Analytical Chemist at Eurofins

Brunswick Township, Minnesota, United States -

Full Time

Start Date

Immediate

Expiry Date

24 Dec, 25

Salary

65000.0

Posted On

25 Sep, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Analytical Chemistry, Problem Identification, Report Writing, Protocol Review, SOP Writing, Training, Experiment Setup, Good Laboratory Practices, Record Keeping, Safety Compliance, Flexibility, Computer Proficiency, Instrumentation Skills, Responsibility, Organization, Adaptability

Industry

Medical and Diagnostic Laboratories

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 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 Organization 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 Organizations. It also has a rapidly developing presence in highly specialized 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 decentralized 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. Job Description Assist the Study Director with all phases of study design, scheduling and conduct. Act proactively to identify problems and potential problems. Assist in writing, reviewing and editing reports, protocols and SOP’s. Training other staff members. Set-up and conduct experiments in accordance with Protocol and SOP's. Efficiently carry out procedures necessary to complete each project with minimal supervision. Accurately prepare all solutions needed for analysis. Meticulously maintain precise records of all experiments in accordance with good laboratory practices. Wash glassware as needed and maintain a clean working environment. Follow all PSL safety requirements. Must be flexible with changing business needs. Ability to safely wear a respirator required. Other duties as assigned. Qualifications B.S. degree or equivalent experience (0-2 years) in analytical chemistry is preferred. Computer proficiency and instrumentation and skills are desirable. The individual holding this position must be of highest integrity and have a very strong sense of responsibility and be willing and able to work with little or no supervision. He/she must be mature, willing to learn new skills, well organized, capable of adapting to a broad spectrum of responsibilities and able to maintain meticulous and accurate records. Adherence to Good Laboratory Practices (GLP) is of utmost importance. Additional Information Position is full-time, Monday-Friday 8am-5pm. Candidates within a commutable distance of South Brunswick, NJ are encouraged to apply. Annual Salary 55,000-65,000 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 USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.

Responsibilities

Assist the Study Director with study design, scheduling, and conduct. Conduct experiments, maintain records, and ensure compliance with safety and laboratory practices.