Hot Medical Affairs Jobs

Senior Regulatory Affairs Specialist

Life Science Recruitment are sourcing a Senior Regulatory Affairs Specialist for our client who are a global medical device company. This position is responsible for coordinating, preparing, and maintaining regulatory submissions and documents on a global level for Europe, the United States, and other countries. Roles & Responsibilities • Determines global regulatory pathways for various projects including product classification and type of regulatory submission or rationale required. • Participates on various teams to define regulatory requirements of ...

Location: Galway,

Regulatory Affairs Associate

Regulatory Affairs Associate Our client is looking for a regulatory affairs associate who will deal with the compliance and approval of products. This person will also be responsible for determining and supporting regulatory activities. Responsibilities • Use technical solutions for problem solving • Improve quality of projects • Use strong writing skills to clearly define and describe technical information • Analyse customer complaints • Identify trends and corrective actions • Review and assess of change control activities for po...

Location: Westmeath,

Clinical Trial Associate

Our Cork city-based biotech client is kicking off a major new recruitment project which will require the hiring of 100+ in-house Clinical Trials experts over 12 months. A superb office and team environment along with salary and benefits package will reward successful candidates here. Responsibilities The Clinical Trial Team provides clinical trial capabilities in support of clinical development. The Associate is accountable to ensure the investigator sites meet requirements to enrol study participants into clinical trials and support ongoing activities during site maintenance and close...

Location: Cork,

Associate Scientist

Life Science Recruitment Cork are currently recruiting a Scientist for a large multinational client in Cork where they will be responsible for Tox Release testing, Clinical Release and Stability testing for Drug Substance and Drug Product, and Stability Lifecycle management.The Clinical Release & Stability Department in Cork, Ireland, is responsible for the biotechnology (Large molecule) scope of the PDMS product portfolio. Education and Experience/Competencies A minimum of Degree in Chemistry, Biochemistry, Pharmaceutical Sciences or ...

Location: Cork,

QA Senior Associate (Contract)

Plant QA Snr Associate Level 4 Dun Laoghaire Overview: The Plant Quality Assurance (PQA) Snr Associate will typically report to a QA Senior Manager and is a core member of the site Quality Assurance team. The PQA Snr Associate will serve as Quality point of contact for manufacturing operations. The site is focused on continuous improvement of all work processes and practices, therefore in addition to routine Quality Assurance duties, PQA Snr Associates may be asked to carry out additional work functions to support site continuous improvement activities. A...

Location: Dublin,