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The latest Regulatory jobs - BETA

Jobs: Regulatory

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Teamleader EU Regulatory Submissions - West Germany - medical device company - up to 80,000 €
Germany
Sep 29
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 Submission Manager – global CRO/Contract research organization - Munich – up to 55,000 €
Germany
Sep 29
We are currently seeking for an energetic and motivated Regulatory Submission Manager to join our clinical team and manage clinical trial application submissions in the European region on a permanent basis full or part time.
Regulatory Operations CMC Austria / CMO
Austria
Sep 29
My client is a globally leading CMO with corporate head offices in the United States. The company has had a great success story in Austria and is thus looking for new members for their Regulatory Affairs team. ...
Head of Regulatory Affairs, CMC, Generics
Austria
Sep 29
My client is a global leader in the pharmaceutical industry. Due to their expansion, they are looking for a new Head of New Submissions and Renewals for their Regulatory Affairs department.Among many other activities, you would be responsible for leading a team of 6 - 10 members, for all regulatory tasks and activities related to new submissions, for developing and executing regulatory strategies and also for ensuring compliance with all regulatory guidelines. ...
Regulatory Manager/Senior Manager - Full Lifecycle - Central London - Pharma
London
Sep 29
Regulatory Affairs Manager / Senior Manager - London; my client is a growth pharmaceutical organization focused on areas of unmet medical need in key therapy areas. Due to expansion they are looking to hire a regulatory manager or senior manager (experience dependent).In this position you will be responsible for supporting the senior director with an upcoming MAA submission for a centralised NCE. following this you will be pivotal in the approval and responses to questions. ...
Regulatory Manager / Senior Regulatory Manager - Devices (Class III) and CE Markings
Buckinghamshire
Sep 29
Regulatory Affairs Senior Manager - Devices - Class III; my client is a diversified healthcare organisation and global manufacturer of Class III devices. They are looking for a Senior Regulatory Manager to drive registration of new products, maintenance of technical files and obtaining of CE markings for Europe. You will have extensive experience within the field of devices registration and a desire to work within a dynamic environment. ...
Regulatory Imports Manager
Hertfordshire
Sep 29
Vacancy: Regulatory Imports ManagerSalary; £45,000- £50,000 per annumLocation: HertfordshireA dynamic Pharmaceutical Company in Hertfordshire are currently looking for a Regulatory Imports Manager to join their team on a permanent basis.Ideally the Regulatory Imports Manager will have an understanding of where to purchase and distribute EU products. ...
Associate Director - Start Up and Regulatory
Surrey
Sep 29
Currently working with a Global CRO in the South London area that is in need of an Associate Director of Study Start Up & Regulatory activities. Our client is offering a competitive salary paired with excellent benefits and office environment.
Senior Manager Regulatory Affairs - Medical Devices
Buckinghamshire
Sep 29
Full-time permanent position considering candidates at manager or senior manager level within regulatory medical devices. Medical devices and CE Marking experience is essential - Competitive package available
Regulatory Affairs Manager - Russia
St. Petersburg
Sep 29
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. ...
Associate Director of Regulatory Affairs – Sweden
Switzerland
Sep 29
Are you ready to become a key stakeholder in a leading global pharmaceutical company’s regulatory activities? Ready to feel valued and recognized at work? Looking to add more to your extensive experience?
Executive Director, Clinical Regulatory Consultant-135745
Europe, Middle East and Africa-UK-England-Cambridge
Sep 29
We are seeking an Executive Director to join our global PPD Consulting group in the EMEA region as Clinical Regulatory Consultant. This is primarily for the therapeutic areas of gene therapy and rare disease.The role can be office or home based in any of the European countries where PPD has an office.PPD are seeking a candidate based in the EMEA region to join the Global Product Development team. ...
Regulatory Affairs Manager for leading global Pharma (Switzerland)
Switzerland
Sep 29
Do you have a passion for Regulatory Affairs? Feel you are ready to use your extensive experience to guide a team? Looking for your next challenge? THEN I HAVE THE OPPORTUNITY FOR YOU! After an exclusive partnership with a top global Pharmaceutical company, I am seeking experienced Regulatory Affairs professionals to join the company in a senior management position.
Regulatory Affairs Officer - Pharma and Medical Devices
Dublin, Republic of Ireland
Sep 28
Our client, a growing Dublin based pharmaceutical company are currently recruiting for a Regulatory Affairs Officer for medical devices.
Regulatory Affairs Officer - Medical Devices
Dublin, Republic of Ireland
Sep 28
Our client, a growing Dublin based pharmaceutical company are currently recruiting for a Regulatory Affairs Officer for medical devices.
Regulatory Affairs Associate - Barleben, Germany
Germany
Sep 28
My client is a globally focussed Diagnostics company looking to expand their regualtory team in Germany.
Senior Regulatory Affairs Manager, 80-100%
Zürich
Sep 28
Senior Regulatory Affairs Manager, 80-100%
Director for Regulatory Affairs, Biologics
Zürich
Sep 28
Global Regulatory Affairs Director/Associate Director
Regulatory Affairs, Global Strategy Lead, EU
Basel
Sep 28
A medium sized global bio-pharmaceutical company is currently seeking a Regulatory Affairs, Global Strategy Lead to join their global Regulatory Affairs team. There are 3 positions available and they have arisen due to a departmental restructure. They have restructured themselves to enable effective coverage of regulatory responsibility and allow for more specialist, effective coverage of products and Regions.
Regulatory Affairs Consultant-Nepal
Nepal
Sep 28
Regulatory Affairs Consultant- 3-6 Month Contract-Home based/Remote Nepal Level: Regulatory Affairs Consultant- Nepal (Nepalese speaking) Contract: 3-6 months Type of contract: Part time Location: Nepal (remote working/homebased) Summary We are looking for a Regulatory Affairs Consultant to manage local regulatory affairs activities for Nepal. The successful candidate will be a Nepalese speaking consultant responsible for providing local regulatory information and translations. ...
Regulatory Affairs Consultant- Ukraine
Ukraine
Sep 28
Regulatory Affairs Consultant- 3-6 Month Contract-Home based/Remote Ukraine Level: Regulatory Affairs Consultant- Ukraine Contract: 3-6 months Type of contract: Part time Location: Ukraine (remote working/homebased) Summary We are looking for a Regulatory Affairs Consultant to manage local regulatory affairs activities for Ukraine. The successful candidate will be responsible for providing local regulatory information and advice as well as preparing local submissions for Ukraine. ...
Senior Associate Regulatory
New Jersey
Sep 28
This is a great oppotunity for a Senior Associate Regulatory to join a well-established organisation based in the US.Smmary of postion:Independently authors, compiles, reviews and submits high-quality regulatory submissions to the FDA within company timelines and in accordance with regulatory guidelines and applicable federal laws. Plans, coordinates and writes, clear, concise and accurate, responses to inquiries from FDA resulting from their review of the submissions. ...
(Senior) Manager, Regulatory Affairs - International Pharma, London
London
Sep 28
Planet Pharma are recruiting a (Senior) Manager of Regulatory Affairs on behalf of our client, an international Pharmaceutical Company in London
Pyschem Chemist - Opportunity to get into Regulatory Affairs
Brussels
Sep 28
This is a position, where you will be focussing on your chemistry experience and at the same time have the chance to be trained into regulatory affairs for de agrochemical sector. You will be part of the EU regs team and be the core expert on psychical Chemistry, mostly monitoring studies based within your field of expertise. At the same time you will get training into regulatory affairs and be in charge of checking the physchem part of the crop protection dossiers.
Regulatory Submissions Coordinator
London or Stirling
Sep 28
Medpace is seeking a Regulatory Submissions Coordinator for our Clinical Operations team in the UK.
Regulatory Submissions Coordinator / Senior Regulatory Submissions Coo
Germany
Sep 28
A global, full-service Clinical Research Organization (CRO) specializing in a multitude of therapeutic areas. Who continue a steady growth and are looking to add to their team!
Senior Regulatory Affairs Manager (CMC)
Cambridge
Sep 28
i-Pharm Consulting are recruiting for…ROLESenior Regulatory Manager (CMC)LOCATION: Cambridge RATE: Negotiable ROLE: Established Biotech are looking for a Senior Regulatory Affairs Manager to work in their EU CMC team on an initial 12 month contract.The core focus will be to assist others in the compilation of complex CMC documentation (including variations as well as quality sections of the IMPD and CTD). ...
Senior Regulatory Affairs Manager (CMC)
Middlesex
Sep 28
i-Pharm Consulting are recruiting for…ROLESenior Regulatory Manager (CMC)LOCATION: Middlesex RATE: Negotiable ROLE: Established Biotech are looking for a Senior Regulatory Affairs Manager to work in their EU CMC team on an initial 12 month contract.The core focus will be to assist others in the compilation of complex CMC documentation (including variations as well as quality sections of the IMPD and CTD). ...
Regulatory Associate (12 Month Contract)
Middlesex
Sep 28
i-Pharm Consulting are recruiting for…ROLERegulatory Associate (12 Month Contact)LOCATION: Commutable from Maidenhead, Uxbridge & Slough RATE: Negotiable ROLE: Leading healthcare company are looking for a regulatory associate to join them on a 12 month contract which could lead to either an extension or permanent placement.The activities you will get involved with include product licensing, submitting new applications globally, CMC post-approval & working with PV on PSUR submissions. ...
Senior CMC Regulatory Manager – Pharmaceutical consulting company - Munich – up to 150,000 €
Germany
Sep 27
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.
Senior Regulatory Medical Writer (CTD) UK
Wales
Sep 27
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 Regulatory Medical Writer (CTD) Germany
Germany
Sep 27
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.
Interim Regulatory Affairs specialist
Enkhuizen
Sep 27
For a freelance project with start-date November, my team and I are now urgently looking for a Regulatory Affairs specialist for one of the world’s most famous consumer health/pharmaceutical organization, to be based in the Utrecht region. The project is for six months to replace someone temporarily.You will report directly to the RA/Quality Director and you will be working closely together with three other RA specialists. ...
FREELANCE: Regulatory Affairs Coordinator - Belgium
Belgium
Sep 27
Regulatory Coordinator - EMEABelgiumMy client is a truly global and highly prestigious pharmaceutical company. We are urgently seeking a Regulatory Coordinator to join their EMEA team, with any successful applicant to be office based in Belgium. The initial contract will be for 12 months with long term plans for extension. ...
Regulatory Affairs Lead
Denmark
Sep 27
We are currently searching for an experienced regulatory professional in Denmark to manage a team of 11 in one of the bigger pharmaceutical companies in the area.
Regulatory Affairs Senior Manager
England
Sep 27
Regulatory Affairs Senior Manager: Hertfordshire - flexibility for 2 days home working Contract duration: 6 months. This is a very unique opportunity to join a consultancy which is working on behalf of some of the world's leading biotech's developing some of the most exciting orphan drugs on the market.
Freelance Clinical and Regulatory Start Up Manager
Austria
Sep 27
Premier Research are a growing global CRO focused on delivering high quality clinical research projects to their diverse client base. With industry leading expertise in Paediatrics, Analgesia, Oncology and CNS we are looking for career focused individuals who want to be a part of our growth
Regulatory Affairs Associate Director \ Regulatory Affairs Director
England
Sep 27
Regulatory Affairs Associate Director \ Regulatory Affairs Director: Hertfordshire - Maybe a couple of day's home working for the right candidate. Salary: Up to £80,000 - £95,000 per annum. Regulatory Professionals are working with an exciting CRO with a fantastic team
Regulatory Affairs Specialist - 5 months contract
Switzerland
Sep 27
ProClinical are currently recruiting for a Regulatory Affairs Specialist with a focus on CMC and API submission on behalf of our client. Our client is part of a leading global pharmaceutical organization and specialized in pharmaceuticals and medical devices. The role will be based in the German part of Switzerland and is a 5 month contract. ...
Chemist - Regulatory Affairs - Agrochemicals
Brussels
Sep 27
In the Position you will be part of a growing agrochemical company. Joining now gives you strong opportunities to progress within the business and to develop in a project leader role. You will be the expert within your field of experience and be monitoring studies within your knowledge field. Furthermore you will be in charge of proofreading the pyschem part of regulatory dossiers, giving you a great change to gain extra experience in this field.
Regulatory Affairs Manager (m/w) im Raum Schönenbuch
Arlesheim
Sep 27
Regulatory Affairs Manager (m/w) im Raum SchönenbuchUnser Kunde ist bekannt für eine vielseitige und verantwortungsvolle Aufgabe in einem dynamischen, unabhängigen und renommierten Unternehmen. Für die Abteilung im Bereich International Affairs, suchen wir für eine neu geschaffene Position einen Regulatory Affairs Manager zum nächstmöglichen Eintrittstermin. ...
Senior Regulatory Affairs Associate
Wiltshire
Sep 27
Senior Regulatory Affairs Associate Rate: Competitive salary + Benefits Package - 25 days holiday, pension, healthcare, bonus Location: Wiltshire A new vacancy has arisen for a proficient Regulatory Affairs Senior Associate
CH - Regulatory Expert - Normal
Schaffhausen
Sep 27
A leading multinational pharmaceutical, and medical devices company currently have an attractive job vacancy available for a CH Regulatory Expert to be based in their office in Schaffhausen, Switzerland. ...
Consultant, Clinical Trial Regulatory Services
Prague
Sep 27
PAREXEL is looking for experienced Regulatory Professional to join their team in Prague.
Regulatory Operations Manager (m/w) RIMS
Frankfurt am Main
Sep 26
Regulatory Submissions Manager (m/w) RIMSOffice-based in Frankfurt, Germany / full-time, unlimitedJob Description:- Participate in the daily activities and workload of site regulatory operations team, ensuring compliance with all SOPs and internal standards- Responsible for project management and implementation of various informations systems such as electronic data management systems (eDMS), regulatory information management systems (RIMS) and submission management systems (SMS) as per the ...
Line Manager for Study Start Up and Regulatory Affairs - Italy - Get in contact now for more details
Milan, Italy
Sep 26
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.
Regulatory Affairs Global CMC Biologicals role covering EU/US/Japan/Emg/LatAm – Associate Director Level - Direct Line management
South-East / M4 / M25 West / Near Heathrow
Sep 26
Coordinate and drive global regulatory CMC strategy for complex submissions and determine and drive the execution of regional CMC regulatory plans in line with the global regulatory strategy. If you wish to apply for this role send your CV to cv@advregulatory.com or call Theo Moore or Matt Greig in the London office on +44 (0)20 7801 3380.
Regulatory Affairs CMC Biologicals Role - Snr Executive / Associate Level - Join a Biologics company with a Great Pipeline
South-East / M4 corridor / M25 West
Sep 26
Within this dynamic regulatory affairs environment you will be working in a mixed role covering early phase or late phase drug development and supporting EU sometimes Global product registrations & line extensions of biotechnology products/projects. If you wish to apply for this role send your CV to cv@advregulatory.com or call Theo Moore or Matt Greig in the London office on +44 (0)20 7801 3380.
Regulatory Affairs CMC Biologicals Role - Sne Excutive Level - Receive great training and real career development... Brussels
Brussels
Sep 26
Gain experience in Global product registrations & line extensions of biotechnology products/projects and receive great training and the opportunity to cross into new therapy areas across a variety of formulations. 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.
Global Regulatory Affairs CMC Associate Director – Brussels – Strategic Global CMC role for Biologicals - Great Salary + Car + Bonus + LTis
Brussels
Sep 26
Advanced Regulatory are now recruiting for a highly innovative and hugely successful pharmaceutical client who are expanding and developing their Global CMC department. 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 Manager / Senior Regulatory Affairs Officer
Surrey
Sep 26
Our client are a branded generics company looking to bring the regulatory function in-house and are looking for an experienced regulatory professional to join their team to oversee this. Looking for a regulatory professional who can work autonomously with at least 5 years regulatory experience. Management experience would be good, or someone looking to move into management, however there is no people management required at present only functional management. Competitive package available
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 - Manage E2B submissions per standardized operating procedural document; review ICSRs for local reportability, make submit/no submit determination, monitor successful transmission.
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.
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. ...
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 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
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.
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
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. ...
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.
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.
jobs : 100 +
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