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Cmc Program Manager Jobs in Ridgeway, SC (NOW HIRING)

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Cmc Program Manager information

See Ridgeway, SC salary details

$36.7K

$102.4K

$149.7K

How much do cmc program manager jobs pay per year?

As of Sep 15, 2026, the average yearly pay for cmc program manager in Ridgeway, SC is $102,445.00, according to ZipRecruiter salary data. Most workers in this role earn between $75,800.00 and $126,300.00 per year, depending on experience, location, and employer.

What is a CMC Program Manager?

CMC Program Managers are professionals responsible for overseeing the Chemistry, Manufacturing, and Controls (CMC) aspects of pharmaceutical or biotechnology product development. They coordinate cross-functional teams to ensure that drug development activities related to product formulation, manufacturing, quality, and regulatory submissions are completed on time and within budget. Their role is crucial in advancing products through clinical development to commercialization while ensuring compliance with global regulatory requirements.

What are the key skills and qualifications needed to thrive as a CMC Program Manager?

To thrive as a CMC Program Manager, you need expertise in chemistry, manufacturing, and controls (CMC), project management experience, and an advanced degree in life sciences or a related field. Familiarity with regulatory submission systems, quality management tools, and certifications such as PMP or Six Sigma are highly valued. Strong leadership, cross-functional communication, and problem-solving skills help manage diverse teams and complex projects effectively. These skills ensure the successful development, regulatory compliance, and timely delivery of pharmaceutical products.

What are some typical challenges a CMC Program Manager faces when coordinating cross-functional teams?

A CMC Program Manager often encounters challenges in aligning the goals and timelines of diverse teams such as process development, analytical, regulatory, and manufacturing. Communication gaps and shifting priorities can complicate project execution, especially when managing external partners or contract manufacturing organizations. Proactive stakeholder engagement and clear documentation are essential to ensure that everyone remains on track and regulatory requirements are met. Successfully navigating these complexities is key to advancing products efficiently through the development pipeline.

What is the difference between Cmc Program Manager vs Cmc Project Manager?

AspectCmc Program ManagerCmc Project Manager
CredentialsTypically requires a Bachelor's degree in life sciences, engineering, or related field; often certifications like PMP or PgMPUsually holds a Bachelor's degree in a relevant field; PMP certification is common
Work EnvironmentOversees multiple projects within a program, coordinating cross-project activities in biotech or pharma industriesManages individual projects, focusing on specific deliverables within the CMC scope
Employer & IndustryPharmaceutical, biotech, or life sciences companies managing complex product developmentSimilar industry, often within the same companies, focusing on specific project execution

The Cmc Program Manager oversees multiple related projects, ensuring alignment with strategic goals, while the Cmc Project Manager focuses on executing individual projects within the CMC domain. Both roles require similar credentials and work in the same industry, but differ in scope and responsibilities.

Cmc Program Manager jobs near you

Director Analytical Services

Columbia, SC • On-site

THE RITEDOSE CORPORATION
Pharmaceutical and Medicine Manufacturing • 501 - 1,000 employees
Learn more about THE RITEDOSE CORPORATIONexternal

$133K - $173K/yr

Full-time

Re-posted 10 days ago

Key responsibilities

  • Lead and oversee all analytical testing activities for development and commercial products

  • Serve as the primary technical and operational contact during onboarding and execution phases

  • Ensure compliance with GMP regulations, oversee investigations, and implement CAPAs

Job description

The Director of Analytical Services is responsible for the strategic and operational leadership of the Analytical Services Laboratory, including oversight of laboratory personnel, resource planning, and execution of analytical activities supporting development programs and commercial products.
Specifically, Director of Analytical Services is responsible for overall management of the Analytical Services Laboratory including supervision of laboratory personnel, management of department budget, assignment of projects, and management of laboratory resources to meet analytical project development and method validation/transfer timelines, as well as commercial quality testing requirements. The Director of Analytical Services serves as a key customer and quality contact for all analytical related items in support of new product development activities and commercial product testing.
This role is accountable for delivering a high-performance laboratory operation defined by efficiency, throughput, data integrity, and professional output, while ensuring timely execution of analytical development, method validation/transfer, and commercial quality testing.
The Director serves as the primary operational and technical point of contact for customers beginning with project proposal support for all analytical activities and pricing. Following the engagement of the new customer, the Director is responsible for leading onboarding, execution, and ongoing communication to ensure a high-quality and predictable client experience.
Responsibilities:
  • Leadership & Execution:
    • Lead and oversee all analytical testing activities for development and commercial products
    • Serve as primary technical and operational contact during onboarding and execution phases
  • Quality and Compliance:
    • Ensure compliance with all GMP regulations
    • Oversee investigations to ensure a thorough conclusive closure of the investigation
    • Ensure appropriate CAPA's are drafted and implemented in a timely manner
    • Knowledge of EU/ROW regulatory aspects
  • Data Integrity:
    • Ensure strong data integrity and right-first-time execution
  • Technical Oversight:
    • Ensure resources for all testing (RM, in-process, finished product, validation, stability and Development)
  • Laboratory Operations:
    • Ensure compliance, inspection readiness, and proper lab conditions
  • Cross-Functional Collaboration:
    • Partner with Quality, Manufacturing, MS&T, Regulatory, Supply Chain, Engineering
    • In coordination with Regulatory and Development manage and oversee CMC authoring for internal and customer regulatory filing
    • Participate in compiling regulatory responses for any regulatory requests

  • Training & Organization:
    • Build scalable organization and training systems
    • Ensure SOP, safety, and cGMP compliance
  • Client Experience:
    • During new customer engagement provide accurate details based on project scope analytical services activities and pricing
    • Own customer onboarding and communication
    • Act as escalation point for analytical issues
  • Operational Excellence:
    • Drive throughput, efficiency, and predictability
    • Establish and Manage KPIs including TAT, on-time delivery, backlog, productivity
  • Financial & Resource Management:
    • Manage budget with focus on efficiency and resource utilization
    • Support financial performance through efficiency improvements

  • Advanced degree with 12-15+ years of experience in GMP analytical labs
  • 8-10 years leadership experience
  • Strong analytical/Scientific knowledge and Background
  • CDMO or contract lab experience preferred
  • Knowledge in polymer E&L in drug finished dosage preferred
  • Strong knowledge of cGMP and data integrity (FDA, EU etc.)
  • Experience with LIMS systems and effective laboratory planning
  • Experience with KPIs, capacity planning, and efficiency improvements
  • Strong leadership and communication skills with ability to participate in and contribute to a team-oriented work environment by developing positive working relationships with other departments
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About Ritedose

Sourced by ZipRecruiter

Industry

Pharmaceutical and medicine manufacturing

Company size

501 - 1,000 Employees

Headquarters location

Columbia, SC, US

Year founded

1995

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