NCBiotech
Almac Group is a group of established businesses at the forefront of the Pharmaceutical industry. Our Company is a recognized global knowledge-based leader for the research, development and delivery of pharmaceutical services. Almac Group's services extend from drug discovery through all areas of clinical trials to the commercialization of pharmaceutical products. Our commitment to Discovery, Development and Delivery in conjunction with our long term partnerships with the majority of the world’s leading pharmaceuticals guarantees a secure future for everyone.
Clinical Laboratory Supervisor Position Overview:
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:
7‑day rotation: Sunday‑Wednesday or Wednesday‑Saturday
Responsibilities
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 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, or clinical laboratory science, or medical technology from an accredited institution
B.S. or M.S. 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. or Ph.D. in chemical, biological, medical, or 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
401(k) company contribution
Professional development programs/ continuous learning opportunities
Company Information Almac is an exceptional, award‑winning, drug development solutions provider at the forefront of the pharmaceutical industry. We are a privately owned organization that has organically grown over 50 years now employing over 7,500 highly skilled personnel worldwide. Our US Headquarters is located at Souderton, PA with additional operations scattered around the US and Europe. ‘Partnering to Advance Human Health’ is more than just a tagline – it is our way of life.
Embracing diversity is at the heart of enhancing Almac Group’s unique culture and reflects our fundamental belief that all people deserve equality, inclusivity and the opportunity for advancement. We are committed to cultivating a welcoming, supportive, and inclusive environment for all. Together, we will build on the strength in our diversity and deliver exceptional solutions to advance human health globally.
Almac Group, Inc.
is an Equal Opportunity Employer
– Minorities, Women, Protected Veterans, Disabled – Proudly embracing diversity in all of its expressions.
Almac provides reasonable accommodations to people with disabilities who need assistance completing the application process. Please email us at ADARequest@almacgroup.com to request assistance.
#J-18808-Ljbffr
Clinical Laboratory Supervisor Position Overview:
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:
7‑day rotation: Sunday‑Wednesday or Wednesday‑Saturday
Responsibilities
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 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, or clinical laboratory science, or medical technology from an accredited institution
B.S. or M.S. 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. or Ph.D. in chemical, biological, medical, or 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
401(k) company contribution
Professional development programs/ continuous learning opportunities
Company Information Almac is an exceptional, award‑winning, drug development solutions provider at the forefront of the pharmaceutical industry. We are a privately owned organization that has organically grown over 50 years now employing over 7,500 highly skilled personnel worldwide. Our US Headquarters is located at Souderton, PA with additional operations scattered around the US and Europe. ‘Partnering to Advance Human Health’ is more than just a tagline – it is our way of life.
Embracing diversity is at the heart of enhancing Almac Group’s unique culture and reflects our fundamental belief that all people deserve equality, inclusivity and the opportunity for advancement. We are committed to cultivating a welcoming, supportive, and inclusive environment for all. Together, we will build on the strength in our diversity and deliver exceptional solutions to advance human health globally.
Almac Group, Inc.
is an Equal Opportunity Employer
– Minorities, Women, Protected Veterans, Disabled – Proudly embracing diversity in all of its expressions.
Almac provides reasonable accommodations to people with disabilities who need assistance completing the application process. Please email us at ADARequest@almacgroup.com to request assistance.
#J-18808-Ljbffr