Regulatory Publishing & Submissions Jobs in Regulatory Affairs

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Manager, Regulatory Medical Writing

Volt Europe are working on an EXCLUSIVE BASIS with a Global Pharmaceutical company to support the growth of their Global Medical Writing team. Part of this includes a key hire for a Manager of Regulatory Medical Writing to be based in their offices. Key requirements: * Prepares, edits and reviews clinical documents * Contributes to all document creation/review/approval SOPs *...

Salary:
Neg
Location:
Scotland
Date Posted:
20-Jan-2017
Job Type:
Permanent

Senior Regulatory Affairs Consultant

An internationally known biotechnology company has an opening for a Senior Regulatory Affairs Consultant job at their Berkshire office. The company has a strong reputation for developing innovative therapies for neurological diseases and employs approximately 7,000 people worldwide. The role would be at a manager / senior manager level and would be for initially 6 month with possible extension to...

Salary:
£50 - 60 per hour
Location:
Berkshire
Date Posted:
24-Jan-2017
Job Type:
Contract/Interim

Senior Regulatory Affairs Associate, CMC - 12 month contract

An excellent opportunity has arisen within the CMC team of a leading Biotech company based in London on a 12 month contract basis. You will ideally have between 1-3 years of CMC Regulatory experience and a strong knowledge of Regulatory Affairs. Responsibilities: -The Regulatory Professional will contribute in implementation of regional strategies by leading the execution of the preparation of...

Salary:
£25 - £30 p hour
Location:
London
Date Posted:
24-Jan-2017
Job Type:
Contract/Interim

Regulatory Affairs Officer

A excellent opportunity has arisen for a Regulatory affairs officer to join a specialist pharmaceutical company based in West Sussex. Within this role you will be responsible for performing & reviewing regulatory affairs activities, including the maintenance of New Product Registrations and the maintenance of existing Product Registrations world-wide. Responsibilities: * Ensure regulatory systems, such as Regulatory Database /trackers are...

Salary:
£30k - £35k pa + Bonus and benefits
Location:
West Sussex
Date Posted:
18-Jan-2017
Job Type:
Permanent

Senior Regulatory Operations/ Publishing Associate - top salary

Do you want to work for one of the best employers in the industry? This top Biopharma has an exciting Regulatory Operations/Publishing/Submissions role for a candidate with 3-5 year's experience. From a career point of view, this is an outstanding company to get on your CV. You will possess good experience and a thorough understanding of Electronic and Paper Publishing...

Salary:
£42,000 to £52,000, bonus and benefits
Location:
Cambridgeshire
Date Posted:
24-Jan-2017
Job Type:
Permanent

Regulatory Affairs Associate - Oxford

An excellent opportunity has arisen for a Regulatory Affairs Associate to join a growing Pharmaceutical company based in Oxfordshire on a permanent basis. Within this role you will be responsible for supporting registration and maintenance of products across Europe. Responsibilities: *Support the preparation, review, and submission of regulatory submissions as appropriate, (i.e: including marketing applications, clinical trial applications, amendments, variations, ...

Salary:
£35k - £38k pa
Location:
Oxfordshire
Date Posted:
18-Jan-2017
Job Type:
Permanent

Senior Regulatory Affairs Manager

JOB TITLE Senior Regulatory Affairs Manager LOCATION Spain Zaragoza// office or home based BENEFITS Generous package (Salary + Benefits) ROLE/DESCRIPTION * Compile and check pharmaceutical quality documentation (Module 3, QOS, IMPD, ASMF etc.) for national and international markets * Prepare Gap Analyses of pharmaceutical quality dossiers in the context of marketing authorization projects, Due Diligence * Set up responses to...

Salary:
Neg
Location:
Spain
Date Posted:
24-Jan-2017
Job Type:
Permanent

Regulatory Affairs Manager

Regulatory Affairs Manager - Biopharmaceutical - Austria - Salary Upon Application If you would like to apply for the position or wish to learn more about the role and company please call Daniel on [Phone number removed] or email your CV with a brief covering note to [Email address removed] An exciting new opportunity has arisen with one of our...

Salary:
Neg
Location:
Tirol
Date Posted:
18-Jan-2017
Job Type:
Permanent

Senior Regulatory Associate (CMC)

i-Pharm Consulting are recruiting for ROLE Senior Regulatory Associate (CMC) LOCATION: Uxbridge or Cambridge RATE: Negotiable ROLE: * The Regulatory Professional will contribute in implementation of regional strategies by leading the execution of the preparation of CMC components of filings for one or more products according to the CMC timelines under the direction of the regional lead. * Responsible for...

Salary:
Neg
Location:
Uxbridge
Date Posted:
24-Jan-2017
Job Type:
Contract/Interim

Contract Regulatory Specialist (Italy - Home) - Novella Clinical

Novella focuses on providing excellent training and career development opportunities, encouraging growth from within our talented work force. Novella specialises in leveraging technology and Clinical Research and continues to improve the quality and service across a broad range of therapeutic areas including Oncology and Medical Devices. Our parent company is one of the World's leading not profit research organisations, and...

Salary:
Competitive
Location:
Italy
Date Posted:
20-Jan-2017
Job Type:
Contract/Interim

Regulatory Affairs Specialist (UK, Permanent and Contract)

Novella focuses on providing excellent training and career development opportunities, encouraging growth from within our talented work force. Novella specialises in leveraging technology and Clinical Research and continues to improve the quality and service across a broad range of therapeutic areas including Oncology and Medical Devices. Our parent company is one of the World's leading not profit research organisations, and...

Salary:
Competitive
Location:
Stevenage
Date Posted:
20-Jan-2017
Job Type:
Contract/Interim
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International Regulatory Strategy Product Lead

International Regulatory Strategy Product Lead - Global Pharmaceutical Company - London - £competitive salary and benefits The Company A leading pharmaceutical company with an exciting pipeline, new offices and great working environment. * Excellent career progression opportunities * Flexible working conditions * International reach The Role Define regulatory strategy for specific therapy areas covering international markets (APAC, LATAM, EAMEA, Japan)...

Salary:
£competitive
Location:
London
Date Posted:
18-Jan-2017
Job Type:
Permanent

Manager, Regulatory Records - Study Start Up (United Kingdom)

Do you want to be a 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...

Salary:
Negotiable
Location:
Camberley
Date Posted:
21-Jan-2017
Job Type:
Permanent

Regulatory/ QA Compliance Specialist

ProClinical has a new vacancy at a pharmaceutical company working in research and development of highly effective and innovative medications. This job vacancy is for a Regulatory/ QA Compliance Specialist to join their team at their offices in Cambridge, UK. The company is one of the industry's most well-known brands and specialises in R&D in 3 major areas; respiratory, oncology...

Salary:
Highly Competitive
Location:
Cambridge
Date Posted:
20-Jan-2017
Job Type:
Permanent

Director Regulatory Affairs CMC, Biosimilars

This is an opportunity for a skilled and experienced Regulatory Affairs and CMC professional to play a pivotal role within an excellent team; ultimately providing access to high quality biologics to more patients all over the globe. You will be working on a first class portfolio and pipeline with particular focus on the fields of oncology and inflammatory disorders. The...

Salary:
negotiable
Location:
Switzerland
Date Posted:
20-Jan-2017
Job Type:
Permanent

Medical Writer (Regulatory)

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. The Phase II-IV Medical Writing group, which is part of the Biostatistics Department, includes Writers who prepare documents in support of clinical trials and who assist...

Salary:
competitive
Location:
Cambridge
Date Posted:
17-Jan-2017
Job Type:
Permanent

Senior Regulatory Manager (Lausanne)

My client is a specialty pharmaceutical company with a focus on development of novel drug candidates. Working in partnership with medium to large pharma they have an enviable record of developing drugs which have high value impact for patients worldwide. They are looking for a Senior Regulatory Affairs Manager to join their team in Lausanne, Switzerland. Job Role and Requirements:...

Salary:
Highly Competitive
Location:
Lausanne
Date Posted:
19-Jan-2017
Job Type:
Permanent

Regulatory Affairs Associate

Regulatory Affairs Associate Greater Boston Area My client is an entrepreneurial mid-sized firm based in the Greater Boston area. They already have 1 highly successful drug on the market, and are making great strides in their new project already. Partnered already with 3 larger firms, there are very strong career prospects, and now is an exciting time to get on...

Salary:
Competitive + Good Company Benefits
Location:
Boston
Date Posted:
19-Jan-2017
Job Type:
Permanent

Regulatory Affairs Submissions Specialist

Regulatory Affairs Submissions Specialist Salary: Negotiable, based on experience Location: Brussels, Belgium Summary Regulatory Affairs Submissions Specialist required to coordinate regulatory submissions within the EMEA region. The successful candidate will be responsible for the planning, review and submission of regulatory documents. Responsibilities * The Regulatory Affairs Submissions Specialist will be responsible for planning, reviewing and coordinating of submissions activities for...

Salary:
Neg
Location:
Brussels
Date Posted:
24-Jan-2017
Job Type:
Permanent

Regulatory Affairs Lead

Regulatory Affairs Lead A fantastic opportunity for an experienced Regulatory Professional to join a global CRO. You will act as Regulatory Lead on Complex Regulatory projects by preparing and reviewing Regulatory submissions to support CTA's and MAA's. All candidates must be eligible to work in the UK. JOB TITLE Regulatory Affairs Lead LOCATION Berkshire BENEFITS Generous Salary Excellent on-going career...

Salary:
£0.00 pa
Location:
Berkshire
Date Posted:
23-Jan-2017
Job Type:
Permanent

Head of Regulatory Affairs - Global New Product Submissions, Generics

This is an exciting opportunity to make a real impact at one of the most important pharma companies in the world through achieving multiple successful new product submissions across the globe. You will lead a fantastic team of motivated Regulatory Professionals (6 directly and a number more on a dotted line) to ensure successful CMC documentation for successful regulatory submissions....

Salary:
negotiable
Location:
Germany, Switzerland
Date Posted:
20-Jan-2017
Job Type:
Permanent

Regulatory Submissions Manager

Regulatory Submissions Manager - Home-based My client, a leading Regulatory Affairs CRO, is looking for an experienced CTA candidate to join their development team as a CTA Submissions Manager. My client works with over 400 global pharmaceutical and biotechnology customers and they need a strong candidate to work co-ordinate and lead CTA Submissions. Candidates must be eligible to work in...

Salary:
£0.00 pa
Location:
England, Home Based
Date Posted:
23-Jan-2017
Job Type:
Permanent

Regulatory Affairs Manager

Edelway is a pan-European Pharma Consultancy. One of our best clients, a global, pharmaceutical company based in Vaud Area, Switzerland and Barcelona Area, Spain is currently looking for experienced Regulatory Affairs Manager. Responsibilities: - Strategy and Execution. - Plans and manages regulatory submissions (e.g. clinical trial and marketing applications) for products within the portfolio in compliance with global filing plans...

Salary:
Competitive
Location:
Canton De Vaud, Barcelona
Date Posted:
20-Jan-2017
Job Type:
Permanent
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