Process Chemist: Principal Scientist
Location:
Posted:
November 23, 2016
Reference:
1042893


About the company
A career at the company offers opportunity, ownership and impact.

All over the world, the company colleagues work together to positively impact health for everyone, everywhere. Our colleagues have the opportunity to grow and develop a career that offers both individual and company success; be part of an ownership culture that values diversity and where all colleagues are energized and engaged; and the ability to impact the health and lives of millions of people. the company, a global leader in the biopharmaceutical industry, is continuously seeking top talent who are inspired by our purpose to innovate to bring therapies to patients that significantly improve their lives.

Role Description
We are seeking a synthetic organic chemist to join the Process Chemistry group within Chemical Research and Development (CRD) in Groton. CRD, as part of Worldwide R&D in Pharmaceutical Sciences, is responsible for the development of process technology for the production of active pharmaceutical ingredients (API). CRD scientists engage in all facets of development from small scale synthesis in support of Discovery programs, to the development of the commercial synthetic route. CRD scientists partner with manufacturing specialists for API synthesis in kilo-lab and pilot plant facilities, as well as provide support for technology transfer to the company manufacturing sites and third party facilities.

The successful candidate will have a working knowledge of process chemistry, and will design, enable and develop scalable processes to pharmaceutical drug candidates, applying innovative chemistries, new technologies and statistical experimental design approaches in a laboratory setting. The ability to work on multi-disciplinary teams involving chemists, analysts, engineers, and technologists and to represent CRD on cross-functional teams is essential.

Responsibilities
The successful candidate would propose and identify efficient and robust synthetic routes for the preparation of API's. This position requires laboratory experimentation, leadership on API project teams and close collaboration with scientists from Analytical R&D and other disciplines such as engineering to further develop synthetic routes into safe, efficient and robust processes. Interpretation of analytical data to drive synthetic experimental plans and the ability to utilize tools such as electronic notebooks to document information are essential. The successful candidate would also be responsible for participating in the preparation of technical transfer documents for manufacture internally or at third parties.

The successful candidate would lead unit of work teams or smaller API project teams. A strong working knowledge of current Good Manufacturing Processes (GMP) is desired. Compliance on safety and regulatory requirements is expected and documented through our internal training program.

The successful candidate would also represent CRD on cross disciplinary programs within Pharmaceutical Sciences and contribute to continuous improvement work in the department and advancement of the Process Chemistry discipline through technology, workflow or business impact.

Qualifications
PhD. in Organic Chemistry, with 3-6 years of pharmaceutical R&D experience in Process Chemistry required.

State of the art knowledge of modern synthetic methodology, including aspects of asymmetric synthesis, green chemistry, catalysis and physical organic chemistry as it relates to reaction mechanism is expected. The ability to employ analytical tools, computational and statistical methodology, and automated laboratory technologies to enhance process development efficiency is desirable. Excellent written and oral communication skills, the ability to effectively influence the work of others, and a general knowledge of drug development and the pharmaceutical industry are key.

PHYSICAL/MENTAL REQUIREMENTS
Laboratory work requiring standing.
Working at a computer.
Ability to use sound scientific judgment and analyze data to advance programs.

NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS
Travel is required on occasion in support of external manufacture or to participate in scientific conferences.

Other Information - Internal
Colleagues who are issued an Incident Final Warning (IFW) on or after January 1, 2016, are not eligible to post and compete for a position for a period of 12-months from the date an IFW is issued.

EEO & Employment Eligibility
the company is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status. the company also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA. the company is an E-Verify employer.
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