Validations/ Verifications Engineer

Katalyst HealthCares and Life Sciences

$90K — $120K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in a Technical or Scientific discipline
  • 5+ years of experience in the medical device industry
  • Experience in Process Verifications/Validations
  • Experience in Design/Process Failure Modes Effects and Analysis
  • Strong problem-solving and decision-making skills
  • Strong initiative and project leadership experience
  • Design Quality Engineering and Design Control experience

Responsibilities

  • Conduct Process Verifications/Validations
  • Execute Design/Process Failure Modes Effects and Analysis
  • Read and inspect blueprints using GD&T techniques
  • Manage personnel to prevent delays and ensure smooth implementation
  • Collaborate with senior leadership on long-term strategic planning
  • Perform risk management and execute product testing
  • Oversee Quality System compliance, including corrective actions and risk management

Benefits

  • Opportunities for professional growth and development
  • Collaborative work environment with a focus on innovation
  • Involvement in cutting-edge medical device projects
  • Access to advanced tools and methodologies like Six Sigma and Lean
  • Support for continuing education, especially for advanced degrees or certifications
Full Job Description
Role Descriptions:

Must Have Technical/Functional Skills

Desirable Skills:

Skills: EIS: Medical Device & Regulations ~EIS: New Product Development (NPD) Methodology and Management

Experience Required: 4-6

5+ years of work experience in medical device industry

Required:
• A bachelor's degree in Technical or Scientific discipline

• 5+ years of work experience in medical device industry
• Experience conducting Process Verifications / Validations
• Experience conducting Design and/or Process Failure Modes Effects and Analysis
• Excellent problem solving and decision-making skills
• Interpersonal skills that foster collaboration as they relate to technical situations
• Strong initiative and follow-through in executing project responsibilities, overcoming obstacles, and balancing multiple priorities effectively through strong technical and/or project leadership experience
• Design Quality Engineering experience
• Design Control experience

Preferred:
• An advanced degree
• A bachelor's degree in mechanical engineering or Bioengineering
• New Product Development experience
• Experience with Blueprint reading/literacy/inspection methods & techniques including GD&T
• Strong experience with Design Excellence, Six Sigma, or Lean
• Spanish as a second language

Roles & Responsibilities:
• Conducting Process Verifications / Validations
• Design and/or Process Failure Modes Effects and Analysis
• Blueprint reading/literacy/inspection methods & techniques including GD&T
• People Management: ability to ensure small delays don't derail critical items and work with embedded team on site to ensure smooth implementation.
• Strategic Mindset: ability to think bigger picture and work with Senior leadership on long term strategy for area/site.
• Performing risk management, execute product testing
• Work on Quality System, including, but not limited to corrective & preventive actions, nonconforming materials, risk management, and medical device regulations

Generic Managerial Skills, If any:
• Required to have good communication skills both written & verbal and be computer literate (Word, Excel, outlook Email - a must).
• Strong interpersonal, organizational, written and oral communication skills
• Dependable, somewhat assertive, reasonably organized, resourceful and communicative with an ability to adapt and learn quickly as well as follow verbal and written instruction, detail oriented.

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