Quality Assurance Manager (Clinical Diagnostic)
- Employer
- Labcorp
- Location
- Shardlow, United Kingdom
- Salary
- Competitive
- Start date
- 23 Mar 2021
- Closing date
- 21 Apr 2021
View more
- Discipline
- Quality, QA / QC
- Hours
- Full Time
- Contract Type
- Permanent
- Experience Level
- Experienced (non-manager)
Job Details
Covance by Labcorp is looking to hire a QA Manager, with Clinical Diagnostis experience to join our expending team in our new site in Shardlow.
The main responsabilities will be:
- Manage ISO 15189 accredidation
- Ensure appropriately trained resources are available, whilst providing guidance and consultation for the team, in order to make sure that tasks are completed according to procedural requirements
- Ensure the consistent implementation, use and review of SOPs
- Escalate issues to management in a timely manner, implementing appropriate solutions including preventative actions
- Negotiate with functional and operational internal stakeholders to improve quality and increase efficiencies
- Analyse and interpret data in order to lead functional process improvement initiatives to drive efficiencies and effectiveness of Regulatory Compliance & Quality Assurance (RC&QA) processes
- Lead and effectively manage constructive crucial interactions with clients or regulatory agencies
- Lead functional process improvement initiatives to drive efficiencies and effectiveness of Regulatory Compliance & Quality Assurance (RC&QA) processes
- Interpret applicable quality regulations/standards and create appropriate policies and procedures
- Lead interactions with clients or regulatory agencies
- Recruit, train, coach and develop individuals based on their development or business needs
- Complete thorough, timely and well documented performance evaluations providing objective feedback to the individual
- Ensure Regulatory Compliance and Quality Assurance (RC&QA) management responsibilities, as indicated in applicable controlled documents, are followed
- Perform other duties, as assigned by management
Education/Qualifications:
- A minimum of a Bachelor's Degree in Life Sciences preferred (or equivalent Life Science experience)
- Experience may be substituted for education.
- 5 to 8 years in regulatory environment (ISO 15189), with Clinical diagnostics experience
- Experience & regulatory expertise of industry quality systems/standards
- Ability to interpret applicable regulations/standards
- Experience in leading process improvement initiatives
- Ability to communicate and negotiate internal stakeholders effectively
- Ability to supervise resources in a single geographic location
Company
At Labcorp, we believe in the power of science to change lives. We are a leading global life sciences company that delivers answers for crucial health questions —because we know that knowledge has the potential to make life better for all. Through our unparalleled diagnostics and drug development capabilities, we provide insights and accelerate innovations that not only empower patients and providers but help medical, biotech, and pharmaceutical companies transform ideas into innovations. Here, you can join our more than 70,000 employees, serving clients in more than 100 countries, as we work together to make a real impact on people’s lives. Join us in our pursuit of answers.
- Website
- https://careers.labcorp.com/global/en
- Location
-
Maidenhead Office Park
Westacott Way
Littlewick Green
Maidenhead
SL6 3QH
United Kingdom
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