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Jobs: (Regulatory)

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Senior European Regulatory Director
Dublin
Dec 10
If you’re a senior regulatory affairs professional with broad and deep leadership experience in the discipline who’s open to an exciting opportunity I’d love to tell you about a role that I’m handling. My client is a young, exciting pharma / biotech company working exclusively in the orphan / ultra orphan disease space. ...
Regulatory Affairs Specialist/Manager
Dublin, Republic of Ireland
Dec 10
On behalf of our client, a global pharmaceutical company, we are currently recruiting for a Regulatory Affairs Specialist/Manager
Experte für Regulatory Affairs Systeme
Hamburg
Dec 10
Experte für Regulatory Affairs Systeme (m/w) Office-based in Wedel Sie haben Spaß an der Betreuung von Software Systemen und bringen idealerweise Erfahrung im Regulatory Affairs mit? Dann ist das genau die richtige Stelle für Sie! Das Unternehmen:Mein Kunde ist ein renommiertes Pharmaunternehmen. Freuen Sie sich auf ein kollegiales Arbeitsumfeld mit flachen Hierarchien. ...
CMC Regulatory Affairs Manager München (m/w)
Germany
Dec 10
Für unseren Kunden aus München sind wir auf der Suche nach einen Regulatory Affairs CMC Manager.Ein schnellwachsendes Unternehmen mit ausgezeichneten Aufstiegsmöglichkeiten und erfolgreichem Work-Life-Balance Programm. Nicht nur die wissenschaftliche Affinität sondern auch eine Team-Orientierte Persönlichkeit ist für das Unternehmen sehr wichtig. ...
Regulatory Manager / Senior RA Manager Join EU MAA team, part of 1st MAA Bio then co-lead 5 new indications Novel MOA Relo Offered
BeNeLux
Dec 10
My client is a well-known bio-pharmaceutical company with a strong pipeline and a stable environment, seeking individuals who want to get ahead in their career, individuals who will apply themselves in order to grow and learn. You will consider this role ...
Senior Regulatory Records Specialist - TMF
England
Dec 7
Why Syneos Health? Join a game-changing company that is reinventing the way therapies are developed and commercialized. Created through the merger of two industry leading companies, INC Research and inVentiv Health, we bring together more than 22,000 clinical and commercial minds to create a better, smarter, faster way to get biopharmaceutical therapies into the hands of patients who need them most.
Senior Study Start Up and Regulatory Specialist - 6 month contract
England
Dec 7
An excellent opportunity for a study start up expert to join on a contract basis.
Senior Study Start Up and Regulatory Specialist
England
Dec 7
An excellent opportunity for an experience study start up specialist to join a leading CRO.
Senior Study Start Up and Regulatory Specialist
England
Dec 7
An excellent opportunity for a study start up specialist to be outsourced to a single sponsor.
Regulatory Affairs Officer
Belgium
Dec 7
Regulatory Affairs Officer, BelgiumAn exciting opportunity has arisen to join a leading CRO and manage their regulatory activities. You will be involved in a wide variety of exciting projects and clinical trials. ...
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OPTION SUISSE Regulatory CMC Director Pure mAbs and Team Management role Development and Marketed, US and Europe and Int’l Majors
Switzerland
Dec 7
OPTION SUISSE ** Regulatory CMC Director *** Pure mAbs & Team Management role ** Development & Marketed, US and Europe & Int’l Majors? This role is based in Switzerland, within easy commute of Lausanne, Geneva, or Bern. The role comes with an advantageous package including RSUs.
Global Regulatory Group Director for Personalized Healthcare
Welwyn
Dec 7
The Global Regulatory Director Personalized Healthcare (PHC) is a global role and is providing regulatory leadership for a portfolio of PHC Projects, in order to support and drive all of its regulatory aspects. ...
Regulatory Data Strategy Leader
Welwyn
Dec 7
Regulatory Data Strategy LeaderThe Digital Revolution is increasing the amount of data available for internal and external use that will bring incredible value to Pharma. This will require that data is made easily accessible to meet strategic business objectives, including data used for regulatory decision making.  The capability required for management and control of data will continue to grow as more and more devices, technologies and services harvest more and more information. ...
Medical Writer Regulatory Affairs Hamburg (m/w)
Germany
Dec 7
Ein Pharma Unternehmen aus Hamburg sucht nach einem Medical Writer für den Regulatory Affairs Aufgabenbereich. Es erwarte Sie eine spannende Tätigkeit in einem wachstumsorientierten Unternehmen mit grossartigen Aufstiegsmöglichkeiten. Das Unternehmen hat eine sehr angenehme Arbeitsatmosphäre und bietet konstante Weiterbildungsoptionen an. ...
Regulatory Affairs Assistant
Belgium
Dec 7
Regulatory Affairs Assistant, BelgiumAn exciting opportunity has arisen to join a leading CRO and be involved in their regulatory activities. You will be involved in a wide variety of exciting projects and clinical trials. ...
Regulatory Affairs Manager
Galashiels
Dec 6
An opportunity has arisen for a Regulatory Affairs manager to come and join the team at an R&D based life sciences company that has a global footprint within biotechnology.
Regulatory Affairs Manager
Watford
Dec 6
An incredible opportunity for a Regulatory Affairs manager has arisen to join a market leading Pharmaceutical company providing medical solutions within Dermatology.
Regulatory Affairs Manager
Hemel Hempstead
Dec 6
An opportunity has arisen for a Regulatory Affairs manager with an eye for detail to come and make an impact in a market leading company that has a huge success within Pharmaceuticals.
Regulatory Affairs Manager
Aylesbury
Dec 6
A requirement for a Regulatory Affairs manager has come up, to join an innovative Regulatory consultancy with a dominance and a proven track record of success within the Lifesciences sector.
Regulatory Affairs Line Manager
Belgium
Dec 6
Regulatory Affairs Line Manager, BelgiumA leading Global Pharmaceuticals Company is looking to add to their renowned RA department. If you’re an RA line manager with 6+ years of experience, this role may be the next step for you in your career. ...
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Regulatory Affairs Manager
Hertford
Dec 6
A requirement for a Senior Regulatory Affairs manager has come up, to join a leading and extremely reputable Global Research and Development-Based company specialising in the Pharmaceutical industry.
Regulatory Affairs Director / Post Marketing / Dynamic Biopharma / West of London
Oxford
Dec 6
Regulatory Affairs Director; Project Leading & Managing; mainly Post-marketing activity; Top Biopharma; West of London location
Senior Regulatory Affairs Manager, Home Counties
Greater London
Dec 6
We are recruiting for an excellent opportunity for a Senior Regulatory Affairs Manager to join a global pharmaceutical company in the Home Counties on a...
Senior Regulatory Affairs Manager Emerging Markets Home Counties
Greater London
Dec 6
We are recruiting for an excellent opportunity for a Senior Regulatory Affairs Manager Emerging Markets to join a global pharmaceutical company in the Home Counties...
Senior Regulatory Affairs Manager in Home Counties
Greater London
Dec 6
We are recruiting for an excellent opportunity for a Senior Regulatory Affairs Manager to join a global pharmaceutical company in the Home Counties on a...
Sr SSU and Regulatory Specialist - Bulgaria
Bulgaria
Dec 6
Here at Syneos Health we are looking for Senior Site Start-Up and Regulatory Specialist to join our team in Bulgaria. The position is either office or home-based in Sofia.
Senior Regulatory Affairs Specialist
Watford
Dec 6
Main purpose of role Develop and applies intermediate knowledge and understanding of the regulatory and legal frameworks, regulatory requirements, legislation, processes and procedures. Key tasks * Assesses regulatory intelligence to assist in the development of local, regional, and global regulatory strategies * Evaluates the regulatory environment and contributes to providing internal advice throughout the product lifecycle (e.g. ...
Regulatory Submission Manager
England
Dec 6
We've had an exciting position released working with a London based global organisation. The company have an excellent reputation on the market and are known for their high level of employee retention, exciting pipeline and innovative approach to the sciences.
US Regulatory: Based RTP, NC OR Remote RA Manager or Senior Regulatory Manager Support complex lifecycle strategies, Line Extensions on mAbs
Remote, Relocate or work in RTP, NC
Dec 6
Work remotely with regular visits to the HQ, or you can already commute to RTP, Raleigh-Durham, North Carolina, or relocate to RTP, which is offered and well-funded by our client.
Regulatory and Public Affairs Lead HC Provider Central Europe Relo and Housing Allowance Build Reg Intell with Public Affairs
Central Europe
Dec 6
To apply or enquire, please contact me, Matt Greig, on UK +447918679405 or send me a full CV to matt@advregulatory.com and I will contact you by return. I am available for telephone calls after work all week, if this is easier, on the same number.
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Regulatory Affairs Manager-152208
Europe, Middle East and Africa-UK-England-Cambridge,
Dec 6
PPD has a new opportunity for a Regulatory Affairs Manager to join our Regulatory Affairs team.  This is a fantastic new opportunity to advance your regulatory career in an exciting and fast paced environment. ...
Manager (m/w) Regulatory Affairs - Stuttgart
Stuttgart
Dec 5
Mein Kunde ist ein recht junges und kleines Unternehmen der Medizintechnik und sucht aktuell einen Zulassungsexperten bzw. eine -Expertin auf internationaler Ebene (EU und USA) für das Portfolio (Implantate und Instrumente).
Regulatory Affairs Manager - London Based
London
Dec 5
Regulatory Affairs Manager - London Based
Senior Medical Writer Regulatory Affairs (m/w)
Germany
Dec 5
Ein Pharma Unternehmen aus Norddeutschland sucht nach einem Senior Medical Writer für den Regulatory Affairs Abteilung. Eine spannende Tätigkeit in einem deutschen Pharmaunternehmen mit einem grossartigen Team. Das Unternehmen hat eine sehr angenehme Arbeitsatmosphäre und bietet konstante Weiterbildungsoptionen an. ...
Regulatory Affairs Manager - CMC
Oxford
Dec 5
Due to our continued growth we are looking for a Regulatory Affairs Manager - CMC to join our CDS team. The purpose of this role is to develop and execute Regulatory CMC strategies for gene therapy products in clinical development and commercial products primarily in the EU and US markets (pre- and post- approval).
Regulatory Affairs CMC GRL, Director Level - This a gloabl role with a growing company in a beautiful part of the world
Geneva, Switzerland
Dec 5
My client is a Geneva based Global Biotechnology company who are looking for a bright and ambitious professional to take the lead on developing global regulatory CMC strategies for early phase projects through global registrations. Contact Theo Moore on + 44 (0) 207 801 3384
Regulatory CMC Director mAbs and Team Mngt role Have strong EU strategy – gain global for both NBEs and Marketed M4 Corridor
London
Dec 5
Regulatory CMC Director *** Pure mAbs and Team Management role ** Have strong EU strategy – gain global for both NBEs and Marketed? This role can be based in the West of London area, within an easy commute of West London, Surry, Bucks, Berks and Middlesex and Herts.
Regulatory and Compliance Global Director Based UK, BeNeLux QMS and PI for the global regulatory function With Relocation
UK M4 or BeNeLux
Dec 5
You will see yourself as someone who can provide solutions into the value chain, by working with different sub teams, different functions and in a role where you will report to the senior management team member (the global RA leadership team), for an individual with a truly remarkable reputation >>>
Regulatory Affairs Officer
Rep. Ireland
Dec 5
On behalf of our client, a leading pharmaceutical company based in the South-East of Ireland, I am  recruiting for a Regulatory Affairs Officer.
OPTION BELGIQUE Sr / Regulatory Programme Manager EU and GRL Career Pathway No mature products GAIN RA Dev and NEW Lifecycle
Belgium
Dec 5
This role will appeal to individuals who want to work in a Global HQ where 70% of ALL decisions are made in the same building! This role is based in Belgium, comes with an attractive salary, bonus, and a great deal of opportunity to grow. This company has a track record of developing individuals from Manager and Senior to the Global Regulatory Lead level!
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Regulatory Affairs Clinical Trial Manager
Basel Area
Dec 5
Our client, an dynamic medium-sized bio-pharmaceutical company headquartered in Switzerland, covering multiple therapeutic areas, is looking for a Regulatory Affairs Clinical Trial Manager for 12 months contract based in the Basel area. The ideal candidate should have 3 years of previous experience working for the pharmaceutical industry being responsible for the compilation and completion of Clinical Trial Applications within an International Regulatory Affairs team.
Regulatory Affairs CMC Director – Cover early and late phase dev. projects - Lead EU and US submissions - Switzerland -
Geneva, Switzerland
Dec 5
Work on Global CMC projects and have real autonomy, scope and responsibility for your own varied product portfolio. You will need at least 10 years of Regulatory affairs CMC experience and be ready for a role where you have real autonomy, scope and responsibility for a varied product portfolio, managing multiple products in different stages of development. Call Theo Moore or Matt Greig in the London office on +44 (0)20 7801 3380.
Regulatory Affairs CMC Director Global Role Great package Great Pipeline Geneva
Geneva
Dec 5
This role is based in beautiful Geneva, where you will receive a wonderful work life balance for an organisation that is growing and developing its pipeline and also its regulatory team. Call Theo Moore or Matt Greig in the London office on +44 (0)207 801 3384 for full details. Or send your CV with a covering note to cv@advregulatory.com to have a confidential discussion about this or other potential roles or career options in regulatory affairs!
Regulatory Affairs Snr Project Manager – EU and then Global role covering early and late stage dev. projects to CeP leadership
Brussels, Belgium
Dec 5
This is a rare opportunity where you can grow and develop to be the lead for both EU and US markets, for large molecules in a medium sized organization with a flat structure that likes to give regulatory staff the opportunity to reach their potential. Contact Theo Moore on +44 (0) 207 801 3384 or email me in confidence via theo@advregulatory.com
Regulatory Affairs CMC Manager
Rep. Ireland
Dec 4
On behalf of my client we are sourcing a candidate for the role of Regulatory Affairs CMC Manager.   This is a permanent role.
Regulatory Affairs Manager
Netherlands
Dec 4
Regulatory Affairs Manager, NetherlandsAn exciting Pharma/Biotech is looking for an experienced RA Manager to join their growing RA department in the Netherlands. ...
Manager Regulatory Affairs and Sicherheitsbeauftragte/r (MDR)
Baden-Württemberg
Dec 4
Manager Regulatory Affairs (m/w) und Sicherheitsbeauftragte/r (MDR)Baden-WürttembergBewerbungsfrist: 14.12.2018
Regulatory Affairs Labelling Associate Director Global Role Strong tracking, systems and coordination Brussels Relo Offered
Belgium
Dec 4
Are you working packaging, artworking or regulatory labeling and want to be part of a global regulatory team (yes, they will consider non regulatory applicants) to be part of a Centre of Excellence push to revitalise their global regulatory labeling and artworking department, for this company which is expanding ...
Regulatory Affairs Advisor
Buckinghamshire
Dec 4
The client,a leading consumer food business, is looking for a Regulatory Affairs Advisor to join the company on a 12 month fixed term contract. The role is to make sure that packaging labels are in line and adhering to EU legislation. The desired candidate will be responsible for exporting to various markets and interacting with relevant people in regulatory areas in required countries.
Regulatory Affairs Associate
Cambridge
Dec 4
Regulatory Professionals are collaborating with a global bio-pharmaceutical company with a strong pipeline including treatments for a variety of products.
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Regulatory Affairs Manager
Hertford
Dec 4
Regulatory Professionals are now collaborating with a leading Pharmaceutical consultancy who are looking for a Regulatory Affairs Manager to join there Hertfordshire team.
Regulatory Affairs Manager
Hertford
Dec 4
Regulatory Professionals are collaborating with an established Pharmaceutical company, who are currently undergoing expansion.
SSU and Regulatory Specialist II - Russian Federation
Russia
Dec 4
Performs assigned activities within the country that lead to start-up of investigative sites in all phases of clinical trials.  Responsible for delivery, with moderate oversight from the SSU Country Manager and specialist knowledge in one or more of the following functional areas: investigator site contracts, ethics and regulatory submissions, and reviews of essential documents required for site initiation.
CMC Regulatory Affairs Manager Norddeutschland (m/w)
Germany
Dec 4
Für unseren Kunden aus Norddeutschland sind wir auf der Suche nach einen Regulatory Affairs CMC Manager.Ein schnellwachsendes Unternehmen mit ausgezeichneten Aufstiegsmöglichkeiten und erfolgreichem Work-Life-Balance Programm. Nicht nur die wissenschaftliche Affinität sondern auch eine Team-Orientierte Persönlichkeit ist für das Unternehmen sehr wichtig. ...
Regulatory Affairs Manager (m/w)
Germany
Dec 4
Ein weltweit agierendes Unternehmen sucht nach Regulatory Affairs Manager (m/w) in Ostdeutschland.Sie werden für die Betreuung der Arzneimittel Zulassungsprojekten verantwortlich sein. Eine familiäre Atmosphäre sowie die internationale Ausrichtung machen den Arbeitsalltag abwechslungsreich und angenehm. Wenn für Sie das Work-Life-Balance äußerst wichtig ist, wäre es eine ausgezeichnete Stelle für Sie. ...
Regulatory Affairs Associate in Cambridge
Cambridge
Dec 3
CK Group are recruiting for a Regulatory Affairs Associate to join a company in the Pharmaceutical industry at their site based in Cambridge on a...
Regulatory Submissions Manager
München (81249)
Dec 3
My client, an expanding Clinical Research Organisation are currently seeking to recruit a Regulatory Submissions Manager to join their Clinical Operations team. This position plays a key role in the clinical trial management process. The role will be based from my client’s offices in Munich. The role:Responsible for the collation and review of electronic and Paper CTA’s, Publishing, Production, dispatch, logging and archiving for regulatory submissions and Notifications. ...
Regulatory Affairs Global Labelling Lead Ops, Op Excel and Implementation Full relocation offered, Associate Director Grade
Brussels, Belgium - with Full Re-location
Dec 3
This is a global role with global delivery, to manage and improve end to end art working, as an Operational Excellence deliverable, in a company which is expanding, has distinct innovator molecules. This is graded as an Associate Director position.
Regulatory CMC Senior Manager Want to gain more region, be promoted and developed and work in a quickly expanding biotech Switzerland
Switzerland
Dec 2
New position to support a pipeline of biological products, with several assets in early development, 1 in global submission and 1 in preparation for BLA, yes, the role is global and includes both the EU and USA. To apply for this role which is on exclusive to Advanced Regulatory (soon to be ADV Talent Partners), please apply to me, in confidence, Oli Dimitrov, on + 44(0)2078013380 or send a full CV to oli@advregulatory.com
Regulatory Affairs Manager, CMC Biologics 12 Months Contract Provide Strategic leadership for CMC bio projects
Cambridgeshire, UK
Dec 2
We have a leading Biopharmaceutical client who is looking for an experienced and motivated Regulatory CMC Manager to take the lead on several EU projects. This is a 12 months contract role based in Cambridgeshire, UK.
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Regulatory Affairs Manager, CMC Biologics 12 Months Contract Provide Strategic leadership for CMC bio projects
Hertfordshire, UK
Dec 2
We have a great opportunity for an Interim Regulatory CMC Biotech Consultant to join a dynamic and expanding, international Biotechnology Company. This is a 12 month contract role with great options to work 3 days a week from home.
Team Director Regulatory CMC Biologicals (mAbs) Ireland Big team, decent pipeline, great people
Ireland
Dec 2
You will have a strong track record in regulatory strategy leadership for CMC for biologicals and some team management either full line or fuller matrix, and want to take on more of a people leadership role, in a company where behaviours and success factors, are important mantras in management roles.
Regulatory Affairs Consultant
Dublin, Leinster,Ireland
Dec 2
PAREXEL sucht gegenwärtig in Europa einen Regulatory Consultant mit guten Deutschkenntnissen für eine Tätigkeit mit Schwerpunkt auf dem Erstellen klinischer Zulassungsdokumente.Ein Consultant sollte ein gutes Verständnis der durch PAREXEL angebotenen Dienstleistungen besitzen. Ein Consultant sollte darüber hinaus über solide fachliche Expertise verfügen und in der Lage sein, sich weitergehendes Expertenwissen anzueignen. ...
Senior Regulatory Manager - Join a dynamic Biotech and work in the dev. space with a great pipeline offering training to become a GRL - Brussels
Brussels, Belgium
Dec 1
With their focus on natural, long-term growth, this amazing organisation depends on the contributions of talented and committed professionals to drive through progress. In turn, they make sure your work environment leaves you the space you need to attend to your personal goals, meet your family obligations, and pursue your professional development. Contact Theo Moore or Matt Greig NOW on +44 207 801 3384 or email us via CV@AdvRegualtory.com
Regulatory Affairs Snr Project Manager – EU and then Global role covering early and late stage dev. projects to CeP leadership
Brussels, Belgium
Dec 1
This is a rare opportunity where you can grow and develop to be the lead for both EU and US markets, for large molecules in a medium sized organization with a flat structure that likes to give regulatory staff the opportunity to reach their potential. Contact Theo Moore on +44 (0) 207 801 3384 or email me in confidence via theo@advregulatory.com
Regulatory Affairs Labelling Associate Director Global Role Strong tracking, systems and coordination Relo Offered
Relocation Offered
Dec 1
Are you working packaging, artworking or regulatory labeling and want to be part of a global regulatory team (yes, they will consider non regulatory applicants) to be part of a Centre of Excellence push to revitalise their global regulatory labeling and artworking department, for this company which is expanding ...
Regulatory Affairs Consultant with German -1 year limited contract
Warsaw, Masovian Voivodeship,Poland
Dec 1
The contract is 1 year limited with possibility of extension.As part of a multi-national project team, you will help to coordinate the compilation, review and submission of regulatory agency applications for local projects in compliance with regulatory requirements as well as internal and client standard operating procedures (SOPs). Your knowledge of clinical trial regulations will enable you to support the team for the development of optimized clinical trial submission strategies. ...
Regulatory Physician
Belgium
Nov 30
My client are a leading biotechnology company who are currently seeking an experienced and motivated Medical Doctor to join their Clinical Development Team. They have a great work environment, where you will be able to make strategic decisions that could be defining global outcomes!
Senior Associate, Regulatory Submissions - UK or EU
Anywhere in the UK/EU
Nov 30
Senior Associate Regulatory Submissions, candidates can be based anywhere in the UK/EU.
Regulatory and Public Affairs Officer (Mngr / Sr Mngr) Multiple EU locations, Drive regulatory and access planning for an expanding private H/C provider
Multiple EU Locations
Nov 30
We have a permanent opportunity for a Regulatory and Public Affairs Officer with a highly successful and rapidly expanding international clinical diagnostic and patient treatment organization, which has 200 plus medical centres in Western and Eastern Europe. f you wish to apply for this role, please send your CV with a contact number to oli@advregulatory.com or alternatively, to have a confidential discussion, please call me Oli on UK +44.207.801.3388
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Regulatory CMC Contractor
Hertfordshire
Nov 30
Regulatory Professionals is collaborating with a leading pharmaceutical firm who are looking for a Regulatory CMC Consultant.
Regulatory Affairs Manager
Cambridge
Nov 30
As a global leader in developing medicines within Oncology, a requirement has arisen in the Regulatory team for a Regulatory Affairs Manager.
Regulatory Affairs CMC Consultant
Netherlands
Nov 30
Regulatory Affairs CMC Consultant An amazing opportunity to work within a great Regulatory Affairs department for a Global Pharmaceutical Company has become available.Job Title: Regulatory Affairs CMC Consultant Location: Netherlands Contract / Freelance position - HomebasedContract Length: 6+ Months – 0. ...
Regulatory Affairs Officer
Runcorn
Nov 30
My client a food supplements organisation have opened a new vacancy within their Regulatory team, they are looking to recruit a Regulatory Affairs Officer on a permanent basis to be based at their offices in North West England.The role:My client is looking for a Regulatory professional to ensure the appropriate licensing and compliance of their product range to ensure the products are safe and meet the needs of their customers and Regulatory expectations. ...
DIRECTOR OF GLOBAL REGULATORY AFFAIRS - Europe
Europe
Nov 30
At PRA we know our greatest strength is our people. We have a commitment to employee development and a culture that values innovation. Where great minds work everything is possible.
Regulatory Affairs Officer
Belgium
Nov 30
Regulatory Affairs Officer, BelgiumAn exciting opportunity has arisen to join a leading CRO and manage their regulatory activities. You will be involved in a wide variety of exciting projects and clinical trials. ...
Regulatory Affairs Associate
Switzerland
Nov 29
Main Responsibility Internal Training support: * Supporting and participating (as necessary) for training relevant content. * Developing training material under supervision.Internal Communication support: * Support the MDR training & communication work stream. * Maintain and establish an Intranet page about the internal MDR project. * Maintain communication matrix under supervision. * Responsible to prepare MDR related Newsletters. ...
Senior Regulatory Affairs Specialist
Switzerland
Nov 29
Main Responsibility Medical Device Regulation implementation project * Prepare training material for RA and other departments. * Provide training for the different sites regarding MDR. * Support and participate in Industry Organization WG`s with relevance for RA. * Author and support guidance documents and procedures to ensure MDR compliance. ...
Associate Director Regulatory Affairs - Emerging Markets - High Wycombe
High Wycombe
Nov 29
Mary Bolt at CK Clinical is recruiting for an Associate Director Regulatory Affairs - Emerging Markets to join a highly established research-based pharmaceutical company with a...
Associate Director Regulatory Affairs - EMEA - High Wycombe
High Wycombe
Nov 29
Mary Bolt at CK Clinical is recruiting for an Associate Director Regulatory Affairs - Emerging Markets to join a highly established research-based pharmaceutical company with a...
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Regulatory Affairs Manager
Belgium
Nov 29
Regulatory Affairs Manager, BelgiumInternational Pharmaceuticals company is looking for an RA Manager to join their well-established RA department in Belgium. ...
Head of Regulatory, Quality and Safety Affairs - Eastern Europe
Czech Republic
Nov 28
An exciting opportunity to join a dynamic, game-changing team within a rapidly growing healthcare company with a diverse portfolio. The role scope is to be the functional country head of the regulatory, quality and safety operations in Czech and Slovak Republic.
Head of Regulatory Affairs
Surrey
Nov 28
My Client a Global Food products organisation has opened a new vacancy within their Regulatory team and is looking to recruit a Head of Regulatory to be based at their offices in either Surrey or Gloucestershire.The Role:To manage all aspects of the Regulatory Affairs Department ensuring that they develop, deliver and grow a full range of services that add value and support for our Food and Drinks Industry clients. ...
Regulatory Affairs Consultant
Belgium
Nov 28
Senior Regulatory Affairs Consultant, BelgiumAn exciting CRO working on a variety of projects, requires a Senior Regulatory Affairs Consultant. This will include working with Medicinal Products and Medical Devices.Job Title: Senior Regulatory Affairs Consultant Location: BelgiumSalary: Very Competitive hourly rateContract Length: 6-12 Month0. ...
Regulatory Affairs Specialist in Switzerland
Switzerland
Nov 28
Regulatory Affairs Data Analyst For this role we are looking for a RA specialist with strong IT skills able to support the local franchise Regulatory...
Regulatory Affairs Specialist in Switzerland
Switzerland
Nov 28
Project name: MDR RA-Tech Files CK Group are recruiting for a Regulatory Affairs Specialist to support a local franchise Regulatory team for various activities in...
Regulatory Affairs Officer II - CMC
England
Nov 28
As a REGULATORY AFFAIRS OFFICER II - CMC you will be expected to prepare and/or reviews CMC regulatory submissions to support clinical trial and marketing authorization activities for either internal and/or external clients. Provides regulatory support for assigned projects. At IQVIA™ your work will also impact healthcare around the world as you will be involved with the most important drugs and the highest-profile clients.
Regulatory Affairs Project Manager in Zuchwil
Zuchwil
Nov 28
Regulatory Affairs Project Manager - Zuchwil Jocelyn Blackham is recruiting for a Regulatory Affairs Project Manager to join a company in the Medical Device industry at...
Regulatory Affairs Officer II - LCM
England
Nov 28
As REGULATOR AFFAIRS OFFICER II - CMC you will be expected to prepare and/or reviews regulatory submissions to support clinical trial and marketing authorization activities for either internal and/or external clients. Provides regulatory support for assigned projects. At IQVIA™ your work will also impact healthcare around the world as you will be involved with the most important drugs and the highest-profile clients.
Senior Regulatory Affairs Officer - CMC
England
Nov 28
As SENIOR REGULATORY AFFAIRS OFFICER - CMC you will be expected to prepare and/or reviews CMC regulatory submissions to support clinical trial and marketing authorization activities for either internal and/or external clients. Provides regulatory support for assigned projects. At IQVIA™ your work will also impact healthcare around the world as you will be involved with the most important drugs and the highest-profile clients.
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Senior Regulatory Affairs Officer - LCM
England
Nov 28
A career at IQVIA™ as a SENIOR REGULATORY AFFAIRS OFFICER will connect you to great opportunity to achieve professional success. At IQVIA™ your work will also impact healthcare around the world as you will be involved with the most important drugs and the highest-profile clients. With clear career paths, a supportive working environment and a flexible working culture, our employees are empowered to drive their careers forwards to match their goals.
Senior Regulatory Labelling Associate (Cambridge or Uxbridge)
Cambridge or Uxbridge
Nov 27
Amgen Regulatory Labelling team are looking for an enthusiastic team player who is detail-oriented and has excellent verbal and written communication skills. Your key role will be to support the EU Labelling managers in executing Labelling tasks.
Regulatory Product lead
London
Nov 27
ProClinical currently has a fantastic opportunity for you to join an international pharmaceutical organisation as a Regulatory Product lead (UK & Ireland) based in London. This company focus on developing treatments for conditions where the impact of the medicines can make an immediate and tangible difference. They provide treatments in Neuroscience, Rare Diseases and other medical sectors. ...
Regulatory Affairs Associate
Middlesex
Nov 27
Our client, a globally recognized pharmaceutical company are hiring immediately and require a senior regulatory affairs associate to join their established team. Key Responsibilities: • The Regulatory Professional under the direction of a Regional Regulatory Lead will lead compilation of CMC regulatory packages for submission and may be the lead for a program under supervision. • Collect and / or create country specific documents for regulatory filings worldwide. • Compile and maintain CTA/MA
Regulatory Affairs Manager - Uxbridge or Cambridge
Uxbridge
Nov 27
Lucy Stendall at CK Group is recruiting for a Regulatory Affairs Manager to join a company in the Pharmaceutical industry at their site based in...
Senior Regulatory Affairs Manager- Oncology- 28082
Uxbridge
Nov 27
My Client a Global Pharmaceutical Company has opened a new vacancy within their Regulatory team and is looking to recruit a Regulatory Affairs Senior Manager- Oncology on an initial 6 month contract to be based in their offices in either Middlesex or Cambridge.The Role:This role will provide regional regulatory support across multiple products. ...
Regulatory Affairs Manager- CTA- EU- 28291
Uxbridge
Nov 27
My Client a Global Pharmaceutical Company has opened a new vacancy within their Regulatory team and is looking to recruit a Regulatory Affairs Consultant on an initial 6 Month basis to be based at their offices in Cambridge or Uxbridge.The Role:Maintain all the required licenses in order to support clinical trials and further development of IMPD’s; market commercially approved medicinal products as well as regulatory compliance, with a focus on patient safety. ...
Regulatory Associate- CTA- 28337
Uxbridge
Nov 27
My Client a Global Pharmaceutical Company has opened a new vacancy within their Regulatory team and is looking to recruit a Regulatory Affairs Associate on an initial 12 month contract to be based in their offices in Middlesex.The Role:The Regulatory Professional under the direction of a Regional Regulatory Lead will assist in the creation and submission of regulatory documents and may be the regulatory lead for a program under the supervision of a more experienced regulatory lead. ...
Regulatory CMC Manager
Cambridgeshire
Nov 27
Hobson Prior has an exciting new Regulatory CMC (Chemistry, Manufacturing and Control) Manager job on offer with an exciting research-based biopharmaceutical company based in Cambridge. You will be joining a rapidly developing client who researches, develops and commercialises drugs.
Senior Regulatory Project Manager
Buckinghamshire
Nov 27
Hobson Prior is currently recruiting for a Senior Regulatory Project Manager to join a pharmaceutical company based in High Wycombe. You will be responsible for ensuring that all processes are fully compliant with regulatory requirements. The client is renowned for their innovative medical research and development practices, so this is an excellent opportunity for a strategic decision maker to thrive.
regulatory jobs : 100 +
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