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Open nowPosted yesterday

QC Shift Analyst

gehc326 open roles

Where
Cork
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Your applicationOpen nowQC Shift Analystgehc · Cork

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The clock on this job

Early applications get read.

13.5% of postings close within 7 days. Measured by our own scanner across the market. gehc postings stay open a median of 15 days.

Share of postings closed within
  1. 2.3%1 day
  2. 4.6%3 days
  3. 13.5%7 days
  4. 21.8%14 days
  5. 36.6%30 days
  6. 58.9%60 days
This job: posted yesterday

gehc median: 15 days open

The posting

Job Description Summary

QC Finish Product Analysts ensure finished product quality through compliant pharmaceutical testing and documentation. The role combines laboratory analysis, regulatory compliance, investigations, and cross-functional support.

• Analysts perform routine tests, including HPLC, osmolality, iodine analysis, chromatography, pH, and extractable volume testing, while meeting turnaround times and cGLP and cGMP requirements. • Responsibilities include LIMS data management, stability support, investigations, instrument calibration, batch-release documentation, trend reporting, audits, and standard operating procedure control. • The role requires a third-level science qualification, 1 to 2 years of pharmaceutical GMP laboratory experience, strong communication skills, training support, and occasional overtime.

Job Description

Roles and Responsibilities

  • Carry out routine analysis on Finished Product samples ensuring compliance with cGLP/cGMP and that turnaround times are met. The testing carried out includes but is not limited to: HPLC, Osmolality, Organic Iodine, Inorganic Iodine, Thin Layer Chromatography, Free aromatic amines, pH, RI, Trom’s, EDTA, Technical tests, Extractable volume., complaints etc..
  • Assisting in the maintenance of the stability program
  • Actively involved in Investigations e.g. LIR’s. etc..
  • Logging of samples in LIMS
  • Entering results on LIMS, checking results are within specification and also task approval.
  • Ensure compliance with EHS at all times, actively participate in EHS activities.
  • Perform routine instrument calibration checks at appropriate times.
  • Preparation and control of Standard Operating Procedures and ensuring compliance with cGMP guidelines at all times.
  • Completion of Documentation for Batch Release process.
  • Assisting in the provision of trends, CPV etc..
  • Assist in audits.
  • Generation/ reporting of Key performance indicators for the group.
  • Be proactive in approach planning for future and implement improvements in an effective manner.
  • Develop areas of expertise in analytical testing in order to solve technical issues.
  • Ensure compliance with current pharmacopoeias and all regulatory/company guidelines.
  • Interaction with other departments e.g. QA, BU, Sterility assurance etc.
  • Keep colleagues informed of current issues and developments as appropriate.
  • Assist in the training and up skilling of colleagues.
  • Reasonable level of overtime will be required to facilitate the business needs.
  • Liaising with internal and external customers e.g., planning/ QA/ BU etc.
  • Carry out additional duties as deemed necessary by your Group Leader/ Supervisor.

Required Qualifications

  • A third level Science Qualification
  • Minimum of 1-2 years pharmaceutical experience in a GMP regulated laboratory environment.

Desired Characteristics

  • Strong oral and written communication skills. Ability to document, plan, market, and execute programs.

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Additional Information

Relocation Assistance Provided: No

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