Senior C&Q Engineer

Posted 10 Days Ago
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Juncos, PRI
In-Office
Senior level
Pharmaceutical
The Role
The Senior C&Q Engineer develops and implements Commissioning & Qualification strategies, oversees commissioning activities, ensures compliance with regulatory standards, and provides technical guidance.
Summary Generated by Built In

 For C&Q services in the Engineering area.

WHAT MAKES YOU A FIT: 

The Technical Part:

  • Bachelor's Degree in Engineering with four (4) years of Assembly and Packaging Process experience.
  • Bilingual (English & Spanish).
  • Project Management skills.
  • Shift: Administrative and according to business needs.00
  • Experience in:
    • C&Q Strategy & Planning
    • Commissioning Activities
    • Qualification Execution (IQ/OQ/PQ)
    • Documentation & Compliance
    • Cross-functional Coordination

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

  • Develop and implement the overall Commissioning & Qualification strategy aligned with project and regulatory requirements.
  • Develop C&Q plans, schedules, and resource forecasting.
  • Oversee and/or execute commissioning activities including FAT, SAT, and field commissioning.
  • Ensure systems are installed and operate per design specifications.
  • Coordinate with vendors and contractors during startup activities.
  • Review and approve commissioning documentation and test results
  • Author, review, and approve qualification protocols (IQ, OQ, PQ).
  • Ensure traceability from User Requirements Specifications (URS) through testing.
  • Execute or oversee protocol execution and ensure proper documentation of results
  • Ensure all C&Q documentation complies with GMP, FDA, EMA, and internal Amgen standards.
  • Maintain document lifecycle within electronic systems.
  • Support data integrity and ALCOA+ principles throughout qualification activities.
  • Prepare and support validation summary reports.
  • Lead and document risk assessments related to system qualification.
  • Evaluate and manage change controls impacting validated systems.
  • Assess impact of deviations and implement corrective and preventive actions (CAPA)
  • Develop the characterization protocols.
  • Execute the characterization activities.
  • Develop and review the characterization reports.
  • Collaborate with Engineering, Validation, Quality Assurance (QA), Manufacturing, and Supply Chain teams.
  • Interface with system owners and technical authorities.
  • Provide technical guidance and mentorship to junior engineers and project team members.
  •  Support project meetings, status reporting, and stakeholder communication.

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
  • Four years of Assembly and Packaging Process experience
  • Bilingual (English & Spanish)
  • Experience in C&Q Strategy & Planning, Commissioning Activities, Qualification Execution (IQ/OQ/PQ)
  • Project Management skills
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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