Occupation
Quality Control Analyst
A Quality Control Analyst monitors and evaluates products or processes against established quality control processes, using statistical process control and root cause analysis to identify defects and drive corrective action. Common in manufacturing, pharmaceuticals, and food production, they ensure operations align with ISO standards and often apply Six Sigma methodologies to improve consistency. This role suits a detail-oriented, analytical professional working within a quality assurance department.
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Open Quality Control Analyst roles (5)
Analyst I, Research Grade QC mRNA
Beckman Coulter
Full-time · Fargo, ND
This is an entry-level quality control role performing testing and validation work on mRNA products in a research manufacturing environment. The role suits someone with a science degree and basic lab skills who wants hands-on experience in biotech quality assurance.
Listed on Beckman Coulter’s careers site · Apply there ↗
Sr Associate I, Quality Control Microbiology
Biogen
Full-time · Research Triangle Park, NC · $81,000 – $105,000
Quality control microbiology role at a pharmaceutical manufacturing facility responsible for testing drug substances, raw materials, and environmental samples using established assays and procedures. Suits experienced microbiologists who thrive in regulated environments and enjoy mentoring others while maintaining strict data integrity standards.
Listed on Biogen’s careers site · Apply there ↗
Analyst, Quality Control, Chemistry & Stability
Moderna
Full-time
This role involves performing GMP quality control testing for mRNA vaccine manufacturing, including analytical chemistry methods like HPLC and particle analysis to support Chemistry, Release, and Stability functions. It suits someone with analytical chemistry experience who thrives in a regulated, detail-oriented environment and wants to contribute to pandemic preparedness through hands-on lab work.
Listed on Moderna’s careers site · Apply there ↗
Data Reviewer, Quality Control Microbiology
Bristol Myers Squibb
Full-time · Indianapolis, IN · $31 – $38 / hour
This role reviews microbiological quality control data at a radiopharmaceutical manufacturing facility, ensuring compliance with cGMP and regulatory standards. It suits someone with laboratory microbiology experience who can work independently to validate testing results and support a manufacturing environment handling ionizing radiation.
Listed on Bristol Myers Squibb’s careers site · Apply there ↗
Quality Control Analyst I, Research Grade
Beckman Coulter
Full-time · Fargo, ND
This role performs quality control testing and documentation for research-grade biopharmaceutical manufacturing at Aldevron, supporting product development and operations. It suits someone with a scientific background looking to start or progress a laboratory career in the biotech sector.
Listed on Beckman Coulter’s careers site · Apply there ↗
Likely next role (3)
Where Quality Control Analysts commonly go next: Quality Control Systems Manager, Validation Engineer.
Lead Validation Engineer
Bristol Myers Squibb
Full-time · Indianapolis, IN · $124,449 – $150,803
This role leads validation and commissioning activities for a radiopharmaceutical manufacturing facility, ensuring GMP compliance as the operation transitions from construction to clinical and commercial production. It suits someone with deep manufacturing validation expertise who can independently manage complex programs while guiding a technical team through regulatory requirements and process improvements.
Listed on Bristol Myers Squibb’s careers site · Apply there ↗
HSIO Validation Lead – Silicon Co-Design
NVIDIA
Santa Clara, CA · $168,000 – $310,500
This role leads silicon validation for NVIDIA's high-speed interfaces like PCIe and NVLink, debugging across the full stack from protocol behavior through firmware and hardware to resolve critical failures before production. The position suits engineers who combine deep protocol expertise with hands-on lab skills and the judgment to navigate complex system-level problems under schedule pressure.
Listed on NVIDIA’s careers site · Apply there ↗
Senior Validation Engineer
Bristol Myers Squibb
Full-time · Indianapolis, IN · $107,904 – $130,754
This role leads validation and commissioning efforts for a new radiopharmaceutical manufacturing facility, supporting the transition from construction through clinical and commercial operations. It suits experienced validation engineers who can independently manage complex GMP projects while mentoring others in a specialized biotech environment.
Listed on Bristol Myers Squibb’s careers site · Apply there ↗
Roles similar to Quality Control Analyst (157)
From Chemical Technician, Clinical Quality Manager, Data Quality Analyst, Document Control Manager, Document Control Specialist, Food and Agricultural Technologist, Laboratory Analyst, Laboratory Technician, Manufacturing Engineer, QA Manager, Quality Assurance Associate, Quality Technician.
Document Control Manager
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Listed on DriveTime’s careers site · Apply there ↗
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Listed on Oreck Corporation’s careers site · Apply there ↗
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Listed on Voyager’s careers site · Apply there ↗
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Listed on FLIR Systems’s careers site · Apply there ↗
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Listed on Stanley Black & Decker’s careers site · Apply there ↗
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Listed on Rockwell Automation’s careers site · Apply there ↗
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Listed on Vermeer Corporation’s careers site · Apply there ↗
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Listed on Schreiber Foods’s careers site · Apply there ↗
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Listed on Mercury Marine’s careers site · Apply there ↗
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Listed on Marlin Firearms’s careers site · Apply there ↗
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