Quality Control, Raw Materials
: Job Details :


Quality Control, Raw Materials

Randstad Life Sciences US

Location: Norwood,MA, USA

Date: 2024-10-06T02:15:12Z

Job Description:

Associate I, Quality Control, Raw Materials

6 Months

Norwood, MA

Hourly Pay: $34.67 an hour

Shift: M-F, 2nd Shift

Job Summary

Reporting to the Supervisor of Quality Control, Seeking a Quality Control Raw Materials Associate I, Sampler based at their Norwood, MA site. The individual in this role will perform QC Raw Material activities in support of GMP Manufacturing and further support special projects as assigned.

Job Responsibilities

  • Requesting, sampling, and shipping of raw materials
  • Sample coordination including cross functional collaboration with internal and external labs
  • Supporting domestic and international sample shipments
  • Supporting testing for methods including pH, conductivity, TruScan RM spectroscopy, appearance, and dimensional verification
  • Inspect product and raw material retain samples.
  • LIMS (LabVantage) sample logging and result entry
  • Raw material and consumable component inspection and release
  • Clean room gowning and aseptic techniques.
  • Managing/stocking of QC lab supplies and routine lab cleaning.
  • Complete and maintain cGMP documentation for work performed.
  • Maintain a safe laboratory working environment.
  • Foster a positive and inclusive work culture that promotes collaboration, innovation, and continuous improvement.
  • Follow all relevant GxP regulations, guidelines, and company policies to ensure compliance with regulatory and internal requirements.
  • Execute tasks precisely as defined in internal guiding documents including but not limited to standard operating procedures (SOPs) and work instructions.
  • Follow Good Documentation Practices and Data Integrity requirements to ensure data, documentation, and records are completed and maintained for use by the business and available to support audits or inspections.
  • Complete training in assigned required learning plan according to the defined timing and the prescribed requalification cadence.

Education & Qualifications

  • BA/BS in a relevant scientific discipline
  • 0-2 years or 3+ years in a GMP QC laboratory setting
  • • Demonstrated aptitude or ability to learn in order to gain a strong understanding of GxP regulations.

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