Our client a global leader in life sciences and diagnostics is looking for Quality Control Associate in Tucson AZ.
Job Duration: Long Term Contract(Possibility Of Extension)
Job Responsibilities:
The Quality Control Associate will perform testing of raw materials in-process materials and finished goods in a regulated cGMP/ISO 13485 environment. This role is responsible for maintaining accurate documentation supporting quality investigations and ensuring compliance with regulatory standards. The ideal candidate will work cross-functionally to support QC operations reagent manufacturing and continuous improvement initiatives.
Key Responsibilities:
- Perform inspection and testing of raw materials in-process and finished goods.
- Document results complete batch records and generate QC reports.
- Maintain Device History Records (DHR) and ensure compliance with cGMP and regulatory requirements.
- Conduct data analysis and support process monitoring and trending.
- Investigate Out of Specification (OOS) results and support CAPA activities.
- Perform routine maintenance and calibration checks of lab equipment.
- Support environmental monitoring and maintain QC lab readiness.
- Assist in reagent formulation and manufacturing activities.
- Manage lab inventory supplies and vendor coordination.
- Participate in validations method development and process transfers.
Quality & Compliance:
- Ensure adherence to FDA ISO GMP and OSHA standards.
- Maintain accurate documentation for material handling storage and release.
- Support audits safety reporting and quality system compliance.
Qualifications:
- High School Diploma (Associates or Bachelors in Life Sciences preferred).
- 07 years of experience in a laboratory or regulated industry.
- Experience in cGMP/GLP/ISO environments preferred.
Skills & Requirements:
- Strong analytical troubleshooting and data analysis skills.
- Hands-on lab experience (pipetting titration spectroscopy etc.).
- Excellent documentation and organizational skills.
- Ability to work in a fast-paced team-oriented environment.
- Familiarity with Lean/6S practices is a plus.
Company Benefits: Medical Dental Vision Paid Sick leave 401K
If interested please share your update resume at /
Required Skills:
Quality Control
Our client a global leader in life sciences and diagnostics is looking for Quality Control Associate in Tucson AZ. Job Duration: Long Term Contract(Possibility Of Extension)Job Responsibilities:The Quality Control Associate will perform testing of raw materials in-process materials and finished goo...
Our client a global leader in life sciences and diagnostics is looking for Quality Control Associate in Tucson AZ.
Job Duration: Long Term Contract(Possibility Of Extension)
Job Responsibilities:
The Quality Control Associate will perform testing of raw materials in-process materials and finished goods in a regulated cGMP/ISO 13485 environment. This role is responsible for maintaining accurate documentation supporting quality investigations and ensuring compliance with regulatory standards. The ideal candidate will work cross-functionally to support QC operations reagent manufacturing and continuous improvement initiatives.
Key Responsibilities:
- Perform inspection and testing of raw materials in-process and finished goods.
- Document results complete batch records and generate QC reports.
- Maintain Device History Records (DHR) and ensure compliance with cGMP and regulatory requirements.
- Conduct data analysis and support process monitoring and trending.
- Investigate Out of Specification (OOS) results and support CAPA activities.
- Perform routine maintenance and calibration checks of lab equipment.
- Support environmental monitoring and maintain QC lab readiness.
- Assist in reagent formulation and manufacturing activities.
- Manage lab inventory supplies and vendor coordination.
- Participate in validations method development and process transfers.
Quality & Compliance:
- Ensure adherence to FDA ISO GMP and OSHA standards.
- Maintain accurate documentation for material handling storage and release.
- Support audits safety reporting and quality system compliance.
Qualifications:
- High School Diploma (Associates or Bachelors in Life Sciences preferred).
- 07 years of experience in a laboratory or regulated industry.
- Experience in cGMP/GLP/ISO environments preferred.
Skills & Requirements:
- Strong analytical troubleshooting and data analysis skills.
- Hands-on lab experience (pipetting titration spectroscopy etc.).
- Excellent documentation and organizational skills.
- Ability to work in a fast-paced team-oriented environment.
- Familiarity with Lean/6S practices is a plus.
Company Benefits: Medical Dental Vision Paid Sick leave 401K
If interested please share your update resume at /
Required Skills:
Quality Control
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