Posted 13 August, 2026
Job Id: 629909
Scientist, Attribute Sciences, Process Development
Job Description
Target PR Range: 29-39/hr DOE
The Scientist, Attribute Sciences, Process Development develops, qualifies, and transfers phase-appropriate analytical methods supporting small molecule and antibody-drug conjugate (ADC) drug substance and drug product development from early clinical through commercial stages. The role collaborates closely with Process Development DS/DP teams to ensure methods are scientifically sound and compliant with regulatory requirements.
Education
- Ph.D. in Analytical Chemistry, Pharmaceutical Sciences, Chemistry, or related scientific discipline with 1-3 years of industry experience; or
- M.S. with 4-6 years of relevant pharmaceutical industry experience; or
- B.S. with 6-8 years of relevant pharmaceutical industry experience.
Required Technical Experience
- Hands-on experience with HPLC/UHPLC, LC-MS/MS, GC, KF, UV-Vis, FTIR, and related analytical techniques.
- Strong knowledge of method development, qualification, validation, and transfer.
- Experience supporting small molecule and antibody-drug conjugate (ADC) development including impurity characterization, stability studies, and DS/DP analytical activities.
Key Responsibilities
- Develop, optimize, troubleshoot, and qualify analytical methods for characterization, release, stability, and process support.
- Develop stability-indicating methods for critical quality attributes, including assay, impurities, dissolution, water content.
- Support small molecule and ADC process development, optimization, technology transfer, and control strategy development.
- Characterize intermediates, starting materials, drug substances, and drug products for small molecules and ADC programs.
- Build process understanding through impurity profiling and material characterization.
- Plan and execute method qualification and validation in accordance with ICH guidelines.
- Ensure methods are robust, reproducible, and fit for purpose across the product lifecycle.
- Analyze experimental data using sound scientific and statistical approaches.
- Maintain accurate documentation in ELNs and laboratory information systems.
- Author technical reports, development summaries
Equal Opportunity Employer
We are proud to be an equal opportunity employer. We welcome and encourage applications from all qualified candidates regardless of race, sex, gender identity or expression, disability, age, religion or belief, sexual orientation, or any other characteristic protected by applicable laws and regulations. It is our policy not to discriminate against any applicant or employee, and we are committed to fostering a diverse, inclusive, and respectful work environment across all locations in which we operate. We believe that diversity, equity, and inclusion are fundamental to our mission and enhance our ability to serve clients globally. If you have a disability or require any reasonable accommodations during the application or interview process, please inform your recruiter or contact us directly so that we can explore the appropriate arrangements.
Fraud Alert
Candidate safety is a top priority at Planet Pharma. The industry has seen an increase in people falsely representing themselves as recruiters to gather personal information from job seekers. For your safety, do not provide sensitive data to anyone you have not spoken with thoroughly, never provide banking information during the application process and always double check the email address of the Recruiter to ensure it’s from an official Planet Pharma domain (@planet-pharma.com, @planet-pharma.co.uk, and @ppgadvisorypartners.com) and not a domain with an alternative extension like .net, .org or .jobs.