QC Specialist – Compliance
vor 5 Monaten
Working with Us
Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams rich in diversity. Take your career farther than you thought possible.
This position is part of the team “Compliance & Continuous improvement” within Quality Control Laboratory of BMS Boudry site.
The Specialist QC “Compliance & Continuous improvement supports the program implemented by the Manager to maintain a reliable, qualified, and regulatory compliant operation with a project and continuous improvement strategy for Boudry QC Laboratory.
The QC Specialist – Compliance & Continuous Improvement will be required to support inspections (including but not limited to internal, corporate, and regulatory audits) and QC Management to fix associated observations.
This role will be the point of contact to coordinate specific system enhancements, to manage isolated issue, and to provide or coordinate trainings.
As a representative of continuous improvement and experienced collaborator, the Specialist drives specific initiatives and support Sr Specialist or other QC members for specific activities which aim to continuously increase QC Laboratory compliance and performance. This position will be required to participate in coordination meetings, to update documents, to support investigations, or to execute any other actions to ensure Laboratory and Site success.
This position is the back up of Sr Specialist “QC Compliance & Continuous improvement” and can be assigned other tasks related to other QC responsibilities.
Key Responsibilities
Support Compliance in accordance with global cGMP regulations and BMS policies
Support regulatory inspections and internal audits Assist implementation of associated actionAct as QC representative for Projects or support implementation
Bring technical & process knowledge to ensure proper Projects implementation Participate in cross functional meetings Communicate and escalate main information or issues highlighted Execute specific tasks according to Projects needsSupport Continuous Improvement initiatives within laboratories
Maintain QC performance data tools implemented Implement actions defined as part of performance data analyze Gather and report data for KPIs Support implementation of LEAN programs (5S, Gemba, Pareto, Tiers, Gemba …) Support QC improvement initiativesAct as an experience collaborator for the Lab
Act as a delegate of Sr Specialist “Compliance and Continuous Improvement” Create & update procedures or other documentsPromotes safe practices and behaviors
Reports immediately all incidents to EHS, participate in investigations and identify measures to prevent similar accidents in the future. Qualifications & Experience
Uniquely Interesting Work, Life-changing Careers
With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.
On-site Protocol
BMS has a diverse occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:
Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.
BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to . Visit to access our complete Equal Employment Opportunity statement.
BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.
BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.
Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.
-
QC Specialist
vor 1 Monat
Boudry District, Schweiz Bristol Myers Squibb VollzeitTransforming Patients' Lives through ScienceBristol Myers Squibb is a global biopharmaceutical company that is committed to transforming patients' lives through science. We are seeking a highly skilled and motivated QC Specialist - Compliance to join our team.About the RoleThe QC Specialist - Compliance will be responsible for supporting the Compliance and...
-
QC Specialist – Compliance Expert
vor 3 Wochen
Boudry District, Schweiz Bristol Myers Squibb VollzeitKey Responsibilities:Support Compliance in accordance with global cGMP regulations and BMS policiesSupport regulatory inspections and internal auditsAssist implementation of associated actionAct as QC representative for Projects or support implementationBring technical & process knowledge to ensure proper Projects implementationParticipate in cross...
-
Compliance Specialist
vor 1 Woche
Boudry District, Schweiz Bristol Myers Squibb VollzeitBristol Myers Squibb is a global pharmaceutical company committed to transforming patients' lives through science. We are seeking an experienced Compliance Specialist to join our Quality Control Laboratory team in Boudry.This role will be responsible for supporting the implementation of a reliable, qualified, and regulatory compliant operation within the QC...
-
Sr. Specialist Scientist QC Analytical Technical Support
vor 6 Monaten
Boudry, Schweiz Bristol Myers Squibb VollzeitWorking with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms...
-
QC Local data specialist
vor 6 Monaten
Boudry, Schweiz Bristol Myers Squibb VollzeitWorking with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms...
-
Specialist - QC Analytical Technical Support
vor 19 Stunden
Boudry, Schweiz Bristol-Myers Squibb VollzeitWorking with UsChallenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the...
-
QC Data Specialist for Laboratory Operations
vor 4 Wochen
Boudry District, Schweiz Bristol Myers Squibb VollzeitJoin the Bristol Myers Squibb team in a role that combines data management expertise with a passion for laboratory operations.BMS is seeking a skilled data specialist to provide support in the development and maintenance of quality control scheduling and planning systems for drug product, drug substance, packaging items, PPQ, and trial material testing on...
-
Boudry District, Schweiz Bristol Myers Squibb VollzeitTransforming Patients' Lives through ScienceBristol Myers Squibb is a leading pharmaceutical company that is dedicated to transforming patients' lives through science. We are seeking a highly skilled and experienced Senior Scientist to join our QC Analytical Technical Support team in Boudry, Switzerland.Job SummaryThe Senior Scientist will be responsible for...
-
Boudry District, Schweiz Bristol Myers Squibb VollzeitTransforming Patients' Lives through ScienceThe Sr. Specialist Scientist QC Analytical Technical Support role at Bristol Myers Squibb is a challenging and meaningful opportunity to make a real impact on the lives of patients. This position is responsible for leading equipment/systems acquisition and decommissioning activities, providing subject matter...
-
Scientific Technical Support Specialist
vor 4 Wochen
Boudry District, Schweiz Bristol Myers Squibb VollzeitAbout This RoleThe Sr. Specialist Scientist is a key member of the QC Analytical Technical Support team at Bristol Myers Squibb. This role is responsible for leading the acquisition and qualification of analytical equipment and computerized systems, as well as providing subject matter expertise on qualification and troubleshooting.Key ResponsibilitiesLead...
-
Data Quality Specialist
vor 2 Wochen
Boudry District, Schweiz Bristol Myers Squibb VollzeitAbout the RoleThis is a unique opportunity to join Bristol Myers Squibb as a QC Local data specialist. The successful candidate will be responsible for providing support in the development and maintenance of QC scheduling and planning systems, ensuring operational efficiency and meeting testing requirements.ResponsibilitiesDevelop, maintain, and implement...
-
Manager, Quality Control Drug Product
vor 6 Monaten
Boudry, Schweiz Bristol Myers Squibb VollzeitBei Bristol Myers Squibb lassen wir uns von einer einzigen Vision inspirieren - die Veränderung des Lebens von Patienten durch Wissenschaft. In den Bereichen Onkologie, Hämatologie, Immunologie und Herz-Kreislauf-Erkrankungen - und eine der vielfältigsten und vielversprechendsten Pipelines der Branche - trägt jeder unserer leidenschaftlichen Kollegen zu...
-
Manager, Quality Control
vor 6 Monaten
Boudry, Schweiz Bristol-Myers Squibb Vollzeit**Working with Us** Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms...
-
Manager, Quality Control Drug Product
vor 6 Monaten
Boudry, Schweiz Bristol Myers Squibb Vollzeit**Working with Us** Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms...
-
Qc Apprentice
vor 6 Monaten
Boudry, Schweiz Bristol Myers Squibb VollzeitBei Bristol Myers Squibb lassen wir uns von einer einzigen Vision inspirieren - die Veränderung des Lebens von Patienten durch Wissenschaft. In den Bereichen Onkologie, Hämatologie, Immunologie und Herz-Kreislauf-Erkrankungen - und eine der vielfältigsten und vielversprechendsten Pipelines der Branche - trägt jeder unserer leidenschaftlichen Kollegen zu...
-
Boudry District, Schweiz Bristol Myers Squibb VollzeitAbout the RoleThe Sr. Specialist Scientist is part of the Quality Control (QC) department of Bristol Myers Squibb in Boudry, Switzerland. This position is responsible for leading equipment and systems acquisition, qualification, and decommissioning activities. The role provides subject matter expertise on new equipment qualification and troubleshooting of...
-
Qc Apprentice
vor 6 Monaten
Boudry, Schweiz Bristol-Myers Squibb Vollzeit**Working with Us** Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms...
-
Senior Quality Assurance Specialist
vor 3 Wochen
Boudry District, Schweiz Bristol Myers Squibb VollzeitAbout the RoleBristol Myers Squibb is seeking a highly skilled Senior Quality Assurance Specialist to join our External Manufacturing team. The successful candidate will be responsible for ensuring the quality of our products, managing vendor relationships, and maintaining compliance with regulatory requirements.Key ResponsibilitiesSupport the Quality...
-
Quality Assurance Specialist
vor 3 Wochen
Boudry District, Schweiz Bristol Myers Squibb VollzeitTransforming Patient Lives through ScienceBristol Myers Squibb is committed to transforming patient lives through science. We are currently seeking a Quality Assurance Specialist - External Manufacturing to join our team. In this role, you will be responsible for ensuring the quality of our products manufactured at external sites.Key ResponsibilitiesSupport...
-
Bulk Operations Manufacturing Specialist
vor 3 Wochen
Boudry District, Schweiz Bristol Myers Squibb VollzeitTransforming Patients' Lives through ScienceBristol Myers Squibb is a world leader in the development of innovative therapies that transform patients' lives. We are seeking a highly skilled Bulk Operations Manufacturing Specialist to join our team.As a Bulk Operations Manufacturing Specialist, you will be responsible for manufacturing products in compliance...
