Job 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 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
Responsibilities
- Contributes as part of a small team of scientists towards the development/optimization, and qualification/verification of analytical methods to support synthetic molecules analytical development.
- Applies in-depth knowledge of concepts and applications to fit-for-purpose methods development.
- Provided analytical support for process and formulation development related works.
- Reviews and interprets data then communicates results to relevant members.
- Identifies, troubleshoots, and implements resolutions to technical problems/issues.
- Conducts work in compliance with cGMP/GLP, safety and regulatory requirements.
- Writing technical reports for functional area
- Independently plans and designs experiments and operations within expertise.
- Able to clarify requests and provide suggestions and put data into context.
- Works with departmental and/or other function members to execute on assignments, under limited supervision.
- Learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies.
- Effectively communicates complex data/decisions within department.
- Contributes significantly to project related lab works within functional area.
- Coordinates work with members in the team
Qualifications
- Working knowledge of analytical techniques with experience using multiple techniques (LC, GC, Dissolution, Karl Fisher, spectroscopic instruments, etc.) for synthetic molecules.
- Basic understanding of industry practices and standards.
- Experiences on method development and validation for synthetic molecule products
- Strong computer, scientific, and organizational skills.
- Analytical and Problem Solving Skills - Able to troubleshoot critical issues or problems and determine causes and possible solutions using appropriate information
- Ability to work well in a team environment
- Communication Skills - Able to expresses oneself clearly and concisely within team
- Organization - Exercises good time management and prioritization skills and is able to successfully manage multiple tasks simultaneously
- Authorization to work in the United States indefinitely without restriction or sponsorship
- Associates degree in chemistry, biology, pharmacy, engineering, or related pharmaceutical science with 7+ years relevant industry experience
- Bachelor's degree in chemistry, biology, pharmacy, engineering, or related pharmaceutical science with 4+ years relevant industry experience
- Master's degree in chemistry, biology, pharmacy, engineering, or related pharmaceutical science with 2+ years relevant industry experience
Additional Information
Position is full-time, Monday - Friday. 8:00-5:00pm are the hours.Candidates currently living within a commutable distance of Cambridge, MA 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 aM/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.
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