ZipRecruiter

Log In

1

Project Manager Cdmo Jobs in Oregon (NOW HIRING)

Burke Porter Group

Program Manager

Corvallis, OR

Experience * 10+ years of program or project management experience in a CDMO, medical device, biotech, or regulated manufacturing environment. * Demonstrated experience owning program financials ...

Ascential Technologies

Program Manager

Corvallis, OR · On-site

Experience * 10+ years of program or project management experience in a CDMO, medical device, biotech, or regulated manufacturing environment. * Demonstrated experience owning program financials ...

Danaher

Senior Product Manager - Core Proteins

OR · On-site +1

$100K - $130K/yr

At Aldevron, we deliver world-class CDMO services that accelerate the development of groundbreaking ... Experience managing projects in a regulated biotechnology, pharmaceutical, or medical device ...

Telix Pharmaceuticals (AMER)

OR · On-site

This role may include direct people management of one or more Project managers. As a strategic ... CMC/Supply & Vendor (CDMO) Alignment: Partner with Technical Operations, Quality, and external ...

Telix Pharmaceuticals (AMER)

OR · On-site

$72.90K - $93.90K/yr

... and with external CDMO partners, collaborating with all stakeholders to develop and execute ... Manage technical collaborations with multiple contract development/manufacturing organizations ...

Telix Pharmaceuticals (AMER)

OR

$91.40K - $112.40K/yr

... CDMO (Contract Development/Manufacturing Organization) qualification initiatives, technical ... managing external CDMOs to ensure compliance with project timelines/cGMPs, and on-going ...

Aptyx

Business Development Executive East

Myrtle Point, OR · On-site

$120K - $190K/yr

Build, manage, and maintain a robust pipeline of qualified new opportunities aligned with revenue ... Monitor scope changes, commercial risks, and customer expectations throughout the project lifecycle ...

Aptyx

Business Development Executive East

OR · On-site +1

$120K - $190K/yr

Build, manage, and maintain a robust pipeline of qualified new opportunities aligned with revenue ... Monitor scope changes, commercial risks, and customer expectations throughout the project lifecycle ...

People also search for

All JobsProject Manager Cdmo JobsProject Manager Cdmo Jobs in Oregon

Project Manager Cdmo information

What are the key skills and qualifications needed to thrive as a Project Manager in a CDMO (Contract Development and Manufacturing Organization), and why are they important?

To excel as a Project Manager in a CDMO, you need a strong background in project management, life sciences, and regulatory compliance, often supported by a relevant degree and PMP certification. Familiarity with project management software (like MS Project or Smartsheet), quality management systems, and industry-specific regulations such as GMP are typically required. Outstanding organizational, communication, and stakeholder management skills help you effectively coordinate cross-functional teams and client expectations. These competencies are vital for delivering complex projects on time and within budget while maintaining regulatory standards and client satisfaction.

How does a Project Manager at a CDMO typically coordinate between clients and internal teams throughout a project lifecycle?

A Project Manager at a Contract Development and Manufacturing Organization (CDMO) acts as the central point of contact for clients and internal teams, ensuring clear communication and alignment of project goals. They regularly facilitate meetings, track project milestones, and proactively address potential issues or changes in scope. This involves close collaboration with departments such as R&D, manufacturing, quality assurance, and regulatory affairs to meet client expectations and project timelines. Effective project managers also document progress and maintain transparent reporting to both clients and internal stakeholders.

What is a Project Manager CDMO?

A Project Manager CDMO (Contract Development and Manufacturing Organization) is responsible for overseeing pharmaceutical or biotech projects outsourced to CDMOs. They coordinate between clients and internal teams to ensure timely delivery, quality, and compliance with regulatory standards. Their role includes managing project timelines, budgets, and resources, as well as communicating progress and addressing issues that may arise during drug development and manufacturing processes.
What are popular job titles related to Project Manager Cdmo jobs in Oregon? For Project Manager Cdmo jobs in Oregon, the most frequently searched job titles are:
What job categories do people searching Project Manager Cdmo jobs in Oregon look for? The top searched job categories for Project Manager Cdmo jobs in Oregon are:
What cities in Oregon are hiring for Project Manager Cdmo jobs? Cities in Oregon with the most Project Manager Cdmo job openings:
Project Manager Cdmo jobs near you
Senior Manager, Manufacturing Operations

Senior Manager, Manufacturing Operations

Rezolute

Bend, OR

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 17 days ago

Job description

Rezolute is a late-stage rare disease company focused on significantly improving outcomes for individuals with hypoglycemia caused by hyperinsulinism (HI). Our antibody therapy, RZ358 (ersodetug), is designed to treat all forms of HI and has shown substantial benefit in clinical trials and real-world use for the treatment of congenital hyperinsulinism (cHI) and tumor hyperinsulinism (tHI). 

Rezolute is seeking a seasoned professional to support its late-stage and pre-commercial external manufacturing operations. The Senior Manager of Manufacturing Operations will be a proactive, self-directed individual with a strong technical foundation and a clear understanding of the interface between Pharmaceutical Manufacturing, Quality Assurance, and external partners. This role requires the ability to interpret and communicate complex manufacturing information effectively across internal teams, business stakeholders, and CDMO partners. 

This fast-paced role supports execution of manufacturing strategies that ensure reliable, right-first-time, and on-time supply to support global clinical trials and commercialization of RZ358. Reporting to the Senior Director of External Manufacturing, this position supports partnerships with contract development and manufacturing organizations (CDMOs) and contributes to delivery of project milestones across multiple Drug Substance (DS) and/or Drug Product (DP) sites. The individual will work closely with internal SMEs (MSAT and QA), Business stakeholders, and Supplier Relationship Management (SRM) to ensure coordinated execution of manufacturing activities. 

Principle Duties and Responsibilities Include:

  • Support execution of Drug Substance (DS) and/or Drug Product (DP) manufacturing in accordance with approved plans, ensuring alignment with program timelines, supply requirements, and business priorities 

  • Serve as a technically informed liaison to internal SMEs (MSAT and QA), Business stakeholders, and Supplier Relationship Management (SRM) to help ensure manufacturing activities are coordinated and aligned with the Plan of Record (POR) 

  • Apply technical understanding of biologics manufacturing processes to support clear and effective communication across internal teams and CDMOs 

  • Work closely with Supplier Relationship Management (SRM), Business stakeholders, and Procurement (PO) to support scheduling, material readiness, and confirmation of manufacturing operations 

  • Support and help facilitate internal Manufacturing Operations alignment meetings to ensure cross-functional visibility and coordination 

  • Assist in coordination of technology transfer, start-up activities, validation, and clinical/commercial manufacturing to support continuity across CDMO partners 

  • Participate in internal and external technical sub-team meetings, including supplier-facing forums, to ensure consistency in communication and alignment to program and business objectives 

  • Support development and collection of manufacturing risk assessments; track risks and help ensure mitigation plans are progressing and visible to stakeholders 

  • Monitor manufacturing KPIs and communicate trends, risks, or issues to leadership, Business stakeholders, and SRM as appropriate 

  • Coordinate Master Batch Record (MBR) and Electronic Batch Record (EBR) review and approval workflows to ensure completeness and compliance 

  • Support tracking and progression of manufacturing change controls (internal and CDMO) through to closure 

  • Partner with QA and CDMOs to track and support resolution of deviations and investigations 

  • Support alignment of Manufacturing Supply Operational Plans with internal forecasts, program timelines, and business objectives 

  • Facilitate coordination of internal SMEs (QA, MSAT) and stakeholders to support timely execution of program deliverables 

  • Provide input into manufacturing-related scopes of work and contracts to ensure alignment with operational needs, supplier capabilities, and program strategy 

  • Support collaboration with Supplier Relationship Management (SRM) to ensure effective oversight of CDMO performance and partnership health 

  • Support tracking of manufacturing activities against budget and scope in collaboration with Finance, Business stakeholders, and leadership 

  • Contribute to development and use of PMO tools and manufacturing project management best practices 

  • Interface with PMO to support alignment of Tech Ops activities with broader program and business goals 

  • Support readiness activities for late-stage and commercial manufacturing, ensuring processes and documentation are aligned for scale, compliance, and supplier execution 

Qualifications/Requirements:
  • Minimum Bachelor's degree in a relevant scientific discipline 

  • Minimum 8 years of relevant experience (industry, project management, or related), with small to mid-sized biotech experience preferred 

  • Demonstrated technical understanding of biologics (mAb) manufacturing, including Drug Substance (upstream/downstream) and/or aseptic Drug Product operations 

  • Ability to apply technical knowledge to support cross-functional communication and decision-making across Technical Operations, Business teams, and external partners 

  • Experience working with CDMOs and supporting external manufacturing operations; exposure to supplier or business interface is preferred 

  • Strong organizational and project coordination skills, with the ability to manage multiple activities and timelines 

  • Demonstrated ability to work independently in a fast-paced, matrixed environment 

  • Strong attention to detail and ability to track complex deliverables to completion 

  • Effective interpersonal and communication skills, with the ability to work across technical, operational, and business functions 

  • Basic understanding of cGMP requirements and quality systems, including change controls, deviations, and batch record review 

  • Proficiency in Microsoft Teams, Excel, Word, PowerPoint, and Smartsheet 

Rezolute (RZLT) currently anticipates the base salary for Senior Manager Manufacturing Operations role could range from $165,000 to $180,000 and will depend, in part, on the successful candidate's geographical location and their qualifications for the role, including education and experience. This position will also be eligible for an annual performance bonus in accordance with the terms of the applicable plan (depending, in part, on company and individual performance and at the Company's discretion on an individual basis). The compensation described above is subject to change and could be higher or lower than the range described based on current market survey data and the qualifications, education, experience and geographical location of the selected candidate. 

Qualifying employees are eligible to participate in benefit programs such as: 

         Health Insurance (Medical / Dental / Vision) 

         Disability, Life & Long-Term Care Insurance 

         Holiday Pay 

         Tracking Free Vacation Program 

         401(k) Plan Match 

         Educational Assistance Benefit 

         Fitness Center Reimbursement 

We are an Equal Opportunity Employer and do not discriminate against applicants due to race, ethnicity, gender, veteran status, or on the basis of disability or any other federal, state or local protected class. 

We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.
apply for this job

Apply