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 Systems Officer – Grangemouth

Barney Smith is recruiting for a Quality Systems Officer to work for a pharmaceutical intermediates manufacturer in Grangemouth on a 12 month contract.

Working solely on New Process Introduction projects you will be responsible for preparing GMP batch records, generating GMP quality documentation for raw materials and equipment, and performing CAPA investigations.

To apply for this role you must have a proven track record of working in QA within a GMP environment.

For more information, or to apply, click 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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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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Global Raw Material Compliance Coordinator

Jason at CK Science is recruiting for a Global Raw Material Compliance Coordinator to join a global pharmaceutical company at their UK Site in London/Kent on a full time, permanent basis.

Our client designs and supports advanced coating systems, modified release technologies and functional excipients for pharmaceutical dosage form and are looking for someone to manage the Raw Material Risk Assessment programme.

If you have experience in a QC, A or regulatory affairs at an intermediate level, and are competent at the day to day management of base raw material data and specifications in the Oracle Quality Module and Master items, our client would like to speak to you.

For more information on this role and to apply click here

 

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Quality Lead Manager – Hertfordshire

Julie Marshall is recruiting a Quality Lead Manager to join a global manufacturing and supply company on a contract basis.

This contract position lasts until June 2014 and requires a QP to provide effective leadership of a Operational Quality team to ensure that released products have been manufactured and packaged in accordance with cGMP and licensing requirements.

If this positions is of interest click here to read the full job description and to apply

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QA Specialist role based in Cork (12 month contract)

  • Reference: 27443
  • Salary: Competitive
  • Contract: 12 months initally

Hannah Milward at CK Science is recruiting for a QA Specialist working for a global healthcare organisation based at their offices in Cork on a 12 month contract.

Responsible for the Document Management System you will be skilled in quality assurance with previous experience working  in a GMP environment.

Click here for more information or to apply for this position

Pharmaceutical Jobs  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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Regional Quality Assurance Consultant – Berkshire

Reena at CK Science is currently recruiting for a Regional Quality Assurance Consultant to join a Global Consumer Healthcare Organisation. Based in Berkshire, this role is a full time on a 12 month contract

Responsibilities

As a Regional Quality Assurance Consultant you will:

  • Providing QA governance and approval of key deliverables for regional validation.
  • Producing regulation and GxP assessments for the regional validation project.
  • Identifying opportunities for continuous improvement mitigation key risks and resolving issues where key decisions are actually required.
  • Driving regionalisation of business processes
  • Holding monthly regional governance board sessions with key leads.
  • Providing QA oversight and support for Change Management function

Qualifications

The successful Regional Quality Assurance Consultant will have the following qualifications, skills & experiences:

  • BSc or equivalent in a life Science subject
  • Proven experience of operating at senior leadership levels within a quality function 
  • Regional Quality Assurance background
  • Proven track record of driving continuous business improvement and change resulting in benefits being achieved
  • Evidence of working at all levels of the organisation
  • Ability to mentor and provide guidance
  • Team management experience essential

 Benefits

As a Regional Quality Assurance Consultant this is an excellent opportunity to join a Global Consumer Healthcare Organisation, which in return offers a competitive salary.

Reena Dhana - Scientific Recruitment ConsultantHow to apply

Apply online now 

For more information or to apply for the role of Regional Quality Assurance Consultant please contact Reena Dhana on 01438 723 500 or email rdhana@ckscience.co.uk. Alternatively please click on the link below to apply online now.  Please quote reference ST25975 in all correspondence.

Entitlement to work in the EEA is essential.

Are you looking for a job in QA?

Click here to view all CK Sciences QA jobs

Science jobs     Science jobs

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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 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 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.

                                       Click here to search our jobs in science now!

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Director of Quality Assurance Job in North West, UK

Jim Gleeson at CK Science is currently recruiting for a Director of Quality Assurance to join a successful molecular diagnostics company based in the North West, UK.

The role:

As Director of Quality Assurance, you will oversee all Quality Assurance activities for the manufacture of in-vitro diagnostics. Further responsibilities will include:

  • Management of the company’s Quality System
  • Close interaction with senior management and international regulatory authorities
  • Ensuring the highest levels of compliance with all applicable standards and regulations
  • Mentoring and development of staff across QA, QC and Compliance
  • Selection of methods, techniques and evaluation criteria in order to obtain robust results

 

The ideal candidate:

  • Jim is looking for candidates with the following skills, experience and qualifications:
  • Extensive GMP QA management experience, ideally within the diagnostics / medical device arena
  • Experience of hosting and managing FDA and other regulatory inspections (ISO 13485 would be particularly useful)
  • A background in ISO 13485 management would be advantageous
  • Excellent communication skills

 

How to apply:

For more information or to apply for this Director of Quality Assurance position, please contact Jim Gleeson on 01438 870027 or email jgleeson@ckclinical.co.uk. Please quote reference CL22921 in all correspondence.

Not quite what you’re looking for? Click here to search our current Quality Assurance jobs online 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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