Quality Control Specialist, Biochemistry
Quick Summary
Lead Lab Operations: Direct the regular workload for Technicians and other Specialists,
Serve as a Subject Matter Expert (SME) for specialized laboratory equipment, coordinating routine maintenance schedules and ensuring compliance.
Requirements
~2 min read- Education: Bachelor’s Degree in Biochemistry, Biological Sciences, Pharmaceutical Sciences, or a closely related field.
- Experience: 4+ years of relevant experience in a laboratory or quality environment.
- Top Skills: Strong verbal, written, and interpersonal communication skills; proficient computer literacy; and the ability to work with and lead a diverse group of colleagues. Must possess a “quality mindset” with a deep understanding of quality expectations and compliance.
- Advanced degree (M.S. or Ph.D.) in Biology, Chemistry, or an associated science with 2+ years of experience.
- Hands-on experience with HPLC and ELISA techniques.
- Proficiency using Empower and/or Softmax software platforms.
- Direct experience in analytical laboratory operations and leadership or training roles.
- Strong attention to detail and a proven track record of acting as a leader of change.
We offer a comprehensive benefits package focusing on financial, physical, and mental well-being while encouraging our employees to pursue our purpose! Some highlights include:
- Multiple relocation packages
- 8-week parental leave
- 9 Employee Resource Groups
- Annual bonus offering
- Flexible work arrangements
- Up to 6% 401K matching
#LI-HL
#LI-Onsite
Elanco is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status
Elanco may use automated tools, including AI, to support parts of our recruitment process, such as reviewing applications against job‑related criteria and/or transferrable skills. These tools help ensure a consistent, structured evaluation, but they do not make hiring decisions. All decisions involve a human reviewer. For more information on how we handle personal data, please see our Elanco Workforce Privacy Notice.
The QC Specialist is responsible for the daily operations and technical leadership of the Quality Control laboratory. This role serves as a subject matter expert for analytical methods and equipment, owning critical processes including method validation, investigations, and the direction of daily workloads for QC Technicians. The Specialist ensures strict adherence to quality policies while driving continuous improvement and collaborating with leadership to optimize laboratory processes.
Responsibilities
~1 min read- →Lead Lab Operations: Direct the regular workload for Technicians and other Specialists, ensuring QC policies are followed and acting as the primary point of contact for technical instruction or clarification.
- →Method Ownership: Perform regular release testing and lead specialized development experiments, including participating in or owning method validations and technical transfers.
- →Quality Event Management: Regularly lead and own quality events, including deviations, laboratory investigations, and change controls.
- →Technical Review & Audit: Act as a reviewer for QC Technicians and other Specialists; audit inventory management and ensure reagent/material qualifications are maintained.
- →SME Leadership: Serve as a Subject Matter Expert (SME) for specialized laboratory equipment, coordinating routine maintenance schedules and ensuring compliance.
- →Continuous Improvement: Partner with the QC Leader to identify and improve obsolete processes, anticipating potential problems and finding effective solutions to improve lab systems.
- →Compliance & Audit Readiness: Participate in audit activities and proactively prepare the laboratory space for inspections by anticipating potential issues.
- →Safety & Culture: Personify Elanco values of Integrity, Respect, and Excellence while fostering an environment of safety, compliance, and inclusion.
- Location: Elwood, Kansas
- Shift: Primarily day shift; however, the ability to occasionally support manufacturing timelines outside of normal operating hours is required.
- Travel: Minimal travel requirements.
Location & Eligibility
Listing Details
- Posted
- September 10, 2026
- First seen
- September 29, 2026
- Last seen
- September 29, 2026
Posting Health
- Days active
- 0
- Repost count
- 0
- Trust Level
- 23%
- Scored at
- September 29, 2026
Signal breakdown
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