Search Results: 674 vacancies
Provide technical leadership and manage a team for qualification activities and data integrity initiatives in regard to small manufacturing... ...following:
Strong knowledge and understanding of equipment used for QC analysis and operations.
Strong background and familiar with...
As a QC Analyst within Sample Management you will perform a variety of chemical or biological analyses on raw materials, products, in-process materials, or stability samples in support of the company’s quality program.
This role will be a 24/7 shift position.
A typical...
The Associate Manager QA is responsible for all aspects of assigned QA Team; provides leadership and support to direct reports. The Associate Manager QA for Manufacturing Operations provides QA oversight to ensure that drug substance manufacturing activities are compliant with...
...maintain harmonization and electronic data integrity across IOPS sites and compliance with regulatory guidelines.
As a QC Electronic Data Management Specialist, a typical day might include, but is not limited to, the following:
Work with cross-functional teams to define...
...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 quality review...
As a QC Compliance Analyst you will support the QC organization in meeting compliance targets through laboratory investigation and deviation management. The Compliance Analyst will report quality system metrics to the group and identify improvements that can be made in all quality...
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...
...chemical or biological analyses on, products, in-process materials, or stability samples in support of the company’s quality program.
As a QC Analyst within the HPLC Lab, a typical day might include, but is not limited to, the following
Gathering data and documenting test...
As a QC Micro Analyst you would perform testing to ensure cGMP compliance in the manufacturing facility. Responsible for assessing the microbiological quality of products, manufacturing equipment, manufacturing process areas, and facility utilities.
Note, this is a shift...
...defined Quality Control projects. You may additionally support, plan and coordinate operational tasks for other QC projects under the guidance of a Portfolio/Program Manager.
This is a 12-month temporary contract.
A typical day might include, but is not limited to, the...
...responsible for the operational oversite of the QA Microbiology and Lab Support Teams at the... ...organizations and must ensure personnel management (goals, feedback, development plans, priorities... ...Control and Laboratories:
Implements a QC oversight function that will assist in the...
...motivated and detail-oriented Biotechnology QA Sr. Associates to join our quality... ...regulations.
~Collaborate with production and QC teams to ensure product quality throughout... ...of cGMP, FDA, Data Integrity, Quality Risk Management and other biopharmaceutical regulatory requirements...
€40k - €50k per annum
...QC Lab Analyst Job Limerick FRS Recruitment are proud to be recruiting on behalf of an International Biotechnology company in the Mid- West who are looking to significantly expand their Quality Control Operations. Seeking a candidate with min 9-12 months GMP industry experience...
...manufacturing standards policies and procedures
A typical day as a QA Validation Specialist, may include:
Generates, executes and/or... ...to supervise contingent workers.
Other duties assigned by management.
Knowledge Skills & Abilities:
Ability to maintain...
Within this 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...
...analyses on raw materials, products, in-process materials, or stability samples in support of the company’s quality program.
As a Senior QC Analyst in Raw Materials a typical day might include, but it not limited to, the following:
• Gathering data and documenting test...
In this role you will be responsible for providing QA oversight and support to manufacturing activities. Performs and leads activities in support of dispositioning product while ensuring compliance with Quality Assurance (QA) policies and procedures, cGMPs, SOPs, and Regeneron...
...QA Specialist (hybrid)
RK8318
Contract – 12 months
Cork
We’re currently recruiting for an exciting opportunity with an award... ....
Carries out tasks related to the administration of event management systems including Review & Approval of Event, Deviations, and Customer...
Life Science Recruitment
Limerick
4 days ago
...reports
Performing monthly performance feedback meetings with direct reports
Escalating all performance issues to management and/or HR
As a Lead Sr QC Micro Analyst, a typical day might include, but is not limited to, the following
Representing Micro and...
...agency expectations. The position will liase with the IT and broader QA organizations to ensure all aspects of IT related programs are in... ...control and SOPs
Participate and support the Quality Risk Management (QRM) principles in the formal and informal risk assessment initiatives...
