Supply Chain Operator, Cell Therapy in Devens, MA at Bristol-Myers Squibb

Devens, Massachusetts, United States

Bristol-Myers Squibb Logo
Not SpecifiedCompensation
Junior (1 to 2 years)Experience Level
Full TimeJob Type
UnknownVisa
Biotechnology, Pharmaceuticals, Cell TherapyIndustries

Requirements

  • High school Diploma / GED
  • Minimum 4 years of experience in warehousing (preferably GMP) or performing material operations activities
  • Proficiency in MS Office applications
  • Knowledge of cGMP/Pharmaceutical regulations
  • Excellent written and verbal communication skills
  • Demonstrated experience to effectively communicate problem statements and escalate concerns
  • Ability to present data and analyses in an organized, clear and concise manner
  • Ability to coach less experienced group members
  • Ability to work independently for extended periods of time
  • Additional post-secondary education resulting in an Associate’s or Bachelor’s Degree in a relevant discipline is preferred (or equivalent combination)

Responsibilities

  • Execute daily tasks for material receipt and shipments according to the schedule
  • Adhere to safety, quality, and productivity standards in all material operations
  • Maintain a safe work environment in all areas where material operations activities occur
  • Collaborate with cross-functional team members to solve work-related problems and perform routine activities
  • Identify and report any changes needed in documentation and equipment as part of continuous improvement efforts
  • Partner with Cell Therapy Manufacturing & Quality to support the readiness for prompt receipt, inspection and start of processing for patient material
  • Coordinate, pack & ship materials to both domestic and international markets, including hazardous materials
  • Adhere to good manufacturing practices and standard operating procedures
  • Support in maintaining material inventory accuracy using required systems and equipment
  • Support process investigations & CAPAs
  • Provide support and suggestions on special projects such as validation of Material Operations areas
  • Assist in reviewing area documents, such as logbooks & worksheets
  • Review work throughout the work process and at completion, in order to ensure that it has been performed properly, where ability to recognize deviation from accepted practice is required
  • Verify SAP transactions of inventoried materials and their movements
  • Troubleshoot inventory/transaction errors

Skills

Key technologies and capabilities for this role

Materials ManagementMaterial ReceiptMaterial ShipmentsSafety StandardsQuality StandardsProductivity StandardsSupply Chain Operations

Questions & Answers

Common questions about this position

What shifts are available for the Supply Chain Operator role?

DAY and NIGHT shifts are available on a Panama schedule with 12-hour shift patterns (6 a.m. to 6 p.m. or 6 p.m. to 6 p.m.) following a 2-2-3 work cycle that includes weekends and holidays.

What are the main responsibilities of the Supply Chain Operator?

The role involves executing daily tasks for material receipt and shipments, adhering to safety, quality, and productivity standards, collaborating with cross-functional teams, coordinating packing and shipping of materials including hazardous ones, maintaining inventory accuracy, and supporting process investigations.

What is the work location for this position?

The position is based in Devens, MA at the Cell Therapy Facility.

What is the company culture like at Bristol Myers Squibb?

BMS offers a challenging, meaningful, and life-changing work environment with opportunities to grow alongside high-achieving teams, emphasizing balance, flexibility, and reimagining the future of Cell Therapy.

What salary or compensation is offered for this role?

This information is not specified in the job description.

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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