Empleos de Integrated Services For Productivity & Validation, Inc en Puerto Rico

NPI, Change Control, Documentation Review, Validation, C&Q, PPQ, FAT · Requirements · Doctorate OR Masters + 2 years of directly related experience OR · Bachelors + 4 years of directly related experience OR · Associates + 8 years of directly related experience OR · High school/GE ...

Bachelor's Degree in Engineering, preferred Mechanical, Electrical, or Chemical · • Excellent written and verbal communication skills · • Technical writing experience · • Working knowledge and experience with cGMP procedures and engineering practices on pharmaceutical/biotech pro ...

Knowledge on Mechanical Equipment Adjustment/Troubleshooting · Knowledge on PLC Systems Troubleshooting– Rockwell · Knowledge on Vision Systems Troubleshooting/Adjustment– Cognex · Knowledge on cGMP's · Knowledge on Systech Vision System Troubleshooting\Adjustments. · Nice to hav ...

Preventive Maintenance Execution Experience, · Knowledge Reading Drawing (Electrical/Mechanical) · Machine Timing Adjustment Experience · Basic knowledge in PLC/Automation · Hydraulic and Pneumatic System Knowledge · Vision System basic Knowledge · Requirements · •Associate's and ...

· • Relevant experience in a commercial bio pharmaceutical manufacturing environment, preferably supporting formulation and aseptic filling operations. · • Understanding of protein science, formulation and filling processes. · • Experience with process monitoring, data trending, ...

Documentation Clerk assigned to the documentation repository area for the site, and its integrated units, such as SOP, Training, and Change Request systems. · Provides measurement and performs monitoring for compliance through metrics for every unit and/or system as required.  · ...

Preferred candidates will have Validation Experience in Parenteral Manufacturing. · Specifically, experience focused in Aseptic Process Validation, Aseptic Techniques, Environmental Monitoring Performance Qualifications, Environmental Characterizations, Airflow Visualization (Sm ...

Experience with: Veeva · Trackwise · CAPA · Change Control · Requirements · Doctorate degree OR Master's degree and 3 years of Manufacturing Operations experience OR · Bachelor's degree and 5 years of Manufacturing Operations experience OR · Associate's degree and 10 years of Man ...

Aseptic Process, NPI, Change Control, FATs, Validation, and PPQs · Requirements · -Doctorate OR · -Masters + 2 years of directly related experience OR · -Bachelors + 4 years of directly related experience OR · -Associates + 8 years of directly related experience OR · -High school ...

· • GMP knowledge: Strong background in regulated environments with ability to apply GMP in manufacturing and validation. · • Validation expertise: Experience in drafting, executing, and approving validation. · • Time pressure filling: Hands-on experience with time pressure fill ...

Knowledge on PLC Systems Trobleshooting– Rockwell · Knowledge on Vision Systems Trobleshooting/Adjustment– Cognex · Knowledge on cGMP's · Knowledge on Systech Vision System Trobleshooting\Adjustments. · Nice to have - Work experience on FDA regulated industries. · Knowledge on ba ...

Change Control, Documentation Review, Validation, PPQ · Requirements · Doctorate OR Masters + 2 years of directly related experience OR · Bachelors + 4 years of directly related experience OR · Associates + 8 years of directly related experience OR · High school/GED + 10 years of ...

The Process Development Engineering contractor supports the development, validation, and implementation of new manufacturing processes. The role involves equipment and process validation, documentation generation, process optimization, and cross-functional technical collaboration ...