Quality Control Technician

Integrated Resources Inc.; North Haven (CT); On-site; USD 50,000 - 70,000; Full time

Benefits offered by this job

Referral bonus of $500 per candidate referred

Job summary

A leading company in the healthcare sector is seeking a Quality Control Technician in North Haven, CT. The candidate will play a critical role in supporting post-market vigilance investigations, ensuring the quality and safety of medical devices. Ideal for individuals with skills in critical thinking and proficiency in MS Office, particularly Excel and Word.

Qualifications

• Experience in a laboratory environment with laboratory equipment is preferred.
• Experience with medical devices preferred but not required.
• Academic knowledge in scientific research methods is a plus.

Responsibilities

• Support Post Market Vigilance Investigations team activities.
• Conduct follow-ups and manage complaint investigations.
• Perform root cause analysis on returned products.

Skills

Proficient with MS Office

Critical independent thinking

Excellent written and verbal skills

Education

High School Diploma

BS Degree in a Technical curriculum

Job description

Integrated Resources, Inc., is led by a seasoned team with combined decades in the industry. We deliver strategic workforce solutions that help you manage your talent and business more efficiently and effectively. Since launching in 1996, IRI has attracted, assembled and retained key employees who are experts in their fields. This has helped us expand into new sectors and steadily grow.

Job Description

Job Title: Quality Control Technician

Location: North Haven, CT
Duration: 7+ months (possibility of extension)

Job Roles & Responsibility

• The candidate will support the Post Market Vigilance Investigations team's activities for the Surgical Solutions Division.
• These activities include; assist in managing the receipt of incoming physical complaint product, conducting follow ups with accounts and/or International Subsidiaries to rectify discrepancies with product receipt, assisting in managing the process flow of complaint investigations, performing Device History Record Reviews, and performing root cause analysis on product customer returns to ensure high levels of quality, reliability, safety, and efficacy.
• Additional responsibilities include management of clinically applied medical device retains and associated paper records in accordance with Healthcare Record Retention Policies and support staffing needs.

Essential Functions

• Assist PMV Investigations Coordinator with managing receipt of physical complaint product samples, in addition to corresponding with domestic and international accounts to rectify discrepancies in product receipt.
• Assist in the prioritization of complaint investigations.
• Assist in the coordination of sanitization of clinically applied medical device returns and shipment to respective Client Manufacturing facilities, as well as coordinating the investigation process with internal Engineering and Quality groups.
• Test and thoroughly evaluate rudimentary products to determine root cause analysis within a closely monitored time frame.
• Certification with OSHA's BloodBorne Pathogens Standard 29 CFR 1910.1030 and adherence to Corporate and Local Environmental Health and Safety Policies.
• Education Required: High School Diploma
• Education Preferred: BS Degree in a Technical curriculum preferred or equivalent industry experience.
• Experience in a laboratory environment and with laboratory equipment or
  academic knowledge in scientific research methods.
• Experience with medical devices preferred but not required.

Skills/Qualifications:

• Must be proficient with MS Office (with emphasis on Excel and Word).
• Critical independent thinking and timely follow up.
• Excellent written and verbal skills necessary.
  
  
• Organizational Relationships/Scope:
  QD003425-001, Rev A
• Quality Assurance
• Manufacturing
• Research and Development
• Regulatory Affairs
• Legal

Additional Information

We do have referral bonus of $500 per candidate, if you refer any of your friends or colleague who are looking out for the same job.

Thanks & Regards,

Seema Chawhan
Clinical Recruiter
Integrated Resources, Inc.
IT Life Sciences Allied Healthcare CRO
Certified MBE |GSA - Schedule 66 I GSA - Schedule 621I