Manufacturing Manager, Liso-cel CAR-T, Manufacturing Operations at Bristol-Myers Squibb

Summit, New Jersey, United States

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Not SpecifiedCompensation

Senior (5 to 8 years)Experience Level

Full TimeJob Type

UnknownVisa

Biotechnology, PharmaceuticalsIndustries

Requirements

Leads by example and drives team to adhere to BMS values: Inclusion, Accountability, Innovation, Urgency, and Passion
Accountable for ensuring Work Centered Team (WCT) executes Cell Therapy manufacturing according to cGMPs, SOPs, and Work Instructions
Takes personal responsibility for safety, performs regular safety Gemba walks, knows hazards, demonstrates safe behavior, and operates/maintains equipment to prevent injuries
Accountable for Production Records, performs batch record reviews (BRR) or Electronic Batch Record review by exception, ensures ALCOA+ principles, right-first-time documentation, complete/accurate records/logbooks, and resolves errors to meet turnaround times
Performs Cell Therapy manufacturing to maintain hands-on expert knowledge of each Unit Operation, demonstrates good execution to new members, and backfills for absent team members to meet production schedules
Further develops technical expertise in CAR-T manufacturing requirements
Provides Production Scheduling team with daily/weekly/monthly information on WCT production resource availability and tracks actual vs. planned/unplanned absences (holidays, sickness, etc.)
Hires personnel meeting job description criteria, BMS values, budgetary, and fiscal requirements
Sets WCT priorities and adjusts as necessary
Availability for Wednesday - Saturday night shift (5 p.m. - 5:30 a.m., with every other Wednesday off), onsite

Responsibilities

Manage and provide oversight of a Work Centered Team (WCT) executing Cell Therapy manufacturing processes
Ensure WCT maintains a culture of safety, compliance, innovation, and Continuous Improvement in Manufacturing Operations
Report to Senior Manager, Manufacturing
Ensure WCT members work safely and adhere to safety practices

Skills

Key technologies and capabilities for this role

Cell Therapy ManufacturingGMP ComplianceContinuous ImprovementSafety ManagementTeam LeadershipManufacturing OperationsCAR-T Processes

Questions & Answers

Common questions about this position

What is the work schedule for this Manufacturing Manager position?

The shift available is Wednesday - Saturday (with every other Wednesday off), onsite night shift from 5 p.m. to 5:30 a.m.

Is this role remote or onsite?

This is an onsite night shift position.

What are the key responsibilities of the Manufacturing Manager?

The role involves managing and providing oversight of a Work Centered Team (WCT) for executing Cell Therapy manufacturing processes, ensuring a culture of safety, compliance, innovation, and Continuous Improvement, and performing batch record reviews.

What company values does the Manufacturing Manager need to uphold?

The role requires leading by example and driving the team to adhere to BMS values of Inclusion, Accountability, Innovation, Urgency, and Passion.

What makes a strong candidate for this Manufacturing Manager role?

A strong candidate should have experience leading teams in GMP manufacturing environments, particularly in cell therapy, with a focus on safety, compliance, documentation accuracy following ALCOA+ principles, and fostering 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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