Biogen Posted August 19, 2026

Sr. Principal Scientist, Oral Drug Product Development

Cambridge, United States Full time
Notify me about similar jobs

Biogen is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.

About this opportunity

About This Role

Biogen is seeking a  Sr. Principal Scientist, Oral Drug Product Development   to provide scientific   and strategic   leadership   for the development of small molecule oral drug products .   This role leads   s cie nt ifi c   and   en gin eering e ff orts   supp orting   formulation and process development across early- and late-stage programs .   This t e chnical   lead   wil l d rive   enabling technologies for   typ ically   low   so lubil ity   and   lo w perm eabil ity   compounds, clinical manufacturing readiness, technology transfer, and commercialization .    The Sr. Principal Scientist serves as a senior drug product leader   and   mentor   on cross-functional CMC and asset teams, influencing development strategy, manufacturing readiness, and regulatory submissions.   This role   will also   be responsible for   managing external partnerships and   advancing   new technologies   and workflows that strengthen Biogen’s oral drug product development capabilities.

What   You’ll   Do

Lead   formulation design, process development, manufacturability assessment, scale-up, technology transfer, and clinical manufacturing of small molecule oral dosage forms   across all stages of development .

Develop enabling formulation approaches for challenging compounds, including poorly soluble, poorly permeable, unstable, or complex molecules   su ch as   orally   delivered   pe pti des .

Serve as the senior drug product representative on cross-functional CMC and asset teams, driving alignment across regulatory, quality, manufacturing, analytical, clinical pharmacology, DMPK, and external partner functions.

Influence portfolio decisions through assessment of developability, manufacturability, biopharmaceutical performance, technical risk, and investment priorities.

Champion technology transfer, clinical manufacturing readiness, and scale-up activities at internal and external manufacturing sites.   Provide strategic oversight and   establish   manufacturing strategies.

Mentor and develop   scientists and engineers supporting oral drug product development.

Oversee completion of drug product sections for regulatory submissions   and   related   technical documentation.

Identify and implement new formulation technologies, predictive tools, digital workflows, and best practices that improve development efficiency and portfolio execution.

Who You Are

You are an innovative scientific leader with a passion for advancing drug development processes through rigorous science and data-driven decision-making. You excel at transforming experimental findings into development strategies, using deep technical expertise and sound scientific judgment to solve complex drug product challenges. Your expertise drives you to develop cutting-edge solutions ensuring manufacturability, scalability, and readiness for commercialization. You thrive in collaborative environments, influencing strategic decisions, and fostering alignment across diverse functions. Your mentoring skills inspire teams to achieve excellence, while your forward-thinking approach maximizes Biogen's capabilities in oral drug product development.

Required Skills:

PhD in   Pharmaceutical Sciences,   Chemical Engineering, Chemistry ,   or a related scientific discipline   with a minimum of 1 2   years’ experience in oral   drug product   development.

Demonstrated   track record   leading   formulation and process development for oral solid dosage forms from early development through clinical manufacturing and/or late-stage development.

Experience with   scale-up, technology transfer, clinical manufacturing , and external manufacturing organizations.

Strong knowledge of CMC development, regulatory expectations, technical documentation, and phase-appropriate development strategies.

Proven   ability to lead across functions,   influence program strategy, manage technical risk, and communicate effectively with diverse stakeholders.

Experience mentoring, developing , or leading   scientists and engineers.

Preferred  Skills:

Deep   e xpertise   in enabling technologies such as amorphous solid dispersions, spray drying, hot-melt extrusion, lipid-based formulations, modified release, or particle engineering.

Experience with late-stage development, commercial readiness, process characterization, or process validation.

Experience supporting at least one NDA/MAA or commercial product   and regulatory agency interaction experience .

Strong understanding and hands on experience with oral solid dose manufacturing unit operations and manufacturability considerations.

Experience implementing   new technologies , digital tools, knowledge platforms, or best practices across multiple programs.

Demonstrated success managing external CDMO/CMO relationships and technology transfer activities.

Job Level: Management

Additional Information

The base compensation range for this role is: $188,000.00-$259,000.00

Base salary offered is determined through an analytical approach utilizing a combination of factors including, but not limited to, relevant skills & experience, job location, and internal equity.

Regular employees are eligible to receive both short term and long-term incentives, including cash bonus and equity incentive opportunities, designed to reward recent achievements and recognize your future potential based on individual, business unit and company performance.

In addition to compensation, Biogen offers a full and highly competitive range of benefits designed to support our employees’ and their families physical, financial, emotional, and social well-being ; including, but not limited to:

Medical, Dental, Vision, & Life insurances

Fitness & Wellness programs including a fitness reimbursement

Short- and Long-Term Disability insurance

A minimum of 15 days of paid vacation and an additional end-of-year shutdown time off (Dec 26-Dec 31)

Up to 12 company paid holidays + 3 paid days off for Personal Significance

80 hours of sick time per calendar year

Paid Maternity and Parental Leave benefit

401(k) program participation with company matched contributions

Employee stock purchase plan

Tuition reimbursement of up to $10,000 per calendar year

Employee Resource Groups participation

Why Biogen?

We are a global team with a commitment to excellence, and a pioneering spirit. As a mid-sized biotechnology company, we provide the stability and resources of a well-established business while fostering an environment where individual contributions make a significant impact. Our team encompasses some of the most talented and passionate achievers who have unparalleled opportunities for learning, growth, and expanding their skills. Above all, we work together to deliver life-changing medicines, with every role playing a vital part in our mission. Caring Deeply. Achieving Excellence. Changing Lives.

At Biogen, we are committed to building on our culture of inclusion and belonging that reflects the communities where we operate and the patients we serve. We know that diverse backgrounds, cultures, and perspectives make us a stronger and more innovative company, and we are focused on building teams where every employee feels empowered and inspired.  Read on  to learn more about Biogen.

All qualified applicants will receive consideration for employment without regard to sex, gender identity or expression, sexual orientation, marital status, race, color, national origin, ancestry, ethnicity, religion, age, veteran status, disability, genetic information or any other basis protected by federal, state or local law. Biogen is an E-Verify Employer in the United States.

Job details

Seniority
Principal
Function
Manufacturing & CMC
Therapeutic area
Not listed
Location
Cambridge, United States
Employment type
Full time

How this role compares

Computed from every other active Manufacturing & CMC role in our database, not just this employer's listings.

We currently track 683 comparable Principal Manufacturing & CMC roles across 89 biopharma companies.

683Comparable roles tracked
620Currently active
89Companies hiring similar roles
34Countries represented

Salary context

265 of 683 peers report a salary range (USD, annualized)

Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.

This roleSubject Not listed on this posting
Lowest disclosed · Senior Technician Calibration - Maintenance · Mylan Technologies, Inc. $37,000/yr – $80,000/yr
Peer group range $58,500 – $288,000 (median $154,900)

Where these roles are based

Top locations among the 683 comparable roles

United States451
India38
Ireland33
Netherlands23
Germany15
Switzerland14

+ 28 more countries

Seniority mix

683 of 683 peers have a known seniority level

Senior431
Principal137
Director115

Therapeutic area mix

9 of 683 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Vaccines & Infectious Disease4
Oncology3
Respiratory1
Dermatology & Aesthetics1

Similar opportunities

The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.

60%similar
Merck Rahway, New Jersey, United States of America Principal
Same function Same seniority Same country
60%similar
AbbVie North Chicago, IL Principal
Same function Same seniority Same country
60%similar
AbbVie North Chicago, IL Principal
Same function Same seniority Same country
60%similar
AbbVie Pleasanton, CA Principal
Same function Same seniority Same country
60%similar
Sanofi US Services Inc. Waltham, United States Principal
Same function Same seniority Same country
60%similar
Regeneron Pharmaceuticals, Inc (USA) Tarrytown, United States Principal
Same function Same seniority Same country

Notify me about similar jobs

Get an email when we spot other openings like this one – same job function, comparable seniority, roles you'd actually want to see.

Or follow a whole field: get every new Manufacturing & CMC job in the United States, and choose locations and companies.

How we calculate "similar"

No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.

Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.

60%
Principal Scientist/Engineer, Drug/Device Combination Products - Device Characterization
Merck · Rahway, New Jersey, United States of America · Principal
Function Therapeutic area Seniority Country
60%
Principal Scientist I, Biologics Drug Product Development
AbbVie · North Chicago, IL · Principal
Function Therapeutic area Seniority Country
60%
Principal Scientist, Biologics Drug Product Development (DPDT)
Regeneron Pharmaceuticals, Inc (USA) · Tarrytown, United States · Principal
Function Therapeutic area Seniority Country
60%
Senior Principal Microbiologist
Lilly · Concord, North Carolina, United States of America · Principal
Function Therapeutic area Seniority Country
Unmatched or unknown dimensions score exactly the same: 0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.