Position is directed toward optimization of existing chemical routes and development of alternate chemistry toward key synthetic intermediates and APIs. Carries out multistep chemical synthesis and product isolation/purification operations in the laboratory, independently or as part of an integrated team. Chemist utilizes modern analytical tools to determine identity and purity of products made during projects. Communication with clients in regular team meetings; prepares R&D reports at the conclusion of projects.
Responsibilities:
Organic Chemistry Knowledge: Strong understanding of the Principles of Organic Chemistry, some process development experience.
Cross Discipline Knowledge: Improved understanding of the principles of cross-functional departments, including analytical chemistry and engineering.
GMP/Regulatory Knowledge: Demonstrated understanding of GMP as it relates to current work. With less manager input, can help to advise clients on key regulatory strategies.
Instrumentation: Demonstrated ability to use, train, investigate root cause issues with HPLC, GC, good understanding of MS, uses automated reactors, may have some experience with In-situ reaction monitoring.
Communication: Good written and oral communication skills, ability to handle client requests with manager review.
Problem Solving: Able to solve problems in the workplace and helps to lead investigations with manager support.
Time Management: Good understanding of time management and can self-organize with or without supervision.
Leadership: Regularly seeks to share ideas and learning across the group/site; pushes new initiatives from the ground up.
Technical Documentation and Review: Ability to write and review reports and technical documents with minimal RFT errors, keep current lab notebook while practicing GDP.
External Influence: Actively participates in regular internal project team meetings, including submission of key technical reports; organizes group level initiatives within the larger scientific team.
Industry Credibility and Rapport: Known as a solid scientific contributor within the department/group
Operational Excellence: Able to support key OE initiatives.
Change Orientation: Locally supports changes associated with larger Cambrex initiatives.
Qualifications:Ph.D. in Chemistry or related field with minimum 2 years’ experience or M.S. in Chemistry or related field with minimum 6 years’ experience or B.S. degree in Chemistry or related field with 10 years of experience in lab environment, pharmaceutical experience preferred.
Hands on experience in pharmaceutical/chemical process development.
Excellent verbal and written communication/interpersonal skills, organizational skills, and the ability to work in a diverse team environment are essential.
Proficiency with Microsoft software (SharePoint, Word / EXCEL / PowerPoint), and Chemdraw is expected.
| Location | High Point, North Carolina |
| Job Type | Full-time |
| Industry | Biotechnology/Pharmaceuticals |
| Company Size | 1,000 to 1,499 employees |
| Year Founded | 1981 |
| Website | http://www.cambrex.com |
Cambrex is an innovative life sciences company with a refreshingly human approach. Driven by passion, our pharmaceutical products, expertise and technologies accelerate our customers’ small molecule therapeutics into markets across the world.
With over 35 years of active pharmaceutical ingredient (API) development and manufacturing expertise, a growing team of more than 1,200 experts and a strong presence in the USA and Europe, we are tried and trusted across branded and generic API markets.
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