Quality Assurance (QMS) Specialist

About Streck : Streck is a Nebraska-based manufacturing company that makes a global impact by developing and distributing to labs worldwide. Our products provide confidence for accurate health care testing! Our passions and priorities are focused on taking care of our customers, employees, and giving back to our community. Streck has jobs for every stage of your career. If you are a dependable, hard-working, and team-oriented individual who values meaningful work, Streck is looking for you to join our community of passionate people on a mission!

This position is responsible for quality activities performed within assigned department(s) and for helping ensure compliance with regulatory requirements and internal procedures. Working under general supervision, the Quality Assurance Specialist provides day-to-day quality support to designated departments and serves as a quality leader within their area of responsibility.

• Support investigation and documentation of observations, deviations, and Nonconforming Product/Material Reports, helping identify potential gaps in the quality system.
• Lead Root Cause Analysis (RCA) meetings as part of the Corrective and Preventive Action (CAPA) process, and assist with CAPA plan implementation and effectiveness checks.
• Support implementation of process changes arising from Change Control through training and direct observation.
• Deliver quality training to new hires and provide ongoing training as needed.
• Perform biannual audits of equipment in assigned areas.
• Maintain visibility into operations through routine direct observation, partnering closely with Operations staff on error prevention.
• Assist with writing and revising Standard Operating Procedures (SOPs).
• Collect and analyze quality data and metrics, and help communicate trends to management.
• Participate in continuous improvement initiatives and project validation teams.
• Support review and retention of Device History Records (DHRs).
• Depending on area of assignment, perform batch record and lot file reviews, in-process and final quality checks, packaging line clearance checks, and related inspections across Manufacturing, Fill/Label, Distribution, QC, QC Lab, and/or BCT Facility functions.

What We're Looking For

Education & Experience

• Associate degree required; Bachelor's degree in a STEM or related discipline preferred.
• 1-4 years of related work experience in an FDA-regulated manufacturing environment; relevant quality experience (2-3 years), preferably in an FDA or USDA industry, may substitute for technical education.

Skills & Attributes

• Strong PC skills, including proficiency with Microsoft Word and Excel.
• High attention to detail.
• Quality auditing certification preferred.
• Accountability, customer focus, professionalism, quality orientation, and a strong team focus.

Work Environment

This role is based in a climate-controlled biological/chemical laboratory, with occasional short-duration exposure to cold temperatures in walk-in coolers. The role requires the ability to wear required cleanroom and personal protective equipment for up to two and a half hours consecutively, and involves standing, walking, lifting up to 55 lbs occasionally, and other physical activity described in the full job description. Travel is estimated at up to 5%.

Streck Offerings

We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.