Jobs · Analyst · Rhode Island

Lab Technician - Urgent Need

MillenniumSoft Inc · Warwick, RI · 23 mo ago
AnalystFull-time

Essential Duties and Position Responsibilities

  • Documenting complaint product sample return date.
  • Decontaminate returned product samples.
  • Cook product transfers to/from external manufacturing sites.
  • Evaluate and investigate product sample returns to assist in determining the most probable root cause of the complaint and document accurate investigation findings in the complaint handling system.
  • Maintain the Field Assurance (Bio-Hazard) Lab area. Ensure Lab is clean and in good order. Items are properly labeled as potential biohazard material as received.
  • Support lab biohazard waste disposal in conjunction with facilities.
  • Manage and document thorough and accurate complaint records while ensuring they are processed in a uniform and timely manner and are compliant with Good Documentation Practices (GDP).
  • Identify and escalate quality issues and identify changes in (MDR/MDV) reportability based on sample return condition.
  • Serve as an active participant during internal and external audits.
  • Complete mandatory training by established due dates and always maintain training compliance.
  • Adhere to departmental processes and systems to ensure regulatory compliance.

Qualifications, Knowledge, and Skills Required

  • Associates degree required. BS/BA preferred.
  • 2-5 years of experience in complaint handling, quality control, manufacturing or related functions in the medical device, pharmaceutical, biotech or equivalent industry.
  • Sound written and verbal communication skills are required.
  • Proficiency in common computer applications such as Microsoft Office (Excel, Word and Outlook).
  • Familiarity with medical, anatomical and physiological terminology preferred.
  • Familiarity with the medical device industry and regulatory requirements preferred.
  • Duties require basic knowledge of mechanical and physical inspection techniques. (Calipers, micrometers, blueprint reading, etc.)
  • Duties require knowledge of inspection/sampling techniques and familiarity with ANSI/ASQZ1.4.
  • Knowledge of FDA Quality System Regulations, ISO 9000, and ISO 13485

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