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Make your mark for patients We are looking for a RIM Operations Systems Manager, curious, structured, and people-focused, to join us in our Regulatory Community Excellence team, based in our Raleigh, NC location. About…
Kyowa Kirin is a fast-growing global specialty pharmaceutical company that applies state-of-the-art biotechnologies to discover and deliver novel medicines in four disease areas: bone and mineral; intractable…
The Specialist (m/w/d) QA CAPA Management oversees customer-related deviation management and quality reporting within a pharmaceutical manufacturing environment. The role involves coordinating investigation strategies, approving CAPA measures, and representing quality processes during audits using GMP standards.
The Specialist QA Supplier Quality Management oversees supplier qualification and monitoring within a GMP-regulated environment. The role involves managing the supplier quality system, handling deviations and CAPAs, and coordinating quality agreements and audits.
The Specialist QA Document & Training manages GMP-compliant training and documentation systems, including LMS and eQMS, while supporting audits and process improvements. The role requires a background in natural sciences and experience in quality assurance within a pharmaceutical environment.
The Specialist QA Change Control Management oversees and improves the GMP-compliant change control processes at a biopharmaceutical manufacturing site. The role involves coordinating changes, moderating governance boards, ensuring data integrity, and supporting audits and international stakeholders.
Manages a team overseeing compliant document control for a gene-therapy manufacturer, using an eQMS like Veeva Vault to maintain SOPs, batch records, and regulatory documentation.
Oversee quality assurance for AAV gene therapy manufacturing, reviewing batch records, ensuring cGMP compliance, and supporting cleanroom operations in a biotech facility.
About Us Lupa is building a category defining product the industry has never seen before. We’re the AI-native operating system for veterinary practices and pet parents, replacing the fragmented, clunky systems vets…
Who we are: Kymera is a clinical-stage biotechnology company pioneering the field of targeted protein degradation (TPD) to develop medicines that address critical health problems and have the potential to dramatically…
Oversee clinical quality and GCP compliance for drug development programs, leading audits and inspections while advising teams on regulatory requirements.
Job Description Implement the Marketing programs in the territory achieving the Sales objectives. Shift and gain market share for the products promoted, by performing the following duties observing and enforcing the…
Job Description Associate Principal Scientist, Regulatory CMC Digital Innovation Rahway, NJ or West Point, PA Our Company is a global health care leader with a diversified portfolio of prescription medicines, vaccines…
Job title: R2868818 Associate Director Incentive Compensation Location: Cambridge, MA About the job: Our Team: The Associate Director, Incentive Compensation is responsible for overseeing the execution and delivery of…
GSK remains committed to achieving bold commercial ambitions for the future. By 2031, we aim to deliver £40 billion in annual sales, leveraging our existing strong performance momentum to significantly increase our…
At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for…
A QA specialist at GE Healthcare ensures product quality by handling deviations, CAPAs, complaints, and SOPs while supporting projects and cross-functional teams in a fast-paced environment. Core tasks include GMP compliance, batch documentation, and problem-solving for pharmaceutical manufacturing and regulatory processes.
Parexel is seeking experienced CMC (Chemistry, Manufacturing, and Controls) professionals to join us as a Regulatory Affairs Consultant CMC Author to support our client. This position requires expertise in regulatory…
By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice…
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