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Formulation Development Cmc Jobs in Columbia, MD

Moderna

Intern, CMC Development (Summer 2027)

Baltimore, MD · On-site +1

$20 - $60/hr

The CMC Development organization at Moderna is looking for top talent in science and engineering to ... Optimize the impact of formulation and processing conditions on the stability of mRNA drug products ...

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Astrazeneca

Regulatory Affairs Director

Gaithersburg, MD

$162K - $213K/yr

... to the development, commercialization and life cycle management of assigned oncology products ... Craft the health authority engagement strategy and interaction plan, drive the formulation of the ...

AstraZeneca

Regulatory Affairs Director

Gaithersburg, MD · On-site

$162K - $213K/yr

... to the development, commercialization and life cycle management of assigned oncology products ... Craft the health authority engagement strategy and interaction plan, drive the formulation of the ...

AstraZeneca

Regulatory Affairs Director

Gaithersburg, MD · On-site

$162K - $213K/yr

... to the development, commercialization and life cycle management of assigned oncology products ... Craft the health authority engagement strategy and interaction plan, drive the formulation of the ...

AstraZeneca

Regulatory Affairs Director

Gaithersburg, MD · On-site

$162K - $213K/yr

... to the development, commercialization and life cycle management of assigned oncology products ... Craft the health authority engagement strategy and interaction plan, drive the formulation of the ...

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All JobsFormulation Development Cmc JobsFormulation Development Cmc Jobs in Columbia, MD

Formulation Development Cmc information

See Columbia, MD salary details

$29

$50

$95

How much do formulation development cmc jobs pay per hour?

As of Sep 5, 2026, the average hourly pay for formulation development cmc in Columbia, MD is $50.50, according to ZipRecruiter salary data. Most workers in this role earn between $34.38 and $80.87 per hour, depending on experience, location, and employer.

What is formulation development CMC?

Formulation Development CMC (Chemistry, Manufacturing, and Controls) refers to the process of designing and optimizing the composition of a drug product, ensuring it is safe, effective, and stable for patient use. This role involves selecting appropriate excipients, developing the manufacturing process, and generating the data required to support regulatory submissions. CMC professionals collaborate with research, quality, and regulatory teams to ensure that the drug product meets all necessary standards throughout its lifecycle.

What are the key skills and qualifications needed to thrive as a formulation development CMC specialist?

To thrive as a Formulation Development CMC specialist, you need expertise in pharmaceutical sciences, chemistry, and regulatory guidelines, often supported by an advanced degree in a relevant field. Familiarity with analytical techniques, formulation equipment, and regulatory submission systems like eCTD is crucial. Strong problem-solving skills, attention to detail, and effective collaboration are essential soft skills in this role. These competencies ensure the successful development, optimization, and regulatory approval of safe and effective pharmaceutical products.

What are some typical challenges faced by professionals in formulation development CMC, and how are they addressed?

Professionals in Formulation Development CMC often encounter challenges such as ensuring formulation stability, meeting regulatory requirements, and scaling up from laboratory to manufacturing. Addressing these challenges requires close collaboration with analytical, regulatory, and manufacturing teams, as well as staying current with evolving guidelines. Effective project management, rigorous experimental design, and proactive risk assessment are key strategies to successfully navigate these complexities and ensure timely progress of drug development projects.

What is the difference between Formulation Development Cmc vs Formulation Scientist?

AspectFormulation Development CmcFormulation Scientist
CredentialsBachelor's or Master's in Pharmacy, Chemistry, or related fields; industry certificationsBachelor's or Master's in Pharmaceutical Sciences, Chemistry, or related fields
Work EnvironmentPharmaceutical or biotech R&D labs, manufacturing settingsResearch labs, development facilities, pharmaceutical companies
Industry UsageRegulatory submissions, product development, manufacturing supportFormulation research, experimental design, product optimization

Formulation Development Cmc focuses on developing formulations suitable for regulatory approval and manufacturing, often involving documentation and compliance. Formulation Scientists primarily conduct research and experiments to create and optimize formulations. While both roles require similar educational backgrounds and work in related environments, Cmc roles emphasize regulatory and manufacturing aspects, whereas Scientists focus on experimental research and innovation.

What are popular job titles related to Formulation Development Cmc jobs in Columbia, MD?

For Formulation Development Cmc jobs in Columbia, MD, the most frequently searched job titles are:

What cities near Columbia, MD are hiring for Formulation Development Cmc jobs?

Cities near Columbia, MD with the most Formulation Development Cmc job openings:

Formulation Development Cmc jobs near you
Infographic showing various Formulation Development Cmc job openings in Columbia, MD as of August 2026, with employment types broken down into 1% As Needed, 82% Full Time, 14% Part Time, and 3% Contract. Highlights an 91% Physical, 3% Hybrid, and 6% Remote job distribution, with an average salary of $105,044 per year, or $50.5 per hour.

Senior Scientist, Process Development

Scorpion Therapeutics

Gaithersburg, MD • On-site

$114 - $182/hr

Other

Posted 6 days ago

Job description

Your Contribution
  • Develop and qualify scale-down models for downstream purification processes to support monoclonal antibody manufacturing
  • Execute studies and FMEA assessments to establish critical process parameters and proven acceptable ranges for process characterization
  • Lead development, optimization, and characterization of downstream processes, including scale-up, virus/impurity clearance, and resin/membrane lifetime
  • Conduct downstream process unit operations such as depth filtration, chromatography, viral inactivation, viral filtration, tangential flow filtration, and formulation
  • Collaborate with cross-functional teams to design experiments, analyze results, support technology transfers, and meet project timelines
  • Contribute to CMC documentation by drafting process descriptions, characterization reports, QbD risk assessments, and other technical reports
  • Drive the creation of best practices and workflows for process development in a fast-paced environment
A Good Match
  • PhD in Biomedical Engineering, Chemical Engineering, Biochemistry or related discipline with 6+ years of relevant experience (including post-doctoral training), or MS with 8+ years of industry experience
  • 6 years' experience in global pharma PD or MS&T for monoclonal antibodies or related biologics
  • Expertise in downstream process development including scale-up and technology transfer
  • Proven ability to design and execute process characterization studies using scale-down models that inform PPQ strategy
  • Strong understanding of biologics CMC processes including PPQ/BLA readiness; antibody or ADC development preferred
  • Demonstrated technical leadership within cross-functional teams and programs
  • Willingness to travel domestically and internationally as required
Benefits
  • Expected Pay Range: $113,600/year to $181,600/year + benefits, annual bonus & equity
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