Analytical Sciences Data Review Group Leader

Eurofins USA PSS Insourcing Solutions • Rensselaer, NY

1d • Onsite

About The Position

At Eurofins PSS, we work with leading international companies across the pharma, medical device, food, cosmetic & consumer products industries - who all trust us with their mission-critical testing. For 20 years, our international network of teams have served clients at their sites, across 20 countries. PSS® is part of Eurofins Scientific, an international life sciences company, providing a unique range of analytical testing services across multiple industries, through a network of over 950 laboratories in 60 countries, and c.a. 63,000 employees. Life at Eurofins is a meritocracy, where people are empowered to make decisions and are rewarded for their success, allowing them to advance quickly. Become your most extraordinary self with support and development throughout your career. The Analytical Sciences Data Review Group Leader is responsible for reviewing GMP data generated by testing personnel for compliance to governing procedures, managing and coordinating the team's workload, and ensuring timely communication with clients and customer teams.

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

Benefits

• Excellent full-time benefits, including comprehensive medical coverage, dental, and vision options
• Life and disability insurance
• 401(k) with company match
• Paid vacation and holidays

What This Job Offers

• Job Type: Full-time
• Career Level: Manager
• Number of Employees: 5,001-10,000 employees