QA Laboratory Lead, Connaught
|Job Title:||QA Laboratory Lead, Connaught|
|Contact Name:||Larry O’Leary|
|Job Published:||over 1 year ago|
Our client a healthcare manufacturer based in Connaught, now seeks a QA Laboratory Lead who is responsible for managing the Laboratory Data Integrity Program, LIMS application and Laboratory Training Program.
This Lead is responsible for the successful execution of strategic Data Management and Development projects for the Analytical Laboratory. This individual will be tasked with leading and managing initiatives and projects in the areas of data management, data governance and quality, and laboratory training and development.
Additionally this individual will be responsible for managing the Analytical Lab?s Data Integrity Program.
Responsibilities for QA Laboratory Lead, Connaught:
Provide motivation to the team and take appropriate corrective action on performance management as required.
Hold performance meetings according to company policy.
To take an active role in the recruitment of team members.
Actively participate in the training and certification of new employees.
Ensure that all aspects of the area of responsibility are fully staffed and that any constraints are managed appropriately.
Ensure all activities are completed in line with regulatory (QA and EHS) and corporate requirements.
Provide required data per project/schedule timelines to support laboratory operations.
Provide team KPI data.
Attend Departmental and APEX meetings; Safety, Green Team Meetings
Hold the agreed number of Team Meetings and Andon Board meetings.
Any other meeting as directed by the area Manager.
Provide review and approval of local and corporate documents.
Work directly with the other Laboratory Leads to ensure that all testing is completed as per schedule/ project timeline.
Ensure review of data and reports generated within the team within agreed timelines.
Work to ensure that sufficient technicians are proficient in team tasks.
Requirements for QA Laboratory Lead, Connaught:
Bachelor?s Degree in Science or similar technical qualification.
Proven track record in a quality discipline in the FDA, EU regulated industry.
Proven track record in direct people management
Knowledge of laboratory GMP and Data Integrity standards
Ability to articulate clearly when dealing with external bodies e.g. Regulatory bodies
Excellent conflict handling skills
Larry on 01-2302400 / email@example.com
The RFT Group, BioPharmaceutical Division specialise exclusively in the recruitment of scientists, engineers and executives for the biotechnology, pharmaceutical and medical device sectors. For a list of all our current vacancies, view our website http://www.rftgroup.ie/
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