Clinical Quality

vor 5 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 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.

**Position Summary**

The Director, Therapeutic Area (TA) Quality Lead will be mainly responsible for managing the Therapeutic Area activities from a quality perspective and delivering the full range of quality related activities in support of the TA. The incumbent is a single point of contact for R&D Quality for the Therapeutic Area.

**Key Responsibilities**
- Design and implement end-to-end quality strategy for respective Therapeutic Area Ensure successful Health Authority (HA) engagement.
- Manage for cause, critical and/or complex quality issues as well as serious breaches for the TA;
- Engage in appropriate activities to support product submissions.
- Establish strong partnership with business stakeholders.
- Interaction with leadership in R&ED and GDD, Patient Safety and Regulatory to influence decisions impacting quality and compliance related to the TA
- Interactions with peers in R&D Quality and Global Quality
- Interactions with external auditors from partner companies and health authority inspectors during the conduct of health authority inspections
- Contact with appropriate technical, supervisory and management personnel internally and externally (BMS sites, vendors, partners etc.) in the conduct and reporting of potential serious breaches, inspections, and audits
- External engagement as needed with industry/trade/QA associations, regulatory agencies, vendors, and licensing partners as well as pharmaceutical company peers
- Internal engagement as needed with relevant R&D partners and corporate functions

**Other**
- Lead multidisciplinary or cross-functional work/project teams; serve as part of strategic team(s) within the group/discipline
- Lead and/or contribute to the implementation of large-scale initiatives and/or organizational changes (such as functional optimization) that affect the department
- Act as a highly credible technical/ functional expert; routinely provide technical/functional guidance/coaching to direct and indirect reports/peers within the line or crosslines
- Drive quality into the business through proactive quality support, mentoring and/or coaching and consultation.
- Provide guidance and expectations to the business to enable execution of external and internal regulations on a global and cross functional level
- Provide input in the global audit plans based on identified signals/trends/risks/gaps
- May influence the external environment through interactions with regulators, trade associations, or professional societies
- Actively share knowledge with others across multiple disciplines and across lines through existing knowledge sharing processes and systems

**Research and Development Quality is responsible for the following**:

- Defines and oversees the global quality strategy for early R&D Development up to phase IV Projects and ensure that GxP Quality Management Systems are implemented and in use
- Translate QMS elements into the R&D processes and ensure feedback to the central QMS team
- Lead the Quality and Compliance R&D Escalation Process
- Ensure GLP systems are in place, studies are audited and lead analytical path of Translational Medicine
- Oversee the Data generation and data integrity from laboratory work and non-clinical phase projects
- Ensure Quality is Designed into non-clinical trials and clinical protocols using data and information from discovery phase, non-clinical and clinical studies
- Oversee process development, manufacturing and release of clinical supplies to clinical trials protocols
- Advice on Franchises (including Cell Therapy) and Clinical Operations development projects
- Lead Qualification of vendors and manage external Quality Systems
- Execute GCP and Pharmacovigilance audits and support GCP and Pharmacovigilance Regulatory inspections
- Ensure that GxP follow-up CAPA activities are completed
- Oversee study centers, countries, investigators and connect with PV, Medical Affairs and Regulatory Affairs
- Contribute to develop Quality Management Systems training elements

**Qualifications & Experience**
**Education and Experience**:

- B.S. and/or M.S. in Chemistry, Biology, or Health or Quality related field or equivalent combination of education, training, and experience
- Minimum 10 years QA experience or relevant experience in medical quality management, biomedical science, clinical development, or regulatory compliance

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