Sr. Specialist, Engineering (onsite)

Merck Merck · Pharma · NJ

This role is for a Manufacturing Engineering Lead at Merck, supporting specialty dosage forms and oral solid dosage (OSD) GMP development activities. The lead will be responsible for technical decisions during their shift, ensuring safety, quality, and equipment performance. Key responsibilities include evaluating production status, troubleshooting equipment, authoring GMP documentation, and leading improvement initiatives. The role requires a Bachelor's degree in Engineering or Science with at least 5 years of GMP manufacturing experience.

What you'd actually do

  1. Own technical decisions for the shift and act as the primary production engineering point of contact for Non‑Sterile operations.
  2. Evaluate safety, quality, and equipment status; make real‑time technical determinations on next steps, including stop‑work when risk warrants; escalate and document per cGMP expectations.
  3. Serve as owner and trainer for key equipment with emphasis on specialty setups (e.g., spray drying, autoinjector assembly, potent‑processing isolators).
  4. Lead room readiness and equipment readiness: plan/execute room setup; equipment assembly/disassembly; cleaning; line clearance; changeover.
  5. Author, execute, and close GMP documentation (batch records, logs, investigations, CAPA, change controls); ensure data integrity in MES (e.g., PAS‑X) and ALCOA principles.

Skills

Required

  • Bachelor’s degree in Engineering or Science (e.g., Mechanical, Chemical, Biomedical) or equivalent GMP manufacturing experience.
  • 5+ years in GMP clinical or commercial manufacturing (OSD or specialty dosage forms) with hands‑on equipment setup, cleaning, and troubleshooting.
  • Demonstrated knowledge of cGMP, data integrity, batch documentation, investigations, and CAPA.
  • Experience with OCT, FCT and encapsulation manufacturing; spray dryers, autoinjector assemblies, isolators (OEB4/OEB5), or comparable specialty equipment.
  • Strong problem solving and root‑cause analysis skills; ability to lead and train operators/technicians on the floor.
  • Ability to work second shift on‑site in classified GMP suites.

Nice to have

  • MES experience (e.g., PAS‑X) and proficiency with electronic logbooks and quality systems.
  • Exposure to potent compound handling and containment strategies; respirator/gowning certification a plus.
  • Lean/Six Sigma certification or practical application; familiarity with TPM/RCM and basic reliability tools.
  • Working knowledge of EHS risk assessment (JSA/WRAs) and equipment qualification/validation basics.