Quality Technician - Night Shift at Phillips Medisize
Letterkenny, County Donegal, Ireland -
Full Time


Start Date

Immediate

Expiry Date

18 Jun, 25

Salary

0.0

Posted On

19 Mar, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Testing, Communication Skills, Market Data

Industry

Pharmaceuticals

Description

Your Job
As a Quality Technician, you will be responsible for performing inspections and tests on finished devices to ensure compliance with specifications and quality management systems. You will actively participate in maintaining our quality culture and contribute to the company’s goals and KPIs, while upholding our environmental and safety policies.
Our Team
Are you passionate about quality assurance and eager to contribute to a dynamic team? Join our Quality Department as a Quality Technician on the Night Shift and become an integral part of ensuring our products meet the highest standards.

WHO YOU ARE (BASIC QUALIFICATIONS)

  • Minimum of a Leaving Certificate standard in education
  • Experience in a Quality, Inspection, or Engineering function
  • Working knowledge of ISO 13485/15378 and FDA 21 CFR Part 820
  • Analytical approach to issues and testing techniques
  • Excellent communication skills
    At Koch companies, we are entrepreneurs. This means we openly challenge the status quo, find new ways to create value and get rewarded for our individual contributions. Any compensation range provided for a role is an estimate determined by available market data. The actual amount may be higher or lower than the range provided considering each candidate’s knowledge, skills, abilities, and geographic location. If you have questions, please speak to your recruiter about the flexibility and detail of our compensation philosophy.

WHO WE ARE

Phillips Medisize, a Molex company, collaborates with industry leaders to design and manufacture drug delivery systems, medical devices and diagnostic tools that save and improve the quality of life for millions of patients annually. With our dedicated team of 6,000+ employees in 29 locations around the world, we share our customers’ mindset that every product is critical to a healthcare provider and their patients somewhere in the world. Molex is a multi-sector global electronics brand owned by Koch, Inc., one of the world’s largest privately held companies. Discover your potential to make a difference
At Koch, employees are empowered to do what they do best to make life better. Learn how our business philosophy helps employees unleash their potential while creating value for themselves and the company.
Additionally, everyone has individual work and personal needs. We seek to enable the best work environment that helps you and the business work together to produce superior results.

LI-JO

Responsibilities
  • Perform inspection and testing on all finished devices as per the relevant specifications
  • Ensure compliance with the Quality management systems in place (ISO 13485/15378/ 14001/FDA 21CFR Part 820) and other relevant standards.
  • Perform environmental monitoring of cleanrooms as per the frequency in place.
  • Perform cGMP Audits of the Manufacturing and Warehouse Areas.
  • Carry out duties in accordance with Quality, Environmental Health and Safety policies of PMLK and GMP.
  • Contributes to the achievement of the company goals and KPI’s and maintain compliance with MBM guiding principles. Responsible for self-training on MPS divisional documentation in Molex.edu learning management system.
  • Active participation in the quality culture, CIP and recognition programs, the recognition and rewards and “shout out” programs RRE - produce a minimum of 2 cards per year
  • Carry out environmental monitoring of all the production areas.
  • Report on any out-of-specification conditions on the environmental monitoring on a monthly basis. Perform inspections and tests on outgoing product in order to determine compliance with specification and suitability for use.
  • Ensure that non-conforming products in the area assigned are appropriately controlled and dealt with. Perform cGMP Audits of the Manufacturing and Warehouse Areas
  • Continuously audit and monitor practices in assigned area to ensure compliance to procedures and conformance to specifications.
  • Perform standard and non-standard tests for evaluation and qualification of new processes, products, materials and equipment in an accurate and timely manner.
  • Maintain paperwork records and documentation relating to quality operations in an orderly fashion so that information is easily traceable. Prepare formal and informal reports from information generated.
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