Microneedle Drug Delivery CRO/CDMO
Hours: 8:30 AM–5:30 PMSales: +86 10 8928 7035Business: bd@casmn.com
CASMN — Beijing CAS Microneedle TechnologyStart a Project
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CASMN CAREERS

Careers

Join CASMN in developing and scaling microneedle technology.

Open positions

Business Development

Responsibilities

  • Develop and maintain relationships with pharmaceutical, vaccine and biologics companies, CROs/CDMOs, research institutes, aesthetic medicine brands and distributors in China and abroad.
  • Advance licensing in and out, technology licensing, co-development, commissioned research, CDMO services and distribution partnerships.
  • Own lead generation, needs assessment, proposal discussions, quotations, negotiations, contracting and payment follow-up.
  • Represent CASMN at trade shows, roadshows and online meetings to promote its microneedle platform.
  • Coordinate project execution with R&D, regulatory affairs, legal, finance and quality teams.
  • Track policy, competitor activity and deal precedents to inform BD strategy and market intelligence.

Qualifications

  • Bachelor’s degree or higher in pharmacy, pharmaceutics, pharmacology, biomedicine, bioengineering or a related field.
  • At least 3 years in pharmaceutical BD, pharma partnerships, CRO/CDMO sales or international business.
  • Use English as a working language for email, calls, proposals, presentations, negotiations and contract discussions.
  • An established industry network in China or abroad, such as pharma R&D, BD or project leads, vaccine companies, CROs/CDMOs, aesthetic medicine brands, distributors or investors.
  • Familiarity with drug development and licensing, co-development and CDMO models. Knowledge of NMPA, FDA or EMA regulatory requirements is preferred.
  • Strong communication, negotiation and coordination skills, ability to work under pressure, and availability for domestic and international travel.
Apply by emailjingwang@casmn.com

Pharmaceutical Formulation R&D

Responsibilities

  • Screen formulations and develop processes. Use QbD and DoE to identify CQAs, CMAs and CPPs and guide optimization.
  • Prepare and evaluate samples, including IVRT/IVPT, sterility, endotoxins, CCIT, protein stability, microneedle strength and insertion, drug loading and release.
  • Support bench-to-pilot scale-up, process validation and technology transfer with manufacturing sites or CMO/CDMO partners.
  • Study material and packaging compatibility and stability, and maintain laboratory records.
  • Write experimental protocols, study reports, SOPs and relevant CTD pharmaceutical sections.
  • Monitor technology and regulatory developments, research technical topics and collect materials for patent filings.
  • Work with regulatory, quality, manufacturing and procurement teams while following GMP, data integrity and laboratory EHS requirements.

Qualifications

  • Bachelor’s degree or higher in pharmacy, pharmaceutics, pharmaceutical engineering, biopharmaceuticals, polymer materials or a related field.
  • Spoken English skills, overseas study, experience at a foreign pharmaceutical company or cross-border project experience are preferred.
  • Junior formulation researcher: Bachelor’s degree with at least 1 year of R&D experience, or a master’s degree as a recent graduate or with 1 year of experience. Perform assigned experiments under guidance.
  • Mid-level formulation engineer: Bachelor’s degree with at least 3 years, master’s degree with at least 2 years, or a recent PhD. Independently lead a workstream or key module.
  • Senior formulation engineer / project lead: Bachelor’s degree with at least 8 years, master’s degree with at least 5 years, or PhD with at least 3 years of R&D experience. Initiate projects, lead end-to-end development and manage a team of 2–5.
Apply by emailjingwang@casmn.com