Scientist, Clinical Supply Operations
2 weeks ago
**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.
Our Clinical Supply Operations is responsible for the supply of drug product administered to patients in clinical studies worldwide. In Global Product Development and Supply the team works closely with our partners to deliver quality products safely, efficiently and on time while operationalizing the innovative technologies that will deliver the transformative medicines of tomorrow. As a member of our team, you will get the chance to play a pivotal role to positively impact patients' lives while developing professionally to achieve your own career goals.
**Position Summary**:
The Clinical Supply Operations Scientist will lead the manufacture of oral solid dosage products in a cGMP environment, ensuring strict adherence to applicable regulatory, safety, and company policies and procedures. In addition, the Scientist will be responsible for leading a variety of engineering projects in support of oral solid dosage manufacturing operations.
**Role and Responsibilities**:
- Leads the manufacture of assigned oral solid dosage product batches and completes all required documentation
- Supports successful technical transfer and scale-up of new products
- Participates in new technology evaluation and implementation
- Establishes plans for managing workload with efficient resource utilization and within designated timeframes. Effectively adjusts plans to deal with changes and obstacles.
- Troubleshoots and resolves manufacturing related issues.
- Effectively supervises assigned pharmaceutical development technician(s) to ensure efficient batch execution.
- Strictly adheres to departmental, Company, and Regulatory policies, procedures, and regulations.
- Communicates effectively with management, quality unit, peers and colleagues within and outside the department for all manufacturing, quality and safety related issues.
- Participates in SOP writing and review.
- Participates in selected initiatives leading to the improvements on cGMP compliance, safety compliance and productivity.
**Experience & Qualifications**:
- B.S. in engineering, pharmaceutical sciences, or related discipline
- 3+ years relevant experience in pharmaceutical manufacturing and/or formulation or related field
- Strong written, verbal and interpersonal communication skills are required to communicate effectively and contribute to multidisciplinary project teams.
- Additional experience with cGMP requirements and process automation systems would be beneficial.
**Why You Should Apply**
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 with the resources to pursue their goals, both at work and in their personal lives.
**Uniquely Interesting Work, Life-changing Careers**
**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 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.
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