3mo
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Clinical Supply Chain CDMO Project Manager
Cambridge or Wrexham or London
$92k-$134k/yr OnsiteFull Time
5+ YOE5+ years’ pharma experience with international exposure; project management; experience with Clinical Packaging, Distribution and CDMOs; English fluent.
6d
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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
2mo
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Business Development Manager - CDMO - Therapeutics/Life Science
Milford, Massachusetts, United States
$120k-$170k/yr RemoteFull Time
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.
4w
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Global Key Account Manager - CMO/CDMO
United States or Minnesota or Minneapolis or Boston or New York City
$130k-$170k/yr RemoteFull Time
8+ YOEBachelor's degree,8+ years key account management,experience managing >$10M global manufacturing accounts,proven sales results,forecasting and metrics experience,proficient with Microsoft Office and SalesForce,ability to travel ~30%.
Microsoft Office, SalesForce
3mo
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Director, CMC, Drug Product
Burnaby or Boston
$181k-$213k/yr HybridFull Time
10+ YOE10+ MgmtPhD/ MSc with 10+ years pharma/biotech management; late-stage drug product manufacturing, CDMOs, cGMP; regulatory filings; leadership and budgeting.
cGMP, CDMO, FMEA, CPP, QA, IND/NDA/MAA
3mo
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Associate Director, Oligonucleotide Development
Waltham, Massachusetts, United States
$159k-$195k/yr OnsiteFull Time
8+ YOEPhD or equivalent with 8+ years in oligonucleotide process chemistry, CMC strategy, CDMO management, and regulatory submissions.
PMO synthesis, ASO synthesis, cGMP, analytical development, CDMO management
3mo
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Senior Director, Biotherapeutics
Boston, Massachusetts, United States
OnsiteFull Time
Extensive biotherapeutics experience, antibody engineering, CDMO collaboration, developability assessment, IND readiness, and leadership of matrix teams.
CDMO management, IND support, high-throughput screening, biotherapeutics design, protein expression systems
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
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
3mo
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Associate Director, CMC Product Development – Small Molecule
Boston or Durham
$198k-$211k/yr HybridFull Time
7+ YOE7+ years in small-molecule drug product development; Ph.D. preferred; leadership of formulation and manufacturing programs; CDMO oversight; strong regulatory documentation experience.
CDMO Management, Regulatory Submissions (IND/IMPD/NDA), DoE, QbD, CQAs, CPPs, Stability Testing, Container-Closure
6d
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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.
3mo
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Senior Project Manager
Devens, Massachusetts, United States
$140k-$155k/yr OnsiteFull Time
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.
Project Management, cGMP, ICH, P&L management, Client/vendor coordination
2d
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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
3mo
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Senior Director, Analytical Research & Development
Boston, Massachusetts, United States
$230k-$270k/yr OnsiteFull Time
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.
HPLC, GC, LC-MS, LC-MS/MS, HPLC-FLR, qToF, IR, qNMR, Thermal analysis, Dissolution
2d
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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.
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