The latest Quality jobs - BETA

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.

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.

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.

Job summary • QA Auditor required for Global Pharma in Wavre, Belgium • Candidates must speak fluent English • Contract initially for 6 months, contract likely to be extended • Freelancers welcome to apply

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.

A global Pharmaceutical company is seeking a Quality Systems Manager to head up and lead all the QMS activities across the company, including the implementation of new systems and process. The client has an exciting pipeline of works as well as a thriving performance driven culture, and offers an opportunity to work in a unique offering in a pivotal role. ...

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.

Quality Associate – 6 months – Walloon Brabant (Belgium)

My client is urgently looking for a quality associate as responsible for reviewing and approving protocols and reports (ANALYTICAL METHOD TRANSFER) from local R&D teams to ensure compliance with Quality requirements as defined in procedures, standards and guidelines. ...

Key Accountabilities:
* Supports the quality aspects of the supplier evaluation process to approve the new Contract Manufacturing Operations.
* Manages and monitors the execution of the actions needed to mitigate any risks as identified in the project risk assessment.
* Ensure the Technical agreements are in place with the CMOs in advance of manufacturing commencing.
* Coordinates completion of CAPAs following supplier audits. ...