Accessibility Links

Regulatory Affairs Recruitment

The regulation of products and devices is long established but can prove extremely complicated. Regulatory Affairs was established to bridge the gap between government, notified bodies, regulations and Life Sciences companies. Regulatory Affairs
professionals play a vital role as the leading department to provide strategic advice for difficult decisions in a drug or device lifecycle. Regulatory professionals have a core responsibility to; develop and plan which markets to sell a product/ device in, encouraging best practice of current legislation, ensuring product documentation is submitted to the correct relevant authorities and investigating new legislation and guiding through them.

The development of products and devices can often take 10-15 years; Regulatory Affairs ensures that every product and device in the pharmaceutical, biotechnology and medical device industries has the relevant license, patient safety and product efficacy to be brought to market.

Our Regulatory Affairs team is structured to reflect the specialisms within this area and provides clients with superior recruitment services from our global hubs.

Latest jobs

Account Manager
  • Job type: Permanent
  • Location: Paramus, New Jersey
  • Salary: US$85000 - US$105000 per year
  • Description The Account Manager will support the Account Director and Medical team in the development and execution of Promotional Medical Education tactics for HCP audiences.
Senior Medical Writer
  • Job type: Permanent
  • Location: Chicago, Illinois
  • Salary: Negotiable
  • Description A progressive agency is looking for a Senior Medical Writer with a passion for oncology to work remotely.
Quality Assurance Validation Manager
  • Job type: Permanent
  • Location: Charlotte, North Carolina
  • Salary: Targetted Bonus + Excellent Benefits
  • Description Quality Assurance Validation Manager North Carolina Excellent Salary + excellent bonus + excellent benefits An innovative research-based global pharmaceutical company is seeking a QA Validation
Scientist - Contractor
  • Job type: Contract
  • Location: Bridgewater, New Jersey
  • Salary: Competitive
  • Description Scientist - Contractor A global biopharmaceutical company is looking to bring on a scientist/senior scientist to their Analytical Development team in Bridgewater, New Jersey for a 6 month contract
Process Development Scientist
  • Job type: Contract
  • Location: South San Francisco, California
  • Salary: Competitive
  • Description Title: Process Development Scientist Company Summary An exciting biopharma company is looking to bring on a Process Development Scientist on a 6-month contract basis
CSV Engineer
  • Job type: Contract
  • Location: Cambridge, Massachusetts
  • Salary: Negotiable
  • Description EPM Scientific is partnering up with an exciting g industry leader who is looking t expand their CSV team. Do to resent growth and the beginning of new projects, they are seeking a CSV engineer who