Laboratory Manager- ICP

Astrix Inc

$100K — $120K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in Chemistry, Biology, or a related scientific discipline.
  • 5+ years of analytical or Quality Control laboratory experience in regulated environments.
  • Previous supervisory experience in a laboratory setting.
  • Strong understanding of analytical laboratory equipment and testing methods, especially ICP-MS and titration.
  • Experience with raw material, in-process, and finished-product testing in manufacturing contexts.
  • Familiarity with regulations like cGMP, cGLP, ISO, USP/FCC, HACCP, or similar standards.

Responsibilities

  • Lead day-to-day activities of the Quality Control laboratory, including planning and scheduling.
  • Supervise, train, and develop laboratory personnel with a focus on safety and quality.
  • Oversee testing of raw materials and products to support manufacturing and product release.
  • Investigate product issues and coordinate corrective actions for out-of-specification results.
  • Support maintenance and troubleshooting of laboratory instruments, particularly ICP-MS.
  • Ensure compliance with quality and regulatory requirements in laboratory documentation.
  • Track laboratory performance metrics and operational needs.
  • Collaborate with Quality, Production, Engineering, and Technical teams to resolve issues and enhance processes.

Benefits

  • Medical insurance
  • Dental insurance
  • Vision insurance
  • Life and AD&D insurance
  • 401K plan and vacation time
Full Job Description
Pay Rate Low: 100000 | Pay Rate High: 120000

At this time, Astrix cannot transfer nor sponsor a work Visa for this position.

This is an excellent opportunity for an experienced ICP laboratory professional ready to take ownership of a high-impact lab operation within a manufacturing environment. In this role, you'll lead and develop a team of laboratory technicians, oversee critical analytical testing and product release activities, and work closely with Quality, Operations, Engineering, and Technical teams to solve problems and improve processes.

Pay : $100k-$120k
Schedule : M-F 8a-5p
Type of Job : Direct Hire/Permanent
Location : Ashtabula, OH

Benefits Offered:

  • Medical
  • Dental
  • Vision
  • Life/AD&D
  • 401K and Vacation

Laboratory Manager- ICP Daily Tasks: What you will do:
  • Lead the day-to-day activities of the Quality Control laboratory, including workload planning, testing priorities, and technician scheduling.
  • Supervise, train, and develop laboratory personnel while maintaining a strong focus on safety, quality, and accountability.
  • Oversee testing of raw materials, in-process samples, and finished products to support manufacturing and timely product release.
  • Review analytical results, investigate testing or product issues, and coordinate corrective actions when results fall outside specifications.
  • Support laboratory instrumentation, including ICP-MS, titration equipment, calibration, validation, preventive maintenance, and troubleshooting.
  • Maintain laboratory documentation and ensure testing activities meet applicable quality and regulatory requirements.
  • Track laboratory performance, testing turnaround times, supplies, standards, and other operational needs.
  • Partner with Quality, Production, Engineering, and Technical teams to resolve manufacturing issues and improve processes.
  • Identify opportunities to improve testing methods, laboratory efficiency, consistency, and overall quality performance.

Laboratory Manager- ICP Qualifications/Requirements:
  • Bachelor's degree in Chemistry, Biology, or another related scientific discipline.
  • 5+ years of analytical or Quality Control laboratory experience, preferably within chemical manufacturing, pharmaceutical, food, or another regulated manufacturing environment.
  • Previous experience supervising or leading laboratory personnel.
  • Strong understanding of analytical laboratory equipment and testing methods; experience with ICP-MS and titration is highly desirable.
  • Experience supporting raw material, in-process, and finished-product testing within a manufacturing operation.
  • Working knowledge of regulated quality practices such as cGMP, cGLP, ISO, USP/FCC, HACCP, or comparable standards.

We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you!

INDBH
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