Quality Assurance Specialist

Overview

Hennessy Research Associates - a Kemin Company is hiring a Quality Assurance Specialist.

We’re looking for a QA specialist or a professional with regulatory experience in animal vaccine manufacturing who thrives in a hands-on, team‑oriented environment. If you enjoy working collaboratively to ensure high‑quality outcomes, this role could be a great fit

As a Quality Assurance Specialist at HRA - Kemin, you’ll be a true partner in the field, working side‑by‑side with a well‑aligned team spanning manufacturing, QC, and regulatory functions to keep operations moving with precision and momentum. You’ll take the lead on batch record review, material release, and customer investigations, while also overseeing equipment intake, managing calibration schedules, and coordinating with external vendors. Skilled in equipment validations and overall equipment management, you’ll play a key role in keeping our systems audit‑ready and performing at their best.

This position is based on-site at our Lenexa, Kansas location.

Join the Kemin Team and Transform Lives!

We are a privately held, family-owned-and-operated global biotechnology company driven by curiosity and committed to transforming the quality of life for people, pets, and the planet.

We create solutions that strengthen health and wellbeing, provide nutrition and immune support for pets and production animals, safeguard the planet’s natural resources, and protect the global food supply chain for generations to come.

We supply over 500 specialty ingredients for various industries, including human and animal health and nutrition, pet food, aquaculture, nutraceutical, food technologies, crop technologies, textiles, biofuels, and animal vaccines.

We employ 3,500 global employees and operations in 90 countries, including manufacturing facilities in Belgium, Brazil, China, Egypt, India, Italy, San Marino, Singapore, South Africa, and the United States.

As a valued member of our team, you'll enjoy a comprehensive benefits package designed to support your financial, physical, and professional well-being:

• Competitive Financial Package: Enjoy a rewarding salary, uncapped bonus opportunities, a 401k match program, and generous paid vacation and holidays.
• Career Development and Advancement: Unlock your potential with opportunities for growth and development throughout your entire career.
• Continued Learning Opportunities: Grow your skills with our in-house learning platforms, offering thousands of training resources both live and online, and take advantage of tuition reimbursement for external post-secondary pursuits.
• Service Opportunities: Make a positive impact with paid time off for volunteering in your community
  

Responsibilities

• Independently determine the disposition of finished products, raw materials and
  packaging.
• Review batch records and laboratory analysis results for accuracy and completeness.
• Independently create and review certificates of analysis.
• Perform lot tracing.
• Lead internal audit(s) and report findings, with minimal supervision.
• Lead monthly GMP audits, report findings, and issue corrections, with minimal supervision.
• Assist with Corrective Action/Preventive Action (CAPA) investigations and follow up regarding customer complaints, deviations, and non-conformities.
• Support external audit(s) of service and raw material suppliers, as needed.
• Support audits with regulatory agencies and certifying bodies, as needed.
• Support the document control system and training database
• Create, update and follow Standard Operating Procedures (SOPs), policies and forms.
• Maintain proper quality documentation.
• Support Change Management tasks.
• Prepare communication for customers, with minimal supervision.
• Provide input for customer questionnaires, with minimal supervision.
• Review and request supplier documents, as needed.
• Create and distribute reports, as needed.
• Must work closely with cross functional teams (including Operations, Quality Control, R&D, Regulatory, and other groups).

Qualifications

• Education and Experience:Associates Degree with 5 years of related experience, or Bachelor’s Degree with 3+ years of related experience.
• Previous manufacturing, warehouse, inventory, inspection, internal and external auditing,
  GMP, or other related experience preferred

• Skilled in equipment validations and overall equipment management

• Must have and maintain an insurable driving record.
• Must be able to work independently and as a team.
• Must have a solid understanding and adherence to the Servant Leadership philosophy.
• Must be a self-starter.
• Must be able to use computer systems, MS Office, M3, LIMs, etc.
• Must have attention to detail.
• Strong written and oral communication skills.
• Familiarity with SPC principles and practices.
• Previous experience in manufacturing and quality control (QC) within human or animal vaccine industry
• Familiarity with Standard Operating Procedures (SOPs) and process validation
• Exposure to diagnostic testing is a plus
• Background in vaccine production (human or animal) is highly beneficial

We are an equal opportunity employer. We consider all qualified applicants without regard to race, color, creed/religion, national origin, ancestry, citizenship or immigration status (where applicable), sex, sexual orientation, gender identity or expression, pregnancy/childbirth/breastfeeding or related conditions, age (40+), disability (including the use of a service animal), genetic information, marital status, familial or caregiver status, military or veteran status, status as a victim of domestic violence, reproductive health decision‑making, and any other status protected by applicable federal, state, or local law. We also prohibit retaliation for raising concerns or participating in an EEO process. Applicants who need a reasonable accommodation to apply or interview can email