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Quality Assurance Assistant

Reed
Posted 7 days ago, valid for 13 days
Location

Cambridge, Cambridgeshire CB2 8AG, England

Salary

£24,000 - £28,800 per annum

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Contract type

Full Time

In order to submit this application, a Reed account will be created for you. As such, in addition to applying for this job, you will be signed up to all Reed’s services as part of the process. By submitting this application, you agree to Reed’s Terms and Conditions and acknowledge that your personal data will be transferred to Reed and processed by them in accordance with their Privacy Policy.

Sonic Summary

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  • The Regulatory and Product Support Assistant position is a hybrid role based in Cambridge, requiring attendance at the site.
  • The job entails managing documentation, assisting with regulatory submissions, and performing administrative tasks to ensure compliance and support product activities.
  • Candidates must have a Bachelor's degree in a Life Science field and at least 2 years of experience in a regulatory, compliance, or product support environment.
  • The salary for this role is competitive and dependent on the candidate's experience.
  • Key skills required include strong organizational abilities, proficiency in Microsoft Office, and excellent communication skills.

Regulatory and Product Support Assistant

Location: Hybrid – need to be able to attend Cambridge siteHours: 37.5 hours per weekSalary: Competitive and will depend on experience 

Reed Scientific have partnered with an industry leading Biotech at the forefront of diabetes research. My client has an immediate requirement for someone to support the regulatory and product compliance functions. You will manage documentation, assist with regulatory submissions, and perform administrative tasks to ensure smooth operations including maintaining compliance with relevant regulations and support product-related activities.

Key Responsibilities

  • Regulatory Support:
    • Prepare and submit regulatory documents, including applications, registrations, and reports, and maintaining an organized and up-to-date database of regulatory documents, approvals, and correspondence.
  • Administrative Tasks:
    • Draft and format regulatory documents, letters, and other correspondence.
  • Product Support:
    • Provide technical support to external partners and customers by responding to inquiries or complaints in line with regulatory guidelines.

Qualifications and Experience

  • Bachelor’s degree in a Life Science related field
  • 2 years of experience in a regulatory, compliance, or product support environment, with a basic understanding of regulatory requirements for medical device software development (e.g., ISO 13485).
  • Strong organizational skills and attention to detail.
  • Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint) and document management systems.
  • Excellent communication skills, both written and verbal.

If you are passionate about making a difference in the field of diabetes management and meet the qualifications, please follow the link to apply.

Apply now in a few quick clicks

In order to submit this application, a Reed account will be created for you. As such, in addition to applying for this job, you will be signed up to all Reed’s services as part of the process. By submitting this application, you agree to Reed’s Terms and Conditions and acknowledge that your personal data will be transferred to Reed and processed by them in accordance with their Privacy Policy.