Senior Research Associate - Protein Science (Genentech - On-site)
We are seeking a talented Senior Research Associate to join Protein Sciences Department in Drug Discovery organization. We seek a highly organized and collaborative research associate to purify and characterize therapeutic antibodies and proteins. The candidate will be expected to purify large numbers of antibodies by high throughput antibody purification, perform QC and distribute them to users. The candidate will also contribute to protein purification and characterization method development strategies.
Responsibilities:
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Purify and characterize therapeutic antibodies and proteins. (Purify large numbers of antibodies by high throughput antibody purification, perform QC and distribute them to user).
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Contribute to protein purification and characterization method development strategies.
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Interact closely with scientists daily, necessitating excellent written and oral communication skills.
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Explore and apply new techniques and technologies to solve antibody purification and characterization challenges.
Knowledge, Skills and Abilities:
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Self-motivated, enthusiastic, cooperative and reliable.
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The ability to adapt to changing demands whilst operating under pressure to deadlines.
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The ability to work accurately and with attention to detail.
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Good interpersonal skills and the ability to work well with other scientific staff.
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Must have a demonstrated track record of ability and initiative to work independently in a collaborative team-oriented setting in line with the vision/mission of the group.
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Strong organizational and time management skills.
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Good verbal communication skills.
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Ability to repeatedly lift and bend with the ability to lift up to 50lbs over head when needed.
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Ability to maintain excellent laboratory records.
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Computer proficiency.
Education and Experience:
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BS, or MS in biochemistry, biophysics or related field with relevant industry experience.
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A minimum 2 + years of protein purification and characterization experience is required.
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Must be a team player and willing to work in a core facility.
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Be highly motivated, detail oriented, efficient and thrive in a fast-paced environment.
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Demonstrated strong multi-tasking ability.
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Mass spec background is a plus.
This job description is intended to describe the general content of the job, and to identify the essential functions of and requirements for the performance of this job. It is not to be construed as an exhaustive statement of duties, responsibilities, or requirements. Because job requirements evolve with the changing needs of Evotec business, this description is subject to change and may be modified at any time, whether formally or informally.
The base pay range for this position at commencement of employment is expected to be $68,640 to $95,000. 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.
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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.
