Quality Assurance Lab Specialist

Filtration Group; Louisville (CO); On-site; USD 60,000 - 65,000; Full time

Benefits offered by this job

Family leave

Health and wellness benefits

Health insurance

Paid Parental Leave

401k with Company Matching

Job summary

Molecular Products, Inc. is seeking a Quality Assurance Lab Specialist in the Louisville/Denver area to perform QA tests, manage toxic gases, and operate GC equipment while ensuring compliance with FDA, GMP, and ISO standards in a laboratory setting.

The role requires a science degree, QA lab experience, and strong analytical skills. Proficiency in MS Office, safety awareness, and clear communication are essential. Benefits include health insurance, 401k with company matching, and parental leave.

Qualifications

• Bachelor’s degree in science, chemistry, bio-chemistry, chemical engineering, related or equiv. QA laboratory experience.
• Strong analytical and problem-solving skills.
• Safety oriented.
• Knowledge of ISO 9001 and/or ISO 13485 Quality Management System Requirements
• MS Office - Beginner to intermediate knowledge in Word, Excel and Access
• Excellent written and verbal communication skills

Responsibilities

• Performs quality control tests following procedures including adsorbent performance using challenge gases, toxic gases.
• Tracks and handles toxic gases in compliance with local laws and regulations, including the shipping and receiving of items.
• Operate GC’s and associated equipment for the physical properties (moisture content, particle size distribution, apparent density)
• Must be comfortable performing statistical data analysis, maintaining test control charts
• Follows process workflow and safety guidelines and protocols.
• Ability to complete basic preventive maintenance, equipment cleaning, work space cleaning, equipment calibration as required
• Ability to create lab scale sample generation.
• Ensure compliance with company policies and business practices including FDA Regulations, GMP, and ISO Medical Device Quality System Requirements.
• Investigate and troubleshoot product or production issues
• Develop corrective actions, solutions and improvements when necessary.
• Comfortable working in a lab environment.
• Computer skills are a must as well as detail oriented.
• Final Product Release – review final product data for conformance to requirements.
• Incoming Inspection – sample and inspect incoming material for conformance to requirements
• Manage Non-conforming material and deviations for assigned products.
• Reports on product performance trends proactively.
• Other duties as assigned

Skills

Analytical skills

Problem solving

Safety oriented

Written & verbal communication

Education

Bachelor’s degree in science/chemistry/biochemistry/chemical engineering

Tools

MS Office (Word, Excel, Access)

Job description

Overview

Molecular Products, Inc. (now part of Parker Hannifin), a global market-leading provider of filtration consumables that drives innovation and delivers solutions across a broad spectrum of applications and end-markets, with a focus on life sciences, indoor air quality and industrial technologies.

Molecular Products, Inc is looking for a Quality Assurance Lab Specialist Ibased in Louisville/Denver area who is a U.S. Person.

Responsibilities

• Performs quality control tests following procedures including adsorbent performance using challenge gases, toxic gases.
• Tracks and handles toxic gases in compliance with local laws and regulations, including the shipping and receiving of items.
• Operate GC’s and associated equipment for the physical properties (moisture content, particle size distribution, apparent density)
• Must be comfortable performing statistical data analysis, maintaining test control charts
• Follows process workflow and safety guidelines and protocols.
• Ability to complete basic preventive maintenance, equipment cleaning, work space cleaning, equipment calibration as required
• Ability to create lab scale sample generation.
• Ensure compliance with company policies and business practices including FDA (Food & Drug Administration) Regulations, GMP (Drug and Device Manufacturing Practices), and ISO (International Organization for Standardization) Medical Device Quality System Requirements.
• Investigate and troubleshoot product or production issues
• Develop corrective actions, solutions and improvements when necessary.
• Comfortable working in a lab environment.
• Computer skills are a must as well as detail oriented.
• Final Product Release – review final product data for conformance to requirements.
• Incoming Inspection – sample and inspect incoming material for conformance to requirements
• Manage Non-conforming material and deviations for assigned products.
• Reports on product performance trends proactively.
• Other duties as assigned

Benefits and Pay:

• Salary $60,000 - $65,000
• Family leave
• Health and wellness benefits
• Health insurance
• Paid Parental Leave
• 401k with Company Matching

Qualifications

Required:

• Bachelor’s degree in science, chemistry, bio-chemistry, chemical engineering, related or equiv. QA laboratory experience.
• Strong analytical and problem-solving skills.
• Safety oriented.
• Knowledge of ISO 9001 and/or ISO 13485 Quality Management System Requirements
• MS Office - Beginner to intermediate knowledge in Word, Excel and Access
• Excellent written and verbal communication skills

Desired:

• Familiar with standard analytical techniques

More about Us

Molecular Products, Inc. is now part of Parker Hannifin. We're a global market-leading provider of filtration consumables that are designed to drive innovation and deliver solutions across a broad spectrum of applications and end-markets, with a focus on life sciences, indoor air quality and industrial technologies. With a global workforce of nearly 65,000 dedicated team members and a footprint that spans 43countries, we are committed to partnering closely with our customers to further our mission.Cultivating Talent and building strong Teams are critical to our success. We know that fulfilling our mission is only possible when we foster an entrepreneurial culture built on a foundation of trust, in which our leaders exhibit a strong bias for action. Join us as we build a truly remarkable company that will long outlast us!

__

This is a general description of the Duties, Responsibilities and Qualifications required for this position. Physical, mental, sensory, or environmental demands may be referenced to communicate the way this position traditionally is performed. Whenever necessary to provide individuals with disabilities an equal employment opportunity, we will consider reasonable accommodations that might involve varying job requirements and/or changing the way this job is performed, provided that such accommodations do not pose an undue hardship.

We arecommitted to creating an inclusive work environment for all team members, regardless of race, gender, religion, sexual orientation, age, disability, genetics, veteran status, marital status, or any other characteristic protected by law. We believe the work we do and the mission we spread is at it’s best when everyone feels free to be their most authentic self.