Merck Posted October 31, 2026

Principal Scientist, High Throughput Production and Automation Group Leader, Discovery Biologics

Boston, Massachusetts, United States of America FULL_TIME
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About this opportunity

Job Description

Principal Scientist, High Throughput Production and Automation Group Leader, Discovery Biologics

We are on a quest for cures and are committed to be the world’s premier, most research-intensive biopharmaceutical company. Our teams combine leading drug discovery capabilities and world-class R&D with the purpose of turning breakthrough science into life-changing medicines.

We are seeking a scientific leader experienced in the intersection of protein sciences and automated solutions for the role of Principal Scientist (Director level) in the Boston Discovery Biologics group, which is an end-to-end vertically integrated Discovery organization. The candidate will serve a central role in the group by leading the molecular biology and high throughput protein production team within the Biologics Production and Engineering group in addition to matrix oversight of automated experimental solutions for the broader Boston Discovery Biologics organization. They will oversee the execution of high throughput production queue that translates our protein engineering team and hit identification team’s designs into screening sets of fit-for-purpose therapeutics. They will work closely with the Early Biotherapeutics Characterization team to streamline handoffs for deeper characterization and developability analysis of produced molecules prior to their release to project teams. The ideal candidate will have a deep expertise in the design and hands-on execution of semi to fully automated high throughput approaches as they’re applied to biologics discovery. They will leverage their experiences advancing therapeutics from discovery into the clinic to optimize our ways of working and contribute to the success of all pipeline programs. The candidate’s holistic understanding of drug discovery will assist our organization as it directly integrates computational and wet-lab approaches with state-of-the-art automation to accelerate the discovery, engineering, and characterization of novel biologics in the pre-IND pipeline.

As a people manager, they will invest in the growth and development of current and future staff to create a culture of collaboration and accountability that enables shared success. They will work closely with their team members to leverage strengths and identify opportunities to continually expand technical skillsets and enterprise thinking. They will work to support the department’s efforts to recruit highly skilled key talent to the organization and be a champion for inclusion. We recognize that our team is our strength, and we are committed to creating an inclusive environment for all employees. Successful candidates must demonstrate inclusive behaviors in working with a group of researchers to drive our core mission.

 

What you will do:

Provide scientific and strategic leadership to a team of 4 FTEs

Lead continuous improvement of our physical and digital workflows as well as guiding future automated workflow expansion to continue delivering on tomorrow's therapeutic pipeline

Manage outsourcing CROs for molecular biology and protein production to maximize the impact of our internal resources

Effectively partner with teams within Discovery Biologics and across multidisciplinary interfaces to achieve organizational objectives

Manage our fleet of liquid handlers (Dynamic Devices, TECAN, Hamilton) and associated peripheral equipment

Leverage programmatic leadership experience to support and co-lead Discovery Biologics therapeutic programs in collaboration with Therapeutic Areas

Foster a culture of scientific excellence and collaboration by mentoring and developing scientists, leveraging individual strengths to build a high-performing, engaged team

Stay abreast of external advancements in relevant scientific fields and promote the external reputation of Discovery Biologics

Be a champion for an inclusive culture

QUALIFICATIONS

Education:

Ph.D. in Biochemistry, Computational Biology, Protein Engineering, Physics, Bioengineering, Molecular Biology, Chemistry, Pharmaceutical Science or related STEM field with 8+ years relevant industry experience, Master's with 12+ years relevant industry experience or Bachelor's with 14+ years of relevant industry experience in biochemistry or related field

Relevant experience to include a record of increasing responsibility and independence in a similar industrial setting

 

Required Experience and Skills

Experience supporting biologic therapeutic discovery programs

Extensive production group leadership experience with a track record of talent acquisition, retention, and development

Deep expertise in state-of-the-art high throughput molecular biology and protein production methodology

Experienced in the development, adaption, and continued usage of integrated, automated biologic production and characterization platforms including automated data capture

Ability to thrive in a fast-paced matrixed reporting model in which your team will work on multiple projects in parallel

Established external reputation through high-impact publications, presentations, and/or scientific community engagement

Preferred Experience and Skills:

Therapeutic project leadership experience resulting in candidate selection and beyond

Experience in protein therapeutics beyond antibodies including higher valency and complexity Fc containing therapeutics, fusion proteins, and antigens

Leadership experience in the design and deployment of integrated walkaway automated biologic production and characterization platforms

#EligibleforERP

Required Skills:

Antibody Discovery, Assay Development, Automation, Biologics, Expression Vectors, High-Throughput Screening, Molecular Biology Techniques, People Management, Protein Expression and Purification, Structural Biology, Therapeutic Proteins

Preferred Skills:

Current Employees apply HERE

Current Contingent Workers apply HERE

US and Puerto Rico Residents Only:

Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Please click here if you need an accommodation during the application or hiring process.

As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics.  As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities.  For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit:

EEOC Know Your Rights

EEOC GINA Supplement​

We are proud to be a company that embraces the value of bringing together, talented, and committed people with diverse experiences, perspectives, skills and backgrounds. The fastest way to breakthrough innovation is when people with diverse ideas, broad experiences, backgrounds, and skills come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively.

Learn more about your rights, including under California, Colorado and other US State Acts

The primary location for this posting is:

USA - Massachusetts - Boston (MA Parcel B Laboratory)

Where required by law, the compensation range for this role is provided below.

The salary range for the primary location of this role is:

$194,100.00 - $305,600.00

This range reflects the Company's reasonable expectation of the base salary applicable to this role at the time of posting. An employee’s position within the salary range will be based on several factors including, but not limited to relevant education, qualifications, certifications, experience, skills, geographic location, government requirements, and business or organizational needs. The successful candidate will be eligible for annual bonus and long-term incentive, if applicable.

We offer a comprehensive package of benefits. Available benefits include medical, dental, vision healthcare and other insurance benefits (for employee and family), retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days. More information about benefits is available at https://jobs.merck.com/us/en/compensation-and-benefits .

Additional location(s): Please note the salary range above applies to the Primary Location of the position. Where a role has other listed locations, different compensation guidelines may apply. You may find the salary ranges for additional locations below. If the salary range is not listed for the location you are applying to, our Talent Acquisition team will provide further information to you relevant to your location.

Additional location(s) Compensation Information:

San Francisco Residents Only:  We will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance

Los Angeles Residents Only:  We will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles’ Fair Chance Initiative for Hiring Ordinance

Search Firm Representatives Please Read Carefully 

Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company.  No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.

Employee Status:

Regular

Relocation:

Domestic/International

VISA Sponsorship:

Yes

Travel Requirements:

10%

Flexible Work Arrangements:

Not Applicable

Shift:

Not Indicated

Valid Driving License:

No

Hazardous Material(s):

OEB4

Job Posting End Date:

12/4/2026 *A job posting is effective until 11:59:59PM on the day BEFORE  the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.

Requisition ID:R423992

Job details

Seniority
Principal
Function
Manufacturing & CMC
Therapeutic area
Not listed
Location
Boston, Massachusetts, United States of America
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 634 comparable Principal Manufacturing & CMC roles across 88 biopharma companies.

634Comparable roles tracked
588Currently active
88Companies hiring similar roles
29Countries represented

Salary context

229 of 634 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 $150,000)

Where these roles are based

Top locations among the 634 comparable roles

United States413
India45
Ireland30
Netherlands16
Germany15
China13

+ 23 more countries

Seniority mix

634 of 634 peers have a known seniority level

Senior403
Principal125
Director106

Therapeutic area mix

6 of 634 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Vaccines & Infectious Disease3
Dermatology & Aesthetics1
Respiratory1
Oncology1

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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.

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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.