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For your reference, we have included the original job posting below.
Scientist - Small Molecule Chemical Process Research and Development
Job Number:
44994699
Company Name:
Amgen
Job Location:
Cambridge, MA US
Job Categories:
Science & Biotech Healthcare & Medical
Scientist - Small Molecule Chemical Process Research and Development
Amgen, a biotechnology pioneer, discovers, develops and delivers innovative human therapeutics. Our medicines have helped millions of patients in the fight against cancer, kidney disease, rheumatoid arthritis and other serious illnesses.
As an organization dedicated to improving the quality of life for people around the globe, Amgen fosters an inclusive environment of diverse, committed and highly accomplished people. People who respect each other but compete intensely to win. Together, we live the Amgen values as we continue advancing science to serve patients.
We are currently seaking a Scientist to work with Small Molecules in our Chemical Process Research and Development space.
A Scientist in the CPR&D Department is responsible for development of the technology to prepare Amgen's small molecule API candidates through all phases of development. The Scientist will participate in drug substance development teams and be expected to develop innovative solutions to prepare small molecule drug candidates.
KEY RESPONSIBILITIES OF THIS STAFF MEMBER INCULDE:
SCIENTIFIC/TECHNICAL • Develop technology to deliver Amgen's API candidates in a practical, efficient and safe manner. • Participate in drug substance teams and collaborate cross-functionally with analytical and drug product representatives to delivery drug substance manufacturing processes in a phase appropriate manner. • Work cross-functionally to deliver CMC regulatory documents and supporting documentation in support of Amgen's small molecule regulatory filings. • Work with external partners to deliver key intermediate or drug substances in support of Amgen's small molecule pipeline. • Deliver processes amenable to cGMP operation and carry out deliveries of drug substance in a cGMP manufacturing environment.
TEAM EXPERIENCE • Demonstrates ability to effectively participate on drug substance development teams as a team member or primary department representative • Represents the department in various departmental and interdepartmental committees that address scientific and administrative initiatives • Participates in and can direct team efforts directed at advancing development/technology programs within the department • Applies team experiences to facilitate cohesiveness and build team spirit
ORAL AND WRITTEN COMMUNICATION • Authors, or provides direction for the authorship of, technical reports or regulatory submissions which may require minimal additional editing. • Gives effective presentations within the department and to senior management with minimal supervision. • Actively creates, generates, and presents paper/presentations at scientific meetings. • Capable of organizing and conducting effective meetings. • Learns and applies facilitation and listening skills.
SUPERVISING OTHERS [MAY HAVE DIRECT REPORT(S)] • Ensures that safe laboratory practices are followed. • Trains less-experienced staff. • Demonstrates ability to direct the activities of others.
LEADERSHIP AND INFLUENCE • Identifies resources and develops timelines for project activities. • Learns to organize, plan, and control multiple project activities effectively to meet corporate timelines. • Effectively and actively participates on one or more project team with demonstrated ability to occupy a leadership role.
Basic Qualifications • Doctorate degree OR • Master's degree & 6 years of scientific experience OR • Bachelor's degree & 8 years of scientific experience
Preferred Qualifications • Ph.D. in Organic Chemistry and 0-5 years of relevant experience in the pharmaceutical or related industry which includes participation and contribution to scientific project teams • A BS Scientist with a minimum of 10+ years pharmaceutical industry or MS scientist 8+ years of relevant experience in the pharmaceutical or related industry which includes participation and contribution to scientific project teams. • Experience with the techniques associated with the synthesis, purification and characterization of organic molecules • Experience solving issues of reaction design and/or synthetic route selection. • An scientific track record which may include peer reviewed publications, scientific conference participation • Experience with the use of analytical instruments (HPLC, NMR, IR and MS) and interpreting the scientific data based upon these techniques. • Demonstrated communication and scientific writing skills.
