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QC Scientist
Limerick
Project Engineer
Limerick
Validation Lead
Limerick
Process Engineer
Dublin North
QC Manager
Dublin
R&D Manager
Galway
Head of R&D
Galway
Data Scientist
Limerick
Senior R&D Engineer
Limerick City
Process Engineer
Limerick
Quality Engineer
Limerick
Data Scientist
Limerick
Consultant




Search Results for Quality Control Manager
Job Title. Location Salary Actions

Quality Manager (Laboratory Diagnostics)

Our client is a leading organisation in the manufacture of Laboratory Diagnostic solutions. They are currently seeking a full time, permanent Quality Manager who will report to the Director of Quality & Regulatory. This is a brand new position in the company, due to their success in developing new products. The sucessful person shall be joining an established Quality team and will be responsible for 3 direct reports. The role is based full-time on site in our clients Manufacturing facility. A senior level role suitable for someone who likes to work in a fast-paced R&D en...

Location: Limerick,
Quality Manager (Laboratory Diagnostics)
Limerick Not Disclosed

QC Associate Manager (LO A007956)

Summary: Oversees the laboratory quality control testing of in-process, stability, and final drug products. Has technical responsibility for all bioanalytical aspects of QC testing. Essential Duties and Responsibilities include, but are not limited to, the following: • Coordinates with members of Manufacturing, Stability, and Business Ops to provide analytical support. • Manages QC Analysts, distributes work load, and monitors progress. • Manages product testing to ensure efficient and compliant operations. • Review...

Location: Limerick,
QC Associate Manager (LO A007956)
Limerick Not Disclosed

QC Manager-Technical Resources (LO A007957)

Summary: Perform, review and manage assay development, characterization, optimization, transfer, validation and investigation for QC chemistry or QC Biochemistry group. Provide technical support, guidance and supervision for release, stability, and in-process testing and assay development. Essential Duties and Responsibilities include, but are not limited to, the following: • Perform, review and manage assay development/validation for QC Chemistry or QC Biochemistry group. • Review new test procedures and assays. • Ma...

Location: Limerick,
QC Manager-Technical Resources (LO A007957)
Limerick Not Disclosed

QC Manager-chemistry (LOA007664 )

Summary: The successful candidate will be responsible for development, implementation and management of the QC Chemistry department for a cGMP biopharmaceutical manufacturing facility. Essential Duties and Responsibilities include, but are not limited to, the following: • Lead and coordinate the startup of a new laboratory building including ensuring monitoring and communicating timeline. • Ensure construction adherence to plan. • Lead a team of six or more individuals to order equipment and supplies to facilitate occupation of the n...

Location: Limerick,
QC Manager-chemistry (LOA007664 )
Limerick Not Disclosed
Other Quality Control Jobs
Job Title Location Salary Actions
QC In Process Analyst - HPLC Cork Not Disclosed

Quality Control Manager Career Profile

Quality Control Manager

Duties and Responsibilities:
  • Responsible for overseeing and prioritizing product testing in the following areas according to establish procedures and production timelines
  • Responsible for providing supervision and direction for the professional supervisory staff in Quality Control department and oversees
  • Responsible for managing department budget
  • Responsible for the support of product COA release
  • Responsible for part 11 compliance throughout the laboratory in addition to support for the automated chromatography and laboratory information system
  • Responsible for directing and reviewing all investigations due to out of specification or out of trend data and reporting these occurrences to upper management.
  • Responsible for maintaining adequate laboratory supplies to meet operational expectations
  • Ensure cGMP compliance with methods, procedures, instruments and employee training
  • Maintain a laboratory safety and hazardous material disposal program to ensure support of environmental Health and Safety guidelines
  • Review and provide recommendations for improvement to new and current methods and specifications including GTM's and SOP's
Qualifications
  • Generally a BSc degree or higher is required. Relevant experience in a scientific discipline closely related to pharmaceutical operations is strongly preferred.
  • A minimum of five years of supervisory experience in a Quality Control laboratory environment is required.
    • Possess a specialized knowledge of document systems, analytical methods and instrumentation
    • Requires advance skills in prioritizing workflow
    • Excellent problem solving skills and good communication skills, both oral and written.
    • Proficiency in the use of Microsoft Office products as well as other software utilized within the scope of this position.