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. 

• 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