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Quality Control Technician I: Chemistry

2 months ago


Norwood, Massachusetts, United States Randstad Life Sciences US Full time

Contract Position

Location: Norwood, MA

Pay Rate: $30-38/hour

Available Shifts:

Sunday to Wednesday, Day Shift: 8:00 AM - 6:00 PM

OR

Wednesday to Saturday, Evening Shift: 2:00 PM - 12:00 AM

OR

Sunday to Wednesday, Night Shift: 10:00 PM - 8:00 AM

OR

Wednesday to Saturday, Night Shift: 10:00 PM - 8:00 AM

In this position, you will conduct cGMP Quality Control Chemistry assessments for various samples including release, stability, and in-process evaluations. This role may also involve supporting specific projects as required.

Key Responsibilities

  • Conduct routine analytical chemistry evaluations, including wet chemistry techniques such as APP, osmolarity, particle analysis, and dynamic light scattering.
  • Perform basic HPLC analyses and NaOH plate reader-based assays to support manufacturing process testing as necessary.
  • Assist with special projects as assigned.
  • Help troubleshoot assay methodologies and equipment as needed.
  • Engage in data entry and support data trending activities.
  • Provide general laboratory support tasks, including reagent preparation, sample management, equipment upkeep, and laboratory cleanliness.
  • Contribute to the development of Standard Operating Procedures (SOPs), protocols, and reports as required.
  • Enter sample results into LIMS (LabVantage) and execute electronic assay forms.
  • Support the stability program.
  • Manage and stock QC laboratory supplies.
  • Complete and maintain cGMP documentation for all tasks performed.
  • Participate in the creation of quality system records, including lab events, deviations, and CAPAs as necessary.
  • Establish and uphold a safe laboratory environment.
  • Adhere to all relevant GxP regulations, guidelines, and company policies to ensure compliance with both regulatory and internal standards.
  • Execute tasks precisely as outlined in internal guiding documents, including but not limited to SOPs and work instructions.
  • Follow Good Documentation Practices and Data Integrity requirements to ensure that data, documentation, and records are accurately completed and maintained for business use and available for audits or inspections.
  • Complete training as per the assigned learning plan within the defined timelines and requalification schedules.
  • Perform additional duties as assigned.

Education & Qualifications

  • Education: Bachelor’s degree in a relevant scientific field.
  • Experience: 0-2 years of laboratory experience.
  • Demonstrated ability to learn and understand GxP regulations.
  • A commitment to making a significant impact as part of a dynamic, transformational organization that values being Bold, Relentless, Curious, and Collaborative.