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

Education and Experience

• 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    

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. The candidate may be asked to travel occasionally (domestically and internationally) for conferences, seminars, and project specific needs (approximately 5% travel).

•  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.