Overview We are looking for an analyst for our Immunology Department to cover a temporary leave.
Responsibilities Perform the work in an environment of compliance with Good Laboratory Practices (GLP).
Perform the work in an environment of compliance with Good Laboratory Practices and GMP.
Support engineers, designers, and project managers with document access, version control, and compliance requirements.
Type of Contract : Full Time / Permanent.
Ensure compliance with Group or local Data Protection policies.
Collaborating in the creation and implementation of compliance policies at the local level.
Enhance compliance processes by identifying opportunities to improve adherence to regulatory requirements and internal company standards.
Coordinate and manage product security and privacy compliance activities.
Audit and / or compliance related roles experience in multinational environments.
Escalating high-risk Correspondent Banking financial crime compliance issues.
Coordinate mitigation tasks to ensure compliance with current regulations.
Responsible for drafting and / or maintaining updated corrective and / or preventive actions.
Conduct / oversee completion of Pre-Study Visits, Site Initiation Visits, Interim Monitoring Visits, and Close-Out Visits, to determine clinical trial protocol.
If you are ready to provide strategic direction and medical expertise to the company's product portfolio; Support development of key medical strategies aligned with the company’s products.
Qualifications Perform the analysis of biological drugs and antibodies (proteins, peptides,...) in biological matrices (plasma, serum,...) of samples from clinical and preclinical studies.
Higher Education Laboratory of Clinical laboratory.
Experience in immunological methods such as RIA, ELISA, ECLA.
Experience in cell assays will be a plus.
Good command of English.
Experience in working in GLP environments.
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Head • Barcelona, Catalonia, España