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

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 ...

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 ...

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 ...

Associate Project Manager

Cranbury, NJ · On-site

$49K - $96K/yr

PMP certificate can be a plus. * 0-5 years of project management experience in pharmaceutical, biotechnology, or CDMO industries preferred. * Strong understanding of CMC development and manufacturing ...

... project management, cosmetics, beauty, personal care, OTC products, or contract manufacturing industries preferred. * Experience within cosmetics manufacturing, CDMO/CMO, skincare, or beauty industry ...

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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 Aug 27, 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.

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 are the key skills and qualifications needed to thrive as a project manager in a CDMO, 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.

What are popular job titles related to Project Manager Cdmo jobs in Edison, NJ?

For Project Manager Cdmo jobs in Edison, NJ, the most frequently searched job titles are:

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.

MSAT CDMO Manager

Springfield, NJ • On-site

Lantheus
Pharmaceutical and Medicine Manufacturing • 501 - 1,000 employees

$111K - $185K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 13 hours ago


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. 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.

Applicants have rights under Federal Employment Law: Employee Polygraph Protection Act (EPPA); Family and Medical Leave Act (FMLA)
For California Applicants: Family Care & Medical Leave & Pregnancy Disability Leave; California Law Prohibits Workplace Discrimination & Harassment; Your Rights and Obligations as a Pregnancy Employee
For Ohio Applicants: Know Your Rights: Equal Employment Opportunity is the Law