Quality Control Associate
$45 - $58 per hourRandstad
As a QC Analyst II, you will support various activities within the QC department. Key responsibilities include executing analytical method transfers for raw materials within a cGMP environment in Quality Control. You will conduct biological, chemical, and physical analyses on raw materials, in-process samples, drug substance, and final product samples, as well as samples collected from manufacturing areas. Salary: $45 - $58 per hour Shift: First Work hours: 8 AM - 5 PM Education: Bachelors Responsibilities Conduct biological, chemical, and physical analyses on samples including raw materials, initial, in‑process, and final products, and samples collected from environmental monitoring according to SOP and pre‑approved protocols. Drive implementation of new methodologies or new sample types into existing QC laboratory methods. Support investigation of nonconformances and troubleshoot unexpected results. Handle multiple tasks concurrently, including testing and inventory management, in a timely manner. Review test data and overall documentation practices (CGDP). May perform release functions in LIMS or other computerized systems. Support generation and documentation of validation protocol deliverables. Draft and update QC SOPs as required. Perform test equipment maintenance and calibrations as required. May perform other duties as assigned. Essential Functions Work in a smoke‑free environment. Wear steel toe shoes. Manually lift up to 50 lbs. Stand for 5 hours at a time. Skills Quality Control Quality Assurance Laboratory/Sciences GMP manufacturing GDP Laboratory functions Product Inspection Production Control Pharmaceutical Qualifications Minimum 2 years of experience Experience level: Experienced Bachelor's degree 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. We offer a comprehensive benefits package, including medical, prescription, dental, vision, AD&D, life insurance, short‑term disability, and a 401(k) plan (based on eligibility). This posting is open for thirty (30) days. Qualified applicants in San Francisco with criminal histories will be considered for employment in accordance with the San Francisco Fair Chance Ordinance. Qualified applicants 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. We will consider for employment all qualified Applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance. For reasonable accommodation, please contact HR support at View email address on click.appcast.io. #J-18808-Ljbffr
- ...department. Key responsibilities are to execute analytical method transfers, including raw materials, for use in a cGMP environment in Quality control. You will be responsible for conducting biological or chemical and physical analyses on raw materials, in-process samples, drug...Suggested
$28 - $32 per hour
...Specialist to join our team. The QA/QC Specialist assists the Quality Systems Manager (Burbank facility), Regulatory Manager or Radioassay... ...(Valencia facility) in maintaining an effective Quality Control Program, which consistently delivers high quality Company products...SuggestedHourly payWork at office- Quality Control Specialist, Microbiology In this vital role, you will provide technical and operational leadership for the QC Microbiology... ..., data review, investigation collaboration, and approval of associated documentation. Generate and maintain complete, accurate,...SuggestedContract workWork experience placementFlexible hoursWeekend work
$45 - $58 per hour
...department. Key responsibilities are to execute analytical method transfers, including raw materials, for use in a cGMP environment in Quality control. You will be responsible for conducting biological or chemical and physical analyses on raw materials, in-process samples, drug...SuggestedHourly payTemporary workShift work$45 per hour
...department. Key responsibilities are to execute analytical method transfers, including raw materials, for use in a cGMP environment in Quality control. You will be responsible for conducting biological or chemical and physical analyses on raw materials, in-process samples, drug...SuggestedHourly payPermanent employmentTemporary workWork experience placementLocal areaShift work- BioSpace is seeking a Senior Associate Quality Assurance in Thousand Oaks, California, to oversee drug product manufacturing areas while ensuring... .... This role involves daily oversight and various quality control responsibilities to maintain product integrity. The ideal...
- Drug Product Quality Assurance Specialist What you will do In this vital role within the... ...Quality oversight to operational activities associated with the aseptic Drug Product... ...and Preventive Actions (CAPAs), Change Controls and document revision, review and approval...Flexible hours
$45 - $58 per hour
...California. This role includes conducting analyses on samples collected from various manufacturing processes and supporting the quality control team in investigation and troubleshooting tasks. The position requires a Bachelor's degree and a minimum of two years of...Hourly payTemporary work$60k - $85k
...driven individual to join our team as a Quality Assurance Specialist reporting to the... ...teams to develop and implement quality control processes, ensuring that our offerings meet... ...supporting documentation; completion of associated records and logs; communication of...Work experience placement- Join Initial Therapeutics, Inc. as a Senior Associate in Quality Control - Microbiology. This role involves supporting the QC Microbiology and Environmental Monitoring team, conducting investigations and microbiological testing, and maintaining laboratory compliance. The...
$22 - $32 per hour
...in Life Sciences or related field or the equivalent combination of education and/or experience. Typically 1 plus years of related quality assurance or manufacturing experience in a GMP pharmaceutical or medical device industry. Tasks and Expectations Evaluate documentation...Summer work- ...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...
$85k - $106.5k
...Quality Control Analyst III in Camarillo, CA Build your future at Curia, where our work has the power to save lives. Curia is a global contract development and manufacturing organization (CDMO) with over 30 years of experience partnering with pharmaceutical and biotech...Contract workWork experience placementWork at officeFlexible hoursNight shiftWeekend work- ...are looking for a motivated and hands-on Quality Operations Specialist to join our team.... ...Review analytical data, test results, and associated documentation to support batch... ...development Manage and support change control activities, including impact assessments...Full timeVisa sponsorshipWork visaMonday to Friday
$45 per hour
...department. Key responsibilities are to execute analytical method transfers, including raw materials, for use in a cGMP environment in Quality control. You will be responsible for conducting biological or chemical and physical analyses on raw materials, in-process samples, drug...Hourly payPermanent employmentTemporary workWork experience placementLocal areaShift work$50 per hour
...advance your pharmaceutical career with a global industry leader? We are seeking a detail-oriented QC Analyst II to support critical quality control operations in a cutting-edge cGMP manufacturing facility. This is a fantastic on-site opportunity to drive analytical...Hourly payContract workTemporary workWork experience placementLocal area- ...Amgen SA in Thousand Oaks, California, seeks a Senior Associate Quality Assurance professional to provide oversight for Drug Product manufacturing. This role includes reviewing electronic batch records and ensuring compliance with GMP standards. The ideal candidate will...Shift work
- Amgen is seeking a Senior Associate Quality Assurance in Thousand Oaks, CA, to oversee Drug Product manufacturing and ensure adherence to quality processes. The ideal candidate will have a strong background in GMP, effective communication skills, and the ability to support...
- SSi People is looking for an MCS Senior Associate Quality Assurance in Thousand Oaks, California. This role requires delivering real-time quality assurance support in a drug substance production facility. Responsibilities include providing compliance support and overseeing...Shift work
- ...complaints. Candidates should hold a Bachelor's Degree in Life Sciences or a related field, with at least 1 year of experience in quality assurance or manufacturing in a GMP environment. Strong attention to detail, project management skills, and proficiency in word processing...
- BioSpace is seeking a Drug Product Quality Assurance Specialist in Thousand Oaks, California. This role involves ensuring compliance with cGMP standards and providing quality oversight for drug product manufacturing. The ideal candidate will have a Bachelor's degree in...
- Amgen Inc. (IR) is looking for a Drug Product Quality Assurance Specialist in Thousand Oaks, California. This full-time role involves overseeing quality assurance in drug product manufacturing operations, ensuring compliance with regulatory and cGMP standards. The ideal...Full time
- Amgen SA is seeking a Drug Product Quality Assurance Specialist in Thousand Oaks, California. This role involves providing quality oversight for operational activities associated with aseptic drug product manufacturing, ensuring adherence to cGMP requirements while collaborating...
- Amgen is seeking a Drug Product Quality Assurance Specialist in Thousand Oaks, CA. This role involves ensuring quality oversight of aseptic drug product manufacturing and compliance with regulatory requirements. The ideal candidate will possess significant experience in...
- A biopharmaceutical company in Thousand Oaks, California is seeking a Quality Operations Specialist. The role encompasses ensuring GMP compliance, supporting batch documentation review, and collaborating with cross-functional teams. Ideal candidates will have a Bachelor...Full time
- ...processing solutions to its clients and serves the Community Association Management industry nationwide through its technology‑forward... ...to perform at your best. Together we win! The Opportunity The Quality Assurance Analyst is responsible for performing quality assurance...Local areaImmediate startFlexible hours
$70.3k - $85k
...ask for an accommodation or an alternative application process. Quality Assurance Specialist Full-time Regular Professional Camarillo,... ...regulatory requirements and industry standards. Draft, revise, and control critical quality documents, technical specifications, and...Full timeTemporary workWork at officeMonday to Friday$55k - $90k
...international community. EBAD seeks an experienced Quality Professional, inspector, or... ...verification that manufactured product and associated processes are compliant to defined... ...including configuration management and document control Experience reviewing and revising...Work at office$75k - $112k
...The Quality Assurance Specialist is responsible for planning, designing, executing, and documenting software testing activities across... ...requirements based on contract needs Must comply with all ITAR/EAR export control regulations Background check required Avum, Inc. is an Equal...Contract workLocal areaRemote work- ...Job Description Job description Immediate Opening! Quality Associate - Data Entry We are seeking a highly detail-oriented Quality... ...including quality inspections, corrective actions, and change control in a pharmaceutical or medical device environment. Understanding...Work experience placementImmediate start
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