Associate Specialist Production Planning at Bristol-Myers Squibb

Bothell, Washington, United States

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Not SpecifiedCompensation

Junior (1 to 2 years), Mid-level (3 to 4 years)Experience Level

Full TimeJob Type

UnknownVisa

Biotechnology, PharmaceuticalsIndustries

Requirements

0-3 years preferred; 1+ years of scheduling experience in cGMP manufacturing environment desired
Experience in scheduling cell therapy manufacturing preferred
Experience in material planning and/or finite scheduling in a medium to high volume environment
Knowledge of scheduling platforms preferred
Knowledge of forecasting, capacity planning, and production planning
Knowledge of cGMP regulations and FDA guidance applicable to biologics and cell therapy (or related) manufacturing
Ability to work independently on projects or problems of moderate scope to meet objectives; troubleshoots and identifies causes and suggests solutions
Attention to detail and ability to perform with a high degree of accuracy
Source of imaginative, thorough, and innovative solutions to a wide range of difficult problems
Experience in lean, operational excellence, six sigma, or continuous improvement, and process mapping preferred
Ability to influence key stakeholders of internal and external teams
Excellent communication and presentation skills as well as the ability to effectively communicate across all levels of the company
Strong analytical and problem-solving abilities
Expert in Microsoft Office programs
Availability for schedule: Wed - Sun 8am-5pm, with training Mon-Fri for first 60 days

Responsibilities

Plans and schedules production related activities at the cell therapy manufacturing facility
Provides manufacturing operations with a plan that maximizes efficiency, resources, and capacity
Achieves on time delivery within budget
Works on projects/matters of moderate complexity
Evaluates and develops scheduling tools and provides technical expertise
Plans and schedules production schedules to meet product demand at the site
Plans and schedules all associated production and support activities including intermediates, product shipment, facility and equipment maintenance
Works with Document Control to ensure all documents (i.e. batch records and packaging records) are ready for Manufacturing
Builds strong relationships and communication with all functions
Provides exceptional customer service
Supports an environment that encourages continuous improvement, best practices and appropriate risk taking

Skills

Key technologies and capabilities for this role

Production PlanningSchedulingCapacity PlanningForecastingcGMPFDA RegulationsCell Therapy ManufacturingBiologics ManufacturingDocument ControlBatch Records

Questions & Answers

Common questions about this position

What is the work schedule for this position?

The schedule is Wednesday through Sunday from 8am to 5pm, with training scheduled Monday through Friday for the first 60 days.

What is the salary range for this role?

This information is not specified in the job description.

What key skills are required for the Associate Specialist Production Planning role?

Required skills include knowledge of forecasting, capacity planning, and production planning; knowledge of cGMP regulations and FDA guidance for biologics and cell therapy; strong analytical and problem-solving abilities; excellent communication and presentation skills; and expertise in Microsoft Office programs.

What is the company culture like at Bristol Myers Squibb?

The culture emphasizes challenging, meaningful, and life-changing work in a flexible environment with high-achieving teams, opportunities for growth, and support for continuous improvement, best practices, and appropriate risk-taking.

What makes a strong candidate for this position?

Strong candidates have the ability to work independently on projects of moderate scope, attention to detail with high accuracy, experience in lean, operational excellence, six sigma, or continuous improvement, and the ability to influence stakeholders and provide innovative solutions.

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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