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SL Controls provides Equipment System Integration solutions to manufacturers, particularly those in the life sciences and technology sectors. Due to the ongoing growth and expansion of our business, we have a number of exciting engineering career opportunities available.
The roles are based in various locations across Ireland as well as in our office in the USA. Our engineers deliver cutting-edge Smart Factory and Industry 4.0 solutions, so the work is rewarding and challenging. We also offer excellent opportunities for career progression.
The Role:
* 6 Month Fixed Term Contract
* Westport, Mayo
* Onsite role
Role Brief:
In this role, you will be responsible for the qualification/validation of laboratory equipment, systems, and processes for an NNIT client. You will revalidate a range of mission-critical systems. All validation activity will be performed in line with GMP, FDA, and other regulatory requirements. You will work with client management and business units to ensure all projects are delivered on time and within budget.
Primary Responsibilities:
* Support equipment validation and potentially some CSV activities.
* Oversee, coordinate, guide, and implement the site validation master plan under prospective, concurrent, and retrospective validation studies in a timely manner, with the relevant engineers. Ensure that all validation requirements are met for any new process, equipment, or change to existing process or equipment.
* Actively work on validation projects, being the departmental point person and completing all associated project documentation in line with current corporate and regulatory expectations.
* Participate in risk assessment processes for all business units & participate in design review processes for all business units.
* Track and generate weekly metrics (GTW QMS, EHS, Compliance Wire, etc.)
* Facilitate the PQR review process, Regulatory Review Process, and Laboratory Equipment Review Process as required to meet project timelines.
* Provide support for audit preparation, direct audit interaction, and involvement in audit responses.
* Support and comply with internal EHS requirements, procedures, and policies. Ensure continued conformance to the EMS within the department.
Skills Brief:
* At least 2 years validation experience in a regulated environment.
* Proven experience of setting up change controls.
* Excellent project management skills.
* Strong critical thinking skills.
Preferred:
* 1 year Pharma or Life Sciences manufacturing sector validation experience.
Person Brief:
* A Bachelor's or Master's degree in a relevant field such as engineering, pharmaceutical science, quality, or regulation.
* This role is more suited to someone recently graduated with ideally 2 years of experience.
* A team player looking to gain more experience and develop their career in the Pharma manufacturing sector.
* Currently holds a valid work permit allowing immediate work in Ireland.
* Resides locally or can relocate quickly, with own transport, as public transport is limited.
Opportunity Brief:
This is an excellent opportunity to work with global industry leaders, developing and improving industry-leading technology solutions. NNIT Ireland offers a supportive environment focused on employee development and wellness, with a competitive compensation package rewarding high performers.
Company Brief:
NNIT Ireland specializes in Equipment System Integration and System Support. We assist top multinational companies in the medical device and pharmaceutical sectors to achieve Six Sigma and OEE targets. Over 20+ years, we have grown from a Sligo-based enterprise into an international business with offices in Galway, Limerick, Leinster, and Florida, USA. We pride ourselves on expertise in industrial IT integration and regulatory compliance supporting global end users, OEMs, and technology providers.
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