Pharmiweb ChannelsAll | PharmaCo | Clinical Research | R&D/BioTech | Sales/Mktg | Healthcare | Recruitment | Pharmacy | Medical Comms

Pharmiweb.com RSS Feed Pharmiweb.com RSS Feeds

Pharmiweb.com RSS Feed PharmiWeb Candidate Blog

Pharmiweb.com RSS Feed PharmiWeb Client Blog

Advertising

The latest Regulatory jobs - BETA

Jobs: Regulatory

Quick Job Search
Search For:
Any Word All Words Exact Phrase Boolean Search
Job Title Only Broad Search
Sort By Date Posted Last updated Company

Regulatory Affairs Specialist in Basel
Basel
Sep 26
Regulatory Affairs Specialist in BaselOur client is well known for a dynamic environment and engaged and passionate people who appreciate the opportunity to shape the future and be part of the creation of impact. ...
Regulatory Affairs Director - Emerging Markets
Cambridge
Sep 26
My client is a top 10 pharmaceutical organisation with a broad therapy focus and an envious pipeline within Oncology, CVS and Respiratory to name a few of their therapy areas. Due to expansion they are looking to hire a number of Regulatory Directors within their emerging markets function. This would be focused on specific early stage therapy areas and late stage individual products. Geographic spread would be across Latam, MEWA, CIS/Russia and Asia Pacific. ...
Global Data Quality and Standards Regulatory Operations Manager
England
Sep 26
Top 20 pharma company based in Hertfordshire is currently looking for a Regulatory professionals who have had exposure to clinical disclosure documents. Successful candidate will be working in the Reg Ops department in a team which has a clear structure for career progression.
Submissions Specialist - Global Safety Reporting - Regulatory Reporting
High Wycombe
Sep 26
Submissions Specialist - Global Safety Reporting/High Wycombe/6 Month Contract/To £28 Per Hr
Global Head Regulatory Affairs
UK - London, Home Counties - Home based
Sep 26
My start-up Bio-Pharmaceutical client is looking to appoint a Head of European Regulatory Affairs. This is a leadership position, the Head of Global Regulatory Affairs is responsible for all regulatory matters across the portfolio of existing medical and device products, as well as advising on business development opportunities from a regulatory perspective.
Head of Regulatory Affairs, FDA Submissions
Zug
Sep 24
Head of Regulatory Affairs, FDA Submissions, Zurich/Zug, Highly Successful Pharmaceutical Company, Switzerland
Regulatory Affairs Manager, Niche Products
Bern
Sep 24
Regulatory Affairs Manager, Niche Products, Bern/Basel/Lucerne, Pre and Post Approval
EU Regulatory Affairs Manager, Zurich
Zürich
Sep 24
Regulatory Affairs Manager, Biologics, Global Role
Regulatory Operations Specialist
Aachen,Germany
Sep 24
Our client, an international research-based pharmaceutical company is looking for a Regulatory Operations Specialist (m/f) office-based in Aachen on a fixed-term-contract via DOCS initially limited until end of 2016. The company operates in the areas of pain treatment, women’s health, inflammation, neurology, perioperative care, cancer supportive care, serves customers internationally and is present in 32 countries with affiliates in Europe, Australia, Latin America and...
Regulatory Affairs Manager (Contract)
Germany
Sep 23
This is a superb opportunity for an experienced Regulatory Affairs manager/consultant to join a worldwide pharmaceutical company in a long term contract position. Our client...
NEW ROLE Regulatory CMC Biologicals Lead Mngr / Sr Manager Have DP Gain DS Structured career ladder West of London / M4 Corridor
England
Sep 23
Our client is seeking to hire an individual with good RA CMC lifecycle submissions and BLA/NDA subs for new countries (first filing but mostly injector and supplemental registrations) who wants to consolidate their expertise and develop their worldwide subs experiences, for a complex product, which’s going through major changes.
Regulatory Affairs Manager - Switzerland
Switzerland
Sep 23
**Regulatory Affairs Manager - Switzerland**
Regulatory Officer
England
Sep 23
This leading global Pharma with a large portfolio within generics, is currently growing out their Regulatory Affairs team. Covering a large therapeutic range, this company provides high quality OTC and generic products globally
Regulatory and Site Services Specialist
USA
Sep 23
Full Time-Office Based in 1 of our US offices with the option to work from home 2 days per week. Our US offices are located in Cary, NC, Wilmington, NC, King of Prussia, PA, & Bristol, TN
Regulatory Affairs- EU, USA, Australasia
Leatherhead
Sep 23
To support the Global Regulatory Affairs management in: - Preparation of post authorisation regulatory documentation in Europe - Preparation of CTAs for clinical programs in USA, Australasia and Europe - Identification of regional-specific requirements for registration in European markets - Development of templates suitable for e-CTD filing
Associate Director- Regulatory Affairs- Clinical
MARLOW
Sep 23
Overview of duties - Experience with European CTA’s and procedures, create CTA knowledge database and update accordingly - Experienced in line management and development of a Regulatory team - Assist in strategy, operational support -Responsible for CTA submissions across the full lifecycle - Lead project management across the full CTA portfolio and contribute expertise to the wider European Regulatory teams
Regulatory Affairs Manager
Copenhagen
Sep 23
A Fantastic opportunity for a Regulatory Affairs Manager to join a dynamic, fast growing Pharmaceutical Consultancy to work with the EU Regulatory team in leading...
Freelance Study Start Up and Regulatory Specialist Position
France
Sep 23
Our client is a global top 10 CRO, a full-service clinical research organisation, providing Ph I-IV clinical development services for the pharmaceutical, biotech and medical device industries, globally across 6 continents. Our client is actively seeking an experienced Study Start Up (SSU) Specialist to join them on an initial 6 month contract.
2 x Regulatory Affairs Specialists - Devices - Brand New Roles
München (81249)
Sep 23
Are you a Regulatory Affairs Professional looking the the Medical Devices field? Looking for a new opportunity? Click here...
Regulatory Affairs Manager - Russia
Moscow
Sep 23
Regulatory Affairs Manager in St. Petersburg or Moscow – Excellent opportunity to work for stable global CRO! We search for our client ideal candidate for position Regulatory Affairs Manager for well-established international CRO based in Russia. We are looking for candidate for full time position to be either office based or home-based. You will have several years of experience in regulatory affairs. It is an excellent opportunity to join global CRO with life / work balance position. ...
Regulatory Team Leader - Agrochemical Company
Brussels
Sep 23
This is a senior Position for a growing agrochemical company. You wil be part of the European Regulatory team and be in charge of 6 people that will report directly to yourself. They will be focussing on making different product registrations throughout Europa. This is a position where you have the change to lead a team and grow your career within the company, whilst at the same time still be in touch with the Technical regulatory work yourself.
Senior Regulatory Executive , CMC-Uxbridge
Uxbridge
Sep 23
Mary Tilston is recruiting for a Senior Regulatory Executive - CMC to join a science-led global healthcare company at their site based in Uxbridge on a...
Cosmetics Regulatory Manager - Massive Portfolio - Spain
Tarragona
Sep 23
This is an exciting time to join a company who research, develop, manage and distribute all of their own products on in one place where you will have a 360 degree view of the product life cycle because you will be managing the cosmetovigilance function of this organisation.
Regulatory Affairs Manager (m/w)
Mannheim
Sep 23
Regulatory Affairs Manager (m/w)Office-based in MannheimWir suchen ab sofort zur Unterstu¨tzung unseres Regulatory Affairs Teams zur Projektfu¨hrung fu¨r europäische Zulassungsverfahren und Life cycle management eine/n Regulatory Affairs Manager (m/w). Ihre Aufgaben: - Planung und Durchführung von Zulassungsverfahren (MRP, DCP, CP und rein nationalen Verfahren) sowie von Life Cycle Verfahren (Variations, Renewals u.a.). ...
Associate Director, EMEA Clinical Trial Regulatory Affairs
Berkshire
Sep 23
This role, for a leading Pharmaceutical company, will be focussed on Clinical Trial applications and ethics submissions. The company you will be working for have a global portfolio of products. You will be preparing complex regulatory submission packages for the EMEA. You will need a comprehensive understanding of Regulatory Authority interactions. You will be directing CTA project management and be involved in SOP development.
REGULATORY AFFAIRS ASSOCIATE (RAA) - Bulgaria
Sofia Bulgaria
Sep 23
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 (RAA) and help realize your career potential.
MEDICAL DEVICE/REGULATORY AFFAIRS OPPORTUNITY UK
England
Sep 23
Are you looking to work in a small, growing company? Work within a close, communicative department that recognise your hard work? Value a strong work culture? THEN I HAVE THE OPPORTUNITY FOR YOU! This is a very rare and niche opportunity, that will allow you to grow with the company and progress in the future! Don’t miss out! Apply now!
Regulatory Affairs Specialist EMEA
Belgium
Sep 22
Regulatory Affairs Specialist EMEA– 12 Months Contract- Immediate start Belgium Level: Regulatory Affairs Specialist EMEA Contract: 12 months’ minimum Location: Germany, EU Summary We are looking for a Regulatory Affairs specialist with commercial experience to work with a renowned pharmaceutical company. The successful candidate will have sound knowledge in post approval regulatory activities. ...
Regulatory Affairs Project Manager
Germany
Sep 22
Regulatory Affairs Project Manager – 12 Month Contract- Germany Level: Regulatory Affairs Project Manager Contract: 12 months minimum Location: Germany, EU Summary We are looking for a Regulatory Affairs Project manager with commercial experience to work with a renowned pharmaceutical company. The successful candidate will have full life cycle management experience and proven experience in project management. ...
Regulatory Affairs CMC Labelling Consultant
Switzerland
Sep 22
Regulatory Affairs CMC Labelling Consultant– 3 Months Contract, Home based/Remote, Switzerland Level: Regulatory Affairs CMC Labelling Consultant Contract: minimum 3 Month Contract Location: Home based/Remote (Switzerland) Summary We are looking for a Regulatory Affairs labelling to consultant to manage CMC and labelling activities for EU. The successful candidate should have a strong grasp of labelling requirements for relevant regulatory authority as well as experience with CMC module 3. ...
Regulatory Specialist - Agrochemical - home working
England
Sep 22
Regulatory Specialist - Agrochemicals - Work from home!Join a company that is dominating their field in a niche product area. Owned by a larger company but yet maintaining it's small company feel, our client offers flexibility (home working), a diverse working culture, flat hierarchy and considerable autonomy. Whilst not necessarily a run of the mill agrochemicals, this is still a growing area and one that for sure will interest you.
Teamleader EU Regulatory Submissions - West Germany - medical device company - up to 80,000 €
Germany
Sep 22
Suchen Sie eine neue Herausforderung als Teamleiter? Wollen Sie das Monitoring und die Umsetzung von regulatorischen Aktivitäten in EU übernehmen? Sind Sie interessiert sich an Einreichungen in den USA zu beteiligen? Dann ist diese Stelle wie für Sie geschaffen.
Regulatory Manager - Agrochemical - home working
England
Sep 22
Regulatory Project Manager - Agrochemicals - Work from home!Join a company that is dominating their field in a niche product area. Owned by a larger company but yet maintaining it's small company feel, our client offers flexibility (home working), a diverse working culture, flat hierarchy and considerable autonomy. Whilst not necessarily a run of the mill agrochemicals, this is still a growing area and one that for sure will interest you.
Senior Manager, Regulatory CMC, Switzerland
Zürich
Sep 22
Senior Manager, Regulatory CMC, Switzerland, Small molecules, Pre and Post Approval, Start-up atmosphere
Regulatory Affairs Manager
Berkshire/London
Sep 22
Regulatory Affairs Manager: Berkshire/London Permanent Role. Salary: £45,000-£55,000 per annum + benefits package. A proactive Regulatory Affairs Manager is required to join this fast-expanding pharmaceutical company
Regulatory Submissons Manager
London
Sep 22
One of our clients, a medium-sized CRO, is looking for a Regulatory Submissions Manager to be based in London.Job Tasks Manage and execute all aspects of global start-up according to Sponsor specifications;Perform quality checks on submission documents and site essential documents;Informed consent form preparation, review and approvalPresent during bid defenses and auditsSite management Requirements More than 5 years of experience in clinical research, preferably with a CRO. ...
Senior Regulatory Affairs Associate
England
Sep 22
Senior Regulatory Affairs Associate Duration: Minimum 6 months: Wiltshire Rate: up to £50 per hour (Depending on Experience) Suitable for: Regulatory Associate, Senior Regulatory Associate, Regulatory project manager
Regulatory Affairs Manager, 60-100%
Zug
Sep 22
Regulatory Affairs Manager, 60-100%, Bio-tech and small molecules, potential for new submissions to the Swiss market
Senior Regulatory Affairs Advisor - Food Supplements
Wiltshire
Sep 22
Senior Regulatory Affairs Advisor - Food Supplements. 6 months. Rate: Highly Competitive. Location: Wiltshire. Regulatory professionals are recruiting on behalf of a respectable pharmaceutical firm that has undergone unparalleled growth over the past decade.
Medical Editor (Regulatory) Contract- Home-Based
England
Sep 22
Medical Editor (Regulatory) Contract- Home-BasedFocus on CSRs, IBs, protocols, summaries and overviews.This is a home-based role, which is very rare in pharma and super convenient if that's what you are after! Furthermore this is a varied position with a focus on virtual team leadership and spearheading statistic consulting: not a regular boring job, actually very interesting.
Regulatory Affairs - Chemical Industry - Belgium
Antwerp
Sep 22
I am specialized in recruiting for regulatory affairs within the chemical industry in Belgium. This means I have a very good understanding of the industry and that I am up to date with available regulatory roles throughout the country. I can keep you up to date with relevant positions for yourself, even on a speculative basis. By doing this you will save time and will not miss out on new opportunities that might be suitable.
Team leader Regulatory Affairs
Sweden
Sep 22
Compiling and coordination of variations in close cooperation with the central Regulatory Affairs team Compiling Summaries of Product Characteristics (SPCs), patient information leaflets (PILs) and labelling texts and keeping them up to date Approving artwork and proof reading Training and support for new employees and junior members of the team The local regulatory expert for central functions as well as the Health authority Archiving, tracking and...
Drug Safety Associate Regulatory Intelligence
Southampton, Hampshire
Sep 22
As part of our Safety Reporting Group in ICON’s Global Regulatory Affairs Department, our DSA’s contribute to our culture of process improvement, perform expedited and periodic safety reporting, maintain projects and liaise with Sponsors, ICON project managers and investigational sites as required.
Regulatory Labelling Compliance Specialist
Hertfordshire
Sep 22
• Leading Pharma Company • 12 month contract initially • Freelance opportunity • Welwyn Garden City, Hertfordshire • Start ASAP
Regulatory Study Start Up Manager - Sweden - Top 10 CRO
Uppsala
Sep 22
Regulatory Study Start Up Manager - Sweden - Top 10 CRO
Global company looking for Global Regulatory Manager – Health
England
Sep 22
My client is inspired by a vision of a world where people are healthier and live better, while making the right kind of social and environmental impact. This opportunity offers the chance to work with a large number and wide variation of projects and products making it possible to widen and broaden your skill set. I’m looking for a Global Regulatory Manager. ...
FREELANCE Regulatory Labelling Compliance Specialist
Hertfordshire
Sep 22
Freelance: Regulatory Labelling Compliance SpecialistUK, Office based (home working consideration after 3 months)12 month renewable contractRole and responsibilities: * Works with DRA affiliates, regulatory program management and Regulatory product managers to promote local PI compliance with client led labelling policies and standards * Proactively identify existing and/or potential compliance issues/gaps, evaluate/communicate potential business impact and advise GPO on corrective/preven ...
Quality and Regulatory Affairs Director
Illinois
Sep 21
Director, Quality and Regulatory Affairs needed for one of the oldest continuing Manufacturing Companies in the United States!Quality and Regulatory Affairs | DirectorElgin, Illinois+ +...
Senior CMC Regulatory Affairs Manager – Pharmaceutical consulting company - Munich – up to 140,000 €
Germany
Sep 21
We are looking for an experienced CMC Regulatory Affairs Manager who wants to use his knowledge in an international operating consulting company with a broad varieties of projects. You can expect an open environment, exciting projects and superb benefits inclusive an opportunity of flexible home-based working.
Regulatory Affairs Manager – medium sized pharma company – Hamburg – 60,000 €
Germany
Sep 21
We are looking for an experienced Regulatory Affairs Associate to join our regulatory affairs team on permanent basis. You can expect to work in a small but well established company with a good family environment and exciting tasks.
Regulatory and Start-Up Specialist 1 (f/m) - office based in Espoo, Finland
Helsinki
Sep 21
PURPOSE Perform tasks at country level associated with Regulatory, Start-up (RSU) and Maintenance activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements andcontractual/budgetary guidelines. May participate in feasibility and/or site identification activities. ...
Graduate Regulatory Affairs Opportunity - Chemistry Background
Brussels
Sep 21
I am currently working for multiple companies in the chemical industry. To support there growth, they are looking to get junior candidates on board that are looking for a career with strong career progression and training and development from day 1!
Regulatory Manager Agrochemicals - Home Office possibility
Germany
Sep 21
Regulatory Manager Agrochemicals - Home Office possibility
Regulatory Documentation Scientist
Basel
Sep 21
Regulatory Documentation ScientistLeading Pharmaceutical company6 month contractFreelance opportunityFull time office based Basel
Senior Regulatory Information Management Consultant (Contract)
Middlesex
Sep 21
i-Pharm Consulting are recruiting for…ROLESenior Regulatory Information Management Consultant (Contract Role)LOCATION: West LondonSALARY: £60-£70 per hour ROLE: Leading Biotech are looking for a Senior Regulatory Information Management Consultant to work on an IDMP project. The role will focus on Data Migration from Insight to the new system and also involve project management as well as managing a small team of consultants. ...
REGULATORY AFFAIRS ASSOCIATE (RAA) - Czech Republic
Czech Republic
Sep 21
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 (RAA) and help realize your career potential.
MEDICAL DEVICE - SENIOR REGULATORY AFFAIRS POSITION
England
Sep 21
My client, an international specialist health care company, are looking for experienced Regulatory Affairs professionals with a strong medical device background, to join their growing team in a specialist role. If you are ready to work in a developing company, that cover a wide range of territories, and work with cutting edge Regulatory science including combination products, THEN APPLY NOW!
Technical and Regulatory Specialist - REACh, HSE
Cheshire
Sep 21
Our client is an impressive organisation experiencing significant growth over the past few years with their unique product manufactured using resins. Offering a broad product line and range with a strategy to diversify, this family grown business is keen to reward those who commit long term. This is provided through bonus and pension schemes that give the impression this company cares about its staff.
Global Regulatory Affairs Lead
Basel
Sep 20
A market leading biopharmaceutical company focused on new innovation, further development and tackling unmet medical needs. With a diverse portfolio working globally around the world. They are currently searching for a Global Regulatory Affairs Lead to join their European Headquarters in Switzerland. This is an opportunity to utilise various technical skills in a strategic position.
Associate Director Global Regulatory Affairs – global pharma company – Frankfurt – 120,000 € plus bonus
Germany
Sep 20
We are looking for an experienced Regulatory Affairs Manager who wants to use his knowledge about global strategy development in one of the biggest pharmaceutical organizations worldwide. You can expect an open environment, life-changing projects and excellent benefits.
Head Regulatory Affairs – medium sized pharma company – Hamburg - competetive
Germany
Sep 20
We are looking for an experienced Regulatory Affairs Manager to lead our regulatory affairs team on permanent basis. You can expect to work in a small but well established company with a good family environment and exciting tasks.
Head of Regulatory International Austria
Austria
Sep 20
Ich habe momentan eine ganz spezielle Vakanz als Head of New Submissions and Renewals im Bereich Regulatory Affairs. Das Unternehmen ist weltbekannt, ein wahrer Industrieführer und Pionier.Sie würden... ...
Regulatory Affairs CMC Manager (Germany)
Paris
Sep 20
An exciting opportunity for a CMC Regulatory Affairs Manager to join a dynamic, fast growing Pharmaceutical consultancy and work with the Regulatory Affairs team in...
Regulatory Affairs CMC Manager (Germany)
Vienna
Sep 20
An exciting opportunity for a CMC Regulatory Affairs Manager to join a dynamic, fast growing Pharmaceutical consultancy and work with the Regulatory Affairs team in...
Regulatory Affairs CMC Manager
Frankfurt am Main
Sep 20
An exciting opportunity for a CMC Regulatory Affairs Manager to join a dynamic, fast growing Pharmaceutical consultancy and work with the Regulatory Affairs team in...
Regulatory Affairs Manager
Madrid
Sep 20
A Fantastic opportunity for a Regulatory Affairs Manager to join a dynamic, fast growing Pharmaceutical Consultancy to work with the EU Regulatory team in leading...
Study Start Up and Regulatory Manager - Italy
Italy
Sep 20
Study Start Up & Regulatory Manager - Italy Location: Milan, Italy Salary: Flexible for the right candidate Reference Number: J23348 Want to be a Subject Matter Expert within SSU & Regulatory Matters?
Regulatory Affairs Associate - Healthcare
Berkshire
Sep 20
Regulatory Affairs Associate - Healthcare Location: Berkshire Salary: £35,000 - £40,000 + Benefits package Reference: J25163 •Do you want to work for one of the biggest consumer health companies in the world?
Regulatory Affairs Associate - 12 month FTC
Berkshire
Sep 20
Regulatory Affairs Associate - 12 month FTC Location: Berkshire Salary: Generous salary + Benefits package Reference: J25158 Do you want to work for one of the biggest consumer health companies in the world?
Regulatory Affairs Consultants
Netherlands
Sep 20
Regulatory Consultants with Medical Device submissions needed in different countries around Europe.
Senior Regulatory Associate
Cambridge
Sep 20
Our client, a leading U.S. Biotech whose therapy area's include Oncology, Liver disease and HIV have a fantastic new open requirement in their team.As a result of substantial company growth we have an exciting Senior Associate position available at their Cambridge office. ...
Senior Medical Writer - Regulatory Germany
Germany
Sep 20
an experienced Regulatory Medical Writer to join a market leading and prestigious consultancy. This opportunity will allow you to deal with international clients after completing an extensive training program. In this role you will also be able to contribute to the success of the company by having your opinion heard. The service you will provide is more than just writing, you will be an essential part of the clinical development teams across different therapeutic areas.
Senior Medical Writer - Regulatory UK
Wales
Sep 20
Regulatory Medical Writer to join a market leading and prestigious consultancy. This opportunity will allow you to deal with international clients after completing an extensive training program. In this role you will also be able to contribute to the success of the company by having your opinion heard.The service you will provide is more than just writing, you will be an essential part of the clinical development teams across different therapeutic areas.
Line Manager for Study Start Up and Regulatory Affairs - Italy - Get in contact now for more details
Milan
Sep 20
My client is looking to extend their Ethics and Regulatory department in Italy and are seeking an experienced Manager Study Start Up & Regulatory. The role is an absolutely pivotal role and comes with vast amounts of opportunities for learning and development. You will be required to ensure the continuous improvement of quality of all Regulatory and Start-up components at the project level across Europe.
Senior/Principal Regulatory Affairs Specialist - EMEA-134542
Europe, Middle East and Africa-UK-England-Cambridge, Europe, Middle East and Africa-Spain, Europe, Middle East and Africa
Sep 20
PPD is recruiting for an experienced Senior or Principal Regulatory Affairs Specialist.    In this role you will provide regulatory advice and carry out projects in the provision of regulatory affairs services.  You will also act as liaison with internal and external clients in the provision and marketing of regulatory affairs services. ...
Regulatory Affairs Manager - Switzerland
Switzerland
Sep 19
**Regulatory Affairs Manager - Vaccines - Switzerland**
Sr. Regulatory Affairs Specialist
Philadelphia
Sep 19
Sr. Regulatory Affairs Specialist needed for Global Med Device Company!  Regulatory Affairs Philadelphia | PA Medical Device experience$70,000-$110,000 + bonus +...
Head of Regulatory Affairs /Leadership/Generics
Austria
Sep 19
My client is an industry leader developing and producing generics. Due to their ever-increasing success and expansion, they are looking for a Head of New Submissions and Renewals. Among others, you would be responsible for leading a team of 10 Registration Managers, for all regulatory tasks and activities regarding new submissions and renewals, for generating regulatory guidance documents and for developing regulatory strategies. ...
Senior ISS Coordinator (f/m) in the field of Regulatory and Study Start Up - office-based in Brussels
Brussels
Sep 19
PURPOSE Support the delivery of activities as determined by the appropriate country, regional lead, global lead or team. May conduct specific tasks under guidance of senior staff. Responsibilities may include all or some of the activities listed at any one time. ...
Regulatory Affairs and Risk Manager - Medical Devices
Warwickshire
Sep 19
Regulatory Affairs & Risk Manager - Medical Devices. Warwickshire. Our client is a medical device developer of complex (software/electronic) portable patient monitoring systems, they are a developing company who are creating jobs, due to further growth
Customer Quality Regulatory Specialist II
United States
Sep 19
This Customer Quality Regulatory Specialist job is with one of the most renowned global pharmaceutical, medical device and consumer health organisations located in the US. The organisation is a top 10 pharma company and employs over 100,000 professionals worldwide.The Customer Quality member will be responsible for supporting Post Market Regulatory Affairs activities associated with complaint handling and MDR submissions. ...
Regulatory Affairs - Expansion of a multinational FMCG company
England
Sep 19
NonStop Pharma has been appointed to conduct a search to fuel the major expansion of a multinational FMCG company’s Regulatory Affairs department. If these opportunities aren’t for you we offer a bonus for any successful referrals of €250, £250 or 300CHF Amazon-Voucher .My client is currently investing in new product development and expansion into new territories. ...
Regulatory Approval Specialist (6 Month Contract)
Cambridge
Sep 19
i-Pharm Consulting are recruiting for…ROLERegulatory Approval Specialist (6 Month Contract)LOCATION: Cambridge RATE: Negotiable (Above Market Average)ROLE: As the Regulatory Approval Specialist your core focus will be too review, compile, prepare and submit CTA applications to MoH and IEC’s across the UK and Ireland. ...
Medical Writer (Regulatory)-135454
Europe, Middle East and Africa-UK-England-Cambridge, Europe, Middle East and Africa
Sep 17
As part of our on-going growth, we are currently recruiting for a Senior Medical Writer to join our rapidly expanding team of over 90 regulatory writers based in Europe, North American and Asia Pacific. ...
Manager, Global Corporate Regulatory Affairs Process and Systems
Paris
Sep 16
A growing and innovative Biotech has an urgent need for a Manager, Global Corporate Regulatory Affairs Process, Systems and Compliance. You will be based in Paris and be responsible for ensuring compliance and quality assurance of RA systems and processes. You will be managing a team of 3 system support specialists who are responsible for compliance.
Regulatory Affairs Specialist-CAPA Role-Medical Devices-Suisse
St. Gallen
Sep 16
Gain an interesting, cross-functional role within regulatory affairs and quality today with this regulatory affairs specialist role. This is a great opportunity within regulatory affairs to expand your skills into CAPA. This will allow you to gain invaluable expertise and develop your career within both regulatory affairs and quality. Apply now to find out more about this fantastic role within regulatory affairs and quality with a world leading medical device company!
Regulatory Affairs Manager - Russia
Moscow
Sep 16
Regulatory Affairs Manager in St. Petersburg – Excellent opportunity to work for stable global CRO!We search for our client ideal candidate for position Regulatory Affairs Manager for well-established international CRO based in Russia. We are looking for candidate for full time position to be either office based or home-based. You will have several years of experience in regulatory affairs. It is an excellent opportunity to join global CRO with life / work balance position. ...
Manager, Regulatory Systems and Quality Control
Paris
Sep 16
A superb opportunity to join a global pharmaceutical company within their structured and effective Regulatory team. Within this position you will hold key responsibility within the pharmaceutical development process and would have the responsibility to implement yourself into key projects ensuring the effectiveness of systems, compliance of projects and management of the team.
Chemistry Graduate - Start opportunity in Regulatory Affairs
Aalst
Sep 16
My client is global company, producing a wide variety of products into different industries. For this reason they have an extensive regulatory department dealing with all chemical regulations. To support their growth they have an entry level position available, where you will be trained into a regulatory professional from day one.
Regulatory Affairs Freelancer-Documentation Control Project
Lausanne
Sep 16
Our client in Lausanne, a leading medical device company are going through an exciting FDA and documentation project in their regulatory department. This is a flexible contract which you will be able to mould around current projects and commitments. If you are an experienced regulatory affairs professional within the medical device industry, with specific experience within the FDA apply today for a fast moving role.
Clinical and Regulatory Start Up Manager
France
Sep 16
The role of a Clinical and Regulatory Start Up Manager will be required to ensure the continuous improvement of quality of all Regulatory and Start-up components at the project level. This is a global position and will be largely home-based. ...
Clinical and Regulatory Start Up Manager
Madrid
Sep 16
The role of a Clinical and Regulatory Start Up Manager will be required to ensure the continuous improvement of quality of all Regulatory and Start-up components at the project level. This is a global position and will be largely home-based. ...
Sr./Regulatory Affairs Associate
West Chester
Sep 16
Location: West Chester, PA (50% travel primarily West Chester) + Home based remainderSummary:The Senior/ Regulatory Affairs Associate will be responsible for administering the day-to-day regulatory affairs operations. ...
Manager, Study Start-up and Regulatory (Italy) – LEADING CRO
Italy
Sep 16
After a recent partnership with one of the top 10 global CRO’s, I am looking for experienced professionals with a Regulatory affairs background to be appointed at a senior level. If you feel you have what it takes, APPLY NOW!
Freelance Study Start Up and Regulatory Specialist - Cambridge
Cambridgeshire
Sep 15
Freelance Study Start Up and Regulatory Specialist - 3 month contract - Global CRO - Multiple Rolesi-Pharm Consulting are seeking on behalf of a Global CRO Freelance Study Start Up and Regulatory Specialists. Our client is a leader in clinical research and development and has strong relationships with a large number of global pharmaceutical companies.
Manager, Global Regulatory Processes, Systems and Compliance
Palaiseau
Sep 15
A growing and innovative Biotech has an urgent need for a Manager, Global Regulatory Affairs Process, Systems and Compliance. You will be based in Paris and be responsible for ensuring compliance of RA systems and processes. You will be managing a team of 3 system support specialists who are responsible for compliance.
Senior Regulatory Affairs Specialist
Limerick
Sep 15
Senior Regulatory Affairs Specialist required for global medical device compan
Regulatory Affairs Specialist
Limerick
Sep 15
Global medical device company has a number of vacancies for Regulatory Affairs Specialists!
Interim Director of European Regulatory Affairs - Munich
Munich, Germany
Sep 15
An exciting opportunity to join a Munich biosimilars company as Interim Director of European Regulatory Affairs. This role is focussed on authoring and submission of pre-approval CMC, and new MAAs, to the EMA. The successful individual will be required to lead a team of 3 regulatory affairs professionals in the authoring and submission of pre-approval CMC modules 2 and 3, and new license applications to European markets for biosimilar products.
Regional Artwork Coordinator (Regulatory affairs)
Hertfordshire
Sep 15
A full time permanent position with a global pharma company in Hertfordshire for a Regional Artwork Coordinator. To coordinate the packaging artwork projects through to print ready solutions to company and Worldwide Regulatory Affairs compliance. Competitive package available
jobs : 100 +
Advertising
Subscribe
to the latest Regulatory jobs

Enter your email address:

Delivered by
FeedBurner



Share | | |
Site Map | Privacy & Security | Cookies | Terms and Conditions

PharmiWeb.com is Europe's leading industry-sponsored portal for the Pharmaceutical sector, providing the latest jobs, news, features and events listings.
The information provided on PharmiWeb.com is designed to support, not replace, the relationship that exists between a patient/site visitor and his/her physician.