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.

In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to over 47,000 staff across a network of more than 900 independent companies in over 50 countries and operating more than 800 laboratories. 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, as well as providing innovative clinical diagnostic testing services, as one of the leading global emerging players in specialised clinical diagnostics testing.

 In 2019, Eurofins generated total revenues of EUR € 4.56 billion, and has been among the best performing stocks in Europe over the past 20 years.

• Manages Manufacturing, Metrology and Materials Management Groups
• Plan/schedule all manufacturing activities
• Quote Manufacturing activities
• Write Protocols, Master Batch Records, Standard Operating Procedures, Specifications and Replies to Audit Observations
• Subject Matter Expert for all audits involving manufacturing -  Regulatory and Sponsor
• Able to work in manufacturing.
• Proactive to address work issues at the individual level for all three areas. 
• Provides goals and development plans for various group members.  Reviews group members twice per year.
• Writes and maintains Master Supply Agreements.
• Develop solutions for technical problems.  Major decision maker in the implementation of new technologies or approaches.  Expand technical expertise into multiple areas.  Support and drive LEAN initiatives.
• Provide manufacturing consultation for clients when needed.
• Commitment to occasional overtime as needed for manufacturing project completion.
• Strong Communicator, both orally and written. Interacts with Project Directors in a clear, timely and professional manner.
• Responsible for cGMP operation of manufacturing area.
• Guide and mentor junior staff to successfully complete projects and grow technical knowledge
• Demonstrate leadership qualities including:
• Effective in communication and ability to train groups on processes.
• Display of confidence
• Demonstrate motivation and take initiative
• Follow through on assignments
• Identify speaking or publishing opportunities and drive to publication or presentation.  Works with Business Development and Marketing to provide training materials or participate in Webinars.
• Complies with Health, Safety & Environmental responsibilities.  Conducts all activities in a safe and efficient manner.

The ideal candidate would possess:

• Expertise in sterile fill-finish operations
• Ability to execute manufacturing procedures of moderate complexity with minimal errors.
• Proficient in at least two core techniques (e.g.; Protein formulation development, small molecule formulation development, topical formulations, lyophilization, DSC, or Rheology etc.).
• Ability to participate in manufacturing and filling operations.
• Experience making topical products
• Good dexterity
• Mechanical inclination
• Positive attitude; willingness to learn
• Solution Driven
• Good work habits (organized efficient, accurate, careful, safety conscious, punctuality, etc.)
• Attention to detail
• Good oral and written communication
• Understanding of instrumentation
• Client service focused

Basic Minimum Qualifications:

• Doctorate’s degree, Master’s degree, or Bachelor’s degree in chemistry, biochemistry, biology or closely related physical science from a four-year college/university or equivalent education and training:
• Ph.D. or Master’s degree and >5 years related experience or Bachelor’s degree and >15 years related experience

Position is full-time, Monday - Friday 8:00am - 5:00pm.  Candidates currently living within a commutable distance of San Diego, CA 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 is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.