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All Analytical Development Cmc Jobs (NOW HIRING)

BridgeBio Pharma

Director, Analytical Development

$144K - $159K/yr

Responsibilities Support Analytical (CMC) activities associated with the formulation of ... Work closely with your Analytical Development colleagues and external CROs/CMOs collaborators to ...

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$89K

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$287.5K

How much do all analytical development cmc jobs pay per year?

As of Aug 19, 2026, the average yearly pay for all analytical development cmc 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 the difference between All Analytical Development Cmc vs Analytical Scientist?

AspectAll Analytical Development CmcAnalytical Scientist
CredentialsBachelor's or Master's in Chemistry, Pharmaceutical Sciences, or related fields; relevant certificationsBachelor's or Master's in Chemistry, Pharmaceutical Sciences, or related fields; relevant certifications
Work EnvironmentPharmaceutical or biotech R&D labs, manufacturing supportResearch labs, quality control, or manufacturing settings
Industry UsageUsed in CMC (Chemistry, Manufacturing, and Controls) documentation and developmentCommonly used in analytical testing, method development, and validation

All Analytical Development Cmc professionals focus on developing and validating analytical methods specifically for CMC documentation and regulatory submissions. Analytical Scientists often work on analytical testing and method development across various stages of product development. While both roles require similar educational backgrounds and work environments, All Analytical Development Cmc roles are more specialized in CMC processes, whereas Analytical Scientists may have broader analytical responsibilities.

What is the job description of analytical development?

Analytical development involves designing, validating, and implementing analytical methods to characterize and ensure the quality of pharmaceutical products. Professionals in this field use techniques such as chromatography, spectroscopy, and other laboratory tools, often working in regulated environments that require compliance with Good Manufacturing Practices (GMP). The role typically requires strong laboratory skills, attention to detail, and knowledge of regulatory standards.
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All Analytical Development Cmc jobs near you
Infographic showing various All Analytical Development Cmc job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 83% Full Time, 14% Part Time, and 2% Contract. Highlights an 90% Physical, 3% Hybrid, and 7% Remote job distribution, with an average salary of $191,412 per year, or $92 per hour.

Director Analytical Services

THE RITEDOSE CORPORATION

Columbia, SC • On-site

$133K - $173K/yr

Full-time

Re-posted 13 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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