Research Associate - Site based - Framingham, MA

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Framingham, MA
63K-87K Annually
Biotech • Pharmaceutical
The Role

Cyprotex, an Evotec company, specializes in ADME-Tox and Biosciences including both in vitro (laboratory experiments) and in silico (computer modelling) approaches. Cyprotex was founded in 1999. The Company serves the Pharmaceutical and Biotech, Cosmetics/Personal Care and Chemicals Industries as well as academia and not-for-profit organizations. Over 1700 organizations trust Cyprotex for their ADME-Tox and Bioscience research needs.

The team is looking for a highly motivated Research Associate that will be responsible for routine screening of compounds in various in vitro ADME/Tox assays and maintaining mammalian cells. Training opportunities will be provided for high throughput screening, cell culture and LC-MS/MS.

 

Job Responsibilities

·         Responsible for planning and conducting high and low throughput in vitro ADME assays, processing data to a high quality of standards, and within specified time frames.

·         To assist the Scientist with validation and investigative assays.

·         To monitor and maintain stock consumables where required.

·         To help with the validation and routine maintenance of laboratory equipment.

·         To provide support to the Senior Scientist, Laboratory Supervisors and Senior Research Scientist when trouble shooting.

·         Identifies, within their group, where support is required and manages their own time sufficiently to provide this support.

·         To follow safety regulations and quality control procedures.

·         To report any issues of concern and discuss/advise scientific strategy with the Laboratory Supervisor and/or Senior Research Scientist.

Qualifications

We would look at graduate with cell culture or LC MS experience as we could train.

·         BA/MS or equivalent experience in a relevant Biological or Chemical scientific discipline with experience working within industry (pharma or CRO).

·         Effective communication and organizational skills, and the ability to troubleshoot and multitask under pressure of deadlines are important.

·         Plate based screening is a plus.

·         Cell culture experience is a plus

·         LC-MS/MS experience is a plus

 

 

The base pay range for this position at commencement of employment is expected to be $63,000 to $87,000; Base salary offered may vary depending on the individual’s skills, experience and competitive market value. Additional total rewards include discretionary annual bonus, comprehensive benefits to include Medical, Dental and Vision, short-term and long-term disability, company paid basic life insurance, 401k company match, flexible work, generous paid time off and paid holiday, wellness, and transportation benefits.

Evotec is an Equal Opportunity Employer.  All qualified applicants will receive consideration for employment without regard to race, gender, age, disability, genetic information, gender expression, gender identity, national origin, religion, sexual orientation, or veteran status.

 

Federal contractors are required to maintain a drug-free workplace as mandated by the Drug-Free Workplace Act of 1988. This federal requirement supersedes state laws that permit the use of cannabis

Evotec (US) Inc. is an Equal Opportunity Employer.  All qualified applicants will receive consideration for employment without regard to race, gender, age, disability, genetic information, gender expression, gender identity, national origin, religion, sexual orientation, or veteran status.

The Company
HQ: Hamburg
5,042 Employees
On-site Workplace

What We Do

Evotec is a biotechnology company that is committed to advancing drug discovery and development. Through flexible business models, we collaborate with pharmaceutical companies, biotechs, foundations, and government agencies on a substantial scale. We believe that by working together, we can make a difference in the lives of patients.

Our Pipeline Co-Creation model represents our adaptable, multi-modality, fully integrated end-to-end approach to drive collaborations and services across all phases of drug discovery and development – from discovery of novel targets to achieving Proof of Concept in the clinic and into commercial manufacturing.

We aspire to contribute data-driven disease understanding and early disease relevance in humans to bring the probability of success up. We select the right modality, which is then propelled forward on our platforms by our passionate people striving for the fastest and most effective ways towards patient impact. This is enabled by convergence of human ingenuity with data and AI.

We also offer specific solutions, products, and CRO/CDMO-like services, always in support of the Biopharma R&D innovator. Our more than 4,000 scientists work closely with numerous partners concurrently, delivering fully integrated research and development portfolios or individual projects with the highest quality standards and efficiency, coupled with great science, passion, engagement, and communication.

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