Material Operations Associate, Lead at Bristol-Myers Squibb

Bothell, Washington, United States

Apply Now

Not SpecifiedCompensation

Mid-level (3 to 4 years), Senior (5 to 8 years)Experience Level

Full TimeJob Type

UnknownVisa

Pharmaceuticals, Biotechnology, ManufacturingIndustries

Requirements

Proficient knowledge of current GMP regulations
Strong interpersonal and communication skills
Knowledge of quality management systems – Veeva Vault

Responsibilities

Provides on the floor support, guidance, and leadership to staff for setting priorities and accomplishment of departmental daily task objectives
Coordinates cross functionally with customer groups on workflow activities and priorities
Builds and leads Bothell Site Supply Chain compliance programs and processes
Supports Bothell Site Supply Chain in collecting and analyzing data to improve processes, reporting, and communication
Leads cross-functional initiatives that ensures clinical and commercial readiness of the cell therapy programs
Serves as the point of contact for Supply Chain projects and operational excellence initiatives
Owns and drives completion of change controls, deviations, and CAPAs
Serves as SME for Supply Chain organization for all quality records
Manages timelines, escalates critical issues, and maintains status dashboards to management
Develops process flow diagrams, process outlines, and documentation to assist in evaluating and optimizing operations
Coordinates between site-level and global colleagues on implementing new projects, representing the interests of Site Supply Chain in project teams led by other functions
Identifies strategic and operational issues both internally and externally, developing proposals, outlines, and implementing solutions
Seeks and supports continuous process improvement projects both within the department and across site initiatives
Manages creation, implementation, and compliance for all documentation, procedures, and policies
Builds and maintains positive relationships with all functions at the Bothell site, as well as with external customers and stakeholders
Champions and fosters a positive and successful collaborative culture, aligned with BMS existing culture
Creation and Management of KPI’s to monitor Supply Chain Quality and Compliance performance
Performs other tasks as assigned

Skills

Key technologies and capabilities for this role

Supply ChainGMPLeadershipContinuous ImprovementChange ManagementKPI DevelopmentProcess Implementation

Questions & Answers

Common questions about this position

What benefits does Bristol Myers Squibb offer?

Bristol Myers Squibb offers a wide variety of competitive benefits, services, and programs that provide employees with resources to pursue their goals both at work and in their personal lives.

Is this a remote position or does it require on-site work?

This information is not specified in the job description.

What are the key responsibilities of the Material Operations Associate, Lead?

The role involves providing on-the-floor leadership, coordinating tasks and priorities, ensuring GMP compliance, driving continuous improvement, managing change controls and CAPAs, and leading cross-functional initiatives for clinical and commercial readiness.

What is the company culture like at Bristol Myers Squibb?

The culture is described as challenging, meaningful, and life-changing, with uniquely interesting work, opportunities to grow alongside high-achieving teams, and a focus on balance and flexibility.

What makes a strong candidate for this role?

Strong candidates will have leadership experience in supply chain operations, expertise in GMP processes and quality records like change controls, CAPAs, and deviations, and the ability to drive cross-functional projects and continuous improvement initiatives.

Bristol-Myers Squibb

Develops and delivers biopharmaceutical medicines

About Bristol-Myers Squibb

Bristol Myers Squibb (BMS) develops and delivers medicines aimed at treating serious diseases, focusing on areas like cancer, autoimmune diseases, and heart conditions. The company conducts extensive research and development to create new drugs, which are sold after receiving regulatory approval. BMS also produces generic drugs, offering affordable alternatives that meet the same quality standards as their branded counterparts. What sets BMS apart from competitors is its dual focus on both innovative and generic medicines, enhancing access to healthcare. The company's goal is to improve patient outcomes while maintaining a commitment to sustainability and corporate responsibility.

New York City, New YorkHeadquarters

1887Year Founded

$33,706.1MTotal Funding

IPOCompany Stage

Biotechnology, HealthcareIndustries

10,001+Employees

Benefits

Flexible Work Hours

Hybrid Work Options

Professional Development Budget

Risks

Increased competition in oncology from emerging biotech firms like ArsenalBio.

BMS's lawsuit over the 340B Drug Pricing Program may lead to regulatory challenges.

Rapid AI and digital tech evolution may pose integration challenges for BMS.

Differentiation

BMS focuses on innovative cancer treatments through collaborations like ArsenalBio for T cell therapies.

The company emphasizes digital health technologies, enhancing clinical trial management and patient engagement.

BMS offers both innovative and generic medicines, increasing affordable healthcare solutions.

Upsides

BMS's partnership with Medidata enhances clinical research processes and patient outcomes.

The collaboration with AI Proteins advances novel miniprotein-based therapeutics, expanding therapeutic modalities.

BMS's global license agreement with BioArctic expands its portfolio in neurodegenerative diseases.

Land your dream remote job 3x faster with AI

Try Jobo Free