Process Sciences Supervisor at Eurofins Lancaster Laboratories Professional Scientific Services, LLC in Rensselaer, New York

Job Description:

Company Description



The work we do at Eurofins matters, and so do our employees. At Eurofins, we put a focus on your professional growth. We provide our employees the ability to break into the biopharmaceutical industry and grow from the bottom up. We have the supportive teams and tools available to invest in you while also affording you work-life balance and a competitive benefits package.


Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies.


If you're looking for a rewarding career, apply with us today!



Job Description




Technical Responsibilities

• Ability to work independently and as part of a team in a client facing environment.


• Self-motivated, adaptable, and a positive attitude


• Excellent communication (oral and written) and attention to detail


• Communicating findings and recommendations at group meetings


• Participating in and/or leading cross-functional teams to support optimal client services


• Gathering, trending, and analyzing performance related data to drive consistency and timeliness in multiple teams supporting Process Sciences Laboratory functions


• Independently investigating team quality events and preventing reoccurrences in support of Process Sciences operations


• Documenting all training


• Training new employees on related lab responsibilities relevant to the supervised functional areas


• May support reviewing, editing, and revising controlled documents (batch records, logbooks, SOPs, etc.) in accordance with cGMP standards to ensure compliance with written procedures

• Leading direct reports, group leaders and their teams, and serving clients in technical settings, such as laboratories or manufacturing facilities


• Disseminate administrative communications


• Demonstrate and promote the company vision


• Proactively plan and multitask to maximize productivity


• Capture and meet all quality and productivity metrics, and demonstrate strong teamwork and collaboration


• Coordinate scheduling, allocation ofresponsibilities, andnew hire on-boarding process


• Coordinates training program


• Development of teambuilding strategies and initiatives


• Continuous improvement of operational excellence


• Support group leader professional development


• Coordinating and participating with candidate interviews


• Performs peer review of data.

• Scientific background with hands on laboratory experience


• Strong leadership skills


• A good understanding of day-to-day business operations


• Demonstrate strong client service skills, teamwork, and collaboration


• Strong computer, scientific, and organizational skills


• Excellent communication (oral and written) and attention to detail


• Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude


• Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies

• Bachelor's degree in Life Sciences, Chemistry, or related field. Other degrees may be considered with relevant experience.


• 2+ years of experience in a cGMP setting


• 2+ years of previous dynamic team leadership experience


• Understanding of biologics manufacturing operations


• Organized and have a strong attention to detail


• Can prioritize multiple assignments and changing priorities


• Ability to learn and utilize computerized systems for daily performance of tasks

• 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


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