Senior Scientist 2 - Chemical Research & Development
Cambrex
Summary
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.
Job description
Job Overview
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
- Carry out multistep organic syntheses, isolation, and purification of targeted products under supervision or direction of a senior member of the team.
- Must possess a basic understanding of modern organic synthesis methodologies.
- The chemist must have a fundamental understanding of modern analytical and spectroscopic techniques and may possess the ability to interpret the corresponding data and spectra.
- Must demonstrate a proficiency to carry out laboratory syntheses and purification techniques on scales ranging from milligrams to several kilograms.
- Require minimal supervision and be able to coordinate project activities and resource usage.
- Demonstrate ability to write comprehensive reports at the conclusion of projects for internal and customer use.
- With manager input, assist in advising clients on key regulatory guidance.
- Work to ensure that a spirit of teamwork and cooperation always exists within the group.
- Conduct laboratory operations in a safe manner. Maintain familiarity with the company's chemical hygiene plan. Exhibit 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.
- This position works with and handles hazardous materials and wastes. Must have the appropriate qualifications to read, understand, apply, and communicate written and verbal information regarding handling and managing hazardous wastes. Training is required within 6 months of assuming duty and once a year thereafter.
- Responsible for recognizing emergency situation concerning hazardous materials and wastes.
Qualifications/Skills
- 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.
Education, Experience & Licensing Requirements
- 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.
Requirements
- 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
- Hands on experience in pharmaceutical/chemical process development
- Strong understanding of the Principles of Organic Chemistry
- Some process development experience
- Demonstrated understanding of GMP as it relates to current work
- Demonstrated ability to use, train, investigate root cause issues with HPLC, GC
- Good understanding of MS
- Uses automated reactors
- Good written and oral communication skills
- Excellent verbal and written communication/interpersonal skills
- Organizational skills
- Ability to work in a diverse team environment
- Proficiency with Microsoft software (SharePoint, Word/EXCEL/PowerPoint) and Chemdraw
- Must have appropriate qualifications to read, understand, apply, and communicate written and verbal information regarding handling and managing hazardous wastes
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.