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Cambrex

Global CDMO for drug substances

Postdoctoral Scientist - Chemical Research and Development

Bioprocess & BiomanufacturingConfirmed live in the last 24 hours
Full-timeHigh Point, NC, USANo salary listedIn-person

About the Job

Requirements

  • A Ph.D. in Organic Chemistry, Medicinal Chemistry, or a closely related discipline is required.
  • No prior industry experience is necessary, but hands-on laboratory experience is essential.
  • A basic understanding of modern organic synthesis methodologies is required.
  • A fundamental understanding of modern analytical and spectroscopic techniques is required, with ability to interpret associated data and spectra.
  • Proficiency in laboratory synthesis and purification techniques at scales ranging from milligrams to several kilograms is required.
  • Ability to coordinate project activities and resource usage with minimal supervision is required.
  • Ability to write comprehensive reports for internal and customer use is required.
  • Understanding of Good Manufacturing Practice as it relates to current work is required.
  • Ability to use and investigate issues with high-performance liquid chromatography and gas chromatography is required.
  • Ability to write and review reports and technical documents, maintain a current laboratory notebook, and practice Good Documentation Practices is required.
  • Ability to read, understand, apply, and communicate written and verbal information about hazardous-waste handling and management is required; training must be completed within six months of assuming duty and annually thereafter.
  • Microsoft Office applications (Word, Excel, and PowerPoint), SharePoint, and ChemDraw proficiency is expected.
  • Strong verbal and written communication, interpersonal, and organizational abilities are required.
  • Ability to handle client requests with manager review is required.
  • Ability to solve workplace problems and assist with investigations with manager support is required.
  • Ability to self-organize with or without supervision is required.
  • Regular use of personal protective equipment, including supplied-air respirators, negative-pressure respirators, gloves, safety glasses, and shielding clothing, is required.
  • The role requires regularly walking and standing, visual acuity, talking, fingering, and occasional exertion of up to 25 pounds of force.

Responsibilities

  • Carry out multistep organic syntheses, isolate and purify targeted products under the supervision or direction of a senior team member.
  • Assess product identity and purity using modern analytical techniques throughout the project lifecycle.
  • Attend frequent meetings with the assigned mentor.
  • Participate in client meetings.
  • Coordinate project activities and resource usage with minimal supervision.
  • Prepare comprehensive reports at the conclusion of projects for internal and customer use.
  • Assist in advising clients on key regulatory guidance with manager input.
  • Work cooperatively within the group.
  • Conduct laboratory operations safely, maintain familiarity with the company chemical hygiene plan, and follow safe work practices.
  • Coordinate project-related equipment and activities with manufacturing and Good Manufacturing Practice operations.
  • Maintain a clean and safe laboratory work area.
  • Recognize emergency situations involving hazardous materials and wastes.
  • Participate in internal project team meetings, submit key technical reports, and organize group-level initiatives within the scientific team.
  • Support key operational excellence initiatives and locally support changes associated with broader company initiatives.

Desired Qualifications

  • Some process development experience is preferred.
  • Basic understanding of cross-functional departments, including analytical chemistry and/or engineering, is preferred.
  • Experience with in-situ reaction monitoring and/or automated reactor platforms may be beneficial.

About the Company

Cambrex

Global CDMO for drug substances

Cambrex is a global contract development and manufacturing organization (CDMO) that provides drug substance development and manufacturing across the entire drug lifecycle, plus analytical and IND enabling services. It uses a range of specialized technologies—such as continuous flow chemistry, handling of controlled substances, liquid-phase peptide synthesis, solid-state science, material characterization, and production of highly potent APIs—to develop and manufacture drug substances for clients. The company differentiates itself with over 40 years of experience, a staff of about 2,000 experts, and a global footprint in North America and Europe, offering end-to-end capabilities from early development through commercial-scale manufacturing. Its goal is to help clients bring new medicines to market by delivering integrated, reliable drug substance development and manufacturing and related analytical support.

Company size
1,001-5,000
Company stage
IPO
Headquarters
East Rutherford, NJ
Founded
1981

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