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