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Quality Control Analyst - Master Data Management (Temporary Assignment 2 years)

04.03. | Temporary | 100%

Quality Control Analyst - Master Data Management (Temporary Assignment 2 years)

Share This Page Quality Control Analyst - Master Data Management (Temporary Assignment 2 years) Qlty Assurance Methods Boudry, , Switzerland Full time R1522455_EN 2/24/2020 4:03:46 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. The Quality Control Analyst - Master Data Management is part of the Technical Support team of the Quality Control (QC) department of Celgene, Switzerland. The main responsibility of the position will be to perform Master Data Management activities in StarLIMS and Oracle and associated GMP document updates in support of Commercial product launches and Variations and New Product Introductions. In addition, the QC Analyst – MDM will act as a StarLIMS Superuser providing support and training to End-Users of the QC laboratories of Celgene International in Boudry/Couvet as well as supporting investigations and resolution of LIMS issues. Your Duties and Responsibilities Represent QC in Commercial Product Launches and Variations meetings Evaluate change controls for impact on LIMS master data and associated QC documentation Creates, maintain and update master data objects in LIMS and Oracle Update associated GMP documents and procedures Provide first line contact with QC End Users and QA e-Systems in case of LIMS issues Lead or support investigations in case of LIMS-related deviations Assist with errors and solve problems with minimum guidance; perform simple data fixes Create and maintain local StarLIMS related standards and procedures Own or support change controls for LIMS changes Perform all activities in compliance to cGMP requirements and applicable standards and procedures Comply to EHS rules and safe work practices per applicable procedures Provide end user training and on-the-job training for new employees where required Perform other tasks as assigned Your Profile? CFC as Laboratory Technician or BS degree in Science, Computer Science or a related field A minimum of 2 years of relevant work experience in a GMP regulated environment (or equivalent). Previous experience in a GMP QC role a plus General computer Literacy (Microsoft Office) Good knowledge of basic coding and code reviews is a plus Good knowledge of LIMS and Oracle applications a plus Professional command of French and English, verbal and written Good technical writing skills Proven time management skills and a strong attention to detail Proven analytical and problem-solving skills Ability to work independently and compliantly 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 © 2018 Bristol-Myers Squibb Company

04.03.2020
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

Labels (1)

Training Company
Training Company

Celgene, A Bristol Myers Squibb Company

Route de Perreux 1Boudry

Industry

Healthcare

Year of foundation

1896

Labels (1)

Training Company
Training Company
Salary

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