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Commercialization Project Manager Jobs in Boca Raton, FL

Acuity_Sandbox

Sales Manager

Delray Beach, FL · On-site

Idea generation and creativity in this position are a must, as are the ability to work with deadlines, manage and complete sales projects through commercialization, and develop creative techniques in ...

Acuity_Sandbox

Sales Manager

Delray Beach, FL · On-site

Idea generation and creativity in this position are a must, as are the ability to work with deadlines, manage and complete sales projects through commercialization, and develop creative techniques in ...

NEXA

Product & Partner Marketing Specialist

Hollywood, FL · On-site

$80K - $95K/yr

This role manages launch execution from planning through commercialization, including timelines ... The ideal candidate is a highly organized, results-oriented marketer with strong project management ...

NEXA

Product & Partner Marketing Specialist

Hollywood, FL · On-site

$80K - $95K/yr

This role manages launch execution from planning through commercialization, including timelines ... The ideal candidate is a highly organized, results-oriented marketer with strong project management ...

ASR Group

Packaging Engineer

Boca Raton, FL

This position will play a critical role in driving projects from concept through commercialization ... Ability to manage multiple projects in a fast-paced environment * Strong critical thinking and ...

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All JobsCommercialization Project JobsCommercialization Project Manager JobsCommercialization Project Manager Jobs in Boca Raton, FL

Commercialization Project Manager information

See Boca Raton, FL salary details

$42.2K

$91.6K

$146.6K

How much do commercialization project manager jobs pay per year?

As of Jul 18, 2026, the average yearly pay for commercialization project manager in Boca Raton, FL is $91,632.00, according to ZipRecruiter salary data. Most workers in this role earn between $71,200.00 and $107,200.00 per year, depending on experience, location, and employer.

What is a Commercialization Project Manager?

A Commercialization Project Manager is a professional responsible for guiding new products or services from development to market launch. They coordinate cross-functional teams, manage timelines and budgets, and ensure that products meet market requirements and regulatory standards. Their role is critical in bridging the gap between product development and successful market entry, often working closely with marketing, sales, R&D, and operations teams. They also monitor project performance and adjust strategies to ensure successful commercialization and profitability.

What is the difference between Commercialization Project Manager vs Product Manager?

AspectCommercialization Project ManagerProduct Manager
CredentialsTypically requires project management certifications (PMP), industry-specific knowledgeOften holds degrees in business, marketing, or related fields; may have certifications like Scrum or Agile
Work EnvironmentCoordinates cross-functional teams to bring products to market, often in manufacturing or tech industriesFocuses on product development, strategy, and lifecycle management, usually in tech or consumer goods
Employer & Industry UsageUsed in manufacturing, tech, healthcare sectors for product launch and commercializationCommon in tech, retail, and consumer goods for managing product offerings

While both roles involve bringing products to market, the Commercialization Project Manager primarily oversees the execution and launch process, ensuring timely delivery. The Product Manager focuses on product strategy, development, and lifecycle management. Understanding these differences helps organizations assign the right responsibilities and professionals for successful product commercialization.

What are some common challenges faced by Commercialization Project Managers during product launches, and how can they be addressed?

Commercialization Project Managers often face challenges such as coordinating cross-functional teams, managing tight deadlines, and aligning diverse stakeholder expectations during product launches. Successfully addressing these challenges involves establishing clear communication channels, setting realistic timelines, and proactively identifying potential bottlenecks. Regular status updates and collaborative planning sessions can help ensure that all team members are aligned and any issues are resolved quickly, leading to a smoother launch process.

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

To thrive as a Commercialization Project Manager, you need expertise in project management, product development, and go-to-market strategies, often supported by a degree in business or a related field. Familiarity with project management tools like Microsoft Project, Agile methodologies, and certifications such as PMP are commonly required. Strong leadership, stakeholder management, and effective communication skills set outstanding candidates apart. These abilities are crucial for successfully launching products, coordinating cross-functional teams, and achieving business objectives within set timelines.
What are popular job titles related to Commercialization Project Manager jobs in Boca Raton, FL? For Commercialization Project Manager jobs in Boca Raton, FL, the most frequently searched job titles are:
What job categories do people searching Commercialization Project Manager jobs in Boca Raton, FL look for? The top searched job categories for Commercialization Project Manager jobs in Boca Raton, FL are:
Commercialization Project Manager jobs near you
Associate Director, CMC Analytical Development, Separation

Associate Director, CMC Analytical Development, Separation

Syncromune

Fort Lauderdale, FL • On-site, Remote

$165K - $200K/yr

Full-time

Posted 23 days ago

Job description

The Associate Director of CMC Analytical Development will oversee the execution of the analytical strategy for drug substance and drug product development across all phases of clinical development and commercialization. This role is responsible for overseeing method development, validation, transfer, and lifecycle management to ensure compliance with regulatory requirements and alignment with company objectives.
Principal Duties and Responsibilities include the following:
  • Define and implement analytical development strategies to support CMC programs from early development through commercialization.
  • Provide technical leadership in analytical sciences, including chromatography, spectroscopy, and characterization techniques.
  • Guide analytical development activities at CDMO and CTL, including method development, optimization, transfer, validation, troubleshooting, and lifecycle management for GMP test methods for DS and DP.
  • Guide extended characterizations in support of comparability and regulatory applications.
  • Foster collaboration with cross-functional groups including Process Development, Quality, and Regulatory Affairs.
  • Author and review analytical sections of regulatory submissions (IND, IMPD, NDA, BLA).
  • Ensure adherence to GMP, ICH, and FDA guidelines for analytical activities.
  • Drive continuous improvement and innovation in analytical technologies and processes.
Supervisory Responsibilities:
  • Indirect Reports: supervise CDMO, CTL, and external resources (such as consultants)
Qualification Requirements:
Education:
  • Ph.D. or M.S. degree in Analytical Chemistry, Pharmaceutical Sciences, Biochemistry, or a related field.
Experience:
  • Must have 5+ years of pharmaceutical or biotechnology industry experience specializing in analytical development.
  • Must have working knowledge of cGMP, ICH, and regulatory guidelines.
  • Must have hands-on experience managing global CTLs and CDMOs.
  • Must have strong technical expertise in separation science, such as liquid chromatography or mass spectrometry.
  • Must have strong technical experience in at least one of the modalities: monoclonal antibody and/ or oligonucleotide.
  • Must have experience in method development, validation, and lifecycle management for QC methods.
  • Good to have experience in complex drug products, such as co-formulation, multi-components, conjugates, etc.
  • Good to have experience in extended characterization & comparability studies to support BLA submission.
  • Good to have experience in authoring technical and scientific documents for regulatory submissions, including IND and BLA filings.
  • Good to have late phase experience, such as PPQ and commercialization.
  • Candidates proficient in both English and Mandarin are highly encouraged to apply.
  • Ability to work in a fast-paced virtual environment.
  • Flexibility to travel domestically and internationally as required.
  • Excellent communication, leadership, organizational and project management skills.
Working Conditions:
  1. Specify work environment:
  • Work from home.
  • Domestic and international travel up to 25%.
  • Regularly required to stand, sit, talk, hear, and use hands
  • Prolonged periods of sitting and standing

Syncromune is an Equal Opportunity Employer.
The Company is required to provide a reasonable estimate of the salary range for this job in certain states and cities within the United States. Final determinations with respect to salary will take into account a number of factors, which may include, but not be limited to, the primary work location and the chosen candidate's relevant skills, experience, and education.
Expected US salary range: $165-$200K
This position generally is eligible for cash incentive compensation, equity incentive compensation, and employee benefits under the Company's benefit plans.
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