Quality Control Scientist

Infotree Global Solutions; Chaska (MN); Presencial; USD 61 992 - 68 880; Tempo parcial

Resumo da oferta

A leading medical equipment manufacturer is seeking a Quality Assurance Scientist to ensure product quality and regulatory compliance in their Chaska operations. The ideal candidate should possess a science or engineering degree with significant experience in quality assurance within regulated industries. Responsibilities include overseeing manufacturing processes, collaborating with technical teams, and driving continuous improvement initiatives. This contract position emphasizes a mid-senior level of experience and offers a competitive pay rate of $45.00/hr - $50.00/hr.

Qualificações

• Minimum of 5 years of relevant experience with a Bachelor's degree.
• Minimum of 3 years of relevant experience with a Master's degree.
• Proven experience in regulated industries.

Responsabilidades

• Provide Quality Assurance oversight and support for manufacturing processes.
• Ensure adherence to design change procedures and corporate policies.
• Collaborate with teams to address non-conforming products.
• Evaluate quality system performance and lead improvement events.

Conhecimentos

Quality Assurance oversight

Regulatory compliance

Cross-functional collaboration

Quality system performance metrics

Formação académica

Bachelor's degree in science or engineering

Master's degree in science or engineering

Doctoral degree in a relevant field

Descrição da oferta de emprego

Job Title

Quality Assurance Scientist

Contract Duration

05 months

Base Pay Range

$45.00/hr - $50.00/hr

Job Description

We are seeking a highly skilled and experienced Quality Assurance Senior Scientist to join our team as an on‑site contractor. This critical role is dedicated to upholding product quality and ensuring regulatory compliance within our Reagent Manufacturing operations.

Key Responsibilities

• Provide comprehensive Quality Assurance oversight and support for Reagent manufacturing processes, including SOP approvals, equipment record approvals, nonconformances, out‑of‑specification events, etc.
• Ensure rigorous adherence to design change procedures, corporate policies, and global regulations (e.g., FDA QSR, ISO), proactively offering guidance and making informed decisions to prevent deviations and non‑conformances.
• Collaborate effectively with cross‑functional teams to swiftly identify, contain, and disposition non‑conforming product.
• Interact proficiently with development, technical operations, and manufacturing personnel to sustain high quality standards, minimize rework and waste, and optimize product satisfaction.
• Establish and drive daily management actions for quality processes, ensuring alignment with broader departmental and organizational initiatives.
• Evaluate quality system performance metrics and lead continuous improvement events to enhance process efficiency and overall effectiveness.

Qualifications

• Bachelor's degree in a science or engineering discipline with a minimum of 5 years of relevant experience.
• Master's degree in a science or engineering discipline with a minimum of 3 years of relevant experience.
• Doctoral degree in a relevant field.
• Proven experience performing Quality Assurance functions within a regulated industry.

Seniority Level

Mid‑Senior level

Employment Type

Contract

Job Function

Quality Assurance, Research, and Analyst

Industries

Medical Equipment Manufacturing, Biotechnology Research, and Manufacturing

Location

Minneapolis, MN