Quality Lab Lead - 3rd Shift (Chem QC)

Actalent

Kokomo (IN)

On-site

USD 65,000 - 72,000

Full time

1 hour ago
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Benefits offered by this job

Medical, dental, and vision insurance
Company-paid life and AD&D insurance
401(k) with company matching
Generous PTO
Career growth opportunities

Job summary

Actalent seeks a Quality Laboratory Supervisor to lead a QC lab in Kokomo, IN on a third-shift schedule. You will manage technicians, validate test data, and ensure materials and finished products meet specifications in a chemical manufacturing setting.

The role emphasizes safety, GMP awareness, equipment calibration, data integrity, and collaboration with Production, Engineering, and Quality teams. Benefits and opportunities to influence continuous improvement are offered.

Qualifications

  • High School Diploma or GED.
  • At least 3 years of experience in quality, laboratory, or manufacturing roles.
  • 2-3 years of supervisory experience overseeing direct reports (preferred but strongly valued).
  • Hands-on laboratory experience with Gas Chromatography (GC).
  • Experience with ICP-MS or elemental analysis techniques.
  • Experience with XRF instrumentation and methods.
  • Experience with rheology and viscosity testing.
  • Experience performing moisture, density, conductivity, solids content, and particle size analyses.
  • Proficiency with LIMS and ERP systems, including strong laboratory documentation practices.
  • Knowledge of chemistry, laboratory operations, quality assurance, and quality control principles.
  • Familiarity with GMP or similar quality and compliance frameworks in a manufacturing or laboratory setting.
  • Ability to interpret and review analytical data, identify anomalies, and ensure compliance with specifications.
  • Strong leadership skills with the ability to direct, coach, and develop laboratory staff.
  • Solid organizational skills with the ability to manage multiple priorities and meet deadlines in a fast-paced environment.
  • Strong commitment to safety and adherence to established procedures and regulatory requirements.

Responsibilities

  • Lead, supervise, and mentor laboratory personnel, including scheduling, training, performance guidance, and day-to-day workflow coordination.
  • Oversee daily laboratory operations to ensure testing of raw materials, in-process materials, and finished products is completed accurately, safely, and on schedule.
  • Review and approve laboratory test results, ensuring compliance with specifications, standard operating procedures, and quality requirements.
  • Support and participate in investigations involving quality issues, non-conforming materials, and customer or internal complaints, including root cause analysis and corrective actions.
  • Ensure all laboratory equipment is properly maintained, calibrated, and functioning according to established standards.
  • Maintain accurate and complete laboratory documentation and records in alignment with quality system requirements and regulatory expectations.
  • Promote and enforce laboratory safety practices, good housekeeping, and adherence to environmental, health, and safety regulations.
  • Support internal and external audits by providing laboratory data, documentation, and explanations of testing procedures.
  • Contribute to continuous improvement initiatives focused on laboratory efficiency, data integrity, and product quality.
  • Collaborate with Production, Engineering, and Quality teams to support cross-functional manufacturing operations and resolve technical or quality-related issues.
  • Ensure proper use of LIMS, ERP systems to maintain data accuracy and traceability.

Skills

Laboratory leadership
GC operation
ICP-MS
XRF
Rheology testing
LIMS/ERP
Data review & QA
Regulatory compliance
Safety compliance
Cross-functional collaboration

Education

Associate's or Bachelor's degree in science/tech field

Tools

Gas Chromatography (GC)
ICP-MS
XRF instrumentation
Rheometer
LIMS
ERP systems

Job description

Actalent seeks a Quality Laboratory Supervisor to lead a QC lab in Kokomo, IN on a third-shift schedule. You will manage technicians, validate test data, and ensure materials and finished products meet specifications in a chemical manufacturing setting.

The role emphasizes safety, GMP awareness, equipment calibration, data integrity, and collaboration with Production, Engineering, and Quality teams. Benefits and opportunities to influence continuous improvement are offered.

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