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Project Manager Cdmo Jobs in Charleston, SC (NOW HIRING)

Project Manager Cdmo information

See Charleston, SC salary details

$41.6K

$90.4K

$144.6K

How much do project manager cdmo jobs pay per year?

As of Sep 5, 2026, the average yearly pay for project manager cdmo in Charleston, SC is $90,362.00, according to ZipRecruiter salary data. Most workers in this role earn between $70,200.00 and $105,700.00 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 Charleston, SC?

For Project Manager Cdmo jobs in Charleston, SC, the most frequently searched job titles are:

What cities near Charleston, SC are hiring for Project Manager Cdmo jobs?

Cities near Charleston, SC with the most Project Manager Cdmo job openings:

Infographic showing various Project Manager Cdmo job openings in Charleston, SC as of August 2026, with employment types broken down into 82% Full Time, 16% Part Time, and 2% Contract. Highlights an 84% Physical, 3% Hybrid, and 13% Remote job distribution, with an average salary of $90,362 per year, or $43.4 per hour.

Sr. Project Manager - Drug Product , Pharma , CDMO

Alcami Corporation

Charleston, SC • On-site

Full-time

Re-posted 24 days ago


Key responsibilities

  • Coordinate a multidisciplinary project team to ensure the accurate and timely completion of project tasks, including contract writing, project planning, and management activities.

  • Develop, track, and communicate project plans, timelines, budgets, and status updates to internal teams and clients, while managing contract requirements and implementing change orders.

  • Facilitate team meetings, drive interdepartmental collaboration, and assist with business development and regulatory activities related to drug development projects.


Alcami rating

7.8

Company rating: 7.8 out of 10

Based on 9 frontline employees who took The Breakroom Quiz


Job description

 

At Alcami, we deliver reliable solutions that unlock the potential of transformative medicines from discovery to commercialization, through trusted partnership with our clients, recognized industry expertise and proven regulatory track record.

Are you interested in joining our team? 

Job Summary

The Senior Project Manager will coordinate a multidisciplinary project team to assure the accurate and timely completion of all contract writing and managing, ERP, invoicing, designing and implementing project plans, acting as the primary liaison with the project team and client communicating project information to appropriate staff members. The Senior Project Manager may serve as program manager and assist clients with their drug development programs. The Sr. Project Manager may also be called upon to participate in the corporate management process and shall actively engage in and support business development efforts.

On-Site Expectations
  • Hybrid role with up to 40% expected on-site, depending on project requirements.
  • 1st Shift: Monday - Friday, 8:00am - 5:00pm.
Responsibilities
  • Develops and tracks the project development plan using Smartsheet.
  • Identifies and tracks critical path/activities, risks, contingencies and alternatives.
  • Communicates out-of-scope activities both internally and externally.
  • Implements Change Orders.
  • Facilitates team meetings with client and project team; setting-up sub-team meetings as necessary.
  • Drives strong interdepartmental collaborations to drive task completion and maintain project timelines.
  • Develop a strategy and work with project teams and clients to manage their contract needs.
  • Develop and approve proposals and contracts for assigned clients and projects in conjunction with the appropriate project team members.
  • Manage contract requirements for each assigned project through ERP and project teams.
  • Communicate budget requirements and status to all team members for each assigned project.
  • Design, implement timelines, and coordinate a detailed project operational plan for each assigned project.
  • Provide project status information both internally and externally at strategic level.
  • Provide input and feedback to Senior Management, Line Manager, or individual team members performance.
  • Provide mentorship to Associate Project Manager(s) and Project Managers specific to projects assigned to them.
  • Serve as proxy for the management of project managers as needed.
  • Assist with business development efforts through ongoing contact with new and assigned clients.
  • Assist with regulatory preparation, submission and overseeing project teams within the program.
  • Other duties as assigned.
Qualifications
  • BA/BS in related field with 5-8+ years pharmaceutical experience.
  • Must have 5 years Project Management experience managing multi-disciplinary project teams.
  • FDA regulation/ICH Guidelines.
  • U.S. Drug Development process.
  • Project Management Operations.
  • Budgets.
  • ERP, QMS, CRM, and MS Suite.
Knowledge, Skills, and Abilities
  • Computer proficient.
  • Communication (verbal and written) and presentation skills.
  • Excellent organizational skills.
  • Ability to multi-task.
  • Strong negotiation skills.
  • Presentation skills.
  • Leadership skills.
  • Mentoring skills.
Travel Expectations
  • Travel required to manufacturing locations to host clients and site visits.
Physical Demands and Work Environment

The physical demands and work environment characteristics described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, you will regularly be required to use hands to finger, handle, or feel; reach with hands and arms; talk or hear and smell. The employee is frequently required to sit. The employee is occasionally required to stand; walk and stoop, kneel, crouch, or crawl. The employee must regularly lift and/or move up to 10 pounds, frequently lift and/or move up to 25 pounds and occasionally lift and/or move up to 50 pounds. Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception and ability to adjust focus.

The noise level in the work environment is usually quiet with periods of higher noise elevations when present in warehouse or manufacturing areas. The employee may be required to gain access to lab personnel via general lab or manufacturing areas only for work discussions or follow-up or be required to tour clients through the various facilities. The employee is required to wear the appropriate personal protective equipment to perform the job duties. Such personal protective equipment may include, but not limited to safety eyewear, various types of respirators/breathing apparatus, lab coats, full protective body coverings, various types of gloves, etc.

Employment Type: FULL_TIME

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