Additionalinformation

Additional Information

This role is a full-time, permanent position Monday-Friday 8am-4:30pm. Candidates currently located within commutable distance to Cambridge, MA are encouraged to apply. This position is based on-site with the occasional requirement to commute to a secondary site within 10-15 minute range.

Excellent full-time benefits include:

• Comprehensive medical coverage, dental, and vision options
• Life and disability insurance
• 401(k) with company match
• Paid vacation and holidays
• Eligibility for yearly goal-based bonus & merit-based increases
• Compensation: $45.00-$50.00 per hour based on education and relatable industry experience.

Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Companydescription

Company Description

The work we do at Eurofins Professional Scientific Services matters, and so do our employees. At Eurofins PSS, we put a focus on your professional growth. We provide our employees the ability to break into the biopharmaceutical industry and grow from the bottom up. We have the supportive teams and tools available to invest in you while also affording you work-life balance and a competitive benefits package.

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.

If you’re looking for a rewarding career, a place to call home, apply with us today!

Jobdescription

Job Description

Position Summary:

The Analytical Process Senior Scientist will be responsible for executing the development / optimization / implementation of analytical methods for small molecule characterization. Another key responsibility is to execute routine sample testing in support of process development activities. Additional responsibilities will be to participate in writing/review of documentations, performing data trending analysis, and supporting other activities in the laboratory as needed.

Responsibilities:

• Perform analytical testing on small molecule pharmaceutical samples using methods such as HPLC(MS), GC(MS), KF, and NMR
• Execute method development and optimization activities
• Analyze experimental data and properly document experiments (electronic lab notebook and records).
• Support process development activities and the execution of required analyses.
• Generate protocols and reports on performed experiments.
• Perform routine laboratory equipment maintenance.
• Perform other laboratory based activities, as required.
• Travel between different client laboratory sites, as needed.
• Compliance with Client SOP and policies related to laboratory work.

Qualifications

Basic Minimum Qualifications:

• A Bachelor’s Degree in chemistry or related scientific discipline is required. Advanced Degree preferred.
• A minimum of 6 years of experience working in a laboratory setting with bachelors degree and 2 years of experience in a laboratory setting with an advanced degree is required
• A working knowledge of common analytical instrumentations, including HPLC, GC, KF, NMR, and hands-on experience with at least of one of the above techniques.
• Excellent oral and written communication skills, good interpersonal skills and ability to work effectively in a team environment.
• Ability to react quickly to changes in project priorities and timelines.
• Highly self-motivated, organized, and detail-oriented, with a can-do attitude
• Must be eligible to work in the United States indefinitely without restriction or sponsorship.

Preferred Qualifications:

• Experience with chromatography data management software (Empower/ Chemstation/ Openlab) is a plus.
• Understanding of pharmaceuticals development and cGMP principles is a plus.