QC Metrology Supervisor

Simtra BioPharma Solutions

$75K — $95K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in a physical science or related field
  • 5+ years of experience with quality control instruments
  • Previous leadership experience preferred
  • Proficient in Microsoft Word, Excel, and Outlook
  • Knowledge of instrument repair and calibration systems
  • Familiarity with QC documentation

Responsibilities

  • Manage the daily operations of the QC Metrology department
  • Provide timely Metrology support to various production QC areas
  • Oversee new instrument projects to ensure compliance and timely qualification
  • Calibrate analytical instruments to meet standards
  • Develop and execute validation protocols for analytical instruments
  • Manage SOPs for both new and existing instruments
  • Participate in continuous improvement teams for efficiency and quality

Benefits

  • Medical & Dental Coverage
  • Flexible Spending Accounts
  • 401(k) with Company Match
  • Paid Time Off and Paid Holidays
  • Education Assistance Program
  • Employee Ownership Plan
  • Short and Long-Term Disability Insurance
Full Job Description
The Quality Control Metrology Supervisor manages the activities in the QC Metrology department and the analysts that perform instrument maintenance and instrument projects in support of the company's quality program. This role works as part of the quality control function, training, and leading others within the laboratory. This position reports to Quality Control Chemistry Manager.

The responsibilities:
  • Manages the daily activities of the QC Metrology department.
  • Ensure timely Metrology support to Production, QC Chemistry, QC Microbiology, QC Critical, Incoming Quality Control and other current Good Manufacturing Practices (cGMP) production areas where analytical instruments are deployed.
  • Manage new instrument projects to ensure timely and compliant installation and qualification.
  • Calibrate analytical instruments for conformance to established government, commercial, and specification standards.
  • Develop and execute validation protocols (Installation Qualification/Operational Qualification/Performance Qualification) for analytical instruments.
  • Manage standard operating procedures (SOPs) on new and existing instruments.
  • Responsible for instrument re-certification with outside standard laboratories, which includes performing incoming inspections and documentation reviews on these instruments.
  • Write, revise and review SOPs.
  • Participate in continuous improvement functions (Lean initiatives) teams, which increase efficiency, solve problems, generate cost savings, improve customer service activities, and improve quality.
  • Perform/assist in internal assessments/investigations by collecting and analyzing accurate, objective evidence regarding risks and their magnitude.
  • Serve as a technical resource for process and/or product development activities.
  • Participate in client and regulatory audits and responds to audit observations.
  • Serve as project Subject Matter Expert (SME) on lab instruments and processes.
  • Understands advanced biological and chemical assays requiring precise analytical skills and understanding of biology and chemistry principles.
  • Can operate advanced laboratory equipment (HPLC, UV, Karl Fischer, pH meter, etc.).
  • Has a thorough knowledge of the US and EU pharmacopeias and a working knowledge of JP pharmacopeia.
  • Ensure that data integrity requirements are maintained.
  • Initiates and authors Laboratory Investigation Reports.
  • Performs general laboratory/personal area clean-up.
  • Identifies and leads special projects that involve new methods, instrumentation, and technologies.


The requirements:
  • Bachelor's degree required, preferably in a physical science related field
  • Minimum of 5 years of experience with QC instruments
  • Previous leadership experience preferred.
  • Computer proficiency in Microsoft Word, Excel, and Outlook and the ability to use enterprise software.
  • Knowledge of instrument/software/documentation repair and calibration systems required.
  • Knowledge and navigation skills of QC documentation required.


Physical / Safety Requirements:
  • Must be able to wear personal protective equipment.
  • Duties may require overtime work, including nights and weekends.
  • Use of hands and fingers to manipulate office equipment is required.
  • Position may require sitting or standing for long periods of time.
  • This position requires handling of laboratory chemicals.
  • Must be able to qualify for 20/40 corrected vision.


In return, you'll be eligible for[1]:
  • Day One Benefits
    • Medical & Dental Coverage
    • Flexible Spending Accounts
    • Life and AD&D Insurance
    • Supplemental Life Insurance
      • Spouse Life Insurance
      • Child Life Insurance
    • 401(k) Retirement Savings Plan with Company Match
    • Time Off Program
      • Paid Holidays
      • Paid Time Off
      • Paid Parental Leave and more
    • Adoption Reimbursement Program
    • Education Assistance Program
    • Employee Assistance Program
    • Community and Volunteer Service Program
    • Employee Ownership Plan
  • Additional Benefits
    • Short and Long-Term Disability Insurance
    • Voluntary Insurance Benefits
      • Vision Coverage
      • Accident
      • Critical Illness
      • Hospital Indemnity Insurance
      • Identity Theft Protection
      • Legal and more
    • Onsite Campus Amenities
      • Workout Facility
      • Cafeteria
      • Credit Union

[1] Current benefit offerings are in effect through 12/31/26

Disclaimer

This job description is intended to provide the minimum knowledge, skills and abilities necessary to perform the job. It may not be inclusive of all the duties and responsibilities of the job. Simtra reserves the right to make modifications based on business requirements.

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