job summary: Immediate opportunity for a Process Development Associate with one of the world's leading biotechnology companies located in Thousand Oaks, CA. The ideal candidate is a recent Bachelor's or Master's graduate in a life sciences field with hands-on lab experience, particularly in protein purification techniques such as filtration, chromatography, and UF/DF. While mammalian cell culture experience is beneficial, a strong foundation in protein p
job summary: Immediate opportunity for a Process Development Associate with one of the world's leading biotechnology companies located in Thousand Oaks, CA. The ideal candidate is a recent Bachelor's or Master's graduate in a life sciences field with hands-on lab experience, particularly in protein purification techniques such as filtration, chromatography, and UF/DF. While mammalian cell culture experience is beneficial, a strong foundation in protein p
job summary: The Staff Quality Engineer, Software will be the subject matter expert on providing guidance to the organization and the software teams in establishing policies and procedures for Software Design Control. This individual will be an integral part of the software development life cycle process in informing, guiding, and evaluating the teams' adherence to practices that would ensure compliance to required regulatory requirements. SKILLS REQUIRED
job summary: The Staff Quality Engineer, Software will be the subject matter expert on providing guidance to the organization and the software teams in establishing policies and procedures for Software Design Control. This individual will be an integral part of the software development life cycle process in informing, guiding, and evaluating the teams' adherence to practices that would ensure compliance to required regulatory requirements. SKILLS REQUIRED
job summary: The Pivotal Drug Substance Technologies organization develops, characterizes and supports clinical drug substance manufacturing processes for all late-stage programs. The successful candidate will be responsible for support of the development, characterization, scale-up and support of upstream and downstream processes to enable clinical advancement of company programs. location: Newbury Park, California job type: Contract salary: $2
job summary: The Pivotal Drug Substance Technologies organization develops, characterizes and supports clinical drug substance manufacturing processes for all late-stage programs. The successful candidate will be responsible for support of the development, characterization, scale-up and support of upstream and downstream processes to enable clinical advancement of company programs. location: Newbury Park, California job type: Contract salary: $2
job summary: The Associate of Manufacturing will work in a dynamic production environment at the Company Thousand Oaks Site supporting development, clinical, and launch activities.Under general supervision, employee will perform operations in the Manufacturing area.Operations will be performed according to Standard Operating Procedures (SOPs). location: Newbury Park, California job type: Contract salary: $28.00 - 30.36 per hour work hours: 7
job summary: The Associate of Manufacturing will work in a dynamic production environment at the Company Thousand Oaks Site supporting development, clinical, and launch activities.Under general supervision, employee will perform operations in the Manufacturing area.Operations will be performed according to Standard Operating Procedures (SOPs). location: Newbury Park, California job type: Contract salary: $28.00 - 30.36 per hour work hours: 7
job summary: Sr. Pharmacovigilance (PV) Operations Manager | Remote | West Coast This critical role is responsible for managing and overseeing PV operations across clinical development programs, ensuring seamless collaboration with PV vendors. You will play a key role in preparing for the initiation of two global Phase 3 trials, ensuring all PV activities are in place. Your expertise in global trial management, study document review, and vendor oversight
job summary: Sr. Pharmacovigilance (PV) Operations Manager | Remote | West Coast This critical role is responsible for managing and overseeing PV operations across clinical development programs, ensuring seamless collaboration with PV vendors. You will play a key role in preparing for the initiation of two global Phase 3 trials, ensuring all PV activities are in place. Your expertise in global trial management, study document review, and vendor oversight
job summary: We are seeking a Sr. Data Analyst to join the Clinical Systems Analytical & Reporting (CSAR)-Analytics team within Global Development Operations. This role will enhance our analytical reporting capabilities and support business continuity across multiple clinical system technology enhancement projects. Key responsibilities include contributing to analytics initiatives supporting critical business functions relying on data from eTMF, EDC, CTMS
job summary: We are seeking a Sr. Data Analyst to join the Clinical Systems Analytical & Reporting (CSAR)-Analytics team within Global Development Operations. This role will enhance our analytical reporting capabilities and support business continuity across multiple clinical system technology enhancement projects. Key responsibilities include contributing to analytics initiatives supporting critical business functions relying on data from eTMF, EDC, CTMS
job summary: Join a leading biopharmaceutical company in Thousand Oaks, CA, for an immediate opening as a Quality Assurance Associate. This is an excellent opportunity to contribute to a successful and growing organization. location: Newbury Park, California job type: Contract salary: $25.00 - 30.36 per hour work hours: 9 to 5 education: High School responsibilities: Under general supervision, this position is responsible for sampling a
job summary: Join a leading biopharmaceutical company in Thousand Oaks, CA, for an immediate opening as a Quality Assurance Associate. This is an excellent opportunity to contribute to a successful and growing organization. location: Newbury Park, California job type: Contract salary: $25.00 - 30.36 per hour work hours: 9 to 5 education: High School responsibilities: Under general supervision, this position is responsible for sampling a
job summary: At Company, every challenge is an opportunity. And every opportunity brings the potential to change lives. Our shared mission to serve patients has driven our status as one of the world's preeminent biotechnology companies, reaching over 10 million patients worldwide. Leverage your high-level expertise to lead and forge partnerships that advance the biotechnical and biopharmaceutical science that can turn the tide of serious, life-interrupt
job summary: At Company, every challenge is an opportunity. And every opportunity brings the potential to change lives. Our shared mission to serve patients has driven our status as one of the world's preeminent biotechnology companies, reaching over 10 million patients worldwide. Leverage your high-level expertise to lead and forge partnerships that advance the biotechnical and biopharmaceutical science that can turn the tide of serious, life-interrupt
job summary: As a trusted staffing and recruitment partner, we are committed to connecting you with the perfect opportunity at a global leader in biotechnology. Leveraging our extensive network, we provide access to top-tier roles that allow you to grow and make a meaningful impact in the healthcare and life sciences industries. This company is dedicated to discovering and developing innovative therapies that address serious diseases, with a focus on onco
job summary: As a trusted staffing and recruitment partner, we are committed to connecting you with the perfect opportunity at a global leader in biotechnology. Leveraging our extensive network, we provide access to top-tier roles that allow you to grow and make a meaningful impact in the healthcare and life sciences industries. This company is dedicated to discovering and developing innovative therapies that address serious diseases, with a focus on onco
job summary: As the largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. We supply prestigious life sciences and biopharma companies with job seekers like you to achieve their bus
job summary: As the largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. We supply prestigious life sciences and biopharma companies with job seekers like you to achieve their bus
job summary: A major pharmaceutical company who work to benefit patients wherever they live by uniting worldwide talent and resources with their vision. KEY SKILLS: PharmacovigilanceDrug safetyPhase 1-3 clinical study experienceProtocol, IB, ICF developmentSMC, DMCSAE and aggregate data review and analysisSignal detection and signal evaluationDSUR authoring location: Telecommute job type: Contract salary: $85 - 100 per hour work hours: 9 t
job summary: A major pharmaceutical company who work to benefit patients wherever they live by uniting worldwide talent and resources with their vision. KEY SKILLS: PharmacovigilanceDrug safetyPhase 1-3 clinical study experienceProtocol, IB, ICF developmentSMC, DMCSAE and aggregate data review and analysisSignal detection and signal evaluationDSUR authoring location: Telecommute job type: Contract salary: $85 - 100 per hour work hours: 9 t
job summary: This is an 18-month onsite contract role based in Thousand Oaks, CA, with potential for extension. The position supports Drug Product Quality Assurance by providing daily compliance oversight on the manufacturing floor. Key responsibilities include batch record review, SOP approvals, MES and Maximo system updates, and minor deviation/CAPA record approvals. The role requires a detail-oriented team player with quality experience and the ability
job summary: This is an 18-month onsite contract role based in Thousand Oaks, CA, with potential for extension. The position supports Drug Product Quality Assurance by providing daily compliance oversight on the manufacturing floor. Key responsibilities include batch record review, SOP approvals, MES and Maximo system updates, and minor deviation/CAPA record approvals. The role requires a detail-oriented team player with quality experience and the ability
job summary: Under general supervision, this position will perform routine procedures and testing in support of the lab. location: Newbury Park, California job type: Contract salary: $24.00 - 27.32 per hour work hours: 9 to 5 education: High School responsibilities: Performing routine laboratory proceduresRoutine analytical testingDocumenting, computing, compiling, interpreting, and entering dataMaintaining and operating specialized equ
job summary: Under general supervision, this position will perform routine procedures and testing in support of the lab. location: Newbury Park, California job type: Contract salary: $24.00 - 27.32 per hour work hours: 9 to 5 education: High School responsibilities: Performing routine laboratory proceduresRoutine analytical testingDocumenting, computing, compiling, interpreting, and entering dataMaintaining and operating specialized equ
job summary: The Sr. Associate Quality Assurance position supports Company's Quality Assurance program under the Plant QA organization providing daily oversight of the Drug Product manufacturing areas. Under general supervision, the role provides support and compliance oversight to Manufacturing and Facilities and Engineering staff in the execution of their processes, procedures, and use of quality systems. location: Newbury Park, California job type:
job summary: The Sr. Associate Quality Assurance position supports Company's Quality Assurance program under the Plant QA organization providing daily oversight of the Drug Product manufacturing areas. Under general supervision, the role provides support and compliance oversight to Manufacturing and Facilities and Engineering staff in the execution of their processes, procedures, and use of quality systems. location: Newbury Park, California job type:
job summary: As the world's largest staffing and recruitment agency in the world, we can commit to find you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. We supply prestigious life sciences and biopharma companies with job seekers like you to achieve thei
job summary: As the world's largest staffing and recruitment agency in the world, we can commit to find you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. We supply prestigious life sciences and biopharma companies with job seekers like you to achieve thei
job summary: As the largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. As the world's leading provider of diagnostic information services, our client is committed to sharing our
job summary: As the largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. As the world's leading provider of diagnostic information services, our client is committed to sharing our
job summary: As the largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. We supply prestigious life sciences and biopharma companies with job seekers like you to achieve their bus
job summary: As the largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. We supply prestigious life sciences and biopharma companies with job seekers like you to achieve their bus
job summary: This Sr Associate position is a laboratory-based position, responsible for analysis of process development samples, multiple instrument operation, analytical method development, sample management, data analysis and reporting. Candidate will work in a cross-function laboratory with following GMP and safety compliance. location: Newbury Park, California job type: Contract salary: $25.37 - 29.98 per hour work hours: 9 to 5 education:
job summary: This Sr Associate position is a laboratory-based position, responsible for analysis of process development samples, multiple instrument operation, analytical method development, sample management, data analysis and reporting. Candidate will work in a cross-function laboratory with following GMP and safety compliance. location: Newbury Park, California job type: Contract salary: $25.37 - 29.98 per hour work hours: 9 to 5 education:
job summary: PRIMARY OBJECTIVE OF POSITION: Under minimal supervision, the Quality Specialist, Stability supports the stability program under regulatory requirements and ISO 13485 and runs stability studies from initial batch/lot selection to final report generation and study destruction; works closely with Quality, R&D, and Operations to assure appropriate batch/lot selection, initiation, and execution of Stability studies in a compliant and timely man
job summary: PRIMARY OBJECTIVE OF POSITION: Under minimal supervision, the Quality Specialist, Stability supports the stability program under regulatory requirements and ISO 13485 and runs stability studies from initial batch/lot selection to final report generation and study destruction; works closely with Quality, R&D, and Operations to assure appropriate batch/lot selection, initiation, and execution of Stability studies in a compliant and timely man
job summary: This is a high level contract role, requiring Direct Global Regulatory Labeling Operations Project Management experience in the Pharma/Biotech industry, as deep knowledge of pharmaceutical labeling regulations, compliance, and processes are critical for this role. The Labeling Project Manager is responsible for all activities associated with the development, creation and execution of labeling for assigned product lines for domestic and/or i
job summary: This is a high level contract role, requiring Direct Global Regulatory Labeling Operations Project Management experience in the Pharma/Biotech industry, as deep knowledge of pharmaceutical labeling regulations, compliance, and processes are critical for this role. The Labeling Project Manager is responsible for all activities associated with the development, creation and execution of labeling for assigned product lines for domestic and/or i
job summary: Seeking a self-motivated and detail-oriented Quality Complaints Sr Associate to join a fast-paced team. Ideal candidates will have a Bachelor's degree, a keen eye for GDP / GMP compliance, and strong organizational and communication skills. This role involves handling returned product samples, performing evaluations and documentation, and ensuring compliance with quality standards. location: Newbury Park, California job type: Contract
job summary: Seeking a self-motivated and detail-oriented Quality Complaints Sr Associate to join a fast-paced team. Ideal candidates will have a Bachelor's degree, a keen eye for GDP / GMP compliance, and strong organizational and communication skills. This role involves handling returned product samples, performing evaluations and documentation, and ensuring compliance with quality standards. location: Newbury Park, California job type: Contract
job summary: We are seeking a Regulatory Submission Manager to support global regulatory initiatives and ensure compliance with regulatory requirements for investigational and marketed products. Role involves working closely with cross-functional teams and regulatory leads to support submission activities, labeling development, and strategic regulatory guidance. The ideal candidate has a strong background in regulatory submissions and document review, as
job summary: We are seeking a Regulatory Submission Manager to support global regulatory initiatives and ensure compliance with regulatory requirements for investigational and marketed products. Role involves working closely with cross-functional teams and regulatory leads to support submission activities, labeling development, and strategic regulatory guidance. The ideal candidate has a strong background in regulatory submissions and document review, as
job summary: We are seeking a Clinical Site Contracts Specialist to manage end-to-end processes for clinical site contracts and consulting agreements, ensuring smooth study start-up and trial operations. If you're detail-oriented, proactive, and passionate about negotiation and collaboration, this is your chance to contribute to critical clinical research initiatives. Apply today to take the next step in your career-let's start the conversation! locati
job summary: We are seeking a Clinical Site Contracts Specialist to manage end-to-end processes for clinical site contracts and consulting agreements, ensuring smooth study start-up and trial operations. If you're detail-oriented, proactive, and passionate about negotiation and collaboration, this is your chance to contribute to critical clinical research initiatives. Apply today to take the next step in your career-let's start the conversation! locati
job summary: We are seeking a highly skilled Senior Manager - CMC Regulatory to lead the planning, preparation, and submission of global regulatory CMC-related content for clinical trial applications, marketing applications, and periodic reports. This role involves ensuring compliance with US and international regulatory requirements, collaborating with cross-functional teams, and providing strategic guidance on manufacturing changes to optimize regulator
job summary: We are seeking a highly skilled Senior Manager - CMC Regulatory to lead the planning, preparation, and submission of global regulatory CMC-related content for clinical trial applications, marketing applications, and periodic reports. This role involves ensuring compliance with US and international regulatory requirements, collaborating with cross-functional teams, and providing strategic guidance on manufacturing changes to optimize regulator
