Entry Level Quality Control Manager Jobs
New grad quality control manager jobs are open to recent graduates and entry level candidates with zero to two years of experience, where strong internship work or hands-on project experience can matter more than a long resume. Most openings are on-site roles across Manufacturing, Biotechnology & Pharmaceuticals, and Consulting & Professional Services, with employers like Sanmina, Cardinal Health, and RQ Construction hiring at this level now.
Find JobsOverview
Showing 5 of 235+ Entry Level Quality Control Manager jobs
As a QC Analytical Scientist, you will support various Quality Control activities within the AQC department. Key responsibilities are to transfer and execute analytical methods, including raw materials, for use in a cGMP environment in Quality control, both analytical quality control methods (AQC) and Quality Control Microbiology methods (QCM).
Responsibilities:
- Drive analytical method validation/ transfer of laboratory methodologies.
- Support the execution and issue resolution (e.g., discrepancies) and completion approval of test plans/protocols.
- Support troubleshooting of analytical methods.
- Ensure laboratory equipment is maintained in a validated state and that all analytical methods transferred follow company and regulatory requirements.
- Responsible for protocol and report generation and other technical documents as required. This may include supporting raw material qualification for new products.
- Use sound scientific principles and statistical techniques to solve problems and make recommendations.
- May Support the installation, operational qualification (IOQ), maintenance and troubleshooting of instrumentation in the AQC group.
- Responsible for deliverables to ensure timelines and milestones are met.
- Bachelor's degree in biotechnology, Microbiology, Pharmacy, Chemistry or equivalent.
- Minimum of 1 year of analytical development or validation experience in Pharmaceutical, Biopharmaceutical or related manufacturing environment, or an advanced degree.
- Strong technical writing skills and able to write generate technical documents and reports that meet company and regulatory requirements.
- Knowledge of analytical methods and operations with strong emphasis in problem-solving.
- Knowledge about analytical method validation.
- Intermediate statistical knowledge and experience with data analysis.
- Knowledge concerning cGMP, especially lab related topics such as method validation and unexpected results investigation.
- Basic knowledge about regulatory requirements concerning analytical instrumentation, and test methods.
- Substantial knowledge and understanding in terms of regulatory standards requirements e.g., CGMP, QSR, USP, 21CFR, ICH etc.
- Ability to complete tasks with minimal direction, demonstration of basic project management skills.
- Ability to multi task in a highly dynamic and diverse environment.
- Attention to detail, good organization, and time management skills to meet deadlines.
- Proficient in Microsoft Office.
- Strategically and business-oriented thinking.
- The overall physical exertion of this position requires light to medium work.
- Working Environment.
- Normal office and laboratory environment.
- May need to work in controlled or clean room environments requiring special gowning.
- May work around chemicals such as alcohol, acids, and buffers that may require respiratory protection.
- Able to work more than 8 hours a day or 40 hours a work week as needed.
- Nice to have the KNEAT Program, not required.
- Experienced in reviewing and approving Life Cycle Validation Documents including:
- Familiar with paperless validation software for life sciences.
- Commissioning, Installation, Operational and Performance Qualification protocols and reports for Equipment, Facilities & Utilities at Biopharmaceutical Manufacture plant.
- Computer System Validation protocols and reports, including SCADA, MES.
- QC/Micro Laboratory Instrument Qualification and method validation.
As a QC Analytical Scientist, you will support various Quality Control activities within the AQC department. Key responsibilities are to transfer and execute analytical methods, including raw materials, for use in a cGMP environment in Quality control, both analytical quality control methods (AQC) and Quality Control Microbiology methods (QCM).
Responsibilities:
- Drive analytical method validation/ transfer of laboratory methodologies.
- Support the execution and issue resolution (e.g., discrepancies) and completion approval of test plans/protocols.
- Support troubleshooting of analytical methods.
- Ensure laboratory equipment is maintained in a validated state and that all analytical methods transferred follow company and regulatory requirements.
- Responsible for protocol and report generation and other technical documents as required. This may include supporting raw material qualification for new products.
- Use sound scientific principles and statistical techniques to solve problems and make recommendations.
- May Support the installation, operational qualification (IOQ), maintenance and troubleshooting of instrumentation in the AQC group.
- Responsible for deliverables to ensure timelines and milestones are met.
- Bachelor's degree in biotechnology, Microbiology, Pharmacy, Chemistry or equivalent.
- Minimum of 1 year of analytical development or validation experience in Pharmaceutical, Biopharmaceutical or related manufacturing environment, or an advanced degree.
- Strong technical writing skills and able to write generate technical documents and reports that meet company and regulatory requirements.
- Knowledge of analytical methods and operations with strong emphasis in problem-solving.
- Knowledge about analytical method validation.
- Intermediate statistical knowledge and experience with data analysis.
- Knowledge concerning cGMP, especially lab related topics such as method validation and unexpected results investigation.
- Basic knowledge about regulatory requirements concerning analytical instrumentation, and test methods.
- Substantial knowledge and understanding in terms of regulatory standards requirements e.g., CGMP, QSR, USP, 21CFR, ICH etc.
- Ability to complete tasks with minimal direction, demonstration of basic project management skills.
- Ability to multi task in a highly dynamic and diverse environment.
- Attention to detail, good organization, and time management skills to meet deadlines.
- Proficient in Microsoft Office.
- Strategically and business-oriented thinking.
- The overall physical exertion of this position requires light to medium work.
- Working Environment.
- Normal office and laboratory environment.
- May need to work in controlled or clean room environments requiring special gowning.
- May work around chemicals such as alcohol, acids, and buffers that may require respiratory protection.
- Able to work more than 8 hours a day or 40 hours a work week as needed.
- Nice to have the KNEAT Program, not required.
- Experienced in reviewing and approving Life Cycle Validation Documents including:
- Familiar with paperless validation software for life sciences.
- Commissioning, Installation, Operational and Performance Qualification protocols and reports for Equipment, Facilities & Utilities at Biopharmaceutical Manufacture plant.
- Computer System Validation protocols and reports, including SCADA, MES.
- QC/Micro Laboratory Instrument Qualification and method validation.
See All 235+ Entry Level Quality Control Manager Jobs
Find roles that match your experience and apply in just a few clicks.
Find JobsEntry Level Quality Control Manager Job Market
Who's Hiring
- Sanmina7
- Cardinal Health6
- RQ Construction6
- Catalent Pharma Solutions6
- Oldcastle Infrastructure5
Top Industries Hiring
- Manufacturing35
- Biotechnology & Pharmaceuticals21
- Consulting & Professional Services18
- Construction & Real Estate17
- Medical Devices14
Entry Level Quality Control Manager Jobs: Frequently Asked Questions
How do I get an entry level quality control manager job?
Employers hiring at the entry level prioritize candidates who can demonstrate hands-on attention to detail, familiarity with inspection processes, and basic knowledge of quality standards like ISO or Six Sigma fundamentals. Internships, lab coursework, or any experience tracking defects or documenting processes gives you a real edge. Tailoring your resume to each posting and highlighting any relevant certifications, even entry-level ones, helps you stand out.
Which companies hire entry level quality control managers?
Companies hiring entry level quality control managers right now include Sanmina, Cardinal Health, and RQ Construction, based on current listings on Migrate Mate as of July 2026. Manufacturing firms, consumer goods companies, and food and beverage producers are among the most active employers at this level, as they maintain large QC operations that regularly bring on junior candidates.
Are there remote entry level quality control manager jobs?
Yes, though most quality control roles involve on-site inspection work. About 1% of entry level quality control manager openings are remote or hybrid as of July 2026, typically covering documentation, reporting, or supplier-facing coordination duties that can be done off-site. If remote flexibility matters to you, filter your search by work setting to see which current openings qualify.
Are these new grad quality control manager jobs?
Yes, many of the listings here are new grad and junior roles that explicitly welcome recent graduates with little or no professional experience. A new grad-friendly posting typically states zero to two years of experience required, accepts internship or academic project work as qualifying experience, or notes that a portfolio or relevant coursework will be considered. Look for language like "entry level," "training provided," or "new graduates encouraged to apply."
Which industries hire the most entry level quality control managers?
Entry Level quality control manager roles concentrate in Manufacturing, Biotechnology & Pharmaceuticals, and Consulting & Professional Services, based on current listings on Migrate Mate as of July 2026. These sectors drive the most entry level hiring because they run high-volume production or regulated processes that require dedicated QC oversight, creating consistent demand for junior candidates who can grow into broader quality management responsibilities.