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Cmc Technical Operations Jobs (NOW HIRING)

Pathos

Director, CMC - Biologics & ADC

New York, NY · On-site

$210K - $250K/yr

This is a foundational hire on the Pathos CMC/Technical Operations team. You will help build and scale the chemistry, manufacturing, and controls function from an early stage, working shoulder-to ...

Pathos

Director, CMC - Biologics & ADC

Manhattan, NY · On-site

This is a foundational hire on the Pathos CMC/Technical Operations team. You will help build and scale the chemistry, manufacturing, and controls function from an early stage, working shoulder-to ...

Pathos AI

Director, CMC - Biologics & ADC

Manhattan, NY · On-site

This is a foundational hire on the Pathos CMC/Technical Operations team. You will help build and scale the chemistry, manufacturing, and controls function from an early stage, working shoulder-to ...

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Cmc Technical Operations information

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$35.5K

$91.3K

$144.5K

How much do cmc technical operations jobs pay per year?

As of Sep 10, 2026, the average yearly pay for cmc technical operations in the United States is $91,282.00, according to ZipRecruiter salary data. Most workers in this role earn between $71,000.00 and $111,500.00 per year, depending on experience, location, and employer.

What is CMC Technical Operations?

CMC Technical Operations refers to the Chemistry, Manufacturing, and Controls (CMC) functions within pharmaceutical and biotechnology companies. This area is responsible for overseeing the development, scale-up, manufacturing, and quality control of drug products. CMC Technical Operations ensures that products are manufactured consistently, meet regulatory requirements, and maintain high quality throughout their lifecycle. The team often collaborates with research, regulatory, and quality assurance departments to bring safe and effective medicines to market.

What are the key skills and qualifications needed to thrive as a CMC Technical Operations professional, and why are they important?

To thrive in CMC Technical Operations, strong expertise in chemistry, manufacturing, and controls (CMC), regulatory compliance, and pharmaceutical development is essential, often supported by a degree in life sciences or engineering. Familiarity with quality management systems, process validation, and regulatory submission tools like eCTD is typically required. Excellent problem-solving, cross-functional collaboration, and project management skills help professionals excel in this role. These abilities are critical for ensuring product quality, regulatory approval, and efficient progression from development through commercial manufacturing.

What are some common challenges faced by professionals in CMC Technical Operations, and how can they be overcome?

Professionals in CMC (Chemistry, Manufacturing, and Controls) Technical Operations often encounter challenges such as managing complex regulatory requirements, coordinating cross-functional teams, and ensuring seamless technology transfer from development to manufacturing. Staying organized and maintaining clear communication with regulatory, quality, and manufacturing groups is crucial. Proactively identifying potential bottlenecks and maintaining flexibility can help address unforeseen technical issues, ultimately supporting timely product commercialization.

What is the difference between Cmc Technical Operations vs CMC Regulatory Affairs?

AspectCmc Technical OperationsCMC Regulatory Affairs
Required CredentialsBachelor's in Chemistry, Pharmaceutical Sciences, or related field; technical certificationsBachelor's or higher in Life Sciences, Regulatory Affairs, or related; certifications like RAC
Work EnvironmentLaboratories, manufacturing facilities, technical teamsRegulatory agencies, corporate offices, compliance teams
Employer & Industry UsagePharmaceutical manufacturing, biotech companiesPharmaceutical companies, regulatory agencies
Common Search & ComparisonYesYes

While Cmc Technical Operations focuses on manufacturing processes, technical troubleshooting, and product development, CMC Regulatory Affairs handles regulatory submissions, compliance, and communication with authorities. Both roles are essential in the pharmaceutical industry but serve different functions within the product lifecycle.

What are popular job titles for Cmc Technical Operations?

Popular job titles for Cmc Technical Operations:

Infographic showing various Cmc Technical Operations job openings in the United States as of September 2026, with employment types broken down into 1% As Needed, 84% Full Time, 12% Part Time, 1% Temporary, 1% Contract, and 1% Nights. Highlights an 93% Physical, 2% Hybrid, and 5% Remote job distribution, with an average salary of $91,282 per year, or $43.9 per hour.

Product Technical Operations Scientist

Fort Detrick, MD • On-site

VENESCO LLC
51 - 200 employees
Learn more about VENESCO LLCexternal

$135K - $150K/yr

Full-time

Re-posted 17 days ago

Job description

Description:

Product Technical Operations Scientist


Venesco LLC is seeking Product Technical Operations Scientists to provide Chemistry, Manufacturing and Controls (CMC), investigational product, manufacturing, quality, and nonclinical support across the medical product lifecycle to facilitate successful product development and regulatory approvals.   


Requirements:

 Duties and Responsibilities 

  • Support manufacturing strategy development. 
  • Review product specifications and manufacturing records. 
  • Support investigational product accountability and logistics. 
  • Review analytical and bioanalytical validation activities. 
  • Participate in manufacturing audits and inspections. 
  • Review stability programs and quality documentation. 
  • Support CMC content for regulatory submissions. 
  • Evaluate manufacturing risks and quality deviations. 
  • Support nonclinical study review activities. 
  • Participate in integrated product teams. 

Minimum Qualifications 

  • Bachelor's or Master's degree in Pharmaceutical Sciences, Chemistry, Biology, Engineering, or related field. 
  • Minimum 5 years of CMC or pharmaceutical development experience. 
  • Knowledge of FDA regulatory requirements, GMP, and GLP. 
  • Experience supporting regulated product development. 


Venesco, LLC, is an equal opportunity and affirmative action employer. Venesco is committed to administering all employment and personnel actions on the basis of merit and free of discrimination based on race, ethnicity, religious affiliation, gender, gender identity or expression, sexual orientation, national origin, protected veteran status, or status as an individual with a disability. Consistent with this commitment, we are dedicated to the employment and advancement of qualified minorities, women, individuals with disabilities, protected veterans, persons of all ethnic backgrounds and religions according to their abilities.

For more information on Venesco, LLC., visit https://venesco.com.