External Quality Associate Director m/f/d

Our Quality Assurance group ensures every single material inside our products is manufactured, processed, tested, packaged, stored and distributed aligned with our incredibly high standards of quality and meets all regulatory requirements. Partnering across our internal manufacturing facilities, external contract manufacturers and suppliers we create an interdependent global manufacturing network dedicated to deliver a compliant, reliable supply to customers and patients on time, every time, across the globe.
We are seeking a growth and improvement minded External Quality Associate Director that can help drive our Strategic Operating Priorities in Europe and APAC regions.

Invent | Pursue the Most Promising Internal and External Science to Address Significant Unmet Medical Needs
Execute | Prioritize Resources Behind Our Key Growth Drivers (Oncology, Vaccines, Select Specialty Areas, Animal Health) While Optimizing Our Base Business)
Adapt | Develop Our People, Culture and Business Model to Evolve with a Dynamic Landscape
Diverse Talent | We are committed to providing an inclusive and welcoming environment with supporting leadership behaviors because having a high-performing, engaged workforce is critical to our ability to deliver innovative solutions to patients and customers around the world
Values and Standards | Our Steadfast Commitment to Our Values and Standards will Continue to Guide Us as We Take on New Opportunities and Will Always be Fundamental to Our Success - They are a Competitive Advantage for Us

Key Responsibilities

Provides Quality oversight over one or more External Entities or projects that will manufacture or tests cell banks, biologic drug intermediates, biologic drug substances, or biologic drug products or both on behalf of our Company for product and analytical technology transfer.
Serve as the quality project lead for Technology Transfer, New Product Introduction and Analytical Transfers to Contract Manufacturing and testing sites.
Assist in managing the end-to-end processes of transfers including but not limited to: Due Diligence, Feasibility Studies, Protocols/Reports, PPQ, PAI Readiness and Quality System Oversight Implementation.
Works with a team of quality project leads and cross functional transfer teams.
Reports to the Quality Director, EQA, for general advice and instruction concerning Quality Operations, but functions independently

Education

Bachelor's or Master's degree in a Science, Engineering, or related area of study.

Required

Work independently and as a Team member with Integrity | Precision | Accomplishment | Motivational Ambition | Respect
Seven years or greater relevant pharmaceutical or biotechnology industry with a thorough knowledge of Quality Systems, Quality Assurance and Quality Control
Solid knowledge of global GMP and regulatory requirements
Proficient in analyzing complex product, production and testing issues and have demonstrated scientific problem solving capabilities
Experience with supporting regulatory inspections
Principled and strong interpersonal, communication, coaching, motivation, negotiation, and persuasion skills to build strong relationships

Preferred

Biologic and/or vaccine Quality Assurance and Quality Control
Contract Manufacturing Oversight (CMOs, Labs, etc.)
Experience with working in regulated environment and with new product introductions / product transfers.
ADC experience preferred
IPI, QSAT and SAP for deviation and CAPA management experience preferred.

Our Manufacturing & Supply Division is dedicated to being the most trusted supplier of biopharmaceuticals worldwide. Our facilities, along with our external contractors, suppliers, and partners, create a reliable global manufacturing network that's devoted to delivering a high-quality, reliable supply to customers and patients on time, every time.
THE COMPANY
Our company has had a presence in Switzerland since 1963. With a regional office and manufacturing/packaging facility, Lucerne is considered the center of operations. Approximately 1,000 people work collaboratively at the four Lucerne locations (Tribschenstrasse, Citybay, Schachen and Kriens). A fifth location has been established in Zurich, aimed at accelerating the development and commercialization of many of our company's medicines and vaccines, which supports our mission to save and improve lives around the world.
We are proud to be certified as a 'Top Employer Switzerland' and 'Top Employer Europe' showing the company's commitment to our employees and the community around us.
Our Tribschenstrasse office, located in the city of Luzern has a rich diversity of employees at this location including Global Supply Chain Management, Regional External Manufacturing and one of our European Finance Hubs. The site also serves as our regional and local headquarters for our company's Animal Health Division in Switzerland.
Employee Status: Regular
Relocation: No relocation
VISA Sponsorship: No
Travel Requirements: 25%
Flexible Work Arrangements: Not Applicable
Shift: Not Indicated
Valid Driving License: No
Hazardous Material(s): N/A
Job Posting End Date: 11/28/2024

A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.

Requisition ID: R320007
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