Quality Control
Listed on 2026-07-30
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Quality Assurance - QA/QC
Quality Control - QC Analysts/Managers, QA Specialist - Analyst/Manager
We are seeking a highly skilled Method Validation / Analytical Chemist III to join our Quality Control team in Houston, TX. In this senior-level role, you will independently perform analytical method validations, verifications, technical transfers, and routine testing for clinical submission materials, including raw materials, finished products, st abilities, and cleaning validations. The ideal candidate will possess a Bachelor's degree in Chemistry, Biochemistry, or a related scientific discipline, backed by 5+ years of hands-on laboratory experience operating and troubleshooting advanced instrumentation such as HPLC, GC, CE, ICP, FTIR, and dissolution apparatus.
To excel in this position, you must have at least 2 years of experience in a strict GLP or cGMP environment, technical writing skills to author SOPs and validation protocols, and the seniority required to conduct peer data reviews, document laboratory investigations, and assist management with employee training and regulatory audit preparations.
salary: $58,240 - $90,999.99 per year
shift:
First
work hours: 8 AM - 4 PM
education:
Bachelors
We are seeking a highly skilled Method Validation / Analytical Chemist III to join our Quality Control team in Houston, TX. In this senior-level role, you will independently perform analytical method validations, verifications, technical transfers, and routine testing for clinical submission materials, including raw materials, finished products, st abilities, and cleaning validations. The ideal candidate will possess a Bachelor's degree in Chemistry, Biochemistry, or a related scientific discipline, backed by 5+ years of hands-on laboratory experience operating and troubleshooting advanced instrumentation such as HPLC, GC, CE, ICP, FTIR, and dissolution apparatus.
To excel in this position, you must have at least 2 years of experience in a strict GLP or cGMP environment, technical writing skills to author SOPs and validation protocols, and the seniority required to conduct peer data reviews, document laboratory investigations, and assist management with employee training and regulatory audit preparations.
- method validation (5 years of experience is preferred)
- HPLC (5 years of experience is required)
- GLP (5 years of experience is required)
- troubleshooting (2 years of experience is required)
- cGMP (2 years of experience is required)
- Years of experience: 2 years
- Experience level:
Experienced
Equal Opportunity
Employer:
Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.
At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants.
If you require a reasonable accommodation to make your application or interview experience a great one, please contact
Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc.
In addition, Randstad offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility).
This posting is open for thirty (30) days.
Experience- Experienced
- 2 years
- Bachelors (required)
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