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Project Manager Cdmo Jobs in Edison, NJ (NOW HIRING)

The MSAT CDMO Manager provides technical and people leadership for MSAT activities supporting ... Lead multiple MSAT projects, including full technology transfer execution from initiation through ...

New

As an international Contract Development and Manufacturing Organization (CDMO), we support the ... Manage projects in the allocated area and escalate complex issues to more senior colleagues or ...

MSAT CDMO Manager

Springfield, NJ · On-site

$111K - $185K/yr

The MSAT CDMO Manager provides technical and people leadership for MSAT activities supporting ... Lead multiple MSAT projects, including full technology transfer execution from initiation through ...

New

As an international Contract Development and Manufacturing Organization (CDMO), we support the ... Manage projects in the allocated area and escalate complex issues to more senior colleagues or ...

As an international Contract Development and Manufacturing Organization (CDMO), we support the ... Manage projects in the allocated area and escalate complex issues to more senior colleagues or ...

Sales Manager

Jersey City, NJ · On-site

$135K - $150K/yr

The manager will collaborate cross-functionally with product development, project management, and ... , CMO, and/or CDMO environment. * Experience in the Nutraceutical, Vitamin, Supplement, or ...

Cambrex is a leading global contract development and manufacturing organization (CDMO) that ... The position requires experience in budgeting, project management, and system-related initiatives ...

Cambrex is a leading global contract development and manufacturing organization (CDMO) that ... The position requires experience in budgeting, project management, and system-related initiatives ...

Cambrex is a leading global contract development and manufacturing organization (CDMO) that ... The position requires experience in budgeting, project management, and system-related initiatives ...

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Showing results 1-20

Project Manager Cdmo information

See Edison, NJ salary details

$46.1K

$100K

$159.9K

How much do project manager cdmo jobs pay per year?

As of Jul 30, 2026, the average yearly pay for project manager cdmo in Edison, NJ is $99,964.00, according to ZipRecruiter salary data. Most workers in this role earn between $77,600.00 and $117,000.00 per year, depending on experience, location, and employer.

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 does a project manager at a pharmaceutical company do?

A project manager at a pharmaceutical company oversees the planning, execution, and completion of drug development and clinical trial projects. They coordinate teams, manage budgets, ensure regulatory compliance, and track project timelines using tools like Gantt charts and project management software. Their role ensures projects meet scientific, regulatory, and business objectives efficiently.

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 the highest paying project manager?

The highest paying project managers are often those working in industries like technology, finance, or pharmaceuticals, with senior roles such as Program Manager or Portfolio Manager earning top salaries. Certifications like PMP and experience managing large, complex projects can also contribute to higher compensation, especially in regions with high demand for project management expertise.

Can I make 100k as a project manager?

Project managers, especially in the pharmaceutical or biotech industries, can earn $100,000 or more annually depending on experience, location, and certifications like PMP. Senior project managers or those working in high-demand sectors often have higher earning potential, with salaries influenced by project complexity and company size.

What is the highest paying job in pharmaceuticals?

In the pharmaceutical industry, senior roles such as Vice President of Research and Development or Chief Scientific Officer tend to be the highest paying positions, often earning six-figure salaries. Project Managers in CDMO companies with extensive experience and advanced certifications can also earn high compensation, especially when overseeing large-scale projects or managing multiple teams.
What cities near Edison, NJ are hiring for Project Manager Cdmo jobs? Cities near Edison, NJ with the most Project Manager Cdmo job openings:
Infographic showing various Project Manager Cdmo job openings in Edison, NJ as of June 2026, with employment types broken down into 3% As Needed, 1% Full Time, 95% Part Time, and 1% Nights. Highlights an 87% Physical, 4% Hybrid, and 9% Remote job distribution, with an average salary of $99,964 per year, or $48.1 per hour.

$111K - $185K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 3 days ago

New


Job description

Lantheus (NASDAQ: LNTH) is the leading radiopharmaceutical-focused company, delivering life-changing science to enable clinicians to Find, Fight and Follow disease to deliver better patient outcomes. Headquartered in Massachusetts with offices in New Jersey, Canada, Germany, Sweden, Switzerland and United Kingdom, Lantheus has been providing radiopharmaceutical solutions for nearly 70 years.

Today, we’re expanding our portfolio and pipeline across oncology, neurology and cardiology. Through recent acquisitions, along with strategic partnerships across the life sciences ecosystem, we are accelerating our efforts to advance precision medicine and improve patient outcomes around the world.

At Lantheus we are purpose-driven, and every employee plays a vital role in our success. We’re dedicated to cultivating a high-growth, forward-thinking culture where innovation thrives and diverse perspectives drive meaningful progress.

Join us and be part of a company where your contributions make a real impact, because we know someone’s health is in our hands.

Summary of role

We are seeking a Manager of CDMO Manufacturing Science & Technology (MSAT) for our Springfield location.  The MSAT CDMO Manager provides technical and people leadership for MSAT activities supporting pharmaceutical and/or radiopharmaceutical drug product manufacturing across internal and external manufacturing networks. This role is accountable for execution of multiple technology transfer and manufacturing support projects while ensuring alignment with cGMP requirements and business objectives.

The MSAT CDMO Manager leads MSAT staff, interfaces with senior stakeholders, and ensures delivery of technically sound and compliant manufacturing solutions.

This position is based in New Jersey and requires a presence on-site 5 days per week, and open to applicants authorized to work for any employer within the United States.

Responsibilities

  • Lead multiple MSAT projects, including full technology transfer execution from initiation through commercial manufacturing.
  • Lead and manage team staff, including assignment of work, prioritization of activities, mentoring, and technical development of team members.
  • Serve as primary MSAT technical lead for assigned manufacturing sites and external partners.
  • Oversee and approve deviation investigations, CAPAs, and change controls.
  • Provide technical oversight for process validation, qualification, and lifecycle management activities.
  • Review and approve technical documentation including tech transfer packages, validation strategies, and regulatory support documents.
  • Provide strategic input into control strategies, process robustness, and continuous improvement initiatives.
  • Lead, mentor, and develop MSAT scientists; assign work and manage priorities.
  • Collaborate with Quality, Manufacturing, Validation, Supply Chain, and Regulatory Affairs to ensure aligned execution.
  • Represent MSAT during regulatory inspections, audits, and governance forums.
  • Actively promote safety culture and Lantheus values.

Basic Qualifications

  • Bachelor’s degree with 7+ years of relevant experience; Master’s degree with 5+ years; or PhD with 3+ years of relevant experience.
  • Demonstrated experience leading tech transfer and manufacturing support activities in a regulated environment.
  • Prior experience managing or leading technical teams.
  • Strong understanding of cGMPs and regulatory expectations.

Other Requirements

  • Willingness to work onsite and travel up to ~20% as required.
  • Strong leadership, communication, and decisionmaking skills.
  • Ability to manage multiple complex technical initiatives concurrently.
  • Strong organizational, communication, and problem-solving skills.
  • Experience with radiopharmaceuticals is preferred.
  • Understanding GMP/GLP principles.
  • Knowledge of hazardous material safety and cGMP requirements.
  • Strong attention to detail and documentation accuracy
  • Previous lab experience in Manufacturing and/or Quality Control at an aseptic processing facility is preferred.
  • Previous experience in Quality, Compliance and/or Manufacturing of radiopharmaceutical products is preferred.

Core Values

The ideal candidate will embody Lantheus core values:

  • Let people be their best
  • Respect one another and act as one
  • Learn, adapt, and win
  • Know someone’s health is in our hands
  • Own the solution and make it happen

The pay range for this position is between $111,000 and $185,000 annually.

Actual base pay offered may vary depending on a number of factors such as job-related knowledge, skills and experience. Employees in this position are eligible for a discretionary performance-based cash incentive, and depending on the level of the role may be eligible for a discretionary annual equity award. Benefits for this position include a comprehensive health benefits package that includes medical, prescription drug, dental, and vision coverage. Other offerings include life and disability benefits, pre-tax accounts, a 401(k) with company contribution, and a variety of other benefits. In addition, employees are eligible for a generous time off package including paid vacation, holidays, sick days, and paid parental leave. Interested candidates can apply at Lantheus.com. Applications for this position will be accepted until 9/1/2026.

Lantheus is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's actual or perceived race, color, creed, religion, national origin, ancestry, citizenship status, age, sex or gender (including pregnancy, childbirth, related medical conditions and lactation), gender identity or gender expression, sexual orientation, marital status, military service and veteran status, disability, protected medical condition as defined by applicable state or local law, genetic information, or any characteristic protected under applicable federal, state, or local laws and ordinances.

Any applicant requiring an accommodation in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should make a request to the Lantheus Talent Acquisition team at talentacquisition@lantheus.com.

Lantheus is an E-Verify Employer.