Associate QA Compliance Engineer

Posted 22 Days Ago
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Limerick, Munster
In-Office
Junior
Software
The Role
The Associate Quality Engineer will support QA operations, implement and manage the Quality Management System, conduct audits, and ensure compliance with regulations in a collaborative environment.
Summary Generated by Built In

Associate QA Compliance Engineer



Kneat enables regulated organizations to move from paper-based validation to intelligent, digitized, paperless solutions. And we do it through the ongoing development of a powerful, purpose-built software platform. In 2014, after 8 years of intensive software development, we launched the world’s most advanced validation software to help revolutionize the speed, precision, transparency and intelligence of validation in the Life Sciences sector. The solution is now used by some of the world’s leading Life Sciences companies. 

 

As Kneat continues to expand, we are looking for an Associate QA Compliance Engineer to join our QA Compliance Department.

Position Summary  

Reporting to our QA Compliance Manager the Associate QA Compliance Engineer, will be responsible for supporting daily quality operations associated with software development and delivery and supporting the implementation and management of all aspects of the Quality Management System (QMS) within the organization.

 

The successful candidate will work collaboratively with software developers, IT staff, account managers, other QA personnel, and business stakeholders to ensure that quality and compliance are the cornerstone of all aspects of the company’s operations, and that all customer, business, and regulatory requirements are met to the highest degree of satisfaction.

 

Primary Responsibilities  

  • Support the implementation and continuous improvement of Kneat’s integrated management system (IMS).
  • Internal IMS audits and input into management reviews.
  • Ensuring that all project documentation is delivered into the QMS.
  • Approval and management of project documentation and other project deliverables, ensuring that projects are always audit-ready. Maintain QA dashboard and metrics.
  • Regulatory and customer audit support; always ensuring audit readiness.
  • Supporting external vendor audits.
  • Assessment of compliance systems on ongoing basis to identify opportunities for process improvement.
  • Reporting to management on the conformance/compliance state of our QMS based on internal audits.
  • Supporting the customer complaints process.
  • Tracking and monitoring the implementation of corrective actions to provide assurance that deficiencies have been addressed.
  • Provision of training on quality systems and methodologies to company personnel.
  • Advising relevant personnel on the status of investigations and associated corrective actions and commitments, as appropriate.
  • Review and approval of qualification/validation documentation.

 

This is not a QC Test Engineer role nor a Validation Engineer role.





Minimum qualifications 

  • Degree or higher in a science, engineering, IT, or similar discipline. (experience will be considered in lieu of education)
  • 2+ years of experience working in a Quality Systems or Quality Assurance related role.
  • Understanding of ISO9001:2015 requirements and/or requirements for systems qualification in a regulated environment.
  • Experience in change control, risk analysis, root cause investigation, complaint handling, non-conformances, corrective actions, etc.
  • Effective writing and communication skills.
  • A passion for quality in a leading-edge technology-based organization.
  • Ability to work well independently or on a team.
  • Proven knowledge and understanding of IT/Life Sciences industry regulations, including FDA and GxP requirements.
  • Experience of participating in customer vendor audits

 

What We Offer You 

 At Kneat, we truly value ideas and collaboration so we’ve created an environment that builds, protects and celebrates teamwork. Our strong culture is central to our continued success. 

 We offer programs and rewards that one would expect from a highly successful and growing technology company: 

 A fantastic culture, team, energy, and a high-growth successful company

  • Competitive salary and benefits
  • Flexible work arrangements
  • Health benefits
  • Training & professional development

 

We invite interested applicants to share their resume and cover letter. 

We operate on a hybrid working basis. 

Applicants must have a permanent Irish working visa. 

Successful applicants will be subject to references and a background check.

 

 

Reasonable Accommodations Statement: To perform this job successfully, an individual must be able to perform the aforementioned duties and responsibilities satisfactorily. Reasonable 

accommodations may be made to enable qualified individuals with disabilities to perform these essential functions. Kneat is an equal opportunity employer 

 

Top Skills

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The Company
HQ: Limerick, Limerick
295 Employees
Year Founded: 2006

What We Do

We digitize validation for Life Sciences. Our purpose-built software makes validation easier, faster and smarter for BioPharma and Medical Device companies.

Kneat is a 21 CFR Part 11 and EudraLex Annex 11 compliant enterprise platform that eliminates paper and gives users an unprecedented capability to create, manage, access and mine validation data. Use Kneat to manage any validation, commissioning or qualification process and never go to paper again.

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