Technical Product Engineer

  • Madison, WI
  • Posted 4 days ago | Updated 8 hours ago

Overview

On Site
Full Time

Skills

PS
PostScript
Boost
Interfaces
Business Development
GMP
Manufacturing
Customer Facing
Supply Chain Management
Documentation
Line Management
NPI
Product Management
Facilitation
Presentations
Management
Process Improvement
Quality Management
Science
Biology
Technical Support
Technology Transfer
Technical Writing
Good Manufacturing Practice
ISO 9000
QMS
Sales
Procurement
Quality Assurance
Project Management
Performance Management
Preventive Maintenance
Training
SAP BASIS
Military
Law
Recruiting
Promotions
Human Resources
Legal
Regulatory Compliance
Reporting

Job Details

Work Location: Madison, Wisconsin
Shift: No
Department: LS-PS-JI Operations A
Recruiter: Anthony Johnson

This information is for internals only. Please do not share outside of the organization.

Your Role:

Mirus Bio has an immediate opening for a Technical Product Engineer that will use their expertise and technical background to boost the connectivity between our Quality, Operations, Product Management, and Commercial Teams. This role will serve as the technical Subject Matter Expert (SME) for our current and future products and drive technical and operational enhancements for our product portfolio. This role interfaces directly with our manufacturing partners and test labs to drive efficiencies and oversee external production activities. This role works closely with the Director of Strategy, Product, and Business Development, Senior Quality Manager, and their teams to influence product line decisions by understanding the customer need, knowing the product manufacturing controls and limits, and driving quality assurance expectations of our products.

We are currently on the lookout for a hands-on individual to join our passionate team. If you are someone who thrives in a collaborative, innovative, and fast-paced environment, join us in shaping the future of our industry and be a part of a team that continues to redefine possibilities. This role works cross-functionally with all departments within Mirus Bio and is a full-time on-site position.

Duties and Responsibilities:
  • Technical SME for formulation, fill, finish for our current and future products driving product and portfolio improvements for both internal operations and customer objectives and supporting both GMP and RUO portfolios.
  • Drive efficiencies and oversee routine production activities at our manufacturing partners and test labs, including technical review of production batch records and associated documentation.
  • Drive final product multisourcing production activities with our manufacturing partners.
  • Owner of critical internal and customer facing documentation including Product Specifications, Product Regulatory Support Packets, Customer Operational/Supply Chain/QA FAQ's, Mirus Quality Supplier Survey, etc. Includes creation, maintenance, and improvements to this documentation.
  • Lead operational product line management activities during the NPI processes including creation of product specifications, product item cards, product labels, and driving product portfolio consistency.
  • Create connectivity between Quality, Operations, Product Management, Support and Commercial Teams by facilitating internal conversations and decisions regarding our products.
  • Compile information and author comprehensive operational technical reports and presentation materials for use with internal and external stakeholders.
  • Project manage and drive product process improvements using Mirus Bio's Quality Management System (QMS) including authoring change controls.
  • Demonstrate behavior outlined within the Mirus Bio Employee Handbook.
  • Perform other duties as assigned by Director of Operations.

Who You Are

Minimum Qualifications:
  • Bachelor of Science (B.S.) degree in Biology, Engineering or related field with commensurate work experience.
  • At least 5 years' experience in highly technical roles focused on products and product applications such as technical support, field application specialist, technology transfer, technical writing, etc.
  • At least 2 years' experience in the cell and gene therapy industry and/or biosciences tools industry.

Preferred Qualifications:
  • Excellent cross-functional communicator comfortable working with all levels in an organization.
  • Strong background working in a cGMP environment, navigating an ISO certified QMS, and supporting quality assurance.
  • Able to effectively translate technical concepts into user-friendly content suitable for diverse audiences, including laboratory scientists, researchers, sales teams, procurement teams, and quality assurance teams.
  • Prefer regulatory and/or quality assurance experience.
  • PM certification or training through an accredited program is preferred.

Travel Requirements:
  • Ability to travel independently 5% of the time, including overnight travel.
  • Ability to drive a vehicle; Must have current and valid U.S. driver license.

The Company is an Equal Employment Opportunity employer. No employee or applicant for employment will be discriminated against on the basis of race, color, religion, age, sex, sexual orientation, national origin, ancestry, disability, military or veteran status, genetic information, gender identity, transgender status, marital status, or any other classification protected by applicable federal, state, or local law. This policy of Equal Employment Opportunity applies to all policies and programs relating to recruitment and hiring, promotion, compensation, benefits, discipline, termination, and all other terms and conditions of employment. Any applicant or employee who believes they have been discriminated against by the Company or anyone acting on behalf of the Company must report any concerns to their Human Resources Business Partner, Legal, or Compliance immediately. The Company will not retaliate against any individual because they made a good faith report of discrimination.
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