Lead Operator — GMP Manufacturing Leader (Second Shift)

ThermoFisher Scientific

Frederick (MD)

On-site

USD 32,000 - 41,000

Full time

14 days+

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Benefits offered by this job

Healthcare plans
Vision plan
Commuter benefits
Tuition reimbursement
Paid time off
Parental leave
Disability insurance
401(k)
Stock Purchase Plan

Job summary

Thermo Fisher Scientific in Maryland is seeking a Lead Operator to join our manufacturing team on the second shift. You will mentor a team, ensure consistent production processes, and drive operational excellence with safety and quality at the forefront.

You will coordinate daily activities, troubleshoot issues, review batch records, and collaborate across functions to meet delivery goals while upholding cGMP standards and strict PPE protocols.

Qualifications

  • Four years of manufacturing experience with demonstrated leadership.
  • Strong knowledge of cGMP, ISO standards and regulatory requirements.
  • Ability to read and interpret manufacturing documentation and SOPs.
  • Experience implementing lean manufacturing and continuous improvement.

Responsibilities

  • Lead and mentor a manufacturing team to ensure consistent production execution.
  • Coordinate daily manufacturing activities and resolve complex issues.
  • Review batch records and ensure compliance with safety and quality standards.
  • Collaborate with cross-functional teams to meet production goals.

Skills

Leadership
cGMP knowledge
ISO standards
Manufacturing documentation
Troubleshooting
Continuous improvement
Cross-functional coordination
ERP proficiency
Microsoft Office
SOP interpretation

Education

Bachelor's in Engineering/Chemistry/Biology or related

Tools

ERP platforms
Manufacturing software

Job description

Thermo Fisher Scientific in Maryland is seeking a Lead Operator to join our manufacturing team on the second shift. You will mentor a team, ensure consistent production processes, and drive operational excellence with safety and quality at the forefront.

You will coordinate daily activities, troubleshoot issues, review batch records, and collaborate across functions to meet delivery goals while upholding cGMP standards and strict PPE protocols.

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