CQV QA Specialist - Pharma Validation & Compliance
Clough AMEC.
Clough AMEC. is seeking an MCS Quality Assurance Specialist to work in Thousand Oaks, CA. The ideal candidate should have over 1 year of experience in commissioning, qualification, and validation processes in pharmaceutical manufacturing. This role focuses on supporting the Quality Assurance program and providing oversight of critical processes in GMP areas. Candidates will play a key role in ensuring compliance and quality at the ATO Plant. #J-18808-Ljbffr Clough AMEC.
$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...Suggested- 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...Suggested
- ...manufacturing adherence to GMP standards. Responsibilities include providing PQA support, reviewing batch records, and ensuring compliance with quality documentation. Ideal candidates should have a relevant degree and experience in GMP environments. This role is suited...Suggested
- MCS Quality Assurance Specialist job at Aequor. Thousand Oaks, CA. Ideal... ..., Qualification, and Validation experience. This position supports... ...Qualification and Validation (CQV) processes in Cell Banking,... ...the role provides support and compliance oversight to Manufact #J-188...Suggested
$50 - $76.42 per hour
The Fountain Group is currently seeking a Senior Quality Compliance Specialist for a prominent client of ours. This position is located in Newbury... ...and budget. Responsibilities: Drive analytical method validation/ transfer of laboratory methodologies Support the...Suggested$60k - $85k
...a driven individual to join our team as a Quality Assurance Specialist reporting to the Quality Engineering Lead based in Moorpark,... .../or internal audit experience preferred. Knowledge of FAIR validation and verification process requirements a plus. Quality system...Work experience placement$91k - $114.2k
...Job Description Quality Assurance (QA) Specialist III in Camarillo, CA Build your future... ...'s role will include identifying compliance risks in the operation prior to and during... ...and approve protocols and executed validation documentation • Work in...Contract workImmediate start- ...Quality Assurance Associate, Biopharma Medical Device This position will provide operational QA support of a clinical drug product packaging and labeling team. Primary responsibilities will include review and approval of printed clinical labels, finished clinical pack...Shift work
- Quality Assurance Associate, Biopharma Location: Thousand Oaks, CA. Employment Type: Contract Business Unit: Plant Quality Assurance Incoming and Packaging Duration: 3 years with possible conversion to FTE 3 Key Consulting is hiring a Quality Assurance Associate for...Contract workShift work
- ...Quality Assurance program under the Plant QA organization providing daily oversight of... ..., the role provides support and compliance oversight to Manufacturing and Facilities... ...Top Must-Have Skill Sets: Must have Pharma industry experience Experience in manufacturing...
- ...activities. Under general supervision, the role provides support and compliance oversight to Manufacturing, Facilities, Engineering, Supply... ...to get extended by the hiring manager. Red Flags: No Plant QA Experienced. Interview process: Video Skype Panel...Work experience placementFlexible hoursNight shiftDay shiftAfternoon shift
- 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
- ...We are looking for a motivated and hands-on Quality Operations Specialist to join our team. How you will add value to 20BLOC The... ...Specialist supports the Quality Assurance function by ensuring compliance with Good Manufacturing Practice (GMP) requirements. This role...Full timeVisa sponsorshipWork visaMonday to Friday
- ...Employment Type: Contract Business Unit: Plant QA Drug Substances Duration: 18+ months (... .... Notes: 100% Onsite. Must have Biotech/ Pharma experience required. Must be able to work... ..., the role provides support and compliance oversight to MFG and F&E staff in the execution...Contract 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...
- ...requires delivering real-time quality assurance support in a drug substance production facility. Responsibilities include providing compliance support and overseeing manufacturing operations. Candidates should possess a high school diploma or higher with relevant...Shift work
- 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...Flexible hours
$70.3k - $85k
...We are looking for a Quality Assurance Specialist to join our team in Camarillo! This is... ...Management System (QMS) to ensure full compliance with regulatory requirements and industry... ...verification, and closure. Support validation protocols (IQ/OQ/PQ) for production equipment...Full timeTemporary workWork at officeLocal areaMonday to Friday- 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...Rotating shiftDay shiftAfternoon shift
- ...Associate will be responsible for performing environmental monitoring, personnel monitoring, and microbiological testing to ensure compliance with industry standards and regulations. The successful candidate will work closely with the Quality Control team to support the...
- 100% onsite role at Thousand Oaks, CA Must be flexible in terms of schedule. Schedule is an 8 hour shift with a 30min lunch. Local Candidates only. No relocations Lab Based Job Bachelor's degree. Nice to have: documentation practices, GMP, previous ...Work experience placementSummer workLocal areaRelocationFlexible hoursShift work
- Quality Complaints, Senior Associate, GMP/Medical Device Job Title: Quality Complaints, Senior Associate, GMP/Medical Device Location: Thousand Oaks, CA. Employment Type: Contract Business Unit: Product Complaints & Surveillance Duration: 1+ years with likely...Contract work
$27 - $29 per hour
Payrate: $27.00 - $29.00/hr. Responsibilities: Receive, clean, and evaluate product complaint return samples. This includes but is not limited to photographs, x-rays, and written inspections. Interface with various sites and business partners Manage...Hourly payFull timeLocal areaFlexible hours- ...Job Description Job Description Job Summary: The Quality Specialist is responsible for creating, reviewing, and submitting First... ...supporting continuous improvement and maintaining regulatory compliance throughout the manufacturing process. Key Responsibilities:...Work at office
- ...QUALITY CONTROL (QC) SPECIALIST Located in Thousand Oaks, California, 20BLOC is a small privately held development-stage biopharmaceutical... ...Write SOPs, analytical protocols and written reports in compliance to cGMP as needed. Perform the day-to-day operation of the...Full timeVisa sponsorshipWork visaMonday to Friday
$92k - $114k
...Quality Control Auditor, you will review, test, and analyze information, reports or data to determine if the applicable process is in compliance with internal policy or regulations. You will assist by performing transactional testing of various loan servicing functions...- Merck & Co. is seeking candidates for a lab-based 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...
$74k - $89k
20BLOC in Thousand Oaks, California, is seeking a motivated Quality Control (QC) Specialist to support our QC and analytical lab operations. This role is essential to ensure compliance with testing requirements and regulatory standards. Qualified candidates should have...$22 - $32 per hour
...containers of up to 50lbs. Role may involve transporting samples to different buildings across campus. This role will be excluded from Winter and Summer shutdowns, and is expected to work during shutdowns excluding federal holidays. #J-18808-Ljbffr Planet Pharma GroupSummer work$92k - $114k
...seeking a Servicing Quality Control Auditor in Westlake Village, CA. Your role involves reviewing various loan servicing functions for compliance, conducting quality control reviews, and identifying discrepancies. Required qualifications include 2+ years of experience in...
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