A brand new TA Manager (Life Science/MedComms) role in Marlow offering the chance to join a busy and growing TA team for our client in the healthcare agency space. You will manage a portfolio of vacancies with a focus on recruiting for Medical Writer and Account Manager/Director roles. You will be adept at filling hard-to-fill roles, an ace sourcer, and someone one who relishes the chance to join a busy, growing and vibrant business. Hybrid working available
- New TA Manager role - chance to join a growing TA team in MedComms/Pharma
- Based in Marlow / hybrid working. Recruit for Medical Writers and Account Mgrs
This role is to provide pre clinical expertise to support Medical Writing activities for product lifecycle management and regulatory submissions.
- Excellent opportunity to join a global leading pharmaceutical business
- Great opportunity to be apart of a dynamic team working on exciting projects
This is an exciting opportunity to join a rapidly expanding CRO as QA Manager. My Client is looking for a QA expert to join their small QA team and assist in auditing, regulatory inspections and validation.
- Rapidly expanding CRO, in last 10 years has grown to over 250 staff
- Brilliant benefits on offer from this country
- CDISC data standard experience.
- Based in the UK.
- Opportunities for career progression.
- Work/life balance.
- CDISC data standard experience.
- Based in the UK.
- Opportunities for career progression.
- Work/life balance.
- CDISC data standard experience.
- Based in the UK.
- Opportunities for career progression.
- Work/life balance.
- CDISC data standard experience.
- Based in the UK.
- Opportunities for career progression.
- Work/life balance.
Leads Regulatory Affairs MDR projects with small to medium complexity to develop and commercialize new products for the company
- Fantastic opportunity to be apart of a global Medical Device Business
- Great opportunity to be apart of a dynamic team working on exciting projects
I have an exciting opportunity as Quality Assurance Manager within a Medical Device company in Hampshire. My client is looking for a QMS, GMP and ISO13485 expert to join their rapidly expanding company to manage the quality team and to ensure the company is prepared for all QMS related audits.
- Aid in the development and manufacture of cutting edge medical devices
- Join a growing team
As a Senior Verification Engineer you will be responsible for developing product verification strategies as the business looks to drive innovative and new medical device products to market
- An exciting opportunity to join a leading global medical device business
- Developing cutting-edge medical technologies for global supply
To combine knowledge of scientific, regulatory and business issues to enable products that are developed, manufactured and distributed to meet applicable regulatory requirements and applicable technical standards
- Opportunity to be a part of a global med-tech company
- Excellent career progression opportunities
Project manager within an SME Pharmaceutical, specialising in Early Access Programs. You will be working in a fast-paced environment, leading localised and global projects.
- Rapidly expanding pharmaceutical with great career growth opportunities
- Flexible working
- EAP Senior Project manager in a fast-growing SME.
- Overseeing various Expanded Access studies.
- Flexible working - 3 days at home, 2 days on-site.
- Opportunities for career progression
This role is a great opportunity for someone looking to up skill themselves in project management, working on a global scale influencing clinical operations as well as the study execution team.
- Hybrid project speicalist and Senior CTA role to provide versatility
- Likely extension and competitive hourly rate
Exciting new opportunity to join a fast growing CRO as a Head Of Regulatory Affairs - EAP
- Rapidly Expanding
- Expanded Access Program Experience is Essential
As Regulatory Affairs Specialist you will assist in the preparation and submission of regulatory applications and registrations as assigned including Design Dossier, Technical Files, 510(k)'s, CSDT files annual reports.
- Work with talented and dynamic people
- Excellent career development opportunities
To produce extremely high quality documents from early stage clinical development to marketing authorisation and beyond, for a high calibre, innovative client base.
- A fantastic opportunity to join a high performing, market leading business
- The chance to work remotely and to be involved in high profile projects
The role requires a technically strong commercial thinker who will enjoy an autonomous finance role in a growing life science/tech business with a global presence.
- Market leading business within the Life Science, hybrid working
- Opportunity to join a fast growing business with lots of progression.
- Flexible working - four days at home and one day on-site.
- Health Economics modelling.
- Flexible working - four days at home and one day on-site.
- Health Economics modelling
