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Cmc Project Manager Jobs in Florida (NOW HIRING)

The CMC will provide customer support at various touchpoints throughout customer journey. This ... Participate in projects, special assignments, and other duties as directed by management. * Deliver ...

The CMC will provide customer support at various touchpoints throughout customer journey. This ... Participate in projects, special assignments, and other duties as directed by management. * Deliver ...

The CMC will provide customer support at various touchpoints throughout customer journey. This ... Participate in projects, special assignments, and other duties as directed by management. * Deliver ...

The CMC will provide customer support at various touchpoints throughout customer journey. This ... Participate in projects, duties, and other tasks assigned by management. Strive to achieve world ...

The CMC will provide customer support at various touchpoints throughout customer journey. This ... Management and Supervisors. โ€ข Participate in projects, duties, and other tasks assigned by ...

The CMC will provide customer support at various touchpoints throughout customer journey. This ... Participate in projects, duties, and other tasks assigned by management. * Strive to achieve 'world ...

The CMC will provide customer support at various touchpoints throughout customer journey. This ... Participate in projects, duties, and other tasks assigned by management. Strive to achieve 'world ...

Supervisor, Manufacturing

Gainesville, FL ยท On-site

$54K - $74K/yr

... CMC development, apply expertise in analytical and process development and GMP manufacturing ... project management, research, and development, etc. to help facilitate successful projects to ...

Janitor

Gainesville, FL ยท On-site

$13 - $16.50/hr

Report any maintenance or safety issues to the supervisor. * Assist with special cleaning projects ... Contemporary Management Concepts (CMC) is an Equal Opportunity Employer. We are committed to ...

Lab - QC Technician

Rockledge, FL ยท On-site

$17.50 - $22/hr

Laboratory & Technical Manager FLSA Status: Non-Exempt Position Summary The QC Technician plays a ... Perform color matching using spectrophotometer technology and CIELAB/CMC data analysis. * Prepare ...

Lab - QC Technician

Rockledge, FL

$17.25 - $21.75/hr

Laboratory & Technical Manager FLSA Status: Non-Exempt Position Summary The QC Technician plays a ... Perform color matching using spectrophotometer technology and CIELAB/CMC data analysis. * Prepare ...

Showing results 41-60

Cmc Project Manager information

See Florida salary details

$33.6K

$78.5K

$126.7K

How much do cmc project manager jobs pay per year?

As of Aug 6, 2026, the average yearly pay for cmc project manager in Florida is $78,485.00, according to ZipRecruiter salary data. Most workers in this role earn between $62,000.00 and $96,000.00 per year, depending on experience, location, and employer.

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 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 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 cities in Florida are hiring for Cmc Project Manager jobs? Cities in Florida with the most Cmc Project Manager job openings:
Infographic showing various Cmc Project Manager job openings in Florida as of August 2026, with employment types broken down into 100% Full Time. Highlights an 92% In-person, and 8% Remote job distribution, with an average salary of $78,485 per year, or $37.7 per hour.

Principal Consultant, Advertising & Promotion Strategy

Opus Regulatory

Miami, FL โ€ข On-site

Full-time

Re-posted 29 days ago


Job description

About Opus Regulatory:
For more than 30 years, Opus Regulatory has provided strategic guidance to industry partners through expert consultants in key practice areas: Regulatory Strategy, CMC, Labeling, Ad Promo, Medical Review, and Medical Information. Our team of senior-level leaders and innovators provides project-specific contributions or ongoing support through the regulatory process. Opus provides customized solutions to meet the challenges and restrictions faced by our clients - from startup biotechs to mid-to-large size pharmaceutical companies.

We're looking for several Principal Consultant, Regulatory Affairs Advertising + Promotion roles (Associate Director to VP levels) who will primarily be responsible for the daily support or management of regulatory requirements for one or more drug products, providing leadership on advertising and promotional materials, and developing and maintaining relationships with key client staff and regulatory bodies. We have a robust client portfolio offering a variety of projects including therapeutic areas.

Responsibilities include:

  • Act as a key regulatory affairs expert within a client regulatory team, providing expertise on regulatory strategy, process, filing, best practices, etc. in conjunction with client leadership.
  • Provide strategic and operational leadership for promotional, educational, and investigative communications
  • Review and evaluate materials submitted by client teams to ensure that the content, quality, and format comply with applicable laws, regulations, and client policy.
  • Uses extensive knowledge of country specific regulatory requirements (US, EU and ICH) and the ability to apply knowledge both strategically and operationally to development projects and marketed product regulatory issues to support clients' corporate goals.
  • Manage launch preparation of promotional material for one or more products.
  • Provide support and guidance to regulatory teams on RA requirements for one or more drug products.
  • Maintain knowledge of changing regulatory requirements and advise teams as appropriate.
  • Represent the client regulatory affairs team in other client meetings or workstreams; provide support for ancillary projects.

Qualifications:

  • Must have a minimum of 6 years of experience in pharmaceutical regulatory affairs specializing in Advertising and Promotion.
  • Bachelor's degree required; Advanced degree in a science discipline preferred.
  • Experience across multiple therapeutic areas is highly desirable.
  • Demonstrated global and international experience is required.
  • Proven project management skills to support the planning and coordination of regulatory submissions and appropriate regulatory inspections.
  • Ability to work independently and innovatively in tackling operational challenges.

Opus Regulatory is an Equal Opportunity Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.

Opus is committed to providing benefit-eligible employees with a comprehensive benefits package designed to support your health, financial well-being, and work-life balance. We offer medical, dental, vision, and prescription drug coverage for employees and their eligible family members. Additional benefits include Life Insurance, Short-Term Disability (STD), and an Employee Assistance Program (EAP), a 401(k) plan, and more. To support time away from work, we provide a paid time off package, which includes 20 vacation days, 5 sick days, & 10 paid company holidays annually.