SRG, the leader in the Life Sciences human capital industry, is looking for a full-time, contract Quality Engineer III to join our client's pharmaceutical manufacturing team in Anasco, Puerto Rico.

*At this time we can only accept candidates currently living in Puerto Rico.

MUST HAVES:

• Bachelor Degree is required.
• 7+ years of experience (manufacturing environment, within the FDA regulated industry
• Experience with production documentation and Quality Assurance/Regulatory
• Knowledge of FDA 21CFR 820, ISO-13483:2003, CMDR, MDD (93/42/EEC), TGA, PAL
• Written and verbal communications skills in Spanish and English

JOB RESPONSIBILITIES:

• Non-Conformance Investigations. Execution and QA Review.
• CAPA (Root Cause) investigations. Execution and QA Review.
• Knowledge in Statistical Tools.
• Analytical, and compliance / technical writing skills.
• National and International regulatory requirements.

** Only candidates selected to be moved forward in the recruitment process will be contacted by SRG's Recruitment Team to schedule a conversation.

Impellam Group and its brands are equal-opportunity employers committed to diversity and inclusion. All qualified applicants will receive consideration without regard to race, color, religion, gender, sexual orientation, pregnancy or maternity, national origin, age, disability, veteran status, or any other factor determined to be unlawful under applicable law. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application, interview process, pre-employment activity, and the performance of crucial job functions.

If you require additional disability considerations, modifications, or adjustments please let us know by contacting HR-InfoImpellamNA@impellam.com or fill out this form to request accommodations.