Senior Scientist I - Chemical Research and Development
Job DescriptionCompany InformationYou Matter to Cambrex.
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 2,400 professionals servicing global clients, Cambrex is a trusted partner in branded and generic markets for API and dosage form development and manufacturing.
Your Work Matters.
At Cambrex, we strive to build a culture where all colleagues have the opportunity to:
engage in work that matters to our customers and the patients they serve learn new skills and enjoy new experiences in an engaging and safe environment strengthen connections with coworkers and the community We're committed to attracting and nurturing a passionate team of valued professionals in our fast-paced and growing company.
We offer a competitive benefits package that includes medical, dental, vision, Life, LTD, retirement savings and more!Your Future Matters.
Known for our customer-focused scientific and manufacturing excellence, as well as our strong commitment to quality and safety, we offer a range of career and growth opportunities across our global network of locations.
Together with our customers, we aim to improve the quality of life for patients around the world.
Start a career where You Matter by applying today!Job OverviewThe Senior Scientist III - Chemical Research and Development is directed toward optimization of existing chemical routes and development of alternate chemistry toward key synthetic intermediates and APIs.
The senior scientist will carry out multistep chemical synthesis and productisolation/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 the course of projects.
Communication with clients in regular team meetings; prepares R&D reports at the conclusion of projects.
ResponsibilitiesCarry 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 review, 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 six months of assuming duty and once a year thereafter.
Responsible for recognizing emergency situations concerning hazardous materials and wastesQualifications/SkillsOrganic Chemistry Knowledge:
Strong understanding of the Principles of 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 industrial GMP and practical application to Cambrex programs; ability to help identify risks for regulatory compliance or violation of site SOP.
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 communicate with clients without manager supervision.
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, though still requires regular check-in with manager.
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 author and review key 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; ability to work with management to develop key local laboratory-based initiatives.
Industry Credibility and Rapport:
Recognized scientific leader within the Cambrex organization, locally and possibly beginning to extend to other sites.
Education, Experience & Licensing RequirementsPh.
D.
in Chemistry or related field with minimum 4 years' experience or M.
S.
in Chemistry or related field with minimum 8 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.
SDL2017 Recommended Skills Api Analytical Chemistry Chemical Process Chromatography Consulting Coordinating Estimated Salary: $20 to $28 per hour based on qualifications.
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 2,400 professionals servicing global clients, Cambrex is a trusted partner in branded and generic markets for API and dosage form development and manufacturing.
Your Work Matters.
At Cambrex, we strive to build a culture where all colleagues have the opportunity to:
engage in work that matters to our customers and the patients they serve learn new skills and enjoy new experiences in an engaging and safe environment strengthen connections with coworkers and the community We're committed to attracting and nurturing a passionate team of valued professionals in our fast-paced and growing company.
We offer a competitive benefits package that includes medical, dental, vision, Life, LTD, retirement savings and more!Your Future Matters.
Known for our customer-focused scientific and manufacturing excellence, as well as our strong commitment to quality and safety, we offer a range of career and growth opportunities across our global network of locations.
Together with our customers, we aim to improve the quality of life for patients around the world.
Start a career where You Matter by applying today!Job OverviewThe Senior Scientist III - Chemical Research and Development is directed toward optimization of existing chemical routes and development of alternate chemistry toward key synthetic intermediates and APIs.
The senior scientist will carry out multistep chemical synthesis and productisolation/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 the course of projects.
Communication with clients in regular team meetings; prepares R&D reports at the conclusion of projects.
ResponsibilitiesCarry 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 review, 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 six months of assuming duty and once a year thereafter.
Responsible for recognizing emergency situations concerning hazardous materials and wastesQualifications/SkillsOrganic Chemistry Knowledge:
Strong understanding of the Principles of 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 industrial GMP and practical application to Cambrex programs; ability to help identify risks for regulatory compliance or violation of site SOP.
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 communicate with clients without manager supervision.
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, though still requires regular check-in with manager.
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 author and review key 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; ability to work with management to develop key local laboratory-based initiatives.
Industry Credibility and Rapport:
Recognized scientific leader within the Cambrex organization, locally and possibly beginning to extend to other sites.
Education, Experience & Licensing RequirementsPh.
D.
in Chemistry or related field with minimum 4 years' experience or M.
S.
in Chemistry or related field with minimum 8 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.
SDL2017 Recommended Skills Api Analytical Chemistry Chemical Process Chromatography Consulting Coordinating Estimated Salary: $20 to $28 per hour based on qualifications.
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