- Location: United States
- Type: Contract
- Job ID: 10623
- Work Setting: On-Site
- Posted: September 25, 2026
- Closing Date: September 23, 2027
- Tax Status: W2
Consultant, Process Development / Manufacturing Support
Biopharma | Technical Operations | CMC Development
Our client, a clinical-stage biopharmaceutical company advancing innovative oncology therapies, has engaged GForce Life Sciences to identify a part-time Process Development / Manufacturing Support Consultant. This individual will support Technical Operations, manufacturing, process development, and CMC initiatives across late-stage programs.
Biopharma | Technical Operations | CMC Development
| Summary |
| Duties / Expectations of Role |
- Review and analyze process development and manufacturing data
- Assess process performance trends and support decision making
- Review batch records and technical documentation
- Support process characterization and manufacturing readiness activities
- Partner with process development scientists and CDMOs
- Assist with technology transfer, technical reporting, and CMC documentation
| Mandatory Requirements |
- BS or MS in Chemical Engineering, Chemistry, or related discipline
- 5-7+ years pharmaceutical industry experience
- Small molecule API development experience
- Background in Technical Operations, Manufacturing, or Process Development
- Strong analytical and documentation skills
| Nice to Have |
- Chemical Engineering background preferred
- Process chemistry experience
- API manufacturing experience
- CDMO and technology transfer experience
- Commercial readiness and validation support experience
| Term & Start |
- Part-time consulting engagement
- Approximately 20 hours per week
- Remote
- Target start: Early 2027
- Potential accelerated start for exceptional candidate