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LondonPermanent£65,000 - £85,000All encompassing- but the CSV expert will primarily be responsible for a number of projects requiring validation work in a GMP environment.
The opportunity to be part of an amazing, fast growth, entrepreneurial business
The opportunity to influence decision making and drive growth.
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SloughPermanentWorking collaboratively with the relevant Global and country teams to establish and implement the regulatory strategies within agreed timescales to bring competitive advantage to RB brands.
Manage/ oversee regulatory strategies and the preparation of regulatory documents targeted at the UK Market.
Join a global blue-chip brand with unrivalled opportunity
Utilise your regulatory knowledge in the biocides space
Save job View job - OxfordTemporary£18,000 - £21,000
With significant direction from a Technician II/Scientist I you will take responsibility for preparing and conducting of T-SPOT.
Operate as a scientist in routine testing, ensuring that the Quality Management System, including ISO 9001:2008, ISO 13485:2003, and ISO 17025:2005, is adhered to at all times and in all aspects of the job6 month contract....Possibly suit a recent science graduate
With supervision you will be preparing and conducting of T-SPOT
Save job View job - BasingstokeTemporary
Execute product regulatory submissions, converting/creating medical device technical documentation according to the requirements of the regulations applicable to the UK.
Implement the Quality Management System so that it aligns with the corporate QMS system and reflects that the UK has left the EU.12 month contract based near Basingstoke
UK MDR QMS Quality Management Systems Auditing
Save job View job - CambridgePermanent
This is a fantastic opportunity for a regulatory professional to boost their career in a rapidly expanding Regulatory team.
Rapidly expanding Pharmaceutical company.
Sunday Times 10 Tech Track ones to Watch 2020
Save job View job - HertfordshirePermanent
An opportunity has arisen in the QA department for a QA professional to join this well established organisation.
work in a first class manufacturing facility
Join a remarkable healthcare group
Save job View job - EnglandPermanent
Exciting Opportunity to join a international and growing pharmaceutical business as an Account Director - Early Phase.
Must Have Early Phase Experience
Home Working
Save job View job - LondonPermanent£30,000 - £70,000
Exciting opportunity to join a global growing pharmaceutical business as a Regulatory Affairs - Publishing Manager.
Must have Publishing Experience
Growing Global Pharmaceutical Experience
Save job View job - LiverpoolTemporary£17 - £23 per hour
Looking for Experience working in Secondary (Fill/Finish) and/or aseptic operations
12 month contract in Liverpool for a QA Associate12 month contract - Liverpool based
Need experience working in Secondary (Fill/Finish) and/or aseptic operations
Save job View job - EnglandPermanent
Exciting opportunity to join a global medical device company as a Senior Regulatory Affairs Manager - Medical Devices . The role involves managing 3 direct reports.
Global Medical Device Business
Must have line management experience
Save job View job - MaidenheadTemporary
12 month contract for an already experienced Global Clinical Study Director
Strong development pipeline and possibility to lead Phase 2 and support on Phase 3 trials for an experienced Global Clinical Study Director12 month contract for a Global Clinical Study Director
You must have already operated at Director level
Save job View job - Alderley EdgePermanent£50,000 - £55,000
The Data Scientist NLP position will provide the Text Analytics Data Scientist with the opportunity to develop systems that enable the analysis and interpretation of large-scale, complex and time specific datasets. This member of the team will need an understanding of how to develop efficient text-mining and analytics solutions in our privacy conscious and commercially sensitive setting.
Opportunity to work on Google size amounts of raw data
Opportunity to tinker with latest NLP techniques
Save job View job - CambridgePermanent£100,000 - £110,000
Managing external suppliers to ensure that Pharmaceutical R&D projects run effectively and efficiently.
A fantastic opportunity to manage a portfolio of cutting edge R&D providers
An opportunity to work with the very best!
Save job View job - LiverpoolTemporary
To co-ordinate the validation activities within the production facilities at Liverpool to ensure that the appropriate site and regulatory standards are applied and work is completed in a timely manner.
To perform accurate and reliable laboratory tests and generate, report and approve results to cGMP standard, in accordance with current company requirements and SOPs.6 month contract based in Liverpool
Experience needed: Validation of lab computerized equipment
Save job View job - ColchesterPermanent
In this role you will lead the quality activities in GLP environment, establish goal and maintain the Quality standard
Well established Research & Development Organization
Provide QA leadership in GLP environment
Save job View job - EnglandPermanent
Exiting opportunity to join a rapdly expanding BiotechEmerging Biotech
life science background essential
Save job View job - OxfordPermanent£35,000 - £45,000
You'll be driving the industrialisation of new projects, and improving existing production lines for a technology-led medical devices company. As a Manufacturing Engineer, you'll work alongside more experienced team members to source equipment, train operators, and drive efficiencies.
You'll be at the forefront of the medical device sector
Many of the current leadership team have progressed through the company
Save job View job - Burton-On-TrentPermanent
You'll be QA Manager for a solid-dose pharmaceuticals manufacturing SME, leading a team responsible for general QMS activity. Your team will have eight QA specialists, and you'll be tasked with coaching and developing them to ensure they become future stars in the industry, as well as growing your own career by taking on more responsibility.
Be a key player in an SME pharmaceuticals manufacturer
Grow your career - take the next step and keep developing
Save job View job - South East EnglandPermanent£90,000 - £150,000
To be the Qualified Person - Quality Manager.
To set up a first class QMS to safeguard end users.A
An opportunity to create, own and run with a Quality Management System
Save job View job - High WycombeTemporary
Be the Key strategic partner to the Commercial Lead shaping the 3-5 year therapy area strategy.
Contract roleLead/support the development of the market access strategy for new products
Deliver the market access plan for our new products
Save job View job - OxfordTemporary£400 - £450 per day
A Principal Medical Writer role in an innovative business
An opportunity to work with the very best on cutting edge therapies.A Principal Medical Writer role in an innovative business
6 month contract, likely to extend
Save job View job - CardiffTemporary£56,000 - £56,100
Based in Cardiff you will lead a multi-partner, research and development programme jointly funded by the Welsh Government and the European Union through the European Regional Development Fund.
This role represents a unique and exciting opportunity to lead a £23.5 million programme that is helping to advance the development and adoption of innovative solutions for better health and wellbeing.Opportunity to provide strategic oversight and direction to the programme
Part time role, 15 hours per week, based in Cardiff.
Save job View job - LondonPermanent£60,000 - £70,000
To produce high quality, scientifically accurate, client focused content across a variety of innovative and traditional platforms.
A Principal Medical Writer role in an innovative business
An opportunity to work with the very best on cutting edge therapies.
Save job View job - EnglandPermanent
Exciting opportunity has arisen for a Business and Competitive Intelligence specialist to join a growing pharmaceutical business.
Must have pharmaceutical experience
Remote Based
Save job View job - CambridgeTemporary
Biomedical Scientists Band 6 - Histopathology
Lab based -contract roleInterim Biomedical scientist Contract role
Pathology Experience Essential
Save job View job - MaidenheadTemporary
Veeva Submissions Vault system implementation.
Looking for experience with Veeva - validation, training and testing.Veeva Systems Implementation Project
6 month contract +
Save job View job - OxfordshirePermanent£55,000 - £65,000
You'll be driving the industrialisation of new projects, and improving existing production lines for a technology-led medical devices company. As a Senior Production Engineer, you'll naturally set the pace and culture in the engineering team for the more junior members to follow.
You'll be at the forefront of the medical device sector
Many of the current leadership team have progressed through the company
Save job View job - LondonPermanent£75,000 - £90,000
To own, develop and manage premium medical content in hematology and oncology.
A high profile role with an innovative medical content provider
An opportunity to work with global experts in Oncology and Hematology
Save job View job - BedfordshirePermanent
Very exciting opportunity for a Regulatory Affairs Associate to join a high growth and ambitious pharmaceutical business.
Rapidly Expanding Pharmecutical Company
Times Tech Track 100 Company
Save job View job - LondonPermanent
Exciting opportunity to join the global regulatory affairs team as the Senior Regulatory Affairs Manager.
Global Pharmacetuical Company
Must have pre and post approval experience
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