Adecco
Location
Lenexa, KS | United States
Job description
Are you eager to leverage your quality assurance expertise in a cutting-edge scientific environment? Then look no further! Adecco is thrilled to partner with a leading global provider of scientific instruments, software, and services for laboratories, and they're seeking a talented Quality Assurance Specialist to join their team in Lenexa, KS.
The Quality Assurance Specialist will review batch records, identify documentation errors, and coordinate with Operations to raise or resolve issues as part of the quality assessment of products. This person will support the quality notification investigation team with data entry and complaint processing when required. Additionally, this team member will be responsible for filing and document retrieval as needed.
Top reasons to work with Adecco:
Weekly Pay
Upskilling opportunities through the Adecco Aspire Academy
Benefit offerings include medical, dental, vision, life insurance, short-term disability, additional voluntary benefits, EAP program, commuter benefits and a 401k plan. Our program provides employees the flexibility to choose the type of coverage that meets their individual needs.
Available paid leave may include Paid Sick Leave, where required by law; any other paid leave required by Federal, State, or local law; and Holiday pay upon meeting eligibility criteria.
Job Details:
Type: Full-time (40 hours/week)
Length: 3 months; Temp to hire opportunity.
Pay: $24.00/hour
Shift/Hours: Monday – Friday, 8:00 AM – 4:30 PM
Requirements:
High School Diploma or Equivalent
Prior experience in inventory control
1+ years of experience in QA, QC, or manufacturing within a regulated environment such as medical device, pharmaceutical, or food manufacturing.
Background in medical device, cGMP, or ISO-certified environment preferred.
Data entry skills and familiarity with inventory management systems such as SAP.
Working knowledge of various computer software programs such as Teams and Excel.
Self-motivated and able to work in a team environment
Able to work in a filing room environment and lift up to 50 lbs. for document archival, as needed
Description:
Review production batch documentation for compliance with cGMP good documentation requirements.
Communicate effectively and coordinate tasks with Manufacturing and Quality Control to facilitate timely release of products.
Process 100% inspection rework activities and stock adjustments.
Aid in processing quality notification investigations
Track and trend functional metrics.
Support compliance initiatives and Regulatory and Customer Audits.
Assist with continuous improvement projects and participate in lean activities.
Job tags
Salary
$24 per hour