The latest Quality jobs - BETA

Head of QA, International BioPharma, Build your team

This is a great opportunity for experienced quality professionals within the quality assurance area to further advance their career by running the quality team on site. This is a key position and one where you will also be involved in the recruitment of more members of your team. You will be able to have a great impact on the organisation as a whole.

A Line Manager of QC position has become available due to the expansion of my client- a leading Biopharmaceutical company with offices throughout Europe.

You will be responsible for leading a team of 5 QC professionals at brand new state of the art facilities in Southern Germany. You will be in charge of expanding this team to 10 by the end of 2013.

This is a once-in-a-career opportunity to join a company which are making a big name for themselves as a leader in bio-therapi

QA Risk Co-ordinator, Frankfurt, Implement New Systems

A brand new position has arisen within an international bio-tech company in the Frankfurt area. You will join as the Quality Assurance risk co-ordinator and you will take on a key role in creating and developing the risk management processes on multiple sites. Due to the role you are undertaking my client is looking for experience within risk management HAACP/FMEA regulations in a QA GMP setting.

Austin Fraser is currently looking for a number of QC Analysts in both the North east and South West where you will be working with a global pharmaceutical services company delivers early to mid-phase drug development solutions. All positions of which have come about due to expansion and volume of work.

We are looking for candidates with API experience and would have ideally worked in a CRO or CMO environment. ...

** exceptional opportunity to join a growing biotech **URGENT**

inVentiv Health Clinical, formerly PharmaNet/i3, is a leading provider of global drug development services to pharmaceutical, biotechnology, generic drug, and medical device companies. With 7,000 employees in more than 36 countries, inVentiv Health Clinical offers therapeutically specialized capabilities for all phases of clinical development, bioanalytical services, and strategic resourcing from a single clinical professional to an entire functional team. ...

A rapidly growing bio-pharmaceutical company is now looking for a Quality Assurance Manager to lead the team of 20 people across Netherlands.

Our Swiss based client, a leading company in the manufacture of Medical Device Products for the treatment of Orthopaedic conditions, is currently recruiting for a Senior Quality Engineer. This specialist role is for someone with experience and certification in Nondestructive testing techniques, but who will also take on a leadership role in supervising personnel carrying out this testing.

For a major Pharma client we are urgently looking for a "Franchise Operational QA Manager" - contract starting ASAP for approx. 6 months (with extension option). You will be a member of the Pharma Development QA team and provide Quality & Compliance Guidance for the development & implementation of Corrective and Preventive Actions (CAPA) - apply now: erika.ganev@harveynash.com

Keyword: Development QA groups, Audits, Quality Plan, Audit

Urgent Vacancy for a global business based in Switzerland. Global candidates considered.

Our client, a diverse pharmaceutical business, capable of supplying healthcare products to the Retail Pharmacy, Hospital and FMCG sectors, has a vacancy for a Supply Quality Administrator.
SAP, Word, Excel, Administration, Organisational skills

• Operational QA Manager • Leading Pharma company • 6 month contract– freelancers only • Office based Basel, Switzerland

I have a fantastic opportunity for a Senior QA GMP Specialist to join a global biotechnology company in Leuven. My client is offering an excellent salary package and a great career prospect.

The QA GMP Manager is responsible for GMP QA activities. The person will ensure there is appropriate GMP compliance and governance to comply with relevant regulations and guidelines. She/he works in close collaboration with the Global Head of Quality to ensure the development and the implementation of quality systems, processes and polices to support activities throughout our business. You will ensure drug substance and drug product are released to meet business and regulatory expectations.

*** OPTION - CLINICAL QUALITY ASSURANCE - GCP *** NORTH GERMANY Based in Northern Germany, our client is one of the top 10 leaders in pharmaceutical development. This is a new role within an existing team of 6-10 clinical quality experts enabling you to grown within this expanding organization! Contact Marc Van de Voorde on +41 (0)41 710 51 00 or +44(0)207 801 33 85, alternatively send your CV in full to marc@advregulatory.com.

A leading pharmaceutical company based in Surrey is recruiting for a Quality Assurance Manager. A fantastic opportunity with a global innovative company that is living in exciting times and it is hoped the Quality team will grow. Great potential to develop and succeed.

An exemplary opportunity has become available with a prestigious pharmaceutical firm that are highly dedicated in the development, production and marketing of speciality and generic medicines.

We are an international player on the medical devices sector and due to our continuous growth, we are looking to reinforce our QARA department (based inGhent) with a new talent.



Your responsibilities:



* · Ensure all the regulatory obligations within the R&D department
* · Preparing the files for submissions
* · Ensure the quality standards are met
* · General support activities to the business (audits, training, etc .. ...

Duties

* IEC 60601 Medical/electrical equipment safety standards
* Risk management
* Design control
* New product quality plans, validation plans, specifications, are properly established
* Process improvements to improve product quality and manufacturability
* Design and Develop forms and instructions for recording, evaluating, and reporting quality data
* Interface with suppliers to improve or resolve quality issues
* Gauge R&R Studies, IQ, OQ, ...

Senior Quality Assurance Auditor is responsible for conducting audits of on-going clinical research and data management projects, as well as assisting with handling other QA program initiatives.

Working for a Major Top-10 Pharmaceutical company that works in developing innovative medical devices, biopharmaceutical medicines, vetinary products and orthopaedic products. The main aim of this role is as an administrative Quality Analyst to consolidate Supplier Database and PSL. The responsibilities of this position include the support and consulting for the development of corrective action plans and corrective actions at suppliers.

German Speaking Life Science Graduate - Germany

This is a rare opportunity for a German speaking science graduate with some experience in GMP/QA to join a rapidly growing pharmaceutical company in Germany.

The position will offer you the chance to gain industry experience within Quality Assurance at junior managerial level with the potential for career progression within the business. ...

We are looking for an exceptional individual to join a global Pharmaceutical company leading the Global GCP and GVP function.

This an English speaking position site based in Germany with the organisation welcoming applicants from both inside and outside the EU with full relocation assistance provided.

Leading Medical Devices Company require a Manager of their Quality Assurance Department

An outstanding opportunity to join one of the worlds leading contract research organizations and be part of a dynamic and growing international company. Join PRA as a Quality Assurance Auditor and help realize your career potential.

Introduction
Our client is seeking an individual with existing skills in QA to join their team managing the quality of supplies for use in clinical trials. Based in Hampshire, this is a great time to join this growing and respected company.

Contract - Pharmaceutical - QA - Quality Assurance - 6 months - Scotland

Clinical Compliance, GCP, Quality Assurance – Fantastic new opening for an Associate Clinical Compliance Manager (GCP, QA) to join this innovative, growing Biotech from their European HQ in Surrey. The position will give you full oversight and ownership on all compliance and QA activities within Europe, documentation review, internal process audits and SOPs in place.

I am currently working alongside an excellent biopharmaceutical company that discovers, invents, develops, manufactures, and commercializes medicines for the treatment of serious medical conditions. They are looking for GCP Auditors and Senior Auditors to join their successful team based in New York State, USA.

SENIOR QA ROLE!

Experienced QA specialist required by Novella Clincal for Associate Director role. Must have experience of auditing to GCP.

As a Clinical Auditor you will responsible for the independent planning and conducting of audits several key clients across the business.

If you are looking to join an organisation with continuing career progression, excellent benefits and the chance to grow with your role this is an excellent position for you. One of the current Assistant Director of Quality Assurance joined this organisation as a Clinical Trials Auditor. The role can be based in any of their European Offices.

Hannah Milward at CK Science is recruiting a Shift QC Analyst on a temporary basis for the duration of approximately 7 months. The Shift QC...

My client is an award winning Medical Device Company who have leading products within multiple fields. They are now looking to strengthen their European Regulatory team with the appointment of their newest RA & QA Manager to be based in Southern Germany. This is a combination role that requires substantial experience in both disciplines with leadership skills also being critical for the successful candidate.

My client is a large and well established pharmacuetical company looking for a Quality Specialist to lead and develop Quality Systems, ensuring they are efficient and effective.

Our client are a leading contract lab testing organisation based in Middlesex offering a great opportunity as a Deputy Quality Assurance Manager.

Our client are an expanding medical device manufacturer based in Leicester who are seeking an experienced QA Technician/Engineer - Risk Management.

We are looking for an exceptional individual to join a global Pharmaceutical company leading the Global GCP and GVP function.

This an English speaking position site based in Germany with the organisation welcoming applicants from both inside and outside the EU with full relocation assistance provided.

Een medical device bedrijf in Zuid-Holland is op zoek naar een ervaren QA officer.
Deze organisatie heeft haar hoofdkantoor in Nederland waar 300 mensen werken. De QA/RA afdeling bestaat uit ongeveer 8 mensen; dit zijn allemaal specialisten die werken op verschillende niveaus en daarboven staat een manager. ...

My client based in the Ticino part of Switzerland, is a global leader in their specialist field within the development of medical devices for the human skeleton. Due to the continued development of their product lines and distribution channels they are looking to recruit a qualified Quality Complaints Specialist to join their team. The main purpose of this position is to support the Deviation, Quality Event and Non-conformation processes within manufacturing.

A fantastic opportunity has arisen within a rapidly expanding pharmaceutical organisation for an experienced Quality Manager/QP to join their successful company.

Based inNorthern Ireland, the global company have a fantastic reputation for offering innovative scientific and commercial expertise to the life sciences industry. Due to a significant period of growth, an exciting opportunity has arisen for a Quality Manager/ QP to play a significant role in the companies’ future success. ...

A leading pharmaceutical company based in Surrey is recruiting for a Quality Assurance Manager. A fantastic opportunity with a global innovative company that is living in exciting times and it is hoped the Quality team will grow. Great potential to develop and succeed.

I am working alongside a very interesting and developing Pharmaceutical company to find an experienced GCP Auditor who would like to join a growing Quality Assurance division. An excellent opportunity has arisen to work in one of the most exciting areas of modern medicine within this innovative pharmaceutical company. They are offering the flexibility of up to 4 days a week home based and 1 day in the office in Cambridge.

*** Before starting your application, please ensure that you have familiarised yourself with this requirements. Applications that do not meet our minimum requirements will not be considered. ***

Our client is a leading pharmaceutical company which is active worldwide manufacturing more than 4 billion drugs in form of tablets, capsules, ampoules, vials and transdermal therapeutic systems per year. ...

HEAD QC MICROBIOLOGY (F/M)

My client an international company based in Switzerland is looking for a Head QC Microbiology to join their manufacturing site.

My client an international company based in Switzerland is looking for a Quality Control Supervisor. The main responsibility is to set up GMP/GLP QC labs and to validate all tests in accordance of international regulations and to plan QC testing schedule and resource. This position is expected to spend at least 25-50% of the time in the QC laboratories assisting with equipment qualifications, assay trouble shooting, and managing assay validations.

I am currently working with a leading Generics client based in home counties who are looking for a Pharmacovigilance Officer to join their team on a permenent basis. You will need to have good experience of PV an d of writing PSURs.

Senior Clinical Quality Assurance Auditor My client is global Pharmaceutical company who specialise in the development and manufacture of therapeutics that target the treatment of CNS disorders and Oncology. They are currently seeking a Senior Clinical Quality Assurance Auditor to be based in their Clinical Development Office.

A leading, global Pharmaceutical Company are looking to bring on board a RA QA Consultant, for a 6 month contract, to their site in Switzerland.

This role will perform Management Reviews per protocol to ensure adequate review of quality and reliability data associated with the Quality Management System.

Role:

- Perform Management Reviews per protocol per schedule. ...

An independent and globally operating Swiss-based biotechnology company with a comprehensive range of services for pharmaceutical and biotechnology companies seeks to hire a QA Manager to work on site close to Basel.

This is an ideal opportunity to apply for a position where you will see the effect your work has on the companies quality structure (as opposed to many of the larger Pharmaceutical conglomerates). ...