CMC & Manufacturing, Science and Technology Drug Substance Lead
Listed on 2026-03-03
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Healthcare
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Pharmaceutical
CMC & Manufacturing, Science and Technology Drug Substance Lead
- Full-time
- Sobi
Location:
United States
Statistics show that women and underrepresented groups tend to apply to jobs only if they meet 100% of the qualifications. Sobi encourages you to change that statistic and apply. Rarely do candidates meet 100% of the qualifications. We look forward to your application!
At Sobi, each person brings their unique talents to work as a team and make a difference. We are dedicated to developing and delivering innovative therapies to improve the lives of people who live with a rare disease. Our edge comes from our team of people and our commitment to patients.
Our mission and culture at Sobi North America get us excited to come to work every day, but here are a few more reasons to join our team:
- Competitive compensation for your work
- Generous time off policy
- Opportunity to broaden your horizons by attending popular conferences
- Emphasis on work/life balance
- Collaborative and team-oriented environment
- Making a positive impact to help ultra-rare disease patients who are in need of life saving treatments
Location Requirement: This position may be based on either the U.S.West Coast (ideally near San Diego,CA) or the East Coast (ideally near Raleigh,NC or Boston, MA). The role requires periodic travel between both locations to support cross‑site collaboration and business needs.
The CMC & Manufacturing, Science and Technology Drug Substance Lead will be responsible for:
- Experienced subject matter expert (SME) and process ownerfor Drug Substance(DS) synthesisofa smallmoleculeused inoraldosage forms.
- Lead the technical work streams of a manufacturing process transfers from development to commercial site and between commercial sites, scale-up activities, process validations and oversees manufacturing of Drug Substance small molecules at external manufacturers for projects in clinical and commercial phase.
- Experience in collaborating effectively with external manufacturing partners and to oversee all technical drug substance synthesis aspects (GMP and non-GMP steps).
- Lead internal activities related to external manufacturing such as process change assessments, major/critical deviations, risk assessments and CAPAs.
- Review and supervise design, set up, execution and documentation of DS related technical studies (CMC development as well as commercial operations), process and equipment qualifications and validations.
- Write and review applicable sections in registration files, variations and market expansion.
- Issue, review and approve applicable internal and external SOPs and fully oversee correctness and compliance of external manufacturing instructions.
- Contribute during set up of new analytical specifications and stability programs and review changes thereof.
- Support in sourcing evaluation of new Drug Substance small molecules, oral dosage forms alternative contract manufacturers and participation in developing supply and quality agreements.
- Be aware of modern synthetic organic chemistry methodologies, advancements, understand and introduce new technologies and how they may be applicable to process innovation, cost or yield improvement.
Education / Learning Experience /
Work Experience:
- University education in Chemistry, Pharmacy or similar.
- 10+ years of experience of development and manufacturing of Drug Substance small molecule, non‑sterilized dosage forms for clinical and commercial use. Ideally for more than 2 molecules.
Skills / Knowledge /
Languages:
- Recognized expert in synthetic organic chemistry and process R&D; experience with deuterated molecules is a plus.
- Scientific and technical background of CMC development and GMP‑compliant manufacturing for small molecule drug substance.
- Experience of working with external manufacturers.
- Demonstrable experience of working in cross functional team with ability to lead functional teams, prioritize and be an effective decision maker.
- Experience of regulatory guidelines (FDA & EMA), regulatory authorities communication and filing documentation.
- Fluent in English, intermediate to full proficiency in Chinese is a plus.
Personal Attributes:
- Strong cross‑functional team player with a strong track record…
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