Quality Control Analyst

1097517
  • Job type

    Temporary
  • Location

    Cork
  • Working Pattern

  • Specialism

    Quality Assurance
  • Industry

    Pharmaceuticals
  • Pay

    DOE

QC Analyst, Lab testing, shift

QC Separations Analyst – Days
Contract: 12 months
Location: Ringaskiddy, Onsite
Shift may be possible.
Competitive salary Open to experience levels.

Position Summary:

This position is responsible for carrying out tasks and projects related to testing procedures, equipment and lab utilities as required by Good Manufacturing Practice (GMP).

Partners with other Departments to ensure that all QC testing activities are completed in an efficient manner.

There is a high volume of complex process data to manage, in addition there are a high number of methods and different technologies within the lab. Analysis includes: cSDS, cIEF, SE-HPLC, IEX- HPLC, Reverse Phase HPLC, Mass Spec

Knowledge of Empower is the most sought-after skill. Team of 22.

General Scope of Responsibilities:
  • Achieves a high level of competency in laboratory methods and procedures to support in process and release testing of biotechnology products.
  • Review and approval of laboratory test results.
  • Performs analytical testing activities in relation to method validation and technical transfer activities to ensure that all methods meet ICH, USP and EP guidelines.
  • Executes validation, operation, maintenance, calibration and troubleshooting of equipment and it’s associated software.
  • Write/executes reports and reviews IQ/OQ and PQ protocols to ensure that all relevant equipment is qualified for cGMP use.
  • Ensures that all testing is completed, reviewed and approved within agreed turnaround times.
  • Ensures QC activities are carried out in compliance with product license commitments, cGMP and company quality standards.
  • Trains other QC analysts in laboratory methods and procedures when required.
  • Writes/updates and reviews TMs, SOPs and WIs as required.
  • Writes and reviews invalid assays, non-conformances and deviations as required.
  • Actively participates in JSI lean initiatives such as Kaizen, 6S and Gemba.
  • Is an active member of the QC group and provide assistance with other group activities as required.
  • Communicates relevant issues to the QC Team Leader promptly.
  • Maintains and develops knowledge of analytical technology as well as cGMP standards.

Specific Testing Experience Required
  • HPLC
  • Capillary Electrophoresis
  • UPLC/Mass Spec (desirable)

Key Competencies Required:
  • Excellent interpersonal skills
  • Ability to operate as part of a team is critical.
  • Excellent communication skills both written and verbal.
  • Good knowledge of LIMS, Trackwise and Electronic documentation systems.
  • Good knowledge of Microsoft Office applications such as word, Excel, PowerPoint
  • Experience working in a high throughput laboratory environment.
  • Excellent technical writing skills.
  • Customer focus.
  • Attention to detail.
  • Strong problem-solving skills.
  • Results and performance driven.
  • Adaptable and flexible.

Qualifications And Experience:
  • BSc (Honors) in a scientific/technical discipline.
  • Experience in a QC laboratory-testing environment within the biological and/or pharmaceutical industry.
  • Demonstrated knowledge and testing experience in an FDA/HPRA approved QC laboratory.


#1097517

Talk to Emma Davidson, the specialist consultant managing this position

Located in Hays Recruitment, Cork, 54 South Mall, CorkTelephone: +35315827794
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