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Open nowPosted 11 days ago

Specialist Quality Complaints

Workable (global search)108,016 open roles

Where
Juncos, Puerto Rico
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Your applicationOpen nowSpecialist Quality ComplaintsWorkable (global search) · Juncos, Puerto Rico

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The clock on this job

Early applications get read.

7.9% of postings close within 7 days. Measured by our own scanner across the market. Workable (global search) postings stay open a median of 7 days.

Share of postings closed within
  1. 1.6%1 day
  2. 3.6%3 days
  3. 7.9%7 days
  4. 14.9%14 days
  5. 34.0%30 days
This job: posted 11 days ago

Workable (global search) median: 7 days open

The posting

We are seeking a Specialist Quality Complaints to support the product complaint system at a biopharmaceutical manufacturing site in Juncos, Puerto Rico. This role leads and manages product complaint investigations and performs data analysis and trending of complaint information to proactively detect signals and take timely, appropriate action.

Key Responsibilities

  • Keep the complaints database current as factual information becomes available, and accurately summarize closed investigations.
  • Review and approve complaint investigations to ensure they are concise, clear and science-based.
  • Follow up on corrective and preventive actions (CAPAs) resulting from investigations through completion.
  • Depending on complaint complexity, conduct and document investigations directly.
  • Translate highly technical investigations into simple, concise documents understandable by non-technical reviewers.
  • Communicate and escalate complaints, represent the site on the product complaint network, and prepare and issue closure letters.

Requirements

Education (one of the following)

  • Doctorate degree; OR
  • Master's degree + 2 years of directly related experience; OR
  • Bachelor's degree + 4 years of directly related experience; OR
  • Associate's degree + 8 years of directly related experience; OR
  • High school diploma/GED + 10 years of directly related experience

Preferred Qualifications

  • Experience in project management, root cause analysis and CAPA determination
  • Quality mindset and deep knowledge of GMP compliance
  • Proficiency in Microsoft Office (Excel, Outlook) and Microsoft Teams

Key Skills

  • Strong project management skills; experience leading cross-functional teams and handling multiple projects simultaneously (a must)
  • Excellent written and verbal communication, including facilitation and presentation skills; excellent technical writing
  • Able to work in a team-oriented, matrix environment with diverse departmental groups
  • Self-motivated, detail-oriented, able to prioritize and meet deadlines
  • Leadership, problem-solving, analytical, influencing and customer service skills in a GMP environment
  • Ability to evaluate issues, make decisions and determine when to escalate

Benefits

  • Contract position: approximately 5.5 months (October 2026 – March 2027), with possible extension
  • Shift: Administrative shift
  • Days: Monday to Friday, 8 hours/day (40 hours/week)
  • On-site in Juncos, Puerto Rico
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