This entry-level scientific role provides structured training in chemical research and development, focusing on optimizing existing synthetic routes and exploring alternative chemistry for key intermediates and active pharmaceutical ingredients (APIs). The Postdoctoral Scientist will independently or collaboratively perform multistep chemical syntheses, including isolation and purification, and utilize modern analytical techniques to assess product identity and purity throughout the project lifecycle.
Responsibilities
Carry out multistep organic syntheses, isolation, and purification of targeted products under supervision or direction of a senior team member
Coordinate project activities and resource usage with minimal supervision
Write comprehensive reports at the conclusion of projects for internal and customer use
Assist in advising clients on key regulatory guidance with manager input
Work to ensure a spirit of teamwork and cooperation always exists within the group
Conduct laboratory operations in a safe manner, maintaining familiarity with the company’s chemical hygiene plan and exhibiting safety awareness and safe work practices
Work closely with manufacturing and GMP operations to coordinate project-related equipment and activities
Maintain a clean, safe laboratory work area
Handle hazardous materials and wastes, with appropriate qualifications to read, understand, apply, and communicate written and verbal information regarding handling and managing hazardous wastes
Recognize emergency situations concerning hazardous materials and wastes
Requirements
Basic understanding of modern organic synthesis methodologies
Fundamental understanding of modern analytical and spectroscopic techniques, with the ability to interpret corresponding data and spectra
Proficiency to carry out laboratory syntheses and purification techniques on scales ranging from milligrams to several kilograms
Good understanding of the Principles of Organic Chemistry; some process development experience preferred
Basic understanding of the principles of cross-functional departments, including analytical chemistry and/or engineering
Demonstrated understanding of GMP as it relates to current work
Good fundamental understanding and ability to use/investigate issues with HPLC, GC; may have some experience with In-situ reaction monitoring and/or automated reactor platforms
Good written and oral communication skills, ability to handle client requests with manager review
Able to solve problems in the workplace and helps to lead investigations with manager support
Good understanding of time management and can self-organize with or without supervision
Millions of jobs, with real people getting hired every day
200,000+
New jobs added daily
7,000,000+
Verified job listings
1,000,000+
Tailored applications submitted
Strong demonstration of sharing key ideas across the group
Ability to write and review reports and technical documents with minimal RFT errors, keep current lab notebook while practicing GDP
Actively participate in regular internal project team meetings, including submission of key technical reports
Organize group-level initiatives within the larger scientific team
Known as a solid scientific contributor within the department/group
Able to support key OE initiatives
Locally support changes associated with larger Cambrex initiatives
Ph.D. in Organic Chemistry, Medicinal Chemistry, or a closely related discipline is required
Hands-on experience in a laboratory setting is essential
Strong verbal and written communication skills, along with interpersonal and organizational abilities
Proficiency in Microsoft Office applications (Word, Excel, PowerPoint), SharePoint, and Chemdraw
Benefits
Healthcare
Life insurance
Retirement planning
Important Details
Program duration: minimum of 10 to 12 months
Schedule: daily work performed primarily in a laboratory setting; walking and standing required regularly; some active work, exerting up to 25 pounds of force occasionally
Regular use of basic PPE (personal protective equipment) such as supplied air respirator, negative pressure respirator, gloves, safety glasses, shielding clothing
About the Company
Cambrex is a leading global contract development and manufacturing organization (CDMO) that provides drug substance, drug product, and analytical services across the entire drug lifecycle. With more than 40 years of experience and a growing team of over 2,000 professionals servicing global clients, Cambrex is a trusted partner in branded and generic markets for API and dosage form development and manufacturing.