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Cmc Scientist Jobs (NOW HIRING)

GenScript/ProBio

CMC Analytical Scientist

Pennington, NJ · On-site

$80K - $110K/yr

The position reports to the Sr. Scientist, is ideally suited for a professional with extensive ... Collaborate closely with other teams in CMC and coordinate cross-functional activities to support ...

Cardinal Health

$31.50 - $40.41/hr

We currently have a career opening for a Scientist I - CMC What Chemistry, Manufacturing and Controls contributes to Cardinal Health The Scientist I - CMC supports regulatory activities for pre ...

GenScript/ProBio

CMC Analytical Scientist

Hopewell, NJ

$80K - $110K/yr

The position reports to the Sr. Scientist, is ideally suited for a professional with extensive ... Collaborate closely with other teams in CMC and coordinate cross-functional activities to support ...

GenScript/ProBio

CMC Analytical Scientist

Pennington, NJ · On-site

$80K - $110K/yr

The position reports to the Sr. Scientist, is ideally suited for a professional with extensive ... Collaborate closely with other teams in CMC and coordinate cross-functional activities to support ...

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How much do cmc scientist jobs pay per hour?

As of Jul 7, 2026, the average hourly pay for cmc scientist in the United States is $42.08, according to ZipRecruiter salary data. Most workers in this role earn between $31.49 and $48.56 per hour, depending on experience, location, and employer.

Do pharmaceutical scientists make a lot of money?

Pharmaceutical scientists, including those working as CMC (Chemistry, Manufacturing, and Controls) scientists, typically earn competitive salaries that vary by experience, education, and location. According to industry data, the median annual salary for pharmaceutical scientists ranges from $70,000 to over $120,000, with senior roles and specialized skills commanding higher pay. Factors such as advanced degrees, certifications, and expertise in regulatory requirements can influence earning potential.

What are CMC jobs?

CMC jobs refer to roles in Chemistry, Manufacturing, and Controls within the pharmaceutical and biotech industries. These positions involve developing, manufacturing, and ensuring the quality of drug products, often requiring knowledge of regulatory standards, Good Manufacturing Practices (GMP), and laboratory skills.

What are CMC Scientists?

CMC Scientists, or Chemistry, Manufacturing, and Controls Scientists, are professionals who focus on the development, production, and quality control of pharmaceutical products. They play a critical role in ensuring that drugs are manufactured consistently, safely, and according to regulatory standards. Their responsibilities include designing experiments, analyzing data, and preparing documentation required for regulatory submissions. CMC Scientists often work closely with other departments such as regulatory affairs, quality assurance, and manufacturing to ensure product integrity throughout the drug development process.

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

To thrive as a CMC (Chemistry, Manufacturing, and Controls) Scientist, you need a strong background in chemistry, pharmaceutical sciences, or chemical engineering, typically supported by an advanced degree and industry experience. Familiarity with analytical instrumentation, regulatory submission tools, and quality management systems such as GMP are essential. Strong problem-solving, project management, and communication skills help coordinate cross-functional teams and manage complex projects. These capabilities ensure regulatory compliance, efficient development processes, and the successful delivery of safe, effective pharmaceutical products.

What are some common challenges CMC Scientists face when collaborating with cross-functional teams during drug development?

CMC Scientists often work closely with regulatory, analytical, and manufacturing teams to ensure a drug's quality and compliance throughout development. A common challenge is aligning timelines and priorities, as different teams may operate on varying schedules or have distinct objectives. Effective communication and flexibility are essential to manage the complex data requirements, address technical hurdles, and respond to regulatory feedback. By fostering strong cross-departmental relationships, CMC Scientists can help streamline processes and mitigate potential delays.

What is a CMC scientist?

A CMC scientist specializes in Chemistry, Manufacturing, and Controls (CMC) within the pharmaceutical industry, focusing on developing and ensuring the quality of drug products. They work on formulation, process development, and regulatory documentation, often using laboratory techniques and regulatory guidelines to support drug approval processes.

What is the highest paid scientist job?

In the field of CMC (Chemistry, Manufacturing, and Controls) science, senior roles such as Director of CMC or Vice President of CMC typically have the highest salaries, often exceeding $150,000 annually. These positions require extensive experience, leadership skills, and expertise in regulatory compliance and drug development processes.
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Cmc Scientist jobs near you

CMC Analytical Scientist

GenScript/ProBio

Pennington, NJ • On-site

$80K - $110K/yr

Other

Re-posted 16 days ago

Job description

About ProBio

ProBio, a subsidiary of GenScript, is a global CDMO offering end-to-end services from discovery to GMP for plasmids, antibodies, and cell & gene therapies. We bring together multidisciplinary expertise to accelerate development and manufacturing through customized, and comprehensive services. ProBio has established companies in the United States, the Netherlands, South Korea, and China (Hong Kong, Shanghai, and Nanjing) and other regions to serve global customers, and has helped customers in the United States, Europe, Asia Pacific and other regions obtain more than 150 IND approvals since October 2017

Position Overview:

The position reports to the Sr. Scientist, is ideally suited for a professional with extensive technical knowledge, and a proven track record of developing and carrying out processes, that are suitable for use in GMP manufacturing of a wide range of clinical trial materials, and participating in the technology transfer. There is a great opportunity to lead and evolve this function within a CDMO business, to support a broad portfolio and advance the manufacturing capabilities to deliver products to the client projects that transform the lives of patients.

Responsibilities:

  • Support the set-up, development and maintenance of a GMP QC-Analytics Lab
  • Generate and characterize engineered cell lines, including production of MCB and WCB for cell-based assay development.
  • Develop, optimize, and execute molecular and cellular assays to assess vector performance using qPCR/ddPCR based assay, Western blot, ELISA and Flow cytometry.
  • Independently plan, perform, analyze, and interpret experiments, present clear data summaries and recommendations to cross-functional teams and clients.
  • Prepare technical reports, study summaries, and presentation materials to support decision-making.
  • Collaborate closely with other teams in CMC and coordinate cross-functional activities to support tech transfer and CMC activities.
  • Drive continuous improvement by identifying and implementing new tools, technologies, and best practices in CGT CMC analytics.
  • Ensure compliance with BSL-2 biosafety standards, cGMP, and applicable regulatory requirements.

Qualifications:

  • Ph.D. with 2+ years or M.S. with 3+ years in Molecular Biology, Cell & Gene Therapy, Biochemistry, or related field.
  • Demonstrated hands-on experience in lentiviral vector release testing and characterization (required).
  • Expertise in molecular and cell biology techniques, including qPCR, ddPCR, ELISA or DNA Sequencing/Analysis.
  • Hands-on experience with Western blotting and flow cytometry for protein and cell-based analyses.
  • Exposure to NGS-based methods for vector or genome characterization is a plus.
  • Working knowledge of Good Documentation Practices, data integrity, and ALCOA+ principles.
  • Strong problem-solving skills with the ability to work independently and collaboratively in a team environment.
  • Excellent interpersonal, verbal, and written communication skills.
  • Familiarity with regulatory requirements and guidance from agencies such as FDA and ICH; experience with EU Annex 1 and laboratory audits is a plus.

Pay range is estimated between $80k - $110k based on skill set and experience.

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