Entry Level Senior Quality Manager Jobs
New grad senior quality manager jobs welcome recent graduates and entry level candidates with zero to two years of experience, where a strong internship record or quality-focused portfolio can carry more weight than years on a resume. Most openings are on-site roles across Technology & Software, Medical Devices, and Distribution & Wholesale, with employers like Cardinal Health, OrganOx, and BD hiring at this level now.
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INTRODUCTION
QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and enthusiastic to join our team. In this role, you’ll work with a highly enthusiastic team, contributing in a world-class manufacturing industry in Puerto Rico & USA.
Responsibilities:
- Develops, modifies, applies and maintains quality standards and protocol for processing materials into partially finished or finished materials product.
- Collaborates with engineering and manufacturing functions to ensure quality standards are in place.
- Devises and implements methods and procedures for inspecting, testing and evaluating the precision and accuracy of products and production equipment.
- Designs or specifies inspection and testing mechanisms and equipment; conducts quality assurance tests; and performs statistical analysis to assess the cost of and determine the responsibility for products or materials that do not meet required standards and specifications.
- Ensures that corrective measures meet acceptable reliability standards and that documentation is compliant with requirements.
- May specialize in the areas of design, incoming material, production control, product evaluation and reliability, inventory control and/or research and development as they apply to product or process quality.
- Equipment & Process Validation
- Quality Systems & Change Control
- Regulatory Compliance & Manufacturing Change Management
QUALIFICATIONS
- Bachelor’s or Master’s degree in Mechanical, Industrial, Electrical Engineering, or related field preferred.
- Experience in FDA/ISO-regulated manufacturing environments, including GMP compliance, inspection readiness, ISO 13485, CAPA, nonconformance management, change control, document control, and risk management.
- Knowledge of validation and manufacturing processes, including equipment, process, product, and software validation (IQ/OQ/PQ), risk-based validation, and manufacturing controls.
- Proficiency in problem-solving, risk assessment, and data analysis tools, including FMEA, 5 Whys, Fishbone, SPC, DOE, capability analysis, trending, and process monitoring.
- Experience with quality and business systems (e.g., Minitab, JMP, Excel, Power BI, SAP) and strong communication, collaboration, continuous improvement, and critical-thinking skills; Lean Six Sigma certification and automation/programming experience are preferred.
- Availability for 1st shift and 2 shift
Quality Consulting Group, LLC is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, protected veteran status, disability status, or any other characteristic protected by law.
INTRODUCTION
QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and enthusiastic to join our team. In this role, you’ll work with a highly enthusiastic team, contributing in a world-class manufacturing industry in Puerto Rico & USA.
Responsibilities:
- Develops, modifies, applies and maintains quality standards and protocol for processing materials into partially finished or finished materials product.
- Collaborates with engineering and manufacturing functions to ensure quality standards are in place.
- Devises and implements methods and procedures for inspecting, testing and evaluating the precision and accuracy of products and production equipment.
- Designs or specifies inspection and testing mechanisms and equipment; conducts quality assurance tests; and performs statistical analysis to assess the cost of and determine the responsibility for products or materials that do not meet required standards and specifications.
- Ensures that corrective measures meet acceptable reliability standards and that documentation is compliant with requirements.
- May specialize in the areas of design, incoming material, production control, product evaluation and reliability, inventory control and/or research and development as they apply to product or process quality.
- Equipment & Process Validation
- Quality Systems & Change Control
- Regulatory Compliance & Manufacturing Change Management
QUALIFICATIONS
- Bachelor’s or Master’s degree in Mechanical, Industrial, Electrical Engineering, or related field preferred.
- Experience in FDA/ISO-regulated manufacturing environments, including GMP compliance, inspection readiness, ISO 13485, CAPA, nonconformance management, change control, document control, and risk management.
- Knowledge of validation and manufacturing processes, including equipment, process, product, and software validation (IQ/OQ/PQ), risk-based validation, and manufacturing controls.
- Proficiency in problem-solving, risk assessment, and data analysis tools, including FMEA, 5 Whys, Fishbone, SPC, DOE, capability analysis, trending, and process monitoring.
- Experience with quality and business systems (e.g., Minitab, JMP, Excel, Power BI, SAP) and strong communication, collaboration, continuous improvement, and critical-thinking skills; Lean Six Sigma certification and automation/programming experience are preferred.
- Availability for 1st shift and 2 shift
Quality Consulting Group, LLC is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, protected veteran status, disability status, or any other characteristic protected by law.
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Who's Hiring
Top Industries Hiring
- Technology & Software
- Medical Devices
- Distribution & Wholesale
- Consulting & Professional Services
- Media & Entertainment
Entry Level Senior Quality Manager Jobs: Frequently Asked Questions
How do I get an entry level senior quality manager job?
Focus on quality-related coursework, internships, or lab experience that shows you can identify defects, document processes, and support compliance audits. Certifications like CQI or an ASQ Certified Quality Improvement Associate credential signal commitment at the entry level. Tailor your resume to each posting, highlight any exposure to ISO standards or quality management systems, and apply to roles that explicitly welcome new graduates or candidates with limited experience.
Which companies hire entry level senior quality managers?
Companies hiring entry level senior quality managers right now include Cardinal Health, OrganOx, and BD, based on current listings on Migrate Mate as of August 2026. At this level, manufacturers, healthcare organizations, and government contractors tend to post the most openings, often pairing junior hires with experienced quality leads for on-the-job mentorship.
Are there remote entry level senior quality manager jobs?
Yes, though most entry level roles in this field are on-site given the hands-on nature of quality inspection and compliance work. About 15% of entry level senior quality manager openings are remote or hybrid as of August 2026, and those positions typically focus on documentation, auditing, or supplier quality functions that can be performed without a physical presence on the production floor.
Are these new grad senior quality manager jobs?
Yes. This page includes new grad, recent graduate, and junior roles alongside other entry level postings. A new grad-friendly listing typically welcomes zero to two years of experience, counts internships or co-ops toward the requirement, and accepts a strong academic project or quality-related portfolio in place of full-time work history. Look for postings that say 'new graduates encouraged to apply' or list internship experience as equivalent.
Which industries hire the most entry level senior quality managers?
Entry Level senior quality manager roles concentrate in Technology & Software, Medical Devices, and Distribution & Wholesale, based on current listings on Migrate Mate as of August 2026. Those sectors drive hiring at this level because they operate under strict regulatory or customer-quality requirements, creating a steady need for junior quality professionals who can support audits, corrective actions, and process documentation from day one.