IpsenEuronext Paris: IPN: Develops medicines for oncology, neuroscience and rare diseases.
5+ YOE5+ years’ pharma experience with international exposure; project management; experience with Clinical Packaging, Distribution and CDMOs; English fluent.
Business Development Manager - CDMO - Therapeutics/Life Science
Milford, Massachusetts, United States
$120k-$170k/yrRemoteFull Time
LGC Group: Global life sciences measurement tools and laboratory services provider.
Bachelor’s degree; proven success in pharma/biotech/CDMO sales; strong understanding of drug development and regulatory landscape; excellent communication; able to manage long sales cycles; multilingual a plus.
Xenon PharmaceuticalsNASDAQ: XENE: Developing therapeutics for neurological and psychiatric disorders.
10+ YOE10+ MgmtPhD/ MSc with 10+ years pharma/biotech management; late-stage drug product manufacturing, CDMOs, cGMP; regulatory filings; leadership and budgeting.
LonzaSIX Swiss Exchange: LONN: Manufactures medicines and provides development services for healthcare companies.
8+ YOEBachelor's in life sciences or business required (advanced preferred),8+ years in biotech/pharma/CDMO business development or sales,proven new-business track record,knowledge of biologics and CDMO services,Salesforce and Microsoft Office proficiency,ability to travel up to 50%.
Director, Commercial Manufacturing & Process Engineering
Waltham, Massachusetts, United States
$184k-$253k/yrRemoteFull Time
Deciphera Pharmaceuticals: Developing targeted kinase inhibitors for the treatment of cancer.
10+ YOE10+ years in pharmaceutical/biopharmaceutical CMC development, commercialization, and manufacturing; leadership; cGMP; CDMO/CMO experience; travel up to 30%.
Director, Peptide Process Development (Cambridge, MA, US, 02142)
Cambridge, Massachusetts, United States
$197k-$267k/yrOnsiteFull Time
AlnylamNasdaq: ALNY: Developing and commercializing RNA interference (RNAi) therapeutics for diseases.
10+ YOEPhD with 10+ years in peptide or conjugate process development; experience leading CDMO collaborations and GMP manufacturing; strong regulatory documentation experience.
PCI Pharma Services: Integrated pharmaceutical development, manufacturing, and global packaging services.
7+ YOE5+ MgmtBachelor’s or Master’s in life sciences or business; 7+ years Biotech/Pharma; PM experience; CDMO preferred; leadership; proficiency with PM tools.
Microsoft Word, Microsoft Excel, Microsoft Access, Microsoft Project, Smartsheet
Rhythm PharmaceuticalsNASDAQ: RYTM: Develops precision medicines for rare neuroendocrine and obesity diseases.
5+ YOE1+ MgmtBachelor's degree in a scientific discipline; 5+ years in pharma QA/compliance; experience with CDMOs, sterile products, and cGMP; strong regulatory knowledge.
Senior Director, Commercial Manufacturing, Science and Technology
United States or Waltham or Boulder
$240k-$280k/yrRemoteFull Time
Cogent BiosciencesNASDAQ: COGT: Develops precision therapies for genetically defined diseases
20+ YOE12+ MgmtLead CDMO CMC lifecycle for late-stage to commercial, 20+ years biotech/pharma; strong regulatory, vendor management, and cross-functional leadership.
cGMP, CDMO coordination, Process Validation, IND, IMPD, CMC, Regulatory Filings
Genetix Biotherapeutics: Developing and commercializing curative gene therapies for rare diseases.
7+ YOEBachelor’s in STEM; 7+ years in regulated biopharma with cGMP; lot disposition/batch review; CMOs/CDMOs experience; GMP docs; electronic systems usage.
eQMS, LIMS, Document Management Systems, Batch Record Management
Associate Director, CMC Product Development – Small Molecule
Boston or Durham
$198k-$211k/yrHybridFull Time
Beeline Medicines: A clinical-stage biotechnology focused on precision therapies for autoimmune and inflammatory diseases.
7+ YOE7+ years in small-molecule drug product development; Ph.D. preferred; leadership of formulation and manufacturing programs; CDMO oversight; strong regulatory documentation experience.
Veranova: Global pharmaceutical developer and manufacturer focused on quality, compliance, and patient outcomes.
6+ YOEBachelor's in Chemistry, Chemical Engineering, Pharmaceutical Sciences, or related field; 6-8 years pharma CDMO PM experience; strong PM, regulatory, and financial acumen.
Kymera TherapeuticsNASDAQ: KYMR: Develops targeted protein degradation medicines to treat human diseases.
15+ YOEPhD and 15+ years pharmaceutical experience in early-stage formulation development, expertise in preformulation, biopharmaceutics, enabling technologies, GMP/regulatory knowledge, and CRO/CDMO management.
Crescent BiopharmaNASDAQ: CBIO: Develops novel oncology therapies and antibody-drug conjugates for cancer.
8+ YOEBachelor's in life sciences,8+ years GMP QA experience for biologics,experience with CDMOs,tech transfer,PPQ,BLA support,knowledge of global GMP and regulatory submissions.
Senior Director, Analytical Research & Development
Boston, Massachusetts, United States
$230k-$270k/yrOnsiteFull Time
Seaport Therapeutics: Develops oral neuropsychiatric medicines using a proprietary technology platform.
12+ YOE6+ MgmtMS or PhD in analytical chemistry with 12–15+ years in small-molecule analytical development; leadership experience; CDMO management; regulatory liaison; strong LC/GC and spectroscopic skills.
Vertex PharmaceuticalsNASDAQ: VRTX: Develops and sells prescription drugs for serious genetic diseases.
10+ YOE10+ years sourcing/CDMO experience in pharmaceuticals, strong negotiation and supplier management, leadership and team development, contract and risk management, analytical skills, familiarity with GMP and regulatory standards.