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US_Process Engineer III

S San Francisco, CA 94080

Posted: 05/20/2024 Job Number: 72279

Job Description

Process Engineer 
Location: New Richmond, WI
Hourly rate: $35.00 - $61.00
Contractor benefits: Medical, Vision, Dental, 401k
Onsite 75% of the time in New Richmond, WI

•    The Process Engineer will be responsible for providing drug delivery device production innovation support to project teams industrializing combination drug delivery devices for parenteral pharmaceutical therapeutics at the company.
•    The candidate has in depth experience in high volume manufacturing processes and methodologies and process development to support clinical and commercial production activities within the company’s device development programs. This includes engaging both internal partners and external manufacturing partners and component suppliers.
•    The Process Engineer will be responsible for, and initiate, projects within engineering areas. Including defining critical steps and resources, and developing practical and thorough solutions to complex problems. The candidate will work with limited direction and may provide guidance to and coordinate work activities of other personnel. The work is reviewed with a focus on long-term perspectives, as the candidate establishes his/her own work priorities and timelines.

•    B.S advanced degree in Engineering, with preference for Mechanical Engineering, or the equivalent.
•    At least 3 years of experience in the industry and/or academia (including advanced studies) after receiving Bachelors’ degree.
•    In depth experience in high volume manufacturing processes and methodologies, with an emphasis in plastic molding and mechanical assembly is expected.
•    Demonstrated success in liaising with engineering and manufacturing resources.
•    Experience working with control systems to be used in production and batch release.
•    Strong expertise with statistical handling and interpretation of data, technical report writing and reviewing.
•    Familiarity with risk management tools; develop FMEAs of the products and ability to assess changes, non-compliances, etc., with risk assessment methods.
•    At least 3 years’ experience supporting process development from feasibility to New Product Introduction
•    Design Controls for regulatory compliance & filing (ISO 13485, etc.): GDP/GLP/GMP, Design History Files, User Requirement Specifications (URS), Factory/Site Acceptance Testing (FAT/SAT), test protocols, technical reports, control systems to be used in production and batch release and risk management tools (methods, FMEAs, non-compliances, etc.).
•    Assembly equipment, Functional Testers, Smart-scopes, Height gauges, Vision Systems.
•    Interaction with Equipment/Process: Plastic Heat stake, Plastic Laser welding, Laser Etching, Zebra Printers, Leak tests (pressure decay), flow test, Bbbble test, drop test, pull test, semi-automated and automated.
•    Full data and statistical analysis (JMP, Minitab) and Design of Experiments, and providing detailed review of data with an emphasis on statistics.
•    Strong skills in relevant modeling and design tools, design controls and/or statistical analysis. Examples may include: Monte Carlo Simulations, Tolerance Analysis, Finite Element Analysis.
•    Six Sigma (Green/Black Belt): DMAIC and DFSS
•    Design for Manufacturability, Molding.

•    Provide DFM/DFA assessment of container-device, and development of testing methods to assess container and deliver system quality and functionality for existing and new technologies.
•    Use of state-of-the-art technology to lead process development to enable clinical and commercial production in our worldwide network.
•    Extensive application of tools to assess design process capabilities such as tolerance analysis, design of experiments, design for reliability, quality by design, design for six sigma, failure modes effect analysis.
•    Characterize and evaluate critical process parameters (CPPs) using appropriate tools such as DOEs, components of variance, house of quality, etc., leveraging electromechanical presses and custom fixtures to run simulations in the lab.
•    Characterize material attributes (MAs) using appropriate tools such as tolerance analyses, empirical / mechanistic modeling with Monte Carlo simulation, etc.
•    Support or lead evaluations and investigations applying the most appropriate root cause analysis tools and methodologies.
•    Procure lab-scale clinical manufacturing equipment. Design, fabricate, and procure fixtures for device assembly and testing.
•    Author / review documentation related to clinical and commercial equipment qualification activities including pFMEAs, FAT, IOQ, and PQ. Author / review process validation protocol(s) and report(s).
•    Author / review SOPs for clinical/ commercial manufacturing (including labeling, packaging, preventative maintenance, and equipment operation).
•    Provide engineering technical leadership to internal cross functional team and external development partners and component suppliers.
•    Recommend assembly processes and techniques that provide the most cost effective, robust and reliable performance for medical devices.

•    Understand, implement, and maintain Roche Pharma Quality Policy and Pharma Quality System (PQS) in the department.
•    Developed Root Cause Analysis on manufacturing defects and collaborated in the completion of Engineering Change Request (ECR), Material Review Board (MRB), and Corrective and Preventive Action (CAPA).
•    Use (and create and implement, if necessary) local procedures and templates ensuring alignment with current versions of PQS documents and best practices.
•    Assist with resolving issues arising from internal quality assessments/audits, regulatory inspections and notified body interactions, and aid in driving closure of inspection issues by preparing appropriate responses and corrective action resolutions.
•    Create and review discrepancy, change and risk management documents for PTDU-D and Devices Teams, as appropriate.
•    Ensure compliance of training to PQS and job-related requirements.

•    Responsible for transfer of design to commercialization.
•    Ensure product quality and design requirements are traced through the equipment development, process development and validation process.
•    Draft, review and/or approve design control documents (i.e. DHF documents) to support device development deliverables using available templates, such as protocols and reports, failure modes effects and analysis, risk management plans, change management plans and design review meeting minutes.
•    Employ good document practices (GDP) when recording data, maintaining archives and drafting and reviewing documents.
•    Participate in hazards analysis and design assessments and reviews.
•    Utilize electronic document archive system and collaborate with Document Control team to ensure document compliance with PQS standards and DHF regulations.
•    Interfaces and Collaboration.
•    Regularly interface with leaders in Contract Manufacturing, Procurement, Quality, Complaints and Regulatory Affairs.
•    Regularly interact at a detailed technical level with design engineers, equipment and production engineers.
•    Support supplier selection through assessment of supplier capabilities for existing equipment and custom automation development, acceptance and installation.
•    Collaborate with internal / external teams to translate design requirements into clinical and commercial processes.

Must be U.S. Person for purposes of Export Compliance.

EEO Statement Apollo Professional Solutions, Inc. is an equal opportunity employer. We provide equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, marital status, age, national origin, ancestry, disability status, medical condition, pregnancy, genetic information, protected veteran status, gender, sexual orientation, gender identity or expression, or any other status or characteristic protected under federal, state, or local law.

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