Quality Control Associate: GMP Analytics, Flexible Hours
Aditi Consulting
An established industry player in pharmaceutical manufacturing is seeking a dedicated Quality Assurance Associate. This role involves performing routine laboratory procedures, conducting analytical testing, and ensuring compliance with safety guidelines and regulatory requirements. Ideal candidates will demonstrate strong communication skills, attention to detail, and the ability to manage multiple priorities in a dynamic environment. Join a team that values flexibility and continuous improvement while contributing to vital research and manufacturing processes in biotechnology. This is an exciting opportunity to grow your career in a supportive and innovative setting. #J-18808-Ljbffr Aditi Consulting
$45 - $58 per hour
...responsibilities include executing analytical method transfers for raw... ...within a cGMP environment in Quality Control. You will conduct biological,... ...areas. Salary: $45 - $58 per hour Shift: First Work hours: 8 AM... ...Laboratory/Sciences GMP manufacturing GDP Laboratory...SuggestedHourly payTemporary workLocal areaShift work$25 - $27 per hour
...related field, OR a candidate with hands‑on QC GMP experience who may not hold a degree. Highly trainable and eager to learn analytical testing techniques in a regulated QC lab.... ...and related activities in support of Quality Control operations. The role requires adherence...SuggestedContract workWork at officeMonday to Friday- Quality Control Specialist, Microbiology In this vital role, you will... ...collaboration, and approval of associated documentation. Generate... ...experience in a fast‑paced, flexible GMP laboratory. Ability to... ...triage and close deviations and analytical test result assessments in...Flexible hoursContract workWork experience placementWeekend work
- BioSpace is seeking a Senior Associate Quality Assurance in Thousand Oaks, California, to oversee... ...involves daily oversight and various quality control responsibilities to maintain product integrity. The ideal candidate will bring GMP experience and a strong understanding of...Suggested
$44.97 - $46.52 per hour
...Group is currently seeking a Quality Compliance Specialist for a prominent... ...,CA . Job Title: Quality Control Validation Scientist Location: Onsite (Mon-Fri, Flexible: 8:00 AM-5:00 PM or 9:00 AM-6:... ...will support Quality Control Analytical (AQC) activities in a cGMP...Flexible hoursWork at office- ...responsibilities are to execute analytical method transfers, including... ...use in a cGMP environment in Quality control. You will be responsible for... ...collected from manufacturing areas. Hours: Mon-Fri 8am to 5 or 9am to 6... ..., pharmaceutical or similar GMP manufacturing environment is...Work experience placementWork at officeLocal areaShift workWeekend work
- ...career. Drug Product Quality Assurance Specialist What... ...activities associated with the aseptic Drug... ...Actions (CAPAs), Change Controls and document revision,... ...monitoring systems within GMP manufacturing environments... ...insurance, and flexible spending accounts A discretionary...Flexible hours
- ...Responsibilities include conducting various biological and chemical analyses in a cGMP environment, handling multiple tasks and maintaining quality standards. The ideal candidate will have a strong background in science, preferably with a bachelor’s degree, and a minimum of 2...
- 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...
- ...are looking for a motivated and hands‑on Quality Systems Specialist to join our team. How... ...compliance with Good Manufacturing Practice (GMP) requirements. This role is responsible... ...oversight of quality Events and Change Control. The Quality Systems Specialist works closely...Full timeVisa sponsorshipWork visaMonday to Friday
$45 per hour
...responsibilities are to execute analytical method transfers, including... ...use in a cGMP environment in Quality control. You will be responsible for... ...areas. salary: $45 - $58 per hour shift: First work hours... ...Laboratory/Sciences GMP manufacturing GDP Laboratory...Hourly payPermanent employmentTemporary workWork experience placementLocal areaShift work- ...skills Ability to follow instructions and GMP procedures accurately Ability to work... ...to HPLC, pH, Density, Osmolality, FT-IR, analytical balances, micropipettes, or analytical laboratory... ..., deviations, invalid assays, and other quality system activities Support laboratory...
- ...Thousand Oaks, California seeks a Senior Associate Quality Control - Microbiology to support the QC... ...and equipment operation in a fast-paced GMP laboratory. The ideal candidate will have... ...benefits package is offered along with flexible work models. #J-18808-Ljbffr AmgenFlexible hours
- Amgen is seeking a Senior Associate Quality Assurance in Thousand Oaks, CA, to oversee Drug Product manufacturing and ensure adherence to quality... .... The ideal candidate will have a strong background in GMP, effective communication skills, and the ability to support manufacturing...
- ...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 and...
- Amgen in Thousand Oaks, CA is seeking a Drug Product Quality Assurance Specialist to provide quality oversight for aseptic Drug Product... ...compliance with cGMP and support deviations, CAPAs, change controls, and document management within the Quality Management System....
- Associate Quality Control - TIM Lab Analyst Join Amgen's mission of serving patients living with serious... ...Report, evaluate, trend and approve analytical data. Troubleshoot, solve problems... .... Must be detail oriented. Must be flexible and adaptable to changing priorities...Flexible hoursWork experience placementWork at office
- ...motivated and hands-on Quality Operations Specialist... ...Manufacturing Practice (GMP) requirements. This... ...batch documentation and analytical data, management of... ...data, test results, and associated documentation to support... ...and support change control activities, including...Full timeVisa sponsorshipWork visaMonday to Friday
- 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
- A leading consulting firm in California is seeking a Senior Associate, Quality Assurance to oversee Drug Substance manufacturing areas and ensure compliance within a GMP environment. The role involves real-time QA support, along with responsibilities like batch record review...Full timeContract work
$85k - $106.5k
...Quality Control Analyst III in Camarillo, CA Build your future at Curia, where our work has the power to save lives. The Quality Control... ...or GLP pharmaceutical industry environment Willing to work flexible hours (nights and weekends), as‑needed (overtime eligible)...Flexible hoursFull timeContract workWork experience placementWork at officeNight shiftWeekend work$22 - $32 per hour
...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 and operation...Summer work- Las Virgenes Municipal Water District is seeking a Quality Assurance/Quality Control Specialist. This role is pivotal in maintaining the laboratory... ...’s degree in a relevant science and three years of analytical experience are required. The position is based in Calabasas...Local area
- ...general supervision of the Water Quality Supervisor, a Quality Assurance/Quality Control Specialist maintains the water... ...(TNI) standards. Reviews analytical and QA/QC data generated by laboratory... ...A California Water Environment Association (CWEA) Laboratory Analyst Grade...Work at officeLocal area
- BioSpace is seeking a Senior Associate for Quality Control in Microbiology in Thousand Oaks, California. This role involves supporting the QC Microbiology... ...health insurance, retirement savings plans, and flexible work options. Join BioSpace and contribute to innovative...Flexible hours
- 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
$76.41k - $94.38k
...complaints for compliance and accuracy. Audit monthly complaint quality, sub‑servicer functions, and internal complaint operations.... ...adherence to procedures and regulatory requirements. Conduct quality control reviews of internal complaint operations’ primary processes,...$45 per hour
...responsibilities are to execute analytical method transfers, including... ...use in a cGMP environment in Quality control. You will be responsible for... ...areas. salary: $45 - $58 per hour shift: First work hours... ...Control biotechnology GMP Laboratory functions...Hourly payPermanent employmentTemporary workWork experience placementLocal areaShift work$50 per hour
...Analyst II to support critical quality control operations in a cutting-edge... ...on-site opportunity to drive analytical excellence and ensure the... ...Contract salary: $50 - 58 per hour work hours: 9 to 5... ..., pharmaceutical, or similar GMP manufacturing quality operations...Hourly payContract workTemporary workWork experience placementLocal area$84k - $105.6k
...Quality Control Microbiologist III – Camarillo, CA The Quality... ...support activities associated with Change Control,... ...environment with QC Analytical and Quality Assurance... ...industry experience in a GMP sterile finish or... ...environment Willing to work flexible hours (nights and weekends)...Flexible hoursNight shiftWeekend work
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