Pharmavise Corporation · 3 months ago
Supplier Quality Assurance Engineer II — Medical Device (Hybrid — Arden Hills, MN) Contract
Saint Paul, Minnesota, United States
Full-time, Contract
Hybrid
Entry, Mid Level
1+ years expPharmavise Corporation is a Fortune 500 Medical Device company seeking a Supplier Quality Assurance Engineer II. This role is essential for leading supplier performance improvement and collaborating with cross-functional teams to address component-related challenges throughout the supply chain.
Food and BeverageHealth Care
Responsibilities
Drives improvement and corrective actions in the quality of components sourced from outside suppliers
Assess & drive reactive as well as proactive supplier project(s)/investigations partnering with Supplier Engineering, Manufacturing/Test operations, Commercial Sourcing, Design Assurance, R&D
Develops solutions to a variety of complex problems of diverse scope and complexity where analysis of data requires evaluation of identifiable factors
Exercises authority and judgment within generally defined practices and policies in selecting methods and techniques for obtaining solutions
Has a broad knowledge of a variety of alternatives and their impact on the business unit
Plans and organizes non-routine tasks with approval
Initiates or maintains work schedule and priorities
Plans and organizes project assignments and maintains project schedules
Works under general direction regarding the direction and progress of projects and special assignments
Independently determines and develops approach to solutions
Interprets, executes and recommends modifications to company policies
Assists in establishing departmental policies and procedures
Work is reviewed upon completion for adequacy in meeting objectives
Establishes and cultivates a wide range of business relationships to facilitate completion of assignments
Interacts with suppliers
Participates in determining goals and objectives for projects
May lead projects within the function or department and/or represents a specialized field in larger project teams
Influences middle management on business solutions
Contributes to the completion of specific programs and projects
Failure to obtain results or erroneous decisions or recommendations would typically result in serious program delays and considerable expenditure of resources
In all actions, demonstrates a primary commitment to patient safety and product quality by maintaining compliance to the Quality Policy and all other documented quality processes and procedures
Assures that appropriate resources (personnel, tools, etc.) are maintained in order to assure Quality System compliance and adherence to the Quality Policy
Establishes and promotes a work environment that supports the Quality Policy and Quality Systems
Qualification
Required
BS degree in an Engineering related field, such as: Mechanical Engineering, Materials Engineering, Chemical Engineering, Electrical Engineering, or similar technical degree with 2-3 years related experience
Experience in Quality Management Systems, regulatory compliance, and risk management
Experience with problem solving quality tools, Corrective/Preventive Actions (CAPA), Technical Documentation
Preferred
Experience with or lead auditor certification to ISO13485, 9001, TS16949 standards
Ability to communicate cross functionally with suppliers, team members and leadership
Highly organized and detail-oriented with ability to manage multiple projects and prioritize effectively
Company
Pharmavise Corporation
♦𝐄𝐱𝐜𝐞𝐥𝐥𝐞𝐧𝐜𝐞 𝐭𝐡𝐫𝐨𝐮𝐠𝐡 𝐐𝐮𝐚𝐥𝐢𝐭𝐲♦: 𝐏𝐡𝐚𝐫𝐦𝐚𝐯𝐢𝐬𝐞, 𝐲𝐨𝐮𝐫 𝐬𝐭𝐫𝐚𝐭𝐞𝐠𝐢𝐜 𝐋𝐢𝐟𝐞 𝐒𝐜𝐢𝐞𝐧𝐜𝐞𝐬, 𝐇𝐞𝐚𝐥𝐭𝐡𝐜𝐚𝐫𝐞 𝐚𝐧𝐝 𝐆𝐨𝐯𝐞𝐫𝐧𝐦𝐞𝐧𝐭 𝐬𝐨𝐥𝐮𝐭𝐢𝐨𝐧𝐬 𝐩𝐚𝐫𝐭𝐧𝐞𝐫.
11-50 employees
Funding
Current Stage
Early StageTotal Funding
unknown2020-04-04Seed
Leadership Team
Ricardo Joseph
Founder and CEO
Company data provided by crunchbase