• Computer Science Degree or similar
• At least 3 years in QA Automation role
• Experience creating / adding to / maintaining test automation frameworks
• Knowledge of Agile methodologies
• Experience testing REST APIs
• Experience with cloud tech i.e. AWS
• Experience with Jenkins or similar

• Very Competitive salary
• Healthcare
• Excellent working environment
• Fantastic career progression potential
• Stock options

• Lead and be the subject matter expert in the assigned process engineering group.
• Provide daily guidance and communication to Engineering Technicians through daily PVD, email and follow up meetings as appropriate.
• Provide support to operations to optimize existing processes and to ensure that production goals are met.
• Monitoring equipment performance to lead/support improvement activity to reduce downtime events and yield losses.
• Drive process improvements through identification of problem areas/opportunities and collaboration with internal groups and external vendors using Lean/Six Sigma and project management techniques.
• Lead the complete validation of new and existing equipment including acceptance trials, debugging, process development, and final validation.
• Development and coordination of related documentation, including standard operating procedures, set-up guides, validation documentation.
• Engage with vendors on the development, design, and evaluation of equipment and/or processes requiring novel and innovative approaches in technology.
• Liaise with corporate R&D in the development of new projects and ensure that project timelines are met.
• Participate in the continuous improvement programs.
• Coordinate planned maintenance activities and process parameter records.
• Support the requirements of ISO13485 and quality system procedures including promoting and complying with cGMP.
• Assist with QNs, customer complaints and CAPA investigations.

Do you want to work for a vibrant, exciting company operating in one of the fastest growing markets online today?

I am working closely with a leading multinational eCommerce company that provide an online marketplace which allows their users to access a vast range of royal-free digital media content.

Currently undergoing a period of growth, I am looking to speak with a talented, passionate and experienced QA Engineer to join this companies Software QA team in Dublin. The perfect candidate will have excellent testing skills, be detail oriented, and will thrive working in a highly technical environment.

This person will work across various teams using a number of tools and technologies and the company are looking for someone with a proven record in enabling the delivery of quality software and engaging throughout the full SDLC.

Duties of the role:

•Interact with PM and Dev teams to gain a strong understanding of the project and the testing objectives.
•Maintain and expand existing testing documentation for product and solutions.
•Work within an Agile environment (using JIRA).
•Protect the overall of quality, security and performance.
•Execute/analyse manual testing and write, execute, and maintain automated tests using the Robot Framework.
•Setup/maintain test environments.
•Support production deployment of applications.

What you need:

•1 - 3 years' experience in QA (at least 1 year to be within an agile environment).
•Excellent understanding of the full Software Development Lifecycle.
•At least 1 years' experience of automated web application test tools (Selenium, Protractor, Robot, etc).
•Knowledge of databases and writing SQL.
•Exposure to/experience in managing frequent releases.
•Excellent communications skills.
•Exposure to PHP, Postgres, Linux implementations (Desirable).
•ISTQB Certification (Desirable).

Please apply at the link provided or contact me for more information on this role and the fantastic package on offer! Call 087 695 0048 or email niall.gormley@stelfox.com

Please note:
We have a number of similar positions currently, and in the future, which we would like to discuss with you should you indicate your interest in this role. When we receive your application for this role, we will contact you to advise you of our process for other similar positions.
Stelfox is fully compliant with GDPR regulations and you can read more in our privacy policy here: https://www.stelfox.com/privacy-policy-gdpr/
Your shared data will not be disclosed or transferred to a third party data controller or data processor located outside the EEA unless we have obtained your express consent.
We look forward to working with you.

• Providing support for ISO13485 Quality System.
• Ensuring alignment to all BD, external and appropriate regulatory requirements.
• Supporting production personnel in relevant continuous improvement activities (Six Sigma).
• Day to day Leadership/Management of New Product Quality Engineering Team. Lead and develop the team through involvement, delegation, and regular reviews of performance as established in IIGs (goals).
• Setup & Management of Key quality systems elements relating to direct production support such as the non- conformance system, incident reporting system and customer complaint analysis.
• Liaise with the R&D Department to ensure compliance to Product Specifications
• Ensure all CAPAs under your responsibility are completed in compliance with all regulatory and procedural commitments
• Develop and implement validation strategy for IQ/OQ and PQ requirements.
• Ensure verification activities undergo test method validation to ensure consistent operation of the test equipment and results for the intended use

• Third level qualification in an Engineering or Science Field (a postgraduate qualification in a related area would be advantageous).
• A minimum of 5 years work experience in an ISO 9001/2000 or ISO 13485 environment, coupled with a background in Medical Devices/Pharmaceutical Industry.
• Experience in the preparation of Technical Documentation.
• At least 3 years supervisory experience.
• Knowledge of Statistical Process Control and Six Sigma methodologies (Greenbelt Certification would be advantageous).
• Experience in CAPA system management.

• Computer Science Degree
• ISTQB certification
• At least 3 years in QA role
• Experience with test automation tools such as Selenium
• Strong SQL skills
• Experience in an Agile environment

• Competitive Salary
• Healthcare
• Pension
• Remote working flexibility post COVID-19

• Lead and be the subject matter expert in the assigned process engineering group.
• Provide daily guidance and communication to Engineering Technicians through daily PVD, email and follow up meetings as appropriate.
• Provide support to operations to optimize existing processes and to ensure that production goals are met.
• Monitoring equipment performance to lead/support improvement activity to reduce downtime events and yield losses.
• Drive process improvements through identification of problem areas/opportunities and collaboration with internal groups and external vendors using Lean/Six Sigma and project management techniques.
• Lead the complete validation of new and existing equipment including acceptance trials, debugging, process development, and final validation.
• Development and coordination of related documentation, including standard operating procedures, set-up guides, validation documentation.
• Engage with vendors on the development, design, and evaluation of equipment and/or processes requiring novel and innovative approaches in technology.
• Liaise with corporate R&D in the development of new projects and ensure that project timelines are met.
• Participate in the continuous improvement programs.
• Coordinate planned maintenance activities and process parameter records.
• Support the requirements of ISO13485 and quality system procedures including promoting and complying with cGMP.
• Assist with QNs, customer complaints and CAPA investigations.

IPS is hiring! We are looking for 2 talented Senior Process Engineers to join our industry leading Process Engineering team at our office in Dublin, Ireland.

The Senior Process Engineer is responsible for designing and implementing manufacturing processes, and, supporting utilities on a scale that can range from developmental pilot plant, to full commercial production. In this role we require a candidate who has process design and operations experience in pharmaceutical facilities, which include biologic and organic synthesis Active Pharmaceutical Ingredients.  

Job Duties and Responsibilities:

• Assist the Lead Process Engineer with conceptual design deliverables such as Process Flow Diagrams, and, Material and Energy Balances.
• Design utilities generation and distribution systems for new and existing manufacturing processes, including Utility Sizing models.
• Generate Process P&IDs that include, process control strategy and CIP/SIP functions, if appropriate. Also, generate P&IDs for critical utility systems, such as Pharma Water, Clean Steam, Process Gases, Heat Transfer Systems and Process Waste.
• Perform engineering studies for expanding, improving or automating existing facilities without supervision.
• Produce Equipment specifications and Equipment Datasheets for process equipment and instrumentation. 
• Support the delivery of Vendor packages through Scoping, Specification, Detailed Design, Construction and CQV.
• Generate Process Calculations to support design.  
• Support Process Safety and Environmental studies including HAZOP, ATEX, Risk Assessment, COSHH and implementation of EU/ ISO standards.  
• Assume ownership of the process-related aspects of a portion of a large project or an entire small project, and provide technical support to the project design team. 
• Make use of and participate in development of company design and production tools, including process simulation and smart P&IDs.
• Establish and maintain excellent working relationships with clients and members of the IPS design team. 
• Special projects as assigned.

• Minimum of 8 years of process engineering design experience, in the Biopharmaceutical industry.
• Process design and operations experience in pharmaceutical facilities, which include biologic and organic synthesis Active Pharmaceutical Ingredients.  
• Bachelor’s or Master’s Degree in Chemical / Biochemical Engineering.
• Proven experience generating PFDs, P&IDs, process equipment data sheets as well as supporting calculations, studies and narratives.
• General knowledge of Pharma system design and applicable codes in process engineering.  
• Has demonstrated strong time management skills and the ability to manage projects, problem solve and communicate effectively with co-workers.
• At this time, IPS are not currently hiring individuals for this position who now or in the future would require sponsorship for employment visa status.

About Us

IPS-Integrated Project Services is a global leader in developing innovative and cost-effective solutions for the engineering, construction, commissioning and qualification of complex pharmaceutical and biotech research and manufacturing facilities. With technical expertise spanning R&D to pilot-scale to large-scale production, our team specializes in the technology, trends and regulatory environment to successfully deliver capital projects and improve operations. For over thirty years, we have applied unique LEAN methodologies throughout the project life cycle, continually finding ways to do things better and more efficiently, delivering higher quality and controlling costs. Headquartered in Blue Bell, PA, IPS is a multi-national company with over 1,450 professionals worldwide and offices in California, Indiana, Kansas, Massachusetts, New Jersey, North Carolina, Pennsylvania, Brazil, Canada, China, Germany, Ireland, Singapore, Switzerland, UK and four locations in India. Visit our website at www.ipsdb.com.

Specialties

Process Architecture, Process Design, Engineering, Construction, Commissioning, Qualification, LEAN Project Delivery, Strategic Master Planning, Energy Conservation Management, Project Controls, Program/Project Management, Operations/Logistics Strategy and Planning, EPCMV and Staffing Services.

IPS is an equal opportunity, affirmative action employer of protected veterans (M/F/D/V).

Attention Search Firms / Third Party Recruiters:  IPS is not seeking assistance or accepting unsolicited resumes from search firms for employment opportunities with IPS. Regardless of past practice, all resumes submitted by search firms to any employee at IPS via-email, the Internet or directly to hiring managers at IPS in any form without a valid written search agreement in place for a specific position will be deemed the sole property of IPS, and no fee will be paid in the event a candidate is hired by IPS as a result of the referral or through other means.