Senior Quality Assurance Manager

Company
Synteract
Location
United Kingdom
Salary
Competitive
Posted
26 Jan 2021
Closes
25 Feb 2021
Ref
28932-DR
Hours
Full Time
Contract Type
Permanent
Experience Level
Experienced (non-manager)
Senior Quality Assurance Manager - Remote (Anywhere, UK)

This position can be located anywhere in the UK

Who We Are

Synteract ® , a Syneos Health ® company, is a leading full service Contract Research Organization (CRO) with a successful three-decade track record of supporting emerging biotech and pharmaceutical companies. With our mission of Bringing clinical trials to life TM , we provide customized Phase I through IV services globally, offering expertise across multiple therapeutic areas, including notable depth in oncology, dermatology, general medicine, infectious disease and vaccine, neuroscience, pediatrics, and rare and orphan diseases.

Position Overview

As the Senior Quality Assurance Manager, you will prepare for and participate in, audits and inspections. You will ensure compliance with applicable regulatory requirements including setting of QA targets. You will write QA SOPs and Work Instructions, and ensure compliance with SOP training and utilization, as well as assisting in the creation of study-related quality assurance planning. You will manage a team of 4 in the UK and US.

Specific tasks would include:
  • Supervisory responsibilities include providing guidance, direction and training to select personnel on tasks to be performed as well as timekeeping and performance management responsibilities.
  • Defines audit schedule, approve audit plans and ensure audits are completed on time including reporting and follow up to closure.
  • Conduct, manage, and follow up audits.
  • Author the writing and revision of Controlled Documents.
  • Captures QA metrics; assists in analysis and reporting.
  • Oversight of QA Risk Management Plans for clinical studies.
  • Hosts, facilitates and participates in external audits, facilitates and contributes to audit responses.
  • May participate in the development, review and approval of software validation documentation; ensures QA review of executed validation materials.
  • Ensures feedback questionnaires are issued. Analyzes feedback questionnaire data and issue escalation as appropriate.
  • Manages issue escalation and resolution, ensuring CAPAs are created as needed, followed, and closed.
  • Ensures QA documentation files are maintained.
  • Offers support and training to departments involved in clinical research.
  • As required, assists QA Director with budgeting.
  • Serves as back-up to other QA team members across job functions as needed.
  • Monitors changes in GCP and notifies relevant departments of notable changes.

Qualifications
  • Bachelor's degree in a related field of study and 8+ years' experience, or equivalent combination of studies and relevant work experience inclusive of substantial quality management oversight and 1-2 years experience effectively managing others.
  • Expansive knowledge of Quality Management Systems.
  • Advantageous: passed training in QA Systems according to ISO9001.
  • ICH-GCP body of knowledge and the conduct of clinical trials.
  • Proficiency in Microsoft Word, Excel, and PowerPoint, Outlook.
  • Effective verbal and writing skills; English + local language, if relevant.


If you're passionate about bringing clinical trials to life, we encourage you to apply today!

Synteract's policy is to provide equal employment opportunity and affirmative action in all of its employment practices without regard to race, color, religion, sex, national origin, ancestry, marital status, protected veteran status, age, individuals with disabilities, sexual orientation or gender identity or expression or any other legally protected category. Applicants for positions with Synteract must be legally authorized to work in the country which they are applying and verification of employment eligibility will be required as a condition of hire. The Company will not sponsor applicants [to this position] for work visas.

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