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Cmc Director Analytical Jobs (NOW HIRING)

BridgeBio Pharma

Director, Analytical Development

$144K - $159K/yr

Communicate and coordinate with internal Analytical, CMC, QA, Regulatory, Project Management and consultants, as well as with external CROs/CMOs counterparts. Manage critical analytical review of ...

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Cmc Director Analytical information

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$89K

$191.4K

$287.5K

How much do cmc director analytical jobs pay per year?

As of Sep 11, 2026, the average yearly pay for cmc director analytical in the United States is $191,412.00, according to ZipRecruiter salary data. Most workers in this role earn between $94,000.00 and $249,000.00 per year, depending on experience, location, and employer.

What is a CMC Director Analytical?

A CMC (Chemistry, Manufacturing, and Controls) Director Analytical oversees the analytical strategy and operations within pharmaceutical and biotechnology companies. They are responsible for ensuring that analytical methods used in drug development, manufacturing, and quality control meet regulatory standards. This role involves leading teams, managing method development and validation, interpreting complex data, and collaborating with cross-functional teams to support product development from early stage through commercialization. CMC Director Analytical professionals also play a key role in preparing regulatory submissions and responding to agency queries.

What are some typical challenges a CMC Director Analytical might face when leading cross-functional teams in drug development projects?

A CMC Director Analytical often navigates challenges such as aligning analytical method development with evolving project timelines and regulatory requirements. Coordinating effectively with chemistry, manufacturing, and regulatory teams can be complex, especially when managing multiple projects at different development stages. Additionally, ensuring data integrity and compliance across global sites requires strong communication and organization. Overcoming these challenges often involves proactive planning, fostering a collaborative team culture, and staying updated on industry best practices.

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

To thrive as a CMC Director Analytical, you need deep expertise in analytical chemistry, regulatory requirements (ICH, FDA, EMA), and a relevant advanced degree (such as a Ph.D. in chemistry or related field). Experience with analytical instrumentation (e.g., HPLC, GC, mass spectrometry), data management systems, and knowledge of GMP/GLP guidelines are typically required. Strong leadership, strategic planning, and effective communication skills help drive cross-functional projects and manage teams efficiently. These competencies ensure robust analytical strategies, regulatory compliance, and successful product development in the pharmaceutical industry.

What is the difference between Cmc Director Analytical vs Cmc Manager Analytical?

AspectCmc Director AnalyticalCmc Manager Analytical
ResponsibilitiesOversees global CMC analytical strategies, leads teams, and ensures regulatory complianceManages daily analytical operations, supports development, and implements testing protocols
Required CredentialsAdvanced degree (PhD/MSc), extensive industry experience, leadership skillsBachelor's or Master's degree, relevant industry experience, technical expertise
Work EnvironmentStrategic, cross-functional leadership, often in corporate or R&D settingsOperational, laboratory-focused, team management within R&D or manufacturing

The Cmc Director Analytical typically holds a higher leadership role with strategic responsibilities, while the Cmc Manager Analytical focuses on daily operations and technical management. Both roles require strong scientific credentials, but the director's scope is broader, often involving global oversight and regulatory strategy.

What are popular job titles related to Cmc Director Analytical jobs?

For Cmc Director Analytical jobs, the most frequently searched job titles are:

Infographic showing various Cmc Director Analytical job openings in the United States as of September 2026, with employment types broken down into 100% Full Time. Highlights an 67% In-person, and 33% Hybrid job distribution, with an average salary of $191,412 per year, or $92 per hour.

Director Analytical Services

Columbia, SC • On-site

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

Full-time

Re-posted 6 days ago

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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