Senior Mechanical Engineer II in Gaithersburg

Energy Jobline ZR

Gaithersburg (MD)

On-site

USD 115,000 - 140,000

Full time

14 days+
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Benefits offered by this job

Health benefits
Retirement savings
Paid time off
Professional development
Bonus eligibility

Job summary

Energy Jobline ZR is seeking a Senior Mechanical Engineer II in Gaithersburg, MD to lead the design of GMP manufacturing systems and sterile consumables. You will create SolidWorks models, perform tolerance and FEA analyses, and drive validation activities across cross-functional teams.

The role requires 8+ years of mechanical design experience in regulated environments, with hands-on work on sterile single-use systems and bioprocessing technologies.

Qualifications

  • BS in Mechanical Engineering; MS preferred
  • 8+ years of mechanical design experience in regulated environments
  • Experience in medical device, bioprocessing, pharma, or regulated industries
  • Hands-on experience with sterile single-use systems or fluid assemblies
  • Strong knowledge of fluid systems, pumps, valves, manifolds, and flow paths
  • Experience with sealing interfaces, tolerance analysis, and complex mechanical systems
  • Proficient in SolidWorks; PDM experience
  • Familiarity with DFx, manufacturability, reliability, and cost optimization
  • Experience with bioprocessing systems such as bioreactors or filtration technologies
  • FEA experience; COMSOL is a plus
  • Knowledge of GMP environments and cleanroom-compatible design
  • Familiarity with ISO 13485, ISO 9001, ISO 10993, ISO 14971, and design controls
  • Experience with validation, testing, and engineering documentation
  • Prototyping and fabrication experience (CNC, molding, 3D printing)
  • Strong communication, collaboration, and problem-solving skills
  • Ability to travel domestically up to 10–15%

Responsibilities

  • Lead mechanical design and development for GMP manufacturing systems and consumables
  • Create CAD models, drawings, BOMs, and ECOs in SolidWorks
  • Perform tolerance analysis, FEA, and root cause investigations
  • Support prototyping, testing, and design verification activities
  • Design sterile single-use bioprocessing and fluid handling systems
  • Develop and execute validation and testing protocols
  • Support design transfer and DHF documentation
  • Collaborate with engineering, manufacturing, quality, and suppliers
  • Mentor junior engineers and provide technical guidance
  • Ensure compliance with GMP, regulatory, and engineering standards
  • Develop SOPs and engineering documentation

Skills

SolidWorks
FEA
PDM
CAD modeling
Prototyping

Education

B.S. in Mechanical Engineering
M.S. preferred

Tools

SolidWorks
COMSOL

Job description

Job Title: Senior Mechanical Engineer II

Location: Gaithersburg, MD (Onsite)

Hours/Schedule: Monday – Friday, Standard Business Hours

Compensation: $115,000 – $140,000 + bonus eligibility

Type: Direct Hire

Overview

A growing life sciences and bioprocessing organization is seeking a Senior Mechanical Engineer II to support the design and development of advanced mechanical systems and sterile consumable technologies used in GMP manufacturing environments. This is a highly collaborative, hands-on engineering role offering exposure to innovative bioprocessing technologies, cross-functional development teams, and complex product development initiatives.

Responsibilities
  • Lead mechanical design and development for GMP manufacturing systems and consumables
  • Create CAD models, drawings, BOMs, and ECOs in SolidWorks
  • Perform tolerance analysis, FEA, and root cause investigations
  • Support prototyping, testing, and design verification activities
  • Design sterile single-use bioprocessing and fluid handling systems
  • Develop and execute validation and testing protocols
  • Support design transfer and DHF documentation
  • Collaborate with engineering, manufacturing, quality, and suppliers
  • Mentor junior engineers and provide technical guidance
  • Ensure compliance with GMP, regulatory, and engineering standards
  • Develop SOPs and engineering documentation
Requirements
  • B.S. in Mechanical Engineering required; M.S.
  • 8+ years of mechanical design experience
  • Experience in medical device, bioprocessing, pharma, or regulated industries
  • Hands-on experience with sterile single-use systems or fluid assemblies
  • Strong knowledge of fluid systems, pumps, valves, manifolds, and flow paths
  • Experience with sealing interfaces, tolerance analysis, and complex mechanical systems
  • Proficient in SolidWorks; PDM experience
  • Familiarity with DFx, manufacturability, reliability, and cost optimization
  • Experience with bioprocessing systems such as bioreactors or filtration technologies
  • FEA experience ; COMSOL is a plus
  • Knowledge of GMP environments and cleanroom-compatible design
  • Familiarity with ISO 13485, ISO 9001, ISO 10993, ISO 14971, and design controls
  • Experience with validation, testing, and engineering documentation
  • Prototyping and fabrication experience (CNC, molding, 3D printing, etc.)
  • Strong communication, collaboration, and problem-solving skills
  • Ability to travel domestically up to 10–15%
Benefits

Our client provides a comprehensive benefits package including medical, dental, and vision coverage, retirement savings options, paid time off, professional development opportunities, and bonus eligibility.

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