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Company

Original Job Post

Bristol Myers Squibb · 2 days ago

Principal Engineer

Devens, MA

Full-time

Hybrid

Mid Level

$119K/yr - $149K/yr

4+ years exp

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Responsibilities

Complete CAPAs, standalone actions, and proactive initiatives in the BMS Quality system

Manage implementation of new technology projects and transfers into commercial manufacturing

Implement process improvement projects to improve robustness, scalability and COGs for cell therapy products

Partner with teams responsible for automation project deliverables to align strategy and identify global best practices for network

Participate in new technology committees, as needed

Interface with vendors of custom and configurable equipment to plan for GMP requirements of future technologies

Ensure Technical requirements are addressed throughout lifecycle of new solutions while ensuring focus on quality and manufacturing requirements

Author technical reports and change controls to support product lifecycle and support regulatory submissions

Partner with system integration teams, business process owners and other global teams to align process data handling initiatives within the technology projects

Collaborate with Regulatory, CMC, and other stakeholders to enable new technologies at commercial manufacturing sites within existing regulatory and operational constraints

This position may require up to 20% of travel

Qualification

Find out how your skills align with this job's requirements. If anything seems off, you can easily click on the tags to select or unselect skills to reflect your actual expertise.

Cell therapy processesRisk assessmentTechnical supportCGMP manufacturingEngineering leadershipTechnology transferProject managementValidation projectsTeam interactionManufacturing supportProblem-solvingInterpersonalLeadershipCommunicationTime managementDetail-oriented

Required

Degree in Biochemical or Chemical Engineering or Sciences: Minimum of a Bachelor's degree with 9+ years of experience, Master's degree with 6+ years or Ph.D. degree with 4+ years of experience

Familiarity with cell therapy processes is preferred.

Ability to effectively lead cross functional teams, meet deadlines, and prioritize responsibilities.

Experience working in a self-driven, performance/results oriented, fast paced matrix environment.

Excellent problem-solving skills, including issue resolution

Ability to assess risk and develop contingency plans for process risks

Able to manage time and elevate relevant issues to management and governance forums.

Detail oriented with excellent verbal and written communication skills.

Strong interpersonal and leadership skills to work with teams in different functions and organizations

The candidate must have demonstrated verbal, written, and communication skills including ability to present complex information clearly and concisely, with a successful proven history of working with technical teams.

Experience should include technical support of a cGMP manufacturing facility, including strong knowledge and engineering leadership for cell therapy manufacturing and processing equipment, manufacturing support and technology transfer.

Proven track record of managing Tech Support, development and/or validation projects

Demonstrated leadership skills, and the ability to interact with and lead diverse groups and teams are essential.

Proven project management skills (organization, collaboration, multi-tasking, and communication), attention to detail, and the ability to perform well in a team-based environment are required

Prior experience in/knowledge of cell therapy preferred

Prior experience facilitating/participating in Risk Assessments preferred

Preferred

Prior experience in/knowledge of cell therapy preferred

Prior experience facilitating/participating in Risk Assessments preferred

Benefits

Medical, pharmacy, dental and vision care

BMS Living Life Better program and employee assistance programs (EAP)

Financial well-being resources and a 401(K)

Short- and long-term disability, life insurance, supplemental health insurance, business travel protection, and survivor support

Paid national holidays and optional holidays, Global Shutdown days between Christmas and New Year's holiday, up to 120 hours of paid vacation, up to two (2) paid days to volunteer, sick time off, and summer hours flexibility

Parental, caregiver, bereavement, and military leave

Adoption and surrogacy reimbursement, fertility/infertility benefits, support for traveling mothers, and child, elder and pet care resources

Tuition reimbursement and a recognition program

Company

Bristol Myers Squibb

Glassdoor

3.8

At Bristol Myers Squibb, we work every day to transform patients’ lives through science.

Founded in 1887

New York, New York, USA

10,001+ employees

http://www.bms.com

H1B Sponsorship

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