The latest Quality jobs - BETA

Senior Validation Expert in Quality Assurance – Netherlands

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. ...

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.

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 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.

Job title: Software Quality Assurance Specialist

Salary/Rate: £ 25,000-£35,000

Benefits: Holidays, Pension, Private Health Care, Life assurance, Gym membership, Flexible Working Hours

Area: Hertfordshire

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. ...

About the role This is your chance to join world leader in the healthcare industry. A truly global company, with manufacturing plants across the world- this role can be based in any major city within Europe! Best of all, in this role- you will have the opportunity to see the world while you work (expenses paid!).

SEC is working closely with a major global Pharma company to find highly motivated individuals for a business critical assignment. ...

Great permanent senior opportunity - Global QA GMP Auditor for Microbiology - based in Germany , in an international, global pharmaceutical company.
Qualifications
-Experience: min. 8 years experience in the pharmaceutical or biopharmaceutical industry, e.g. in Pharma Production, Quality Assurance, Quality Control, Development, Audit experience desirable
-Prior Auditing experience desirable
For more information's please contact directly with Agness +44

This major top-10 Pharmaceutical / Devices Company works in developing innovative medical devices, biopharmaceutical medicines, vetinary products and orthopaedic products. This is a long-term contract and the main purpose of the role is determining and reporting on the state of compliance of the quality system versus regulatory standards. Also you have to perform CAPA verification of effictivness as necessary.

This company is looking for someone to join their growing firm as a Pharmacovigilance Quality Officer. The successful candidate will take full responsibility to assist in the global pharmacovigilance activities within GPS-UK for the companies Laboratories Inc. in accordance with Company, United Kingdom & international standards and regulatory requirements, as assigned.

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

To perform remediation activities generated from the Management Review Legacy Reviews to ensure adequate product and process risk review.

Role:

- Perform Management Review remediation per schedule. ...