Senior Project Engineer
Contract W2
Contract Independent
Contract Corp To Corp
On-site
$100 - $110/hr
Talent Software Services, Inc
Fitment
Dice Job Match Score™
📊 Calculating match score...
Job Details
Skills
- MEDICAL DEVICE
- DEVICE DEVELOPMENT
- COMBINATION PRODUCT DEVELOPMENT
- DESIGN HISTORY FILE
- DESIGN TRACEABILITY MATRIX
- PROJECT ENGINEER
- ENGINEER
Summary
Senior Project Engineer
Job Summary: Talent Software Services is in search of a Senior Project Engineer for a contract position in Novato, CA. The opportunity will be for six months with a strong chance for a long-term extension.
Position Summary: The client''s Technical Operations group is responsible for creating our drugs for use in clinical trials and for scaling production of those drugs for the commercial market. These engineers, technicians, scientists, and support staff build and maintain clients'' cutting-edge manufacturing processes and sites, provide quality assurance and quality control to ensure we meet regulatory standards, and procure the needed goods and services to support manufacturing and coordinate the worldwide movement of our drugs to patients.The Medical Device and Combination Products Engineer (Sr Engineer 2, Level 8) is responsible for the development of medical device components of drug-device combination products. Primary activity is to manage and support design control, risk management, and human factor engineering. The Engineer will lead internal device teams and will represent BioMarin to interact with technology and service providers, and contract manufacturers (CMOs) to ensure that all required activities are defined clearly and performed in a timely manner. This person will mainly be focused on ensuring Device Development activities are performed per Regulatory guidance, industry practices, and client''s SOPs. He/she will lead, support, and coordinate between various internal functions as well as external parties to ensure that devices/combination products meet predefined requirements.
Primary Responsibilities/Accountabilities:
Qualifications:
University degree in Engineering or related scientific discipline preferred, with 8-10 years related experience in medical device/combination product development.
Preferred:
If this job is a match for your background, we would be honoured to receive your application!
Providing consulting opportunities to TALENTed people since 1987, we offer a host of opportunities, including contract, contract to hire, and permanent placement. Let''s talk!
Job Summary: Talent Software Services is in search of a Senior Project Engineer for a contract position in Novato, CA. The opportunity will be for six months with a strong chance for a long-term extension.
Position Summary: The client''s Technical Operations group is responsible for creating our drugs for use in clinical trials and for scaling production of those drugs for the commercial market. These engineers, technicians, scientists, and support staff build and maintain clients'' cutting-edge manufacturing processes and sites, provide quality assurance and quality control to ensure we meet regulatory standards, and procure the needed goods and services to support manufacturing and coordinate the worldwide movement of our drugs to patients.The Medical Device and Combination Products Engineer (Sr Engineer 2, Level 8) is responsible for the development of medical device components of drug-device combination products. Primary activity is to manage and support design control, risk management, and human factor engineering. The Engineer will lead internal device teams and will represent BioMarin to interact with technology and service providers, and contract manufacturers (CMOs) to ensure that all required activities are defined clearly and performed in a timely manner. This person will mainly be focused on ensuring Device Development activities are performed per Regulatory guidance, industry practices, and client''s SOPs. He/she will lead, support, and coordinate between various internal functions as well as external parties to ensure that devices/combination products meet predefined requirements.
Primary Responsibilities/Accountabilities:
- Drive device and combination product development-related engineering activities on critical pipeline products. This includes component and sub-assembly design, creating design history files, and leading technical project team meetings.
- Create and own technical documentation (e.g., testing protocols, reports, SOPs, work instructions, etc.)
- Manage / support device development, including regulatory activities.
- Support all regulatory filings and related activities.
- Manage / Support all stages of design control for class II/III medical devices.
- Interface with key stakeholders and outside experts/vendors to define project/product requirements to meet client''s Pipeline portfolio.
- Specify test requirements and acceptance criteria to satisfy quality and regulatory needs (e.g., Design Verification Testing, DVT).
- Lead/support risk analyses, such as hazard identification, FTA, FMEA, etc., associated with devices.
- Provide support to device component manufacturing and final product assembly with CMO.
- Support human factor engineering studies with the clinical sciences group.
- As needed, facilitate product and process improvement through appropriate change controls and documentation.
- Knowledge of regulations and standards (e.g., cGMP/QSR/ICH/ISO/AAMI/ANSI/FDA/EMA)
- Working knowledge of design software packages, e.g., SolidWorks an advantage.
Qualifications:
University degree in Engineering or related scientific discipline preferred, with 8-10 years related experience in medical device/combination product development.
- University degree in Engineering or related scientific discipline preferred. Prefer MS with 8+ years or BS with 10+ years'' experience.
- Experience managing cross-functional programs is highly desirable.
- Experience leading and coordinating human factor engineering studies
- Experience working in an outsourced environment and working with contract research, development, and manufacturing organizations is highly desirable.
- Excellent written and verbal communication skills.
- Must be comfortable with leading without authority, uncertainty, and change.
Preferred:
- Device development, combination product development, auto injector, prefilled syringe, needle safety device, on-body injector, on-body device, vial and syringe development
- Design history file, risk management (dfmea, ufmea, pfmea), design traceability matrix, design verification, design validation, process development
- Design verification testing, report writing. Developing test methods
- Design for assembly, design for manufacturability
- Design input requirements, user requirements
- Design output specification
- Experience in working with external device component companies, vendors, and CDMOs
If this job is a match for your background, we would be honoured to receive your application!
Providing consulting opportunities to TALENTed people since 1987, we offer a host of opportunities, including contract, contract to hire, and permanent placement. Let''s talk!
Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.
- Dice Id: talmn001
- Position Id: 26-04161
- Posted 7 days ago
Company Info
We pride ourselves in making sure that diversity in the workplace is at the forefront of our business. Our Founder, Dave Iacarella, is an Army Veteran who is committed to giving back to fellow Veterans. We are proud of our history of transitioning military Veterans into the workforce with companies that value their service. TALENT helps companies meet their veteran and diversity spend initiatives and requirements. We are committed to supporting veteran and diverse organizations.
Create job alert
Never miss an opportunity! Create an alert based on the job you applied for.Similar Jobs
It looks like there aren't any Similar Jobs for this job yet.
Search all similar jobs