About this opportunity
Viridian Therapeutics, Inc. lists this Director, Formulation and Drug Product Development opportunity in waltham, Massachusetts. Review the employer’s description below for duties, qualifications and application requirements.
Job description
Location 221 CRESCENT ST STE 103A,Waltham, MA, ,United States
Base Pay $200,000.00 - $245,000.00 / Year
Employee Type FT Exempt
Required Degree Doctorate
Travel 15%
At Viridian, we are focused on developing best-in‑class medicines for people living with autoimmune and rare diseases. Leveraging our team’s expertise in antibody discovery and engineering, we have created a robust pipeline of differentiated investigational therapeutic candidates for well-validated targets.
Reporting to the Executive Director, Drug Development, the Director, Formulation and Drug Product Development will provide scientific and technical leadership for formulation and drug product development activities across Viridian's biologics pipeline. This individual will be responsible for developing and advancing formulation strategies, drug product processes, and manufacturing approaches from early development through commercialization, with a focus on monoclonal antibodies and other protein therapeutics. The role requires the ability to integrate formulation science, drug product process development, stability data, product quality understanding, and regulatory expectations into phase‑appropriate development strategies.
This role is based in our Waltham, MA headquarters. Our office‑based employees are required to work in the office three (3) days a week.
Responsibilities (including, but not limited to):
Lead formulation development activities for biologic products, including formulation design, excipient selection, stability strategy development, and support of clinical and commercial dosage forms
Develop scientifically sound formulation and drug product development strategies that balance product quality, manufacturability, patient needs, regulatory expectations, and program timelines
Design, oversee, and interpret formulation development, process development, characterization, and validation studies using risk‑based and data‑driven approaches
Apply a strong understanding of protein structure, degradation pathways, formulation mechanisms, and product quality attributes to guide development decisions and address technical challenges
Utilize analytical data and product characterization results to investigate stability trends, define formulation risks, support root‑cause analyses, and enable informed decision‑making
Lead drug product process development activities, including fill‑finish process development, scale‑up, technology transfer, process characterization, and process validation
Provide technical leadership for external CDMOs and manufacturing partners supporting formulation development, drug product development, technology transfer, and commercial readiness activities
Review and approve technical protocols, reports, manufacturing documentation, investigations, change controls, and development plans
Serve as the drug product development representative on cross‑functional project teams and contribute to overall CMC strategy and program execution
Author and review drug product and formulation sections of regulatory submissions, health authority responses, and other technical documents
Assess technical risks, develop mitigation strategies, and drive resolution of formulation, manufacturing, and product quality challenges
Maintain awareness of emerging technologies, industry trends, and regulatory expectations relevant to biologics formulation and drug product development
Qualifications:
Ph.D. in Pharmaceutical Sciences, Chemistry, Chemical Engineering, Biochemistry, Biology, or a related scientific discipline with 8+ years of relevant industry experience strongly preferred; or
M.S. with 10+ years of relevant industry experience; or
B.S. with 12+ years of relevant industry experience
Demonstrated experience supporting products from early clinical development through late‑stage development, process validation, and commercial readiness
Experience working with external CDMOs and managing outsourced development and manufacturing activities
Deep understanding of protein formulation science, including degradation pathways, stabilization mechanisms, excipient selection, and formulation optimization
Strong foundation in analytical characterization techniques and the ability to use analytical data to guide formulation and process development decisions
Demonstrated expertise in experimental design, data analysis, interpretation of complex datasets, and application of scientific principles to solve technical challenges
Experience with high‑concentration protein formulations, lyophilized products, or other challenging biologic dosage forms
Experience supporting combination products, including prefilled syringes and autoinjector presentations
Strong written, verbal, and executive‑level communication skills; able to operate with significant autonomy, sound judgment, and high accountability in a fast‑paced matrix environment
Strong commitment to ethical standards
Proficient with Microsoft Office suite (i.e., Word, PowerPoint, Excel, Outlook, SharePoint, etc.)
Ability to travel up to 15%
The salary range for this position is commensurate with experience
Viridian offers a comprehensive benefits package including:
Competitive pay and stock options for all employees
Medical, dental, and vision insurance
Short- and long-term disability coverage
Life, Travel and AD&D
401(k) Company Match with immediate company vest
Employee Stock Purchase plan
Generous vacation plan and paid company holiday shutdowns
Various fertility, mental, financial, and proactive physical health programs
Viridian Therapeutics, Inc. provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination, harassment, or retaliation of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by Federal, State, and Local laws. Viridian will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.
Viridian Therapeutics, Inc participates in E-Verify, the federal program for electronic verification of employment eligibility.
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Worksite address
waltham, MA, 02254, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.