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Regulatory-affairs Jobs
Find regulatory-affairs jobs from top employers and recruitment agencies on Just4Medical.co.uk. Search and apply now, or join for the very latest Jobs by Email. |
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» Your search returned 262 jobs. Showing page 1 of 11 pages.
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Content: regulatory affairs
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Clinical Project Manager (Medical Devices)
Home Based with regular office presence in Kent (UK) required
£85,000 DOE + Bonus + Pension
Our client, an established international medical device specialist, is recruiting for an experienced Clinical Project Manager (Medical Devices).
The ideal candidate will have expertise .. |
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Location:
Kent, Kent
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Hours:
Full Time
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Salary:
£80000 - £85000/annum Bonus
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Regulatory CMC Manager
I am looking for a CMC regulatory specialist for Drug/Device production
So if you have worked with regulatory CMC and drug-device combo product and would like to work with a rapidly growing company, then this is your chance!
I am working with a growing Biotech company there is rapidly scaling up for lau.. |
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Location:
Copenhagen, Copenhagen
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Hours:
Full Time
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Salary:
£75546 - £83940/annum
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Regulatory Affairs Director – Biologics/ATMP - Leading Consultancy
Nonstop Pharma are representing a Regulatory Consultancy Company who is seeking to appoint a Regulatory Affairs Director who has strong experience of working on Biologics or ATMPs. You will be working for a consultancy who is dedicated to providing high qu.. |
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Location:
Essex, Essex
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Hours:
Full Time
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Salary:
£60000 - £110000/annum Additional Benefits
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QUALITY ASSURANCE AND COMPLIANCE MANAGER – CRO / LIFE SCIENCES / BIOTECH / PHARMA
BASED BALLINA – COUNTY MAYO - WEST COAST OF IRELAND
BASE SALARY 65-80,000 EUROS PLUS BENEFITS (INC RELOCATION)
With major sites across Europe, ESS Recruits client has built a global CRO company uniquely designed to meet the .. |
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Location:
Ireland, Ireland
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Hours:
Full Time
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Salary:
£65000 - £80000/annum 65-80,000 EUROS PLUS BENEFITS (INC R
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Regulatory CMC VP, Director and Associate Director for BioPharma.
I am looking for a VP, director and Associate director of Biopharma production.
So if you have worked Biologics CMC Regulatory and is looking for a step up, then this is your chance. I got positions in Denmark, Switzerland and Ireland right now, with more oppor.. |
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Location:
Limerick, Limerick
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Hours:
Full Time
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Salary:
£75546 - £135143/annum
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Quality Manager - Medical Devices/Pharma/Life sciences/Healthcare
Salary £Excellent + 10% Bonus (£7K) + Shares + Car
Our client is looking for a permanent Quality Manager to be based at their headquarters near Warwick and Birmingham. Reporting to the Director of Quality and Regulatory Affairs, our client is looking .. |
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Location:
Warwick, Warwickshire, Warwick, Warwickshire
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Hours:
Full Time
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Salary:
£70000 - £73000/annum (DOE) + Bonus + Shares + Benefits
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Are you a Senior Regulatory professional with an in depth understanding of the drug development process? Do you have exposure to Phase I and Phase II trials? Would you like to work in a consultancy environment working across a number of projects, helping shape the direction of the organisation? Please get in contact for a confid.. |
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Location:
Cambridgeshire, Cambridgeshire
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Hours:
Full Time
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Salary:
£70000 - £90000/annum
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Blackfield Associates are currently partnered with a market leading Medical Device organisation based in East Switzerland. Our client is looking for a Regulatory Manager to manage a small team within their regulatory affairs department.
As a Regulatory Affairs Manager you will be responsible for preparation of technical documen.. |
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Location:
Switzerland, Switzerland
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Hours:
Full Time
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Salary:
£92472 - £107884/annum
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PAY RATE AS REQUIRED.
Order Number: PAD68201
Position: CMC OTC Regulatory Affairs
CMC Post Marketing Support
Location: Egham, TW20 9NW
Duration: Initialy 12 months
Hourly Rate: On Application
This role supports the FMCG Client Central Regulatory Affairs Group.
* The role provides regulatory support for our clients mark.. |
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Location:
TW20, Egham, Surrey, TW20, Egham, Surrey
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Hours:
Full Time
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Salary:
£99999/annum Salary As Required by candidate
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Order Number:68201
Position:CMC OTC Regulatory Affairs
CMC Post Marketing Support
Location:Egham
Duration:Approx. 12 months
Hourly Rate:On Application
This role supports the FMCG Client Central Regulatory Affairs Group.
·The role provides regulatory support for our clients marketed OTC products in the Health Care G.. |
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Location:
Egham, Surrey, Egham, Surrey
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Hours:
Full Time
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A new opportunity has arisen with a market-leading Healthcare company working as a Senior Pharmacovigilance Manager. They are seeking an experienced and dynamic individual to take on this role based at their head office in Berkshire working closely alongside the team in the UK. The successful candidate will be responsible for en.. |
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Location:
Reading, Berkshire
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Hours:
Full Time
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Our client, a medical device manufacturer requires a Chief or Director of Quality & Regulatory Affairs (QARA) who will be responsible for developing, implementing and maintaining a Quality and Regulatory strategy and for ensuring Regulatory Compliance in the company’s chosen markets and all other future expansion marke.. |
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Location:
Birmingham, West Midlands (County), Birmingham, West Midlands (County)
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Hours:
Full Time
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Regulatory Affairs Specialist
Medical Devices – High Wycombe
£35,000 - £45,000
Our client is a fast growing Medical Device company that is going through rapid year and year growth.
They have developed a ground breaking product that has endless medical applications and a constant growth of clinical data to back .. |
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Location:
High Wycombe, Buckinghamshire
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Hours:
Full Time
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Salary:
£35000 - £50000/annum
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Nursing Home Manager Job Specification - Nursing Home Manager; To take joint responsibility with the operations manager as the person-in-charge for the dayto- day running of the home. To take full professional accountability in respect of the clinical management of the home. To promote a caring environment for service users thro.. |
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Location:
Weymouth, Dorset, Weymouth, Dorset
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Hours:
Full Time
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Salary:
£55000 - £65000/annum
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Arevna Partners are currently seeking a Regulatory Specialists to support a Global Medical Device client based in Switzerland. The role will require compliance to the European Medical Device Regulation (MDR) ensuring the continuation of supply post EU MDR implementation.
The successful Regulatory Specialist will need to meet th.. |
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Location:
Switzerland, Switzerland
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Hours:
Full Time
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Salary:
£90000 - £100000/annum
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Polytec are looking for a highly experienced Senior Development Project Manager on behalf of our South Cambridgeshire based, Biotechnology client. The successful candidate will take full responsibility for the co-ordination, planning and management of our client's development-stage programmes to ensure they are delivered on .. |
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Location:
Cambridge, Cambridge
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Hours:
Full Time
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Order Number: 68201
Position: CMC OTC Regulatory Affairs
CMC Post Marketing Support
Location: Egham
Duration: Approx. 12 months
Hourly Rate: On Application - Please quote hourly rate required.
This role supports the FMCG Client Central Regulatory Affairs Group.
* The role provides regulatory support for our clients mark.. |
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Location:
Egham, Surrey, Egham, Surrey
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Hours:
Full Time
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I am currently working with a Medical Device company based in Gloucestershire who are looking for a permanent RA Specialist to join the team.
The RA Specialist will ideally have at least 2 years’ experience working within the Medical Devices industry and have a strong understanding of Clinical Studies.
The RA Specialist .. |
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Location:
Gloucestershire, Gloucestershire
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Hours:
Full Time
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Salary:
£35000 - £40000/annum £35k - 40k per year
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Medical Writer-Flexible Hour Contract-Oxford, UK
Start date: ASAP, but we will look at those wishing to start from September 2018
NonStop Recruitment are looking for an immediate need as a medical writer searching for their next consultant mission. Our client have just won some exciting new projects and due to this have an exc.. |
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Location:
Oxford, Oxford
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Hours:
Full Time
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Salary:
£300 - £400/day
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This is an exciting new instruction for an EMEA Product Registration Associate with a key client in the area.
The role is being presented on a long-term contract basis and is likely to run for up to 12 months.
Applications are therefore invited from individuals with a regulatory background who have perhaps previously worked wi.. |
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Location:
Folkestone, Kent
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Hours:
Full Time
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Role Title: Quality Officer
Employment Type: Permanent
Location: North West of the UK
Role Summary.
* My Client are a Pharmaceutical Company, who are looking for a Quality Officer to complete their team
Role Responsibilities
* Complete tasks handed out via management
* Work via GMP Regulations
* Complete SOP’s c.. |
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Location:
Cheshire, Cheshire
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Hours:
Full Time
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Salary:
£35000/annum
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Our client is an established Pharmaceutical Manufacturing business. They are looking to recruit a Data Integrity and Validation Officer to join the team on a permanent basis.
This position will be responsible for ensuring the business operates under applicable regulatory policies for documentation and data integrity/guidelines .. |
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Location:
Wiltshire, Wiltshire
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Hours:
Full Time
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Salary:
£65000 - £70000/annum
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Chase Resourcing are delighted to announce that we are looking for a Business Unit Manager for one of our clients based in Galway.
The successful candidate will have responsibility and leadership for overall operation of a Business Unit. Implements systems and strategies to ensure a safe work environment, maximize profitable gr.. |
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Location:
Ireland, Ireland
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Hours:
Full Time
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This role supports our clients Central Regulatory Affairs Group in Egham. The role provides regulatory support for their marketed OTC products in the Health Care.
Our client has a highly successful global health care business and the job will require liaising with local RA managers and / or consultants in regulatory affairs dep.. |
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Location:
TW20, Egham, Surrey, TW20, Egham, Surrey
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Hours:
Full Time
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Salary:
£33 - £50/hour PAYE Only. No ltd or umbrella
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Director of Quality – Pharma
Please note, you must be from a pharmaceutical background, and have worked in a Director level role within the pharmaceutical environment to be considered.
Purpose of the role: -
* To drive the Quality function with a determination to deliver excellence in all aspects of company operations.. |
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Location:
NP22, Nant-y-bwch, Blaenau Gwent, NP22, Nant-y-bwch, Blaenau Gwent
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Hours:
Full Time
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chatham , Kent
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