Qp

Job Description Piramal Pharma Solutions is a leading global CDMO of advanced drug development and manufacturing solutions to the pharmaceutical industry.
To act as the key contact point for all QA and GMP issues on the Morpeth Site, for products imported into or manufactured on behalf of the Morpeth Site.
1.
Responsibilities and Key Tasks QP specific activities •Act as QP for all products manufactured and packaged at the Morpeth site •To ensure product is made in accordance with manufacturing licences and equivalent marketing authorizations •Assure product, process and facilities comply with national and global regulatory requirements in alignment to the Morpeth site policies •Provide quality oversight of all activities on site and of subcontractors •To actively participate in/chair Site Quality Review Team Meetings •To ensure any significant quality or compliance issues are escalated to senior management •To review and approve quality documentation •To conduct internal audits and advise on corrective action •To conduct external audits of supplies vendors, contractors and service providers •Provide support for customer visits and audits •Provides pro-active support for and initiates quality improvements within Manufacturing and Quality •Deliver training Critical Tasks