Associate Engineer, Shift Engineering, Devens Biologics Digital Plant at Bristol-Myers Squibb

Devens, Massachusetts, United States

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Not SpecifiedCompensation

Junior (1 to 2 years)Experience Level

Full TimeJob Type

UnknownVisa

Biotechnology, PharmaceuticalsIndustries

Requirements

Minimum education of a bachelor’s in engineering or equivalent degree or combination of education and technical experience
Minimum of two (2) years' experience with Process Control Systems or Manufacturing Systems
Knowledge and/or application of computerized systems
Demonstrated troubleshooting skills
Understands the expectations of working in regulated industries such as Biotech, Pharmaceutical, and Medical Devices
Excellent written and verbal communication skills
Strong interpersonal skills and the ability to work in a team environment
Availability for 7:00am - 7:00pm shift on a rotating schedule including holidays and weekends

Responsibilities

Support the 24/7 operation of all GMP computerized systems (including Process Automation Systems, and Manufacturing Execution Systems) utilized at the Devens Biologics site
Develop the technical and communication skills required to effectively support and troubleshoot complex automated and computerized systems while working in a cross functional organization
Follow applicable standard operating procedures while working with validated systems
Investigate the root cause of incidents, propose resolutions, and escalate issues accordingly
Leverage and develop documentation within the knowledge base to resolve issues encountered and facilitate the troubleshooting of future incidents
Act as the site point of contact for planned and unplanned outages
Perform periodic system administration related activities to ensure systems operate within prescribed specifications
Support the configuration, testing and implementation of process control solutions to a variety of complex technical problems
Provide excellent customer service to internal stakeholders
Provide troubleshooting, root cause analysis, development of resolutions to Incidents, Investigation support, Information and Data requests, and technical support for Biologics Manufacturing Processes in a timely manner with escalation as needed
Provide application service management, outage management, life-cycle management, and compliant change implementation for business critical computerized systems

Skills

Key technologies and capabilities for this role

GMPProcess Automation SystemsManufacturing Execution SystemsTroubleshootingRoot Cause AnalysisIncident ManagementChange ManagementBiologics Manufacturing

Questions & Answers

Common questions about this position

What is the work schedule for this role?

The position involves a 7:00am - 7:00pm shift on a rotating schedule that includes holidays and weekends.

What are the minimum education requirements?

A minimum of a bachelor’s degree in engineering or equivalent degree, or a combination of education and experience, is required.

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.

What is the company culture like at Bristol Myers Squibb?

The culture emphasizes challenging, meaningful, and life-changing work alongside high-achieving teams, with opportunities for growth and a focus on balance and flexibility.

What skills are essential for success in this role?

Key skills include troubleshooting and root cause analysis of computerized systems, technical support for manufacturing processes, strong communication in a cross-functional team, and following SOPs with validated systems.

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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