Search Results: 158 vacancies
Responsible for implementing microbiologically based initiatives as part of the QA Microbiology team at IOPS Raheen. Aspects of investigation activities, training, project implementation, and data collection and analysis will be utilized. Knowledge of Biopharmaceuticals and...
In this role you will be responsible for providing QA oversight and support to manufacturing activities. Performs and leads activities... ...and Regeneron Standard Requirement Documents.
As a Senior QA Specialist a typical day might include, but is not limited to, the following...
...requirements and support, follow and implement company manufacturing standards policies and procedures
A typical day as a QA Validation Specialist, may include:
Generates, executes and/or reviews master and completed cleaning validation protocols, summary reports and associated...
...implement on daily basis a quality culture and any other company manufacturing standards, policies and procedures.
As a Principal QA Validation Specialist, a typical day might include, but is not limited to, the following:
Having strong knowledge and understanding of...
...Hobson Prior are in search of a dedicated Principal QA who will provide exemplary quality leadership, invaluable guidance, and meticulous... ...details or to talk directly to a life sciences recruitment specialist directly, please select "Contact me" at the top of this page....
...role you will be responsible for the management and leadership of the Quality Assurance Operations function. This role will be part of the QA Operations site management team and is a key leader in the cross functional support of the manufacturing activities. This role will...
...for and training of individuals in the specific Quality System and/or Quality Program assigned.
~Provide coaching and mentoring to other QA reps, to provide appropriate and timely solutions to compliance in a business focused fashion.
Key Responsibilities:
~Co-ordinates...
...QA Associate
My client are seeking highly motivated, talented Quality Assurance Associate to support their new Biologics Manufacturing Facility. The ideal candidate is an organised and a methodical professional who fosters a positive team environment. Main Purpose and Objectives...
...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 is not limited to, the following:
Leading a technical...
Job Title: Facilities Maintenance Specialist (CMMS Coordination)
Department: Facilities Maintenance
Summary: Responsible for the administration, coordination and completion of tasks on BMRAM to maintain the required cGMP state of the Computerised maintenance management system...
Limerick
9 days ago
A QA Validation Technical Writer is required by Careerwise recruitment to work with our Limerick based biotech client on a 12-month contract position.
Role of this position
Execution of SIP/ cleaning and continuing validation protocols.
Writing and approving Deviations...
...Summary: The Quality System Specialist participates in maintaining site compliance of operations inclusive of but not limited to Manufacturing... ..., Facilities Maintenance, Engineering, Materials Handling, and QA Validation in accordance with mandated regulatory requirements and...
...this role you will be responsible for supporting the Environmental, Health and Safety for the Limerick IOPS location.
As an EHS Specialist a typical day might include, but is not limited to, the following:
Developing, implementing and monitoring environmental, health...
...scale commercial manufacturing production program. You will be heavily involved in technical transfer of processes.
As a Process Specialist-Formulation a typical day might include, but is not limited to, the following:
Liaising with the process science/technology...
Within this role you will be responsible for Procurement activities related to the assigned categories of spend.
As a Temp Sourcing Specialist a typical day might include, but is not limited to the following:
Responsible for end-to-end management of assigned categories,...
The QC Compliance Specialist will be responsible for managing QC's Change Controls/CAPAs and Workflows.
In this role a typical day might include, but is not limited to, the following:
Coordination and documentation of QC quality records including but not limited to, Change...
...Summary: This role is responsible for the operational oversite of the QA Microbiology and Lab Support Teams at the Raheen site. This person is the leader for these two organizations and must ensure personnel management (goals, feedback, development plans, priorities, etc.)...
...Regulatory Change Oversight, iii) Regulatory Risk Management, and iv) Regulatory Strategy & Sustainability.
The Technical Regulatory Specialist supports both the Regulatory Change Oversight and Regulatory Risk Management pillars, connecting the dots across regulation...
...UL Hospitals Group is hiring Clinical Nurse Specialist (CNS)- Ophthalmology
Purpose of the Post:
The purpose of this Clinical Nurse Specialist Ophthalmology post is to:
Deliver care in line with the five core concepts of the role set out in the framework for the...
...alignment with company brand to activate audience support of company goals and preserve company culture and reputation. The Communications Specialist creates internal communication plans and content across a variety of channels and platforms in alignment with organizational goals...
