QC Supervisor

Company Description

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 is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. Eurofins is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. The Group also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.

In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to 55,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 50 countries. Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.

In 2020, Eurofins generated total revenues of EUR € 5.4 billion, and has been among the best performing stocks in Europe over the past 20 years.

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 QC functions
• Independently investigating team quality deviations and preventing reoccurrences in support of QC operations
• Documenting all training
• Training new employees on GMP related responsibility 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

Leadership Responsibilities

• 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 of responsibilities, and new 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.

  The Ideal Candidate would possess:

• 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

Qualifications

• 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

Additional Information

We have various openings on first, second and t