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Cmc Management Jobs (NOW HIRING)

Reporting to the Program Management & Operations organization, the CMC Project Manager partners with CMC, Manufacturing, Analytical Development, Quality, Regulatory Affairs, Supply Chain, Clinical ...

CMC Project Manager ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven ...

Manage timelines and deliverables for CMC workstreams, ensuring alignment with project goals. * Prepare and coordinate CMC documentation for AR, DSUR, and responses to regulatory authority questions.

Head of CMC

Redwood City, CA · On-site

$277K - $416K/yr

Program & Project Management: Build and own the integrated CMC program plan: a single resource-loaded timeline spanning cell line development, upstream, downstream, analytical, formulation, DS and DP ...

Project management skill is plus * Author and review CMC sections of regulatory submissions, including IND, NDA, and MAA applications. * Ensure documents align with FDA, EMA, and ICH regulatory ...

$183K - $330K/yr

The CMC Product Lead ensures seamless integration of program strategy with the Target Product ... Accountable for the strategy of the resource and financial management of the team, including ...

CMC Writer

Paramus, NJ · On-site

$45 - $50/hr

TekWissen is a global workforce management provider headquartered in Ann Arbor, Michigan that offers strategic talent solutions to our clients world-wide. Job Title: CMC Writer Location: Paramus, New ...

Showing results 41-60

Cmc Management information

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$81K

$118.8K

$157.5K

How much do cmc management jobs pay per year?

As of Sep 13, 2026, the average yearly pay for cmc management in the United States is $118,816.00, according to ZipRecruiter salary data. Most workers in this role earn between $94,000.00 and $132,000.00 per year, depending on experience, location, and employer.

What is CMC management?

CMC management refers to the oversight and coordination of Chemistry, Manufacturing, and Controls (CMC) processes in the development and production of pharmaceuticals or biologics. This includes ensuring the quality, safety, and consistency of drugs by managing formulation, manufacturing protocols, analytical testing, and regulatory documentation. Effective CMC management is critical for meeting regulatory requirements and ensuring that products are safe and effective for patients. Professionals in this field work closely with research, development, quality assurance, and regulatory teams to bring new therapies to market.

What are the key skills and qualifications needed to thrive in CMC management?

To succeed in CMC (Chemistry, Manufacturing, and Controls) Management, you need a deep understanding of pharmaceutical development, regulatory requirements, and process optimization, often supported by a degree in chemistry, pharmacy, or related fields. Familiarity with quality management systems, regulatory submission platforms, and industry standards like ICH guidelines is crucial. Strong leadership, project management, and cross-functional communication skills help drive complex projects and effective collaboration. These capabilities ensure products meet safety, efficacy, and compliance standards throughout the drug development lifecycle.

What are some common challenges faced by professionals in CMC management, and how can they be addressed?

Professionals in CMC (Chemistry, Manufacturing, and Controls) Management often encounter challenges such as navigating complex regulatory requirements across different markets, ensuring consistent product quality during scale-up, and managing cross-functional communication between R&D, manufacturing, and regulatory teams. Addressing these challenges involves staying updated with evolving regulations, fostering strong collaboration among teams, and implementing robust quality management systems. Clear documentation and proactive risk management are also essential to overcome hurdles and ensure smooth product development and approval processes.

What is the difference between Cmc Management vs Cmc Specialist?

AspectCmc ManagementCmc Specialist
CredentialsBachelor's degree in life sciences, regulatory affairs, or related field; often requires experience in CMCSimilar educational background; may require specific certifications in regulatory affairs or quality assurance
Work EnvironmentOversees teams, manages projects, liaises with regulatory agenciesPerforms detailed review, documentation, and data analysis within the CMC process
Employer & Industry UsagePharmaceutical and biotech companies, regulatory agenciesPharmaceutical companies, contract research organizations, regulatory consulting firms

In summary, Cmc Management involves overseeing the entire CMC process, managing teams, and strategic planning, while Cmc Specialists focus on detailed technical work, data review, and documentation within the CMC scope. Both roles require relevant education and experience but differ in scope and responsibilities.

More about Cmc Management jobs

What cities are hiring for Cmc Management jobs?

Cities with the most Cmc Management job openings:

What states have the most Cmc Management jobs?

States with the most job openings for Cmc Management jobs include:

Infographic showing various Cmc Management job openings in the United States as of September 2026, with employment types broken down into 1% As Needed, 82% Full Time, 15% Part Time, and 2% Contract. Highlights an 87% Physical, 2% Hybrid, and 11% Remote job distribution, with an average salary of $118,816 per year, or $57.1 per hour.

Director, Site and CMC Program Management

Indianapolis, IN

Bristol Myers Squibb
Scientific Research and Development Services • 10K+ employees

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 2 days ago


Bristol Myers Squibb rating

8.2

Company rating: 8.2 out of 10

Based on 51 frontline employees who took The Breakroom Quiz


Job description

At RayzeBio, every day is an opportunity to ignite meaningful change. As a wholly-owned subsidiary of Bristol Myers Squibb, RayzeBio blends the nimble, pioneering spirit of an emergent biotech with the global expertise and resources of a leading innovator in oncology. Our mission is to develop transformative radiopharmaceutical therapies that offer new hope for patients living with cancer. Here, you'll join a multidisciplinary team where your ideas are valued, your expertise is amplified, and collaboration is at the heart of everything we do. From day one, expect to make an immediate impact-on our science, on our teams, and most importantly, on patients. Learn more about RayzeBio: https://careers.bms.com/rayzebio/

Position Summary:

The Director, Program Management will provide strategic leadership and operational oversight for Indianapolis site-based and end-to-end CMC programs. This role will serve on the site leadership team, partner with Product Development and Operations leadership, build core program management capabilities, and ensure effective portfolio delivery across process development, supply chain, production, and related functions.

Job Responsibilities:Program Management Strategic Leadership
  • Serve on the Indianapolis site leadership team to drive strategic priorities and ensure alignment with Product Development and Operations leadership.
  • Build and lead the Program Management team, including planning capabilities, systems, processes, governance routines, and KPIs to drive execution.
  • Ensure CMC portfolio delivery by partnering across global product teams, key functions--process development, supply chain, production, quality, regulatory, engineering, and external partners.
  • Translate strategic priorities into integrated plans, timelines, decision points, risk mitigation strategies, and performance reporting.
  • Lead prioritization and escalation discussions to align resources, resolve barriers, and maintain focus on business and patient-impact priorities.
End-to-End CMC and Site Program Execution
  • Manage integrated CMC program planning and execution across site operations, global program teams, Product Development functions, Quality, Regulatory, Finance, and Commercial stakeholders.
  • Coordinate key site and portfolio initiatives, including manufacturing readiness, technology transfer, supply chain planning, engineering projects, CAPA related initiatives, and operational readiness.
  • Identify critical path risks, dependencies, resource constraints, and execution barriers; drive mitigation planning and timely escalation.
  • Facilitate effective governance forums with clear agendas, decisions, actions, owners, and follow-through.
Team and Capability Building
  • Recruit, develop, and manage program management talent to support evolving CMC and site priorities.
  • Define PM accountabilities, decision rights, escalation pathways, standards, tools, templates, and ways of working.
  • Strengthen program management maturity through critical path analysis, scenario planning, executive communication, governance preparation, and performance tracking.
  • Foster a culture of accountability, collaboration, risk management, continuous improvement, and clear communication.
Communication, Governance, and Stakeholder Management
  • Prepare concise updates, dashboards, decision materials, and executive communications for site leadership and governance forums.
  • Translate complex technical, operational, and portfolio information into clear insights, recommendations, and actions.
  • Serve as a bridge across site operations, global program teams, external partners, and enterprise leadership.
  • Promote transparency by surfacing risks, issues, decisions, and trade-offs early through appropriate governance channels.
Education and Experience:
  • Bachelor's degree in life sciences, chemistry, engineering, pharmaceutical sciences, business, or related discipline required; advanced degree preferred.
  • Minimum of 10 years of pharmaceutical, biotechnology, or related life sciences experience, with significant experience in program/project management and CMC, manufacturing, process development, or site operations.
  • Demonstrated experience leading cross-functional, matrixed teams and complex programs with multiple stakeholders, risks, dependencies, and competing priorities.
  • Experience supporting CMC execution, manufacturing readiness, technology transfer, supply chain planning, or commercial readiness strongly preferred.
  • Experience building program management capabilities, operating models, governance routines, dashboards, systems, and KPIs preferred.
  • Prior people management experience preferred.
Skills and Qualifications:
  • Strategic, execution-focused leader able to translate portfolio priorities into actionable plans and measurable outcomes.
  • Strong understanding of drug development, CMC, manufacturing, supply chain, quality, regulatory, and/or radiopharmaceutical environments.
  • Proven ability to influence senior leaders and align cross-functional teams without direct authority.
  • Excellent communication, analytical, problem-solving, prioritization, and executive presentation skills.
  • Demonstrated ability to build teams, implement tools and processes, and drive continuous improvement in a fast-paced environment.
  • Leverages AI to drive program, portfolio, or functional performance through prioritization and scaled adoption
Physical Demands and Work Environment

This role is primarily office-based with occasional travel to site, partner, or manufacturing locations as needed.

If you come across a role that intrigues you but doesn't perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.

Compensation Overview:

Indianapolis - RayzeBio - IN: $203,389 - $246,459

The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee's work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience.
Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit https://careers.bms.com/life-at-bms/.

Benefit offerings are subject to the terms and conditions of the applicable plans in effect at the time and may require enrollment. Our benefits include:

  • Health Coverage: Medical, pharmacy, dental, and vision care.

  • Wellbeing Support: Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).

  • Financial Well-being and Protection: 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support.

Work-life benefits include:

Paid Time Off

  • US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees)

  • Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non-Exempt, Hourly Employees: 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays

Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.

All global employees full and part-time who are actively employed at and paid directly by BMS at the end of the calendar year are eligible to take advantage of the Global Shutdown.

*Eligibility Disclosure: The summer hours program is for United States (U.S.) office-based employees due to the unique nature of their work. Summer hours are generally not available for field sales and manufacturing operations and may also be limited for the capability centers. Employees in remote-by-design or lab-based roles may be eligible for summer hours, depending on the nature of their work, and should discuss eligibility with their manager. Employees covered under a collective bargaining agreement should consult that document to determine if they are eligible. Contractors, leased workers and other service providers are not eligible to participate in the program.

RayzeBio and Bristol Myers Squibb

RayzeBio was acquired by Bristol Myers Squibb (BMS) in 2024 and is a wholly-owned subsidiary of BMS; however, RayzeBio will continue to operate as a standalone organization.

Supporting People with Disabilities

BMS and RayzeBio are dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplaceaccommodations/adjustmentsand ongoing support in their roles. Applicants can request a reasonable workplaceaccommodation/adjustmentprior to accepting a job offer. If you require reasonableaccommodations/adjustmentsin completing this application, or in any part of the recruitment process, direct your inquiries toadastaffingsupport@bms.com. Visitcareers.bms.com/eeo-accessibilityto access our complete Equal Employment Opportunity statement.

Candidate Rights

BMS and RayzeBio will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.

If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information:https://careers.bms.com/california-residents/

Data Protection

We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at https://careers.bms.com/fraud-protection/

Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at TAEnablement@bms.com. Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response.

R1605207 : Director, Site and CMC Program Management

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About Bristol-Myers Squibb

Sourced by ZipRecruiter

Bristol-Myers Squibb is a world-renowned global Biopharmaceutical company headquartered in New York, NY, US. Established in 1887, the company has more than 130 years’ worth of history dedicated to discovering, developing, and delivering innovative medicines that help patients prevail over serious diseases. The company operates in the healthcare industry and thrives on providing a range of pharmaceutical products and services for various medical fields, like oncology, cardiovascular diseases, and immunoscience. Notably, Bristol-Myers Squibb is known for its commitment to relentless research and innovative drug development, which has led to breakthroughs like Opdivo, one of the first immunotherapies.

Industry

Scientific research and development services and pharmaceutical and medicine manufacturing

Company size

10,000+ Employees

Headquarters location

New York, NY, US