The latest Quality jobs - BETA

I am looking for a quality assurance specialist. You will be working with a leading biopharmaceutical company at a very exciting time with market leading products.

Head of Quality/QP, Southern Germany, Top 5 Pharma!

My client is a leading company in the pharmaceutical industry that is looking to expand their quality team. This is a great chance for experienced professionals in quality assurance that are eligible as a qualified person to further their career and gain experience that is second to none.

Some Areas of Responsibility are:

- To develop and implement strategic improvement for the department in order to
meet key business priorities

- To coordinate top level work plans across both QC and QS. Agree priority of
work from internal customers and organise to provide appropriate service levels. ...

My client has one of the longest heritages in the Pharmaceutical industry which has resulted in decades of success. They have key products in multiple therapy areas and part of their success story has been down to only hiring the very best candidates within the industry. They are now looking to add to their talented group with recruitment of their newest ‘QA Compliance Manager’.

This position is with a mid-sized biologics/pharmaceutical company in the Greater Los Angeles area. This company is expanding rapidly, has purchased a new facility, and is running completely off of profit after only a couple years with a marketed product. ...

Our client is currently seeking a QA Manager/Qualified Person (GMP) for their Cambridgeshire location

GCP Quality Manager- Exciting Biotech in Germany



I am recruiting for a hands on GCP Manager at a growing Biotech in Germany, to take responsibility for QMS, Compliance and audit management. This company will offer you the chance to progress your career in a broad position, where you can grow with the organisation at an interesting stage of development.

A fantastic and exciting new opportunity has become available for a Quality Assurance professional to join a leading Pharmaceutical company as a Quality Assurance Representative.

(Re)qualification of equipment and rooms Writing of qualification documents as far as related to Quality Assurance (QA)

Summary

Partners with the Regulatory Affairs, Supply Chain and Pharmacovigilance to assist and participate in the assurance of compliance activities required to ensure that products supplied by the global pharmaceutical company, are in accordance with cGMP their associated Marketing Authorisation, company standards and values.

A rapidly growing biopharmaceutical company is now looking for a Head of QC to lead the team of 70 people across Netherlands.

This is an exciting opportunity to join Phlexglobal, an expanding specialist provider of technology enabled document management solutions to the global clinical research market, as an eTMF Quality Specialist

A senior role -Head of QC- has become available within an pharma industry specialist in Plasma products.

This is an ideal opportunity to gain niche pharmaceutical experience to become an expert and make yourself very valuable. In this high profile role, you will be in charge of 70 members of staff indirectly, with manager reporting directly to you.

You will oversee all QC activity during the development of industry-leading Plasma products in a GLP and GMP environment.

QA Officer! Great Career Experience!

Your role as QA officer will be focused upon the GMP compliance in the manufacturing site. You will be ensuring oversight of all stages of product manufactured ensuring compliance with cGMP's and be responsible for the review and approval of SOP's, validation protocols, deviations and change controls. The role will also involve providing support and working closely with manufacturing, laboratories, MS&T,

A fantastic and exciting new opportunity has become available for a Quality Assurance professional to join a leading Pharmaceutical company as a Quality Assurance Representative. You will be based in Liverpool, a city bursting with history, culture and life.

Job title: Quality Engineer

Salary/Rate: Competitive

Location: Wiltshire

Benefits: Pension, Private Medical Cover, Gym Membership and annual company bonus

A global Medical Device organisation is looking for a Quality Engineer to work in project teams responsible for all activities dealing with validation, risk assessment, test methods validation and statistical assessment of data.

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.

Requirements:
1. Support and oversee all the quality and compliance processes
2. Manage and improve CAPA processes
3. Identify and design improvement processes
4. Liaising with Health Authorities regarding questions and queries
5. Driving and managing global quality plan and timely and efficiently execution
6. Closely cooperation with other involved departments and teams
7. Working and improving SOP according to GCP guidelines
8. ...

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.

If you are interested in re-locating to Switzerland this could be the opportunity for you!

**URGENT** GCP QUALITY ASSURANCE MANAGER ** SMALL BIOTECH ** SWITZERLAND**

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. ...

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 Officer. With thriving Export and Contract Manufacturing Divisions in place, this is an exciting time to join this organisation.

Operational QA Manager - Switzerland Mylene Paumier is recruiting for a Operational QA Manager to join a global pharmaceutical company at their site based in Switzerland...

I am currently working alongside a very exciting and developing company who are looking for a Head of Quality to join their Quality Assurance division. In this position you will report directly to the Managing Director of the company and ensure the Quality department meets the business and customer desirables.

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.

Regulatory Affairs & Quality Manager Standort: Oesterreich Sicherstellung der Kommunikation innerhalb des Konzerns und entsprechend der nationalen und europäischen Vorgaben Leitung des lokalen Qualitäts- und Beschwerdemanagements Implementierung und Optimierung regulatorischer und qualitätsrelevanter Maßnahmen und Prozesse

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 Associate Director of Quality Assurance (QA) in Reading, and help realize your career potential.

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.

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.

Our client is looking for a Global Quality & Compliance Manager to be based in the UK. Applications are welcome from across Europe. A comprehensive relocation support package is provided for those moving to the UK.

Contract - Pharmaceutical - QA Manager - Quality Assurance Manager - 6 Months - Lincolnshire

Vibrant, dynamic and highly stable medical device company is currently looking for a number of quality engineers for their growing department. This is a great opportunity to further develop in a company that truly is a fun and young environment to work in!

Freelance TMF Specialist - UK

My client is a global Pharmaceutical company who are urgently looking for multiple Clinical Project Assistant / Clinical Trial Administrator for a 8 month contract on a daily rate. Ideally you will have a proven track record as a CTA. Please note this is a 5 day week full-time position and you will be based onsite at our client's European HQ North of London.

As the Quality Assurance Auditor you will:



* Support quality management functions

* Undertake various quality assurance and control activities
* Ensure systems and processes comply with applicable laws, regulations
* Implement standard operating procedures, protocols and guidelines.
* Report to the Business Head and work co-operatively with Project Managers, Senior Researchers and Support staff.

A 4 month contract has become available for an ambitious Quality Engineer for a leading medical device manufacturer. Get in touch if you would like to join an up and coming organisation as a Quality Engineer.

Our client is a leader in the production and development medical devices Due to company expansions, they now have a vacancy for an experienced quality engineer to join the team.

The position is available within the quality assurance department of regulated GMP pharmaceutical company. The job functions will involve approval and audit of suppliers, SOP preparation, review and approval of analytical test methods and reports, process documentation preparation, process investigation review, complaint investigation, analysis of data and preparation of trend reports in accordance with current legislation and GMP.

Quality Management System Remediation Consultant – Luzern, Switzerland

Our client are a leading PI distributor seeking an experienced Head of Quality to be based on site in Yorkshire.

Our client are an expanding medical device manufacturer based in Leicester who are seeking an experienced QA Technician/Officer - Document Control.

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.