Quality control Analyst I

AllSTEM Connections; Camarillo (CA); On-site; USD 50,000 - 70,000; Full time

Job summary

AllSTEM Connections is looking for a laboratory technician in Camarillo, California, to support routine QC laboratory testing and various sample management activities. Candidates should have 1-2 years of experience in a GMP QC laboratory and a thorough understanding of laboratory practices.

The ideal candidate will excel in attention to detail and organizational skills while managing routine laboratory tasks. Proficiency in laboratory equipment such as HPLC and micropipettes is strongly preferred.

Qualifications

• 1-2 years of laboratory experience, preferably in GMP QC laboratory or pharmaceutical industry.
• Basic knowledge of ICH, USP, 21CFR Part 210, and 211.
• Experience in a fast-paced GMP QC laboratory environment preferred.

Responsibilities

• Support routine QC laboratory testing for various samples.
• Assist in sample management activities.
• Perform accurate documentation and maintain laboratory records.
• Support laboratory investigations and quality system activities.
• Collaborate with various departments to meet operational priorities.

Skills

Attention to detail

Organizational skills

Time management

Ability to work independently

Familiarity with GMP procedures

Basic lab equipment knowledge

Tools

HPLC

Micropipettes

Analytical balances

Job description

Qualifications

• 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