At Kelly® Science & Engineering , we're passionate about helping you find a job that works for you. How about this one?
We're seeking for Specialists Manufacturing (multiple positions) to work at a premier biotechnology manufacturing client in Juncos, PR .
Let us help you grow at work and discover the next step in your career, all while being a vital part of your community.
Salary: $38.00 hr
Shift: Administrative shift (support a 24/7 manufacturing operations, some remote work is possible)
Why you should apply to be Specialist Manufacturing :
Competitive pay with biweekly direct deposit (W-2)
Hands-on experience supporting critical manufacturing and quality systems in a leading biotechnology environment
Collaborative, fast-paced, and dynamic workplace with growth opportunities
Access to extensive training resources and career guidance
Paid vacation, sick leave, holidays, and eligibility for a Christmas bonus ( Must comply with minimum established requirements to qualify.)
This job might be an outstanding fit if you have the following requirements:
Doctorate OR Master's degree plus 2 years of Manufacturing Operations experience OR Bachelor's degree plus 4 years of Manufacturing Operations experience
Bachelor's degree in engineering or a related technical discipline is a plus
Experience in manufacturing, process development, or quality assurance within the biotech or pharmaceutical industry, with progressively increasing responsibility.
Strong experience managing deviations, non-conformances, investigations, CAPAs, and Change Controls using TrackWise, Veeva, or similar quality systems.
Experience with Root Cause Analysis, deviation assessments, investigation ownership , and technical report writing.
Proficiency in Microsoft Office and SAP (ERP) systems.
Excellent written and verbal communication skills in English and Spanish, including technical writing and presentations.
What's a typical day as Specialist Manufacturing? You'll be:
Supporting the execution of manufacturing and quality systems including non-conformances, process validation, procedures, training, and new product introductions
Serving as a process owner and document owner for manufacturing procedures, ensuring alignment with current operations
Assessing process performance, identifying and implementing process improvements, and providing troubleshooting support on the manufacturing floor
Leading or assisting in deviation investigations, authoring investigation reports, and managing non-conformance (NC) and Corrective and Preventive Action (CAPA) closures
Supporting the establishment and review of process monitoring parameters, collecting and analyzing process data, and preparing quarterly reports
Assisting with process validation protocols, data collection, and execution of validation activities
Participating in regulatory inspections, new product introduction, process or equipment modification projects, and special initiatives
Collaborating with cross-functional teams and supporting change control processes
Helping you discover what's next in your career is what we're all about, so let's get to work. Apply to be Specialist Manufacturing today!
Recruiter Lilly Abouomar 9395454792
SETTPuertoRico
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Why Kelly ® Engineering?
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