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Specialist Quality Complaints
Juncos, PR, US
Scientific
Bachelors Degree
Full Time, Temporary
38.00
Experienced (Non-Manager)
On-site
Biotechnology/Pharmaceuticals
First Shift (Day)
Juncos, PR, US
38.00
Experienced (Non-Manager)
Full Time, Temporary
Biotechnology/Pharmaceuticals
On-site
Scientific
Bachelors Degree
First Shift (Day)
Job details
Kelly® Engineering is seeking Specialist Quality Complaints for a 6 month contract position at a Global Pharmaceutical & Biotechnology client in Juncos, Puerto Rico. If you’re passionate about bringing the latest scientific discoveries to life and are ready to take the next step in your career, trust The Experts at Hiring Experts.
Salary: $38.00 per/hour
Overview
This client is Global Biopharmaceutical company whose mission is to discover, develop and deliver innovative medicines that help patients prevail over serious diseases.
In this role you’ll be responsible for Supporting the product complaint system at Amgen through; leading and managing product complaint investigations, performing data analysis and trending of complaint information to proactively detect signals and take appropriate actions in a timely manner.
This role will give you an opportunity to transform patients’ lives through science by contribute with a global leading biopharma company powered by talented individuals who drive scientific innovation.
Schedule: Administrative shift
Responsibilities:
- Keep the complaints database updated as soon as factual information is available and summarize closed investigations into the database accurately.
- Ensure complaint related investigations are concise, clear and science-based by reviewing and approving such investigations.
- Follow-up on corrective actions derived from investigations through completion.
- Depending on the nature and complexity of the complaint, the specialist may be responsible of conducting and documenting the investigation.
Qualifications:
- Doctorate degree or Master’s degree and 3 years of directly related experience or Bachelor’s degree and 5 years of directly related experience or Associate’s degree and 10 years of directly related experience.
- Experience in manufacturing/packaging deviations, Root Cause Analysis, complaint investigations, project management and compliance.
What happens next:
Once you apply, you’ll proceed to next steps if your skills and experience look like a good fit. But don’t worry – even if this position doesn’t work out, you’re still in our network. That means our team of expert Science & Clinical recruiters will have access to your profile, making your opportunities limitless.
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