GxP Supplier Quality Manager at Roche

Shanghai, Shanghai, China -

Full Time

Start Date

Immediate

Expiry Date

29 Jul, 26

Salary

0.0

Posted On

01 May, 26

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

GxP, Quality Management, Supplier Quality, cGMP, ISO Standards, Regulatory Compliance, Auditing, CAPA, Risk Management, Technical Transfer, Quality Agreements, Process Validation, Investigation Management, MS Office, Google Suite, Communication

Industry

Biotechnology Research

Description

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters. The Position Technical Job Responsibilities Oversee all required quality activities during the lifecycle of a GxP supplier (Source & Select, Implement, Manage and Decommission), including but not limited to: process or method validations, Roche audits, Health Authority inspections, complex investigations, product complaints, and regulatory submissions, as assigned. Develop, negotiate and maintain Quality Agreements and Product Specific Requirements (as appropriate) with GxP suppliers, as well as with Partners, Collaborators and External Sponsors as applicable, and ensure compliance with agreements. Collaborate with GxP suppliers to address any gaps in audit responsiveness, CAPA implementation, deviation reporting and management, complaint management, investigation closure, and change implementation with regards to quality and timeliness with the supplier; and escalate as appropriate. As applicable, manage all required quality activities to support Make Assess Release (MAR) of Roche products including approval of master process documentation, batch documentation review, resolution of investigations, assessment of changes, and monitor and report GxP Supplier quality performance. As applicable, release, reject or quarantine Roche products (drug substance or API, bulk drug product, and semi-finished and finished products) and medical devices produced within the area of responsibility per applicable Roche requirements, cGMP and the schedule. Support RP and QP Declaration and Certification requirements as applicable. As applicable, collaborate with GxP suppliers to maintain the manufacturing processes and the Specifications and Analytical Methods (SAM) in a validated state and compliant with the regulatory dossier, including stability testing programs. Also includes quality oversight for direct material changes, certifications, supplier specifications and internal release specifications, and other documentation. As applicable, develop and maintain quality risk management plans; utilize risk management tools to identify and mitigate supplier quality and compliance risks, ensuring suppliers are in a state of compliance. As applicable, manage or lead quality deliverables supporting technical transfers for manufacturing, testing, packaging and product launches at external sites As applicable, engage in supplier improvement initiatives to solve complex manufacturing or quality problems. Functional Job Responsibilities Collaborate and manage relationships across internal and external partners to ensure quality expectations are aligned with Roche objectives. Notify Senior Management of potential quality or regulatory issues that may impact product quality or regulatory compliance. Troubleshoot and drive the resolution of quality issues, fostering effective interdepartmental and cross-functional partnerships. Approve documents as authorized and described by Roche policies, procedures and job descriptions. Be accountable for behaviors described in Roche Code of Conduct. Deliver business outcomes in support of departmental objectives. Maintain and communicate work priorities to meet goals and timelines. Ensure timely completion of all job-related training requirements prior to performing GMP-job functions and strive to continuously improve on knowledge and skills in quality, compliance and technology. Communicate new and updated regulatory requirements and applicable Roche expectations to GxP suppliers as applicable and evaluate systems in place. Perform other quality related activities and projects in order to ensure quality and compliance and enable continuous improvement. Identify, support and/or lead continuous improvement initiatives that may benefit External Quality and other organizations. As applicable, deputize for the designated PTQX Leader or a peer and assist with their duties if and when required. May mentor and/or coach colleagues within and outside the organization. TDT QSPOC role The TDT QSPOC (Quality Single Point of Contact) for Investigational Medicinal Products (IMP): may mentor and/or coach colleagues within and outside the organization. Is a strategic matrix leader role in the Technical Development Team (TDT) and responsible for strategic end-to-end product quality oversight until pivotal go. Works cross-functionally for the assigned molecules or products, providing leadership for quality oversight. The TDT QSPOC collaborates with IMP Quality Operations, TDTs, Early Stage Technical Development Committees and the IMPQ Leadership Team to develop and implement a product quality strategy and plan. Other QSPOC roles May also assume QSPOC role as it applies to other teams, for example: in TPTs, Tech Transfer project teams, CDMO governance teams (JPTs, etc.). Delegate of the Swiss Responsible Person As applicable, the GxP Supplier Quality Manager is assigned as delegate of the Swiss Responsible Person a) for commercial products in Switzerland (“Fachtechnisch verantwortliche Person, FvP” as defined in SSD-0208222). b) for IMPs in Switzerland (“Fachtechnisch verantwortliche Person, FvP” as defined in delegation matrix GD-0304780 — Attachment to SOP-0201719: Swiss Responsible Person Delegation Matrix for IMP Contract Manufacturing Organisation (Betriebsstandort #1108280) Within this role, the GxP Supplier Quality Manager Is reporting directly to the Swiss RP with respect to lot disposition and related questions for a) commercial products as per SSD-0208222 and b) IMPs as per GD-0304780, as applicable Is responsible for the lot disposition (release or reject) of commercial products (i.e. drug substance or API, bulk drug product, and semi-finished and finished products) or IMPs (i.e. investigational medicinal products e.g., bulk drug product materials, reformulated comparator products, active pharmaceutical ingredients). Ensures that the quality of the commercial products and IMPs produced on behalf of FHLR, Pharma Technical Operations is in accordance with the current SwissMedic Licenses 511265 and 512286. For IMP: documents regulatory restrictions on batch certificates and performs batch certification for Switzerland and RoW countries. Firewalled Projects Participant The incumbent acknowledges that she/he is bound by all confidentiality obligations imposed by her/his Employment Agreement/Proprietary Information Agreement (or in the case of a non-employee, under the contract between Roche and her/himself or her/his employer, agency, or contract company) in connection with her/his access to Confidential Information, including firewalled projects. Before resuming quality oversight and responsibility for a firewalled project, the incumbent confirms that she/he understands that all contents are Confidential Information and that unauthorized disclosure or use of such Confidential Information may result in termination of her/his employment or services and/or legal action. Qualifications and Skills Ideally, a B.A. or B.S. degree in life sciences or equivalent. Previous experience in the pharmaceutical or related industry or an equivalent combination of education and experience. Experience with GxP suppliers such as CMO, CLO and direct material suppliers is a plus. Sound knowledge of cGMP, ISO standards and international regulations for pharmaceuticals. Ability to interpret quality standards as they relate to GxP suppliers. Operational Excellence expertise is a plus. Highly competent in MS office or Google Suite applications including Excel, PowerPoint, Word, and MS Project, etc. Ability to communicate clearly and professionally both in writing and verbally. Fluency in oral and written English is a must. Additional language skills are a plus. This position may require up to 10% domestic and/or international travel. Who we are A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact. Let’s build a healthier future, together. Roche is an Equal Opportunity Employer. We believe it’s urgent to deliver medical solutions right now – even as we develop innovations for the future. We are passionate about transforming patients’ lives. We are courageous in both decision and action. And we believe that good business means a better world. That is why we come to work each day. We commit ourselves to scientific rigor, unassailable ethics, and access to medical innovations for all. We do this today to build a better tomorrow. We are proud of who we are, what we do, and how we do it. We are many, working as one across functions, across companies, and across the world. We are Roche.

Responsibilities

The GxP Supplier Quality Manager oversees quality activities throughout the supplier lifecycle, including audits, investigations, and regulatory compliance. They also manage quality agreements, CAPA implementation, and product release processes to ensure adherence to Roche requirements and cGMP standards.