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  • Job type

    Contract
  • Location

    Uxbridge
  • Working Pattern

    Full-time
  • Specialism

    Regulatory Affairs
  • Industry

    Pharmaceuticals
  • Pay

    Competitive Rates
  • Closing date

    6 Jun 2024

Regulatory CMC Contract | 12 Months

Your new company
Join a leading organisation in the pharmaceutical industry on a 12-month contract. This reputable company operates in either Uxbridge or Cambridge, with the option for remote work. With a focus on global CMC submissions, you'll have the opportunity to work with strict timelines and make a significant impact on the development and marketing of life-changing products.

Your new role
As a Regulatory Affairs Associate (CMC), you'll play a crucial role in supporting the Chemistry, Manufacturing, and Controls (CMC) function. Your responsibilities will include organising and executing regulatory CMC projects and submissions. You'll maintain submission timelines, format documents, schedule meetings, manage reviews, and more. Strong organisational skills, attention to detail, and proficiency in Microsoft Office suite are essential for success in this role. Additionally, your effective communication and interpersonal skills will contribute to successful collaboration with stakeholders.

What you'll need to succeed:
  • Proficient skills in Microsoft Office suite, especially Word, Excel, PowerPoint, and Project
  • Strong organisational skills with attention to detail
  • Excellent time management skills and ability to prioritise workload
  • Project management skills
  • Adept interpersonal and communication skills (both verbal and written)
  • Ability to work both independently and as a member of a team
  • Laboratory background and previous experience in a lab (preferred)

Preferred qualifications:
  • Degree in life sciences, biochemistry, or chemistry
  • Experience in the biopharmaceutical or pharmaceutical industry
  • Familiarity with eCTD structure
  • Motivated with initiative to learn quickly

What you'll get in return
This is an exciting opportunity to work with a renowned organisation in the pharmaceutical industry on a 12-month contract. Additionally, you'll have the chance to enhance your skills and knowledge in CMC and regulatory affairs. The company fosters a supportive and collaborative environment where you can thrive both independently and as part of a team.

What you need to do now
Take the next step in your career and make a significant impact on global CMC submissions. Please click apply now and reach out to Julia Bowden at Hays with any questions.



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