USA - Senior Quality Compliance Specialist
$50 - $76.42 per hourThe Fountain Group
The Fountain Group is currently seeking a Senior Quality Compliance Specialist for a prominent client of ours. This position is located in Newbury Park (Thousand Oaks), CA . Details for the position are as follows: Pay: $50-76.42/hr., based on years of experience. 12-month assignment with possibility for extension or conversion based on performance and budget. Responsibilities: Drive analytical method validation/ transfer of laboratory methodologies Support the execution and issue resolution (e.g., discrepancies) and completion approval of test plans/protocols Support troubleshooting of analytical methods Ensure laboratory equipment is maintained in a validated state and that all analytical methods transferred follow company and regulatory requirements. Responsible for protocol and report generation and other technical documents as required. This may include supporting raw material qualification for new products Use sound scientific principles and statistical techniques to solve problems and make recommendations. May support the installation, operational qualification (IOQ), maintenance and troubleshooting of instrumentation in the AQC group. Responsible for deliverables to ensure timelines and milestones are met. Qualifications: Strong technical writing skills and able to write generate technical documents and reports that meet company and regulatory requirements Knowledge of analytical methods and operations with strong emphasis in problem‑solving. Knowledge about analytical method validation. Intermediate statistical knowledge and experience with data analysis Knowledge concerning cGMP, especially lab related topics such as method validation and unexpected results investigation. Basic knowledge about regulatory requirements concerning analytical instrumentation, and test methods Substantial knowledge and understanding in terms of regulatory standards requirements e.g., CGMP, QSR, USP, 21CFR, ICH etc. If you are interested in hearing more about the position, please respond to this posting with your resume attached. Please forward this posting to any friends or colleagues as we do offer a Referral Bonus for any candidate hired. By applying for this job, you agree to receive calls, AI‑generated calls, text messages, or emails from and its affiliates, and contracted partners. Frequency varies for text messages. Message and data rates may apply. Carriers are not liable for delayed or undelivered messages. You can reply STOP to cancel and HELP for help. You can access our privacy policy at Privacy Policy. #J-18808-Ljbffr
$50 - $76.42 per hour
...A leading staffing agency is seeking a Senior Quality Compliance Specialist in Thousand Oaks, CA. The role involves driving analytical method validation and maintaining regulatory compliance in laboratory settings. Ideal candidates will have strong technical writing skills...Senior- Planet Pharma Group is seeking a Quality Assurance Associate in Thousand Oaks, California. The role involves receiving, cleaning, and evaluating product complaint samples, as well as managing inventory and authoring technical reports. A Bachelor’s Degree in Life Sciences...Senior
- ...position in Thousand Oaks, CA. The role requires a Bachelor's degree in Life Sciences and at least 1 year of related experience in quality assurance or manufacturing within the GMP pharmaceutical or medical device industry. Responsibilities include evaluating product complaint...Senior
- ...Thousand Oaks, California, is seeking a professional to train attorneys and manage legal documentation. The role involves ensuring compliance with company policies, auditing files, and updating case information. Ideal candidates will work in a dynamic environment...Senior
$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...SeniorSummer work- ...Job Title: Quality Complaints, Senior Associate, GMP/Medical Device(JP10448) Location: Thousand Oaks, CA. Employment Type: Contract Business Unit: Product Complaints & Surveillance Duration: 1+ years with likely extensions or conversion to FTE Notes: 100% onsite Posting...SeniorContract work
- ...degree. Nice to have: documentation practices, GMP, previous lab experience. Hiring Manager Notes • What type of qualities/characteristics are you looking for in candidates to work best with your team? Self-motivated individuals interested in gaining...SeniorWork experience placementSummer workLocal areaRelocationFlexible hoursShift work
$27 - $29 per hour
...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. Top 3 Must Have Skill Sets:...SeniorHourly payFull timeLocal areaFlexible hours- ...Job Title: Quality Assurance Senior Associate, Biopharma (JP10382) Location: Thousand Oaks, CA. 91320 Employment Type: Contract Business Unit... ...Under general supervision, the role provides support and compliance oversight to Manufacturing and Facilities & Engineering staff...SeniorContract work
- Our client is seeking a dedicated and detail-oriented Quality Complaints Senior Associate to join a dynamic team focused on maintaining the highest... ...resolution and quality documentation efforts. Maintain compliance with regulatory and company standards during all processes...Senior
- ...Job Title: Quality Assurance Senior Associate – (JP10393) Location: Thousand Oaks, CA. 91320 Employment Type: Contract Business Unit: Plant... ...Under general supervision, the role provides support and compliance oversight to MFG and F&E staff in the execution of their processes...SeniorContract workShift workNight shiftDay shiftAfternoon shift
- Aditi Consulting is seeking a Specialist Business Systems Analyst in Thousand Oaks, California. The role involves providing real-time QA support in a manufacturing setting, focusing on compliance and oversight in a GMP environment. Candidates should have strong critical...Senior
- ...prominent technology firm in California seeks an experienced MCS Senior Associate Quality Assurance to oversee Drug Substance manufacturing... ...providing PQA support, reviewing batch records, and ensuring compliance with quality documentation. Ideal candidates should have a...Senior
- BioSpace is seeking a Senior Associate Quality Assurance in Thousand Oaks, California. In this role, you will ensure GMP compliance for final drug product procedures and documentation. Responsibilities include approving clinical labels, inspecting clinical packs, and supporting...SeniorFlexible hours
$27 - $29 per hour
...Degree in Life Sciences or related field, or equivalent combination of education and/or experience. Typically 1+ years of related quality assurance or manufacturing experience in a GMP pharmaceutical or medical device industry. Top 3 Must Have Skill Sets Attention to...SeniorHourly payFull timeLocal areaFlexible hours$40 - $44 per hour
...experience in engineering and manufacturing, particularly within regulated environments. Responsibilities include leadership in project execution, quality compliance, and validation strategy development. This is a contract position paying $40-$44/hour. #J-18808-Ljbffr...SeniorContract work- SSi People is looking for an MCS Senior Associate Quality Assurance in Thousand Oaks, California. This role requires delivering real-time quality... ...production facility. Responsibilities include providing compliance support and overseeing manufacturing operations....SeniorShift work
- divh2Senior Compliance Officer/h2pLocation: Irvine, CA/ppDuration: 6 month plus contract or... ...meeting respective regulatory compliance. The Senior Compliance Officer - Contractor will... ...planning through reporting and produce quality, timely deliverables./ppObtain...SeniorContract workFor contractorsWork at office
$116k - $182.27k
...Description About the role The Senior Project Management Lead is a... ...phase‑gate deliverables to ensure quality and readiness. Train and coach... ..., budget, quality, and compliance targets. Manage core project planning... ...pay practices. For Location: USA - CA - Thousand Oaks - Rancho...SeniorMinimum wageFull timeTemporary workWork at officeLocal areaFlexible hoursWeekend work- US Tech Solutions is seeking a Senior Associate, Quality Assurance to provide onsite QA support at their Thousand Oaks location. The role involves rotating between day and swing shifts, providing oversight of Clinical/Commercial drug substance production. The ideal candidate...SeniorRotating shiftDay shiftAfternoon shift
- InstantServe LLC is seeking a Senior Compliance Officer based in Westlake Village, CA. This role emphasizes ensuring compliance with federal and state regulations within mortgage lending. Key responsibilities include conducting compliance tests, evaluating loan processes...SeniorContract work
- ...strong experience in project coordination, EHS training, and data analysis tools like Power BI and Excel. With a focus on quality and compliance, the role involves stakeholder engagement and maintaining project documentation. The position offers a hybrid work model and...SeniorContract work
- ...Clinical Supply Chain Senior Associate - Thousand Oaks, CA Pay Rate: $40.00/Hr. on W2 These are 9 Months Contract... ...emphasis on vendor management, logistics oversight, and quality compliance. They should be proficient in managing clinical shipments globally...SeniorPermanent employmentContract work
$34 - $38 per hour
...for a big biopharma leader. Your focus will be enabling effective planning, tracking, and delivery of EHS projects emphasizing quality, compliance, and operational performance. You will engage with stakeholders to support strategy implementation, compliance, and financial...SeniorHourly payContract work- The Steely Group is looking for a dedicated Quality Complaints Senior Associate located in Thousand Oaks, California. This role involves managing product complaint evaluations and ensuring accurate documentation in a fast-paced GMP environment. The ideal candidate should...Senior
- ...Sr. Regulatory Affairs Specialist 100% ONSITE in Westlake Village, California... ...Caldera Medical's Mission - To Improve the Quality of Life for Women! Message from the Hiring... ...documentation for medical device approvals in compliance with EU MDR, MDSAP, NMPA, TGA, ANVISA,...SeniorWork at officeLocal areaWorldwide
$132.77k - $165.98k
Senior Contracts Administrator This position requires a seasoned contracts individual who is skilled in complex negotiation, management... ...the bid/no bid decision for submission. Responsible for the quality and compliance of each submitted proposal through collaborative interaction...SeniorFull timeContract workWork at officeFlexible hours$28.85 - $38.46 per hour
...Job Description Job Description Job Title: Quality Systems Specialist Job Description The Quality Systems Specialist is responsible for... ...environment to coordinate the document control system and ensure compliance with both internal and external requirements....Contract workTemporary workWork at office- Senior Associate Quality Assurance The Sr. Associate QA will be a member of the Amgen Thousand Oaks Clinical Final Drug Product QA team, responsible for ensuring GMP compliance of all final drug product procedures and documentation. The role requires meticulous inspection...SeniorFlexible hours
- Senior Associate Quality Assurance The Sr. Associate Quality Assurance position supports Amgen’s Quality Assurance program under the Plant QA... ...-time troubleshooting and triage with quality and aseptic compliance. Support quality related decision making involving non-routine...SeniorFlexible hoursShift workAfternoon shift
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