Search Results: 253 vacancies
...documentation for equipment, systems, and processes in accordance with regulatory requirements and company manufacturing standards, and oversees a team of Validation Oversight Specialists.
As an Associate Manager in QA Validation Oversight , a typical day might include, but...
...clients using leading technology and exceptional service.
This is an exciting opportunity within the recently-established Regulatory Risk & Oversight Office in Asset Servicing.
The Regulatory Risk & Oversight Office oversees the management of regulatory risk across...
...The primary role of the Senior Regulatory Scientist is to assist in the running of the regulatory affairs by providing input into: regulatory strategies, performing activities associated with obtaining and maintaining regulatory approval to commercialise medical devices in...
...services.
•Family Resource Centers and associated national programmes.
•The statutory regulation... ...12 (1) – (5) of the legislation.
Regulatory Practice Development: The Regulatory... ...notifications of cessations.
•Complete oversight of the tasks associated with the processes...
...Italy and Belgium.
The key responsibilities of the role include:
Lead planning and execution of the daily and periodic regulatory reporting solutions in cooperation with the other senior partners on the team.
Engage with internal departments to evaluate and implement...
...providing professional expertise, leadership, oversight and assisting with strategic planning... ...Regulations, Eudralex Volume 4 and associated Annexes, ISO Standards and ICH, WHO and... ...communicates industry trends as they pertain to regulatory agency findings, expectations, and...
The Associate Manager QA is responsible for all aspects of assigned QA Team; provides leadership... ...Manufacturing Operations provides QA oversight to ensure that drug substance... ...expectations regarding Quality.
Participates in regulatory and customer audits.
Education and...
...and Archives operations. This includes oversight of the following: document workflows, records... ..., projects, and metrics.
As an Associate Manager Document Control, a typical day... ...site leads
Interfacing directly with regulatory or partner inspectors, as needed, to represent...
The candidate will support the development and execution of regulatory strategies for biologic products and combination products for the portfolio assigned and perform the duties outlined below
In this role, a typical day might include the following:
• Support CMC/Combination...
...Regulatory Affairs Manager is required to act as a regulatory expert within our medical technology client's engineering team in Limerick. Our client is looking for the next Quality SME who will participate in multi-functional teams as the regulatory expert in new product development...
...Our client, A leading laboratory in Limerick, are seeking a Senior Regulatory Officer to join their team. This role will provide ongoing support to the regulatory team and to all teams with regulatory and legal requirements.
Please Note: This is a six month fixed term...
...protocols, regulation, and schedule.
Supervises a team responsible for the delivery of the manufacturing compliance records in a cGMP regulatory environment.
Schedules team duties and tasks.
Ensures timely management of quality instance closure.
Authors manufacturing...
...and facilitation of the Approved Supplier List (ASL), support of regulatory inspections, SOP writing and revision and the management of the... ...the maintenance of the Approved Supplier List (ASL) and associated Periodic Review of suppliers.
Interfaces daily with Quality...
...Calibration team, staff leadership, and resource management.
As an Associate Manager or Manager in Calibration a typical day might include,... ...matter expert and presenting related topics & details to regulatory inspectors during inspections
Responsible for all aspects of...
...Sr. Associate - Quality - Biotechnology Operations
Our client, a global biotech company... ...critical role in maintaining the quality and regulatory compliance of the biopharmaceutical... ...improvement initiatives.Quality Assurance Oversight:
~Develop and maintain quality assurance...
Associate Director (Quality Assurance)
Our client, a global biotech, are currently recruiting for an Associate Director Quality Assurance... ...processes including support of GMP and GLP compliance, regulatory inspection readiness, Quality Plan and continuous improvement projects...
...Our client is an industry-leading financial services company and they currently have an exciting opportunity for a Senior Regulatory Reporting Consultant to join their team in Limerick . This position is on an initial 12-month fixed-term contract that may have the possibility...
...be a hybrid model after training completion.
Your new role
An opportunity has arisen for a Senior Consultant within Limerick Regulatory Reporting department and some of the principal responsibilities are as follows:
Responsible for providing unrivalled client satisfaction...
...healthcare better. Plus, we have an award-winning culture and were recently named one of the World’s Best Workplace by Fortune!
Associate Sourcing Manager
Permanent contract, Limerick
Job Summary
The Associate Sourcing Manager will support the development and...
...software such as Endoscan V, SoftMax Pro and DataPro2.
As an Associate Director within IT Applications, a typical day might include,... ...systems such as Service Now advantageous
You have knowledge of Regulatory Asset Manager Systems advantageous
You possess excellent...
