The
Clinical Laboratory Supervisor is responsible for overseeing the day-to-day testing activities in the Diagnostic Services' CLIA accredited Clinical Testing Laboratory. This includes supervision of high complexity molecular testing within global clinical trials, management of scientific staff and accurate reporting of test results across a wide range of technology areas. The post holder will drive continuous improvement and support a culture of scientific integrity and patient care.
SHIFT Sun-Wed or Wed-Sat
Responsibilities include but are not limited to:
- Provide day-to-day supervision of testing personnel and reporting of test results within the high complexity Clinical Testing Laboratory
- Coordinate the activities of junior team members to ensure the completion of clinical testing within agreed timeframes
- Monitor specimen examinations and test analyses to ensure that acceptable levels of analytic performance are maintained at all times.
- Responsible for the generation, revision, and/or review of laboratory or equipment-related SOPs and other quality documents
- Perform molecular biological techniques adhering to the laboratory's quality control policies.
- Ensure that all remedial actions are taken in a timely manner whenever test systems deviate from the laboratory's established performance specifications and leadership is notified as required.
- Be accessible to testing personnel at all times testing is performed to provide on-site, telephone or electronic consultation to resolve technical problems in accordance with policies and procedures.
- Monitor batch manufacturing stock levels and coordinate ordering and testing of new reagent and control batches to ensure adequate supply for clinical testing. Verify reagents, consumables, and laboratory equipment are qualified for use and within expiry.
Required Requirements:
- B.S. in chemical, biological, medical, clinical laboratory science, or medical technology from an accredited institution
- B.S. or MS degree, with 4+ years of training/experience in at least one of the following technologies: qPCR, Nanostring, and/or NGS, OR
- Ph.D., with 1+ year of training/experience in at least one of the following technologies: qPCR, Nanostring, and/or NGS
Preferred Requirements:
- M.S. in chemical, biological, medical, clinical laboratory science, or medical technology from an accredited institution or Ph.D. in chemical, biological, medical, clinical laboratory science, or medical technology from an accredited institution
- ASCP Board Certification as a Specialist in Molecular Biology
- Excellent oral and written communication skills
- Attention to detail
- Experience in a high complexity CLIA testing environment
- Experience with data analysis and reporting of results in at least one of the following technologies: qPCR, Nanostring, and/or NGS
- Substantial experience in troubleshooting molecular laboratory techniques
- Experience preparing for/participating in laboratory audits, from CAP and other regulatory agencies
What can Almac Group offer you? - Medical, Vision & Dental benefits from the 1st of the month following start date
- 20 days PTO per year, accrued monthly following start date
- 12 holidays per year as well as one day for Annual Diversity Day
- Company paid Long and Short-term disability along with Life Insurance
- 401k company contribution
- Professional development programs/ continuous learning opportunities
Want to see our latest job opportunities? Follow us on LinkedInRECRUITMENT AGENCIES PLEASE NOTE: Almac will only accept applications from agencies/business partners that have been invited to work on this role through our portal. Candidate Resumes/CV's not submitted through our portal or directly to Hiring Managers will be considered unsolicited and no fee will be payable. Thank you for your cooperation.
