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Formulation Development Cmc Jobs in Chelsea, MA (NOW HIRING)

Syner-G

Consultant II

Framingham, MA · On-site

Manage the transfer of formulation design to trusted CDMO partners and draft all necessary ... Collaborate effectively with CMC teams; including, analytical development scientists, drug ...

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Formulation Development Cmc information

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$32

$55

$104

How much do formulation development cmc jobs pay per hour?

As of Jul 7, 2026, the average hourly pay for formulation development cmc in Chelsea, MA is $55.30, according to ZipRecruiter salary data. Most workers in this role earn between $37.60 and $88.56 per hour, depending on experience, location, and employer.

What is the role of CMC in drug development?

In formulation development, CMC (Chemistry, Manufacturing, and Controls) ensures the quality, safety, and efficacy of a drug by establishing manufacturing processes, quality standards, and regulatory documentation. Formulation scientists and CMC teams collaborate to develop stable, scalable drug products that meet regulatory requirements throughout development and commercialization.

What is the salary of formulation R&D?

The salary for a Formulation Development CMC professional typically ranges from $70,000 to $130,000 annually, depending on experience, education, and location. Entry-level roles may start lower, while senior positions with specialized skills or certifications can earn higher salaries. Compensation often includes benefits such as health insurance and bonuses.

What is the highest paying job in pharmaceuticals?

In pharmaceuticals, senior roles such as Vice President of Research and Development or Chief Scientific Officer typically have the highest salaries, often exceeding several hundred thousand dollars annually. These positions require extensive experience, advanced degrees, and leadership skills, and they oversee drug development, regulatory strategies, and company innovation.

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.

Is formulation part of CMC?

In formulation development roles within CMC (Chemistry, Manufacturing, and Controls), formulation is a core component, involving the design and optimization of drug formulations to ensure stability, efficacy, and manufacturability. These professionals work with analytical tools, quality standards, and regulatory requirements to develop suitable formulations for clinical and commercial products.

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, and why are they important?

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.
Formulation Development Cmc jobs near you
Vice President, Pharmaceutical Development

Vice President, Pharmaceutical Development

Kymera Therapeutics

Watertown, MA • On-site

$315K - $395K/yr

Other

Posted 11 days ago

Job description

Who we are:

Kymera is a clinical-stage biotechnology company pioneering the field of targeted protein degradation (TPD) to develop medicines that address critical health problems and have the potential to dramatically improve patients' lives. Kymera is deploying TPD to address disease targets and pathways inaccessible with conventional therapeutics. Having advanced the first degrader into the clinic for immunological diseases, Kymera is focused on building an industry-leading pipeline of oral small molecule degraders to provide a new generation of convenient, highly effective therapies for patients with these conditions. Founded in 2016, Kymera has been recognized as one of Boston's top workplaces for the past several years. For more information about our science, pipeline and people, please visitwww.kymeratx.com or follow us onX (formerly Twitter)orLinkedIn. 

How we work:
  • PIONEER: We are courageous, resilient and rigorous in our mission to improve patients' lives through our revolutionary degrader medicines.
  • COLLABORATE: We value trust + transparency from everyone. Our goals are shared, our decisions data-driven and our camaraderie genuine.
  • BELONG: We recognize our differences, inviting curiosity and inclusivity, so that our people are valued, seen, and heard.
How you'll make an impact:
  • Define and lead the company's pharmaceutical development strategy across the portfolio, ensuring alignment with corporate priorities and development timelines
  • Provide strategic leadership for preformulation, biopharmaceutics, and formulation development activities supporting discovery, preclinical, and clinical-stage programs
  • Champion innovation in formulation sciences and enabling technologies to address complex drug delivery and bioavailability challenges
  • Drive development and implementation of phase-appropriate drug product development and manufacturing strategies
  • Lead a high-performing Pharmaceutical Development team, in internal activities and management of an external network of CROs, CDMOs, and strategic partners
  • Establish scalable processes, operational frameworks, and best practices to support portfolio growth
  • Provide strategic oversight of outsourced development and manufacturing activities, ensuring quality, timelines, and technical objectives are achieved
  • Lead CMC-related regulatory strategy for drug product development activities, regulatory submissions and health authority interactions
  • Ensure compliance with applicable GMP and regulatory requirements
  • Represent Pharmaceutical Development in due diligence activities, external collaborations, and interactions with other functions
  • Contribute to risk assessment, resource prioritization, and investment decisions as a member of the Technical Operations leadership team
  • Foster strong cross-functional partnerships across Research, Clinical, Regulatory, Quality, Supply Chain, and Program Management to enable efficient advancement of pipeline programs
Skills and experience you'll bring:
  • Ph.D. in Pharmaceutics, Pharmaceutical Sciences, Chemical Engineering, or related discipline with 18+ years of relevant pharmaceutical industry experience
  • Demonstrated success leading pharmaceutical development strategy from discovery through clinical development, with experience supporting commercialization readiness
  • Strong understanding of preformulation, biopharmaceutics, formulation development, and oral solid dose drug product manufacturing for small molecules
  • Deep expertise in formulation approaches for poorly soluble compounds, including application of enabling technologies to improve bioavailability and product performance
  • Proven track record of advancing programs through IND and clinical development milestones and contributing to successful regulatory submissions
  • Strong knowledge of GMP requirements, regulatory expectations, and evolving industry trends
  • Experience building and managing high-performing teams and external partnerships
  • Excellent communication and leadership skills, with the ability to effectively engage technical teams, executive leadership, external partners, and regulatory agencies
Equal Employment Opportunity

Kymera Therapeutics is proud to be an equal opportunity employer, seeking to create a welcoming and diverse environment.  All applicants will receive consideration for employment without regard to race, color, religion, creed, gender, national origin, age, disability, veteran status, pregnancy, sex, marital status, gender expression or identity, genetic information, sexual orientation, citizenship, or any other legally protected class.

Compensation

  • Kymera offers a competitive compensation package that recognizes both results and capabilities through market-based, performance-driven pay.
  • The anticipated base salary range for this role is $315,000 - $395,000, with eligibility for annual bonus, equity participation, and comprehensive benefits.
  • Actual salary is based on a holistic evaluation of the specific role/level as well as each candidate's depth of experience and the capabilities they bring to the position.

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