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Associate Engineer II

1 month ago

Somerset, United States JCSI Full time

Job Title: Associate Engineer II

Location: Somerset, NJ (On-site)

Employment Type: Full-Time

Seniority Level: Associate

Industry: Pharmaceuticals, Manufacturing

Job Function: Engineering, Project Management


About the Company

JCSI, a recruitment consulting firm, is partnering with Lupin Pharmaceuticals to find an Associate Engineer II to join their team. Lupin Pharmaceuitcals is a global leader in the production of high-quality oral solid and liquid dosage medications. At our Somerset, NJ facility, we focus on operational excellence, safety, and continuous improvement to drive the production of essential medicines. Join a dynamic, collaborative team that values innovation, professional growth, and teamwork, and help us deliver quality products that improve lives worldwide.


Job Summary

Lupin Pharmaceuticals is seeking an Associate Engineer II to support manufacturing and packaging operations at our Somerset, NJ facility. This role is essential to improving operational efficiency, problem-solving, and leading continuous improvement initiatives. Reporting to the Operations Director, you will manage projects and ensure compliance with Good Manufacturing Practices (cGMP) standards, making a significant impact on pharmaceutical production processes.


Key Responsibilities

  • Equipment & Process Expertise: Act as the technical expert in manufacturing and packaging, enhancing equipment performance and process efficiency.
  • Documentation Management: Develop and maintain SOPs, change controls, and qualification protocols.
  • Root Cause Investigations: Lead investigations into process deviations and customer complaints, implementing corrective actions through root cause analysis.
  • Continuous Improvement: Drive lean manufacturing efforts to reduce errors, eliminate waste, and improve safety and product quality.
  • Project Leadership: Oversee capital investment projects, managing scope, timelines, and cross-functional collaboration.
  • Safety & Compliance: Ensure a safe working environment and compliance with cGMP standards.
  • Cross-Functional Collaboration: Work with finance, procurement, quality assurance, and technical teams to achieve project goals.


Qualifications

  • Required:
  • Bachelor’s degree in Engineering (Chemical or Mechanical preferred) OR 15 years of equivalent pharmaceutical experience.
  • 2-6 years of experience in pharmaceutical manufacturing or packaging operations.
  • Proficiency in Good Manufacturing Practices (cGMP) and technical writing for SOPs and protocols.
  • Strong experience in root cause analysis, deviation investigations, and continuous improvement projects.
  • Capital project management experience.
  • Familiarity with lean manufacturing principles.
  • Preferred:
  • Experience with oral solid and liquid dosage forms.
  • Knowledge of Process Safety Management (PSM) and automation in pharmaceutical processes.
  • Hands-on experience with specific pharmaceutical equipment.


Work Hours

Monday to Friday, 8 AM to 5 PM, with occasional off-hour support as required.


Compensation & Benefits

  • Salary: $80K - $90K (commensurate with experience)
  • Annual performance-based bonus: 7.5-10%
  • Relocation assistance available for the right candidate.


Why Join Us?

Lupin Pharmaceuticals fosters a culture of innovation, teamwork, and growth. By joining our team, you’ll contribute to meaningful projects in a dynamic environment where your efforts make a direct impact on patient health and company success.


How to Apply

Interested candidates are encouraged to apply by submitting their resume. Lupin Pharmaceuticals is an equal opportunity employer, committed to creating a diverse and inclusive workplace.