QUALITY SYSTEMS SPECIALIST
20BLOC
Located in Thousand Oaks, California, 20BLOC is a small privately held development-stage biopharmaceutical company, driven by a mission to create breakthrough protein-based drugs to save lives. Our lead product is an innovative solution to provide oxygen to tissues. Check us out at We are looking for a motivated and hands‑on Quality Systems Specialist to join our team. How you will add value to 20BLOC The Quality Systems Specialist supports the Quality Assurance function by ensuring compliance with Good Manufacturing Practice (GMP) requirements. This role is responsible for development and support of the Quality Management System (QMS), including Supplier Qualification and oversight of quality Events and Change Control. The Quality Systems Specialist works closely with Manufacturing, QC, Supply Chain and other cross-functional teams to ensure product quality, data integrity, and regulatory compliance. Key Responsibilities Supplier risk assessment and classification Oversight of supplier audits (on-site and paper audits) Management of Supplier Agreements Quality Systems Development and oversight of electronic Quality Management Systems (e‑QMS) Development of the Deviation and CAPA Quality System, supporting investigations, including root cause analysis and CAPA planning, and quality approval of deviations Development of the Change Control Quality System, including impact assessments and Quality approval Oversight of the document control and GMP training Quality Systems Ensure documentation practices comply with data integrity and GMP requirements Compliance & Continuous Improvement Support internal audits and regulatory inspections, including preparation of documentation and responses Assist in tracking and trending quality events and quality metrics Support risk assessments and continuous improvement initiatives Ensure timely closure of deviations, CAPAs, and change controls Cross-Functional Support Collaborate with Manufacturing, QC, and other departments to resolve quality issues Provide GMP guidance and support to operational teams Participate in training activities related to GMP and quality procedures Education Bachelor’s degree in Life Sciences or a related field Experience 4 years+ of experience in Quality Assurance within a GMP-regulated pharmaceutical environment Experience in Supplier Quality management Experience with e‑QMS Experience managing deviations, change control, training, and document control Working knowledge of regulatory requirements (e.g., FDA, EMA, ICH guidelines) Strong understanding of GMP and pharmaceutical quality systems High attention to detail and strong documentation skills Ability to investigate issues and perform root cause analysis Strong organizational and time management skills Effective written and verbal communication skills Ability to work independently and collaboratively in a team environment Proficiency with electronic QMS systems Please apply at View email address on click.appcast.io – in subject line: Quality Systems Specialist This is a full-time, on-site position located in Thousand Oaks, California, and requires working on-site Monday through Friday. All applicants must be authorized to work in the United States. We are not sponsoring employment visas. Compensation: The salary range for this position is $82,000.00 to $109,00.00 USD annually. This salary range is an estimate, and the actual salary may vary based on various factors, including, without limitation, individual education, experience, tenure, skills, and abilities, as well as internal equity and alignment with market data, including potential adjustments for geographic location. 20BLOC is an equal opportunity employer. All applicants will be considered for employment without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status, or other applicable legally protected characteristics. We offer competitive compensation and benefits including health, dental, vision and life insurance, 401(k) and paid time off. #J-18808-Ljbffr 20BLOC
- 20BLOC in Thousand Oaks, CA is seeking a hands-on Quality Systems Specialist to drive GMP-compliant quality systems and supplier oversight. You will develop and maintain the e‑QMS, deviations, CAPA and change control, ensuring data integrity and regulatory compliance across...Suggested
$26 per hour
...Job Description Job Description At Cydcor, we’re committed to delivering top-quality experiences for our clients and customers. As a Sales Quality & AI Systems Specialist , you’ll play a critical role in measuring and improving sales quality across field sales offices...SuggestedWork at officeRemote work- Quality Control Specialist, Microbiology In this vital role, you will provide technical and operational leadership for the QC Microbiology and... ...ready documentation using electronic laboratory and quality systems (e.g., LMES, LIMS, CIMS, and Veeva). Partner with Quality...SuggestedContract workWork experience placementFlexible hoursWeekend work
$44.97 - $46.52 per hour
The Fountain Group is currently seeking a Quality Compliance Specialist for a prominent client of ours. This position is located in Newbury Park ,... ...Preferred Skills Kneat validation software Paperless validation systems for life sciences Commissioning, Installation,...SuggestedWork at officeFlexible hours- ...Check us out at We are looking for a motivated and hands-on Quality Operations Specialist to join our team. How you will add value to 20BLOC The... ...of quality events, and support of the Quality Management System (QMS). The Quality Operations Specialist works closely with...SuggestedFull timeVisa sponsorshipWork visaMonday to Friday
$25 - $27 per hour
...team. Comfortable with basic computer skills and documentation systems. Familiarity with GMP principles is a plus, but not a strict requirement... ...laboratory testing and related activities in support of Quality Control operations. The role requires adherence to current Good...Contract workWork at officeMonday to Friday$45 - $58 per hour
...method transfers for raw materials within a cGMP environment in Quality Control. You will conduct biological, chemical, and physical... ...). May perform release functions in LIMS or other computerized systems. Support generation and documentation of validation protocol deliverables...Hourly payTemporary workLocal areaShift work$75k - $112k
...The Quality Assurance Specialist is responsible for planning, designing, executing, and documenting software testing activities across Avum's government... ...Experience testing government procurement and acquisition systems, including data exchanges, interfaces, and business...Contract workLocal areaRemote work- ...transfers, including raw materials, for use in a cGMP environment in Quality control. You will be responsible for conducting biological or... ...). May perform release functions in LIMS or other computerized systems. Support generation and documentation of validation protocol...Work experience placementWork at officeLocal areaShift workWeekend work
- ...Overview Under the general supervision of the Water Quality Supervisor, a Quality Assurance/Quality Control Specialist maintains the water quality laboratory’s quality... ...ensure compliance with the laboratory’s quality system. Administers the laboratory’s QA/QC internal...Work at officeLocal area
$30 - $32 per hour
MCS Senior Associate Quality Assurance with GMP and Audit Experience (Onsite Job in Thousand Oaks, CA) Location: Thousand Oaks, CA Employment... ...thrive in fast‑paced, ambiguous environments. Familiarity with systems like C‑Docs, Smartsheets, SharePoint, and QMS tools is a plus....Contract work$89k - $126k
...Worker Type: Regular Summary The Quality Management and Improvement Internal Auditor is responsible for performing quality management systems audits (product, process, or systems) at several AV locations. Position Responsibilities Provide technical subject matter expertise...Permanent employmentContract workWork at officeHome office- ...of patients while transforming your career. Drug Product Quality Assurance Specialist What you will do In this vital role within the Plant Quality... ...the role ensures adherence to cGMP requirements, quality systems, and regulatory expectations while partnering closely with...Flexible hours
- Amgen SA is seeking a Drug Product Quality Assurance Specialist in Thousand Oaks, California. This role involves providing quality oversight for... ...assurance, with a strong understanding of Quality Management Systems and regulatory compliance. Amgen offers a competitive...
- Amgen in Thousand Oaks, CA is seeking a Drug Product Quality Assurance Specialist to provide quality oversight for aseptic Drug Product manufacturing... ..., and document management within the Quality Management System. Cross‑functional collaboration with Manufacturing,...
$76.41k - $94.38k
...complaints for compliance and accuracy. Audit monthly complaint quality, sub‑servicer functions, and internal complaint operations.... ...improvement recommendations. Navigate various mortgage servicing systems such as MSP, MortgageServ, LoanServ, SBO, etc. Qualifications 5...- 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
$26 per hour
...exceptional experiences for our clients and customers. As a Sales Quality & Customer Support Specialist, you’ll play a vital role in improving customer outcomes... ...Word, Outlook) ~ Familiarity with Salesforce or CRM systems ~ Exposure to quality reporting or AI tools like...Work at officeRemote work- Associate Quality Control - TIM Lab Analyst Join Amgen's mission of serving patients living with serious illnesses. Since 1980, Amgen... ...complete, accurate, and concise documentation using electronic systems and laboratory notebook. Participate in audits, initiatives, and...Work experience placementWork at officeFlexible hours
- ...to perform at your best. Together we win! The Opportunity The Quality Assurance Analyst is responsible for performing quality assurance... ...to accommodate remediation of findings. Maintain complete system development records and changes. Comfortable using Excel, Word...Local areaImmediate startFlexible hours
- ...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
$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- 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...Flexible hours
- ...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...
- BioSpace is seeking a Senior Associate Quality Assurance in Thousand Oaks, California, to oversee drug product manufacturing areas while ensuring regulatory compliance and supporting Amgen's Quality Assurance program. This role involves daily oversight and various quality...
- 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...
- ...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...
- 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
- 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 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...
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