Control Center Technician I
: Job Details :


Control Center Technician I

Norwich Pharmaceuticals

Location: Norwich,NY, USA

Date: 2024-12-14T08:19:55Z

Job Description:
SUMMARY OF POSITIONThe Control Center Technician is responsible for providing support to ongoing laboratory activities in a cGMP environment.ORGANIZATION STRUCTUREThe Control Center Technician reports to the Group Leader Laboratory Operations. RESPONSIBILITIESPrimary responsibilities of this role include the following:
  • Responsible for maintaining inventory of laboratory supplies, chemicals,
  • standards and reference drugs; including but not limited to ordering, receiving, stocking, managing expiry and resupply to ensure availability to technical staff when needed.
  • Coordinate sample receipt, inventory and distribution to testing groups
  • Manage laboratory purchase requisitions through approval, PO issuance,
  • ordering, receiving, and invoice approval.
  • Perform laboratory housekeeping, cleaning and maintenance of laboratory
  • apparatus, and glassware washing to ensure availability to laboratory technical staff.
  • Assist with department budget management, including administrative
  • assistance with development of budgets, managing yearly blanket orders, tracking spending against budget amounts and proactively alerting management of spending trends.
  • Manage production sample retain storage, inventory and inspection.
  • Assist with new employee onboarding, desk setup,
  • controlled substance access, computer access, QUMAS, Compliance Wire, SAP US21, and other onboarding as required.
  • Coordinate laboratory controlled substance inventory management and
  • control. Lead regular controlled substance inventories and monthly cycle counts.
  • Manage samples and materials through the OFS process.
  • Data entry and/or review into tables, reports, COA, iStability, SAP, LIMS or other systems as required.
  • Perform basic laboratory procedures in accordance with approved procedures.
  • QUALIFICATIONS
  • High school diploma plus 3 years working experience, or Associate's Degree in a technical discipline.
  • Strong oral and written communication skills.
  • Proficient in computer use (Word, Excel, internet) with ability to learn new computer applications.
  • Ability to follow Standard Operating Procedures and methods.
  • Highly organized and operates with a sense of urgency in a fast paced environment.
  • Strong interpersonal skills and sound judgment.
  • GMP DECISION-MAKING AUTHORITYIdentifies and escalates issues to laboratory management.This role will offer an hourly range that commensurate with experience and demonstrated skills in the $18.00 - $20.00 range. An Equal Opportunity Employer, including disability/vets.
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