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Manage Cdmo Jobs (NOW HIRING)

... CDMO Compliance Officer for its FUJIFILM Biotechnologies business, a world-leading contract ... The individual will play a critical role in helping FUJIFILM Biotechnologies manage new and ...

CDMO Project Manager

Saint Louis, MO · On-site

$89K - $133K/yr

Louis, Missouri Your Role We are looking for a successful, true Project Manager for our Cherokee CDMO (Custom Development Manufacturing Organization) site in St. Louis. In this position you will play ...

Director, QA GMP Operations

Waltham, MA · On-site

$188K - $230K/yr

Manage CDMO performance within Quality Agreement expectations and GMP compliance. * Drive continuous improvement and inspection readiness. * Collaborate cross functionally to ensure pre-approval ...

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How much do manage cdmo jobs pay per year?

As of Sep 13, 2026, the average yearly pay for manage cdmo in the United States is $59,525.00, according to ZipRecruiter salary data. Most workers in this role earn between $42,000.00 and $68,500.00 per year, depending on experience, location, and employer.

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For Manage Cdmo jobs, the most frequently searched job titles are:

Associate Director, External Manufacturing

Madison, WI • On-site

Scorpion Therapeutics
51 - 200 employees

Other

Posted 2 days ago

New


Job description

Responsibilities:
  • Serve as single point of accountability and primary technical/business interface for 1–3 strategic CDMOs supporting drug substance, conjugation, and/or drug product manufacturing.
  • Lead day-to-day CDMO operations: joint operating cadences, governance meetings, escalation pathways, and performance reviews; build trust with CDMO leadership/technical teams.
  • Drive on-time, in-full, in-specification delivery of clinical and commercial supply; monitor KPIs (yield, cycle time, right-first-time, deviation rate, on-time release).
  • Lead and approve technology transfers from internal Process Development into assigned CDMOs.
  • Review/approve batch records, deviations, CAPAs, change controls, investigations, risk assessments, and validation documentation from CDMOs.
  • Develop/execute risk mitigation for critical raw materials, secondary sourcing, and capacity contingency.
  • Partner with Procurement and Legal on commercial terms, statements of work, quality agreements, and capacity reservations.
  • Cross-functional leadership across PD, Analytical Development, Quality, Regulatory, Supply Chain, Program Management, and Clinical Supply; translate program priorities into CDMO deliverables and resolve issues in a matrixed environment.
  • Provide technical oversight of solid-phase oligonucleotide synthesis, purification (HPLC, TFF/UF-DF), lyophilization, ligand conjugation (e.g., GalNAc), and related unit operations.
  • Support drug product formulation, sterile filtration, fill‑finish, and stability.
  • Lead PPQ, validation, and commercial supply readiness; support comparability assessments; partner on demand planning/capacity modeling/S&OP; drive cost‑of‑goods optimization.
  • Contribute CMC sections (IND/CTA/BLA/NDA) and support regulatory interactions, pre‑approval inspections, and inspection readiness; partner with QA on quality agreements/audits.
Requirements:
  • PhD, MS, or BS in Chemistry, Chemical Engineering, Biochemistry, Pharmaceutical Sciences, or related field.
  • 8+ years (or less with PhD) in biopharmaceutical technical operations/external manufacturing/CMC with progressive responsibility.
  • Proven experience managing CDMO relationships as primary technical/business owner (technology transfer, GMP oversight, performance management).
  • Required: synthetic oligonucleotide (siRNA or ASO) manufacturing experience; strong preference for GalNAc conjugates/targeted RNA delivery technologies.
  • Ability to lead/influence in a cross‑functional, matrixed environment (PD, AD, Quality, Regulatory, Supply Chain).
  • Experience supporting late‑stage clinical programs/commercial launches (PPQ; BLA/NDA‑supporting activities).
  • Strong working knowledge of FDA/EMA/ICH GMP and supporting regulatory inspections at CDMOs.
  • Excellent written/verbal communication; translate technical detail into executive recommendations.
Preferred:
  • Lead complex strategy projects with minimal direction.
  • Experience developing operations network strategies for a growing global market.
Onsite:

Based onsite; expected in office five days a week.

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