External Supply Operations Quality Manager (fixed term contract) Autore annuncio: Randstad Italia spa Zona lavoro: Roma Data pubblicazione: 13 novembre 2024 Sigla riferimento: CX423877 Randstad inhouse services, specialty pharma, is looking for a resource on behalf of Pfizer srl to be included in the Rome office in the role of External Supply Operations Quality Manager.
Responsibilities: The ESOQ Manager is accountable for providing quality assurance management of key contractors for Pfizer and for assuring that the products supplied to our patients are manufactured & tested in accordance with c-GMPs, the registration file and any additional country specific requirements.
This is a highly independent position operating with minimal supervision, interacting with high levels of management both at contract manufacturers and within Pfizer.
(S)he will operate as spokesperson for ESOQ and will focus on developing relationships, independently negotiating, developing and communicating Pfizer quality requirements with contract manufacturers.
ESOQ Manager will have significant interactions with many internal business and manufacturing organizations (e.g.
External Supply, Regulatory, Technical Support, Quality, PGS sites and R&D) and will lead virtually-based cross functional teams.
Initiate, review and approve regulatory changes through Pfizer enterprise system (i.e PDM) for changes initiated by or impacting ESOQ managed contractors.
Provide support for the closure of the deficiency letters, CMC Commitments, Regulatory requests for Renewals, New Product registrations and Post approval variations.
Main point of contact for Global Chemistry Manufacturing & Controls (GCMC) department or Local Regulatory Affairs in Pfizer Country Offices (Single market products) for the regulatory activities involving the ESOQ contractors.
As the Regulatory Expert, participate in Virtual Site Operating Teams (VSOT) or similar meetings for ESOQ managed contractors and if needed, participate in Site Quality visits at the contractors.
Support and Perform Lot Disposition for Biotech semi-finished and finished products (if applicable).
Qualifications: Minimally BA/BS Science, Engineering, or related technical discipline with at least 7 years in a GXP setting and/or Regulatory Affairs role.
At least 4 years of Product Quality Assurance experience in a GMP environment.
Aseptic manufacturing experience would be an asset.
Advanced computer skills, MS Office and enterprise systems such as SAP, QTS, PDM, Documentum platforms.
Command of English language required and multi-lingual is a benefit.
Strong verbal and written communication including presentation skills.
Shows strong negotiation skills and is diplomatic in communication with internal and external customers.
Demonstrated ability to manage multiple projects and priorities.
Demonstrated ability to prioritize work, to act and work independently and to report items as required to Team leader.
Demonstrated excellent organization skills.
Demonstrated experience managing complex quality and compliance activities in a manufacturing plant or with a contractor.
Developing personal leadership to manage cross functional projects.
Developing ability to resolve conflicts.
Takes initiatives and is proactive, persistent.
Has a broad GMP and technical know-how to handle emerging issues.
Able to report remotely and deliver work independently.
Up to 20% travel may be required.
A fixed-term position in administration is envisaged with classification according to the chemical collective bargaining agreement and classification commensurate with experience.
La ricerca è rivolta ai candidati ambosessi (L.903/77).
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