Current jobs related to Qa Compliance Specialist - Sligo, Sligo - Gertek Project Management


  • Sligo, Sligo, Ireland Gertek Project Management Full time

    Sligo Based Role GerTEK is an engineering consultancy company specialising in project management, talent solutions and commissioning qualification and validation services. We partner with many of the world's largest life science & technology companies who entrust in us to deliver their most strategic and important projects with our technically strong...


  • Sligo, Sligo, Ireland PE Global Full time

    Social network you want to login/join with:PE Global is currently recruiting for a QA Manufacturing Compliance Specialist on behalf of a leading pharmaceutical company based in Sligo. This is an initial 12-month contract role.ResponsibilitiesEnsure that all products leaving meet the standards required for marketed and investigational drug products.Ensure...


  • Sligo, Sligo, Ireland Cpl Full time

    Company Profile:Our client a leading biopharmaceutical company are hiring for a QA Compliance Specialist III for their state of the art manufacturing facility in Sligo on an initial 12-month contract. If interested in taking your next step into a Senior level QA role in a emerging pharma hub don't hesitate to reach out to myself today for more info or apply...


  • Sligo, Sligo, Ireland Cpl Full time

    Social network you want to login/join with:Quality Operations Compliance SpecialistSummary:Ensure that all products and manufacturing processes meet required quality standards for both commercial and investigational drug products. Provide compliance oversight and support to Operations to ensure adherence to GMP and internal procedures.Key...


  • Sligo, Sligo, Ireland Cpl Full time

    Our client a leading biopharmaceutical company are hiring for a QA Compliance Specialist III for their state of the art manufacturing facility in Sligo on an initial 12-month contract. If interested in taking your next step into a Senior level QA role in a emerging pharma hub don't hesitate to reach out to myself today for more info or apply below.Job...


  • Sligo, Sligo, Ireland Cpl Technology - Tech Recruitment Experts Full time

    6 days ago Be among the first 25 applicantsQuality Operations Compliance SpecialistSummaryEnsure that all products and manufacturing processes meet required quality standards for both commercial and investigational drug products. Provide compliance oversight and support to Operations to ensure adherence to GMP and internal procedures.Key ResponsibilitiesLead...

  • QA Specialist

    2 weeks ago


    Sligo, Sligo, Ireland beBeeQuality Full time

    Quality Assurance RoleWe are seeking a highly skilled Quality Assurance Specialist to join our team. As a Quality Assurance Specialist, you will play a key role in ensuring the quality and safety of our products.The successful candidate will have a strong understanding of Good Manufacturing Practices (GMP) and quality standards. They will be responsible for...


  • Sligo, Sligo, Ireland Cpl Full time

    Join to apply for the QA - Validation Specialist role at Cpl1 week ago Be among the first 25 applicantsJoin to apply for the QA - Validation Specialist role at CplGet AI-powered advice on this job and more exclusive features.Senior Talent Partner at CPL - Science & Engineering : 01 614 6178JO-2506-552925QA Validation Specialist required for expanding biotech...


  • Sligo, Sligo, Ireland CPL Full time

    QA - Validation SpecialistBiotechnologySligo – PermanentI am looking to speak with candidates with Validation experience in a GMP Quality environment for a growth role of QA Validation Specialist.The successful candidate will support review and approval of validation documentation and activities related to the qualification of the facility, equipment and...

  • QA Specialist

    6 days ago


    Sligo, Sligo, Ireland Phibro Animal Health Full time

    About Phibro Animal Health CorporationPhibro Animal Health Corporation is a publicly traded, global organization with a rich history in animal health and nutrition as a manufacturer and marketer of medicated feed additives, vaccines, nutritional specialty products, and mineral nutrition. We strive to be a trusted partner with livestock producers, farmers,...

Qa Compliance Specialist

1 month ago


Sligo, Sligo, Ireland Gertek Project Management Full time
Ger TEK is an engineering consultancy company specialising in project management, talent solutions and commissioning qualification and validation services.

We partner with many of the world's largest life science & technology companies who entrust in us to deliver their most strategic and important projects with our technically strong personnel ensuring all important activities meet both current requirements and client's needs.

We have multiple projects that we support, and we are looking to add to our team, we are interested in talking to you if you fit the criteria outlined below: QA Compliance Specialist Key Responsibilities: Ensure adherence to standards for both marketed and investigational drug products leaving the site.

Guarantee compliance of products and aseptic processes with end-user, regulatory, and company requirements.

Provide quality and compliance oversight for Operations, ensuring manufacturing aligns with site policies.

Conduct quality oversight during aseptic processing, including observing aseptic interventions.

Lead/assist in investigations related to non-compliance in product or manufacturing processes.

Review and audit completed Batch Records and Manufacturing Logs.

Complete quality reviews of operations documentation (SOPs, JSTMs, Risk Assessments).

Perform Line Clearance activities and Incoming Raw Material checks.

Provide Stability Program Support, including sample pulls and weekly checks.

Maintain finished product status and administer Quality Logs (e.g., QA Hold, Sample Request).

Lead daily walkarounds of manufacturing areas.

Drive continuous improvements and streamline processes for compliance.

Offer support as needed.

Education & Key Requirements Third-level degree in a science, quality, or engineering discipline.

Minimum three years' experience in quality/operations in a regulated GMP environment.

Aseptic processing experience in quality or operations is highly desirable.

Strong knowledge of regulatory requirements.

High attention to detail and mental concentration for accuracy and compliance.

Total commitment to quality and maintaining high standards.

Demonstrates integrity, strong work ethic, and supports compliance with c GMP and HPRA/FDA regulations and company policies, procedures and guidelines We offer competitive compensation packages and opportunities for professional growth in a dynamic and innovative work environment.

If you are a motivated QA Compliance Specialist seeking an exciting challenge in the biopharmaceutical industry, we encourage you to apply.

To start the process click the Continue to Application or Login/Register to apply button below.