Senior Process Engineer - Small Molecule/Oligo/Peptide

CRB

Atlanta (GA)

Hybrid

USD 120,000 - 180,000

Full time

4 days ago
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Job summary

CRB seeks a Senior Process Engineer with deep expertise in small molecule manufacturing to join its engineering consulting team. This role supports process design, scale-up, optimization, and regulatory alignment across pharmaceutical projects.

You will lead scope with projects, mentor staff, and coordinate with cross-functional teams, ensuring compliance with cGMP, FDA, EMA, and ICH guidelines, while communicating with clients and internal teams.

Qualifications

  • Bachelor's or Master's in Chemical Engineering (ABET-accredited).
  • 5+ years in small molecule process engineering, consulting or client-facing.
  • Strong knowledge of synthesis, purification, and formulation processes.
  • Experience with design firm or operating company settings.
  • Excellent written and verbal communication.
  • Familiarity with cGMP and regulatory guidance.

Responsibilities

  • Lead design and execution of small molecule API process development and scale-up.
  • Perform site assessments, gap analyses and recommend improvements.
  • Develop PFDs, P&IDs, and mass/energy balances.
  • Translate client requirements into actionable design scope and document decisions.
  • Mentor junior engineers and coordinate with cross-functional teams.
  • Prepare technical reports, proposals, and presentations.
  • Support capital project planning and regulatory alignment.

Skills

Chemical Engineering
Regulatory knowledge
Client-facing

Education

ABET-accredited Chemical Engineering degree

Tools

PFDs & P&IDs
Mass/energy balances
Process simulation

Job description

CRB seeks a Senior Process Engineer with deep expertise in small molecule manufacturing to join its engineering consulting team. This role supports process design, scale-up, optimization, and regulatory alignment across pharmaceutical projects.

You will lead scope with projects, mentor staff, and coordinate with cross-functional teams, ensuring compliance with cGMP, FDA, EMA, and ICH guidelines, while communicating with clients and internal teams.

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