Specialist, Engineering (Onsite)

MSD Malaysia

Rahway (NJ)

On-site

USD 87,300 - 137,400

Full time

7 days ago
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Benefits offered by this job

Medical, dental, vision insurance
401(k) retirement plan
Paid holidays and time off

Job summary

Merck & Co. in Rahway, NJ is seeking a Non-Sterile Specialist, Engineering to provide on-site engineering support for the FLEx center on the second shift, collaborating across Research Labs and Pharmaceutical Sciences for OSD processes.

The role involves maintenance, validation support, deviation investigations, GMP documentation, and coordination of equipment installation and commissioning, with emphasis on quality and regulatory readiness.

Qualifications

  • Strong familiarity with quality, cGMP, safety, and environmental policies and procedures.
  • Familiarity with oral solid dosage drug-product manufacturing equipment and processes.
  • Experience with computerized maintenance and management systems (CMMS).
  • Strong mechanical, electrical, and automation troubleshooting ability.
  • Ability to flexibly adapt to workflow across quality and facility aspects.
  • Effective organizational, communication, and technical writing skills.
  • Strong computer skills.

Responsibilities

  • Maintain facility, utilities, and manufacturing equipment in compliance with GMP and safety requirements while applying reliability maintenance best practices.
  • Support equipment validation from commissioning through decommissioning; manage changes and periodic reviews.
  • Investigate deviations, issue quality notifications, identify root causes, and develop CAPAs.
  • Maintain GMP documentation and support clinical operations.
  • Manage purchase orders, capital requests, and coordinate installation and commissioning of new equipment.
  • Provide engineering and compliance support for non‑sterile process equipment and utilities, and act as a subject‑matter expert during regulatory interactions.
  • Operate with minimal supervision and serve as a technical and compliance resource during second‑shift operations.

Skills

GMP compliance
CMMS
Electrical troubleshooting
Mechanical troubleshooting
Automation troubleshooting
Quality processes
Communication
cGMP

Education

Bachelor’s degree in engineering

Tools

SAP Plant Maintenance
eVal/Kneat
ProCal CCMS
CMMS systems

Job description

Non-Sterile Specialist, Engineering

Position Summary: This engineer provides on‑site engineering support for the Rahway, NJ FLEx (Formulation, Laboratory & Experimentation) center, supporting non‑sterile operations within our company’s Research Labs and Pharmaceutical Sciences groups. Work is performed on the second shift, Monday through Friday. The FLEx facility supports formulation and filling activities for clinical, stability, and developmental supplies for Oral Solid Dosage (OSD) products, including process development, scale‑up, launch, transfer, and optimization for commercial products.

Responsibilities
  • Maintain facility, utilities, and manufacturing equipment in compliance with GMP and safety requirements while applying reliability maintenance best practices.
  • Support equipment validation from commissioning through decommissioning; manage changes and periodic reviews.
  • Investigate deviations, issue quality notifications, identify root causes, and develop CAPAs.
  • Maintain GMP documentation and support clinical operations.
  • Manage purchase orders, capital requests, and coordinate installation and commissioning of new equipment.
  • Provide engineering and compliance support for non‑sterile process equipment and utilities, and act as a subject‑matter expert during regulatory interactions.
  • Operate with minimal supervision and serve as a technical and compliance resource during second‑shift operations.
Qualifications
Education

Bachelor’s degree in engineering plus a minimum of 2 years of related experience supporting pharmaceutical manufacturing operations for oral solid dosage (OSD) formats.

Required Experience and Skills
  • Strong familiarity with quality, cGMP, safety, and environmental policies and procedures.
  • Familiarity with oral solid dosage drug‑product manufacturing equipment and processes.
  • Experience with computerized maintenance and management systems (CMMS).
  • Strong mechanical, electrical, and automation troubleshooting ability.
  • Ability to flexibly adapt to workflow across quality and facility aspects.
  • Effective organizational, communication, and technical writing skills.
  • Strong computer skills.
Preferred Experience and Skills
  • Maintenance and engineering techniques and management, including capital project management.
  • Independent problem‑solving capabilities.
  • Experience with SAP Plant Maintenance (gatekeeping and work‑order prioritization).
  • Experience with eVal/Kneat paperless electronic validation system.
  • Experience with ProCal as a computerized calibration maintenance system (CCMS).
  • Familiarity with planning and scheduling practices and business/financial practices.
Required Skills
  • Adaptability and biopharmaceuticals knowledge.
  • cGMP guidelines, electronic batch records, GMP compliance.
  • Laboratory experiments, mammalian cell culture.
  • Pharmaceutical biology, manufacturing, sciences, pharmacodynamics, pharmacotherapeutics.
  • Process optimization, product formulation, SOP writing.
Compensation

Salary range: $87,300.00 – $137,400.00. Eligible for annual bonus and long‑term incentive, if applicable.

Benefits
  • Medical, dental, and vision healthcare and other insurance benefits for employee and family.
  • Retirement benefits, including 401(k).
  • Paid holidays, vacation, compassionate leave, and sick days.
EEO Statement

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.

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