Senior Manager, Medical Device Package Testing at Eurofins

Lancaster, Pennsylvania, United States -

Full Time

Start Date

Immediate

Expiry Date

13 Jan, 26

Salary

0.0

Posted On

15 Oct, 25

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

GMP, GLP, Quality Assurance, Inventory Management, Personnel Management, Technical Communication, Problem Solving, LEAN Initiatives, Client Confidentiality, Performance Evaluation, Training and Development, Data Review, SOP Preparation, Project Management, P&L Assessment, Conflict Resolution

Industry

Medical and Diagnostic Laboratories

Description

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 laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. It 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. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products. In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. Job Description Applies GMP/GLP in all areas of responsibility, as appropriate Demonstrates and promotes the company vision Regular attendance and punctuality Ensure that the quality policy program is understood, implemented, and maintained; identify, prevent, or correct any departures from the quality system Oversee inventory, maintenance and repair of departmental instruments, tools, equipment, materials and/or products Utilize the MOS to track key performance indicators and drive continuous improvement Manage scheduling of personnel; evaluate personnel performance Participate in interview process, make recommendations for new hires; oversee training and development of staff Ensure department maintains client confidentiality Review, prepare, and approve methods, data, and SOP’s Continually evaluate systems and processes to help improve overall productivity and quality Investigate and solve laboratory problems Support and drive LEAN initiatives and operational improvements – drive projects to completion Support Group Leaders in meeting client objectives and developing staff Communicate with clients on technical and business matters – make yourself available to meet with clients to discuss operations and conduct tours and audits Provide technical input and guidance to clients Lead business review meetings, assessing and understanding P&L’s Be involved in establishing CapEx list for coming year Evaluate pricing structure and provide input for changes Foster motivation and morale Perform and/or assign other duties as requested to ensure smooth operation of department · Perform all functions in support of and in compliance with all state and federal employment regulations Qualifications Bachelor's degree in chemistry, biology, biochemistry, or related degree concentration and at least 5-10 years of laboratory experience. Responsible for the direct management of the leadership employees in the department including Group Leader I-IV. Knowledge of departmental techniques; manage personnel, resolve conflicts, and correct poor performance; attention to detail; tolerance for stress; integrity; computer skills; communicate effective (verbally and written); perform multiple tasks simultaneously; logical thought; make decisions for self and others; independently develop solutions to complex problems. Additional Information Position is full-time, Monday-Friday, 8 a.m.-5 p.m., with overtime as needed. Candidates currently living within a commutable distance of Lancaster, Pennsylvania are encouraged to apply. 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 Eurofins USA Medical Devices is a Disabled and Veteran Equal Employment Opportunity employer.

Responsibilities

The Senior Manager will oversee the quality policy program, ensuring compliance with GMP/GLP standards and managing departmental operations. They will also lead personnel management, including training, performance evaluation, and client communication.