Quality Control Specialist
Work Type: Contract
Location: Carlow
Role Overview:
An exciting opportunity has arisen for a talented QC Associate Microbiology Specialist to join a leading pharmaceutical team in Carlow. The role is perfect for an experienced professional looking to make a significant impact in a fast-paced, cutting-edge environment. This position offers the chance to provide technical support to the Quality Control (QC) Microbiology Laboratory while contributing to the manufacture and supply of high-quality pharmaceutical products.
Key Responsibilities:
The QC Associate Microbiology Specialist will be a key player in the operations of the Microbiology Lab and will take on a range of senior responsibilities, including:
Method Development & Validation: Developing and executing microbiology test methods, project validations, and troubleshooting any issues that arise during validation studies.
Microbiology Support: Providing microbiological expertise for site investigations and ensuring compliance with regulatory standards.
Continuous Improvement: Driving continuous improvement initiatives, including lean lab practices, method optimization, and development.
Documentation & Reporting: Authoring and managing change controls, procedures, test methods, deviations, and ensuring accurate and timely documentation.
Result Authorization: Authorising microbiological sample results to support batch release.
Training & Development: Developing training modules and supporting team development through collaboration and coaching.
Environmental Control: Supporting the environmental control program through trend analysis and corrective/preventative actions.
Regulatory Compliance: Staying up to date with the latest regulatory requirements and ensuring these are applied to all aspects of microbiology testing and procedures.
LIMS System Updates: Managing LIMS system updates and ensuring proper handling of microbiological data.
Experience, Knowledge & Skills:
Proven experience in microbiology testing, method validation, and laboratory operations.
Strong planning and organisational skills, with the ability to work effectively under pressure.
In-depth knowledge of microbiological testing methods such as Bioburden, Endotoxin, and Sterility testing.
Demonstrated experience in change management and continuous improvement processes.
Strong interpersonal skills and the ability to communicate clearly, both verbally and in writing.
Self-starter with a passion for delivering high-quality results and strong commercial acumen.
Ability to work effectively in a high-performance team environment.
Qualifications & Education:
A Bachelor’s Degree or higher in Microbiology or a closely related field.
At least 5 years of experience in the Microbiology Pharmaceutical industry or a similar operating environment.
Strong knowledge in the execution, validation, and development of microbiology test methods.
Demonstrated ability to manage change and lead improvement initiatives.
Carlow, Ireland:
Carlow is a thriving, vibrant community offering a high quality of life. Nestled in the heart of Ireland, it combines the charm of countryside living with excellent amenities, making it a perfect location for work and leisure.
Take the Next Step:
If you're a driven and innovative QC Associate Microbiology Specialist looking for a rewarding role with an established organisation, this is your chance to make a meaningful contribution to the future of the pharmaceutical industry.
For further information on this role please contact Hannah Talbot
Phone: 086 107 0950
Email: engineering@hero.ie
Check out all our open jobs on our HERO Recruitment website – https://www.hero.ie/
Please Note: Under its obligation under the Data Protection legislation, HERO Recruitment will not forward your details to any company without your prior approval.
Data can only be transferred outside of the EEA on the basis of standards contractual clauses, to a country for whom an adequacy decision has been given by the European Commission or where the express permission of the data subject has been given. You have supplied us with your personal data in the process of applying for a position. Our client company may have personnel outside of the EEA who will review your data. We will apply the appropriate criteria in respect of the data transfer depending on the location of those personnel.
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