Entry Level Quality Control Specialist Jobs
New grad quality control specialist jobs are open to recent graduates and entry level candidates with zero to two years of experience, where internship work or hands-on lab exposure can matter more than a long resume. Most openings are on-site roles across Distribution & Wholesale, Medical Devices, and Biotechnology & Pharmaceuticals, with employers like Cardinal Health, Freenome, and Mirus Consulting hiring at this level now.
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mîrus Consulting Group is a local company based in Humacao, Puerto Rico that provides computer system validation and information technology consulting services to pharmaceutical companies and other organizations across the Island and parts of the United States. Its services include the assessment and validation of automation equipment, network infrastructures and business processes, as well as the project management involved.
Position Summary
The Specialist Quality Control is responsible for providing scientific and technical expertise to support microbiology laboratory operations, validation activities, and quality systems compliance. This role leads microbiological method validation and technical documentation efforts for new product introductions, investigates quality events, designs specialized studies, and serves as a key technical resource for microbiology-related testing and regulatory compliance activities in a GMP-regulated environment.
Key Responsibilities
- Prepare, review, and approve technical writing reports associated with microbiological method validations and new product introductions.
- Serve as a technical subject matter expert for microbiological testing activities and laboratory investigations.
- Provide scientific and technical support to the Microbiology Laboratory to ensure compliance with GMP requirements.
- Design, execute, and document special studies to support product, process, laboratory, and quality investigations.
- Perform scientific evaluations of microbiological data and trends to support product quality decisions.
- Support deviation owners by evaluating events, performing technical assessments, identifying root causes, and determining appropriate corrective and preventive actions (CAPAs).
- Collaborate with cross-functional teams including Quality Assurance, Manufacturing, Validation, Regulatory Affairs, and Technical Services to support operational objectives.
- Review and interpret microbiological testing results to ensure compliance with established specifications and regulatory requirements.
Technical Knowledge & Skills
- Technical writing and report generation for Microbiology Method Validations.
- Knowledge of:
- Bioburden Testing
- Bacterial Endotoxin Testing (BET)
- Low Endotoxin Recovery (LER)
- Sterility Testing
- Method Suitability / Method Validation in Microbiology (MMV)
- Mycoplasma Testing
- Experience with deviation investigations, root cause analysis, and CAPA development.
- Knowledge of GMP, GDP, and microbiological laboratory practices.
- Strong problem-solving, analytical, and technical writing skills.
- Ability to communicate effectively with cross-functional teams and management.
- Experience supporting regulatory inspections and compliance initiatives is highly desirable.
Education
- Doctorate degree in a Scientific discipline; OR
- Master’s degree with 2 years of directly related experience; OR
- Bachelor’s degree with 4 years of directly related experience.
This Company is an equal employment opportunity employer. We adhere to a policy of making employment decisions without regard to race, color, religion, sex, sexual orientation, national origin, citizenship, age or disability. We assure you that your opportunity for employment with this Company depends solely on your qualifications.
mîrus Consulting Group is a local company based in Humacao, Puerto Rico that provides computer system validation and information technology consulting services to pharmaceutical companies and other organizations across the Island and parts of the United States. Its services include the assessment and validation of automation equipment, network infrastructures and business processes, as well as the project management involved.
Position Summary
The Specialist Quality Control is responsible for providing scientific and technical expertise to support microbiology laboratory operations, validation activities, and quality systems compliance. This role leads microbiological method validation and technical documentation efforts for new product introductions, investigates quality events, designs specialized studies, and serves as a key technical resource for microbiology-related testing and regulatory compliance activities in a GMP-regulated environment.
Key Responsibilities
- Prepare, review, and approve technical writing reports associated with microbiological method validations and new product introductions.
- Serve as a technical subject matter expert for microbiological testing activities and laboratory investigations.
- Provide scientific and technical support to the Microbiology Laboratory to ensure compliance with GMP requirements.
- Design, execute, and document special studies to support product, process, laboratory, and quality investigations.
- Perform scientific evaluations of microbiological data and trends to support product quality decisions.
- Support deviation owners by evaluating events, performing technical assessments, identifying root causes, and determining appropriate corrective and preventive actions (CAPAs).
- Collaborate with cross-functional teams including Quality Assurance, Manufacturing, Validation, Regulatory Affairs, and Technical Services to support operational objectives.
- Review and interpret microbiological testing results to ensure compliance with established specifications and regulatory requirements.
Technical Knowledge & Skills
- Technical writing and report generation for Microbiology Method Validations.
- Knowledge of:
- Bioburden Testing
- Bacterial Endotoxin Testing (BET)
- Low Endotoxin Recovery (LER)
- Sterility Testing
- Method Suitability / Method Validation in Microbiology (MMV)
- Mycoplasma Testing
- Experience with deviation investigations, root cause analysis, and CAPA development.
- Knowledge of GMP, GDP, and microbiological laboratory practices.
- Strong problem-solving, analytical, and technical writing skills.
- Ability to communicate effectively with cross-functional teams and management.
- Experience supporting regulatory inspections and compliance initiatives is highly desirable.
Education
- Doctorate degree in a Scientific discipline; OR
- Master’s degree with 2 years of directly related experience; OR
- Bachelor’s degree with 4 years of directly related experience.
This Company is an equal employment opportunity employer. We adhere to a policy of making employment decisions without regard to race, color, religion, sex, sexual orientation, national origin, citizenship, age or disability. We assure you that your opportunity for employment with this Company depends solely on your qualifications.
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Who's Hiring
Top Industries Hiring
- Distribution & Wholesale
- Medical Devices
- Biotechnology & Pharmaceuticals
- Consulting & Professional Services
- Delivery & Couriers
Entry Level Quality Control Specialist Jobs: Frequently Asked Questions
How do I get an entry level quality control specialist job?
Employers at this level look for candidates who understand inspection methods, documentation standards, and quality management basics, whether from coursework, internships, or hands-on lab work. A degree in a relevant field such as manufacturing technology, chemistry, or engineering helps, but so does any experience with ISO standards or quality tools. Tailoring your resume to highlight attention to detail and process accuracy gives you a clear edge.
Which companies hire entry level quality control specialists?
Companies hiring entry level quality control specialists right now include Cardinal Health, Freenome, and Mirus Consulting, based on current listings on Migrate Mate as of November 2026. Manufacturers, food and beverage producers, pharmaceutical companies, and defense contractors tend to hire consistently at this level as they need strong entry level pipelines to support inspection and compliance teams.
Are there remote entry level quality control specialist jobs?
Yes, though most quality control roles are on-site given the hands-on nature of the work. About 0% of entry level quality control specialist openings are remote or hybrid as of November 2026, and these tend to be in documentation review, data analysis, or supplier audit support rather than direct product inspection.
Are these new grad quality control specialist jobs?
Yes, these listings include new grad, recent graduate, and junior quality control specialist roles. A posting is typically new grad friendly when it welcomes zero to two years of experience, counts internships or co-ops toward the requirement, or accepts a relevant portfolio of academic or project work in place of full-time history. Look for language like 'entry level,' 'new graduates welcome,' or 'training provided.'
Which industries hire the most entry level quality control specialists?
Entry Level quality control specialist roles concentrate in Distribution & Wholesale, Medical Devices, and Biotechnology & Pharmaceuticals, based on current listings on Migrate Mate as of November 2026. These sectors drive consistent hiring at the entry level because their production volumes, regulatory requirements, and compliance obligations create ongoing demand for inspection and quality assurance support.