QC Analyst - Micro

Cpl Group

Dublin

On-site

EUR 42,000 - 56,000

Full time

9 days ago

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Job summary

Pfizer in partnership with Cpl Group seeks a QC Analyst Micro to join the team on an 11-month fixed-term contract at our Dublin plant in Grange Castle. This onsite role focuses on microbiology testing, calibration of instruments, and timely documentation in a cGMP environment.

The role requires a science/engineering background with strong communication skills; training will be provided and there are opportunities to support QA investigations and audits.

Qualifications

  • Requires degree: Science/Engineering or equivalent (not essential but preferred)
  • Excellent communication and interpersonal skills
  • Incumbents may be asked to perform other duties as required

Responsibilities

  • Perform microbiological testing on finished drug product, in-process materials, stability samples and environmental monitoring
  • Calibrate and use laboratory instrumentation
  • Document analytical results in a timely manner
  • Report non-conformances to the QC Manager
  • Assist in preparation/review of SOPs, reports, and protocols
  • Assist in training of other analysts and ensure training compliance
  • Support validation/qualification of test methods and processes
  • Facilitate investigations and support product investigations
  • Support laboratory inspections and audits
  • Troubleshoot lab methods and instrument issues
  • Maintain trend analysis programs and contribute to QC operations
  • Liaise with internal and external customers
  • Ensure samples analyzed meet batch disposition requirements

Skills

Excellent communication & Interperson

Education

Third level qualification in Science/Engineering or equivalent

Job description

Cpl In partnership with our client Pfizer are seeking a QC Analyst Micro to join the team for an 11 month fixed term contract, Onsite at their state of the art plant in Dublin, Grange Castle. this is an Onsite role.

Job Responsibilities:
  • Perform Microbiological testing analysis on, but not limited to, finished drug product, in process materials, stability samples and environmental monitoring.
  • Responsible for calibration and use of laboratory instrumentation.
  • Complete documentation associated with analytical results in a timely manner.
  • Report and document any non-conformances to the QC Manager.
  • Assist in the preparation and review of area documentation e.g. SOP's, Reports, Protocols.
  • Assist in the training of other analysts.
  • Ensure training compliance within assigned work area and QC.
  • Perform and assist in additional duties as directed by the QC Manager.
  • Ensure relevant assays are performed on samples in support of release test and stability test programs.
  • Support any validation and qualification of test methods and processes.
  • Facilitate laboratory investigations and support associated product investigation.
  • Support Laboratory inspection and audits.
  • Troubleshoot laboratory methods and instrument problems.
  • Establish and monitor trend analysis program.
  • Contribute to the operations of the Quality Control Laboratories.
  • Liaise with all customers both internal and external.
  • Record and review laboratory testing documentation to cGMP standard.
  • Implement and adhere to appropriate levels of cGMP within the laboratory.
  • Promote safety awareness and the established culture of IIF within the assigned work area.
  • Ensure that sample analysis is conducted to meet batch disposition requirements.
To be successful in this role the following are prerequisites to application:
  • Third level Qualification in Science, Engineering or equivalent is preferred though not essential.Exceptions may be considered where relevant skills/experience and correct attitude and behaviours exist (this may be supplemented by further education in parallel)
  • Excellent communication and interpersonal skills
  • This job description indicates the general nature and level of work expected of the incumbent.It is not designed to cover or contain a comprehensive listing of all activities, duties or responsibilities required of the incumbent.Incumbents may be asked to perform other duties as required
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