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Contractor Role Description: Supplier Management This Quality position is considered a global role reporting into the supplier management team within PharmSci QA who is responsible for supporting the Pharmaceutical…
Cell Culture We are seeking motivated and creative individuals to join our gene therapy platform development team. As part of this team, the successful candidate will contribute to ongoing efforts to develop and design…
Job Responsibilities: The Data Management (DM) Quality Associate will: • Review study documentation ensuring data quality is consistent with DM best practices, standards and procedures • Perform Trial Master File QC,…
Job Summary: The Sr. Data Scientist, CORA will support the CORA research director in completing research activities across the analytic team. This role conducts observational database studies to support multiple drug…
Position 1: This role will be responsible for the review of GMP documentation respective to QC Microbiology assay and activities. Review will include: • Environmental monitoring, water data including bioburden,…
Regulatory affairs with Technical Files, or equivalent in an R&D or quality position with hands-on experience in the preparation, review, and/or auditing of medical device DHFs, Risk Management files, and/or DMR’s.…
If you are interested give me a call on 973-606-3290 or you can send me the copy of resume on himanshu.prajapat(at)collabera.com Roles: • The qualified candidate will have current verifiable experience writing code/UI…
Provides phone and desktop support/consulting services and problem resolution. Images and Deploys computers for New Hires and Upgrades. Provides on-site desktop support services and problem resolution. Interfaces with…
Job Description/Requirements The Project Portfolio Manager is accountable and responsible for managing and executing a portfolio of projects at the Andover site. Projects in the portfolio will include procurement and…
Experience on a recent version of AutoCAD, diagrams & facility drawings, and ability to follow CAD standards. AutoCAD 2007 or later (required) Please reach out to me on 630-485-2166; sending your resume to…
SUMMARY OF POSITION: The Senior Manager, Indirect Sourcing, Professional Services will be responsible for a major portion of Medtronic’s global professional services spend which in total is approximately $1 billion…
Looking for a Project Manager or Project Coordinator with Regualatory affairs Experience. To know more about this position or to schedule an interview, please contact: Sagar Rathore 630-485-2166…
• Review and/or create user acceptance test (UAT) plan/ scripts for quality and completeness of electronic data capture (EDC) systems including Electronic Clinical outcome assessment (eCOA) systems. • Perform UAT…
• The Regulatory Submission Delivery Manager is responsible for the coordination of publishing deliverables, in line with the strategic direction of the programs/products • Act as the primary point of contact for…
Job Title: Site Relationship Manager Location: Cambridge, MA Duration: 3 Year+ (Possible Ext.) Job Responsibilities: The Site Relationship Manager (SRM) within Value Based Medicine (VBM) will be responsible for the…
Summary: • Position provides operational coordination for three labs within Research, including the management of moves in the office and laboratory, monitoring and execution of research agreements, and management of…
Our client is a multinational biotechnology company, headquartered in the US, whose goal is to ensure that people everywhere have access to innovative treatments and quality health care. Through working in partnership…
Job Summary The individual will work in the External Quality Assurance Department. This unit oversees contract manufacturing (3rd party manufacturing) operations, supply chain operations and supplier quality functions.…
Primary Duties The Manager, Safety Data Collection, Clinical Trials is responsible for managing the Pharmacovigilance (PV) operations of Pre and Post-approval Clinical Studies globally. The employee supports the Senior…
Client: Direct Client Location: Cambridge, MA Job Title: Safety Data Collection Manager Duration: 1 year Responsibilities • Responsible for managing the Pharmacovigilance (PV) operations of Pre and Post-approval…
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