1

Cmc Project Manager Jobs in Silver Spring, MD (NOW HIRING)

Clinical Project Manager

Baltimore, MD · On-site

$80K - $135K/yr

Clinical Project Manager Salary Range: $80K-$135K Location: Baltimore, MD Unfortunately, we cannot ... 100+ CMC programs , and 1,397 clinical trials across all phases. Our teams are involved in ...

Clinical Project Manager

Baltimore, MD · On-site

$80K - $135K/yr

Clinical Project Manager Salary Range: $80K-$135K Location: Baltimore, MD Unfortunately, we cannot ... 100+ CMC programs , and 1,397 clinical trials across all phases. Our teams are involved in ...

Clinical Project Manager

Baltimore, MD · On-site

$80K - $135K/yr

... 100+ CMC programs, and 1,397 clinical trials across all phases. Our teams are involved in ... The Clinical Project Manager (CPM) is the single, accountable leader for early-phase (FIH, SAD/MAD ...

Project Coordinator

Jessup, MD · On-site

$60 - $80/hr

Minimum of 3 years of experience in customer service, project management, or construction site development We are CMC, a Fortune 500 ® company at the leading edge of our industry. Our construction ...

next page

Showing results 1-20

Cmc Project Manager information

See Silver Spring, MD salary details

$46.5K

$108.6K

$175.2K

How much do cmc project manager jobs pay per year?

As of Sep 12, 2026, the average yearly pay for cmc project manager in Silver Spring, MD is $108,573.00, according to ZipRecruiter salary data. Most workers in this role earn between $85,800.00 and $132,800.00 per year, depending on experience, location, and employer.

What is a CMC Project Manager?

A CMC (Chemistry, Manufacturing, and Controls) Project Manager oversees the development, manufacturing, and regulatory aspects of pharmaceutical products. They coordinate cross-functional teams, manage timelines, and ensure compliance with regulatory requirements. Their role is critical in guiding drug development from early stages to commercialization while maintaining quality and efficiency.

What are the typical responsibilities of a CMC Project Manager in a pharmaceutical company?

A CMC Project Manager is responsible for coordinating cross-functional teams to ensure successful delivery of project milestones related to product development, manufacturing, and regulatory submissions. Their daily tasks often include developing project timelines, managing risk assessments, overseeing documentation, and facilitating communication between technical, regulatory, and quality departments. They play a pivotal role in preparing CMC sections for regulatory filings, supporting process optimization, and troubleshooting manufacturing challenges. This position requires excellent multitasking abilities and close collaboration with internal stakeholders and external partners throughout the product lifecycle.

What are the key skills and qualifications needed to thrive as a CMC Project Manager, and why are they important?

A CMC Project Manager needs strong expertise in Chemistry, Manufacturing, and Controls (CMC) processes, project management certifications (such as PMP), and a background in pharmaceutical or biotech industries. Familiarity with regulatory submission systems, quality management software, and documentation tools is highly valued. Exceptional organizational skills, problem-solving ability, and effective cross-functional communication help candidates excel in this role. These capabilities are critical for ensuring project milestones are met, regulatory requirements are satisfied, and product development remains on track.

What are popular job titles related to Cmc Project Manager jobs in Silver Spring, MD?

For Cmc Project Manager jobs in Silver Spring, MD, the most frequently searched job titles are:

What cities near Silver Spring, MD are hiring for Cmc Project Manager jobs?

Cities near Silver Spring, MD with the most Cmc Project Manager job openings:

Infographic showing various Cmc Project Manager job openings in Silver Spring, MD as of September 2026, with employment types broken down into 84% Full Time, 15% Part Time, and 1% Contract. Highlights an 86% Physical, 2% Hybrid, and 12% Remote job distribution, with an average salary of $108,573 per year, or $52.2 per hour.

Bilingual (English & Chinese) Project Coordinator/Manager - CDMO Service

Germantown, MD • On-site

Other

Re-posted 20 days ago


Job description

Position Summary:

We are seeking an individual with a strong background in viral vector production and/or project management. This position reports to VP of Commercial Strategy

  • Provide project management support to CMC team members including PD, TT and GMP teams in their execution of activities including manufacturing and release of drug substance and drug product, manufacturing process improvements and validation, analytical method development, transfer and validation, and shipping studies.
  • Serve as the primary liaison between uBriGene and clients on CMC activities for the client projects.
  • Collect updates on all CMC activities in the MS Project file on a monthly basis to update % completion or new dates.
  • Schedule, conduct, and draft minutes for PD, TT and GMP team on respective client projects to ensure regular, efficient team, and stakeholder communication.
  • Facilitate robust communication within PD, TT and GMP teams to ensure all functions are aware of the schedule, changes in strategy and impacts to risks and resources.
  • Hold team members accountable for on-time completion of tasks or milestones.
  • Performs critical path analysis and supports scenario planning for CMC deliverables.
  • Provide project coordination and communication, including participation in technical calls and face-to-face meetings, development of agendas, creation of meeting minutes, tracking of action items, and scheduling of follow-up meetings.
  • Support writing, review, and schedule of CMC related regulatory documents and health authority interactions.
  • Assist in preparing presentations, updating corporate project plans, etc.
  • Other responsibilities as needed
II. Requirements Education, Experience, and Skills
  • B.S. or MS. in engineering or biological sciences degree is required
  • > 3 years of experience in biologics manufacturing, preferably in viral vector production
  • Previous project management experience in the biologics production is preferred but not required.
  • Proven experience organizing, planning, and executing large-scale projects from vision through implementation
  • Experience using project management tools (project scheduling and resource management), such as MS Project.
  • Proven analytical, conceptual and problem solving skills are required to evaluate business problems and apply knowledge to identify appropriate solutions.
  • Exceptional team building and stakeholder relationship management skills are required, with the ability to establish rapport, persuade and effectively negotiate with senior management, key stakeholders and functions.
  • Bilingual skills in English and Chinese are preferred.

uBriGene Biosciences, Inc. is an equal employment opportunity employer and does not discriminate against any applicant on the basis of race, color, religion, sex, sexual orientation, gender expression and identity, national origin, ancestry, age, mental and physical disability, genetic information, any veteran status, military status or application for military service, or membership in any other category protected under applicable law.

#J-18808-Ljbffr