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Principal Scientific Engineering Associate Jobs

Engineering Associate Technician - 3rd Shift We're actively seeking qualified candidates for an ... Provide technical support to engineering and scientific teams * Perform technical evaluations and ...

Principal Duties and Responsibilities This information is intended to be descriptive of the key ... Bachelor of Science degree in civil engineering, construction science, or related degree from an ...

Engineering Associate

Kerrville, TX · On-site

$60 - $80/hr

Principal Duties and Responsibilities This information is intended to be descriptive of the key ... Bachelor of Science degree in civil engineering, construction science, or related degree from an ...

... associate tools commonly used in life sciences research and development a plus Basic Qualifications: Ability to effectively communicate, both verbally and through electronic media Ability to work on ...

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Principal Scientific Engineering Associate information

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$36.5K

$109.4K

$182K

How much do principal scientific engineering associate jobs pay per year?

As of Sep 9, 2026, the average yearly pay for principal scientific engineering associate in the United States is $109,393.00, according to ZipRecruiter salary data. Most workers in this role earn between $85,000.00 and $125,000.00 per year, depending on experience, location, and employer.

What is a principal scientific engineering associate?

A Principal Scientific Engineering Associate is a senior-level professional who supports scientific research and engineering projects, often within research institutions or laboratories. They typically design experiments, develop technical solutions, and oversee complex instrumentation or systems. This role involves significant responsibility in planning, executing, and managing scientific programs, as well as mentoring junior staff. Principal Scientific Engineering Associates bridge the gap between scientists and engineers, ensuring research objectives are met efficiently and safely.

How does a principal scientific engineering associate typically contribute to interdisciplinary research teams?

As a Principal Scientific Engineering Associate, you play a pivotal role in bridging the gap between engineering and scientific research teams. You are often responsible for designing and implementing complex experiments, managing technical projects, and collaborating with scientists, engineers, and technical staff to solve challenging research problems. Regularly, you will coordinate with team members from various disciplines to ensure that experimental setups and data analyses align with project goals. This collaborative environment fosters innovation and provides opportunities to mentor junior staff and contribute to strategic decision-making for research initiatives.

What are the key skills and qualifications needed to thrive as a principal scientific engineering associate, and why are they important?

To thrive as a Principal Scientific Engineering Associate, you need advanced scientific knowledge, strong analytical abilities, and a relevant degree (often a master's or Ph.D.) in engineering, physics, or a related field. Familiarity with laboratory instrumentation, data analysis software, and project management tools is commonly required, along with experience in experimental design and implementation. Leadership, problem-solving, and effective communication are vital soft skills for collaborating across multidisciplinary teams and guiding complex projects. These abilities enable successful research outcomes, innovation, and the management of sophisticated scientific initiatives.

What are popular job titles related to Principal Scientific Engineering Associate jobs?

For Principal Scientific Engineering Associate jobs, the most frequently searched job titles are:

Associate Principal Scientist, Small Molecule Chemical Engineering

Rahway, NJ • On-site

Merck & Co.
Pharmaceutical Product Wholesalers • 10K+ employees

$150 - $200/hr

Other

Medical, Dental, Vision, Retirement, PTO

Posted 13 days ago


Merck rating

8.0

Company rating: 8.0 out of 10

Based on 51 frontline employees who took The Breakroom Quiz

43rd of 86 rated pharmaceutical


Job description

Job Description Associate Principal Scientist, Engineering Chemical Commercialization Technology (CCT)

The Chemical Commercialization Technology (CCT) department, part of our Manufacturing Division, is seeking a highly motivated and collaborative scientist to join our team. This position offers the opportunity to provide technical leadership across a varied portfolio of late-stage small molecule development programs while working in a highly integrated environment with research, manufacturing, quality, regulatory and external partners.

The Associate Principal Scientist, Engineering, will leverage deep scientific and engineering knowledge to develop safe, robust, scalable, and commercially viable manufacturing processes. The role encompasses process characterization, technology transfer, process validation, regulatory filing support, commercial launch readiness and global supply support for late-stage pipeline and commercial products.

The successful candidate will lead teams in the application of scientific and risk-based approaches to process understanding and control strategy development. This includes the use of Quality Risk Management (QRM), statistical design of experiments (DOE), process modeling, and data analytics to enhance process robustness and ensure reliable product supply.

This position combines laboratory and pilot-scale experimental work with direct engagement at commercial manufacturing facilities. The scientist will be expected to provide strategic technical leadership during scale-up, process validation, technology transfer and manufacturing investigations while mentoring junior scientists and engineers.

The candidate must demonstrate a strong commitment to safety, quality, and compliance, including adherence to current Good Manufacturing Practices (cGMPs), Good Documentation Practices (GDPs), data integrity principles, and participation in risk assessments, deviation investigations, change control activities and continuous improvement initiatives.

Key Responsibilities
  • Lead technical development, scale-up, and commercialization of small molecule drug substance manufacturing processes.
  • Design and execute process characterization studies to establish process understanding and define commercial operating ranges.
  • Apply Quality Risk Management (QRM), Quality by Design (QbD) and statistical methodologies to develop robust control strategies.
  • Provide technical leadership for technology transfer activities to pilot plant and commercial manufacturing sites.
  • Support process validation, continued process verification, regulatory submissions and post-approval change implementation.
  • Collaborate effectively with Manufacturing, Process Research, Quality, Regulatory, Supply Chain and external partners to resolve complex technical issues.
  • Lead investigations associated with process deviations, yield improvements, impurity control and process robustness.
  • Mentor and develop junior scientists and engineers through technical coaching and project leadership.
  • Drive innovation through the application of advanced process technologies, digital tools, modeling and data analytics where appropriate.
Position Qualifications Education
  • Ph.D. in Chemical Engineering or a related scientific discipline with a minimum of 4 years of relevant industrial experience following completion of the Ph.D.

OR

  • B.S. or M.S. in Chemical Engineering or a related scientific discipline with a minimum of 8 years of relevant industrial experience.
Required Experience and Skills
  • Demonstrated expertise in chemical process development and scale-up for pharmaceutical or specialty chemical manufacturing.
  • Proven ability to independently design, execute, interpret, and communicate experimental studies aimed at improving process understanding, robustness, productivity and control strategy development.
  • Experience supporting technology transfer from laboratory development through pilot plant and commercial manufacturing.
  • Strong technical leadership and project management capabilities in cross-functional environments.
  • Ability to mentor and develop scientists and engineers through technical guidance and coaching.
  • Excellent written, verbal, and presentation communication skills.
  • Strong organizational and time-management skills with the ability to manage multiple priorities.
  • Demonstrated problem-solving capabilities using scientific and engineering principles.
  • Ability to collaborate effectively across technical, quality, regulatory and manufacturing functions.
Preferred Experience and Skills
  • Hands-on experience with unit operations commonly employed in small molecule drug substance API development and manufacturing, including chemical reactions, workup operations, filtration, drying, crystallization and particle engineering.
  • Experience leading process characterization, validation strategy development, and process performance qualification (PPQ) activities.
  • Experience authoring or contributing to regulatory submissions and responding to health authority questions.
  • Expertise in statistical experimental design and data analysis tools (e.g., JMP, Minitab, or equivalent).
  • Experience supporting commercial manufacturing, lifecycle management, and post-approval process changes.
  • Familiarity with mathematical modeling, process simulation, mechanistic understanding and scale-up principles.
  • Experience working with external manufacturing partners and contract development/manufacturing organizations (CDMOs).
  • Knowledge of cGMP requirements and pharmaceutical manufacturing operations.
  • Experience applying digital, data science, or advanced manufacturing technologies to accelerate process development and commercialization.
Required Skills

API Manufacturing, Bioprocessing, Chemical Engineering, Chemical Processes, Commercialization, Manufacturing, Manufacturing Processes, Manufacturing Scale-Up, Manufacturing Technologies, Pharmaceutical Process Development, Process Design, Process Development (PD), Small Molecule Drugs, Technology Transfer

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.

Equal Employment Opportunity

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.

Salary Range

The salary range for this role is

$142,400.00 - $224,100.00

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.

Benefits

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.

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

Employee Status

Regular

Relocation

Domestic

VISA Sponsorship

Yes

Travel Requirements

10%

Flexible Work Arrangements

Not Applicable

Shift

1st - Day

Valid Driving License

No

Hazardous Material(s)

n/a

Job Posting End Date

09/10/2026

*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

R414626

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