Top 3 Senior qa Jobs in Lawrence, Ks

Quality Control Senior Scientist
Plastikon Healthcare —Lawrence, KS
- $90,000 - $105,000 a year
- Full-time
- 5 years
- Master's degree
- Bachelor's degree
- Health insurance
- Dental insurance
Quick Apply
12d
Senior QA Analyst
PSI Services LLC —Olathe, KS
- $115,000 a year
- Full-time
- Hybrid work
- 5 years
- Office
- Java
- Disability insurance
- Health insurance
Quick Apply
Sr. Specialist, Quality Control
Merck —De Soto, KS
- $106,200 - $167,200 a year
- Full-time
- Microsoft Word
- Bachelor's degree
- Travel
- Paid holidays
- Health insurance
12d

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Quality Control Senior Scientist

Plastikon Healthcare -
Lawrence, KS

Quick Apply

Job Details

Full-time
$90,000 - $105,000 a year
12 days ago

Benefits

Health insurance
Dental insurance
401(k)
Flexible spending account
Paid time off
Employee assistance program
Vision insurance
401(k) matching
Life insurance
Referral program
Retirement plan

Qualifications

Biology
Volumetric analysis
pH level monitoring
Teamwork
Empower (software)
Defect resolution root cause analysis
pH meters
pH sensors
High-performance liquid chromatographs
Microbiology testing
GMP
Bachelor's degree
Titration
Medical device manufacturing facility experience
Pharmaceutical analysis
Organizational skills
Biomedical regulatory compliance
Verification of laboratory test methods
Quality control experience within pharmaceutical industry
Microbiological analysis
Fourier-transform infrared (FTIR) spectroscopy
Quality audits
Chemical testing
Test validation method
Validation design
FDA regulations
Audit support
Data analysis software

Full Job Description

Job Overview

We are seeking a dynamic and detail-oriented Quality Control Senior Scientist to lead our quality assurance initiatives within a fast-paced manufacturing environment. The position leads analytical testing, method development, and investigation activities for raw materials, in-process samples, and finished products across medical devices and pharmaceutical manufacturing. This role serves as a technical resource and mentor within the QC laboratory, driving compliance with regulatory standards (FDA, ISO 13485, cGMP) and internal quality specifications, while leading complex investigations and continuous improvement initiatives.

Responsibilities

Lead and perform advanced chemical, physical, and microbiological testing per approved methods (Wet Chemistry, HPLC, FTIR, TOC, pH, conductivity, endotoxin, and bioburden)
Develop, qualify, and validate new and existing analytical test methods; author method validation/verification protocols and reports
Record all test data contemporaneously in laboratory notebooks, worksheets, or electronic data systems in accordance with ALCOA+ data integrity principles
Review and approve analytical data generated by QC Scientists for accuracy, completeness, and compliance prior to release
Lead OOS/OOT investigations and root cause analyses; author and drive CAPA activities to closure
Serve as a subject matter expert during internal and external audits (FDA, ISO, customer), including hosting and presenting to auditors
Author, review, and approve SOPs, test methods, method validations, and other QC documentation
Mentor and provide technical training to QC Scientists and laboratory staff
Oversee instrument qualification, calibration, and troubleshooting programs
Ensure compliance with cGMP, GLP, FDA 21 CFR Parts 210/211/820, and ISO 13485
Partner with Manufacturing, R&D, Regulatory, and Quality Assurance leadership to resolve complex quality issues and support product lifecycle initiatives
Contribute to risk assessments and continuous improvement projects within the QC laboratory

Requirements

Bachelor's degree in Chemistry, Biology, Microbiology, or related science required; Master's degree preferred
5+ years of QC laboratory experience in medical device, pharmaceutical, or related industry setting, including demonstrated method development/validation experience
Advanced proficiency in pH, conductivity, and TOC analysis
Strong competency in wet chemistry techniques including titrations
Demonstrated experience with HPLC, FTIR, and data acquisition software (e.g. Empower)
Working knowledge of FDA regulations, ISO 13485, and cGMP requirements
Proven track record leading investigations, method validations, and audit support
Strong documentation, investigation, and problem-solving skills
ASQ CQE or CQA certification preferred

Competencies & Attributes

Strong attention to detail and commitment to data accuracy and integrity
Demonstrated leadership and mentoring ability within a laboratory setting
Excellent organizational skills with the ability to manage multiple concurrent projects and priorities
Clear and professional written and verbal communication skills, including audit and cross-functional presentation experience
Ability to work independently, exercise sound scientific judgment, and lead cross-functional collaboration
Proactive, quality-first mindset with strong critical thinking and root-cause problem-solving skills

Join us to be part of a passionate team dedicated to excellence in manufacturing quality! We offer an engaging environment where your expertise will directly impact product safety and customer satisfaction while supporting your professional growth in a thriving industry.

#PKJOBS

Pay: $90,000.00 - $105,000.00 per year

Benefits:

401(k)
401(k) matching
Dental insurance
Employee assistance program
Flexible spending account
Health insurance
Life insurance
Paid time off
Referral program
Retirement plan
Vision insurance

Work Location: In person

Quick Apply

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senior qa jobs in lawrence, ks

Quality Control Senior Scientist

Senior QA Analyst

Sr. Specialist, Quality Control

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