Technical Leader Packaging

25.06. | Employee | 100%

Technical Leader Packaging

Share This Page Technical Leader Packaging Manufacturing/Ops Boudry, , Switzerland Part time R1526010_EN 6/16/2020 4:11:44 PM Bristol-Myers Squibb is a global Biopharma company committed to a single mission: to discover, develop, and deliver innovative medicines focused on helping millions of patients around the world in disease areas such as oncology, cardiovascular, immunoscience and fibrosis. Join us and make a difference. We hire the best people and provide them with a work environment that places a premium on diversity, integrity, collaboration and personal development. Through a culture of inclusion, we create a better, more productive work environment. We believe that the diverse experiences and perspectives of all our employees help to drive innovation and transformative business results. MS&T is a science-driven organization dedicated to building in-depth and comprehensive knowledge of our products and their processes. We work across the entire lifecycle of our Pharmaceutical Products and across both internal and external manufacturing/packaging and API Manufacturing. This position leads and/or manages global and strategic (or technically complex) projects for Bristol-Myers Squibb Global Commercial Supply and ensures projects are delivered within agreed timelines, cost and quality targets. Transfers product knowledge into the Global Commercial Supply organization. Provides technical expertise and support to Packaging Operations to improve capacity, quality, cost or to establish root cause. The success of this function requires effective collaboration with Pharmaceutical Development, Contract Manufacturing, Supply Chain, Manufacturing, Packaging Operations, and Regulatory CMC. Responsibilities will include, but are not limited to the following: Manage strategic packaging projects (such as the Technology Transfer of a product from Development) from project initiation to closure including after action reviews. Advocate best practice project methodologies and tools. Develop, write and review project documentation including project plans, test protocols, risk assessments and reports. In collaboration with the responsible Product Steward provide technical/scientific expertise and support to packaging sites. In collaboration with the Technology Leader Packaging, support product, technology or packaging improvements/changes. Assist with writing and reviewing of CMC documentation associated with project or packaging changes. Transfer reliable and well understood packaging processes into Global Supply or within the network. Transfer the knowledge from the sending unit to receiving unit and Product Steward. Ensure knowledge is captured and transferred. Engage with Packaging sites/Development and CRO/CMO’s and advocate the use of scientifically sound principles. Advise on the definition of CQA’s and CPP’s and an appropriate control strategy. Participation in the design, execution and data analysis associated to technical trials/batches associated with the projects. Writing and reviewing project documentation including project plans, test protocols, risk assessments and reports. Update a scientific knowledge base. Advises on Scientific and Business developments (including Technology, Processes, Regulations etc). Applies and advocates the use of Lean and 6 Sigma methodologies. Assist with the development of Standards, guidelines and SOP’s to enhance the quality and robustness of our manufacturing operations, knowledge transfer and technical support processes. Skills/Knowledge Required : Minimum Bachelor’s Degree in Packaging Engineering/Technology, Packaging Development, or similar education in this field. At least 8 years of experience in the Pharmaceutical/Cosmetics/Food industry. Experience in the development/application of packaging design and their implementation. Knowledge and experience of primary, secondary, and tertiary packaging materials. Good working knowledge of QA, cGMP and the Pharmaceutical Regulatory framework Good knowledge of various types pharmaceutical packaging processes/technologies. Good knowledge of Technology Transfer and validation. Demonstrated project leadership/management experience. Experience of multi-site/cross-site project management. Working knowledge Lean and 6 Sigma methodologies. Good leadership skills and ability to influence and work across organizational boundaries. Effective communication skills, good command of English and preferably another European language. Ability to work well as an integral part of a large Project Team. Bristol-Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees the resources to pursue their goals, both at work and in their personal lives. Working with Us By fostering a culture of inclusion, we empower this 21st century workforce to achieve our company's mission of helping patients to prevail over serious diseases. Explore Job Opportunities A clear purpose. An inclusive culture. The chance to work at the top of your field. These are a few of the reasons Bristol-Myers Squibb is the right choice for your next career move. Come Meet Our Team Are you ready for a career where you make a profound difference? We invite you to visit us at one of our events to learn more. For US Applicants Only Bristol-Myers Squibb endeavors to make this website accessible to any and all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process, please contact . This contact information is for accommodation requests only and cannot be used to inquire about the status of applications. The Physician Payment Sunshine Act (Sunshine Act) requires Bristol-Myers Squibb to report any transfers of value, including payments made to reimburse interview-related expenses, for candidates who are US-licensed physicians. U.S. licensed Physicians covered by the Sunshine Act include Doctors of Medicine, Osteopathy, Dentistry, Dental Surgery, Podiatry, Optometry and Chiropractic Medicine who are licensed to practice medicine in the U.S. This information will be reported to the Centers for Medicare and Medicaid Services (CMS) on an annual basis and CMS shall post submitted data on its public database. For more information, Bristol-Myers Squibb is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, protected veteran status, pregnancy, citizenship, marital status, gender expression, genetic information, political affiliation, or any other characteristic protected by law. For our EEO Policy Statement, please . If you'd like more information on your EEO rights under the law, please click here: and Follow Us Powered by

25.06.2020
Employee, 100%

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Celgene, A Bristol Myers Squibb Company

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Celgene, A Bristol Myers Squibb Company

Route de Perreux 1Boudry

Industry

Healthcare

Year of foundation

1896

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Celgene, A Bristol Myers Squibb Company

Route de Perreux 1Boudry

Industry

Healthcare

Year of foundation

1896

Labels (1)

Training Company
Training Company
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