Mativ

QC Laboratory Chemist

Mativ Dallas, TX

Pay found in job post

Retrieved from the description.

Base pay range

$100,000.00/yr - $135,000.00/yr
Description

Position Title: QC Laboratory Chemist - Healthcare Products

location: Dallas, Texas

JOB DESCRIPTION: (quick summary of the role)

Our QC Laboratory Chemist supports Mativ’s Healthcare division. This individual will be responsible for the day-to-day running of the Biomed Quality Laboratory, routine sampling and testing raw materials, intermediates, finished products to ensure compliance with regulatory, internal and customer standards and specifications. You will also be responsible for cleaning and storing tools and equipment; documenting and keeping test records and implementing Good Laboratory practices.

Quality Control Chemist Duties And Responsibilities

  • Conduct routine and non-routine analysis of water and raw materials, in-process samples, and finished products using analytical techniques such as HPLC, GC, FTIR, UV-Vis, and wet chemistry methods as applicable.
  • Provide technical expertise to the business with respect to material analysis.
  • Review internal and 3rd party analytical, microbiological and physiochemical test reports and update test methods, Lab SOPs and Work Instructions as necessary.
  • Document and report analytical and other laboratory findings accurately and promptly, maintaining detailed records in compliance with regulatory guidelines.
  • Support validation efforts with testing as necessary.
  • Document investigate and communicate out-of-specification (OOS) results, NCR and Deviations, identifying root causes and implementing corrective actions as necessary.
  • Participate in regulatory and internal audits/inspections, providing technical expertise as an SME and support to ensure adherence to cGMP and company policies.
  • Collaborate with cross-functional teams including Quality Assurance, Research & Development, and Manufacturing to support product release, stability testing and complaint investigation activities.
  • Stay current with industry trends and regulatory requirements, contributing to continuous improvement initiatives within the Quality Control department.
  • Take ownership of the Quality Lab including HSE, Access restriction and lab equipment Calibration.
  • Perform verification activities to ensure the accuracy and reliability of lab equipment.
  • Perform raw material re-certifications and order lab supplies as necessary.
  • Support compounding/Production by providing in-process testing and preparing Buffers and other chemical solutions as needed.
  • Ensure that bulk and RM retains are stored and easily retrievable.
  • Organize work schedule to complete assigned tasks efficiently, on schedule and right first time.
  • Prepare test solutions, volumetric solutions, and samples used in analysis.
  • Other duties as assigned by management as needed.
  • Support Stability activities by drafting and executing stability protocols and compiling the final reports.
  • Prepare lab reports and perform laboratory data trends analyses.
  • Any other duties as maybe assigned by your direct Supervisor.

qualifications: (Required Education & Skill sets:)

  • Bachelor’s degree in chemistry, Pharmaceutical Science, related field or higher from an accredited institution.
  • Detailed knowledge of quality management systems, current Good Manufacturing Practices, expertise with QC principles and compliance requirements.
  • 5-8 years of relevant laboratory experience, with 4-5 years of QC specific experience.
  • Working knowledge of statistics along with advanced software expertise, such as JMP or LIMS, is optimal.
  • Demonstrated ability to lead technical teams.
  • Demonstrate strong oral and written communication skills.
  • Experienced in leading technical lab investigations.
  • Familiar with USP, Global compendia and ICH guidelines.
  • Understanding of GMP/GLP.
  • At least 3 years Testing experience within the pharmaceutical or related industry.
  • Occasional may be required to lift up to 30 pounds.

What We Offer

As a Mativ employee, you’ll have access to a variety of benefit programs designed to help you no matter

your stage of life.

Medical, dental and vision insurance

Consumer-Driven Health Plan (CDHP)

Preferred Provider Organization (PPO)

Exclusive Provider Organization (EPO)

Company-paid Basic Life Insurance And Additional Voluntary Life Coverage

Paid vacation and competitive personal time off

401(k) savings plan with company match

Employee assistance programs – available 24/7 to you and your family

Wellness and Work Life Support - career development and educational assistance

This posting will close within 90 days of the date posted. We encourage you to apply now!

About Mativ

Mativ Holdings, Inc. is a global leader in specialty materials headquartered in Alpharetta, Georgia. The

company makes material impacts on the world every day through a wide range of critical components

and engineered solutions that solve our customers’ most complex challenges. We manufacture on three

continents and generate sales in nearly 100 countries through our family of business-to-business and

consumer product brands. The company’s two segments, Filtration & Advanced Materials and

Sustainable & Adhesive Solutions, target premium applications across diversified and growing end-

markets, from filtration to healthcare to sustainable packaging and more. Our broad portfolio of

technologies combines polymers, fibers, and resins to optimize the performance of our customers’

products across multiple stages of the value chain. Our leading positions are a testament to our best-in-

class global manufacturing, supply chain, and materials science capabilities. We drive innovation and

enhance performance, finding potential in the impossible.

Mativ and its subsidiaries are Equal Opportunity Employers. Qualified applicants will be considered

without regard to their race, color, religion, sex, sexual orientation, gender identity, national origin,

disability, or status as a protected veteran.
  • Seniority level

    Mid-Senior level
  • Employment type

    Full-time
  • Job function

    Quality Assurance
  • Industries

    Manufacturing

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