Merck & Co.
Principal Scientist, Upstream Process Development Group Lead
USA - New Jersey - Rahway
Get past the screening software and onto a recruiter's desk
hirly rewrites your resume for this job — matching the keywords and skills in the posting, moving your most relevant experience to the top, and writing a cover letter to fit. About 30 seconds.
- Keywords matched to this posting
- Fit score before you apply
- Cover letter included
Matched against 2.6M live jobs from 190,000+ employers in 200+ countries.
Tailor my resume for this job →Apply from your AI assistant
Connect hirly to Claude and ask it to apply to this job. hirly tailors your resume, fills the employer’s form and asks before sending. ChatGPT: manual setup today.
Some employer sites stop an application at a CAPTCHA or sign-in and hand it back with a link. Applying needs a paid plan. Works with any assistant that supports MCP.
hirly's read of this role
- Seniority
- Lead / management
- Country
- US
- Work mode
- On-site / unstated
- First seen by hirly
- 3 Oct 2026
Derived automatically from the posting. Upload your resume above to see how the role scores against it.
the posting
Job Description
Job Description:
Our Scientists are our Inventors. Through innovative thinking, state-of-the-art facilities, cutting-edge science, and technology, we collaborate to deliver the next medical breakthroughs. We are looking for a collaborative, self-motivated scientific leader with expertise in downstream bioprocessing to join Biologics Process Research & Development (BPR&D) as a Senior Principal Scientist.
As a Senior Principal Scientist/Principal Scientist, you will drive various strategic initiatives and translate strategies into implementation for our Company biologics platform. You will collaborate with an immensely creative and collaborative team of scientists and engineers to design upstream, cell-culture processes while developing technical strategies related to upstream processing and recombinant expression of drug candidates in early- and late-stage development.
Responsibilities include, but are not limited to:
Serve as a scientific leader to shape and drive innovation across the Biologics pipeline, strategy, and science.
Anticipate and solve scientific and technical challenges across projects and functional teams, in a fast-paced, multidisciplinary environment.
Lead the development of robust and scalable upstream processes for biologics in various stages of clinical development, as well as process characterization and regulatory filings for successful commercialization.
Improve upstream processes by increasing efficiency and cost-effectiveness through research and innovation, while evaluating technologies and industry best practices.
Collaborate with academia, industry, and vendors to facilitate the development and early adoption of novel process technologies.
Contribute to strategic initiatives; work with senior leaders to establish overall project strategy and guide teams in its execution.
Conceptualize, plan, and execute projects using effective organizational, prioritization, and problem-solving skills.
Stay updated on the scientific and regulatory landscape; contribute scientifically and build your reputation through conference participation.
Represent BPR&D as a upstream bioprocess expert/co-leader in internal and cross-functional project teams.
Direct supervision of 3-5 scientists, accountable for development and growth of a cohesive group and direct reports
Mentor and actively share expertise across teams; guide career development within and outside the group; build strong, collaborative connections in matrix teams
Minimum Education Requirements:
Ph.D. with 10+ years, MS with 12+ years, or BS with 14+ and Ph.D. with 6+ years, MS with 8+ years, or BS with 10+ years of industry experience in Chemical/Biochemical Engineering or a related field for Senior Principal Scientist position and Principal Scientist position, respectively.
Required Experience, Skills, and Competencies :
Strong fundamental knowledge and subject matter expertise in cell-culture process development for biologics, fed-batch cell culture, bioreactor scale-up and scale-down, as well as recent advances, and challenges in the field
Expertise in independently conducting and directing the design, execution, analysis, and documentation of all stages of cell-culture process development
Track record of accomplishments in upstream bioprocessing with a history of peer-reviewed publications and presentations. Strong understanding of cell metabolism and biochemical pathways relevant to bioprocessing.
Knowledge of biologics CMC development.
Ability to adapt to and prioritize complex objectives under tight timelines in a rapidly changing environment.
Experience leading internal and external cross-functional, matrixed teams.
Demonstrated scientific leadership with significant, measurable project impacts across a set of programs.
Action-oriented mindset with a capacity for creativity; ability to take initiative, innovate, iterate, and solve problems.
Supervise, coach and mentor scientists to maximize talent development and utilization.
Excellent interpersonal and communication skills.
Preferred Experience & Skills:
Leadership of CMC development teams.
Experience with continuous biomanufacturing integrated with process-analytical technologies.
Knowhow of intensified inoculum and perfusion process development.
Expertise in media/feed development and relevant chemistry.
High-throughput experimentation, automation, and process control.
Knowledge of microbial fermentation.
Cell culture predictive modeling (omics (transcriptomics, metabolomics, or/and proteomics), metabolic flux analysis); statistics, data-science, machine learning, artificial intelligence.
Process characterization and validation, CDMO supervision, commercialization of biologics.
Required Skills:
Biologics, Bioprocess Engineering, Bioreactors, Cell Culture Process Development, Cell Culture Techniques, Cell Line Development, Chemistry, Combination Products, Commercialization, Downstream Processing, Finite Element Analysis (FEA), Matrix Management, Pharmaceutical Process Development, Process Development (PD), Process Implementations, Quality by Design, Regulatory Filings, Scientific Presentations, Technical Evaluation, Technology Development, Technology Transfer
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 salary range for this role is
$173,200.00 - $272,600.00
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.
San Francisco Residents Only: We will consi
Listed on hirly, a job board. hirly is not the employer: Merck & Co. is hiring for this role.
Similar jobs
- Principal Data Scientist (Credit Risk for Small Business and Commercial)Navy Federal Credit Union · Vienna, VA, United StatesFirst seen today
- Principal Scientist – Analytics Team LeadNovartis · Cambridge (USA)First seen today
- Principal Scientist – Analytics Team LeadNovartis · Cambridge (USA)First seen today
- Staff Scientist - AnesthesiologyWustl · Washington University Medical CampusFirst seen yesterday
- Staff Scientist - Radiation OncologyWustl · Washington University Medical CampusFirst seen yesterday
Browse similar roles
Want this one?
Upload your resume and hirly rewrites it for this job and writes the cover letter — in about thirty seconds, before you sign up.
Tailor my resume for this job