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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
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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.