At GSK, we have bold ambitions for patients, aiming to positively impact the health of 2.5 billion people by the end of the decade. Our R&D focuses on discovering and delivering vaccines and medicines, combining our understanding of the immune system with cutting-edge technology to transform people's lives. GSK fosters a culture ambitious for patients, accountable for impact, and committed to doing the right thing, making sure that we focus our efforts on accelerating significant assets that meet patients' needs and have the highest probability of success. We're uniting science, technology, and talent to get ahead of disease together.
Find out more:
Our approach to R&D
As a key member of our Formulation Science team in Cambridge, MA, you will play a vital role in developing drug product formulations that support projects from discovery through late-stage development. Your core responsibilities will include designing and executing studies, performing in-process testing, and working with cross-functional partners to ensure our drug candidates are safe, stable, and effective.
We are looking for a hands-on problem solver who is conscientious, team-oriented, and communicates with clarity and purpose. If you are a quick learner who takes ownership of your work, you will thrive in this environment. This is more than a job; it's a chance to grow as a leader, make a direct impact on patients' lives, and contribute to GSK's mission of getting ahead of disease together.
Responsibilities
- Design, prepare and test drug product formulations at bench scale to assess stability, compatibility and performance.
- Develop and execute stability studies and stress tests; analyze results and recommend formulation strategies.
- Characterize physicochemical properties using analytical methods such as particle size, pH, viscosity, single-particle measurements, chromatography, and thermal analysis.
- Collaborate with analytical, process development, regulatory and quality teams to support program decisions and documentation.
- Maintain accurate laboratory records, prepare study reports, and present data to project teams.
- Maintain the drug product laboratory space in an organized and in a safe manner
- Troubleshoot experiments, improve methods, and contribute to standard operating procedures.
Work arrangement
This role is on-site and based at Cambridgepark Drive Massachusetts in the United States. You will be expected to work on-site five days a week to interact with team members, execute experiments, train colleagues, collaborate with lab teams, and complete documentation.
Basic Qualifications
- BS, MS or PhD in pharmaceutical sciences, chemical engineering, chemistry, or a related field. BS + 5 years of experience, MS 3+ years of experience, PHD with 0+ years of experience.
- Hands-on laboratory experience preparing and evaluating formulations for small molecules or biologics.
- Experience with stability study design and data interpretation.
- Practical skills with analytical techniques such as HPLC, particle sizing, pH/viscosity measurement, and thermal analysis.
- Strong laboratory documentation practices and experience using electronic or paper laboratory notebooks.
- Good verbal and written communication skills and ability to work in cross-functional teams.
Preferred Qualifications
If you have the following characteristics, it would be a plus:
- MS or PhD in formulation science, pharmaceutics, or related discipline.
- Experience with biologic formulations, lyophilization, or controlled-release systems.
- Familiarity with process development, scale-up considerations and manufacturing hand-offs.
- Strong sense of ownership and personal responsibility, with experience in coordinating with team members to ensure tasks are on track and goals are met successfully.
- Excellent interpersonal skills, demonstrating a patient, thoughtful, and approachable demeanor that fosters a positive and highly collaborative team environment.
- Knowledge of regulatory expectations for formulation development and drug product stability.
- Experience with DOE (design of experiments) and statistical analysis for formulation optimization.
- Prior experience in pharmaceutical or biotech industry environments.
Skills
Biotechnology, Cell Biology, Cross-Functional Teamwork, Data Quality, Following Instructions, Interpersonal Communication, Lab Maintenance, Life Science, Matrix Leadership, Proper Documentation, Scientific Presentations, Scientific Research, Scientific Writing
- If you are based in Cambridge, MA; Waltham, MA; Rockville, MD; or San Francisco, CA, the annual base salary for new hires in this position ranges $89,925 to $149,875. The US salary ranges take into account a number of factors including work location within the US market, the candidate's skills, experience, education level and the market rate for the role. In addition, this position offers an annual bonus and eligibility to participate in our share based long term incentive program which is dependent on the level of the role. Available benefits include health care and other insurance benefits (for employee and family), retirement benefits, paid holidays, vacation, and paid caregiver/parental and medical leave. If salary ranges are not displayed in the job posting for a specific country, the relevant compensation will be discussed during the recruitment process.
Please visit GSK US Benefits Summary to learn more about the comprehensive benefits program GSK offers US employees.
Why GSK?
Uniting science, technology and talent to get ahead of disease together.
People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.
If you require an accommodation or other assistance to apply for a job at GSK, please contact the appropriate Recruitment Staff by emailing us at -
GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law.
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