- Astrix Technology (Los Angeles, CA)
- …We are seeking a QA Document Specialist to join a leading global pharmaceutical manufacturing company. In this role, you'll support the QA department by processing ... etc.) + Minimum 2 years of document control experience within a GMP pharmaceutical or biotech environment + Knowledge of document management systems (Master Control… more
- Astrix Technology (San Bernardino, CA)
- …- 2nd Shift** We're partnering with a rapidly expanding personal care and pharmaceutical manufacturing company in San Bernadino, CA to find a **QA Inspector** who's ... a QC/QA Inspector in a GMP-regulated environment, ideally in personal care or pharmaceutical manufacturing. + Sharp attention to detail and a keen eye for spotting… more
- Astrix Technology (Fremont, CA)
- …Apply for Job Our client, a leading organization in the pharmaceutical and biotechnology manufacturing sector, is seeking a detail-oriented **Manufacturing Assembly ... Minimum 1 year of experience in a GMP-regulated manufacturing environment ( pharmaceutical or biotechnology industry strongly preferred). + Basic computer skills (MS… more
- Astrix Technology (Los Angeles, CA)
- …products for research, clinical development and commercial application to pharmaceutical and biotechnology companies worldwide and offers a comprehensive range ... of services._ **Title:** Quality Assurance Document Control Specialist(Contract) **Location:** Fully Onsite - Torrance, CA **Schedule:** Mon - Fri 8-5pm **Pay rate:** $28-30/hr **Contract:** 3 months with potential for extension The QA Document Control… more
- Astrix Technology (Los Angeles, CA)
- …or engineering discipline + 4-7 years of experience in a GCP-Biologics or pharmaceutical environment. + CQA or other audit certifications are desirable. + Previous ... experience with TMF or electronic document management systems is a plus. We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability… more
- Astrix Technology (Los Angeles, CA)
- …Low: 28 | Pay Rate High: 35 + Added - 24/07/2025 Apply for Job Pharmaceutical Company in Los Angeles, CA is seeking a Production Chemist to join their Production ... team! This is a direct hire opportunity! Eagerly hiring! **Shift:** Monday-Friday 8-5pm, with occasional shift to 2nd (2pm-10pm) **Must have** : 1 year of HPLC **Responsibilities:** + Perform purification process by chromatography, crystallization and other… more
- Astrix Technology (San Diego, CA)
- …plus + Minimum of 3 years of QC experience in a biotech or pharmaceutical GMP environment + Prior experience in a QA department is advantageous, method validation ... + Hands-on expertise with techniques such as HPLC, GC, and Karl Fischer titration + Strong working knowledge of GMP regulations and guidelines (eg, BPF, ICH-Q7, ISO 13485, US/EU Pharmacopeia) + Proven project management skills and ability to meet ambitious… more
- Astrix Technology (Gardena, CA)
- …**Key Responsibilities:** + Review and process batch records (non-regulated to pharmaceutical -grade materials) + Transcribe data into internal databases + Ensure ... compliance with cGDP standards + Generate/review documents (eg, Certificates of Analysis) + Coordinate with labs and departments for documentation needs + Monitor task queues and maintain organized workspace + Assist with QA projects as needed **Training:**… more
- Astrix Technology (Thousand Oaks, CA)
- …working knowledge of GMP, CFR regulations, and quality systems in a pharmaceutical or life sciences environment. + Proven experience with documentation systems such ... as SOPs, CCMS, NCs, and work orders. + Technical expertise in utility, building, and production system maintenance. + Ability to read and interpret technical drawings and schematics. + Strong attention to detail and organizational skills. + Proficient in using… more
- Astrix Technology (Thousand Oaks, CA)
- …and certifications. **Qualifications & Requirements:** + In-depth knowledge of pharmaceutical filling, freeze-drying, and packaging equipment. + Expertise in pumps, ... valves, seals, motors, and lubrication practices. + Strong documentation skills and keen attention to detail. + Solid understanding of cGMP standards and predictive maintenance techniques. + Ability to read, interpret, and update engineering drawings and… more