Senior Specialist, QC Materials Management, Cell Therapy in Devens, MA at Bristol-Myers Squibb

Devens, Massachusetts, United States

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Not SpecifiedCompensation

Senior (5 to 8 years)Experience Level

Full TimeJob Type

UnknownVisa

Biotechnology, Pharmaceuticals, Cell TherapyIndustries

Requirements

Bachelor’s degree, preferably in Chemistry, Microbiology, or related science. Advanced degree preferred
4+ years of relevant work experience, preferably in a regulated environment. An equivalent combination of education and experience may substitute
Experience with material management
Ability to accurately and completely understand, follow, interpret and apply Global Regulatory and cGMP requirements
High problem-solving ability/mentality, technically adept and logical
Ability to communicate effectively with peers, department management and cross-functional peers about task status, roadblocks and needs
Ability to work in a fast-paced team environment, meet deadlines, and prioritize work
Excellent organizational and critical thinking skills

Responsibilities

Serve as the site representative for QC material management program and manage the lifecycle activities of QC laboratory materials
Support onboarding of new materials through document creation and change control
Collaborate with QC network functions and site functions such as QC lab, supply chain and other departments for the management of QC materials
Implement and maintain the QC material inventory management system (e.g., Kanban)
Train others on material management process and procedures as applicable
Perform document revision, project, CAPA, and related tasks and/or continuous improvement efforts
Create, revise, and review technical documents, such as SOPs and working instructions for sample management
Implement 5S and FIFO principles as appropriate
Apply critical thinking skills when working on new procedures or process improvements
Communicate effectively with management regarding task completion, roadblocks, and needs
Perform other tasks as required to support the QC laboratories

Skills

Key technologies and capabilities for this role

QC Materials ManagementLaboratory Supplies ManagementDocument CreationChange ControlSupply Chain CollaborationCell TherapyMicrobiologyAnalytical Testing

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 position remote or onsite?

The role is based in Devens, MA at the CTF facility, indicating an onsite position.

What key responsibilities are required for this role?

Key responsibilities include managing the lifecycle of QC laboratory materials, supporting onboarding of new materials through document creation and change control, collaborating with QC and site functions, implementing inventory systems like Kanban, training others, and applying 5S and FIFO principles.

What is the company culture like at Bristol Myers Squibb?

The culture is 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 position?

A strong candidate will have expertise in QC material management to serve as SME, experience with lifecycle management, document creation, change control, inventory systems like Kanban, collaboration across functions, and skills in training, CAPA, and continuous improvement.

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.

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