Control Center Technician I

Summary Of Position

The Control Center Technician is responsible for providing support to ongoing laboratory activities in a cGMP environment.

ORGANIZATION STRUCTURE

The Control Center Technician reports to the Group Leader Laboratory Operations.

Responsibilities

Primary 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 AUTHORITY

Identifies and escalates issues to laboratory management.

The anticipated base hourly range for this position is $18.00 to $ 20.00 an hour. This position is eligible for Alvogen’s annual discretionary bonus and comprehensive benefits package, consisting of medical and prescription drug coverage (two PPO plans and an HDHP with Health Savings Account and employer contribution), dental, vision, flexible spending accounts. Alvogen’s benefits package also includes a retirement savings program, long-term care coverage, paid time off (176 hours prorated to hire date ) inclusive of sick time, disability benefits, life insurance, a wellness program, and 13 company recognized paid holidays per year. We anticipate this position will be posted on 03/06/2026 and remain open for at least 30 days. To apply, select the apply button and submit your application.

“An Equal Opportunity Employer, including disability/vets.”