1w
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Finance Director, CDMO Operations
Coventry, Rhode Island, United States
$180k-$240k/yr OnsiteFull Time
15+ YOECPA with ~15+ years finance leadership experience in accounting, FP&A, cost accounting, operational finance, manufacturing/CDMO preferred; strong controls, stakeholder management, SAP/Oracle preferred, advanced Excel.
SAP, Oracle ERP, Microsoft Excel
4w
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Global Key Account Manager - CMO/CDMO
Durham or Boston or New York City or Minneapolis
$130k-$170k/yr RemoteFull Time
8+ YOE1+ MgmtBachelor's degree and 8+ years key account management, experience managing >$10M global/manufacturing accounts, sales forecasting, strategic selling, travel (~30%), proficient with Microsoft Office and SalesForce.
Microsoft Office, SalesForce
3mo
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Director/Senior Director, CMC, Drug Substance
Boston or Needham
$222k-$303k/yr HybridFull Time
10+ YOEPhD in Chemistry or Chemical Engineering with 10+ years API CDMO experience; regulatory CMC writing; CDMO selection and tech transfer; extensive cGMP knowledge.
CDMO management, CMC, Regulatory writing, GxP
2mo
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CMC Synthetics Clinical Manufacturing Leader
Cambridge, Massachusetts, United States
$149k-$215k/yr OnsiteFull Time
5+ YOEPharmD or PhD; 5+ years in DS/DP manufacturing; GMP experience; cross-functional with CDMO; international collaboration.
2mo
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Director, Commercial Manufacturing & Process Engineering
Waltham, Massachusetts, United States
$184k-$253k/yr RemoteFull 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%.
JMP, Statistical analysis tools
2mo
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Director, Peptide Process Development (Cambridge, MA, US, 02142)
Cambridge, Massachusetts, United States
$197k-$267k/yr OnsiteFull Time
10+ YOEPhD with 10+ years in peptide or conjugate process development; experience leading CDMO collaborations and GMP manufacturing; strong regulatory documentation experience.
2mo
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Manager, Quality Assurance
Boston, Massachusetts, United States
$110k-$165k/yr HybridFull Time
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.
GMP, CAPA, SOPs, document control
2w
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Director, Biologics Development
Waltham, Massachusetts, United States
$190k-$230k/yr OnsiteFull Time
10+ YOE10+ years biopharma experience in biologics process development, CDMO management, CMC strategy, regulatory authoring (Module 3), and leadership in a matrixed environment.
2mo
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Senior Director, Commercial Manufacturing, Science and Technology
United States or Waltham or Boulder
$240k-$280k/yr RemoteFull Time
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
2mo
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Manager, QA Operations Disposition
Somerville, Massachusetts, United States
$118k-$166k/yr OnsiteFull Time
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
1w
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Senior Director, Formulation Development
Watertown, Massachusetts, United States
$235k-$330k/yr OnsiteFull Time
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.
3d
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Director/Senior Director, GMP Quality Assurance Operations
Waltham, Massachusetts, United States
$200k-$260k/yr OnsiteFull Time
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.
eQMS, DMS, LMS
4d
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Director, Strategic Sourcing
Boston, Massachusetts, United States
$180k-$270k/yr HybridFull Time
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.
Power BI, Tableau, Microsoft Office, ERP
1w
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Senior Director, Drug Product
Waltham, Massachusetts, United States
OnsiteFull Time
10+ YOEPhD or MS/BS with equivalent experience in chemistry/chemical engineering or life sciences; 10+ years biologics drug product experience, CMC and CDMO management, regulatory submission experience.
2mo
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Sr. Business Development Executive - Biotech Solutions (New England)
Boston, Massachusetts, United States
$128k-$192k/yr RemoteFull Time
5+ YOE5+ years quota-carrying field sales or business development in CDMO services; hunter mindset; proven new logo wins and multi-year contracts; willing to travel up to 50%.
1d
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Associate Director, Analytical Development & Quality Control
Boston, Massachusetts, United States
OnsiteFull Time
8+ YOE5+ MgmtPh.D. with ≥8 years or M.S. with ≥11 years in analytical chemistry/radiochemistry; ≥5 years managing CDMOs; experience with analytical method lifecycle, investigations, OOS/OOT, CAPA, and cGMP/ICH requirements.
1d
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QA Product Complaint Manager
Waltham, Massachusetts, United States
$118k-$145k/yr HybridFull Time
5+ YOE5+ years QA experience in biotech/pharma/medical device, Bachelor's in Life Science or Engineering, complaint handling, experience with CDMOs, Veeva eQMS, knowledge of US/global GMP and ICH guidelines.
Veeva Quality Management System, Microsoft Word, Microsoft PowerPoint, Microsoft Excel, Microsoft Outlook, Microsoft SharePoint
2mo
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Principal Scientist, Drug Product Development
Cambridge, Massachusetts, United States
$165k-$200k/yr OnsiteFull Time
8+ YOEPhD in a related field; 8-10+ years drug product development experience for peptides; expertise in parenteral and oral dosage forms; experience with CRO/CDMO and IND/CMC activities; leadership and collaboration skills.
Parenteral formulations, Oral dosage forms, Formulation development, CMC, IND
2mo
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Director, Peptide Process Development
Cambridge, Massachusetts, United States
$197k-$267k/yr OnsiteFull Time
10+ YOEPhD in a relevant scientific discipline, 10+ years industry experience in peptide/POC process development, CDMO management and process transfer experience, regulatory CMC documentation experience, and cross-functional leadership ability.
1d
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Principal Engineer
Waltham, Massachusetts, United States
$173k-$193k/yr HybridFull Time
PhD (>8 yrs) or MS (>15 yrs) in Science/Engineering; expert in small-molecule process development, scale-up, tech transfer, DOE, data analysis, CDMO management; strong leadership and communication.
Process Analytical Technology (PAT)
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