Closed listing
Direct Materials Regulatory Filings Expert
- Mississauga, ON, Canada
Full-time
This opening has closed.
The original listing is kept below for reference.
Job details
- Job type
- Full-time
- Closing date
- Experience
- Experience & Education: BS/MS/PhD in Science, Engineering or Management with at least 5 years of experience in the pharmaceutical, pharmaceutical or medical device industry.
- Posting language
- English
- Posted
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Search current openingsOriginal job description
Archived listing. The details below describe a past opening.
The Position
At Roche, we believe that every patient deserves access to life-changing innovations. As a global healthcare leader operating across pharmaceuticals and diagnostics, we combine cutting-edge science, advanced technology, and a passion for improving lives to address some of the world’s most challenging medical needs. Driven by our commitment to research and sustainable healthcare solutions, we foster an inclusive, collaborative environment where diverse teams are empowered to question the status quo, drive continuous improvement, and redefine what is possible in modern medicine.
The Pharma Technical (PT) Operations Global MSAT & Engineering group takes bold steps to modernize technical operations to enable Roche to deliver medicines for patients more quickly, efficiently and reliably. PTT shapes and accelerates technology innovation and product lifecycle management for tomorrow, while standardizing and driving operational excellence in PT today.
The PTT Direct Materials Certification and Filing Expert, reporting to the PTT Direct Materials Certification and Filing Team Lead, is responsible for providing technical oversight and proactively implementing solutions supporting Direct Materials and distribution networks. The position is accountable for the various filing requirements and appropriate certification of our products, including oversight of current Health Authority regulations regarding biological-derived materials. This role requires innovative, efficient, and sustainable technical solutions to ensure a robust and flexible supply chain and deliver processes that enable distribution of healthy products across the product life cycle.
The Oppurtunity
- Accountable for the design and robust execution of the Certification and Filings business process and oversight of content for Biologics and Synthetic Molecules (e.g., BSE/TSE, GMO, virus-risk)
- Accountable for proactive management of Direct Materials Filing Strategies in alignment with PTR to ensure compliance with relevant Health Authority requirements
- Accountable for building collaborations and work relationships between key stakeholders and user groups including External Quality, Procurement, Planning, QC, QA, Manufacturing, Development, and Regulatory
- Responsible for authoring, reviewing and/or approving Certificates and Filing sections with legalization signature responsibilities for Roche products
- Maintains a state of global inspection readiness at all times and is responsible for implementing compendia changes and/or changes related to Health Authority audits
- Responsible for owning and/or assessing information requests related to material topics to support Product Health
- Lead Direct Material Management data improvement activities, driving successful implementation of programs including data management, systems understanding, and process design
We use artificial intelligence to screen, assess or select applicants for this role.
This posting is for an existing vacancy at Hoffmann-La Roche Ltd.
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.
More about this job
Responsibilities
Oversee direct materials certification and filing strategies, including regulatory content for biologics and synthetic molecules, and author, review, or approve certificates and filing sections. Maintain inspection readiness, implement regulatory and compendial changes, respond to material information requests, and lead data and process improvement initiatives across global stakeholder groups.
Requirements
Requires a BS, MS, or PhD in science, engineering, or management and at least five years of experience in the pharmaceutical or medical device industry; regulatory filings or material specifications experience is an advantage. Candidates should have global team experience, advanced project management skills, working knowledge of ICH guidelines, ISO standards, GMP operations, and health authority regulations, with quality systems and operational excellence knowledge desired.
Skills
- Regulatory Filings
- Direct Materials Management
- Material Specifications
- Project Management
- ICH Guidelines
- ISO Standards
- Pharmaceutical GMP
- Health Authority Regulations
- Quality Systems
- CAPA
- Change Management
- Six Sigma
- Lean
- Regulatory Compliance
- Stakeholder Collaboration
- Data Management
Visa sponsorship
Not detected in the job text
Categories
- Healthcare
- Manufacturing
- Science & Research
- Management & Leadership
- Logistics
Keywords
- Direct Materials
- Certification
- Regulatory Filings
- Biologics
- Synthetic Molecules
- BSE/TSE
- GMO
- Virus Risk
- Health Authority Regulations
- ICH Guidelines
- ISO Standards
- Pharmaceutical GMP
- Material Specifications
- Filing Strategies
- Certificates
- Legalization Signatures
- Inspection Readiness
- Compendia Changes
- Health Authority Audits
- Product Health
- CAPA
- Change Management
- Six Sigma
- Lean
- Project Management
- Data Management
- Process Design
- Supply Chain
- Operational Excellence