MANAGER ESIQ SUPPLIER QUALITY
Descripción de la oferta de empleo
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal.
Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.
Learn more at https://www.
nj.
om/.
External Quality team member having the Quality oversight responsibility of assigned Suppliers as part of Janssen Supply Chain Portfolio, ensuring quality standards are achieved and maintained at suppliers through management, and monitoring.
This role has both site and global interactions, as well as, use of all Global Quality Systems including (NC/CAPA, Audit, Change Control, Escalation, etc.) Acting as the Single Point of Contact (SPOC) for Supplier Quality at the Athens, GA site.
Key Responsibilities.
Planning, execution, and documentation of the qualification and monitoring for suppliers who are sourcing APIs, API materials or DP materials such as excipients, raw or packaging materials, to the Janssen Supply Chain for the manufacture of Intermediates, APIs, or drug products respectively Surveillance on the quality and compliance status for all suppliers under the Account Ownership Performing audits, technical visits, and proactive engagements at suppliers and external manufacturers Management of Change related to supplier and/or external manufacturers (change assessor, action executioner, change approvers) Assessment of deviations, corrective and preventative actions (CAPAs), and complaints concerning suppliers and external manufacturers Provision of all information needed for the release/reject of suppliers in SAP (SAP master data) Establishment of JJ Quality requirements and Quality agreements and periodic review of Quality Agreements Qualification of suppliers for new product introductions Periodic performance measurement for suppliers; including face to face meetings Provide support to JSC local Site during Customer and HA inspections as needed Ensure the supplier Specification agreement and approval management They consistently work with external business partners for the purpose of driving the development of core process reliability at external sites.
Act as SPOC (single point of contact) for local JSC site, representing EQ-SQ in Site related matters.
Involvement in Change Management, escalations, compliance issues, recalls, field action that are related to suppliers and/or to the local JSC site Build an accurate connection with the local JSC site establishing periodical meeting with the site Quality Organization to get and provide updating/alignment about the R&R and any shared activities/objectives Connect periodically (weekly is recommended) with local JSC site, local planning, Global procurement (Quartet approach) to discuss and review of the Supplier Quality ongoing performance Ensure to reach out all appropriate members of EQ that could be requested by the site or any stakeholder (e.
.
HA inspection, Escalation, significant investigation) During the HA inspections.
Support the local site (in presence), being the reference for any SQ related activities as.
Qualifications Education.
A minimum of a Bachelors Degree, preferably with a Science or Engineering focus Experience and Skills.
Required.
A minimum of 6 years of experience in quality management, production, quality control, or R&D in a pharmaceutical and/or biotechnology environment Proven experience in leading external manufacturing operations or Quality Assurance for external manufacturing Ability to collaborate with internal operating companies and R&D partners on a wide variety of product, process, project and compliance related issues.
Works with internal JSC functional groups to broker the vital technical support for external partners Interactions are required with Tech Ops, PDMS, Procurement, EHS, Planning, the different JSC manufacturing sites, but also with the other quality groups within JSC and on enterprise level, such as Compliance, Quality unit API manufacturing, Quality systems and the different Qualified persons.
Familiar with GMP – and International Conference on Harmonization (ICH) - regulation Expert demonstrating extensive knowledge and skills to provide mentorship to others and develop balanced improvements in EQ-SQ Partners with Enterprise and JSC leaders to establish process improvements and pro-active quality achievements.
Exposure to regulatory authorities’ inspections Other.
This position is anticipated to have up to 25% travel Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer.
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.
For more information on how we support the whole health of our employees throughout their wellness, career and life journey, please visit www.
areers.
nj.
om.
Detalles de la oferta
- Sin especificar
- En toda España
- Sin especificar - Sin especificar
- 06/11/2024
- 04/02/2025
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