Senior Analyst 1, QC Testing (2-2-3 Shift)

Position Overview The Sr. Analyst 1, Quality Control (QC) All QC Team is responsible for performing routine testing required for Urgent/STAT testing of manufacturing batch samples, clean utility, environmental monitoring. This role is part of a 24x7 team that supports testing/sampling across all of the QC laboratories required for urgent testing/Manufacturing support. The role will learn and perform testing/sampling across multiple labs in QC. Job Description What You’ll Do: Performs basic testing that spans all of the QC labs (e.g., Bioburden, Endotoxin, HPLC, UV280, TOC, etc.) per department Standard Operating Procedures (SOPs) and test methods for samples associated manufactured batches Executes advanced lab testing and support for all laboratory assays for all samples, and acts as a Subject Matter Expert (SME) and qualified trainer of at least one test Leads sample collection and manages sample logistics for testing Supports testing for all qualification and study directed testing Supports investigation of routine OOS assays and events Conducts qualification and validation protocols Reviews intermediate lab testing results Troubleshoots complex assays Writes and assists with document preparation and review Manages project timelines Assists management with training and on-boarding of new staff as needed Embraces LEAN lab and six sigma principles and applies them to laboratory processes Champions projects and project management as assigned Performs other duties, as assigned Minimum Qualifications: Bachelor's with 2+ years of relevant QC experience OR Master's with 0 years of experience Experience with aseptic production & support 1-3 years in a GMP environment Advanced understanding of GMP, GLP, GDP requirements Advanced knowledge of QC testing and laboratory experience LIMS experience Experience with document control including reviewing and editing technical documents Preferred Qualifications: 4+ years of previous experience working within QC or with GXP or quality systems is an advantage Advanced experience in a GMP QC Laboratory, advanced knowledge of all compendial test methods. Working Conditions & Physical Requirements: Ability to discern audible cues Ability to inspect or perform a task with 20/20 corrected vision, visual acuity, including distinguishing color Ability to ascend or descend ladders, scaffolding, ramps, etc. Ability to stand for prolonged periods of time (Daily up to 60 minutes) Ability to sit for prolonged periods of time (Daily up to 60 minutes) Ability to conduct activities using repetitive motions that include writs, hands and/or fingers. Ability to conduct work that includes moving objects up to 10 pounds. Ability to bend, push or pull, reach to retrieve materials from 18" to 60" in height, and use twisting motions. EEO Information Fujifilm is committed to providing equal opportunities in hiring, promotion and advancement, compensation, benefits, and training regardless of nationality, age, gender, sexual orientation or gender identity, race, ethnicity, religion, political creed, ideology, national, or social origin, disability, veteran status, etc. ADA Information If you require reasonable accommodation in completing this application, interviewing, completing any pre-employment testing, or otherwise participating in the employee selection process, please direct your inquiries to our HR Department (View email address on click.appcast.io). #J-18808-Ljbffr Merck & Co.