Job Description
This is a leadership role providing Quality and Compliance oversight of site operations, inclusive of but not limited to Manufacturing, Quality Systems, Quality Control, Quality Assurance, Facilities Maintenance, Materials Handling, and QA Validation in accordance with mandated regulatory requirements and site expectations.
Responsibilities
* Ensuring compliance with all aspects of Quality for the Raheen site, inclusive of manufacturing, quality systems, quality control, validation, facilities and materials management
* Overseeing site quality systems, including Deviations, CAPA, Change Control, Audits (Internal and External), and Customer Complaints
* Reviewing and approving documents related to area functions, such as failure investigations, change control documents, corrective/preventative action documents, standard operating procedures
* Approving procedures, policies, and instructional documents relating to quality systems to ensure compliance with company policy and local and international regulatory requirements
* Monitoring and trending metrics for site quality systems
* Managing and developing site risk assessment activities and site risk register
* Participating in continuous improvement initiatives
* Participating in regulatory and customer audits
* Collaborating with functional departments to resolve issues and maintain compliance
* Identifying gaps in systems and developing feasible plans for correction
* Training personnel on quality system processes
About This Role
This role might be for you if:
* You have the ability to work independently or as part of a team
* You have experience leading and managing teams
* You are a self-starter with the ability to operate in a multifaceted environment
* You are comfortable working on your own initiative
* You demonstrate expert GMP knowledge
Requirements
To be considered for this position, you should have a BSc/BEng in a scientific discipline or related field with 7+ years of relevant work experience in the pharmaceutical or other related industry.