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Development Scientist

Job in Alabaster, Shelby County, Alabama, 35007, USA
Listing for: Croda
Full Time position
Listed on 2026-06-22
Job specializations:
  • Research/Development
    Research Scientist, Data Scientist
  • Science
    Research Scientist, Data Scientist
Salary/Wage Range or Industry Benchmark: 80000 - 100000 USD Yearly USD 80000.00 100000.00 YEAR
Job Description & How to Apply Below

Croda is a FTSE
100 organization driven around our purpose of Smart Science to Improve Lives™. With over 6,000 employees across 39 countries, we are focused on the research and development of novel and highly sustainable raw materials for the Life Sciences and Consumer Care sectors.

We are passionate and excited about how we can develop and utilize new technologies to shape and inspire changes within an ever‑growing marketplace. As our business looks to deliver its ambitious strategy of growth, we are looking for a Development Scientist to join our Process Development group.

What You’ll Be Doing
  • Responsible for the planning and execution of multi‑step syntheses from laboratory to commercialization, applying sound scientific principles, literature knowledge, and structured experimental approaches such as DoE and QbD.
  • Responsibilities include process development, implementation, technology transfer support, validation activities, and continuous improvement initiatives.
  • Works in a collaborative, cross‑functional environment and is expected to independently plan and execute laboratory work, interpret results, and communicate findings clearly.
  • Own the development, optimization, and scale‑up of robust, safe, and cost‑effective synthetic processes from laboratory through commercial manufacturing scale in compliance with cGMP requirements.
  • Design, execute, and interpret laboratory and pilot‑scale experiments to establish process understanding, identify critical quality attributes (CQAs) and critical process parameters (CPPs), and define appropriate operating ranges.
  • Plan, prioritize, and manage multiple development projects simultaneously, ensuring delivery against timelines, quality standards, and cost targets.
  • Serve as a technical subject matter expert in cGMP manufacturing operations applying fundamental chemistry and engineering principles to resolve complex manufacturing issues, troubleshoot challenges including investigation of deviations, non‑conformances, and process changes; and recommend effective corrective and preventive actions.
  • Evaluate existing manufacturing processes to identify and implement improvements in efficiency, robustness, quality, safety, environmental impact, and regulatory compliance.
  • Author, review, and maintain GMP documentation, including standard operating procedures (SOPs), batch production records (BPRs), validation protocols, and technical reports, ensuring data integrity and compliance.
  • Communicate complex technical information effectively through written reports, presentations, and verbal discussions with internal teams, departmental, site, and global leadership, as well as clients and external collaborators.
Who We’re Looking For Development Scientist I
  • M.S. in organic chemistry or related field (entry‑level; academic research experience preferred), or
  • B.S. in organic chemistry or related field with ~ 1 to 3 years of relevant industrial or academic research experience
Development Scientist II
  • Ph.D. in organic chemistry or related field (entry‑level industry or postdoctoral experience acceptable), or
  • B.S. or M.S. in organic chemistry or related field with ~ 3 to 5 years of relevant industrial experience (cGMP experience preferred)
Development Scientist III
  • Ph.D. in organic chemistry or related field with ~ 3 to 5 years of relevant industrial experience (cGMP experience preferred), or
  • B.S. or M.S. in organic chemistry or related field with ~ 5 to 8 years of relevant industrial experience (cGMP experience preferred)
Additional Competencies
  • Experience in the synthesis and purification of small molecules, notably lipids
  • Working knowledge of cGMP principles and regulated laboratory environments
  • Supports a positive, healthy, and flexible work environment
  • Maintains a well‑documented record of work performed in presentations, laboratory notebooks, batch production records, and Process Development Reports
  • Demonstrates clear understanding of technical issues and the requirements of a viable manufacturing process; has demonstrated independent support on multiple processes
  • Identifies areas where change/continuous improvement is beneficial to the business, and successfully defends and implements…
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