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Pharmaceutical Cmc Jobs (NOW HIRING)

AstraZeneca

Associate Director, CMC Lead

Boston, MA · On-site

$136K - $204K/yr

Define and deliver the pharmaceutical development strategy for the pre-IND/IND-enabling portfolio to drive timely progression to first-in-human readiness. * IND/IMPD Readiness: Lead CMC regulatory ...

AstraZeneca

Associate Director, CMC Lead

Boston, MA · On-site

$136K - $204K/yr

Define and deliver the pharmaceutical development strategy for the pre-IND/IND-enabling portfolio to drive timely progression to first-in-human readiness. * IND/IMPD Readiness: Lead CMC regulatory ...

AstraZeneca

Associate Director, CMC Lead

Boston, MA · On-site

$136K - $204K/yr

Define and deliver the pharmaceutical development strategy for the pre-IND/IND-enabling portfolio to drive timely progression to first-in-human readiness. * IND/IMPD Readiness: Lead CMC regulatory ...

AstraZeneca GmbH

Associate Director, CMC Lead

Boston, MA · On-site

$137 - $205/hr

Define and deliver the pharmaceutical development strategy for the pre-IND/IND-enabling portfolio to drive timely progression to first-in-human readiness. * IND/IMPD Readiness: Lead CMC regulatory ...

CMC Phoenix

PRN Pharmacist

Phoenix, AZ · On-site

$60/hr

College Medical Center Phoenix (CMC Phoenix) is seeking a PRN Pharmacist to join our team and support the Mission, Vision, Values, and Code of Conduct of College Hospitals. The Pharmacist is ...

Telix Pharmaceuticals (AMER)

CMC Program Lead

OR · On-site +1

BA or BS degree in Science, Mathematics, Engineering, or a related scientific discipline required * 10+ years of relevant radiopharmaceutical/pharmaceutical/biopharma CMC experience with 5+ years of ...

CMC Phoenix

Overnight Pharmacist

Phoenix, AZ · On-site

$61 - $64/hr

College Medical Center Phoenix (CMC Phoenix) is seeking a full-time Pharmacist to join our team and support the Mission, Vision, Values, and Code of Conduct of College Hospitals. The Pharmacist is ...

BeiGene USA

Executive Director, Regulatory Affairs, CMC

$153K - $202K/yr

S.-based biologics Regulatory CMC activities and serves as a key partner to the China-based ... BA/BS Degree in scientific disciplines with 14+ years of relevant pharmaceutical experience, MS/PhD ...

Rhythm Pharmaceuticals

Director, Regulatory CMC

Boston, MA · On-site

$182K - $275K/yr

S. degree in a scientific or life sciences discipline with a minimum of 10 years experience in Regulatory CMC, manufacturing, analytical development, quality, or related pharmaceutical development ...

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Pharmaceutical Cmc information

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$14

$19

$25

How much do pharmaceutical cmc jobs pay per hour?

As of Aug 22, 2026, the average hourly pay for pharmaceutical cmc in the United States is $19.78, according to ZipRecruiter salary data. Most workers in this role earn between $17.79 and $21.88 per hour, depending on experience, location, and employer.

What is a pharmaceutical CMC?

Pharmaceutical CMC professionals are experts who manage the Chemistry, Manufacturing, and Controls (CMC) aspects of drug development and production. They ensure that pharmaceuticals are consistently manufactured with the required quality, safety, and efficacy by overseeing the development, scale-up, and regulatory submission processes. Their work involves coordinating formulation, analytical testing, process validation, and compliance with regulatory guidelines, such as those from the FDA or EMA. CMC professionals play a critical role in bringing new drugs to market by ensuring all manufacturing and quality controls meet stringent regulatory standards.

What skills and qualifications are needed to thrive as a pharmaceutical CMC?

To thrive as a Pharmaceutical CMC professional, you need a strong background in chemistry, pharmaceutical sciences, and regulatory compliance, often supported by a relevant degree or advanced qualification. Familiarity with regulatory submission systems (e.g., eCTD), analytical instrumentation, and quality management systems is typically required. Critical thinking, attention to detail, and effective cross-functional communication are vital soft skills for excelling in this role. These skills ensure that pharmaceutical products are developed, manufactured, and documented in compliance with global regulations, supporting product quality and successful regulatory approvals.

What are common challenges faced in a pharmaceutical CMC role, and how can they be addressed?

One of the main challenges in a Pharmaceutical CMC role is ensuring regulatory compliance while managing tight timelines for product development and approval. Professionals must coordinate across cross-functional teams, including R&D, quality assurance, and manufacturing, to ensure all documentation and processes meet evolving regulatory standards. Staying updated with global regulatory requirements and maintaining clear communication channels can help address these challenges. Additionally, adaptability and strong project management skills are essential to navigate unexpected technical or regulatory hurdles that may arise during the drug development lifecycle.

What is the difference between Pharmaceutical Cmc vs Pharmaceutical Quality Assurance?

AspectPharmaceutical CmcPharmaceutical Quality Assurance
Primary FocusDevelopment, manufacturing, and control of drug substances and productsEnsuring product quality through audits, compliance, and process validation
Required CredentialsDegree in pharmacy, chemistry, or related field; knowledge of GMP regulationsDegree in pharmacy, chemistry, or related field; understanding of quality systems
Work EnvironmentLaboratories, manufacturing sites, R&D facilitiesQuality control labs, regulatory agencies, manufacturing oversight
Industry UsageDrug development, formulation, manufacturingQuality management, compliance, validation processes

Pharmaceutical Cmc professionals focus on the development and manufacturing of drug substances, ensuring formulation and process control. In contrast, Pharmaceutical Quality Assurance specialists concentrate on maintaining product quality through audits, validation, and compliance. Both roles require similar educational backgrounds and work within the pharmaceutical industry, but their core responsibilities differ significantly.

What cities are hiring for Pharmaceutical Cmc jobs?

Cities with the most Pharmaceutical Cmc job openings:

What states have the most Pharmaceutical Cmc jobs?

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

What job categories do people searching Pharmaceutical Cmc jobs look for?

The top searched job categories for Pharmaceutical Cmc jobs are:

Pharmaceutical Cmc jobs near you
Infographic showing various Pharmaceutical Cmc job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 80% Full Time, 14% Part Time, 1% Temporary, 3% Contract, and 1% Nights. Highlights an 87% Physical, 2% Hybrid, and 11% Remote job distribution, with an average salary of $41,139 per year, or $19.8 per hour.

Associate Director, CMC Lead

AstraZeneca

Boston, MA • On-site

$136K - $204K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 18 days ago

AstraZeneca rating

8.4

Company rating: 8.4 out of 10

Based on 45 frontline employees who took The Breakroom Quiz

22nd of 86 rated pharmaceutical

Job description

Job Title: Associate Director, CMC Lead
Introduction to role:
Are you ready to lead early-stage CMC strategy that turns precision radioconjugate science into first-in-human reality? As Associate Director, CMC Lead, you will steer development across a portfolio of alpha-emitting, tumor-targeted medicines, shaping IND-enabling plans and building the foundations for reliable, phase-appropriate clinical supply. Your decisions will determine how fast promising candidates move from discovery to patients.
You will join a team pushing the boundaries of oncology through novel radioconjugates and smart combinations, supported by state-of-the-art radiopharmaceutical manufacturing capabilities and an advancing clinical pipeline. How will you prioritize across multiple candidates, balance scientific rigor with speed, and de-risk the path to first-in-human studies? If you thrive in a dynamic, matrixed environment and enjoy solving complex CMC puzzles, this role puts you at the center of impact.
Accountabilities:
  • Phase 0 CMC Strategy: Define and deliver the pharmaceutical development strategy for the pre-IND/IND-enabling portfolio to drive timely progression to first-in-human readiness.
  • IND/IMPD Readiness: Lead CMC regulatory strategy; guide and contribute to authoring high-quality documentation and data packages for IND/IMPD submissions.
  • API/Drug Product/Analytical Integration: Coordinate API, drug product, and analytical development to establish robust, scalable, phase-appropriate processes and methods.
  • Clinical Supply Strategy: Build and execute supply strategies for Phase 0/Phase I, aligning isotope availability, shelf life, and study timelines to ensure on-time, fit-for-purpose clinical material.
  • Portfolio Leadership: Manage multiple early-stage programs; set priorities, balance resources, and adjust strategies as data emerge to protect the critical path.
  • Cross-Functional Influence: Represent CMC on project teams; shape overall program strategies and inform candidate selection through clear, data-driven risk/benefit assessments.
  • Target and Modality Assessment: Evaluate new molecular targets and modalities for CMC feasibility and developability to guide investment decisions.
  • Transition Enablement: Partner with Program Management, Clinical, Research, Regulatory, Quality, and Supply Chain to enable seamless movement of candidates from research into early development.

Essential Skills/Experience:
  • 7+ years of experience in pharmaceutical/biopharmaceutical product development and manufacturing;
  • Minimum education: Bachelor's degree. Advanced degree in Biochemistry, Pharmaceutical Chemistry, Pharmaceutics, Pharmaceutical Science, Chemical Engineering, or related scientific discipline preferred.
  • Demonstrated experience managing early-phase CMC development, including IND-enabling activities, process development, and analytical method development.
  • Strong project leadership skills with the ability to manage multiple concurrent programs at varying stages of maturity.
  • Demonstrated strong interpersonal and communication skills with the ability to collaborate effectively across functions and influence stakeholders at multiple levels of the organization.
  • Ability to develop and implement phase-appropriate pharmaceutical strategies across CMC areas (API, DP, Analytical) aligned with overall program objectives and timelines.
  • Experience working in a matrix environment and leading cross-functional sub-teams to deliver against defined milestones.
  • Strong problem-solving aptitude with the ability to navigate ambiguity and make sound technical and strategic judgments in a data-limited, early-stage environment.

Desirable Skills/Experience:
  • Experience with radiopharmaceuticals or radioconjugates, including awareness of radiochemistry constraints and alpha-emitting isotopes.
  • Prior authorship or leadership of CMC sections for IND/IMPD filings for biologics, conjugates, or complex modalities.
  • Familiarity with clinical supply strategies for short half-life or just-in-time manufactured products.
  • Hands-on application of Quality by Design, design of experiments, and risk management in early development.
  • Track record of successful tech transfer to GMP facilities and effective collaboration with external partners or CDMOs.
  • Understanding of analytical method lifecycle, including phase-appropriate validation and control strategy development.

The annual base pay (or hourly rate of compensation) for this position ranges from $136,514 USD to $204,771 USD. Our positions offer eligibility for various incentives-an opportunity to receive short-term incentive bonuses, equity-based awards for salaried roles and commissions for sales roles. Benefits offered include qualified retirement programs, paid time off (i.e., vacation, holiday, and leaves), as well as health, dental, and vision coverage in accordance with the terms of the applicable plans.
Why AstraZeneca:
Here you will follow the science with the resources to act on it, working alongside radiochemists, data scientists, clinicians, and CMC leaders who challenge assumptions and unlock new solutions together. We invest deeply in understanding disease biology and harness digital, data science, and AI to better predict clinical success, accelerating promising assets without compromising quality. Expect an environment that values kindness alongside ambition, where bold ideas are welcomed, thoughtful risks are supported, and your expertise directly shapes how innovative medicines reach patients sooner.
Call to Action:
If you are ready to lead pivotal CMC decisions that bring precision radioconjugates to first-in-human studies faster, step forward and shape what science makes possible.
#LI-Hybrid
Date Posted
04-Aug-2026
Closing Date
30-Aug-2026
Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.

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About AstraZeneca

Sourced by ZipRecruiter

AstraZeneca is a global, science-led, patient-focused biopharmaceutical company that focuses on the discovery, development and commercialization of prescription medicines for some of the world's most serious diseases. But we're more than one of the world's leading pharmaceutical companies. A place built on courage, curiosity and collaboration - we make bold decisions driven by patient outcomes. Empowered to lead at every level, free to ask questions and take smart risks that write the next chapter for our pipeline and Oncology team. Make a meaningful impact that brings real benefits to society. By applying your knowledge of data, you will help to redefine our industry and ultimately save lives. Work with experts who share a common goal: to accelerate the potential of medicines and the science of tomorrow.

Industry

Pharmaceutical product wholesalers and pharmaceutical and medicine manufacturing

Company size

10,000+ Employees

Headquarters location

Cambridge, Cambridgeshire, GB

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