The latest Quality jobs - BETA

Quality controller required for an international medical device company in the South East for an administrative role dealing with PMS complaints.

Medical Device Regulatory Affairs Specialist required!

PharmaNet/i3 is recognized as a leading provider of global drug development services to pharmaceutical, biotechnology, generic drug, and medical device companies, including therapeutically specialized capabilities for Phase I-IV clinical development, bioanalytical services, and staffing from a single clinical professional to an entire functional team.

Our client, a leading global CRO, provides a comprehensive range of services in Phase I-IV clinical trials to the biopharmaceutical and device industries. They are currently seeking a QA Auditor / Sr QA Auditor for their Dublin site.

Global Pharmaceutical company with extensive manaufacturing facilitie in NE England seeks a Global Quality Systems Manager.

This is a permanent position paying between 45-50000 GBP per annum

To work within supply chain related quality control across the organisation and with suppliers to ensure continual improvement of processes and products, thus helping reduce defects, problems, etc. To drive progress within the organisation and with suppliers by implementation of relevant and timely actions [including corrective and preventive].

Clinical Quality Assurance Associate (Senior) Location: Germany Contract Type: Permanent Salary: Competitive My client is a global Biopharmaceutical company based in Germany who are experiencing phenomenal growth and as a result are now looking to recruit for a Senior Clinical QA Associate to join the team.

Head of Corporate Quality Management position. Excellent salary and package offered. Based in Mainland Europe.

You will be acting as Corporate Quality Administrator (50- 70%) for a successful Biotech company.

A great opportunity has arisen for any QA Systems manager, within one of the biggest names in the Healthcare/pharmaceutical industry. This blue chip organisation not only offers a leading portfolio of products, but also state of the art facilities. Renowned for providing competitive packages and job satisfaction, this is a truly unique opportunity reap the rewards of your accumulated experience.

You will be acting as Corporate Quality Administrator (50- 70%) for a successful Biotech company.

Quality manager

Senior Clinical Quality Assurance Associate Permanent, Office Based North Rhein Westphalia, Germany Are you looking for your next career step within the field of Quality Assurance? If so then this could be the ideal opportunity for you! My client, a renowned, international pharmaceutical company is seeking a Senior Clinical QA Associate, to help drive quality in their clinical activities.

QA Specialist, Carlow, Global Pharmaceutical Company


QA Specialist required for leading Pharmaceutical manufacturing company. Exciting permanent opportunity based in Carlow, Ireland.

Across a number of companies I am looking for strong quality professionals in the Manchester area. These roles cover CSV, Software Validation/Quality, Systems Quality and QUality Engineers. Most of the organisations are global players and are working with interesting medical devices.

An exciting opportunity for a Senior Quality Offer with developmental opportunities!

Great opportunity to join a growing organisation (100% growth year on year) and lead a site Quality function with 5 direct reports. This role has the backing of a wider group for stability but also the freedom of an emerging organisation which gives you the ability to direct strategy.

An excellent opportunity for a QC Technician to join a Medical Device Organisation based in West Sussex on a 1-3 month contract basis

Great opportunity to join a Global Organisations capable of progressing your career more than almost any in the UK. This organisation looks for the best members of staff in the industry and rewards them well for there work.

This role will directly support our vision and mission by ensuring the development and...

Medical Device Company in the South West is seeking a Quality Engineer on a 6 Month Contract to start ASAP

Global Medical Device Company in Sweden is looking for a Quality Technician to join the fast growing Quality Department in Gothenburg – Sweden.

Global Medical Device Company in Switzerland over 50 years in the industry is looking for a Supplier Quality Engineer to join the Quality Department in Zurich.

Global Medical Device Company in Switzerland over 50 years in the industry is looking for a Quality Engineer to join the Quality Department in Zurich.

Global Life Science Company (manufacturing and producing API) in Switzerland is looking for Deputy QA Manager for the QA department in Lausanne area.

Global Medical Device Company in Switzerland over 50 years in the industry is looking for a Quality Engineer (combination products – drug eluting products) to join the Quality Department in Zurich.

Global Medical Device Company in Switzerland over 50 years in the industry is looking for a Quality System Associate to join the Quality Department in Zurich.

You will be acting as Quality Engineer for a successful medical device company based in Zurich. Your main responsibilities will include supporting the project teams during risk assessment of products and production processes, and in the test plans, then evaluating the results.

You will be acting as QA Manager for global company. Your main responsibilities will include responsibility for the commercial and pipeline products which are sill in clinical phase, the approval of interim and final products, process and cleaning validation, change control and the approval of relevant documents. You are the first point of contact for internal and external customers, and will prepare and follow up after audits, and after a period there will be leadership responsibilities.

QA Senior Associate / Manager Localisation: Belgique Type de contrat: CDI Mon client est une société biopharmaceutique internationale basée en Belgique qui connaissent une croissance considérable. Ce site GMP réglementé, il faudra quelqu'un qui a de l'expérience de s'assurer que les produits sont fabriqués et testés selon les politiques de l'entreprise mondiaux et locaux.

A world leading healthcare manufacturer, based in Yorkshire, seeks to appoint a Global Quality Systems Manager. Salary (negotiable based upon experience level) £45 000 - £50 000 For further information regarding this excellent opportunity please contact Steven Winship at Progressive Pharma on 0207 469 5255.

My client is the leader in their therapy field in Medical Devices whose reputation is exemplary. Due to continued success and growth, they are now looking to add a Quality Assurance Specialist to their dynamic team. The opportunity offers excellent training potential as well as career opportunities and would suit ambitious candidates who are looking to progress.

QA Senior Associate/Manager Location: Belgium Contract Type : Permanent My client is a global Biopharmaceutical company based in Belgium who are experiencing considerable growth. This GMP regulated site will require someone who has experience of ensuring that products are manufactured and tested according to global and local company policies.

QA Officer (Medical Devices) Location: Belgium Contract Type: Permanent Salary: Competitive My client is a global Biopharmaceutical company based in Belgium who are experiencing considerable growth.

Senior Clinical Quality Assurance Associate. Location : Germany Contract type : Perm Salary: Competitive My client, a global pharmaceutical company with a great reputation, is seeking a suitably qualified Senior Quality Assurance Associate to assist with all quality aspects of the company.

Commercial QA Specialist Location: Belgium Contract Type : Permanent My client is a global Biopharmaceutical company based in Belgium who are experiencing considerable growth. This GMP regulated site will require someone who has experience of ensuring that products are manufactured and tested according to global and local company policies.

Due to a re-organisation within the Quality and Regulatory departments an opening for a Quality Assurance Manager has arisen. Our UK manufacturing site is located in Kent. The salary on offer for this position is in the region of £55 000+ (negotiable dependant upon experience).

Quality Assurance Manager Permanent, Full Time Various locations across Eastern and Western Europe, Office Based. My client, a full service CRO, is urgently seeking a Quality Assurance Manager. This is an exciting opportunity for an experienced quality professional to make an impact by combining existing internal expertise within a team with oversight of all GxP. The QA manager will develop a strategic vision for the team.

Our client is a leading specialist biotechnology organization offering an excellent opportunity as a Senior Quality Assurance Scientist to be based in Essex. Ideally you will be experienced in; six sigma tools, quality management systems, ISO 9001, auditing and statistical risk management tools.

Our client, a multinational clinical research organization, currently has a vacancy for a Quality Auditor 11. This is a full-time permanent role based in Dublin.

A growing Pharmaceutical company manufacturing Pharmaceuticals and Medical Devices is currently look to hire a new Head of Quality Assurance for their facility.

Clinical QA role at the European HQ of an R&D pharmaceutical company, based in Central London. To maintain awareness of global clinical programmes and project manage assigned projects to ensure adequate QA coverage and that audits of external service providers are performed. An initial fixed-term contract is on offer as maternity cover.

Titel: Quality Engineer 100% (m/f)
Location: Zurich region, Switzerland
Permanent position

Be primarily involved with quality assurance (QA) review of bulk and commercial drug products including Active Pharmaceutical Ingredients (API) batches. Maintain working relationships between QA department and the other departments’ suppliers. The position will support QA activities on the manufacturing site.

Prüfung von Arbeitsdokumenten für die Verpackung von klinischen Prüfmustern auf Einhaltung der externen und internen Vorgaben (Studien-, GMP/GCP- und SOP-Konformität); Kontrolle der Batch-Dokumentation und Studien-beschreibungen; Überprüfung der Auftragsanforderungen, Label Links Reports und Randomisierungen

I am looking for a very highly qualified expert if that’s you then this is your chance to work within one of the most highly qualified, experienced and motivated teams in the industry. Better yet, the company that I am working with is looking for a candidate who can work in their hear office in Switzerland. On top of this I’m looking for ONE exceptional individual to head up the team as the head of QA. Read on and learn more!

You will be acting as a Quality and Compliance Specialist for a large global pharmaceutical company.

You will be acting as QA Specialist (GMP) for a successful pharmaceutical company.

Quality Development Auditor Permanent £Negotiable Leading Pharmaceutical Surrey This fantastic opportunity is with a leading global pharmaceutical based in Surrey. They are looking to bring on board someone with strong GCP knowledge and experience with a clinical research background.

PV/QA/Compliance Permanent role Based in Thames Valley This is a permanent role working for a global pharmaceutical company within the quality department working alongside the Pharmacovigilance department.

We are currently looking to recruit a GCP Auditor.
My client is a well-respected and growing company that believes the details of your career are every bit as critical as the work for you.

The Person
You will be educated to a degree level in biological, physical, health, pharmacy or other related science together with extensive experience in QA auditing and thorough knowledge of GxP standards. You will be fluent in English.

Quality Assurance Trainee Location : Garbagnate Milanese Italy My Client is a growing biotechnology company in Italy and are looking for a Quality Assurance trainee to expanding team. Accompanied by a company tutor, you will have the opportunity to be introduced to the activities of quality assurance of pharmaceutical company operating in accordance with the applicable good Manufacturing Practice (GMP).

Quality Assurance Assistant Location :Austria Full-time/ permanent Job Description - Review of the production and control documents in the context of the release of biopharmaceutical ingredients (Batch Record Review) - Clarification during the batch record review with the management of production, analysis and development

Associate, Documentation Quality Regulatory Affairs Location: Hertfordshire A fantastic opportunity has arisen for a Associate for Documentation Quality, Regulatory Affairs to join a global pharmaceutical company based in Berkshire. The Associate for Documentation Quality, Regulatory Affairs will support the Medical Writers and Regulatory Affairs Authors to ensure data accuracy and formal quality in the documentation used in Clinical Studies and Regulatory Submissions.

Quality Assurance Trainee Location : Garbagnate Milanese Italy Employment type : 6 month contract. My Client is a growing biotechnology company in Italy and are looking for a Quality Assurance trainee to expanding team. Accompanied by a company tutor, you will have the opportunity to be introduced to the activities of quality assurance of pharmaceutical company operating in accordance with the applicable good Manufacturing Practice (GMP).

Quality Assurance Assistant Location :Austria Full-time/ permanent - Review of the production and control documents in the context of the release of biopharmaceutical ingredients (Batch Record Review) - Clarification during the batch record review with the management of production, analysis and development

An Excellent opportunity for a Clinical QA Manager to join a prestigious Clinical Trials Organisation based in London - Fantastic company and EXCELLENT location

Our client are an international medical device company based in Hertfordshire seeking an experienced Quality Engineer. You will have past experience in a similar role,

Our client are an internationaly recognised blue chip pharmaceutical company offering an excellent opportunity as a Quality Manager to be based in the North East in County Durham.

Are you a successful Clinical Administrator looking to for a new challenge? We at Phlexglobal are building a team of Quality Specialists to become part of our eTMF and Document Solutions team to be based in our offices in Amersham.

Our client are a global medium size pharmaceutical company who are seeking an experienced Quality Control Manager to be based at their site in Wales.

Key People are recruiting for a Quality Assurance Manager for our European client based in Switzerland

My client, based in Dorset, is currently seeking an experienced Quality Control Manager on an initial 3 month contract.

QC Scientist required for expanding Dublin based healthcare company!

Doc, Quality, Regulatory Affair Associate required

We are currently looking to recruit a PV Quality & Compliance Manager.
My client is an independent, patient oriented pharmaceutical company with outstanding performance which operates world-wide.

Job Purpose

*Quality & Compliance Manager for PV Business Processes and Subject Matter Expert for PV regulations

My client is one of the most innovative Medical Device companies in the market today who have established a great reputation and client base in the last 10 years. My client is now looking to recruit their newest Head of Quality Assurance for their premises in Switzerland. This position is integral in the business operations and would require the successful candidate to be an acting member of the Senior Management team.

For over 30 years PAREXEL has supported the Bio-Tech and Pharmaceutical industries in helping the development of new drugs and treatments on a global basis. As a leading global biopharmaceutical service provider, we supply knowledge-based contract research, medical communications and consulting services across a broad range of therapeutic areas to the worldwide pharmaceutical, biotechnology and medical device industries

My client is a pharmaceutical company based in the North who requires a Regulatory/ QA Co-ordination Manager. Job Purpose: To manage client liaison in relation to regulatory activities to ensure that each batch of product manufactured for client companies complies with the individual Marketing Authorisations.

My client is a Global Phamaceutical company based in Northern Ireland. Following an audit, they require a QA Compliance Consultant for a mimimum of 6 months, 5 days per week. Home working is an option.

QC CHEMIST

QC LAB MANAGER

Leading Global Medical Device Company is looking for a German Speaking Senior Supplier Quality Manager to be based in Basel – Switzerland.

Global Medical Device Company is looking for a Quality Manager in Sweden (Stockholm and Lund areas)!!! The company is working with various Medical Device products and has manufacturing sites globally.

Global Medical Devices Company in Germany is looking for a Product Quality Engineer for their fast growing department in Cologne. The company is offering great career development opportunities and offers a very competitive salary.

My client is the leader in their therapy field in Medical Devices whose reputation is exemplary. Due to continued success and growth, they are now looking to add a Quality Assurance Specialist to their dynamic team. The opportunity offers excellent training potential as well as career opportunities and would suit ambitious candidates who are looking to progress.

My client is a pharmaceutical company based in the North who require a Regulatory/ QA Co-ordination Manager.

My client, a leading Pharmaceutical/Medical Device company based in the Home Counties, is seeking a Quality Compliance Officer to join their team on a 12 month contract, with the possibility of a full time position on commencement of the contract.

Quality Assurance Manager

International Medical Device Company in Sweden is looking for a Quality Engineer to join the Quality Department in Stockholm area!!!

Medical Device Company in Germany, Cologne area is URGENTLY looking for Senior Quality System Specialist to join their team as soon as possible. MUST BE FLUENT IN GERMAN, WRITTEN AND SPOKEN!

ClinTec International is working on strategic assignments with a major multi-national pharmaceutical company, who is a leader in the global healthcare market. As such we are recruiting for a Quality Assurance Product Specialist to join their expanding global company in Germany.

QA Operations Manager, Dublin, Global Pharmaceutical Company


QA Operations Manager required for a leading Pharmaceutical Company. You will have over 8 years QA Operations experience and a Pharmaceutical Technical background. This is a permanent, full time role based in Dublin.

An exciting opportunity for an experienced Qualified Person to work within the manufacture of sterile products

My client is the leader in their therapy field in Medical Devices whose reputation is exemplary. Due to continued success and growth, they are now looking to add a Quality Assurance Specialist to their dynamic team. The opportunity offers excellent training potential as well as career opportunities and would suit ambitious candidates who are looking to progress

Quality Control Managerial opportunity with a leading contract manufacturer and API specialist in Switzerland. Fluent German is an essential requirement for this role.

My client is a global medical device company and is the largest life sciences company in the world, based in the North of England. They are offering a 6 month contract to a QA Manufacturing support engineer. Job Purpose: To provide Quality Engineering and Process Excellence support in a defined Business Unit / Value Stream environment for In-Process, Finished Product, First Articles & New Product Introduction.

My client is a global medical device company and is the largest life sciences company in the world, based in the North of England. They are offering a 6 month contract to a QA Manufacturing support engineer. Job Purpose: To provide Quality Engineering and Process Excellence support in a defined Business Unit / Value Stream environment for In-Process, Finished Product, First Articles & New Product Introduction.

QA STERILES GMP

Exclusive QA Manager position

Global Medical Device Company is looking for a Quality Manager in Paris – France to start as soon as possible!!! The company is working with various Medical Device products and has manufacturing sites globally. In this role you will be working alongside the International QA Director and will be required to travel around 5% internationally.

Titel: Manager Global Quality Assurance GCP (m/f)
Location: North Rhine-Westphalia
Permanent position

Quality Assurance Management role with a developing specialist pharmaceutical company in Munich.

Based at our EMEA Headquarters in Leamington Spa, Hospira have an opportunity available for a Quality Manager - QP.

Exclusive QA Manager position

My client an international Pharmaceutical company are looking for an International QA Audit Manager to join them at their offices in Scotland. This role will involve extensive travel and you will need sound GCP/GMP knowledge and experience.

Job Purpose:The Senior Quality Specialist independently performs a majority of the process...

Quality, GMP

QA, IS013485 13485