Jason Johal at CK Science is currently recruiting for a QA Service Provider Strategy Lead to join one of the world’s leading research-focused healthcare groups for at their Hertfordshire site on a full time, permanent basis.

This role monitors activities outsourced to Service Providers through periodic risk assessment, risk-based routine audits and provides ongoing support to mitigating actions. It also provides actionable data to Senior Procurement/Outsourcing functional management based on analysis of data (audit/inspection/risk) and identification of trends.

Responsibilities

Joining the international Product Development Quality Assurance (PDQA) team, this position will be assigned to the Laboratory service category (GLP, GCP). Reporting to the Principal Team Lead for Service Provider QA Strategy the ideal candidate will be responsible for the design and implementation of the Service Provider risk management and audit strategy across the GLP, GCP, GPVP areas. The role works in partnership with Procurement/Outsourcing Functions and the PDQA GLP, GCP, PV Strategy Leads to ensure that Risk Assessments are maintained across the inventory of Service Providers engaged globally (gRED, pRED, PD, GPS/gMED) and at Affiliate Level.

As QA Service Provider Strategy Lead you will:

  • Design and implement the PDQA Service Provider risk-based strategy for risk management and audit activities
  • Define/maintain the “audit/risk universe” of Service Providers based on input from Procurement/Outsourcing functions and PDQA GxP Strategy Leads
  • Partner closely with the GxP Strategy Leads, Procurement/Outsourcing Functions to ensure that risk assessments are maintained for Service Providers to determine which audits will be conducted and where risk mitigation activities should occur.
  • Develop and implement a GxP risk based strategy to deliver an audit program and quality oversight model for service providers within service category areas.
  • Assess specific risk areas on an on-going basis, communicate to PDQA senior leadership and propose modifications to PDQA strategy where necessary
  • Assess data/metrics from audits, inspections and risk management activities for compliance trends and risks
  • Develop communication tools (reports/dashboards) for audit and inspection metrics and trends
  • Support regulatory authority GCP inspections at service providers

Qualifications

The successful QA Service Provider Strategy Lead will have the following qualifications, skills & experiences:

  • Bachelor’s degree or equivalent in a scientific or quality related field or equivalent combination of education, training and experience
  • Extensive experience in the pharmaceutical industry and/or quality assurance with excellent knowledge of a GLP or Pharmacovigilance Service Provider Quality role
  • Demonstrated knowledge of GLP, GCP, CSV, PV / drug safety and regulatory requirements
  • Project management experience with proven leadership, mentoring and coaching skills
  • Experience supporting Service Provider sourcing initiatives and/or representing QA on Service Provider Strategic Alliance or Category governance teams
  • Proficiency in the conduct of GxP related audits of Service Providers
  • Experience supporting regulatory authority inspections

Benefits

If successful, you will be joining a QA Service Provider Strategy Lead. In return there is:

  • Attractive salary
  • Excellent benefits
  • Career progression opportunitiesJason Johal - Scientific Recruitment at CK Science

How to apply

Apply online now

To apply for this QA Service Provider Strategy Lead position contact Jason Johal via email: jjohal@ckscience.co.uk or telephone: 01438 723 500. Please quote reference ST25997 in all correspondence. Entitlement to work in the EEA is essential.

Are you looking for a QA job?

Click here to view all CK Sciences QA jobs

 

Healthcare Recruitment - CK Science   Healthcare Recruitment - CK Science

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QA Officer in Newcastle

Graeme Pallas at CK Science is recruiting for a QA Officer to join a pharmaceutical manufacturing company at their site located in QA Officer in Newcastle on a short term contract.

Responsibilities:

As a QA Officer you will be responsible for:

  • Ensuring products and processes are in compliance with ISO9001 and GMP requirements
  • Assist with critical review of production batch records
  • Assist with failure investigations
  • Manage quality systems including Non conformance, deviations, CAPA’s

Qualifications:

As a QA Officer, you will have the following qualifications, skills and experience:

  • Qualification in a science based subject
  • Experience of working in a QA environment
  • Familiar with cGMP

Benefits:

The successful QA Officer will be joining a pharmaceutical manufacturing company at their site in Newcastle.  This is a short term contract initially scheduled to last 3-4 months to cover maternity leave.

Graeme Pallas - Recruiter at CK Science

 How to apply:

Apply online now

For more information or to apply for this QA Officer position, please contact Graeme Pallas on 0191 384 8905 or email gpallas@ckscience.co.uk. Please quote reference DH25920 in all correspondence.

 Looking for a new job in QA?

Click here to view other QA Officer

Pharmaceutical Recruitment    Pharmaceutical Recruitment CK Science

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QA Technician – Southern Scotland

Barney Smith at CK Science is recruiting for a QA technician to join one of the most successful and innovative food companies in Scotland

Responsibilities:

As a QA technician  you will be working a continental shift pattern and will be responsible for:

  • Data collection
  • Process auditing
  • Completing on line checks with detailed analysis and interpretation of results. 

Qualifications:

The successful candidate for this QA technician  must be qualified to minimum HNC or equivalent in a Quality Management of Food Science related discipline or equivalent industrial experience and have a proven track record in QA within the food or biotechnology industry. 

How to apply:Barney Smith - Manager at CK Science

Apply online:

For more information or to apply for this QA technician role please contact Barney Smith on 0191 384 8905 or email bsmith@ckscience.co.uk. Please quote reference DH24485 in all correspondence.

Are you looking for a new job in the food industry? Click here to see our latest jobs

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QA Auditor Job in Sussex

Julie Marshall at CK Science is currently looking for a QA Auditor to join the Quality Auditing team of a successful pharmaceutical company based in Sussex.

This QA Auditor role is a full-time, temporary role. If successful, you will be joining a global company and in return there is an attractive salary, coupled with career progression opportunities.

To be considered for this Quality Assurance Auditor position, you will have the following qualifications, skills and experience:

  • Experience in performing and maintaining compliance audits in line with Regulatory and QMS requirements
  • Experience in leading Audits, including scheduling, planning, executing, reporting and CAPA management
  • A degree (or equivalent) in an appropriate discipline or related experience
  • Knowledge of GMP regulations and in-depth knowledge of Quality Management Systems
  • Certified Auditor/Internal/External
  • Experience within a quality function or from a quality based role within manufacturing

How to apply:

Julie Marshall - Scientific Recruitment Consultant at CK Science

Please contact Julie for more details.

Click here to apply online now.

For more information regarding this QA Auditor position, please contact Julie Marshall at CK Science on 01438 723500 or email jmarshall@ckscience.co.uk. Please quote reference ST24342 in all correspondence.

Not quite right? Click here to search our other Quality Assurance jobs online now.

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Quality Assurance Auditor – Hertfordshire

Reena Dhana is currently recruiting for a Quality Assurance Auditor to be based within the GMP quality department of a global pharmaceutical company who are based in Hertfordshire.  This is initially a temporary contract of 4 months with a strong possibility of extension.

Responsibilities:

As a Quality Assurance Auditor you will ensure compliance to cGMP of all activities related to the development of pharmaceutical products for use in Clinical Trials, including the Quality Management systems and you will carry out Quality compliance reviews/release of Investigational Medicinal Products for use in Clinical Trials. Other duties will include:

  • Auditing and approving procedures and documents from manufacturing
  • Analytical, packaging and service groups
  • Reviewing and approving equipment and facilities qualification
  • Training others as appropriate
  • Assisting with external audits as required.

Qualifications:

The ideal candidate for this Quality Assurance Auditor role will hold a BSc in a Life Science subject (or equivalent) and will have experience gained within relevant departments of Pharmaceutical companies, preferably Quality Assurance. You will have a good working knowledge of cGMPs. An understanding of Clinical Supplies requirements would be advantageous.

How to apply: 

For more information or to apply for this Quality Assurance Auditor role please contact Reena Dhana on 01438 723 500 or email rdhana@ckscience.co.uk.  Please quote reference ST23319 in all correspondence.

                                                            Click here to apply now!

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Quality Assurance Officer – NE England

 

Heather Deagle at CK Science, is currently recruiting a Quality Assurance Officer to join a blue chip pharmaceutical company located in North East England.

Responsibilities:

The successful candidate will work as part of a team but must also be able to work independently. You will be responsible for QA compliance of packaging artwork. This will be achieved by ensuring a consistent and regulatory compliant approach to ensure quality is maintained within the organisation.  Other duties of the role will include coordinating quality meetings, ensuring escalation of issues, effective closure of Corrective and Preventative Actions (CAPA), ensure deviations and complaints reporting systems are functioning in a compliant manner.

Qualifications:

Ideally, you will be qualified in a science related discipline and have worked in a quality assurance role in either the science, artwork or print industries. You will have good communication, problem solving and IT skills.

Duration:

This role  will be on a temporary basis initially until the end of the year, but with a strong possibility of being further extended.

How to apply:

For more information or to apply for this Quality Assurance Officer position, please contact Heather Deagle on 0191 384 8905 or hdeagle@ckscience.co.uk. Please quote reference DH22448 in all correspondence.

 

                                                          Click here to apply online!

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Quality Assurance Officer Jobs, Pharmaceutical

Our client, a major pharmaceutical company located in County Durham, has a number of long term temporary vacancies for Quality Assurance Officers with relevant experience in product release and cGMP compliance. Some but not all of the positions may involve shift working, for which there is a generous shift allowance.


As a Quality Assurance Officer, you will ensure that all products released for sale or further processing comply with cGMPstandards, product quality specifications and regulatory requirements. You will also generate and review product related technical documents, and collate and interpret data such as analytical results/trends and regulatory, validation and engineeringinformation. Working as a  Quality Assurance Officer you will also lead and direct investigative work into products failing to meet requisite standards (and regulatory issues). You will also lead investigative work and develop and agree corrective actions.
Our client is looking for individuals with a strong background in Quality Assurance, good knowledge of cGMP and regulatory requirements and the ability to manage multiple activities concurrently within high volume, complex areas. Excellent communications skills are also required, togetherwith demonstrable leadership and decision-making abilities.

Apply Now

For more information, or to apply for this Quality Assurance Officer position, please contact Graeme on 0191 384 8905 or email gpallas@ckscience.co.uk.

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Quality Assurance Officers (Pharmaceutical Product Release) – County Durham, UK

Our client, a major pharmaceutical company located in County Durham, has a number of long term temporary vacancies for Quality Assurance Officers with relevant experience in product release and cGMP compliance.  Some but not all of these Quality Assurance Officer positions may involve shift working, for which there is a generous shift allowance.

As a Quality Assurance Officer you will have the following responsibilities:

  • You will ensure that all products released for sale or further processing comply with cGMP standards, product quality specifications and regulatory requirements.
  • You will also generate and review product related technical documents, and collate and interpret data such as analytical results/trends and regulatory, validation and engineering information.
  • To lead and direct investigative work into products failing to meet requisite standards (and regulatory issues).
  • You will also lead investigative work and develop and agree corrective actions.

Our client is looking for individuals with a strong background in Quality Assurance, good knowledge of cGMP and regulatory requirements and the ability to manage multiple activities concurrently within high volume, complex areas.  Excellent communications skills are also required, together with demonstrable leadership and decision-making abilities.

 

Apply now

For more information, or to apply for these Quality Assurance Officer roles, please contact Graeme at CK Science on 0191 384 8905 or email gpallas@ckscience.co.uk. Please quote reference DH20139 in all correspondence.

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Global QA Director based in South East, UK

An exciting Global QA Director job has arisen at an international Pharmaceutical company based in the South East of England. This is a Senior Leadership role for Quality Assurance serving both the external client and internal QA Departments.As an experienced Quality Assurance Director, you will act as the primary contact for all client-related QA communication, and the development and implementation of Quality Agreements. Further responsibilities of the role will include:

– Overseeing all quality-related concerns.

– Functioning as a liaison between a single, large-market clients and internal personnel.

– Developing and maintaining strong relationships with client QA senior management.

– Managing the single client’s quality and regulatory matters, CGMP compliance and two-way communication.

– Assuring that client requirements are developed, documented and agreed upon for manufacturing, testing and distribution and return of pharmaceutical clinical supplies.

This QA Director role will encompass all of my clients’ global locations and will interact with personnel in multiple client locations.

The ideal candidate will have extensive managerial QA/regulatory compliance experience in the pharmaceutical, chemical, medical device or biotech industry, as well as strong leadership experience in the field. You will also have an outstanding customer-service orientated background.

This is a rare opportunity for you to make your mark on a prestigious international pharmaceutical company. If you are interested in hearing more about this exciting role, please contact Jason Johal on 01438 723500 or email jjohal@ckscience.co.uk. Alternatively, you can meet Jason and hear more about this role at our YouTube Channel. To apply, click here.

CK Science is the leading independent scientific recruitment agency for science jobs. CK Science provide an all round recruitment service to the chemical, pharmaceutical, biotechnology, waste and environmental and other related industries right across the UK.

We have built a strong client base who appreciate our professionalism, integrity and commitment to finding the right person for the job. Equally important to our success are our candidates, who recognise our dedication to operating in a fair and ethical manner to meet their needs in the current job market.

Keywords: QA jobs, quality assurance jobs, pharmaceutical QA, clinical QA, QA Director, clinical trials, ck science, lab jobs, chemistry jobs, scientist jobs, science jobs, microbiology jobs, biology jobs, analytical jobs, scientific recruitment, biotechnology jobs

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