Job Description
Join Our Team as a Biologics Conjugation Senior Scientist!
We are seeking a strategic and technical scientist with expertise in laboratory start up and operations ideally in a development & commercialization space to support our ever growing and dynamic late-stage biologics pipeline within the expansive Biologics S&T portfolio.
Why You'll Love This Role:
As a Sr. Scientist in Biologics Conjugation Commercialization, you’ll be at the forefront of starting up new lab capabilities for conjugation. Setting up systems and processes to help the lab operate efficiently and effectively.
As the laboratory manager, you will troubleshoot and solve problems for the laboratory and operating systems, and help drive capital planning processes and asset management programs. A key deliverable of our commercialization team is to have qualified scale down models for our conjugation processes, and you will be instrumental in design and establishment of those models to support process characterization, right first time PPQ and regulatory filings. You will engage our program team members to understand their needs and continually look to improve operations by developing efficient solutions that will support business objectives and ensure continuity and Safety, and Environmental compliance.
Key Responsibilities:
Scientific Engagement: Help the Biologics Conjugation Commercialization team with scientific direction and consistent establishment of lab scale down models to be used across our portfolio.
Lab Operations Leadership: Lead daily lab operations, including scheduling, training, inventory management, tiers and operational metrics to enable efficient experimental execution and continuous improvement.
Asset Reliability and Capability Leadership: Lead capital asset startup, equipment ownership, project planning, maintenance, calibration, troubleshooting, and root cause failure analysis to ensure laboratory equipment and systems remain reliable, accurate, efficient, and ready for use.
Compliance, Safety, and Process Safety Leadership: Ensure laboratory activities, systems, and equipment are maintained in compliance with safety, environmental, quality, regulatory, and Process Safety Management requirements, including appropriate controls for work involving potent compounds.
Cross-Functional Collaboration: Unite diverse teams to achieve program goals as One Team. Champion compliance and safety; promote a culture of diversity, inclusion, and equity. Experience and aptitude to work, and collaborate in internal and external cross-functional, matrixed teams.
Project Management: Adaptability and agility to prioritize and deliver complex objectives, often on tight timelines, in a rapidly changing environment.
Recognition: Celebrate team achievements and foster a culture of appreciation.
Innovation: Lead business improvement initiatives and leverage your network to drive change.
Education & Experience:
Bachelor's degree in Chemical Engineering, Bioengineering, Biological Engineering, or a related field with six (6) years of relevant industry experience. OR
Master's degree in Chemical Engineering, Bioengineering, Biological Engineering, or a related field with four (4) years of relevant industry experience. OR
Ph.D. in Chemical Engineering, Bioengineering, Biological Engineering, or a related field with a no minimum relevant knowledge.
What You Bring:
Ability to lead without authority, build trust, and inspire accountability
Ethical, resilient, and committed to excellence
Skilled in risk management, team facilitation, and strategic planning
Exceptional communication and stakeholder engagement skills
Sound judgment and issue-resolution mindset,
Ability to navigate ambiguity, remove barriers, and escalate appropriately to keep work moving.
Preferred Skills:
Laboratory start-up experience
In-depth knowledge of conjugation chemistry techniques.
Experience working in laboratories that handle potent compounds, high-containment materials, or specialized safety controls.
Experience in pilot or commercial scale manufacturing of biological molecules.
Familiarity with late-stage process development, process characterization, scale down model qualification, process validation regulatory submissions, and working with external contract organizations.
Minimum of 3 years experience troubleshooting equipment and utility systems
Minimum of 3 years experience executing/supporting Capital projects/Project Management
Understanding of or experience with Capital and Profit Planning Processe
Experience with Computerized Maintenance Management System (CMMS) software such as SAP, Procal, or Maximo
Experience in using QlikSense, Spotfire, or other data analytical software
Experience in performing root cause analysis
Required Skills:
Antibody Drug Conjugates (ADC), Bioconjugation, Bioreactors, Capital Planning, Capital Project Management, cGMP Regulations, Chemical Engineering, Chromatographic Techniques, Clinical Judgment, Conjugation Chemistry, Design of Experiments (DOE), Detail-Oriented, Good Manufacturing Practices (GMP), Influencing Without Authority, Laboratory Operations, Laboratory Setup, Leadership, Process Design, Process Optimization, Process Scale Up, Project Development, Project Management, Project Resource Management, Root Cause Investigations, Technology Transfer
Preferred Skills:
Current Employees apply HERE
Current Contingent Workers apply HERE
US and Puerto Rico Residents Only:
The salary range for this role is
$117,000.00 - $184,200.00
This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this 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.
You can apply for this role through https://jobs.merck.com/us/en (or via the Workday Jobs Hub if you are a current employee). The application deadline for this position is stated on this posting.
Employee Status:
Regular
Relocation:
Domestic
VISA Sponsorship:
Yes
Travel Requirements:
25%
Flexible Work Arrangements:
Hybrid
Shift:
1st - Day
Valid Driving License:
No
Hazardous Material(s):
n/a
Job Posting End Date:
09/30/2026
*A job posting is effective until 11:59:59PM on the day BEFOREthe listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.
