Jobs in the United States

25+ jobs

Group jobs by employerEmail me new jobs Save this search

Added 16 mins ago
Quality Engineer
Promega
Madison, WI
YOUR ROLE: As a Quality Engineer, you'll lead quality system improvement projects for Promega's medical device business, work governed by ISO 13485 and FDA's Quality Management System…
Added 26 mins ago
Software Engineer I
RTX
United States
Qualifications You Must Have:
Added 29 mins ago
ZZ
Principal Software Development Engineer, Design Systems (Web)
ZINC Zillow, Inc.
Remote, United States
- $185,800 to $312,400 USD / year
Design Foundations brings together design systems, digital accessibility, brand and visual language, content standards, and the AI-enabled tools increasingly used by Product, Design, and…
Added 30 mins ago
Endpoint Security Engineer
Hays
VA
Seeking an experienced cybersecurity engineer to support enterprise Application Whitelisting/Application Control and daily endpoint security operations. The resource should have strong…
Added 31 mins ago
Sr. Software Engineer - Design and R&D
General Motors LLC
Warren, MI
The Global Design and R&D IT team supports the design and research and development of GM production and concept vehicles, from early innovation through production design. We are seeking a…
Added 31 mins ago
Sr. Systems Engineer - Design and R&D
General Motors LLC
Warren, MI
The Global Design and R&D IT team supports the design and research and development of GM production and concept vehicles, from early innovation through production design. We are seeking a…
Added 39 mins ago
Cyber Full Stack Senior Consultant
Deloitte
Kansas City, MO
+ Helping digital platforms improve trust and safety and address online harms
Added 39 mins ago
Cyber Full Stack Manager
Deloitte
Kansas City, MO
+ Leading design, development, integration, deployment, testing, and troubleshooting of production-grade solutions within client environments, including artificial intelligence (AI) and…
Added 44 mins ago
DI
Electrical Hardware Engineer
Dataspeed Inc.
Rochester Hills, MI
- $60,000 to $90,000 USD / year
About the Role We are looking for a hands-on Electrical Hardware Engineer with 1-3 years of experience to join our team and design the electrical systems that turn conventional vehicles…
Added 51 mins ago
Applied AI Engineer - Engineering Simulation & Design Exploration
Bentley Systems, Incorporated
Philadelphia, PA
…by professionals, and organizations of every size, for the design, construction, and operations of roads and bridges, rail and transit, water and wastewater, public works and utilities,…
Added 58 mins ago
Manufacturing Engineer III – 2nd Shift - New Glenn
Blue Origin Personnel, LLC
Space Coast, FL
Writing clear shift handoffs and coordinating with day shift engineering, quality, and production operations
Added 1 hour ago
Senior Computer Vision Architect
Apple
Seattle, WA · Sunnyvale, CA
…programs across many Apple products! We do this by enabling the co-design of computer vision algorithms and systems through a deep understanding of the complexities and trade-offs between…
Added 1 hour ago
Software Development Engineer, Test Tooling
Apple
Cupertino, CA
…critical user flows across the Apple Ads platform. As a Tooling Engineer, you'll help develop tooling and automation to our testing faster and more reliable. That includes test data setup…
Added 1 hour ago
Machine Learning Engineer
Apple
Cupertino, CA
…content to consumers. Are you a results-oriented and versatile engineer who can excel in a fast-paced environment? You will work closely with ML engineers and scientists to design, develop,…
Added 1 hour ago
Software Engineer, Apple Ads
Apple
Cupertino, CA
Architect, design, and implement internet-scale, low-latency, highly-available ad-serving systems in a cloud environment.
Added 1 hour ago
Hardware Systems Design & Integration Engineer - AirPods
Apple
Cupertino, CA
…Lead for an AirPods program, owning the system architecture, design, and development from initial concept through mass production. You will drive critical trade-offs - applying rigorous…
Added 1 hour ago
PM
Network Engineer - Collaboration & Enterprise Connectivity
Prologis Management
Denver, CO
- $83,000 to $114,000 USD / year
As a Network Engineer - Collaboration & Enterprise Connectivity, you will help deliver secure, reliable enterprise connectivity and production-ready voice and conference room experiences…
Added 1 hour ago
Electronic Security Systems Engineer
VTG
Pearl City, HI
Perform C4ISR engineering drafting, drawing reviews, drawing control, and related services required in the design of electronic/communications equipment, systems and installations. Drawings…
Added 1 hour ago
I
Salesforce Commerce Cloud Dev Ops/Release Engineer
iSoftStone
New York, NY
- $75 to $83 USD / hour
iSoftStone, Inc. is Seeking a Salesforce Commerce Cloud Dev Ops/Release Engineer to Join our Team in New York!
Added 1 hour ago
Senior System Safety Engineer
Astrion
Eglin Air Force Base, FL
Astrion has an exciting opportunity for a Senior System Safety Engineer supporting the Agile Weapons Division (AFLCMC/EBX) at Eglin AFB, FL. This division is resposible for acquiring…
Added 1 hour ago
Sr. Automation Engineer
Zifo
Remote, United States
…sciences, biotech, and pharmaceutical organizations. We enable digital transformation across R&D, manufacturing, and quality by delivering data-driven, scalable, and compliant software…
Added 1 hour ago
Senior Data Engineer
Jobgether
Remote, United States
The Senior Data Engineer will lead the design, development, and optimization of enterprise data architectures and business intelligence solutions.
Added 1 hour ago
V&V Automation Engineer
Quest Global
Sunnyvale, CA
Quest Global delivers world-class end-to-end engineering solutions by leveraging our deep industry knowledge and digital expertise. By bringing together technologies and industries,…
Added 1 hour ago
Physical IC Layout Engineer – Analog / PMIC
Glint Tech Solutions LLC
Santa Clara · Santa Clara, CA
Collaborate closely with analog and digital design engineers to ensure layout quality and design integrity.
Added 2 hours ago
Instrumentation & Controls Engineer SME – Hyperscale Data Centers
Jacobs
Portland, OR
…projects. Your expertise will shape project execution, influence design strategy, and strengthen our delivery…

Promega

Quality Engineer

Madison, WI, United States

Apply on careers.promega.com About employer

Applications open in a new tab.

Job details

Apply by: Nov 12, 2027
Posting language: English
Posted: Nov 12, 2026

Original job description

OUR TEAM: The Product Quality and Compliance (PQ&C) team at Promega brings together Product Quality Assurance, Quality Systems, and Compliance in one collaborative organization. We make sure Promega's Research Use Only, IVD medical device, and Active Pharmaceutical Ingredient (API) products meet high quality standards for our customers, and that they comply with regulations across a global portfolio. We cover everything from product release and complaint investigation to quality system processes, audits, and regulatory inspections. We work closely with Manufacturing, R&D, Operations, and Supply Chain to find and fix the root causes of quality issues. We value curiosity, accountability, and practical judgment. We're also adopting AI-supported tools so we spend less time on administrative work and more on improving quality.

YOUR ROLE: As a Quality Engineer, you'll lead quality system improvement projects for Promega's medical device business, work governed by ISO 13485 and FDA's Quality Management System Regulation (QMSR). You'll also be a compliance resource as Promega builds its capabilities in Active Pharmaceutical Ingredient (API) manufacturing. You'll scope and drive projects from charter through implementation and improve key processes. You'll support API nonconformance review and GMP compliance, and investigate escalated complaints. Your work will move between RUO, device and API, often in the same week, and you'll help stakeholders see risks to timeline and quality before they become problems. The role has real room to shape how our quality systems grow alongside Promega's expanding organizational capabilities.

JOB OBJECTIVE: Utilize design, engineering and quality principles and practices to support the design and manufacture of products and implement and improve key business and quality processes. Actively support Promega's growing Active Pharmaceutical Ingredient (API) business by monitoring compliance with GMP and customer requirements across API manufacturing, and lead quality system improvement projects aligned with ISO 13485 and other medical device regulations.

CORE DUTIES:

Works with internal and external stakeholders and managers to define issues, select projects, and prioritize work. Assure projects align with business and quality system objectives. Create project charters, work plans, schedules, issues logs, and risk management plans, as necessary. Actively manages partners, contractors and/or consultants in delivering solutions during project work.
Develops project, process, instrument and product plans addressing key requirements, deliverables, timing, and assignments needed for successful completion. Write or establish methods or procedures to ensure continued and improved process and system performance. Implements project, process, instrument, or product work in collaboration with other partners, departments, or teams. Create assignments and tasks and track completion against stated requirements. Address delays and other barriers in completion of tasks.
Reports and/or presents project, instrument, or product progress/metrics to stakeholders during course of work. Identify issues detrimental to the timeline, budget, or quality of the work, and recommend solutions to overcome identified issues. Ensure source data is verified and accurate. Summarize metrics and support management to present data.
Uses quality, engineering and human factors concepts, design and implement product and process improvements to improve quality and lower costs. Ensure products and processes meet customer, business, and regulatory requirements.
Develops, redesigns, and manages processes which are compliant with customer requirements, the Quality System Regulation (QSR) and ISO13485. Key systems include Process Controls, Supplier Controls, and other related QS sub-systems.
Serves as a compliance resource for contract-manufactured Active Pharmaceutical Ingredient (API) products, monitoring adherence to API quality standards and implementing process improvements to ensure ongoing compliance with external GMP requirements and customer standards.
Supports review of nonconformance documentation for API products, as needed, to ensure compliance with internal procedures and external quality standards.
Occasionally supports customer audits, complaint resolution, and relationship development, as needed.
Use and comply with Complaint Investigation procedures and Promega's Quality System procedures as appropriate to this position. Apply problem-solving skills, while performing investigations and communicate investigational work to internal and external customers as applicable. Recommend further action, as necessary.
Works with management with executive responsibility on urgent/critical activities or projects needed for the business.
Performs other duties as assigned to support departmental and business needs.
Demonstrates inclusion through their own words and actions and is accountable for a safe workspace. Acts with kindness, curiosity and respect for others.
Embracing and being open to incorporating Promega's 6 Emotional & Social Intelligence (ESI) core principles in daily work.
Understands and complies with ethical, legal and regulatory requirements applicable to our business.

KEY QUALIFICATIONS:

Minimum BS degree or equivalent in engineering, technical and/or scientific discipline with minimum 4 years of engineering or design experience.
Minimum of 3 years' experience in project management or supervision, especially in the biotechnology or medical device areas.
Demonstrated adaptability and willingness to learn and effectively use AI-supported tools in daily work, along with working knowledge of role-relevant software such as Visio, Microsoft Project, and CAD in a Windows-based environment.
Demonstrated experience in achieving results in a rapidly changing cross-functional environment.
Strong analytic and presentation skills for problem determination, decision-making and resolution.
Over 2 years' experience in designing, developing, and supporting biotechnology, medical device, or API product lines.
Demonstrated proficiency in digital tools and technology, including Microsoft applications and mobile platforms, with the ability to adapt and leverage emerging technologies, such as artificial intelligence, to improve efficiency, automation, and collaboration.

PREFERRED QUALIFICATIONS:

Independent, self-starter with proven results in problem identification, planning, communication, and project management.
Able to work and communicate well with a diverse scientific, business, and organizational group to achieve improvement and operational results.
Experience in medical device and cGMP systems, especially in understanding requirements, identifying improvement targets, tracking results, and developing products.
Experience in Active Pharmaceutical Ingredient (API) manufacturing or contract-manufactured API compliance, including working knowledge of quality standards governing API products.
Technical knowledge or experience in scientific areas applicable to small molecule drug manufacturing.
Excellent oral and written communication skills, including formal presentations, coaching, and problem resolution.
Ability to articulate technical and interpersonal issues and resolve conflict in a constructive manner to ensure project success.
MS or greater in engineering or technical discipline.

PHYSICAL DEMANDS:

Ability to use a computer/Microsoft Office applications.

At Promega, we value diversity and strive to create an inclusive workplace. We are proud to be an Equal Opportunity Employer, making employment decisions without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, disability, or any other protected class.

Apply on careers.promega.com About employer

More about this job

Skills

Supply chain management
Quality assurance procedures
Regulatory compliance
Good manufacturing practices
Quality control systems
Medical device regulations
Risk management
Collaboration
Manage quantitative data
Documentation
Problem solving
Project management
Biotechnology
Adaptability
Microsoft Visio
Microsoft Project
Microsoft Windows
Presentation skills
Decision making
Communication skills
Coaching
Use a computer
Microsoft Office

Report this job

Work requirements

Jobs in the United States