Mechanical Engineer-1

PROLIM Global Corporation

Warminster, PA

JOB DETAILS
SKILLS
Analysis Skills, AutoCAD, Biotech and Pharmaceutical, Budget Management, CAD (Computer-Aided Design) Software, Communication Skills, Continuous Improvement, Cost Effectiveness Analysis, Cross-Functional, Current Good Manufacturing Practice (cGMP), Drug Manufacturing, Emerging Technology, Establish Priorities, FDA (Food and Drug Administration), Fluid Mechanics and Dynamics, ISO (International Organization for Standardization), Industry Standards, Industry/Trade Analysis, Insurance Regulations, International Health, Leadership, Maintain Compliance, Manufacturing, Mechanical Engineering, Medical Equipment, Multitasking, Performance Tuning/Optimization, Problem Solving Skills, Process Improvement, Product Programs, Product Support, Product Testing, Project/Program Management, Quality Assurance, Regulations, Regulatory Requirements, Research & Development (R&D), Simulation, SolidWorks, System Integration (SI), Team Lead/Manager, Team Player, Testing, Time Management
LOCATION
Warminster, PA
POSTED
30+ days ago

Position Overview:

We are looking for a Mechanical Engineer III to play a key role in the design, development, and optimization of our pharmaceutical equipment. The successful candidate will lead multidisciplinary teams, apply advanced engineering principles, and drive innovation to ensure the delivery of high-performance, reliable, and compliant solutions. This position offers an exciting opportunity to contribute to the advancement of pharmaceutical manufacturing technology and make a meaningful impact on global healthcare.

Responsibilities:

  • Lead the design and development of mechanical components and systems for pharmaceutical equipment, from concept to production.
  • Conduct engineering analyses, including structural, thermal, and fluid dynamics simulations, to optimize performance and ensure compliance with industry standards and regulations.
  • Collaborate with cross-functional teams, including R&D, manufacturing, quality assurance, and regulatory affairs, to ensure seamless integration of mechanical systems into final products.
  • Drive continuous improvement initiatives to enhance product reliability, manufacturability, and cost-effectiveness.
  • Provide technical expertise and guidance to junior engineers and contribute to their professional development.
  • Support product testing, validation, and troubleshooting activities, both in-house and at customer sites.
  • Stay abreast of emerging technologies, industry trends, and regulatory requirements relevant to pharmaceutical equipment design and manufacturing.

Qualification:

  • Minimum of ~8 years of experience in mechanical engineering within the pharmaceutical or medical device industry, with a focus on equipment design and development.
  • Proficiency in CAD software (e.g., SolidWorks, AutoCAD) and engineering simulation tools (e.g., ANSYS, COMSOL).
  • Strong understanding of regulatory requirements, such as FDA cGMP, ISO 13485, and ASME BPE, relevant to pharmaceutical equipment design and manufacturing.
  • Experience leading multidisciplinary engineering teams and driving projects from conception to completion.
  • Excellent problem-solving skills and the ability to apply engineering principles to develop innovative solutions.
  • Effective communication skills, with the ability to collaborate effectively with internal teams and external stakeholders.
  • Proven track record of delivering high-quality, compliant, and commercially successful products on schedule and within budget.
  • Ability to manage multiple projects simultaneously and prioritize tasks effectively.

Benefits:

  • Opportunities for professional development and career advancement within a dynamic and growing organization.
  • A collaborative and supportive work environment where your contributions are valued and recognized.

About the Company

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PROLIM Global Corporation