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

Senior Director, CMC Technical Lead

Boston, MA ยท On-site

$235K - $285K/yr

Join us as a Senior Director, CMC Technical Lead , and you'll be part of a culture that welcomes ... linical, formulation, process and analytical development, manufacturing and regulatory plans.

Apply Early

Senior Director, CMC Technical Lead

Boston, MA ยท On-site

$235K - $285K/yr

Join us as a Senior Director, CMC Technical Lead , and you'll be part of a culture that welcomes ... linical, formulation, process and analytical development, manufacturing and regulatory plans.

Support stability-related input into formulation, process development, control strategy, and change ... Experience working in cross-functional CMC teams within a matrixed development or commercial ...

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Formulation Development Cmc information

See Chelsea, MA salary details

$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.
Senior Director, CMC Technical Lead

Senior Director, CMC Technical Lead

Elektrofi Inc

Boston, MA โ€ข On-site

$235K - $285K/yr

Full-time

Retirement

Posted 2 days ago

Be an early applicant


Job description

Description:

Welcome to an inspired career.

At Halozyme Hyperconโ„ข, a wholly-owned subsidiary of Halozyme Therapeutics, Inc., we are reinventing the patient experience and building the future of drug delivery. We are passionate about the important work we do and constantly strive to do more. We embrace transformation and work hard to innovate for the future. We do this together, as One Team โ€“ we rise by lifting others up and believe in the power of working together for the collective win. Thatโ€™s why we need youโ€”to help us make a significant impact by taking on increasingly complex challenges, leaping beyond the status quo, advancing our mission and making our One Team culture thrive.


Join us as a Senior Director, CMC Technical Lead , and youโ€™ll be part of a culture that welcomes diversity, thinks differently to solve problems, works collaboratively as one team, and delivers meaningful innovations that impact peopleโ€™s lives.


How you will make an impact

Halozyme Hypercon is seeking an experienced CMC Technical Lead to join our Program Management and Portfolio Strategy team. This is a technical role that will lead cross-functional program teams โ€“ from early development through launch. This role will serve as the primary technical and strategic interface between internal cross-functional teams, external partners, and regulatory authorities to ensure successful development of biologics on the Hyperconโ„ข Platform. The role requires dynamic leadership expertise in biologics nonclinical development and CMC and strong decision-making abilities.


In this role, youโ€™ll have the opportunity to:

  • Drive the development and implementation of the integrated scientific, technical, and regulatory strategy of programs in the portfolio ensuring alignment with overall program objectives and regulatory requirements.
  • Partner with the program manager, functional heads, and technical SMEs to integrate nonclinical, formulation, process and analytical development, manufacturing and regulatory plans.
  • Partner with the program manager, functional heads, and technical SMEs to identify risks, and implement mitigation strategies for each program.
  • Support regulatory strategy development and health authority interactions as the lead contributor
  • Act as the primary technical interface between the company and Alliance Partners, ensuring transparent communication and alignment.
  • Facilitate effective decision-making by preparing clear program updates, risk assessments, and recommendations for governance and senior leadership.
  • Facilitate technical governance meetings, decision-making forums, and stage-gate readiness reviews.
  • Serve as the primary interface between the Program team and Company leadership, ensuring that the programโ€™s technical strategy and operational plans are aligned with Elektrofiโ€™s short- and long-term goals.
  • Foster a collaborative, high-performing team environment that encourages accountability and solution-oriented thinking.
Requirements:

To succeed in this role, youโ€™ll need:

  • Advanced degree (BS considered with strong experience) in scientific or engineering discipline.
  • 12+ years of biotech/pharma industry experience, including 5+ years of CMC program leadership in biologics development.
  • Proven ability to lead complex, cross-functional teams in a matrix environment.
  • Ability to operate strategically while also managing tactical execution details.
  • Strong team player who can rapidly build positive relationships, proactively partner across teams with the ability to motivate and influence others and negotiate diplomatically.
  • Deep understanding of end-to-end drug product development, manufacturing, and regulatory expectations for biologics. Experience working with high-concentration and subcutaneous formulations is preferred.
  • Strong understanding of biologics CMC development, from preclinical through clinical stages with regulatory submission experience (IND/CTA, BLA/MAA).
  • Excellent oral and written communication skills, and attention to detail to ensure high quality presentations and regulatory submissions.

In return, we offer you:

  • Full and comprehensive benefit program, including an Employee Stock Purchase Program and 401(k) matching.
  • Opportunities to grow in a culture that prioritizes learning, development and progression through in-house programs and tuition reimbursement.
  • A collaborative, innovative team that works as one to amplify your impactโ€”on your career, the work you do and patientsโ€™ lives.

The most likely base pay range for this position is $235,000-$285,000 per year. Several factors, such as experience, tenure, skills, and particular business needs, will determine an individualโ€™s exact level of compensation. Base salary is only one element of employee compensation at Halozyme. Total compensation could include bonuses, sales incentives, and equity awards.


Equal Employment Opportunity Statement

Halozyme Hypercon, Inc is an Equal Employment Opportunity (EEO) employer. It is the policy of the Company to provide equal employment opportunities to all qualified applicants without regard to race (including traits historically associated with race, including but not limited to: hair texture and protective hair styles), religion, religious creed (including religious dress and grooming practices), ethnicity, color, national origin, ancestry, age (40 and older), genetic information, disability (mental and physical, including HIV and AIDS), reproductive health decision-making, medical leave or other types of protected leave, domestic violence victim status, political affiliation, medical condition (including cancer/ genetic characteristics and information), sex, gender, gender identity, gender expression, sexual orientation, marital or familial status, citizenship, pregnancy (including perceived pregnancy, childbirth, breastfeeding, or related medical conditions), military or veteran status, or any other status protected by federal, state, or local law.


Click here to view the Know Your Rights Poster.


Accessibility and Reasonable Accommodations

Halozyme Hypercon is committed to providing reasonable accommodations for qualified individuals with disabilities and disabled veterans during our application process. If you need assistance or an accommodation due to a disability, contact Human Resources at talentacquisition@halozyme.com.


Halozyme Privacy Notice: Applicant Privacy Notice.


To all agencies, please, no phone calls or emails to any employee of Halozyme Hypercon about this requisition. All resumes submitted by search firms/employment agencies to any employee at Halozyme Hypercon via email, the internet, or in any form and method will be deemed the sole property of Halozyme Hypercon unless such search firms/employment agencies were engaged by Halozyme Hypercon for this requisition and a valid agreement with Halozyme Hypercon is in place. If a candidate submitted outside of the Halozyme Hypercon agency engagement process is hired, no fee or payment of any kind will be paid.




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