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Contact Info
Alan O'Riordan
Life Science

+353873657522
[email protected]
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Details

Quality Supervisor


Reference:AOORAJTG-808155 Location: Dublin
Dublin North
Dublin West
Qualification:DegreeExperience:4-5 Years
Job Type:PermanentSalary: Not Disclosed
May be suitable for: QA Supervisor

Company/ Role Background

My client are currently looking to recruit a Quality supervisor to lead the Quality team. This is an excellent opportunity to lead a team, develop and gain experience within a company were every staff member has a vital role to play in achieving our objectives and making the company a success. The Quality team ensure active, raw material & finished product Quality & Integrity through analysis, compliance & Quality auditing, all driven by a culture of problem solving, teamwork & cross departmental communication to consistently assure delivery of quality products to our customers.

Responsibilities
The main responsibilities of the role include:
• To co-ordinate the day to day operational requirements of the lab
• Coordinating resources & equipment/HPLC usage for busy season
• Preparing lab budget and monitoring of spend
• HPLC Software - Empower Administrator
• Organise & Lead monthly & weekly team meetings
• Oversee yearly PM’s for all equipment & Manage all lab contractors/engineers
• Maintaining equipment issues database & providing training as required
• Perform HPLC Method Validation as required
• Monitor & coordinate the activities of the Rework product database spreadsheet
• To review and approve key documents including reports, SOPs and specifications
• Overseeing & maintaining the laboratory Visual Management Board (VMB)
• Responsible for Performance & Development Reviews for team
• Project Management oversight in the lab
• Lead or contribute to the completion of key Quality related projects
• Coordinate Quality related continuous improvement initiatives
• Identify training needs of Quality team & coordinate training plan to ensure competency in the performance of required tasks.
• Work closely with the manufacturing & packing teams, providing guidance on the implementation of manufacturing and packing process improvement programs in line with Best Practice.
• Plan & maintain monthly auditing programs for Quality processes in manufacturing & production
• Lead the Investigation of formulation and packing quality issues, proposing and implementing root cause solutions
• Organise training & Awareness sessions for Quality, Manufacturing & Packing areas relating to all aspects of quality
• Investigation of quality related customer complaints, using 8 step problem solving methodology
• Liaise with our contract manufactures, ensuring Quality standards & compliance with specification
• Oversight for Quality Actions Tracker & Rework database
• Manage Methods of Manufacture & Finished Product Specifications
• NPI: To assist with the introduction of new products on site in line with project timelines
• Promote health & safety within the laboratory

Essential Qualifications and Criteria

Skills and experience:

• Minimum 4 -5 years’ experience in a manufacturing environment is preferable.
• Pharmaceutical background is preferable.

Essential Qualifications:
A Bachelor’s degree, ideally in Chemistry, Analytical Chemistry or a related Science discipline.

Essential Criteria:
• A good working knowledge of HPLC systems & Empower software is desirable
• Experience in leading a team
• Experience in project management is preferable
• Effective decision-making ability

The successful candidate must be located in Ireland already and available to be onsite 5 days a week.

If you are interested in discussing, apply now or contact me directly on [email protected] / +353 87 365 7522