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This is an onsite role working as part of the Senior Leadership Team reporting into the General Manager in a hands on small to medium sized organisation.
Medical device, pharmaceutical or experience working in a regulated manufacturing industry preferred.
This is a hands-on leadership role in a small, fast-paced environment, ideal for someone who enjoys building systems, developing people, and influencing across the organisation.
The QA Manager will lead audits and take ownership of validation and quality systems compliance.
Strong QA Supervisor / Senior Supervisor ready to step up will also be considered.
Responsibilities Lead and develop the site Quality team Maintain and continuously improve the Quality Management System Oversee all validation activities (process, equipment, facilities) and maintain the Master Validation Plan. xcfaprz
Lead internal, customer and regulatory audits Drive CAPAs, NCRs, deviations and change controls (initiation through closure) Report quality metrics to senior leadership Act as ISO 13485 Management Representative Requirements 5+ years experience in a regulated manufacturing environment Strong quality systems and validation background Experience managing or supervising a team Confident leading audits and regulatory interactions Strong influencing, mentoring and stakeholder engagement skills Experience in a small company environment is advantageous Strong QA Supervisor / Senior Supervisor ready to step up will be considered Please contact me for a confidential discussion or to discuss further.
Deirdre Sheehan Skills: Quality Validation Auditing Benefits: Mobile phone Paid Holidays Canteen Parking Pension Educational assistance Bonus
Sprachkenntnisse
- English
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