Sr. Supplier Quality Engineer

Posted 6 Days Ago
Be an Early Applicant
Juncos, PRI
In-Office
Senior level
Pharmaceutical
The Role
Supports supplier and distribution quality for medical device manufacturing. Responsibilities include establishing approved supplier lists, negotiating quality agreements, qualifying and auditing suppliers, monitoring performance, managing supplier CAPA issues, validating receiving inspection methods, and supporting new product development. The role drives supplier quality improvement, regulatory compliance, sampling strategies, control plans, and supplier qualification while collaborating with engineering and distribution teams. Travel to contract manufacturers and suppliers is required.
Summary Generated by Built In

For Supplier Quality services in the Manufacturing/Engineering area.

WHAT MAKES YOU A FIT: 

The Technical Part:

  • Bachelor's degree in Engineering and a minimum of four (4) years of relevant experience, or an advanced degree with a minimum of two (2) years of relevant experience within the medical devices industry. 
  • Bilingual (English & Spanish).
  • Work Type: Hybrid
  • Shift: Administrative and according to business needs
  • Experience in:
    • Distribution Centers and 3PL's suppliers 
    • Leading Projects
    • SAP, Agile and Trackwise desired.

The Personality Part:    

  • If you have excellent communication skills and aren’t afraid to ask for help when you need it (in addition to your excellent Maintenance skills), this might be the job for you! Sprinkle on a love of the scientific method, teamwork, and, above all else, being ethical, and you just might have what it takes to take on this new challenge. Bring it on!

AS A PIECE OF FITS, YOU WILL: (The day-to-day on the job)

  • Support the Supplier and Distribution Quality organization in identifying and establishing the Approved Supplier List (ASL) for Distributors and 3PLs, negotiating Quality Agreements, monitoring supplier performance, developing and executing audit schedules, and supporting supplier validation and qualification activities.
  • Qualify suppliers according to company standards and may administer a Certified Supplier Program within Receiving Inspection to ensure cost-effectiveness.
  • Monitor parts, materials, and services from acquisition through the manufacturing cycle and communicate and resolve supplier-related problems through the Supplier CAPA process.
  • Develop and prioritize supplier audit schedules to ensure designated suppliers are audited regularly and comply with Good Manufacturing Practices (GMP) and applicable quality standards.
  • Evaluate suppliers’ internal functions and overall performance, providing feedback and recommendations regarding their operations.
  • Provide Pre-Market Supplier Quality Engineering support for New Product Development (NPD), working in partnership with Component Engineering, Post-Market Supplier Quality, and Distribution teams to prevent defects and ensure the quality and reliability of parts, materials, and services.
  • Collaborate with Distribution in the selection of new Distributors and 3PLs.
  • Define Receiving Inspection requirements as required, including associated test method validation.
  • Provide technical guidance and ensure quality compliance throughout the Supplier Quality engagement across the NPD lifecycle for newly qualified parts.
  • Implement strategies to drive product quality and continuous improvement, ensuring purchased products and components are manufactured and qualified in accordance with applicable industry standards, regulatory requirements, and customer requirements.
  • Collaborate with Component Engineers to develop and deliver the Product Acceptance Sampling Strategy, Approved Supplier List coordination, Supplier Owned Quality deployment, and Control Plans for new products.
  • Availability to travel to visit external Contract Manufacturers and Suppliers.

WHO WE ARE:

We are a Service Provider company different from the rest. We pride ourselves in how we treat the most important piece of our company's puzzle: you! We integrate Engineering, Construction, Maintenance, Utilities and Specialized Technical services across the Island (and in the US as well!). Our company is flexible, family-oriented and focused on our resources' well-being, while providing our Pharmaceutical, Medical Device and Manufacturing industry clients with top-notch quality talent. We're FITS! 

Are you the next piece?

Skills Required

  • Bachelor's degree in Engineering and at least four years of relevant medical device industry experience
  • Advanced degree and at least two years of relevant medical device industry experience
  • Bilingual English and Spanish communication skills
  • Experience with distribution centers and third-party logistics suppliers
  • Experience leading projects
  • Experience with SAP
  • Experience with Agile
  • Experience with TrackWise
  • Availability to travel to external contract manufacturers and suppliers
Am I A Good Fit?
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The Company
HQ: Guaynabo, PR
76 Employees
Year Founded: 2008

What We Do

We are a Service Provider company different from the rest. We pride ourselves in how we treat the most important piece of our company's puzzle: you! We integrate Engineering, Construction, Maintenance, Utilities and Specialized Technical services across the Island (and in the US as well!). Our company is flexible, family-oriented and focused on our resources' well-being, while providing our Pharmaceutical, Medical Device and Manufacturing industry clients with top-notch quality talent. We're FITS! Are We The Right Piece For You? We are: Experienced and knowledgeable in the Industry Committed to Safety Always compliant with FDA Regulations & Audits Cost Effective Proven successful track record Over ten (10) years of experience If you'd like to apply to any of our open positions, send us your updated resume in Word or PDF Format to [email protected]

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