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The latest Regulatory jobs - BETA

Jobs: Regulatory

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Regulatory CMC Manager, Biologics, Major Project
Basel
Feb 10
Regulatory CMC Manager, Biologics, Major Project, Early Development, Hands on and strategic input
Regulatory Consultant (Freelance) – Massachusetts – 6 month contract with home working available
USA
Feb 10
Rare opportunity for a Regulatory Affairs Consultant to join one of the world’s top 5 companies, working within the dynamic regulatory team on exciting projects. The Regulatory Affairs Consultant will enjoy the benefit of being able to work from home some days and be provided with a lucrative hourly rate.
Senior Regulatory Associate - Clinical Trials
Berkshire
Feb 10
i-Pharm Consulting are recruiting for…JOB TITLE: Senior Regulatory Associate LOCATION: BerkshireRATE: Negotiable ROLE: Compiling initial CTA (clinical trial application) submissions to relevant Health Authorities, and Ethics submissions to relevant ethics committees. There is also a need to potentially follow up with amendments, and the submissions will be for approval within the EAME region. ...
Regulatory Affairs-Medical Devices-Biotech
Stockholms Län
Feb 10
För min kunds räkning letar jag efter Regulatory Affairs managers till deras Medical device avdelning.
Regulatory Specialist – Career Kisktarter - Paris Region
France
Feb 10
This is an exciting opportunity for a young professional to join a team of passionate individuals where you will be learning from the regulatory team allowing you to develop you regulatory knowledge and advance your career.
Letar efter Regulatory CMC Managers
Stockholms Län
Feb 10
Jag söker efter CMC-professionella med erfarenhet inom pharmaceuticals och medical devices! Har du erfarenhet av att jobba på ett biotech är det ett plus i kanten.
Regulatory Affairs Specialist - ROW role - Cambridge - UK
Cambridge
Feb 10
To apply for this regulatory affairs specialist role please call Julie Cooper on 07951 082482 or email on:julie@mosaicrecruitment.co.uk
Regulatory Affairs Specialist - ROW
Cambridge
Feb 10
To apply for this role please call Julie Cooper on 07951 082482 or email Julie Cooper @julie@mosaicrecruitment.co.uk
Regulatory Affairs Manager - Cosmetics - Nottingham
Midlands
Feb 10
To apply for this regulatory affairs cosmetics role please call Julie Cooper on 07951 082482 Alternatively please send CV to :julie@mosaicrecruitment.co.uk
Regulatory Affairs Associate Manager - Operations- Cambridge
Cambridge
Feb 10
To apply for this associate regulatory affairs operations manager please call Julie Cooper on 07951 082482 Alternatively please send your CV to : julie@mosaicrecruitment.co.uk
Regulatory Affairs Project Manager - consultancy work - Surrey
Surrey
Feb 10
To apply for this regulatory affairs project manager role please call Julie Cooper on 07951 082482 Alternatively please send your CV to- julie@mosaicrecruitment.co.uk
Regulatory Affairs Specialist Cosmetics - Midlands- International role- Exciting new role
Nottingham
Feb 10
To apply for this regulatory affairs cosmetics role please send your CV to;julie@mosaicrecruitment.co.uk or to discuss further please give Julie cooper a call on 07951 082482
Regulatory Affairs Manager - clinical trial work - can be home based anywhere in GERMANY - must speak German
Germany
Feb 10
To apply for this role please call Julie Cooper on 07951 082482 or send me a copy of your CV to: julie@mosaicrecruitment.co.uk
Regulatory Affairs Specialist - EU and US Medical Devices and Biocides role - Midlands
Midlands
Feb 10
To apply for this regulatory affairs medical devices / biocides role please call Julie Cooper on 07951 082482 or send your CV to:julie@mosaicrecruitment.co.uk
Regulatory Operations Consultant-Leading Global Biotech
Uxbridge
Feb 10
Regulatory Operations Consultant-Leading Global BiotechFor the World leaders in Biotechnology I am looking for a Regulatory Operations Consultant to join them on a 12 month contract, to start in March. This is a role that will offer you exposure within a large contracting community and the chance for continuous contract opportunities.
Senior Director, Head of Regulatory
Switzerland
Feb 10
If you wish to apply for this role send your CV with a covering note to cv@advregulatory.com quoting reference number noted above. Alternatively to have a confidential discussion about this or other potential roles or career options, call Matt Greig or Theo Moore, in the UK London office, on +44 (0)207 801 3380.
Regulatory Affairs / Regulatory Affairs Director – lead early stage projects for development US, Europe and International – FULL RELOCATION
Netherlands - close to Amsterdam
Feb 10
This is a Global Regulatory Lead role graded Associate Director. Please call one of Advanced Regulatory’s Principals for Regulatory Affairs, Matt Greig or Theo Moore on +44 (0)207 801 3380 or +44 (0)7918 679 405.
Regulatory Affairs Senior Director / GRL – Geneva – Global role with Team leading…
Geneva, Switzerland
Feb 10
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.
CONTRACTOR Regulatory CMC Bio EU and Intl CMC submissions OR IMPD Writing Up to 3 days a week at home
London M4 corridor/South-East (near Heathrow)
Feb 10
If you wish to apply for this role send your CV with a covering note to cv@advregulatory.com quoting reference number noted above. Alternatively to have a confidential discussion about this or other potential roles or career options, call Matt Greig or Theo Moore, in the UK London office, on +44 (0)207 801 3380.
Senior Associate Regulatory Affairs (CTA) (Contract)
Buckinghamshire
Feb 10
New position!!! We are recruiting for a Senior Associate Regulatory Affairs (CTA) for our client in Buckinghamshire for a 12 month contract position. Competitive rates of pay!!
Regulatory Affairs Executive - Medical Devices - North London \ Hertfordshire
England
Feb 10
Regulatory Affairs Executive - Medical Devices - North London \ Hertfordshire Our client is a medical devices manufacturer with a product portfolio which is distributed worldwide in over 50 countries
Home Based – Regulatory Writer – Global CRO – 12 Month Contract
England
Feb 10
This world leading CRO is after experienced medical writers who can come in on a contract basis and hit the ground running. This position is 100% home based allowing you to work on a range of global projects. This is a brilliant opportunity for anyone that wants to push their career onto the next level in an up to date and innovative organisation.
Regulatory Senior Manager\ Associated Director, Labelling
England
Feb 10
Regulatory Senior Manager\ Associated Director, Labelling : East Anglia OR Home Based Salary - Flexible dependant on candidate Generous benefits package including car or car allowance
Regulatory Affairs Scientist
England
Feb 10
Regulatory Affairs Scientist Locations: Buckinghamshire Salary: £55,000 - £65,000 + Competitive Benefits package
Regulatory Affairs Opportunities
Rep. Ireland
Feb 10
We are actively seeking candidates with Regulatory experience to fulfill a number of new vacancies with our clients.
Regulatory Affairs Officer
Rep. Ireland
Feb 10
On behalf of our client, a global organisation we now have a vacancy for a Regulatory Affairs Officer to be based in their Dublin location.
FREELANCE SENIOR ASSOCIATE - REGULATORY AFFAIRS
Buckinghamshire
Feb 10
Global Pharmaceutical player is currently seeking 3 senior regulatory affairs associates to undertake 12 month contracts. These are hihgly lucrative roles as the hiring client is undergoing some fantastic transformations, further solidifying its industry name. ...
Regulatory Affairs Specialist
Dublin
Feb 10
Our client a leading pharmaceutical manufacturing company now have a vacancy for a Regulatory Affairs Specialist - Medical Devices This is a full time permanent role.
Global Regulatory Affairs Manager, Operations
Basel
Feb 10
Global Regulatory Affairs Manager, Operations, Start-UpProducts
Regulatory Affairs/tech. Dokumentation
Hechingen
Feb 10
Anfertigung der technischen Dokumentation.Mitwirken im Entwicklungsprozess als Schnittstelle zum R&DRisikobewertung der verschiedenen Bauteile und der kritischen LieferantenSteuerung der der Zulassung nach Maschinenrichtlinie in Zusammenarbeit mit verschiedenen Behörden weltweit.
Regulatory Compliance Manager (m/w)
Austria
Feb 10
Regulatory Compliance Manager (m/w)Office-based in ÖsterreichVollzeit, unbefristetAufgaben:- Sie erstellen, kontrollieren und aktualisieren Zulassungsdossiers von Arzneimitteln inKooperation´mit den betroffenen Fachabteilungen.- Sie betreuen die Kunden und Behörden hinsichtlich qualitätsrelevanter und regulatorischerFragestellungen, verfassen Änderungsanträge und beantworten Mängelrügen. ...
Regulatory Officer, Central London
London
Feb 10
An excellent opportunity has arisen for a Regulatory Officer to join a Pharmaceutical company based in central London. Within this role you will be responsible for registering an exciting range of new products and maintaining a European Portfolio. This role has become available due to an ongoing period of growth within the company and your responsibilities will be split across Regulatory, PV and Quality.
Global Regulatory Associate - New Position
Kingston Upon Hull
Feb 10
My client is an established multinational consumer goods company who produce healthcare and well-being products available internationally. They are looking for enthusiastic individuals to join their team as Global Regulatory Associates; this position is an amazing opportunity to build on your regulatory experience and develop yourself and your experience with a blue chip company. ...
Specialist, EMEA Regulatory Labelling (2 Year Maximum Duration Contract) Job
BOUDRY, Neuchâtel, Switzerland
Feb 10
Celgene is a global biopharmaceutical company leading the way in medical innovation to help patients live longer, better lives. Our purpose as a company is to discover and develop therapies that will change the course of human health. We value our passion for patients, quest for innovation, spirit of independence and love of challenge. ...
Sen Regulatory Affairs Specialist - Leadership role - Austria
Austria
Feb 9
Senior Regulatory Affairs Specialist - Leadership role - Austrian Med Tech - English essential with German a bonusWe seek a Senior Regulatory Affairs specialist with several years experience working in the Medical Devies sector to take on key and senior duties at our Austrian site, both hands on and in a mentoring/supervisory capacity.
Regulatory and Quality Officer – Broad Tasks - Belgium
Belgium
Feb 9
The company is specialized in products for hospitals to help critical and chronically ill patients. They have built out a good reputation worldwide so you can be proud of the company you work for. Besides the company and team has an open culture. The communication is clear, informal and fast. In that way you feel comfortable in the work environment and act like yourself.
Senior Regulatory Programme Manager
Home or office based
Feb 9
• 12 month contract • Freelancers only • Office based in Welwyn Garden City or working from home upto 4 days a week • Ideally fully time, however working 4 days a week will also be considered
Global Director, Regulatory Affairs
Zürich
Feb 9
Global Director, Regulatory Affairs, Biologics, Zurich Area
Regulatory Affairs Officer Submissions
Dublin, Republic of Ireland
Feb 9
On behalf of our client, a growing pharmaceutical company, we are currently recruiting for Regulatory Affairs Officers for submissions. These are for permanent and 12 month contract opportunities.
Regulatory Affairs Officer Compliance
Dublin, Republic of Ireland
Feb 9
On behalf of our client, a growing pharmaceutical company, we are currently recruiting for Regulatory Affairs Officers Compliance. These are for contract positions, approx 8 months duration.
Regulatory Affairs Specialist-Long Term Project-Medical Devices
Zürich
Feb 9
A fast moving role within regulatory affairs has come in with a world leading medical device company. Our client are looking for a regulatory affairs specialist to come on board for a long term project ending December 2017. Our client in the process of completing several international projects and are looking for someone to join them during this expansion phase globally.
Regulatory Affairs Specialist II-III
Raynham
Feb 9
An exciting opportunity has arisen to work for a global, leading specialist Medical Device organization that focusses on offering the world’s most comprehensive portfolio of orthopaedic, neuro products and services for joint reconstruction. The position is a Regulatory Affairs Specialist II-III role to be based on site in Raynham, Massachusetts. ...
Cosmetics Regulatory Affairs Professionals – Fast Growth
Hilversum
Feb 9
I am currently working for an exciting fast growing company that is looking for regulatory professionals who are experienced with the cosmetics directive. You will be part of a company that already has a global client portfolio but has ambitous plans in terms of its future development.
UBC - Regulatory Consultant, Research and Clinical Services (London)
United Kingdom, London, England
Feb 9
Responsible for the all-electronic and paper assembly, publishing, production, dispatch, logging and archiving of regulatory submissions.Provide project management oversight (tracking, planning, timelines) for regulatory (MOH) submissionsReview submission documents for content and format corrections.Responsible for monitoring inventory of supplies related to submission preparation and initiate purchase orders.May directly interact with regulatory agencies.
Regulatory CMC Professionals
Denmark
Feb 9
I am specialist headhunter in the Nordics focusing mostly on Regulatory affairs in the Pharmaceutical industry as well as Medical devices.
Regulatory CMC Expert- Big Pharma
Denmark
Feb 9
An opportunity to join a global pharmaceutical company based in Scandinavia as a Regulatory Affairs CMC Expert!
Regulatory Portfolio Project Manager - early development
Oxfordshire
Feb 9
Regulatory Portfolio Manager - Early Development Currently recruiting are a global, innovative pharmaceutical company who are currently driving toward a new, state of the art, innovative Research and Development department across all areas, especially Regulatory Affairs. ...
ASAP - Freelance Regulatory Associate - FRANCE
Paris
Feb 9
ASAP - Freelance Regulatory Associate - 6 Months ContractHi All, One of the industry’s leading CRO’s are actively seeking a talented regulatory affairs associate to join them on a freelance basis at their Paris offices.As a regulatory affairs associate, you will be heavily involved in contributing to Initial clinical trial applications (CTA) as well as making amendments to necessary committees and authorities to support submissions. ...
Regulatory Associate (£35-£45 per hour)
Berkshire
Feb 8
i-Pharm Consulting are recruiting for…JOB TITLERegulatory Associate LOCATION: Berkshire (2-3 days working from home)RATE: £35-£45 per hourLENGTH: 6 MonthsROLE: Submitting and managing initial Clinical Trial Applications and Ethics submissions to Ethics Committees’ in UK and MHRA. ...
Clinical Study-Start up Specialist, Study Start-up, In-house CRA, Regulatory submissions Co-ordinator
UK - South East UK
Feb 8
Clinical Study-Start up Specialist, Study Start-up, In-house CRA, Regulatory submissions Co-ordinator, Regulatory associate, CTA, Clinical Trial Associate – London/ M4 Corridor / Home based. We are currently recruiting for a highly recognised CRO that are growing their study start-up team as a core function. Please contact Zoe Benningfield on 07896 693960 or email zoe@peoplewithchemistry.com
Regulatory Affairs Manager within Medical Devices - EU and FDA
Oxfordshire
Feb 8
As the manager within their global function you will lead activities related to the submission, maintenance and lifecycle management of their medical device products globally. ...
Regulatory Affairs/ Quality Assurance Manager
France
Feb 8
Our client, one of the top 10 Lab Company in the Animal Health is currently looking for a Pharmacist or a Vet specialized in Regulatory affairs and Quality Assurance to work in one of its French Lab
SSU and Regulatory Specialist II - Sweden / Denmark
Sweden
Feb 8
Do you want to be part of a global top 10 CRO? INC Research is a full-service clinical research organization, providing the full range of Phase I to IV clinical development services for the world’s pharmaceutical, biotech and medical device industries. We do this across six continents. We believe that therapeutic and operational experience forms the foundation for taking medicines successfully through clinical development.
SSU and Regulatory Specialist II -Poland
Krakow, Warsaw
Feb 8
Do you want to be part of a global top 10 CRO? INC Research is a full-service clinical research organization, providing the full range of Phase I to IV clinical development services for the world’s pharmaceutical, biotech and medical device industries. We do this across six continents. We believe that therapeutic and operational experience forms the foundation for taking medicines successfully through clinical development.
Trainee Regulatory Affairs-Career Starter-Medical Devices-CH
Arbon
Feb 8
Are you looking to develop your career in regulatory affairs with a leading medical device company? This is a fantastic role for a mechanical engineer with some experience within regulatory affairs to kick start their career in this fantastic regulatory affairs associate role. This opportunity is a great skill enriching role working with innovative medical devices.
Regulatory Submissions Manager
Lille
Feb 8
As a Regulatory Submissions Manager you will be working for a niche bio-pharmaceutical company, which develops medicines for unmet medical needs. The company is at the forefront of developing therapeutic and diagnostic solutions to address patient needs in metabolic and inflammatory diseases currently recruiting for a Regulatory Submissions Manager.
Regulatory Affairs Specialist
Zuchwil
Feb 8
Mary Tilston is recruiting for a Regulatory Affairs Specialist to join a company in the pharmaceutical industry at their site based in Switzerland on a...
Regulatory CMC Expert to Giant Biotech
Denmark
Feb 8
An excellent opportunity to join one of Scandinavia's most expanding and attractive pharmaceutical companies as a Regulatory Affairs CMC Specialist!
CMC Regulatory Manager 2 Years 30h Part-Time
Munich
Feb 8
Seeking an experienced CMC Manager for Regulatory Affairs for a 2 year long maternity cover, part time, 30h/week. The company are also expanding however so this could turn into a full time permanent positions for the right candidate. On the other hand, if anyone is looking for a more short term option with increased flexibility, this would be an excellent role for you as staying within the company after the maternity cover will not be a mandatory requirement. ...
Regulatory Affairs Director-Growing Generics Company-Midlands
Northamptonshire
Feb 8
Regulatory Affairs Director-Growing Generics Company-MidlandsI have a great opportunity for an experienced Regulatory professional to join of the fastest growing generics companies as their Director of Regulatory Affairs. This is a great chance for somebody with a proven management track record to step up into a Director level function and also further enhance their knowledge of global regulations including FDA.
Regulatory Manager – Career Progression - Lyon
Lyon
Feb 8
This is an exciting opportunity for someone to take the nerxt step in there career into a mangement positiion where you will be leading a small team esnuring the registration of biocides throughout Europe offering you the chance to help develop junior staff.
Regulatory Affairs Associate-6 Month FTC-Cheshire
Wiltshire
Feb 8
Regulatory Affairs Associate-6 Month FTC-CheshireMy client, a smaller pharma company in Cheshire are currently looking for a Regulatory Affairs Officer for a 6 month maternity cover. In this position you will gain good exposure to UK regulations as well as working with innovative OTC products in a fast moving environment.
Regulatory Writer - Entry Level - North East
North East England
Feb 8
My client is a Global Leader in the Pharmaceutical Industry. They are currently looking for an enthusiastic, driven individual to join their ever growing team. With this expansion has come an increased focus on training and development. You really will be part of some of the most impressive training in the industry. This kind of opportunity is rare and really shouldn't be missed.
Senior Regulatory Specialist – Cosmetics - Picardie
Picardie
Feb 7
This is an exciting opportunity for an established professional to join the regulatory team of a leading cosmetics brand where you will be instrumental in getting products to market throughout Europe and beyond allowing you to develop you regulatory knowledge and advance your career.
Regulatory Specialist – Global Brand - Antwerp
Antwerp
Feb 6
This is an exciting opportunity to join a company are dedicated to sustainability and growth where you will be part of a company that provides quality phytosanitary products and offers real solutions for crop management offering you the ability to improve the way you perceive crop management and actually expand your experience with it.
Regulatory CMC Expert to Giant Biotech
Denmark
Feb 5
My client, a global pharmaceutical company with focus on developing innovative treatments to their patients, is currently looking for a Regulatory Affairs CMC Specialist to join their expert team. This fantastic opportunity is ideal for someone who is ready for a new challenge while working for one of the multinational leaders in this area.
Regulatory Specialist
Cambridge, England
Feb 5
• Permanent position with Client • Office based Cambridge • Niche Pharma • Start ASAP
Regulatory Affairs Manager - Cosmetics - Nottingham
Midlands
Feb 5
To apply for this regulatory affairs cosmetics role please call Julie Cooper on 07951 082482 Alternatively please send CV to :julie@mosaicrecruitment.co.uk
Regulatory Affairs Associate Manager - Operations- Cambridge
Cambridge
Feb 5
To apply for this associate regulatory affairs operations manager please call Julie Cooper on 07951 082482 Alternatively please send your CV to : julie@mosaicrecruitment.co.uk
Regulatory Affairs Project Manager - consultancy work - Surrey
Surrey
Feb 5
To apply for this regulatory affairs project manager role please call Julie Cooper on 07951 082482 Alternatively please send your CV to- julie@mosaicrecruitment.co.uk
Regulatory Affairs Specialist Cosmetics - Midlands- International role- Exciting new role
Nottingham
Feb 5
To apply for this regulatory affairs cosmetics role please send your CV to;julie@mosaicrecruitment.co.uk or to discuss further please give Julie cooper a call on 07951 082482
Regulatory Affairs Manager - clinical trial work - can be home based anywhere in UK or Europe- can be based in most European countries
Germany
Feb 5
To apply for this regulatory affairs manager role please call Julie Cooper on 07951 082482 or send your CV to : julie@mosaicrecruitment.co.uk
Regulatory Affairs Specialist - EU and US Biocides role and some medical devices work - Midlands
Midlands
Feb 5
To apply for this regulatory affairs medical devices / biocides role please call Julie Cooper on 07951 082482 or send your CV to:julie@mosaicrecruitment.co.uk
Regulatory Affairs Consultant
Hungary
Feb 5
Regulatory Affairs Consultant- 12 Month Contract- Hungary, EU Level: Regulatory Affairs Consultant Contract: 12 months Salary: Negotiable Location: Hungary, EU Summary Regulatory Affairs Consultant is required to manage global regulatory affairs. The successful candidate will be responsible for post approval activities such as maintaining the MAA by ensuring that variation, licences renewals and label changes are updated on a timely manner. ...
Regulatory Consultant
Berkshire
Feb 5
This is a great opportunity for a Regulatory Consultant to join a recognised organisation based in Berkshire, England. This is a 3 month contract role with the possibility of an extension. Job Role:  This Regulatory Consultant job role will include some key accountabilities that are EU market post approval, ensuring regulatory systems such as Regulatory Database /trackers are implemented and kept up to date as well as providing labelling and Artwork support. ...
Manager, Regulatory Affairs
Spain
Feb 5
You will be working for an innovative and growing company based in Spain with an incredible portfolio of established and new medicines. In your role as Regulatory Affairs Manager, you will be working in a global context. You will be involved in the initial set-up all the way to product launch. This will mean you are also involved in strategic decisions on multi-disciplinary international projects.
Principal Regulatory Affairs Executive \ Regulatory Affairs Consultant - Life Cycle Maintenance
England
Feb 5
Principal Regulatory Affairs Executive \ Regulatory Affairs Consultant - Life Cycle Maintenance Duration: Fixed term contract until Jan 2017 Rate/Salary: £55,000 per annum plus benefits
Global Regulatory Affairs Operations Consumer Safety Report CFI Operator
England
Feb 5
Global Regulatory Affairs Operations Consumer Safety Report CFI Operator - Berkshire Rate: £35 per hour. Our client is a global consultancy with offices in New York, India, Philippines and here in the UK.
Strategic Regulatory Affairs Specialist - Medical Devices
Switzerland
Feb 5
Strategic Regulatory Affairs Specialist - Leading Medical Device group based in Switzerland
Regulatory Project Lead - office or home based in Europe - global CRO
Rep. Ireland
Feb 5
We are looking for an experience Regulatory Project Lead to join our European team in the office or work home based and be responsible for regulatory and start-up activities on allocated projects. You can expect a professional environment, challenging tasks and great career progressions.
Team Leader/Senior CMC Regulatory Affairs Manager – Pharmaceutical consulting company - South Germany - no German required
Germany
Feb 5
We are looking for an experienced Regulatory Affairs Manager who wants to use his CMC knowledge in an international operating consulting company and lead a small team of Regulatory specialists. You can expect an open environment, exciting projects and excellent benefits.
Regulatory Submissions Co-Ordinator
Cambridge
Feb 5
A contract author/co-ordinator role within the Device Centre of a global leading healthcare manufacturer. This site based in Cambridge require assistance with a core activity...
Senior Director of Regulatory Affairs
Beijing
Feb 5
Senior Director of Regulatory AffairsAn excellent opportunity has just arisen in China to act as the representative for all RA matters and be an advisor to global companies coming from the US and Europe. ...
Senior Regulatory Associate - 12 Month Contract
Middlesex
Feb 4
i-Pharm Consulting are recruiting for…JOB TITLESenior Regulatory Associate LOCATION: Middlesex or Cambridge RATE: Negotiable with Excellent benefitsROLE: Leading Biologics Company are looking for a Senior Regulatory Associate for a 12 Month Contract. The focus of the project/s will be submitting Clinical Trial Applications via VHP to competent authorities across the EU. There will also be an element of managing sponsors and ensuring all regulatory information is tracked and updated. ...
Regulatory Affairs Project Manager
England
Feb 4
Regulatory Affairs Project Manager Location - Hampshire Salary - £40,000 - £50,000 + Competitive salary package
CMC Manager – Regulatory Author – Global Pharma
Germany
Feb 4
CMC Manager - Regulatory Author - Global Pharma I am currently working with a renowned and leading Pharmaceutical company, who are investing heavily within their Biologics side of the business. To support this growth, as part of their CMC development team, they require a candidate to work with national authorities and write CMC Regulatory Documents throughout the development lifecycle.
Regulatory CMC Manager, Biologics, Major Project
Basel
Feb 4
Regulatory CMC Manager, Biologics, Major Project, Early Development, Hands on and strategic input
Regulatory Affairs Manager
Dublin
Feb 4
To support our EU Consulting team, we are currently looking for an experienced Regulatory Affairs Manager. The role is full time, permanent and office based in Dublin.
Publisher – Regulatory Operations – Cambridgeshire region
Cambridge
Feb 4
This is an outstanding opportunity to join an expanding regulatory operations team in the capacity of publisher. By joining this company who have enjoyed sustained growth over the last decade, you'll find a broad role and avoid the pigeonholing typically you see in top 10 pharma companies. Ultimately gaining new skills, this position suits a publisher with 2-3 years of experience looking to progress.
Formulation Regulatory Officer, Clear Progress
Nottinghamshire
Feb 4
A leading manufacturer of Agrochemical products is looking to appoint a regulatory officer to join their QA and Compliance department on a permanent basis.The focus of the position is to provide support to the production and other technical departments; testing and measuring product performance.The company currently has an extensive product range; allowing the role to offer true diversity giving you the chance to broaden and develop your existing skill set.
Regulatory Affairs Team Leader, Cosmetics - UK
Yorkshire and the Humber
Feb 4
My client is a large pharmaceutical company with historic reputation in the industry and over a century of scientific contributions to healthcare worldwide, so if you are looking to join a company where your work makes a difference, do not hesitate to apply now! They are currently looking for a Regulatory Affairs Team Leader and a team member for the same team, specialized in cosmetics and based in the North! If this sounds like the right position for you, do not hesitate to send your CV across*
Regulatory Affairs Project Manager – Ohio – Rare opportunity to join a leading team
USA
Feb 4
A rare opportunity has become available for a Regulatory Affairs Project Manager to join one of the most dynamic companies within the Ohio area. The Regulatory Affairs Project Manager will be joining a world recognized company which has won several awards within the industry.
Regulatory Affairs Manager– Ohio – Join A World Recognized Company
USA
Feb 4
We are currently recruiting for a Regulatory Affairs Manager to join our vibrant team, based in Ohio. The Regulatory Affairs Manager will be joining an international company and gain exposure within numerous areas of regulatory affairs
Team Lead / Sen Regulatory Aff Specialist - Austrian Med Tech
Austria
Feb 4
Team Lead / Senior Regulatory Affairs Specialist - Austrian Med Tech - global Market leader - English essentialRight in the midst of mountains and scenic landscapes in Austria, our client runs an impressive and cutting edge development and manufacturing facility for electronics based implantable medical devices. It's a new year and foremost on their wishlist is a Senior Regulatory Affairs Specialist with line management duties.
Regulatory Affairs Manager
Berckshire
Feb 3
Do you want to work for a growing pharmaceutical service provider working Global Studies and seeking a challenging and rewarding career in a commercially focussed role?
Regulatory Affairs and Quality Assurance Manager - Medical Devices
England
Feb 3
Regulatory Affairs & Quality Assurance Manager - Medical Devices Sussex Location: This role would suit someone residing in Sussex, Surrey, Hampshire, Middlesex or someone willing to relocate.
CMC Regulatory affairs Lead – Office based in Berkshire
Berkshire
Feb 3
A world leading provider of biopharmaceutical services is looking for your expertise as a Regulatory Affairs Officer within the specialisation of CMC. You will be in charge of preparing and reviewing regulatory submissions to support clinical trial and marketing authorisation activities for internal and/or external clients.
Regulatory Affairs Associate Manager - Operations- Cambridge
Cambridge
Feb 3
To apply for this associate regulatory affairs operations manager please call Julie Cooper on 07951 082482 Alternatively please send your CV to : julie@mosaicrecruitment.co.uk
Regulatory Data Analyst
Buckinghamshire
Feb 3
Natasha Young is recruiting for a Regulatory Data Analyst to join a leading pharmaceutical company, based in Buckinghamshire. This is an opportunity to join a...
Regulatory Affairs Officer within Medical Devices - EU and US
West Yorkshire
Feb 3
As the successful candidate you will be responsible for the following:• Prepare and maintain Medical Device technical files for the company’s Medical Device Products in accordance with current UK and EU legislation.• Ensure regulatory compliance of the Medical Devices registrations in line with current legislation and liaise with the Quality Assurance team and Notified Bodies to effect updates and changes to internal regulatory systems accordingly. ...
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