← All live jobs

Merck

Senior Scientist, Small Molecule Chemical Engineering

Location
Rahway, NJ (NJ)
Posted
Posted today (employer shows the date only)
Source
Workday (employer's applicant tracking system)
Category
R&D/Science
Industry
Pharma/Biotech
Apply on employer site

Application: Workday — account required, long form — you fill it in on the employer's site.

UNTIL never charges to apply and never asks for payment or personal info on behalf of employers.

Apply kitYour saved details, ready to copy

From the employer's posting

Job Description

We are seeking a self-motivated individual to join our Chemical Commercialization Technology (CCT) department, part of our manufacturing division. This is an exciting opportunity to work in a highly collaborative environment with substantial technical responsibility and leadership of internal and external work. If you are passionate about developing safe and robust manufacturing processes and thrive in a dynamic setting, we invite you to apply.

The Senior Scientist, Engineering position leverages scientific/technical experience to develop safe and robust manufacturing processes through process characterization, technology transfer, validation, filing and supply support of late-stage projects in the small molecule pipeline.

The candidate will provide scientific expertise by learning and utilizing Quality Risk Management methodologies and tools for statistical design of experiments. This role involves hands-on experimentation at the laboratory bench and kilo lab scales in addition to technology transfer to commercial manufacturing facilities. The scientist will be expected to exhibit a mindset of safety and quality compliance, which will include following current Good Manufacturing Practices (cGMPs), and participating in risk assessments, deviation investigations, and Good Documentation Practices (GDPs).

Responsibilities

  • Develop safe and robust manufacturing processes through process characterization, technology transfer, validation, filing, and supply support of late-stage projects in the small molecule pipeline.
  • Provide scientific expertise by learning and utilizing Quality Risk Management methodologies and tools for statistical design of experiments.
  • Conduct hands-on experimentation at the laboratory bench and kilo lab scales.
  • Transfer technology to commercial manufacturing facilities.
  • Exhibit a mindset of safety and quality compliance, including following current Good Manufacturing Practices (cGMPs).
  • Participate in risk assessments, deviation investigations, and Good Documentation Practices (GDPs).

Qualifications

Required

  • Bachelor of Science (BS)/Master of Science (MS) in Chemical Engineering with a minimum of five (5) years of required work experience. PhD in Chemical Engineering from an accredited college/university with no industry experience required.
  • Relevant work experience in chemical process development.
  • Demonstrated capability to develop and execute an experimental program to address issues of process design, robustness, and productivity.
  • Highly effective communication and collaboration skills.
  • Good organizational, interpersonal, writing, and time management skills.
  • Ability to operate within a cross-functional process development team.

Preferred

  • Experience performing lab-based research/process development, including performing unit operations common in small molecule drug substance process development such as chemical reactions, work-up, and crystallization.
  • Experience leading regulatory file authoring, validation planning, and execution.
  • Experience guiding internal/external technical discussions.
  • Familiarity with statistical design and analysis tools.
  • Experience with process scale-up and technology transfer, moving from laboratory to pilot plant or factory.
  • Familiarity with concepts and application of current Good Manufacturing Practices (cGMPs) ideally during pharmaceutical drug substance/drug product development and production.
  • Experience with mathematical modeling, theoretical scaling calculations, and Quality by Design principles.

WE2026

Required Skills:

Bioreactors, cGMP Regulations, Chemical Processes, Chromatographic Techniques, Computational Design, Design of Experiments (DOE), Good Manufacturing Practices (GMP), Pharmaceutical Manufacturing, Pharmaceutics, Process Development (PD), Process Development Engineering, Process Optimization, Process Scale Up, Small Molecule Drug Development, Small Molecule Synthesis, Teamwork, 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​

…

Similar live roles