Sr. Scientist, Small-Molecule Drug Substance Development and Manufacturing - #258708
Arcus Biosciences
Date: 1 day ago
City: Hayward, CA
Salary:
$150,000
-
$170,000
per year
Contract type: Contractor

Description
Sr. Scientist, Small-Molecule Drug Substance Development and Manufacturing
Arcus Biosciences is a biotech company focused on immuno-oncology with clinical stage drug candidates in both monoclonal antibody and small molecule areas. Our Small Molecule Drug Substance Development and Manufacturing team has an opportunity for a Senior Scientist position to support our small molecule drug development pipeline.
Position Description
Arcus Biosciences is an Equal Opportunity Employer and prohibits discrimination and harassment of any kind. Arcus is committed to the principle of equal employment opportunity for all employees and does not discriminate based on race, religion, color, sex, gender identify, sexual orientation, age, non-disqualifying physical or mental disability, national origin, veteran status or any other legally protected status. EOE/AA/Vets
Sr. Scientist, Small-Molecule Drug Substance Development and Manufacturing
Arcus Biosciences is a biotech company focused on immuno-oncology with clinical stage drug candidates in both monoclonal antibody and small molecule areas. Our Small Molecule Drug Substance Development and Manufacturing team has an opportunity for a Senior Scientist position to support our small molecule drug development pipeline.
Position Description
- Under supervision of a senior member of the team to contribute to the overall business goals of Small Molecule Drug Substance Development & Manufacturing.
- Develop efficient, phase appropriate synthetic processes for APIs through effective lab scale R&D, which will include but not limited to route design, route scouting and process optimization toward suitable API synthesis for development and commercial production. Design and execute critical experiments to trouble shoot process issues encountered in large scale productions. Conduct lab experiments such as the establishment of process ranges, impurity fate and purges to support process characterization and process validation for late-stage projects.
- Work in a team of Arcus scientists and partner contract development and manufacturing organization teams to develop efficient manufacturing processes for small molecule drug substance preparation under GMP. The projects may encompass clinical stage candidates through commercial launch. Responsibilities will range from initiating process transfer, through scale up, GMP manufacturing and process validation activities.
- Provide technical review of master batch records.
- Provide person-in-plant support for manufacturing at CMO sites as needed by traveling either domestically or overseas.
- Provide concise technical updates to the Small Molecule Drug Substance Development and Manufacturing organization and key stakeholders in partner functions.
- Partner with Drug Product, Analytical Sciences, Quality Control and Quality Assurance to help ensure Arcus’ manufactured GMP drug substances are delivered on time with appropriate quality.
- Contribute to writing / reviewing CMC sections of regulatory filings as needed.
- Ph.D. in Organic Chemistry with at least 3 years of related industry experience, or MS with 6 years or B.S. with 8 years of related industry experience.
- Well trained in modern synthetic organic chemistry, including synthetic methodology, reaction mechanism, and modern analytical methods (NMR, MS and HPLC). Maintain broad up-to-date knowledge of current synthetic organic chemistry field as well as industrial trends through scientific literature and participation in conferences.
- Proven ability to carry out independent in-depth research in the areas of design and implementation of efficient synthetic routes for complex target organic compounds and/or development of new synthetic methodologies. Established track record for strategic thinking and creative problem solving. A good publication record is desirable.
- Excellent interpersonal skills, including clear, succinct, and timely oral and written communications.
- Proven ability to foster collaborative relationships with key stakeholders.
- Excellent organizational skills, with ability to successfully manage multiple priorities.
- Full knowledge and firsthand experiences in small molecule drug substance manufacturing under GMP regulations.
- Late-stage process characterization work experiences to support NDA filing such as process range finding, impurity fate and purges, technical report writing to support NDA filing are highly preferred.
- Frequently stand, walk, twist, bend, stoop, squat, grasp lightly, use fine manipulation, grasp forcefully, perform desk-based computer tasks, use telephone, write by hand, lift, carry, push and pull objects weighing over 40 pounds.
- Occasionally sit, kneel, crawl, reach and work above shoulders, sort and file paperwork or parts.
- Rarely climb, scrub, sweep, mop, chop and mix or operate hand and foot controls.
- Must have correctible vision to perform duties of the job.
- Ability to bend, squat, kneel, stand, reach above shoulder level, and move on hard surfaces for up to eight hours.
- Ability to lift heavy objects, possibly weighing up to 50 pounds.
- Position may require repetitive motion. WORKING CONDITIONS:
- May require working near blood borne pathogens.
- May require work in an environment where animals are used for teaching and research.
- Position may at times require the employee to work with or be in areas where hazardous materials and/or infectious diseases are present.
- Employee must perform tasks that require the use of personal protective equipment, such as safety glasses and shoes, protective clothing and gloves, and possibly a respirator.
- May require extended or unusual work hours based on research requirements and business needs. *Consistent with its obligations under the law, the company will provide reasonable accommodation to any employee with a disability who requires accommodation to perform the essential functions of his or her job.
Arcus Biosciences is an Equal Opportunity Employer and prohibits discrimination and harassment of any kind. Arcus is committed to the principle of equal employment opportunity for all employees and does not discriminate based on race, religion, color, sex, gender identify, sexual orientation, age, non-disqualifying physical or mental disability, national origin, veteran status or any other legally protected status. EOE/AA/Vets
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