QC Micro Analyst (11-Month Contract) - Onsite Dublin

Cpl Group; Leinster; On-site; EUR 42,000 - 52,000; Full time

Job summary

Pfizer is seeking a QC Analyst Micro to join our team on an 11-month fixed-term contract at the state-of-the-art Dublin Grange Castle plant. This is an onsite role.

The successful candidate will perform microbiological testing on finished drug products, in-process materials, stability samples and environmental monitoring, calibrate instruments, document results, and support audits and investigations. Training of others and ensuring cGMP compliance are also expected.

Qualifications

• 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 behaviors exist.
• 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

Responsibilities

• Perform Microbiological testing analysis on finished drug product, in process materials, stability samples and environmental monitoring.
• 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. SOPs, 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 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.

Skills

Communication skills

Education

Science/Engineering degree

Job description

Pfizer is seeking a QC Analyst Micro to join our team on an 11-month fixed-term contract at the state-of-the-art Dublin Grange Castle plant. This is an onsite role.

The successful candidate will perform microbiological testing on finished drug products, in-process materials, stability samples and environmental monitoring, calibrate instruments, document results, and support audits and investigations. Training of others and ensuring cGMP compliance are also expected.