Sr. Director, Manufacturing Technical Operations
- Full-Time
- Carlsbad, CA
- GenMark Diagnostics
- Posted 3 years ago – Accepting applications
Heroes work here!
Do you want to join a company where you can be a hero too?
We deliver innovative, diagnostic solutions that improve the lives of patients and their families and are proud to be one of the heroic diagnostic companies that is in this fight against COVID-19.
As a member of GenMark’s team, you’ll get to be part of an organization where we embody our cultural beliefs in everything we do. The following is a glimpse of what our culture looks like and If you'd like to join us, we encourage you to apply as our company is growing!
- Go Big - We never settle and challenge what’s possible
- Win Together - We are one team with a shared purpose
- Own It - We step up, drive it, and deliver it
- Be Bold - We empower ourselves and other
WHAT YOU'LL DO AT GENMARK!
As the Sr. Director, Manufacturing Technical Operations you will be responsible for the direction and coordination of Manufacturing Technical Operations functions, including manufacturing engineering, process engineering, equipment engineering, and automation functions. This leader will have an excellent understanding of device manufacturing, including working with device development and manufacturing to enable manufacturing at various scales. This leader will foster a strong attitude of collaboration and work closely with all other groups within the organization. This person will provide leadership and oversight to a variety groups within the operations division, including manufacturing and supply chain, in support of commercial product efforts.
ESSENTIAL DUTIES & RESPONSIBILITIES
- Ownership of designing, sustaining and improving manufacturing processes with a critical focus on improving yield and gross margin.
- Work with colleagues across GenMark to ensure efficient and effective production for all product lines.
- Serve as Subject Matter Expert on device manufacturing; supporting development, manufacturing, investigations, process improvements, validations, regulatory filings, technical documents, and inspections.
- Work with suppliers and contract manufacturers on tech transfer, process installation, process qualification, and ongoing manufacturing oversight.
- Lead a team of technical experts to support manufacturing and translate business requirements into process changes in support of product and manufacturing strategies.
- Ensure ongoing technical support for all manufacturing processes both internally and/or at contract manufacturing sites and directing global initiatives and cross-functional teams of subject matter experts in manufacturing.
- Driving innovation and communication of latest industry trends and best practices for process design and manufacturing to ensure consistency.
POSITION REQUIREMENTS
- Minimum of BS degree with a scientific or engineering focus
- 10+ years of operational or engineering experience in a Biotechnology, Medical Device or Pharmaceutical manufacturing environment.
- Demonstrated knowledge of biomaterials and biotechnology device manufacturing.
- Experience establishing and maintaining robust validation and process control strategies.
- Several years leading and managing a team of dedicated engineers, scientists and technicians.
- Strong engineering skills, including facility fit and process engineering assessment into different facilities.
- Strong Lean Six Sigma or alternate continuous improvement skills for root cause analysis.
- An understanding of design control elements required for medical or in-vitro diagnostics devices.
- Able to apply principles of mechanics, microfluidics, and materials to understand the mechanical design of complex plastic parts and assemblies.
- Able to apply basic biologic principles including nucleic acid sample preparation and PCR amplification to understand assay performance on the consumable platform.
- Experience with plastic assembly techniques such as ultrasonic and laser welding.
- Advanced experience with root cause analysis, design of experiments, and data analysis.
- Experience with qualification, verification, and validation requirements as related to parts, equipment and products.
ABOUT GENMARK
GenMark’s ePlex true sample-to-answer system symbolizes the evolution of eSensor technology combined with digital microfluidics. ePlex offers unique solutions to address the most significant challenges facing clinical laboratories, while supporting hospital systems to deliver patient-centered, value-based care. ePlex streamlines the diagnostic workflow from physician order entry to the final test report, and is the only true sample-to-answer solution designed to improve patient care, reduce costs, and increase lab efficiency.
GenMark is headquartered in Carlsbad.