Quality Control Analyst I
AllSTEM Connections
Qualifications:
• Bachelor's Degree in a related field • Strong attention to detail and organizational skills • Ability to follow instructions and GMP procedures accurately • Ability to work independently and manage routine laboratory tasks with minimal supervision • Comfortable performing routine and repetitive laboratory and documentation activities • Strong time management skills and ability to support multiple priorities simultaneously • at least 1-2 years of laboratory experience. (GMP QC laboratory or pharmaceutical industry experience preferred) • Previous experience in a fast-paced GMP QC laboratory environment preferred • Basic exposure to HPLC, pH, Density, Osmolality, FT-IR, analytical balances, micropipettes, or analytical laboratory testing strongly preferred • Familiarity with ICH, USP, 21CFR Part 210, and 211 preferred
Responsibilities:
• Support routine QC laboratory testing using pH, Osmolality, FT-IR, for in-process, finished product, and stability samples testing. • Assist with sample management activities including but not limited to sample login, labeling, tracking, storage, and shipment coordination • Support stability program execution including sample pulls, submissions, inventory management, and tracking activities • Perform accurate documentation and data recording in accordance with cGMP, ALCOA+, and data integrity requirements • Maintain laboratory notebooks, worksheets, logbooks, and electronic records in an audit-ready state • Assist with laboratory investigations including OOS results, deviations, invalid assays, and other quality system activities • Support laboratory maintenance, calibration, housekeeping, and audit readiness activities • Work cross-functionally with QA, Manufacturing, Stability, Microbiology and external laboratories to support testing timelines and operational priorities • Follow approved SOPs, test methods, and other GMP laboratory procedures with minimal supervision • Perform self-review of data and documentation for accuracy and completeness prior to submission for secondary review • Adapt quickly to changing priorities, urgent sample requests, and fluctuating laboratory workload Equal Opportunity Employer / Disabled / Protected Veterans The Know Your Rights poster is available here:
The pay transparency policy is available here:
For temporary assignments lasting 13 weeks or longer, AllSTEM Connections is pleased to offer major medical, dental, vision, 401k and any statutory sick pay where required. We are committed to working with and providing reasonable accommodations to individuals with disabilities. If you need a reasonable accommodation for any part of the employment process, please contact your staffing representative who will reach out to our HR team. AllSTEM Connections participates in the E-Verify program in certain locations as required by law. Learn more about the E-Verify program.
We also consider for employment qualified applicants regardless of criminal histories, consistent with legal requirements, including, if applicable, the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance. Pursuant to applicable state and municipal Fair Chance Laws and Ordinances, we will consider for employment-qualified applicants with arrest and conviction records, including, if applicable, the San Francisco Fair Chance Ordinance. For Los Angeles, CA applicants: Qualified applications with arrest or conviction records will be considered for employment in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act. Additional Skills (none specified)
AllSTEM Representative Contact Info Account Executive:
Broughton
Branch Phone:
View phone number on click.appcast.io
Location:
Ontario, CA
• Bachelor's Degree in a related field • Strong attention to detail and organizational skills • Ability to follow instructions and GMP procedures accurately • Ability to work independently and manage routine laboratory tasks with minimal supervision • Comfortable performing routine and repetitive laboratory and documentation activities • Strong time management skills and ability to support multiple priorities simultaneously • at least 1-2 years of laboratory experience. (GMP QC laboratory or pharmaceutical industry experience preferred) • Previous experience in a fast-paced GMP QC laboratory environment preferred • Basic exposure to HPLC, pH, Density, Osmolality, FT-IR, analytical balances, micropipettes, or analytical laboratory testing strongly preferred • Familiarity with ICH, USP, 21CFR Part 210, and 211 preferred
Responsibilities:
• Support routine QC laboratory testing using pH, Osmolality, FT-IR, for in-process, finished product, and stability samples testing. • Assist with sample management activities including but not limited to sample login, labeling, tracking, storage, and shipment coordination • Support stability program execution including sample pulls, submissions, inventory management, and tracking activities • Perform accurate documentation and data recording in accordance with cGMP, ALCOA+, and data integrity requirements • Maintain laboratory notebooks, worksheets, logbooks, and electronic records in an audit-ready state • Assist with laboratory investigations including OOS results, deviations, invalid assays, and other quality system activities • Support laboratory maintenance, calibration, housekeeping, and audit readiness activities • Work cross-functionally with QA, Manufacturing, Stability, Microbiology and external laboratories to support testing timelines and operational priorities • Follow approved SOPs, test methods, and other GMP laboratory procedures with minimal supervision • Perform self-review of data and documentation for accuracy and completeness prior to submission for secondary review • Adapt quickly to changing priorities, urgent sample requests, and fluctuating laboratory workload Equal Opportunity Employer / Disabled / Protected Veterans The Know Your Rights poster is available here:
The pay transparency policy is available here:
For temporary assignments lasting 13 weeks or longer, AllSTEM Connections is pleased to offer major medical, dental, vision, 401k and any statutory sick pay where required. We are committed to working with and providing reasonable accommodations to individuals with disabilities. If you need a reasonable accommodation for any part of the employment process, please contact your staffing representative who will reach out to our HR team. AllSTEM Connections participates in the E-Verify program in certain locations as required by law. Learn more about the E-Verify program.
We also consider for employment qualified applicants regardless of criminal histories, consistent with legal requirements, including, if applicable, the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance. Pursuant to applicable state and municipal Fair Chance Laws and Ordinances, we will consider for employment-qualified applicants with arrest and conviction records, including, if applicable, the San Francisco Fair Chance Ordinance. For Los Angeles, CA applicants: Qualified applications with arrest or conviction records will be considered for employment in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act. Additional Skills (none specified)
AllSTEM Representative Contact Info Account Executive:
Broughton
Branch Phone:
View phone number on click.appcast.io
Location:
Ontario, CA
Vacancy posted 2 days ago
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