Principal Scientist 1 - Chemical Research & Development
Cambrex
Summary
The Principal Scientist 1 - Chemical Research and Development role 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.
Job description
Job Overview
The Principal Scientist 1 - Chemical Research and Development role 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
- Design and carry out multistep organic syntheses, isolation, and purification of targeted products.
- Possess a strong understanding of modern organic synthesis methodologies.
- Have a thorough understanding of modern analytical and spectroscopic techniques and be able to interpret the corresponding data and spectra.
- Conduct literature searches for specific target compounds and use the literature to base a design of alternate routes to these compounds.
- Demonstrate proficiency to carry out laboratory syntheses and purification techniques on scales ranging from milligrams to several kilograms, and design and implement process modifications.
- Manage projects on-time without supervision with excellent time management.
- Author and review comprehensive reports at the conclusion of projects for internal and customer use.
- Work closely with other chemistry and analytical laboratory staff to coordinate project activities and resource usage.
- Ensure a spirit of teamwork and cooperation exists within the group.
- Conduct laboratory operations in a safe manner and maintain familiarity with the company's chemical hygiene plan.
- Follow responsible actions regarding chemical disposal and maintain compliance with all regulations at the federal, state, and local levels.
- Demonstrate effective communication skills (both interpersonal and presentations) and participate in project team meetings with customers.
- Work closely with manufacturing and GMP operations to coordinate project related equipment and activities.
- Maintain a clean, safe laboratory work area.
Qualifications/Skills
- Organic Chemistry Knowledge: Beginning to demonstrate an understanding of advanced theories in Organic Chemistry/Process Development.
- Cross Discipline Knowledge: Higher level of understanding of the principles of cross-functional departments, including analytical chemistry and engineering.
- GMP/Regulatory Knowledge: Demonstrated understanding of the GMP landscape and fundamental understanding of the industrial regulatory landscape; good understanding of site SOPs and regulatory CMC concerns.
- Instrumentation: Advanced knowledge of HPLC, GC, MS, automated reactor platforms, in-situ reaction monitoring, and ability to train and troubleshoot problems with equipment.
- Communication: Good written and oral communication skills, often leading technical calls with clients.
- Problem Solving: Strong demonstration of problem solving, ability to lead investigations.
- Time Management: Able to maintain timeline of key activities and use time efficiently; ability to handle projects without supervision.
- Leadership: Demonstrated record of mentorship and development of peers, partner lines and ability to support initiatives within the department.
- Technical Documentation and Review: Ability to author and review technical documents with minimal RFT errors; can write new SOP with manager assistance, keep current lab notebook while practicing GDP.
- External Influence: Ability to lead local project teams and steer clients to desired outcomes.
- Industry Credibility and Rapport: Recognized scientific leader within the Cambrex organization.
- Operational Excellence: Actively participates in key operational excellence initiatives.
- Change Orientation: Active participation and support for implementation of Cambrex system level changes/initiative.
Education, Experience & Licensing Requirements
Ph.D. in Chemistry or related field with minimum 6 years' experience or M.S. in Chemistry or related field with minimum 10 years' experience or B.S. degree in Chemistry or related field with 12 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.
Requirements
- Ph.D. in Chemistry or related field with minimum 6 years' experience, or M.S. with minimum 10 years' experience, or B.S. with 12 years of experience in lab environment
- Hands on experience in pharmaceutical/chemical process development
- Strong understanding of modern organic synthesis methodologies
- Thorough understanding of modern analytical and spectroscopic techniques and ability to interpret data and spectra
- Advanced knowledge of HPLC, GC, MS, automated reactor platforms, and in-situ reaction monitoring
- Demonstrated understanding of GMP landscape and regulatory CMC concerns
- Excellent verbal and written communication and interpersonal skills
- Organizational skills and ability to work in a diverse team environment
- Proficiency with Microsoft software (SharePoint, Word, Excel, PowerPoint) and Chemdraw
- Ability to conduct literature searches and design alternate synthetic routes
- Ability to author and review technical documents with minimal RFT errors
- Demonstrated record of mentorship and development of peers
Benefits
- Healthcare
- Life Insurance
- Retirement Planning
Company overview
Cambrex is a leading global contract development and manufacturing organization (CDMO) that provides comprehensive drug substance, drug product, and analytical services across the entire drug lifecycle. With over 40 years of experience and a team of more than 2,000 professionals servicing global clients from sites in North America and Europe, Cambrex has established itself as a trusted partner in both branded and generic pharmaceutical markets. The company specializes in API and dosage form development and manufacturing, offering specialized technologies including continuous flow processing, controlled substances handling, liquid-phase peptide synthesis, solid-state science, and highly potent API manufacturing. Cambrex serves as a critical partner for pharmaceutical companies seeking to accelerate small molecule therapeutics to market, providing end-to-end solutions from early-stage development through commercial manufacturing. Their global network of facilities enables them to support clients with complex regulatory requirements and scale-up needs throughout the drug development process.