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Biotech Quality Control Jobs in Kansas (NOW HIRING)

Bachelor's degree in Biology, Microbiology, Chemistry, Animal Science, Biotechnology, or equivalent experience; * 10+ years' of progressive experience/roles within quality control in USDA-regulated ...

QA Technician

Lenexa, KS · On-site

$20 - $23/hr

The job opportunity is for one of our clients specializing in biotechnology product development ... Communicate effectively and coordinate tasks with Manufacturing and Quality Control to facilitate ...

... Change Control, and Deviation activities. * Ensure compliance with cGMP, quality standards, and ... Bachelor's Degree in Engineering, Biotechnology, Chemical Engineering, Mechanical Engineering, or ...

$16 - $19.50/hr

... and biotech industries encompassing approximately 70 manufacturing locations, 20 Application ... They will also provide quality control and quality assurance with proper samples and product ...

... biotech start-ups to established pharmaceutical companies. Our products, services and solutions ... Serve as the final quality control checkpoint, ensuring alignment across text, tables, figures, and ...

... biotech start-ups to established pharmaceutical companies. Our products, services and solutions ... Serve as the final quality control checkpoint, ensuring alignment across text, tables, figures, and ...

... biotech start-ups to established pharmaceutical companies. Our products, services and solutions ... Serve as the final quality control checkpoint, ensuring alignment across text, tables, figures, and ...

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Biotech Quality Control information

See Kansas salary details

$27.2K

$72.5K

$115.5K

How much do biotech quality control jobs pay per year?

As of Aug 4, 2026, the average yearly pay for biotech quality control in Kansas is $72,528.00, according to ZipRecruiter salary data. Most workers in this role earn between $54,000.00 and $89,200.00 per year, depending on experience, location, and employer.

What does a biotech quality control do?

On a daily basis, a Biotech Quality Control professional performs routine testing and analysis of raw materials, intermediates, and finished products to ensure they meet established specifications. This involves preparing samples, operating analytical equipment, maintaining accurate records, and documenting results in compliance with regulatory guidelines. Quality Control staff also collaborate closely with production, quality assurance, and research teams to troubleshoot issues and support process improvements. Regular internal audits and participation in team meetings are common, making communication and teamwork key parts of the job.

What is a biotech quality control?

A Biotech Quality Control (QC) job involves ensuring that biological products, processes, and facilities meet regulatory and quality standards. QC professionals conduct testing, analyze data, and document results to verify product safety and efficacy. They work with laboratory techniques such as PCR, HPLC, and microbiological testing. The role is critical in maintaining compliance with industry regulations like GMP and FDA guidelines.

What are the key skills and qualifications needed to thrive in biotech quality control?

To excel in Biotech Quality Control, candidates typically need a background in biology, chemistry, or related sciences, with strong knowledge of laboratory techniques and regulatory requirements. Familiarity with laboratory information management systems (LIMS), Good Manufacturing Practices (GMP), and common analytical instruments such as HPLC or PCR is highly valued. Attention to detail, problem-solving abilities, and effective communication are crucial soft skills for this role. These competencies are vital for ensuring that biotech products consistently meet quality and compliance standards essential for patient safety and regulatory approval.

What are popular job titles related to Biotech Quality Control jobs in Kansas? For Biotech Quality Control jobs in Kansas, the most frequently searched job titles are:
What job categories do people searching Biotech Quality Control jobs in Kansas look for? The top searched job categories for Biotech Quality Control jobs in Kansas are:
Infographic showing various Biotech Quality Control job openings in Kansas as of July 2026, with employment types broken down into 89% Full Time, 3% Part Time, 1% Temporary, and 7% Contract. Highlights an 81% Physical, 3% Hybrid, and 16% Remote job distribution, with an average salary of $72,528 per year, or $34.9 per hour.

Sr. Specialist, Quality Control

MSD

De Soto, KS • On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 19 days ago


Job description

Job Description

Join Us in Shaping the Future of Animal Health

Our Animal Health Division is investing $895 million in expanding our manufacturing and research & development facilities in De Soto, Kansas - the state's largest economic development project to date. As a Sr. Specialist, Quality Control you will be part of a world-class team at our Center of Excellence in the Animal Health Corridor, contributing directly to the production of veterinary products that improve animal health and welfare globally. This role combines project leadership/coordination and quality oversight to ensure successful QC laboratory method transfers. The Quality Control Sr. Specialist will ensure laboratory processes and systems are in place to meet Quality Control testing activities associated with the method transfers. The successful candidate will collaborate with crossfunctional teams (Analytical Tech Support, Manufacturing, Validation, Quality Control) to identify gaps and risks, implement appropriate controls, and drive continuous improvement to support the project.

Key Responsibilities

  • Serve as the Project lead for the QC laboratory transfers.
  • Serve as the liaison to the project sponsors, keeping them informed of the status of all project activities and resources
  • Represent the team at project/tier meetings
  • Evaluate site-to-site process/methods
  • Resolve any Project Issues in an effective manner
  • Ensure teams are formed to support the project, and monitor timelines to ensure that each phase is completed on schedule, preventing delays.
  • Coordinate site level activities related to the method transfers.
  • Ensure that deliverables meet quality standards before moving to the next phase
  • Review/approve required test method information (spec sheets, tests, biomaterials/reagents, release criteria).
  • Review/approve protocols and reports associated with the project
  • Support completion of Transfer Complexity assessment.
  • Author the Quality Risk Management Plan, and support gap assessments.
  • Coordinate Change Control plans and review/approve related Change Records.
  • Ensure readiness for sample management (sampling plans - transport and handling)
  • Support Regulatory Affairs with Outline of Production/Special Outline updates

Job Requirements

  • Bachelor's degree in Biology, Microbiology, Chemistry, Animal Science, Biotechnology, or equivalent experience;
  • 10+ years' of progressive experience/roles within quality control in USDA-regulated animal product facilities
  • Experience with USDA regulations and inspection processes in manufacturing environments
  • Relevant practical experience with QC laboratory environments, method transfer, or related quality roles in biologics, vaccines, or similar industries
  • Experience with qualification of facilities, equipment, instruments, and/or utilities.
  • Knowledge of Good Manufacturing Practices (GMP), quality systems, and regulatory expectations.
  • Strong attention to detail, excellent documentation practices, and ability to maintain audit-ready records.
  • Effective communication and interpersonal skills; ability to collaborate with cross-functional teams and external vendors.
  • Proficient with MS Office (Word, Excel, PowerPoint); experience with SAP and electronic quality management systems (Reliance, Veeva) preferred.

Preferred Qualifications

  • Experience leading or supporting method transfers and performing go-sees.
  • Strong project coordination skills and ability to work with cross-functional teams.
  • Experience with implementation of LIMS
  • Excellent written and verbal communication skills.

Physical and Work Environment

  • Primarily office-based with occasional travel between sites.
  • Ability to travel for site visits/go-sees as required.

Required Skills:

Adaptability, Good Manufacturing Practices (GMP), Laboratory Information Management System (LIMS), Laboratory Operations, Manufacturing, Manufacturing Environments, Project Coordination, Quality Control (QC), Quality Control Management, Quality Standards, Technical Transfer, Testing, USDA Regulations

Preferred Skills:

Laboratory Quality Control, Quality Management, Quality Management Systems (QMS)

Current Employees apply HERE

Current Contingent Workers apply HERE

US and Puerto Rico Residents Only:

Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Please click here if you need an accommodation during the application or hiring process.

As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics.As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities. For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit:

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We are proud to be a company that embraces the value of bringing together, talented, and committed people with diverse experiences, perspectives, skills and backgrounds. The fastest way to breakthrough innovation is when people with diverse ideas, broad experiences, backgrounds, and skills come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another's thinking and approach problems collectively.

Learn more about your rights, including under California, Colorado and other US State Acts

The salary range for this role is

$106,200.00 - $167,200.00

This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An employee's position within the salary range will be based on several factors including, but not limited to relevant education, qualifications, certifications, experience, skills, geographic location, government requirements, and business or organizational needs.

The successful candidate will be eligible for annual bonus and long-term incentive, if applicable.

We offer a comprehensive package of benefits. Available benefits include medical, dental, vision healthcare and other insurance benefits (for employee and family), retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days. More information about benefits is available at https://jobs.merck.com/us/en/compensation-and-benefits.

You can apply for this role through https://jobs.merck.com/us/en (or via the Workday Jobs Hub if you are a current employee). The application deadline for this position is stated on this posting.

San Francisco Residents Only:We will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance

Los Angeles Residents Only:We will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance

Search Firm Representatives Please Read Carefully
Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.

Employee Status:

Regular

Relocation:

No relocation

VISA Sponsorship:

No

Travel Requirements:

25%

Flexible Work Arrangements:

Remote

Shift:

1st - Day

Valid Driving License:

Yes

Hazardous Material(s):

N/A

Job Posting End Date:

07/31/2026

*A job posting is effective until 11:59:59PM on the day BEFOREthe listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.