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.

Position Responsibilities Include:

• Support Quality Control Analytical technical writing including change controls, investigations, and documentation practices in support of GMP manufacturing activities
• Participate in the initiation, revision, and completion of change control documentation to ensure audit readiness/compliance
• Work closely with Quality Control Analytical laboratory personnel and cross-functional partners to fully understand and solve problems
• Inform management on progress and concerns
• Route materials through document management systems
• Work independently with minimal supervision and direction
• Maintain compliance with company policies, training requirements, cGMPs and safety standards
• This is a hybrid role with flexibility to work from home but will require work onsite in Andover, MA to meet business needs

Basic Minimum Qualifications:

• Bachelor’s degree in chemistry or related scientific field 
• at least 3+ months of experience in a Pharmaceutical GMP setting
• Have an understanding of biologics manufacturing operations
• Ability to read and interpret SOP’s, operating and maintenance instructions and procedure manuals
• Must be able to identify problems and know when to solve proactively and seek advice
• Proficient with MS Office applications
• Are able to learn and utilize computerized systems for daily performance of tasks such as LIMS, SAP, and Trackwise.

Preferred Qualifications:

• Quality assurance /investigations/change control technical writing experience preferred
• Ability to organize and prioritize work
• Ability to work independently and as part of a team in a client facing environment
• Ability to define problems, collect data, establish facts and draw valid conclusions
• Self-motivated, adaptable, and a positive attitude
• Strong analytical and problem-solving abilities
• Strong written and verbal communication skills

Position is full-time, Monday - Friday 8:00am - 5:00pm. Candidates currently living within a commutable distance of Andover, MA are encouraged to apply. Excellent full-time benefits including comprehensive medical coverage, dental, and vision 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 is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.