ZipRecruiter

Log In

1

Biotech Contract Manager Jobs in Missouri (NOW HIRING)

TekWissen LLC

Logistics Analyst

Creve Coeur, MO · On-site

$25 - $30/hr

... and biotechnology products. Job Title: Logistics Analyst Location: Creve Coeur, MO, USA, 63141 Duration: 6 Months Job Type: Contract Work Type: Onsite * Manage the day-to-day interaction and ...

Amgen

Strategic Sourcing Manager

Kansas City, MO

$125K - $163K/yr

Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest ... Develop and negotiate contracts, ensuring clear scope, deliverables, timelines, and accountability.

Nood

Technical Product Development Manager

California, MO · On-site

$85 - $110/hr

Manage contract manufacturer relationships, including briefing, follow-up, escalation, and driving ... biotech, or consumer goods manufacturing * Experience owning launch timelines across multiple ...

6AM City, LLC

Senior Buyer Planner

California, MO · On-site

$85 - $120/hr

Contract-to-Hire Overview We are seeking an experienced Senior Buyer / Planner to join a high ... Manage procurement and material planning activities for consumables, including: * Wet chemicals

New

kindeva

Senior Project Manager

Bridgeton, MO

Experience within pharmaceutical, biotechnology, or Contract Development and Manufacturing Organization (CDMO) environments. * Project Management Professional (PMP) certification. * Experience with ...

kindeva

Senior Project Manager

Bridgeton, MO

Experience within pharmaceutical, biotechnology, or Contract Development and Manufacturing Organization (CDMO) environments. * Project Management Professional (PMP) certification. * Experience with ...

kindeva

Senior Project Manager

Bridgeton, MO · On-site

Experience within pharmaceutical, biotechnology, or Contract Development and Manufacturing Organization (CDMO) environments. * Project Management Professional (PMP) certification. * Experience with ...

kindeva

Senior Project Manager

Bridgeton, MO

Experience within pharmaceutical, biotechnology, or Contract Development and Manufacturing Organization (CDMO) environments. * Project Management Professional (PMP) certification. * Experience with ...

Pioneer Data

Cell Culture Technician

Chesterfield, MO · On-site

Cell Culture Technician Duration: 18 months contract, extendable up to 48 months Location ... The Technical Associate, Cell Banking role is part of a biotechnology manufacturing team focused on ...

next page

Showing results 1-20

All JobsBiotech Contract JobsBiotech Contract Manager JobsBiotech Contract Manager Jobs in Missouri

Biotech Contract Manager information

What is a biotech contract manager?

A Biotech Contract Manager oversees contracts related to biotechnology partnerships, vendors, research agreements, and regulatory compliance. They negotiate terms, ensure adherence to legal and industry standards, and mitigate risks for their organization. Their role requires collaboration with legal teams, procurement, and scientific departments to support business objectives. Effective contract management helps biotech companies streamline operations, maintain compliance, and optimize financial and operational outcomes.

What are the typical day-to-day responsibilities of a biotech contract manager?

As a Biotech Contract Manager, your daily tasks often include drafting, reviewing, and negotiating a variety of contracts such as research agreements, vendor contracts, and licensing deals. You will regularly collaborate with legal, procurement, research, and finance teams to ensure terms align with company goals and regulatory requirements. Managing timelines, tracking key deliverables, and monitoring compliance throughout the contract lifecycle are also core parts of the role. This position requires balancing multiple priorities and maintaining strong communication with both internal teams and external partners to support the company’s scientific and commercial objectives.

What are the key skills and qualifications needed to thrive as a biotech contract manager?

A Biotech Contract Manager should possess a strong background in contract law, negotiation, and life sciences, often supported by a bachelor's or master's degree in a related field and relevant experience in biotech or pharmaceutical contract management. Familiarity with contract management software, compliance platforms (such as Icertis or DocuSign), and regulatory guidelines like FDA and GxP is highly beneficial. Superior attention to detail, analytical thinking, and excellent interpersonal and communication skills set outstanding professionals apart in this role. These capabilities ensure accurate and efficient contract execution, risk mitigation, and effective collaboration with internal and external stakeholders in a highly regulated industry.

What are popular job titles related to Biotech Contract Manager jobs in Missouri?

For Biotech Contract Manager jobs in Missouri, the most frequently searched job titles are:

What job categories do people searching Biotech Contract Manager jobs in Missouri look for?

The top searched job categories for Biotech Contract Manager jobs in Missouri are:

Biotech Contract Manager jobs near you
Infographic showing various Biotech Contract Manager job openings in Missouri as of August 2026, with employment types broken down into 86% Full Time, 11% Part Time, and 3% Contract. Highlights an 84% Physical, 3% Hybrid, and 13% Remote job distribution.

Senior Manager, Contract Development & Manufacturing

Jobtailor

California, MO • On-site

$180 - $240/hr

Other

Posted 5 days ago

Job description

Overview
  • Provide strategic and operational leadership within Amgen Contract Development and Manufacturing (ACDM)
  • Drive execution of external development and manufacturing activities for Synthetic Drug Substance (DS) programs supporting Antibody Drug Conjugate (ADC) and Small Molecule modalities across clinical and commercial stages.
  • Lead complex, cross‑functional programs with external development and manufacturing partners (CDMOs/CROs) to ensure reliable, compliant, and efficient supply execution.
  • Influence internal and external stakeholders in a dynamic global environment.
  • Serve as the primary interface with CDMOs/CROs and internal cross‑functional teams.
  • Drive sourcing activities including supplier selection, onboarding, scope of work development, and proposal management.
  • Oversee manufacturing operations, technical transfers, compliance, and issue resolution with external partners.
  • Ensure project delivery against quality, compliance, supply, timeline, and cost objectives.
  • Lead risk management, escalation resolution, and operational decision‑making across programs.
  • Build strong internal and external partnerships to support program success and operational excellence.
  • Manage quality systems activities including deviations, investigations, change controls, and CAPAs.
  • Manage budgets, purchase orders, and financial forecasting for external manufacturing activities.
  • Mentor and train ACDM staff and cross‑functional teams and demonstrate strong leadership, collaboration, and accountability.
Requirements
  • Doctorate degree and 2 years of Manufacturing, Operations, Process Development, or External Supply experience OR Master’s degree and 4 years of Manufacturing, Operations, Process Development, or External Supply experience OR Bachelor’s degree and 6 years of Manufacturing, Operations, Process Development, or External Supply experience OR Associate’s degree and 10 years of Manufacturing, Operations, Process Development, or External Supply experience OR High school diploma / GED and 12 years of Manufacturing, Operations, Process Development, or External Supply experience
  • Advanced degree in Chemistry, Chemical Engineering, Pharmaceutical Sciences, or related field preferred.
  • 10+ years of pharmaceutical or biotechnology experience in Synthetic DS development and manufacturing.
  • Experience supporting Small Molecule and/or ADC modalities from development through commercial manufacturing.
  • Proven leadership of external manufacturing programs with CDMOs/CROs in a cGMP environment.
  • Strong knowledge of cGMPs, quality systems, regulatory/CMC requirements, and pharmaceutical operations.
  • Experience with sourcing strategies, supplier management, and commercial supply operations.
  • Strong project management, strategic thinking, and problem‑solving skills.
  • Experience managing deviations, investigations, change controls, and CAPAs with external partners.
  • Demonstrated ability to lead and influence cross‑functional, matrixed teams.
  • Strong communication, collaboration, negotiation, and stakeholder management skills.
  • Self‑starter who thrives in fast‑paced, complex environments and drives continuous improvement.
  • Demonstrated commitment to teamwork, accountability, innovation, and patient focus.
#J-18808-Ljbffr

Apply