Validation Engineer

job
  • Sterling Engineering
Job Summary
Location
Buffalo Grove ,IL
Job Type
Contract
Visa
Any Valid Visa
Salary
PayRate
Qualification
BCA
Experience
2Years - 10Years
Posted
15 Nov 2024
Share
Job Description

Overview:

As a Quality Validation Engineer, you'll play a pivotal role in ensuring the highest quality standards in the manufacturing of medical devices. Join a world-renowned company at the forefront of drug delivery solutions, and be part of a team that is revolutionizing the pharmaceutical and biotechnology industries.


Job Responsibilities:

  • Spearhead the planning, coordination, and execution of validation projects, ensuring seamless development and production of products that meet customer and internal quality objectives.
  • Collaborate with cross-functional teams to investigate and resolve customer complaints, leveraging your problem-solving skills and industry expertise.
  • Evaluate and manage supplier performance, fostering strong partnerships and ensuring mutual understanding of specified requirements.
  • Coordinate and lead the execution of validations, change control activities, and the creation of comprehensive written protocols.
  • Conduct supplier quality evaluations, audits, and implement quality agreements to maintain compliance and foster continuous improvement.
  • Analyze statistical data and develop product specifications, ensuring accuracy and adherence to industry standards.
  • Promote and organize training activities for internal departments, fostering a culture of quality and continuous learning.
  • Collaborate with customers to ensure mutual understanding of requirements and objectives, ensuring their satisfaction.
  • Support and maintain compliance with ISO and FDA QSR quality systems, as well as company policies and initiatives.
  • Identify and execute continuous improvement projects, leveraging Six Sigma tools and methodologies.

Requirements:

  • Bachelor's degree in Engineering, Science, or a related field.
  • 3+ years of experience in a Quality position, preferably in the Medical Device industry (ISO 13485).
  • Proven expertise in technical writing, IQ/OQ/PQ, and equipment validation.
  • Excellent communication skills, with the ability to understand, read, write, and speak English fluently.
  • Proficiency in advanced mathematical concepts and intermediate statistical (SPC) knowledge.
  • Six Sigma experience, training, or certification is preferred. SAP experience is an added advantage.
  • Ability to travel up to 25% domestically and internationally.


Salary: Negotiable, based on experience

Other Smiliar Jobs
 
  • Landisville, PA
  • 3 Hours ago
  • Park Ridge, IL
  • 1 Days ago
  • Itasca, IL
  • 1 Days ago
  • West Chicago, IL
  • 1 Days ago
  • El Dorado, KS
  • 21 Hours ago
  • Crystal Lake, IL
  • 21 Hours ago
  • University Park, IL
  • 21 Hours ago
  • Naperville, IL
  • 21 Hours ago
  • Chicago, IL
  • 21 Hours ago
  • Downers Grove, IL
  • 21 Hours ago
  • Garland, TX
  • 21 Hours ago
  • Hoffman Estates, IL
  • 21 Hours ago
  • Cincinnati, OH
  • 21 Hours ago
  • Mayfield, KY
  • 21 Hours ago