Description
I have an immediate opening for a Quality Control Supervisor with a leading medical device company based in Athlone.The Quality Control (QC) Supervisor is responsible for supervising a variety of work functions that include the inspection and testing of raw materials, component piece parts, and finished goods received from suppliers. The Quality Control Supervisor is also responsible for supervising product release activities.
DUTIES AND RESPONSIBILITIES:
Technical*
* Demonstrates a theoretical understanding of laboratory operations, systems, methods and regulatory compliance.
* Demonstrates an understanding of company priorities, objectives and project timelines.
* Applies scientific judgment to perform work and contribute to milestones related to specific projects.
* Authors documents that impact Quality.
* Works with management to review FTE requirements, annual budgeting and other business needs.
* Responsible for maintaining a compliant training program.
* Reviews SOP's, development studies, validation procedures, change controls, deviations, and investigations to maintain compliance in the laboratory.
* Works independently on problems of diverse scope where the analysis of the situation or data requires in-depth evaluation of various factors.
* Applies knowledge of Good Manufacturing practices (GMP) on a daily basis.
* Performs additional tasks and duties as assigned.
* Works with analysts to develop, optimize and validate test methods, equipment and laboratory systems.
* Manage day-to-day laboratory operations.
Managing People*
* Delegates responsibility and projects to Quality Technicians based on their level of judgment and experience.
* Meets with individual employees on a regular basis to discuss, prioritize, and assign laboratory work and projects.
* Meets with functional group on a regular basis to discuss routine laboratory functions, individual projects, and department goals.
* Manage personnel development, annual performance reviews, and performance issues with minimal guidance.
Discretion*
* Proactively plans and prioritizes laboratory operations and resolves quality and compliance issues.
* Independently exercises judgment for broadly defined practices, procedures and policies to select methods, techniques and evaluation criteria.
* Uses judgment and experience to troubleshoot problems and formulate solutions.
Leadership/Management*
* Supervises Quality Technicians and provides training and mentorship.
* Responsible for coordinating or contributing to complex projects of moderate scope within QC and cross-functionally.
* Provides technical expertise within QC and outside of the department.
* Identify potential development opportunities for employees.
Qualifications/Education:
* Leaving Certificate or equivalent required.
* Higher Third Level education preferred (certificate, degree).
* Three years' experience in a like capacity or equivalent within the Medical Device or Pharmaceutical sectors is preferred.
Skills:
* Proven analytical or problem solving skills.
* Self starter and results oriented.
* Be able to multitask and adapt in a high pace environment.
* Excellent communication skills are required to work efficiently and effectively across all levels of the organization.
* Strong interpersonal and organizational skills.
This is an excellent opportunity to join a growing company during an exciting period for the business. If interested please apply directly to this advert or contact Derek Sheridan on for immediate consideration.