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Quality Assurance In Pharmaceutical Jobs in Kansas

QA Technician

Lenexa, KS · On-site

$20 - $23/hr

Preferred Requirements * 1+ years of experience in QA, QC, or manufacturing within a regulated environment such as medical device, pharmaceutical, or food manufacturing. * Background in Medical ...

In this role, the Quality Assurance Manager will monitor performance, analyze quality trends, implement corrective actions, and leverage standardized quality tools and processes to enhance service ...

Providing positive, professional ongoing training to production employees in regards to customer specifications * Interact with QA Manager and Production Management for analysis projects * Ensure ...

Providing positive, professional ongoing training to production employees in regards to customer specifications * Interact with QA Manager and Production Management for analysis projects * Ensure ...

QA Inspectors are required to lift and move raw material samples and boxed products ... Team member in overall management of the facility. Expect to work on tests and pilot runs of new ...

QA Inspectors are required to lift and move raw material samples and boxed products ... Team member in overall management of the facility. Expect to work on tests and pilot runs of new ...

QA Inspectors are required to lift and move raw material samples and boxed products ... Team member in overall management of the facility. Expect to work on tests and pilot runs of new ...

QA Inspectors are required to lift and move raw material samples and boxed products ... Team member in overall management of the facility. Expect to work on tests and pilot runs of new ...

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Quality Assurance In Pharmaceutical information

What does a quality assurance professional do in the pharmaceutical industry?

A Quality Assurance (QA) professional in the pharmaceutical industry is responsible for ensuring that all products meet established standards of quality, safety, and efficacy. They develop, maintain, and monitor procedures and systems that comply with regulatory requirements such as Good Manufacturing Practices (GMP). QA professionals conduct audits, review documentation, manage deviations, and support continuous improvement to ensure that medications are safe for patients. Their work is critical in preventing errors, ensuring product consistency, and maintaining the trust of regulatory agencies and consumers.

What are the key skills and qualifications needed to thrive as a quality assurance professional in the pharmaceutical industry?

A successful Quality Assurance professional in pharmaceuticals needs a solid background in life sciences or pharmacy, understanding of GMP regulations, and relevant QA experience. Familiarity with quality management systems (QMS), documentation software, and regulatory compliance tools is typically required. Attention to detail, critical thinking, and effective communication are essential soft skills for excelling in this role. These skills ensure product safety, regulatory compliance, and the consistent delivery of high-quality pharmaceutical products.

What are some common challenges faced by quality assurance professionals in the pharmaceutical industry, and how can they be effectively managed?

Quality Assurance (QA) professionals in the pharmaceutical industry often face challenges such as keeping up with evolving regulatory requirements, ensuring consistent documentation, and coordinating cross-functional teams during audits. Managing these challenges requires continuous training, strong attention to detail, and effective communication skills. Collaboration with other departments, such as production and regulatory affairs, is key to identifying issues early and maintaining compliance with Good Manufacturing Practices (GMP). Establishing clear quality procedures and staying proactive with process improvements also help QA professionals maintain high standards and reduce risks.

What is the difference between Quality Assurance In Pharmaceutical vs Quality Control In Pharmaceutical?

AspectQuality Assurance In PharmaceuticalQuality Control In Pharmaceutical
FocusProcesses, compliance, and preventing defectsTesting and inspecting products for defects
ResponsibilitiesDeveloping quality systems, audits, documentationSampling, testing, and analyzing products
CredentialsGMP certifications, quality management trainingLab certifications, analytical testing skills
Work EnvironmentOffice-based, quality departments, manufacturing sitesLaboratories, manufacturing facilities

Quality Assurance In Pharmaceutical focuses on establishing and maintaining quality systems to prevent issues, while Quality Control In Pharmaceutical emphasizes testing products to identify defects. Both roles are essential in ensuring pharmaceutical safety and compliance, but they differ in scope and daily tasks.

Is quality assurance a good career in the pharmaceutical industry?

Quality assurance in the pharmaceutical industry is a stable and growing career, focusing on ensuring products meet safety and regulatory standards. It often requires knowledge of Good Manufacturing Practices (GMP), quality control processes, and relevant certifications. The role offers opportunities for advancement and specialization within the industry.

What does quality assurance do in the pharmaceutical industry?

Quality assurance professionals in the pharmaceutical industry ensure that products meet safety, quality, and regulatory standards throughout the manufacturing process. They develop and implement procedures, conduct audits, and review documentation to prevent defects and ensure compliance with Good Manufacturing Practices (GMP).

What are popular job titles related to Quality Assurance In Pharmaceutical jobs in Kansas?

For Quality Assurance In Pharmaceutical jobs in Kansas, the most frequently searched job titles are:

What job categories do people searching Quality Assurance In Pharmaceutical jobs in Kansas look for?

The top searched job categories for Quality Assurance In Pharmaceutical jobs in Kansas are:

Infographic showing various Quality Assurance In Pharmaceutical job openings in Kansas as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 14% Part Time, 1% Temporary, 4% Contract, and 1% Nights. Highlights an 86% Physical, 2% Hybrid, and 12% Remote job distribution.

Manager, Quality Assurance

Altasciences

Overland Park, KS • On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 9 days ago


Altasciences rating

7.6

Company rating: 7.6 out of 10

Based on 17 frontline employees who took The Breakroom Quiz

59th of 120 rated laboratories


Job description

Your New Company!
At Altasciences we all move in unison to assist and work in the discovery, development, and manufacturing of new drug therapies to get them faster to people who need them. No matter your role, we all play an important part and you will have a significant impact on the health and well-being of people across the globe. By living our values of Employee Development, Customer Focus, Quality and Excellence, Respect and Integrity, we look to foster a passionate and collaborative work environment and we are looking for talented and enthusiastic people, like you, to join our growing team! Whether you're a recent college graduate or seeking your next career opportunity, it's time to discover your future at Altasciences.
We are better together and together We Are Altasciences.
About The Role
The Manager, Quality Assurance is responsible for leading QA staff, resources, and assigned QA activities to ensure effective quality oversight, timely execution, and compliance with applicable internal procedures and external regulatory requirements. The role supports a risk-based quality approach by integrating quality data, audit outcomes, inspection findings, compliance trends, and operational input to guide QA priorities and continuous improvement. The Manager, Quality Assurance also supports inspection readiness, quality issue escalation, staff development, and the effective execution of QA programs within the assigned site, function, or business area.
You'll Do Here
  • Lead and manage QA staff, workload, and priorities to ensure effective execution of QA activities.
  • Provide coaching, performance feedback, and development support to team members.
  • Support hiring, onboarding, training, and ongoing staff development.
  • Promote accountability, consistent QA standards, and professional conduct within the team.
  • Oversee QA programs, including audits, inspections, documentation review, and quality system activities.
  • Ensure QA activities are conducted in compliance with procedures, regulatory requirements, and timelines.
  • Support audit planning and execution using a risk-based approach.
  • Ensure appropriate follow-up and oversight of audit and inspection findings.
  • Apply risk-based approaches to QA planning, prioritization, and issue escalation.
  • Integrate quality data, audit results, inspection outcomes, and trends to identify risks.
  • Monitor quality indicators and escalate significant or recurring issues.
  • Oversee or support quality system activities such as deviations, investigations, root cause analysis, and CAPAs.
  • Ensure quality issues are properly documented, assessed, and resolved.
  • Support quality initiatives and continuous improvement activities.
  • Recommend improvements to processes, procedures, and QA practices.
  • Support preparation, coordination, and follow-up of sponsor audits and regulatory inspections.
  • Participate in inspections as a QA representative, as applicable.
  • Review audit and inspection responses to ensure accuracy and compliance.
  • Maintain effective relationships with internal stakeholders and external partners.
  • Ensure QA activities comply with SOPs, policies, and applicable GxP requirements.
  • Maintain awareness of relevant regulatory requirements and industry trends.
  • Support development and maintenance of SOPs and controlled documents.
  • Monitor and report QA metrics, risks, and performance indicators.
  • Provide updates to QA leadership on key issues and initiatives.
  • Communicate effectively with internal teams and external stakeholders.
  • Support escalation of quality issues as needed.

What You'll Need to Succeed
  • Bachelor degree or higher, in Chemistry, Biochemistry, Biology
  • Minimum of 5 of related experience
  • At least 2 years (of the 5) related supervisory experience
  • MS Word, Excel, Outlook and Power Point
  • Ability to read and interpret technical documents and industry specific manuals.
  • Ability to write advanced reports and correspondence.
  • Ability to speak effectively before groups of customers or employees of the organization
  • Experience in the pharmaceutical industry.
  • Knowledge and understanding of the applicable Canadian, US, European, and ICH pharmaceutical
  • regulations and guidelines, for phase I research studies (i.e., GCP, GLP, and GMP).
  • Detail oriented.
  • Project management and coordination skills.
  • Ability to meet tight deadlines.
  • Tactful, reliable, persuasive, dependable, consistent, flexible.
  • Excellent verbal and written communication skills.
  • Well developed interpersonal skills are required.
  • Personal/professional integrity and proven discretion in handling confidential information.
  • Ability to develop strong trusting relationships in order to gain support and achieve results.
  • Capable of managing multiple conflicting priorities.
  • Must be self-directed, motivated, and have a willingness to take the initiative to identify and anticipate client needs and make recommendations for implementation.
  • Relevant industry experience a plus.

What We Offer
Altasciences offers a wide variety of benefits to help our employees live healthy and fulfilling lives both at and outside of work.
Altasciences' Benefits Package Includes:
  • Health/Dental/Vision Insurance Plans
  • 401(k)/RRSP with Employer Match
  • Paid Vacation and Holidays
  • Paid Sick and Bereavement Leave
  • Employee Assistance & Telehealth Programs

Altasciences' Incentive Programs Include:
  • Training & Development Programs
  • Employee Referral Bonus Program

#LI-AN1
MOVING IN UNISON TO DELIVER A BIG IMPACT WITH A PERSONAL TOUCH
Altasciences is an equal opportunity employer committed to diversity and inclusion. Our goal is to attract, develop and retain highly talented employees from diverse backgrounds, allowing us to benefit from a wide variety of experiences and perspectives. All qualified applicants will receive consideration for employment without regard to age, race, color, religion, creed, sex, sexual orientation, gender identity, national origin, disability or any other protected grounds under applicable legislation. Reasonable accommodations for persons with disabilities during the recruitment process are available upon request. Join us at Altasciences!

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