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Job description

Kindeva is a leading global contract developer and manufacturer (CDMO) with delivery platform expertise in Autoinjector, Inhalation, Transdermal/Intradermal Patch Technologies. We partner with our customers to improve patient outcomes around the world. Together, as One Team, we will manufacture many more tomorrows.

Responsible for Supplier Quality Assurance. Role sets the standard for suppliers & provides Quality oversight for ensuring materials received on site are consistently supplied to agreed specification. Liase with Suppliers and Site Quality and Sourcing to ensure standards are maintained

ROLE RESPONSIBILITIES

• Responsible for annual planning & execution of supplier audits, including audit reports and any required follow up. Escalation of audit related issues to site/global management as needed
• Responsible for update of Supplier Risk Files in MasterControl
• Perform supplier qualification, approval of suppliers and management of approved suppliers in MasterControl. Support supplier/material additions/changes through project involvement
• Support resolution of Supplier quality issues including discussion of quality issues with Suppliers in compliance with Supplier/Quality Agreements
• Appraise Suppliers, through assessments, audits and technical interfaces
• Provide training/awareness to sites as required for Supplier Quality activities
• Participate in Customer/Regulatory audits to site as required

BASIC QUALIFICATIONS

• Degree level or equivalent in Business, Supply Chain, Engineering or Science based.
• Minimum of five years experience within pharmaceutical companies. With previous auditing responsibility
• Good knowledge of GMP, Quality System requirements, international regulations & standards.
• Good verbal & written communication skills, across all levels. Effective in decision making, directing & influencing people. Ability to cope with changing priorities, strong organizational skills and ability to work by self or in teams