Abbvie Product Development Science and Technology (PDS&T) Biologics Analytical-CMC Strategy is responsible for driving the analytical CMC control strategy for late-stage development of biologics. The ...
Abbvie Product Development Science and Technology (PDS&T) Biologics Analytical-CMC Strategy is responsible for driving the analytical CMC control strategy for late-stage development of biologics. The ...
Abbvie Product Development Science and Technology (PDS&T) Biologics Analytical-CMC Strategy is responsible for driving the analytical CMC control strategy for late-stage development of biologics. The ...
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Abbvie Product Development Science and Technology (PDS&T) Biologics Analytical-CMC Strategy is responsible for driving the analytical CMC control strategy for late-stage development of biologics. The ...
Proactively manage CMC aspects of clinical products in early-to-late development to create high quality regulatory submissions that support product development strategy. * Author and review CMC ...
Proactively manage CMC aspects of clinical products in early-to-late development to create high quality regulatory submissions that support product development strategy. * Author and review CMC ...
Director, CMC Team Lead
New Haven, CT · On-site
You will craft the CMC Development Plan, drive decisions at pace, and ensure operational execution aligns to strategy, risk, and value. Do you thrive at the intersection of science, operations, and ...
Director, CMC Team Lead
New Haven, CT · On-site
You will craft the CMC Development Plan, drive decisions at pace, and ensure operational execution aligns to strategy, risk, and value. Do you thrive at the intersection of science, operations, and ...
Director, CMC Team Lead
New Haven, CT · On-site
You will craft the CMC Development Plan, drive decisions at pace, and ensure operational execution aligns to strategy, risk, and value. Do you thrive at the intersection of science, operations, and ...
Director, CMC Team Lead
New Haven, CT · On-site
You will craft the CMC Development Plan, drive decisions at pace, and ensure operational execution aligns to strategy, risk, and value. Do you thrive at the intersection of science, operations, and ...
Lead crossfunctional coordination across Manufacturing, Quality, Analytical Development, Regulatory CMC, Supply Chain, and external partners to resolve complex CMC issues * Manage CMC execution in ...
Lead crossfunctional coordination across Manufacturing, Quality, Analytical Development, Regulatory CMC, Supply Chain, and external partners to resolve complex CMC issues * Manage CMC execution in ...
CMC Writer
Paramus, NJ · On-site
$45 - $50/hr
Hybrid * A Pharmaceutical CMC (Chemistry, Manufacturing, and Controls) Writer plays a crucial role in regulatory submissions by preparing technical documents related to drug development ...
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CMC Writer
Paramus, NJ · On-site
$45 - $50/hr
Hybrid * A Pharmaceutical CMC (Chemistry, Manufacturing, and Controls) Writer plays a crucial role in regulatory submissions by preparing technical documents related to drug development ...
Project Manager
Dallas, TX · On-site
Salary: $80,000 - $95,000/yr At CMC Development & Construction, working together onDeveloping Tomorrow is our motto. Founded in 2016, CMC is a full-service General Contractor firm which provides ...
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Project Manager
Dallas, TX · On-site
Salary: $80,000 - $95,000/yr At CMC Development & Construction, working together onDeveloping Tomorrow is our motto. Founded in 2016, CMC is a full-service General Contractor firm which provides ...
Director of CMC
El Segundo, CA · On-site
$200K - $230K/yr
This role will be responsible for all CMC activities across the external drug development pipeline of Varda's partners. Reporting to the VP, Pharma Program Management), this position requires ...
Director of CMC
El Segundo, CA · On-site
$200K - $230K/yr
This role will be responsible for all CMC activities across the external drug development pipeline of Varda's partners. Reporting to the VP, Pharma Program Management), this position requires ...
The Analytical Development group within the Targeted LNP (tLNP) CMC Development Team at AbbVie is dedicated to advancing state-of-the-art analytical capabilities for tLNP therapeutics development.
The Analytical Development group within the Targeted LNP (tLNP) CMC Development Team at AbbVie is dedicated to advancing state-of-the-art analytical capabilities for tLNP therapeutics development.
Develop, lead, and implement global CMC regulatory strategies to support the clinical development, registration, and post-marketing activities. * Lead the preparation and maintenance of the CMC ...
Develop, lead, and implement global CMC regulatory strategies to support the clinical development, registration, and post-marketing activities. * Lead the preparation and maintenance of the CMC ...
Lead formulation development and CMC activities for late-stage small molecule drug products supporting Phase 3 clinical programs and NDA submission. * Develop and execute formulation and process ...
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Lead formulation development and CMC activities for late-stage small molecule drug products supporting Phase 3 clinical programs and NDA submission. * Develop and execute formulation and process ...
This role manages technical projects across CMC development, life cycle management, and industrial technical initiatives, ensuring alignment across R&D, regulatory, manufacturing, and external ...
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This role manages technical projects across CMC development, life cycle management, and industrial technical initiatives, ensuring alignment across R&D, regulatory, manufacturing, and external ...
Manager, Regulatory Affairs- CMC
Basking Ridge, NJ · On-site
$127K - $190K/yr
This position manages assigned developmental and post marketing projects with a high level of ... Manages CMC development and post marketing projects. * Execution of Strategy and Submissions:
Manager, Regulatory Affairs- CMC
Basking Ridge, NJ · On-site
$127K - $190K/yr
This position manages assigned developmental and post marketing projects with a high level of ... Manages CMC development and post marketing projects. * Execution of Strategy and Submissions:
Director of CMC
Lawndale, CA · Hybrid
The Director of CMC leads the development, optimization, qualification, and transfer of analytical methods; oversees CMC documentation and regulatory-support activities; and provides cross-functional ...
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Director of CMC
Lawndale, CA · Hybrid
The Director of CMC leads the development, optimization, qualification, and transfer of analytical methods; oversees CMC documentation and regulatory-support activities; and provides cross-functional ...
Provide innovative and proactive regulatory strategy for CMC development of gene therapy products for all project teams in early research and all stages of clinical development. * Design and execute ...
Provide innovative and proactive regulatory strategy for CMC development of gene therapy products for all project teams in early research and all stages of clinical development. * Design and execute ...
Lead formulation development and CMC activities for late-stage small molecule drug products supporting Phase 3 clinical programs and NDA submission. * Develop and execute formulation and process ...
Lead formulation development and CMC activities for late-stage small molecule drug products supporting Phase 3 clinical programs and NDA submission. * Develop and execute formulation and process ...
The primary responsibility of this role is to deliver projects in the pharmaceutical CMC development area for ZS clients. This includes serving as a subject matter expert on drug substance and drug ...
The primary responsibility of this role is to deliver projects in the pharmaceutical CMC development area for ZS clients. This includes serving as a subject matter expert on drug substance and drug ...
The Analytical Development group within the Targeted LNP (tLNP) CMC Development Team at AbbVie is dedicated to advancing state-of-the-art analytical capabilities for tLNP therapeutics development.
The Analytical Development group within the Targeted LNP (tLNP) CMC Development Team at AbbVie is dedicated to advancing state-of-the-art analytical capabilities for tLNP therapeutics development.
Lead formulation development and CMC activities for late-stage small molecule drug products supporting Phase 3 clinical programs and NDA submission. * Develop and execute formulation and process ...
Lead formulation development and CMC activities for late-stage small molecule drug products supporting Phase 3 clinical programs and NDA submission. * Develop and execute formulation and process ...
Cmc Development information
See salary details
$29K - $33.7K
7% of jobs
$33.7K - $38.5K
8% of jobs
$42.6K is the 25th percentile. Wages below this are outliers.
$38.5K - $43.2K
11% of jobs
$43.2K - $47.9K
14% of jobs
The median wage is $50.4K / yr.
$47.9K - $52.6K
19% of jobs
$52.6K - $57.4K
13% of jobs
$58.8K is the 75th percentile. Wages above this are outliers.
$57.4K - $62.1K
12% of jobs
$62.1K - $66.8K
8% of jobs
$66.8K - $71.5K
4% of jobs
$71.5K - $76.3K
3% of jobs
$76.3K - $81K
1% of jobs
$29K
$53.4K
$81K
How much do cmc development jobs pay per year?
As of Jun 23, 2026, the average yearly pay for cmc development in the United States is $53,418.00, according to ZipRecruiter salary data. Most workers in this role earn between $42,500.00 and $60,000.00 per year, depending on experience, location, and employer.
Full-time
Medical, Dental, Vision, Retirement, PTO
Posted 13 days ago
AbbVie rating
8.7
Based on 97 frontline employees who took The Breakroom Quiz
13th of 71 rated pharmaceutical
Job description
Company Description
About AbbVie
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube.
Job Description
Abbvie Product Development Science and Technology (PDS&T) Biologics Analytical-CMC Strategy is responsible for driving the analytical CMC control strategy for late-stage development of biologics. The Analytical CMC Strategy team is responsible for ensuring late phase to commercial method development, optimization, validation, advanced characterization, process development support, regulatory authoring, and control strategy for biologics. The team works cross-functionally with process development, regulatory, and quality within the Abbvie network. This role requires a strategic thinker with a strong technical analytical background in gene therapy and tLNP technologies, manage complex projects, and effectively communicate cross-functionally.
Responsibilities:
Qualifications
Additional Information
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:
Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company's sole and absolute discretion, consistent with applicable law.
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html
US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
https://www.abbvie.com/join-us/reasonable-accommodations.html
About AbbVie
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube.
Job Description
Abbvie Product Development Science and Technology (PDS&T) Biologics Analytical-CMC Strategy is responsible for driving the analytical CMC control strategy for late-stage development of biologics. The Analytical CMC Strategy team is responsible for ensuring late phase to commercial method development, optimization, validation, advanced characterization, process development support, regulatory authoring, and control strategy for biologics. The team works cross-functionally with process development, regulatory, and quality within the Abbvie network. This role requires a strategic thinker with a strong technical analytical background in gene therapy and tLNP technologies, manage complex projects, and effectively communicate cross-functionally.
Responsibilities:
- Drives overall analytical control strategy, including justifying appropriate specifications, determining critical quality attributes, assessing product shelf-life, and risk-based comparability strategies for the biologics pipeline.
- Establish collaborations across the organization to ensure delivery of critical analytical BLA enabling activities.
- Setting team strategies, managing resources and defining risk mitigation strategies.
- Communicate project strategy, key issues, and risks to relevant teams and escalate risks and facilitate resolution within/across functional areas.
- Act as the principal contact for all stakeholders and balance conflicting expectations between cross-functional areas.
- Actively participate in yearly FTE planning across the analytical organization
Qualifications
- Bachelor's Degree or equivalent education in Science related field with extensive (typically 18 years) of related work; Master's Degree or equivalent education Science or PharmD or equivalent education with extensive (typically 16 years) of related work; PhD in Science or related field with typically 10 years of related work experience.
- Experience in research and/or development environment.
- Proven ability to innovate with a history of new or improved product releases.
- Interacts well with diverse groups within function and maintains strong working relationships with internal and external collaborators.
- Demonstrated ability to influence others across areas of scientific disciplines.
- Technical background in healthcare, laboratory diagnostics, medical devices or pharmaceutical companies.
Additional Information
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:
- The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future.
- We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.
- This job is eligible to participate in our long-term incentive programs.
Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company's sole and absolute discretion, consistent with applicable law.
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html
US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
https://www.abbvie.com/join-us/reasonable-accommodations.html
About AbbVie
Sourced by ZipRecruiter
AbbVie's mission is to discover and deliver innovative medicines that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas: immunology, oncology, neuroscience, eye care, virology, women's health, and gastroenterology, in addition to products and services across its Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on Twitter, Facebook, Instagram, YouTube, and LinkedIn.
Industry
Scientific research and development services
Company size
10,000+ Employees
Headquarters location
North Chicago, IL, US
Year founded
2013