Quality Project Coordinator at Smart Precise Solutions Inc
Guaynabo, PR 00969, USA -
Full Time


Start Date

Immediate

Expiry Date

09 Nov, 25

Salary

45000.0

Posted On

10 Aug, 25

Experience

3 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Packaging, Biology, Regulated Industry, Qsr, Materials Science, English, Industrial Engineering, Chemistry, Chemical Engineering, Biomedical Engineering, International Standards, Manufacturing

Industry

Pharmaceuticals

Description

POSITION SUMMARY:

Smart Precise Solutions, Inc. is seeking a Quality Project Coordinator responsible for leading and supporting investigations related to raw material non-conformances (NCRs) within the manufacturing and packaging areas for diabetes-related products. This role will serve as a liaison between Quality, Engineering, Manufacturing, Suppliers, and other cross-functional teams to ensure timely, thorough, and compliant closure of non-conformance events in accordance with applicable regulatory standards.

ACADEMIC REQUIREMENTS:

  • Bachelor’s degree in Biology, Chemistry, Biomedical Engineering, Chemical Engineering, Industrial Engineering, Materials Science, or a related scientific/engineering discipline.
  • A master’s degree is a plus but not required.

REQUIRED EXPERIENCE:

  • Minimum of 3 years of experience in a regulated industry (pharmaceutical, medical device, biotechnology).
  • Proven experience managing non-conformances, deviations, or material-related complaints.
  • Familiarity with manufacturing and packaging processes.
  • Hands-on experience with electronic quality systems (e.g., Track Wise, Veeva, Master Control).
  • Strong technical writing skills and ability to work cross-functionally.
  • Bilingual: Spanish and English (written and spoken at a technical level).

REGULATORY KNOWLEDGE:

  • U.S. Regulations:
  • 21 CFR Parts 210, 211, 820 (GMPs and QSR)
  • 21 CFR Part 11 (electronic records and signatures)
  • International Standards:

How To Apply:

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Responsibilities
  • Coordinate investigations for raw material non-conformances in manufacturing and packaging areas.
  • Track and follow up on Corrective and Preventive Actions (CAPAs) associated with NCRs.
  • Collaborate with Quality, Engineering, Production, and Procurement teams to gather objective evidence and determine root causes.
  • Ensure all documentation is accurate and compliant with internal procedures and regulatory requirements.
  • Perform trend analysis and prepare technical reports.
  • Participate in internal and external audits, providing information related to NCR investigations.
  • Manage project timelines and prioritize tasks to meet investigation deadlines.
  • Support continuous improvement initiatives related to raw material quality and process control.
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