ZipRecruiter

Log In

1

Pharmaceutical Development Jobs in Boston, MA (NOW HIRING)

Alkermes

Scientist, Formulation Development

Waltham, MA · On-site

$136/hr

S. / B.S. in Chemical Engineering, Pharmaceutical Sciences, Materials Science, or a related field, with 0-3 / 6+ / 10+ years of pharmaceutical development experience, respectively. Preferred ...

Alkermes

Scientist, Formulation Development

Waltham, MA · On-site

$136/hr

Collaborate effectively within Pharmaceutical Development and cross-functional project teams, fostering a culture of diversity, inclusion, and belonging. * Maintain and grow scientific and technical ...

Sebela Pharmaceuticals Inc.

QC Chemist

Holbrook, MA

$55/hr

Braintree Laboratories, Inc., a part of Sebela Pharmaceuticals, has its contract development and manufacturing organization (CDMO) in Holbrook, MA, offering pharmaceutical-development and in-house ...

Ocular Therapeutix

Analytical Chemist II

Bedford, MA · On-site

Ocular Therapeutix is seeking an Analytical Chemist to support Pharmaceutical Development activities. This role is responsible for laboratory testing to characterize the chemical and physical ...

Sebela Pharma

QC Chemist

Holbrook, MA · On-site

$55K - $60K/yr

Braintree Laboratories, Inc., a part of Sebela Pharmaceuticals, has its contract development and manufacturing organization (CDMO) in Holbrook, MA, offering pharmaceutical-development and in-house ...

next page

Showing results 1-20

All JobsPharmaceutical Development JobsPharmaceutical Development Jobs in Boston, MA

Pharmaceutical Development information

See Boston, MA salary details

$25.5K

$74.3K

$142.3K

How much do pharmaceutical development jobs pay per year?

As of Aug 24, 2026, the average yearly pay for pharmaceutical development in Boston, MA is $74,327.00, according to ZipRecruiter salary data. Most workers in this role earn between $38,000.00 and $96,700.00 per year, depending on experience, location, and employer.

What is a pharmaceutical development?

A Pharmaceutical Development job involves researching, formulating, and optimizing new drug products to ensure safety, efficacy, and regulatory compliance. Professionals in this role work on drug formulation, process development, and scale-up for manufacturing. They collaborate with scientists, regulatory teams, and production staff to bring medications from the lab to market. This field requires strong knowledge of chemistry, biology, and regulatory requirements.

What does a pharmaceutical development professional do?

Professionals in Pharmaceutical Development typically oversee the formulation and optimization of new drug products, conduct lab-based experiments, and analyze test data to ensure product efficacy and safety. They frequently collaborate with cross-functional teams such as quality assurance, regulatory affairs, and manufacturing to advance each stage of product development. Regular responsibilities also include drafting technical reports, maintaining detailed laboratory documentation, and supporting regulatory submissions. The role often requires balancing hands-on lab work with strategic planning, ensuring that all processes comply with industry standards and regulations.

What are the key skills and qualifications needed to thrive in pharmaceutical development?

To thrive in Pharmaceutical Development, you need a strong background in pharmaceutical sciences, chemistry, or related fields, often supported by an advanced degree (MS or PhD) and experience in drug formulation and testing. Proficiency in analytical instrumentation (e.g., HPLC, GC), regulatory compliance systems, and Good Laboratory Practice (GLP) certifications are highly valued. Strong project management, problem-solving abilities, and effective communication skills set top performers apart. These competencies ensure the development of safe, effective pharmaceuticals while navigating complex regulatory requirements and cross-functional team dynamics.

How much do pharmaceutical developers make?

Pharmaceutical developers typically earn a median annual salary of around $80,000 to $120,000, depending on experience, education, and location. Entry-level positions may start lower, while experienced professionals or those with advanced degrees can earn higher salaries, especially in research and development environments.

How to get into pharmaceutical development?

To enter pharmaceutical development, candidates typically need a bachelor's degree in pharmacy, chemistry, biology, or a related field, with advanced roles often requiring a master's or Ph.D. in a relevant discipline. Gaining experience through internships, research projects, or entry-level positions in laboratories is valuable, along with developing skills in laboratory techniques, data analysis, and regulatory compliance. Certifications such as Good Laboratory Practice (GLP) or Good Manufacturing Practice (GMP) can enhance job prospects in this field.

What does a pharmaceutical development do?

A pharmaceutical development professional is responsible for designing, testing, and optimizing processes to create new drugs or improve existing ones. They work in laboratories and manufacturing settings, often using specialized tools and adhering to regulatory standards to ensure product safety and efficacy.

What are the most commonly searched types of Pharmaceutical Development jobs in Boston, MA?

The most popular types of Pharmaceutical Development jobs in Boston, MA are:

What are popular job titles related to Pharmaceutical Development jobs in Boston, MA?

For Pharmaceutical Development jobs in Boston, MA, the most frequently searched job titles are:

What job categories do people searching Pharmaceutical Development jobs in Boston, MA look for?

The top searched job categories for Pharmaceutical Development jobs in Boston, MA are:

Pharmaceutical Development jobs near you
Infographic showing various Pharmaceutical Development job openings in Boston, MA as of August 2026, with employment types broken down into 1% As Needed, 82% Full Time, 14% Part Time, and 3% Contract. Highlights an 90% Physical, 3% Hybrid, and 7% Remote job distribution, with an average salary of $74,331 per year, or $35.7 per hour.

Vice President, Pharmaceutical Development

Watertown, MA • On-site

Kymera Therapeutics
Biotechnology Research and Development • 51 - 200 employees
Learn more about Kymera Therapeuticsexternal

$315K - $395K/yr

Full-time

Re-posted 23 hours 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 visit www.kymeratx.com or follow us on X (formerly Twitter) or LinkedIn.
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.

Apply