- job summary: Seeking a Regulatory Affairs Specialist to support Quality Operations and Regulatory Affairs. This long-term temporary role is essential to maintaining regulatory compliance and supporting consistent, on-time product delivery. The successful candidate will be responsible for handling regulatory submissions, CAPAs, customer complaints, and supporting audits. This role also includes performing regulatory reviews and supporting other areas as njob summary: Seeking a Regulatory Affairs Specialist to support Quality Operations and Regulatory Affairs. This long-term temporary role is essential to maintaining regulatory compliance and supporting consistent, on-time product delivery. The successful candidate will be responsible for handling regulatory submissions, CAPAs, customer complaints, and supporting audits. This role also includes performing regulatory reviews and supporting other areas as n
- job summary: Primary point of contact to lead, manage and coordinate, in partnership with the ContractResearch Organization (CRO), the conduct of clinical trials from study design to close out at a global level in accordance with ICH-GCPOversee the quality and scientific integrity of clinical operations for studies at a global levelCollaborates with cross functional stakeholders to ensure timely and on budget execution of clinical trial deliverablesjob summary: Primary point of contact to lead, manage and coordinate, in partnership with the ContractResearch Organization (CRO), the conduct of clinical trials from study design to close out at a global level in accordance with ICH-GCPOversee the quality and scientific integrity of clinical operations for studies at a global levelCollaborates with cross functional stakeholders to ensure timely and on budget execution of clinical trial deliverables
- 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 oncojob 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: *Regulatory Affairs Specialist* This position assists the Director of Quality Operations (DQO) in maintaining an effective Quality Operations and Regulatory Program, which consistently delivers high quality EZIP products on time. Handles regulatory submissions, CAPAs, customer complaints, conducts regulatory reviews and participates in audits to verify that appropriate current procedures and applicable regulations are followed, and keeps thejob summary: *Regulatory Affairs Specialist* This position assists the Director of Quality Operations (DQO) in maintaining an effective Quality Operations and Regulatory Program, which consistently delivers high quality EZIP products on time. Handles regulatory submissions, CAPAs, customer complaints, conducts regulatory reviews and participates in audits to verify that appropriate current procedures and applicable regulations are followed, and keeps the
- job summary: Perform experiments, organize data and analyze results under minimal supervision. With minimal supervision, plans, conducts or monitors experiments, records and organizes data, analyses results, generates robust and reliable data and/or Ensures that contracted studies are conducted in compliance with the respective protocol and applicable guidelines and regulations. 90% lab work including sample isolation, drying, and testing location: Newjob summary: Perform experiments, organize data and analyze results under minimal supervision. With minimal supervision, plans, conducts or monitors experiments, records and organizes data, analyses results, generates robust and reliable data and/or Ensures that contracted studies are conducted in compliance with the respective protocol and applicable guidelines and regulations. 90% lab work including sample isolation, drying, and testing location: New
- 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! locatijob 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: 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: 7job 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
