Emploi CDI Skaneateles

Roles & Responsibilities: Lead software validation efforts for ATE systems used in testing infusion pumps, patient monitors, or diagnostic devices. Develop validation protocols, test plans, scripts, and reports in alignment with FDA 21 C... - Voir cette offre d'emploi

This is where your work makes a difference. At Baxter, we believe every person—regardless of who they are or where they are from—deserves a chance to live a healthy life. It was our founding belief in 1931 and continues to be our guiding ... - $88000 - 120000 per year - Voir cette offre d'emploi

We want you to help us shape the future of shopping experiences and deliver on our purpose of connecting people with the products and experiences that enrich their lives. Joining SAS Retail Services, an Advantage Solutions company, means jo... - $16 per hour - Voir cette offre d'emploi

Job Description: Serve as the SME for qualification of analytical equipment in a GMP manufacturing setup, ensuring compliance with GAMP 5, FDA 21 CFR Part 11, and EU Annex 11. Responsibilities: Author/execute URS, DQ, IQ, OQ, PQ protoco... - Voir cette offre d'emploi

Roles & Responsibilities: Is a bachelor's degree Required? - Not required, but degree is preferred. I would reference the requirements that we have for our quality analysts, see below. How many years of recent experience does this person... - Voir cette offre d'emploi

Responsibilities: Process Validation and IQ-OQ-PQ Experience in medical parts manufacturing experience is the key, with process validation expertise around 8 to 10 yrs experience. Protocol Review & Compliance: Study and assess Installati... - Voir cette offre d'emploi

Job Description: Self-sufficient go-getter with quality mindset. Associate will be working closely with the supplier quality team to address gaps within supplier quality and distribution systems. They will be expected to pull and review d... - Voir cette offre d'emploi

This is where your work makes a difference. At Baxter, we believe every person—regardless of who they are or where they are from—deserves a chance to live a healthy life. It was our founding belief in 1931 and continues to be our guiding ... - $136000 - 176000 per year - Voir cette offre d'emploi

Responsibilities: Serve as the technical SME for qualification of analytical equipment in manufacturing setup. Author and execute qualification protocols (URS, DQ, IQ, OQ, PQ) in accordance with GAMP 5, FDA 21 CFR Part 11, and EU Annex 1... - Voir cette offre d'emploi

Roles & Responsibilities: Lead software validation efforts for ATE systems used in testing infusion pumps, patient monitors, or diagnostic devices. Develop validation protocols, test plans, scripts, and reports in alignment with FDA 21 C... - Voir cette offre d'emploi