Quality Control Technician

Abbott

Scarborough (ME)

On-site

USD 45,000 - 60,000

Full time

14 days+

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Benefits offered by this job

Medical and Prescription Drug Plans
Dental Plan
Vision Plan
Health Savings Account
Flexible Spending Accounts
Supplemental Life Insurance
Short Term Disability
Long Term Disability
Critical Illness and Accident Insurance
401(k)

Job summary

Abbott is seeking a Quality Control Technician for a 6-month role located in Scarborough, Maine. The candidate will be responsible for performing testing of in-process components and final release testing for Lateral Flow, ELISA, and Molecular products. A minimum of an Associates degree and 1+ years in a laboratory setting is required.

The role also involves troubleshooting, maintaining equipment, and ensuring compliance with GMP/GLP standards. Abbott prioritizes diversity and offers a range of employee benefits.

Qualifications

  • Associates degree in Biology, Chemistry, Life Sciences or related field, or equivalent experience.
  • 1+ years of laboratory and/or quality control experience.
  • 2+ years’ experience in a regulated industry preferred.
  • 2+ years’ experience with GMP, FDA, ISO, and USDA regulations preferred.

Responsibilities

  • Perform testing of in-process components for Lateral Flow, ELISA, and Molecular products.
  • Perform final release testing for Lateral Flow, ELISA, and Molecular products.
  • Troubleshoot technical and quality issues.
  • Undertake new procedures and observe safety precautions.
  • Perform technical procedures and use laboratory equipment.
  • Review batch records.
  • Calibrate/maintain laboratory equipment.
  • Maintain Good Manufacturing/Laboratory Practices (GMP/GLP).

Job description

Title: Quality Control Technician

Location: Scarborough, Maine

Duration: 6 Months

Shifts: 8:00AM - 4:30PM

100% Onsite

Responsibilities
  • Perform testing of in-process components for Lateral Flow, ELISA and Molecular products
  • Perform final release testing for Lateral Flow, ELISA and Molecular products
  • Troubleshooting of technical and quality issues
  • Undertake new procedures and observe proper safety precautions
  • Able to perform technical procedures and use laboratory equipment
  • Review batch records
  • Calibrate/maintain laboratory equipment
  • Maintain Good Manufacturing/Laboratory Practices (GMP/GLP)
Education
  • Associates degree in Biology, Chemistry, Life Sciences or other related technical field or equivalent combination of education and experience
  • 1+ years of laboratory and/or quality control experience
Preferred Qualifications
  • 2+ years’ experience in a regulated industry
  • 2+ years’ experience with GMP, FDA, ISO and USDA regulations
Prior experience in the following areas
  • Pipette experience
  • pH meter o ELISA assays
Competencies
  • Working knowledge of internet sotware, MRP Inventory/Manufacturing software and Mircosoft Office Suite (Outlook, Excel, and Word)
  • Knowledge of enzyme and/or immunochromatographic assays, inspection/measurement systems, systematic troubleshooting, statistics and data analysis

An equal opportunity employer, Abbott welcomes and encourages diversity in our workforce.

  • We provide reasonable accommodation to qualified individuals with disabilities
Consultants Eligible Benefits Upon Waiting Period
  • Medical and Prescription Drug Plans
  • Dental Plan
  • Vision Plan
  • Health Savings Account (for High-Deductible Health Plans)
  • Flexible Spending Accounts (Health, Limited Purpose, Dependent Care, Commuter Parking and Commuter Transit)
  • Supplemental Life Insurance
  • Short Term Disability (coverage varies by state)
  • Long Term Disability
  • Critical Illness, Hospital coverage, Accident Insurance
  • MetLife Legal, MetLife ID Fraud, and MetLife Pet Insurance
  • 401(k)
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