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The latest Regulatory jobs - BETA

Jobs: (Regulatory)

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Regulatory Affairs Specialist (medizinsche Geräte) / junges Unternehmen / Karrieremöglichkeiten
Germany
Jan 18
Eine einmalige Chance als Ingenieur und Regulatory Affairs Specialist im Bereich medizinische Geräte der Klassifizierungen 3, Teil eines global operierenden Unternehmen zu werden. Im süddeutschen...
Expert Regulatory Specialist
Berlin
Jan 18
EPM Scientific are currently looking for an Expert Regulatory specialist to join a diverse and rapidly growing Medtech company who specialize in in-vitro diagnostics. The...
Regulatory Information Management Systems (RIMS) Manager
Wiltshire
Jan 18
Regulatory Information Management Systems (RIMS) Manager Location: Wiltshire Salary: Up to £60,000 per annum + company benefits •Have over 15 years sector expertise and still rapidly growing.
Regulatory Affairs Team Leader
England
Jan 18
This is an excellent opportunity for a regulatory professional to join an international Bipharma within their regulatory department. You will be responsible for developing and managing a small team of regulatory professional focusing on the development and registration of allergy medicines.
Regulatory Affairs Consultant
Dublin
Jan 18
On behalf of our client, a Dublin based regulatory consultancy firm, we are recruiting for a Regulatory Affairs Consultant.
Regulatory Affairs Specialist-Learn New Skills-Medical Devices
Zürich
Jan 18
Exclusive role within regulatory affairs to develop your career within the niche and exciting area of packaging, labelling and documentation for innovative medical devices. You will work closely with a key regulatory affairs management team of a world leading medical device company and gain exposure to exciting international projects and develop your skills in a niche and lucrative area.
Regulatory Affairs Manager (medizinsche Geräte) / globales Unternehmen
Germany
Jan 18
Eine einmalige Chance als Regulatory Affairs Manager im Bereich medizinische Geräte und Produktzulassung der Klasse 1 -3, Teil eines globalen, internationalen Unternehmens zu werden. In...
Associate Director, Regulatory Affairs
London
Jan 18
A superb new opportunity has arisen with a global market leading Pharmaceutical company. They are currently searching for an Associate Director Regulatory Affairs to join their team in the UK. This is a novel position within the organisation which will allow for further growth of the Regulatory Affairs team.
Regulatory CMC Manager
Tyrol
Jan 18
An exciting new opportunity has arisen with one of our leading Biopharmaceutical clients. We are currently searching for a Regulatory CMC Manager, Biopharmaceuticals. Within this position you will be responsible for the compilation of CMC sections of regulatory dossiers for submissions globally. You would be responsible for writing CMC documentation for marketed products and throughout the development of biopharmaceutical products.
Regulatory Affairs Manager
Tyrol
Jan 18
An exciting new opportunity has arisen with one of our leading Biopharmaceutical clients. We are currently searching for a Regulatory Affairs Manager, Biopharmaceuticals. Within this position you will be responsible for the preparation of regulatory documentation for regulatory submissions globally. You would be responsible for the interaction with Regulatory, Health and Competent Authorities globally and support the development of biopharmaceutical products with regulatory input.
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Senior Regulatory Specialist - Medical Devices
Germany
Jan 18
Skills Alliance have partnered with a global Medical Device company to source for a Senior Regulatory Specialist for a position based in Southern Germany. Our...
France Regulatory Lead and Responsible Pharmacist
Paris
Jan 18
Situé dans Paris intra-muros, un laboratoire novateur cherche un Pharmacien Responsable pour diriger son département des Affaires Réglementaires France. Dans cette petite structure au succès prometteur, vous disposerez d'une autonomie importante dans vos projets et dans le management de votre équipe.
Toxicologist - Risk Assessment and Regulatory
Amersfoort
Jan 18
I'm currently working for a global player for the fragrance and flavours industry. The company has been through a rapid growth phase over the last couple of years and is looking to continue this expansion. To support their growth they are looking for an experienced Toxicologist to join the team.
Regulatory Affairs Assistant
Leeds
Jan 18
Regulatory Affairs Assistant Location: Leeds, UK. Contract: 12 months Regulatory Professionals are currently working with a leading pharmaceutical company and are looking for a Regulatory Affairs Assistant on a contract basis.
Regulatory Affairs Officer– Successful Future– Brussels
Brussels
Jan 18
A big pharmaceutical company is looking for a Regulatory Affairs Officer because there Benelux regulatory team needs support. The company has a diverse product portfolio such as vaccines, pharmaceuticals, consumer health,... Because they have spread their successes in different areas you can be more certain about the stability of your job.
Clinical Regulatory Lead - Luzern
Luzern, Switzerland
Jan 18
This position is for a Senior Clinical Research Associate (SCRA) who excels in regulatory issues and has strong submission experience. You will be outsourced to one designated pharmaceutical sponsor.
Regulatory CMC Associate Manager
Basel
Jan 18
Reg CMC Associate Manager wanted for our Basel based client in the pharmaceutical sector. ...
Regulatory Affairs Manager (Medizinprodukte) / junges Unternehmen / Karrieremöglichkeiten
Germany
Jan 17
Eine einmalige Chance als Ingenieur und Regulatory Affairs Specialist im Bereich Medizinprodukte der Klassifizierungen 3 Teil eines global operierenden Unternehmen zu werden. Im süddeutschen Standort...
Near beautiful Canal City GHENT - Regulatory Manager - Medical Devices - NPD , Strategy and Compliance - International role
Belgium
Jan 17
To apply for this role please call Julie Cooper on 07951 082482 or alternatively send your CV in the strictest confidence to: julie@mosaicrecruitment.co.uk
Regulatory Affairs Manager - near historic Ghent and close to the sea - Manage a team of three -NPD , Compliance , Strategy work
Belgium
Jan 17
To apply for this regulatory affairs manager role please call Julie Cooper on 07951 082482 or send your CV to: Julie@mosaicrecruitment.co.uk
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Regulatory Affairs Manager -near to the beautiful canal city of Ghent - Manage a team of three - International role - Medical Devices
Belgium
Jan 17
To apply for this regulatory affairs manager role please call Julie Cooper on 07951 082482 or send your CV to: Julie@mosaicrecruitment.co.uk
Regulatory Electronic Submission Planner
Kent
Jan 17
Good communication skills, written and verbal, and experience with Microsoft Word and Microsoft Excel. Experience and proven track record in regulatory affairs submissions (In NCE’s and or generics).
Regulatory Electronic Submission Planner
Kent
Jan 17
Good communication skills, written and verbal, and experience with Microsoft Word and Microsoft Excel. Experience and proven track record in regulatory affairs submissions (In NCE’s and or generics).
Associate Director, International Regulatory Strategy
Switzerland
Jan 17
Un des leaders de l'industrie pharmaceutique, une biotech innovante et en perpétuelle évolution, est à la recherche d'un Associate Director pour le département de l'International Regulatory Strategy. C'est une entreprise reconnue, possédant un excellent portefeuille de produits. Pour cette opportunité, nous recherchons un candidat parlant couramment anglais, avec un background en neurosciences ou maladies génétiques.
Regulatory Affairs Coordinator - Medical Devices
Paris
Jan 17
ProClinical are currently seeking Regulatory Affairs Coordinators based in Paris, France for a global medical devices project. There are also opportunities in Madrid, Lisbon, Rome, Athens or Tel Aviv.The global medical devices project will require Coordinators to collect Regulatory data and coordinate projects, liaising with Regulatory Affairs, Marketing, Supply Chain etc. The position will give an excellent opportunity for a junior profile to progress in their career. ...
Manager Regulatory Affairs (m/w) Medizintechnik
Karlsruhe
Jan 17
Manager Regulatory Affairs (m/w) Medical DevicesOffice-based in der Nähe von KarlsruheAufgaben:- Erarbeitung und Umsetzung von Zulassungsstrategien und –plänen für neue Produkte weltweit. ...
AD/Director, Data Sciences, Safety and Regulatory (DSSR) Business
reading
Jan 17
PURPOSE Establish and manage an effective Sales plan to maximize Organizational growth for the allocated Business unit(s) for Data Sciences, Safety & Regulatory (DSSR) services in the relevant Geography. To serve as strategic business partner responsible for identifying, developing and expanding new business opportunities in alignment with internal stake holders within Sales, Account Management & Operations (BU & GDN). ...
Associate Director - Regulatory Affairs
USA
Jan 17
My client is an emerging bio-pharmaceutical company whose pipeline spans multiple therapeutic areas through strategic alliances, collaborations and partnerships with academic institutions and pharmaceutical companies.
Regulatory Specialist- world well known Cosmetic Brands
Germany
Jan 17
Regulatory Specialist- world well known Cosmetic Brands My client a global leader and one of the fastest growing entities within the Cosmetic Industry is currently looking for a Regulatory Affairs Manager to join one of it departments in Germany.Products manufactured by my client belong to some of the most famous brands in the world. World leading company gives you an opportunity to work with best specialists within the field and expand your professional network. ...
CMC Regulatory Specialist –Interesting Pipeline- Belgium
Antwerp
Jan 17
A biotech company is looking for a CMC Regulatory Specialist to complement the regulatory team on the CMC part of the dossier (the others are more (pre)-clinical focused). The company has no products on the market yet and has a strong pipeline which means you can be part of the process from pre-marketing stage and have more impact on the company's success by bringing innovative products to the market.
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SSU and Regulatory Specialist I - Study Start Up (South Africa)
Johannesburg
Jan 17
Do you want to be part of a global top 10 CRO? INC Research is a full-service clinical research organization, providing the full range of Phase I to IV clinical development services for the world’s pharmaceutical, biotech and medical device industries. We do this across six continents. We believe that therapeutic and operational experience forms the foundation for taking medicines successfully through clinical development.
Manager, SSU and Regulatory (ITALY)
Cambridgeshire
Jan 17
I am currently representing a great opportunity to work within a top 10 CRO, across 6 continents and to provide the full range of Phase I to IV clinical development services for the world’s pharmaceutical, biotech and medical device industries.
Technical File Reviewer / Medical Devices / ISO13485 / ISO 9001 / Regulatory Affairs / Regulatory
Hertfordshire
Jan 16
Job Title: Technical Reviewer Salary: Up to £65,000 per annum Location: Home Based I am currently working with a Medical Device company who are looking for a Technical Reviewer to join the company in a Home Based role.  The role will require occassional travel within the UK and Europe. ...
Regulatory Affairs Manager – globales Biotechnologieunternehmen – Baden Württemberg - 75,000 € - Teilzeit auch moeglich
Germany
Jan 16
Wir suchen einen motivierten Regulatory Affairs Manager, der sich leidenschaftliche für Patiensicherung sorgt und gerne in einem Familienfreundlichen Unternehmen arbeiten möchte. Als Gegenleistung erhalten Sie spannende Aufgaben, innovatives Produktportfolio und exzellente Karriereentwicklung.
Team Leader Regulatory Affairs Medical Device - global healthcare company - Belgium - 85,000 €
Belgium
Jan 16
We are looking for a Team Leader Regulatory Affairs, who likes to work in a global and diverse company and will take credit for operational, strategical and line management task. You can expect to work in a small but already good developed medical device team with a great environment and exciting product portfolio.
Regulatory CMC administrator
Hertfordshire
Jan 16
A global pharmaceutical company is seeking a Regulatory CMC Administrator to join their team in Hertfordshire, UK. The company employs people all over the world and focuses on developing drugs and treatments for Alzheimer's disease, epilepsy and cancer. Job Role: To provide business support for the maintenance of the Agency Approved Module 3 content in the EDGE Document Management System. ...
Regulatory Specialist
Maidenhead
Jan 16
i-Pharm Consulting are recruiting for…ROLERegulatory Specialist LOCATION: Maidenhead (flexibility to work from home)RATE: £20-£25 per hour ROLE: • Coordinating and assisting with the interpretation and implementation of key legislation (REACH, CLP, and BPR) impacting activities in Europe • Determining, negotiating, collating, reviewing and selecting appropriate data in support of product classifications• Labelling and registrations• Coordinating and assisting the Functional Expert with the ...
Regulatory Affairs Specialist-Innovative Devices-Munich, DE
München (81249)
Jan 16
NonStop Medical Devices are currently looking for a regulatory affairs specialist to join our client, a market leading medical device company.
Regulatory Affairs Manager - Manchester
Manchester
Jan 16
Regulatory Affairs Manager - Manchester •Have been established for over a century! 10,000 employees worldwide and expertise of years and years of professional development. •Uses science and technology as one to create products improving the overall life quality.
Home Based – Regulatory Writer – Global CRO – 12 Month Contract
England
Jan 16
This world leading CRO is after experienced medical writers who can come in on a contract basis and hit the ground running. This position is 100% home based allowing you to work on a range of global projects.
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Argochemical Regulatory Manager - Be the Senior EU Specialist
Amsterdam
Jan 16
My Client is an international Agrochemical Company, with strong expansion plans for the EU market. To support their growth they are looking for a Regulatory Project manager, who will be in charge of the whole EU crop protection portfolio.
Regulatory Affairs Director of CMC – Brussels – Global role with Team Leading
Brussels, Belgium
Jan 16
My client is offering a strong salary at the upper end of the pay scale with a number of strong benefits/initiatives around full re-location, private healthcare, stock options, sign on allowances, housing allowances , fully expensed company car with petrol card, bonus & school fees paid for one of the International Private schools in Brussels. Call Theo Moore or Matt Greig in the London office on +44 (0)20 7801 3380
Regulatory Affairs Global CMC Biological Roles in South-West Switzerland - Great Salary and full Re-location Packages Available
South-West Switzerland
Jan 16
The salary and package is exceptional for this role, including basic salary up to 155,000 CHF + Bonus + shares + full re-location package including housing and a large settling in allowance. To have a confidential discussion about this or other potential roles or career options, call Theo Moore or Matt Greig in the London office on +44 (0)20 7801 3380.
Regulatory Affairs Director / EU and Global regulatory strategies - line management and project management role / Brussels
Brussels
Jan 16
This exciting Biotechnology client based in Brussels is looking for someone special. They seek a regulatory affairs Director with experience of both line management and project management for EU and Global projects with In-depth knowledge of Paediatric Investigation Plans and Orphan Drug Designation applications. Call Theo Moore or Matt Greig in the London office on +44 (0)20 7801 3380.
Regulatory Officer - FMCG Training provided
Leeds
Jan 16
Regulatory Officer - FMCG experience? Training provided!Take the opportunity to work for a leading global brand with 75% of it’s products being the number one seller worldwide in it’s industry. Providing a chance to learn new regulations (pending your experience) and get hands on dossier compiling experience, this is a chance to work with a market leader and progress.Regulatory experience from any industry will be considered. ...
Regulatory Coordinator EMEA
Brussels
Jan 13
Main missions: • to provide procedural, administrative and planning support for new submissions and variation submissions in the EU • to provide administrative regulatory support during filing and review of new submissions, variations / to plan and coordinate new submissions, variations, CHMP referrals, FUM, in order to ensure timely submission • to draft module 1 components • to ensure timely submission in collaboration with managers• to prepare the English Product Information in collaborat ...
Regulatory Specialist - IVD - 6 Months
Gloucestershire
Jan 13
I am looking for a Regulatory Specialist for a 6 month contract based in the West. They are looking for someone to help review and update and develop IVD Technical Files. ...
Senior Regulatory Affairs Officer/ Senior Registration Officer
Hertfordshire
Jan 13
Minimum 12 month FTC to cover a maternity leave with global client based in Herts. Competitive package available. Minimum 18 month post-marketing regs experience required.
Associate Director Regulatory Affairs
Switzerland
Jan 13
The Hydrogen Group has been appointed to search and select an Associate Director Regulatory Affairs, who is looking to contribute their expertise to facilitate and assist a regulatory team on behalf of a growing global pharmaceutical services organisation. This is a great opportunity for a Regulatory Affairs professional to develop and progress into a leading role.The role comes with an attractive salary. The position is based in one of the company's major global hubs.
Regulatory CMC Manager, Biologics, Pre Approval
Neuchâtel
Jan 13
Regulatory CMC Manager, Biologics, Pre Approval, Early Development, Hands on and Project Coverage, Western Switzerland
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Regulatory Affairs Manager, CMC, Austria
Salzburg
Jan 13
Regulatory Affairs Manager, CMC, technical and strategic input, global pharmaceutical company working on products in development and established brands
Regulatory Affairs Manager, Development Products
Basel
Jan 13
Regulatory Affairs Manager/Senior , development products, global HQ, EMA, strategic and hands on focus. Salary package competitive with Big Pharma, relocation help is available and many of the team are ex-pats.
Regulatory Affairs Manager Düsseldorf - projects
Germany
Jan 13
Ein Dienstleisterunternehmen in NRW und Bayern sucht nach einem Junior und Senior Regulatory Affairs Manager.Sie würden in einem familienähnlichen Umfeld arbeiten und Flexibilität bezüglich Arbeitszeiten haben. Darüber hinaus hätten Sie die Gelegenheit an mehreren dynamischen und herausfordernden Projekten teilzunehmen, und auch eng mit anderen Abteilungen zusammenzuarbeiten. ...
Drug Regulatory Affairs Coordinator (80%)
Basel
Jan 13
DRA, Drug Regulatory affairs Coordinator 80%, great chance to join a friendly and stable team working on global submissions.If you are an experienced regulatory affairs administrator then this is a great chance to gain global submissions experience with a well established pharmaceutical company in the Basel area. The team are stable and thanks to new investment, they are targeting a number of new submissions not just in Switzerland, but also across the emerging markets. ...
CMC Regulatory Afffairs Frankfurt Area
Germany
Jan 13
Unser Kunde, eines der schnellst wachsenden Dienstleisterunternehmen im Bereich Regulatory Affairs, sucht nach neuen Regulatory Affairs Spezialisten, die sich gut mit CMC auskennen. Das Unternehmen ist global, hat hunderte von internationalen Kunden und mehrere Standorte in Europa. Momentan gibt es Vakanzen für CMC-Experten in Hessen und NRW. ...
Belgian Post Market Regulatory Specialist
Brussels
Jan 13
Post Market Regulatory Profesionals- Belgium- entry level
Head of Regulatory Czech Republic Prague
Prague
Jan 13
Head of Regulatory- Prague
Junior Regulatory Officer - Get Experience With Crop Protection
Limburg
Jan 13
My client has a big portfolio of crop protection products, that are being sold worldwide. To support the registration process they are looking for a junior candidate, who wants to learn about crop protection registrations. This is an excellent opportunity for someone who is looking to transform his skill-set into a niche area, with loads of career growth opportunities and job stability.
Senior Regulatory Affairs Associate – innovative pharma company – Mannheim – 50,000 €
Germany
Jan 13
We are looking for a Regulatory Affairs Associate, who likes to work in a young and innovative pharma company and will take credit for operational tasks for dossier compilation and submissions. You can expect to work in a small but already good developed company with a great environment and exciting product portfolio.
REGULATORY SUBMISSIONS ASSOCIATE / Maidenhead, United Kingdom
Maidenhead, UK
Jan 13
COVANCE is a leading global drug development services company and we provide support to the Pharmaceutical and Biotechnology industries.
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Regulatory Affairs Manager Russia and GUS states – pharma company in Hamburg – 70,000 Euro
Germany
Jan 13
We are currently seeking for a motivated Regulatory Affairs Manager who will be responsible for regulatory activities within development and post marketing stage. It is an excellent opportunity to work in a dynamic team and contribute to the development of a well-established company, while receiving an attractive salary package.
Senior Associate- Regulatory Affairs CMC-
London
Jan 13
I am currently working on behalf of a global consumer health company who is looking for a Senior Associate specilising in CMC to join their team.
Regulatory Affairs Associate
England
Jan 13
The Hydrogen Group has been appointed to search and select a Regulatory Affairs Associate, on behalf of a global pharmaceutical company. This organisation is currently focused on the rapid expansion of their innovative product portfolio to provide affordable solutions to individuals and their wellbeing.
Quality and Regulatory Affairs Associate
Rep. Ireland
Jan 13
Our client, a global medcial device company with offices in Dublin now have a new vacancy for a Quality & Regulatory Affairs Associate.
VP, Regulatory Affairs
USA
Jan 13
My client is a large firm based in the Cambridge, MA. With over 2 decades of experience at the highest level, this firm already has a strong product portfolio, and is looking for more individuals to take up the reins in Regulatory Affairs
Regulatory Affairs Manager
USA
Jan 13
My client is a large firm based in the Cambridge, MA. With over 2 decades of experience at the highest level, this firm already has a strong product portfolio, and is looking for more individuals to take up the reins in Regulatory Affairs
Regulatory Affairs Officer - Munster
Tipperary, Republic of Ireland
Jan 13
Our client, a pharmaceutical company now have an immediate requirement for a Regulatory Affairs Officer.
Head of Regulatory Affairs - Italy - OTC role
Italy
Jan 13
To apply for the for this regulatory affairs role please call Julie Cooper on 07951 082482 or send your CV to: julie@mosaicrecruitment.co.uk
HEAD OF REGULATORY AFFAIRS - CELL AND GENE THERAPY - CENTRAL LONDON - ENGLAND - £80K - £85K
London
Jan 12
An opportunity to work at a leading CTG (Cell and Gene therapy) organisation as Head of Regulatory Affairs based in London. You will be responsible for the overseeing of products (Cell and Gene Therapy) into early clinical trials, providing clinical, technical and manufacturing regulatory expertise.
Senior Regulatory Affairs Manager - London
London
Jan 12
A fantastic opportunity has risen within an incredibly exciting and pioneering organisation as Senior Regulatory Affairs Manager, based in the heart of London a stone’s throw away from the Thames and within a 10-minute walk from London Bridge station.
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Regulatory Affairs Assistant - Compliance - Medical Devices
Leeds
Jan 12
Regulatory Affairs Assistant / Leeds / 11 Months Contract / Up To £17 Per Hr
Senior Regulatory Affairs Associate - Devices
Oxfordshire
Jan 12
Senior Regulatory Affairs Associate - Devices Salary -£35,000-£39,000 pa Permanent - 37 hours pw Location - Oxfordshire Do you want to work for well-established company with over 70 years' experience?
Regulatory Affairs Associate - Devices
Oxfordshire
Jan 12
Senior Regulatory Affairs Associate - Devices Salary -£35,000-£39,000 pa Permanent - 37 hours pw Location - Oxfordshire Do you want to work for well-established company with over 70 years' experience?
Sr SSU and Regulatory Specialist (United Kingdom)
Camberley
Jan 12
Do you want to be part of a global top 10 CRO? INC Research is a full-service clinical research organization, providing the full range of Phase I to IV clinical development services for the world’s pharmaceutical, biotech and medical device industries. We do this across six continents. We believe that therapeutic and operational experience forms the foundation for taking medicines successfully through clinical development.
SSU and Regulatory Specialist II (Germany)
Munich
Jan 12
At INC Research we appreciate the importance of having experts dedicated to the set up stages of the studies, and for this reason we have a devoted Study Start Up team with departments focused upon Site Identification and Feasibility, Site Contracts, Ethics and Regulatory and Patient Recruitment.
SSU and Regulatory Specialist I
Germany
Jan 12
Do you want to be part of a global top 10 CRO? INC Research is a full-service clinical research organization, providing the full range of Phase I to IV clinical development services for the world’s pharmaceutical, biotech and medical device industries. We do this across six continents. We believe that therapeutic and operational experience forms the foundation for taking medicines successfully through clinical development.
Regulatory Affairs Manager - Ghent - Manage a team of three - International role - Medical Devices
Belgium
Jan 12
To apply for this regulatory affairs manager role please call Julie Cooper on 07951 082482 or send your CV to: Julie@mosaicrecruitment.co.uk
Regulatory Submissions Coordinator
Rotterdam
Jan 12
Medpace is a global, full-service Clinical Research Organization (CRO) specializing in a multitude of therapeutic areas. Our headquarters are located in Cincinnati, Ohio and we are active in over 45 countries across the globe. We continue to steadily grow and are looking to add to our team! Our clinical activities are growing rapidly, and we are currently seeking a full-time, office-based Regulatory Submissions Coordinator to join our Clinical Operations team. ...
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Regulatory Affairs Specialist // North Carolina // Medical Device // 6 Months Initial Contract
USA
Jan 12
The role will primarily involve aiding the development and execution of various FDA and internal submissions including PMAs, 510(k)s, IDEs and various lifecycle management submissions.
Senior Director, Regulatory
San Francisco
Jan 12
The Regulatory Affairs Professional (Director) will be responsible for the comprehensive management of regulatory aspects of the company’s development projects while actively contributing as a member of the project team(s). This position will also require key contributions to department and company initiatives related to regulatory affairs operations and strategy. ...
Global Regulatory Affairs Manager
USA
Jan 12
My client is an entrepreneurial mid-sized firm based in the Greater Boston area. They already have 1 highly successful drug on the market, and are making great strides in their new project already. Partnered already with 3 larger firms, there are very strong career prospects, and now is an exciting time to get on board
Global Regulatory Affairs Director/Associate Director
USA
Jan 12
My client is an entrepreneurial mid-sized firm based in the Greater Boston area. They already have 1 highly successful drug on the market, and are making great strides in their new project already. Partnered already with 3 larger firms, there are very strong career prospects, and now is an exciting time to get on board.
Associate Director - Global Regulatory Affairs
Berkshire
Jan 12
An internationally known biotechnology company has an opening for a Associate Director job at their Berkshire office. The company has a strong reputation for developing innovative therapies for neurological diseases and employs approximately 7,000 people worldwide. Job Role: Responsible for developing and implementing innovative European regulatory strategies for product under development, through application to approval. ...
Regulatory CMC Consultant
Surrey
Jan 12
This pharmaceutical regulatory affairs job is an excellent opportunity to work for a global leader in the life sciences industry. They are currently looking for a Regulatory CMC Consultant to be located in close proximity to London - in Surrey, UK. The company has been established for more than 150 years and is a major supplier to the NHS. ...
Regulatory and Site Services Specialist (W/M)
France
Jan 12
Based in Paris area - Office based
Regulatory Affairs Manager - Ghent - Manage a team of three - International role - Medical Devices
Belgium
Jan 11
To apply for this regulatory affairs manager role please call Julie Cooper on 07951 082482 or send your CV to: Julie@mosaicrecruitment.co.uk
Regulatory Affairs Update Jan 2017
Switzerland
Jan 11
Regulatory Affairs Update January 2017
Regulatory Affairs Manager - Ghent - Manage a team of three - International role - Medical Devices
Belgium
Jan 11
To apply for this regulatory affairs manager role please call Julie Cooper on 07951 082482 or send your CV to: Julie@mosaicrecruitment.co.uk
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Regulatory Affairs Manager - Ghent - Manage a team of three - International role - Medical Devices , Belgium
Belgium
Jan 11
To apply for this regulatory affairs manager role please call Julie Cooper on 07951 082482 or send your CV to: Julie@mosaicrecruitment.co.uk
Regulatory Affairs Assistant
South East
Jan 11
An exciting Regulatory Affairs Assistant opportunity for a junior regulatory professional to join a growing SME pharmaceutical company based in the South East of England....
Regulatory Affairs CMC Professional
Dublin, Republic of Ireland
Jan 11
On behalf of our client, a global pharmaceutical company, we are currently recruiting for 2 Regulatory Affairs Professionals within the CMC Department.
Head of Regulatory Affairs - Italy - OTC role
Italy
Jan 11
To apply for the for this regulatory affairs role please call Julie Cooper on 07951 082482 or send your CV to: julie@mosaicrecruitment.co.uk
REGULATORY AFFAIRS ASSOCIATE - Germany
Regulatory Affairs Associate
Jan 11
An outstanding opportunity to join one of the world’s leading contract research organisations and be part of a dynamic and growing international company. Join PRA Health Sciences as a Regulatory Affairs Associate and help realize your career potential.
Regulatory Officer - Biocides
Leeds
Jan 11
Regulatory Associate - Biocides - leading market opportunityTake the opportunity to work for a leading global brand with 75% of it’s products being the number one seller worldwide in it’s industry. Providing a chance to learn new regulations (pending your experience) and get hands on dossier compiling experience, this is a chance to work with a market leader and progress.Valuing development, our client looks to put employees on a career path and takes pride in it's regulatory department. ...
-Prague- Head of Regulatory Affairs
England
Jan 11
Head of Regulatory- Prague
Junior Post Market Regulatory Specialist -Belgium
Brussels
Jan 11
Junior Post Market Regulatory Specialist urgently needed in Belgium
Senior Regulatory Affairs Office or Manager(Permt/FTC) - EMEA based
Reading
Jan 11
PURPOSE Provide support to mgmt in the promotion and assessment of compliance with regulations, guidelines, and operating procedures. Manage QA oversight of projects, assignments, and training. Conduct independent audits to assess compliance with regulations, guidelines, and operating procedures. Prepare and distribute reports of findings to operations staff, management, and customers. Provide consultation in interpretation of regulations, guidelines, policies, and procedures. ...
Regulatory Affairs Officer 2
Reading
Jan 11
RESPONSIBILITIES Acts as CMC lead/specialist for client projects, may have CMC responsibility for a portfolio of products.  Conducts CMC change control assessments Provides regulatory strategy of CMC submissions worldwide Authors and reviews Module 3 sections Prepares and reviews CMC documentation required to support submissions e.g IMPD updates, MAA, post approval variations and renewals. ...
regulatory jobs : 100 +
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