Qc Bioanalytical Analyst

PE Global (UK)

Swords

On-site

EUR 40,000 - 60,000

Full time

14 days+

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Job summary

PE Global (UK) is recruiting a QC Bioanalytical Analyst for a multi-national Pharma client in Dublin. This contract position involves executing and supporting analytical testing with various assays like HPLC and PCR, ensuring compliance with GMP requirements.

Ideal candidates will have 1-5 years of laboratory testing experience in the Pharmaceutical industry and possess effective communication skills. The role also encompasses maintaining laboratory equipment and participating in audits.

Qualifications

  • 1 – 5 years laboratory testing experience in the Pharmaceutical industry.
  • Relevant experience in GMP settings.
  • Knowledge of regulatory requirements to Irish and European standards.

Responsibilities

  • Execute routine analytical testing with various assays.
  • Support the laboratory testing schedule for efficient QC systems.
  • Calibrate and maintain laboratory instruments.

Skills

Laboratory testing experience in the Pharmaceutical industry
HPLC Analysis
PCR testing
Bioassay methods (ELISA)
Effective communication skills

Job description

PE Global is currently recruiting for a QC Bioanalytical Analyst for a leading multi-national Pharma client based in Dublin

This is a contract position.

Role:
  • Executing and supporting routine analytical testing with assays such as HPLC Analysis (IEX, SEC, RPLC), UV analysis, Capillary Electrophoresis (CE), PCR testing, Bioassay methods (ELISA methods) and a wide range of compendial methods on Release, In-process, Stability samples in compliance with GMP requirements.
  • Executing and supporting routine analytical testing with Raw materials onsite.
  • Follow up-to-date practices with reference to pharmacopoeias, specifications, regulations and industry standards.
  • Support the laboratory testing schedule to achieve an efficient QC system.
  • Receive and manage samples that come into the lab for stability, in-process and release testing.
  • Reagent preparation, cleaning, and routine equipment maintenance.
  • Maintain good housekeeping and hygiene within the laboratory.
  • Calibrate and maintain all designated laboratory instruments.
  • Participate in risk assessments, inspections, audits, incident investigations, etc. and implement and follow-up on corrective / preventative measures.
Requirements:
  • 1 – 5 years laboratory testing experience in the Pharmaceutical industry.
  • Relevant experience and skill sets in their area of expertise that adds value to the business; ideally in a manufacturing, preferably in a GMP setting.
  • Experience and critical skills in the area of expertise that add value to the business; ideally bioassay and DNA testing, chemistry testing and raw material testing.
  • Knowledge of regulatory/ code requirements to Irish, European and International Codes, Standards and Practices.
  • Knowledge of cGMP & Laboratory Quality Systems.
  • Effective communication, presentation and interpersonal skills, to interface effectively with all levels of colleagues and with external customers in a team orientated manner.
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