Analytical Sciences Data Review Group Leader

Eurofins•Rensselaer, NY

4h•$29 - $34•Onsite

About The Position

At Eurofins PSS, we partner with leading international companies in the pharma, medical device, food, cosmetic, and consumer products industries, providing mission-critical testing services. For two decades, our global network of teams has served clients directly at their sites across 20 countries. PSS® is a division of Eurofins Scientific, an international life sciences company with over 950 laboratories in 60 countries and approximately 63,000 employees. Eurofins fosters a meritocratic environment where individuals are empowered to make decisions and are rewarded for their achievements, facilitating rapid career advancement. The Analytical Sciences Data Review Group Leader is responsible for overseeing the review of GMP data, managing a team, and ensuring compliance with established procedures.

Requirements

Bachelor’s Degree (BS) in Chemistry, Life Sciences, or other science-related equivalent
2 years of cGMP experience
2 years of leadership experience
Experience with HPLC/UPLC and UV-Vis Spectrometer instrumentation
Experience with ELISA, MCE, and/or iCIEF techniques
Experience with processing quantitative liquid chromatography data
Strong computer and organizational skills
Excellent communication (oral and written) and attention to detail
A strong integrity and work ethic
A strong work ethic and ability to meet physical demands including, but not limited to, routinely lifting objects of 25 lbs. or more, walking and standing for extended periods of time, pushing or pulling carts and equipment and bending down or reaching for supplies
Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude
Ability to learn new processes, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies
Authorization to work in the United States indefinitely without restriction or sponsorship

Responsibilities

Review of GMP data generated by testing personnel for compliance to governing procedures
Review of logbook entries for completeness and correctness
Confirmation of chain of custody integrity for samples tested
Review of audit trails to confirm adherence to actions executed and any timelines outlined in governing procedures
Timely and efficient communication with testing personnel to address any annotations or corrections needed to ensure compliance with governing procedures
Use of GDP to record activities in logbooks, laboratory notebooks, and electronic systems
Laboratory safety and compliance walkthroughs with documentation of any observations
Completion of all safety and procedural trainings and re-training
Personnel management and development
Manages and coordinates the team's workload
Management of the cross-training and capacity of the team
Monitors and reports all productivity and quality metrics
Proactive and effective communication with client and customer teams
Completes routine laboratory safety walkthroughs and employee compliance checks
Participate in the hiring process and onboarding/training of new hires
Delivers training for new hires and other employees in the department
Participates in overtime and weekend scheduling as required