US
0 suggestions are available, use up and down arrow to navigate them
PROCESSING APPLICATION
Hold tight! We’re comparing your resume to the job requirements…
ARE YOU SURE YOU WANT TO APPLY TO THIS JOB?
Based on your Resume, it doesn't look like you meet the requirements from the employer. You can still apply if you think you’re a fit.
Job Requirements of QA Specialist II:
-
Employment Type:
Full-Time
-
Location:
Houston, TX (Onsite)
Do you meet the requirements for this job?
QA Specialist II
Tailored Management Services Inc
Houston, TX (Onsite)
Full-Time
Title: QA Specialist II
Location: 14905 Kirby Drive, Houston, TX - 77047
Contract: 6+ Months - possibility for extension or FTE conversion
Shift: Night Shift (Sunday to Thursday 11pm - 8am)
Pay Rate:: $30.77 - $51.28/Hour + Benefits
Job Description:
The QA Specialist Level II-Quality Operations represents the QA department ensuring that quality requirements are met. Support manufacturing operations and all support groups related to manufacturing execution. Supports investigations using problem solving tools. Supports corrective actions and change controls as needed. Review and approve GMP master documents and executed GMP documents from QC, manufacturing, material management, and any other department that supports lot production. Other duties include tracking quality records, QA on the floor execution, and overall cGMP compliance.
Bachelor Degree - Life Science or Engineering
GMP experience in the biologics and pharma industry. Working knowledge of equipment/facilities qualifications, GMP and GDP environment
Location: 14905 Kirby Drive, Houston, TX - 77047
Contract: 6+ Months - possibility for extension or FTE conversion
Shift: Night Shift (Sunday to Thursday 11pm - 8am)
Pay Rate:: $30.77 - $51.28/Hour + Benefits
Job Description:
The QA Specialist Level II-Quality Operations represents the QA department ensuring that quality requirements are met. Support manufacturing operations and all support groups related to manufacturing execution. Supports investigations using problem solving tools. Supports corrective actions and change controls as needed. Review and approve GMP master documents and executed GMP documents from QC, manufacturing, material management, and any other department that supports lot production. Other duties include tracking quality records, QA on the floor execution, and overall cGMP compliance.
- Verify the company’s compliance with ISO/GMP quality system requirements and other regulatory guidance as appropriate.
- provide oversight for compliance of CAPA and minor deviations.
- Perform QA walkthroughs and work closely with manufacturing and support groups to resolve any issues identified during the walkthroughs.
- Support activities that involves QA presence on the floor.
- Review Master Batch Records (MBR) and supporting documents to support batch disposition. Perform review/release of Buffer/ media as needed.
- Perform other duties as assigned.
Bachelor Degree - Life Science or Engineering
GMP experience in the biologics and pharma industry. Working knowledge of equipment/facilities qualifications, GMP and GDP environment
- Experience with regulations (US, EU and other)
- Experience in a biopharmaceutical manufacturing environment
- Experience in equipment / facilities / utilities validation activities
- Strong experience in GDP
Get job alerts by email.
Sign up now!
Join Our Talent Network!