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Lab Operations Engineer - Group Leader

Eurofins Scientific
Spring House, USA
Full-time
Senior · 30+ years experience
Onsite
Discovered Today
Communication

Full Job Posting

Required skills

  • Experience in a GLP or GMP laboratory, preferably in a bioanalytical setting.
  • Proven experience in validation activities and associated Quality functions.
  • Demonstrated strong interpersonal skills with the ability to influence others and promote a culture of inclusion, feedback, and empowerment.
  • Highly organized, and multitasking capabilities to manage multiple equipment or system schedules, documents, and maintenance tasks.
  • Strong verbal and written communication skills, with comfort in interacting with diverse on-site and off-site collaborators.
  • Ability to follow Standard Operating Procedures with insight into continuous improvement.
  • Apply general knowledge of company business developed through education or experience.
  • Understand and apply regulatory/ compliance requirements relative to the role.
  • Problem solver/troubleshooter, skilled in Root Cause Analysis (RCA).
  • Position is full-time, Mon-Fri 8am-5pm. Candidates currently living within a commutable distance of Spring House, PA are encouraged to apply. The site is not accessible by public transportation routes/options.
  • 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 PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.
  • 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.
  • In 2021, Eurofins generated total revenues of EUR 6.72 billion, and has been among the best performing stocks in Europe over the past 20 years.

Qualifications

  • Minimum of a Bachelor of Science degree needed (with a minimum of 2 years of relevant experience) or a Master’s degree in engineering science, Information Technology or a related field.
  • Authorization to work in the country indefinitely without sponsorship.
  • Previous leadership experience
  • Experience in a GLP or GMP laboratory, preferably in a bioanalytical setting. Proven experience in validation activities and associated Quality functions. Demonstrated strong interpersonal skills with the ability to influence others and promote a culture of inclusion, feedback, and empowerment. Highly organized, and multitasking capabilities to manage multiple equipment or system schedules, documents, and maintenance tasks. Strong verbal and written communication skills, with comfort in interact
  • Experience in a GLP or GMP laboratory, preferably in a bioanalytical setting.
  • Proven experience in validation activities and associated Quality functions.
  • Demonstrated strong interpersonal skills with the ability to influence others and promote a culture of inclusion, feedback, and empowerment.
  • Highly organized, and multitasking capabilities to manage multiple equipment or system schedules, documents, and maintenance tasks.
  • Strong verbal and written communication skills, with comfort in interacting with diverse on-site and off-site collaborators.
  • Ability to follow Standard Operating Procedures with insight into continuous improvement.
  • Apply general knowledge of company business developed through education or experience.
  • Understand and apply regulatory/ compliance requirements relative to the role.
  • Problem solver/troubleshooter, skilled in Root Cause Analysis (RCA).

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