Pharma Process Scientist/Engineer (Scale-Up)

Merck & Co.

Rahway (NJ)

Hybrid

USD 87,000 - 137,000

Full time

3 days ago
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Benefits offered by this job

Medical, dental, vision benefits
401(k) retirement benefits
Paid holidays
Vacation
Sick days

Job summary

Merck & Co. in Rahway, NJ (and West Point, PA) seeks a Scientist/Engineer for Pharmaceutical Commercialization Technology to drive process development and technology transfer for small molecule solid dosage products. You will work with multi-disciplinary teams across PD, QA, regulatory, and manufacturing to scale from pilot to commercial.

Hybrid work arrangement. The role emphasizes hands-on development, DOE, QbD, data analytics, and collaboration to deliver medicines worldwide.

Qualifications

  • Bachelor's degree with 2 years related experience or Master's with 1 year related experience in Chemical/Biochemical Engineering, Materials Science/Engineering, Pharmaceutical Sciences, or related discipline.
  • Experience with QA, regulatory, and manufacturing interfaces is a plus.
  • Strong communication and collaboration skills are essential.

Responsibilities

  • Plan, conduct, and interpret pharmaceutical process development studies with manager and team support.
  • Participate in drug product working groups and cross-functional interactions.
  • Apply Quality by Design and risk-based approaches to development and design of experiments.

Skills

Strong communication
Team collaboration
Problem solving
DOE concepts
Quality by Design
Data analytics

Education

Bachelor's degree in Chemical/ Biochemical Engineering
Master's degree in Chemical/ Biochemical Engineering

Tools

Process scale-up experience
Technology transfer
cGMP familiarity
Process modeling

Job description

Merck & Co. in Rahway, NJ (and West Point, PA) seeks a Scientist/Engineer for Pharmaceutical Commercialization Technology to drive process development and technology transfer for small molecule solid dosage products. You will work with multi-disciplinary teams across PD, QA, regulatory, and manufacturing to scale from pilot to commercial.

Hybrid work arrangement. The role emphasizes hands-on development, DOE, QbD, data analytics, and collaboration to deliver medicines worldwide.

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