quality control analyst

Agilent Technologies

<div><h2 class="jobSectionHeader">Job Description</h2>
The world's most revolutionary biopharma companies are partnering with Agilent Technologies to advance the next frontier of medicine. Agilent continues to invest in capacity and expansion of its Colorado operations. Join our team of professionals dedicated to the development and commercialization of nucleic acid therapeutics for life changing, lifesaving medicines.
The Quality Control Analyst will conduct routine and non-routine analysis and review to support release, stability testing per Standard Operating Procedures (SOP) and Analytical Methods in accordance with current Good Manufacturing Practices (cGMPs) and regulatory requirements. Has a clear understanding of Good Laboratory Practices (GLPs), cGMPS, and other regulatory requirements.
Effectively engages in continuous improvement of processes and procedures. Proven ability to exercise judgment and appropriately escalate issues to QC management.
Essential duties and responsibilities:<ul><li>
Excellent communication skills, both written and oral</li><li>
Conducts analysis associated with clinical and commercial under current Good Manufacturing Practices (GMP) regulations and guidance per Food and Drug Administration (FDA) and Organization for Economic Co-Operations and Development (OECD) as well as International regulations</li><li>
Performs analysis on APIs (developmental and commercial), final product, and other requested testing as per written procedures</li><li>
Reviews data for compliance to specifications and reports and troubleshoots abnormalities</li><li>
Ensures equipment is performing well and communicates and takes appropriate action as necessary</li><li>
Required to follow good documentation practices</li><li>
Exercises judgment within broadly defined practices and policies in selecting methods, techniques and evaluation criteria for obtaining results</li></ul><h2 class="jobSectionHeader">
Qualifications</h2>
Required:<ul><li>
Bachelor&rsquo;s of Science Degree</li><li>
Relevant lab experience</li></ul>
Desired:<ul><li>
One year experience in Analytical Chemistry or related life sciences field
</li><li>Knowledge of cGMP guidelines</li><li>
Experience with stability testing, HPLC, UV Vis, pH testing, and other analytical testing</li><li>
Knowledge of international regulations (i.e., International Committee on Harmonization (ICH) Q7)</li><li>
Experience with computer software and hardware applications, including Microsoft Word and Excel</li></ul>
Additional Details
This job has a full time weekly schedule. Applications for this job will be accepted until at least March 19, 2026 or until the job is no longer posted.
The full-time equivalent pay range for this position is $27.15 - $42.43/hr plus eligibility for bonus, stock and benefits. Our pay ranges are determined by role, level, and location. Within the range, individual pay is determined by work location and additional factors, including job-related skills, experience, and relevant education or training. During the hiring process, a recruiter can share more about the specific pay range for a preferred location. Pay and benefit information by country are available at: https://careers.agilent.com/locations
Agilent Technologies, Inc. is an Equal Employment Opportunity and merit-based employer that values individuals of all backgrounds at all levels. All individuals, regardless of personal characteristics, are encouraged to apply. All qualified applicants will receive consideration for employment without regard to sex, pregnancy, race, religion or religious creed, color, gender, gender identity, gender expression, national origin, ancestry, physical or mental disability, medical condition, genetic information, marital status, registered domestic partner status, age, sexual orientation, military or veteran status, protected veteran status, or any other basis protected by federal, state, local law, ordinance, or regulation and will not be discriminated against on these bases. Agilent Technologies, Inc., is committed to creating and maintaining an inclusive in the workplace where everyone is welcome, and strives to support candidates with disabilities. If you have a disability and need assistance with any part of the application or interview process or have questions about workplace accessibility, please email job_posting@agilent.com or contact +1-262-754-5030. For more information about equal employment opportunity protections, please visit www.agilent.com/en/accessibility.<h2 class="jobSectionHeader">
Travel Required:
</h2>No<h2 class="jobSectionHeader">
Shift:
</h2>Day<h2 class="jobSectionHeader">
Duration:
</h2>No End Date<h2 class="jobSectionHeader">
Job Function:
</h2>Quality/Regulatory</div>

Quality Control Analyst

Vyriad, Inc.

COMPANY OVERVIEWVyriad is an early stage biotechnology company focused on curing cancer using potent, safe and cost-effective cancer therapies utilizing engineered replication competent viruses designed to selectively and rapidly destroy cancer. Revolutionizing cancer treatment is our long-term goal, requiring curiosity, perseverance, an openness to challenging convention and a commitment to excellence. The challenges are complex, the work pace is fast, and progress is seldom a straight line. All of this makes for an exhilarating environment of collaboration, discovery and fun.GENERAL JOB DESCRIPTION:Responsible for performing routine analytical testing of various sample types, including raw materials, intermediates, and drug substance/products to ensure compliance with GMP and regulatory standards. This analyst position is ideal for an individual transitioning into Quality Control with a baseline understanding of biologic therapeutics and cGMP. The QC Analyst I will execute established analytical methods, maintain accurate records, and uphold the highest standards of laboratory safety and data integrity. Experience in cell-based assays and/or PCR-based analyses is preferred.SUPERVISORY RESPONSIBILITIES:NoDUTIES AND RESPONSIBILITIES:<ul><li>Perform and maintain test systems for GMP manufacturing, and performing assays related to in-production and post-production product quality. Assays in the areas of molecular, biochemical, or cell-based systems.</li><li>Involved in reagent management, routine maintenance of laboratory equipment, and performing robust sample tracking/management.</li><li>Document all testing activities accurately in accordance with cGMP and Good Documentation Practices (GDP).</li><li>Support validation status of release assays, and product stability</li><li>Participate in laboratory housekeeping, calibration, and quality initiatives.</li><li>Work under direct supervision while learning QC systems, methods, and compliance expectations.</li><li>Additional duties as assigned.</li></ul>EDUCATION AND EXPERIENCE REQUIREMENTS<ul><li>Bachelor&rsquo;s degree in a science related field.</li><li>Minimum of 1 year in an industry or a professional setting incorporating GDP.</li></ul>REQUIRED SKILLS AND/OR QUALIFICATIONS:<ul><li>Familiarity with aseptic technique, basic molecular biology, or analytical methods preferred.</li><li>Familiarity with ALCOA+ Principles of GDP, with familiarity of cGMP preferred</li><li>Should be detail-oriented and have the ability to work independently and productively under general direction, routinely exercise initiative and sound judgment to contribute to team objectives.</li><li>Must have demonstrated capacity to comprehend complex protocols and reports, and programs</li><li>Must be flexible in adapting to a variety of responsibilities, work assignments, and priorities.</li></ul>PHYSICAL REQUIREMENTS:<ul><li>Prolonged periods of standing at laboratory benches.</li><li>Prolonged periods of sitting at a desk and working on a computer.</li><li>Must be able to lift up to 15 pounds at times</li></ul>WORK SCHEDULE:<ul><li>Weekends or weeknight work is occasionally required depending on the production schedule or process needs.</li></ul>BENEFITS:<ul><li>Group Healthcare Plan, including company paid dental and vision.</li><li>Short- and long-term disability, life and AD&amp;G insurance.</li><li>Simple IRA with employer match</li><li>Educational assistance program</li><li>Holiday and PTO</li></ul>Job Type: Full-timePay: $52,000.00 - $67,000.00 per yearBenefits:<ul><li>401(k) matching</li><li>Dental insurance</li><li>Employee assistance program</li><li>Flexible schedule</li><li>Flexible spending account</li><li>Health insurance</li><li>Health savings account</li><li>Life insurance</li><li>Paid time off</li><li>Parental leave</li><li>Retirement plan</li><li>Tuition reimbursement</li><li>Vision insurance</li></ul>Education:<ul><li>Bachelor's (Required)</li></ul>Experience:<ul><li>Good Documentation Practices (GDP): 1 year (Required)</li><li>Quality control: 1 year (Required)</li></ul>Ability to Relocate:<ul><li>Rochester, MN 55901: Relocate before starting work (Required)</li></ul>Work Location: In person

Quality Control Analyst I

<div><h2 class="jobSectionHeader">Job Description</h2>
To protect the health and safety of our employees, contractors, customers and communities, employees in the U.S. and Puerto Rico are required to be fully vaccinated against COVID-19, unless an approved exemption has been granted for a medical reason, sincerely held religious belief, or an employee is otherwise exempt under applicable law.
Agilent inspires and supports discoveries that advance the quality of life. We provide life science, diagnostic and applied market laboratories worldwide with instruments, services, consumables, applications and expertise. Agilent enables customers to gain the answers and insights they seek - so they can do what they do best: improve the world around us. Information about Agilent is available at www.agilent.com.
The world's most revolutionary biopharma companies are partnering with Agilent Technologies to advance the next frontier of medicine. Agilent continues to invest in capacity and expansion of its Colorado operations. Join our team of professionals dedicated to the development and commercialization of nucleic acid therapeutics for life changing, lifesaving medicines.
Job Description:
Conducts routine, non-routine analysis and review to support release, stability testing, Environmental Monitoring, Cleaning Verification per Standard Operating Procedures (SOP) and Analytical Methods in accordance with current Good Manufacturing Practices (cGMP) and regulatory requirements. Has a clear understanding of Good Laboratory Practices (GLPs), cGMP, and other regulatory requirements. Actively engages in continuous improvement of processes and procedures. Proven ability to exercise judgment and appropriately escalates issues to QC management.
ESSENTIAL DUTIES AND RESPONSIBILITIES:<ul><li>
Outstanding communication skills, both written and oral</li><li>
Conducts analysis associated with clinical and commercial under current Good Manufacturing Practices (GMP) regulations and guidance per Food and Drug Administration (FDA) and Organization for Economic Co-Operations and Development (OECD) as well as International regulations</li><li>
Performs analysis on APIs (developmental and commercial), final product and other requested testing as per written procedures</li><li>
Review data for compliance to specifications and reports and troubleshoots abnormalities</li><li>
Ensures equipment is performing well and communicates and takes appropriate action as necessary</li><li>
Required to follow good documentation practices</li><li>
Exercises judgment within broadly defined practices and policies in selecting methods, techniques and evaluation criteria for obtaining results</li></ul>
SHIFT: DAY SHIFT Monday - Friday<h2 class="jobSectionHeader">
Qualifications</h2>
Required:<ul><li>
Secondary Education with two years of relevant QC experience</li><li>
Demonstrated knowledge of analytical equipment and instrumentation</li></ul>
Desired:<ul><li>
Bachelor's degree (B.S.)</li><li>
Knowledge of FDA regulations</li><li>
Knowledge of cGMP guidelines</li><li>
Personal leadership skills in a team environment</li><li>
Knowledge of and skills in using computer software and hardware applications, including Microsoft Word and Excel</li><li>
Familiar with the following laboratory disciplines is highly desired:</li></ul>
Bacterial Endotoxin (LAL Analysis)
Bioburden (Membrane Filtration Analysis)
Total Organic Carbon (TOC Testing)
Compressed Gas Monitoring
Environmental Monitoring
UV Analysis
USP &lt;61&gt;
Additional Details
This job has a full time weekly schedule. Applications for this job will be accepted until at least March 19, 2026 or until the job is no longer posted.
The full-time equivalent pay range for this position is $34.00 - $53.13/hr plus eligibility for bonus, stock and benefits. Our pay ranges are determined by role, level, and location. Within the range, individual pay is determined by work location and additional factors, including job-related skills, experience, and relevant education or training. During the hiring process, a recruiter can share more about the specific pay range for a preferred location. Pay and benefit information by country are available at: https://careers.agilent.com/locations
Agilent Technologies, Inc. is an Equal Employment Opportunity and merit-based employer that values individuals of all backgrounds at all levels. All individuals, regardless of personal characteristics, are encouraged to apply. All qualified applicants will receive consideration for employment without regard to sex, pregnancy, race, religion or religious creed, color, gender, gender identity, gender expression, national origin, ancestry, physical or mental disability, medical condition, genetic information, marital status, registered domestic partner status, age, sexual orientation, military or veteran status, protected veteran status, or any other basis protected by federal, state, local law, ordinance, or regulation and will not be discriminated against on these bases. Agilent Technologies, Inc., is committed to creating and maintaining an inclusive in the workplace where everyone is welcome, and strives to support candidates with disabilities. If you have a disability and need assistance with any part of the application or interview process or have questions about workplace accessibility, please email job_posting@agilent.com or contact +1-262-754-5030. For more information about equal employment opportunity protections, please visit www.agilent.com/en/accessibility.<h2 class="jobSectionHeader">
Travel Required:
</h2>Occasional<h2 class="jobSectionHeader">
Shift:
</h2>Day<h2 class="jobSectionHeader">
Duration:
</h2>No End Date<h2 class="jobSectionHeader">
Job Function:
</h2>Quality/Regulatory</div>

Quality Control Microbiology Analyst

Grifols

<div></div><div><div><div><div><div>Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions.</div></div><div> 
<div></div>
</div> 
</div></div><div>Grifols has been a leader in the healthcare industry since 1909 by creating innovative products and services based on the values of ethics, quality and responsibility. Grifols' activities focus on fulfilling the needs of its patients as well as healthcare professionals working in therapeutics, pharmacy, diagnostics and blood banking. For more than 100 years, Grifols has developed, manufactured and marketed product designed to improve human health. Grifols manufactures plasma derived biopharmaceutical products of proven efficacy, quality and safety. For more information, please visit our website: http://www.grifols.com</div> 

<div>
Purpose &amp; Responsibilities of Position:</div> 


The QC Data Trending &amp; Analysis Intern will support the Quality Control department by performing routine trending of key analytical test results. The intern will help identify data outliers, monitor assay stability, and provide weekly updates to QC leadership. This role is ideal for a student interested in quality systems, laboratory operations, or data analytics in a regulated environment.

Key Responsibilities:
<ul>
<li>Evaluate QC results and trends for critical tests across assigned product lines</li>
<li>Analyze test results for out-of-trend or out-of-expectation values</li>
<li>Summarize findings using standardized reporting formats</li>
<li>Notify QC management via email regarding weekly observations</li>
<li>Escalate any potential issues or abnormal trends</li>
<li>Assist in improving the data trending workflow and documentation</li>
<li>Present end‑of‑internship findings and recommendations</li></ul> 


Skills/Qualifications/Education Requirements: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skills, education, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions
<ul>
<li>Candidate must be currently enrolled in 4 year degree program pursuing Bachelor&rsquo;s degree in Mathematics, Biostatistics, Engineering, Data Science, or related field OR currently accepted or enrolled in Master&rsquo;s or PhD program</li>
<li>Candidate must currently have GPA of 3.0 or higher</li>
<li>Strong analytical and organizational skills with attention to detail and ability to follow established procedures</li>
</ul><ul><li>Proficiency with Excel or basic data analysis tools; Microsoft word and PowerPoint</li>
</ul>
<div>The estimated pay scale for Intern role based in California, is $18 - $22 per hour. Final compensation packages will ultimately depend on education, experience, skillset, knowledge, where the role is performed, internal equity and market data. Grifols is a global healthcare organization with employees in 30 countries focused on patient health and providing impactful results. Since our humble beginnings in 1909, Grifols has been a family company that prides itself on its family-like culture. Our company has more than tripled over the last 10 years, and you can grow with us!
</div>
<div>Third Party Agency and Recruiter Notice:
</div>
<div>Agencies that present a candidate to Grifols must have an active, nonexpired, Grifols Agency Master Services Agreement with the Grifols Talent Acquisition Department. Additionally, agencies may only submit candidates to positions that they have been engaged to work on by a Grifols Recruiter. All resumes must be sent to a Grifols Recruiter under these terms or they will be considered a Grifols candidate.</div> 


Grifols provides equal employment opportunities to applicants and employees without regard to race; color; sex; gender identity; sexual orientation; religious practices and observances; national origin; pregnancy, childbirth, or related medical conditions; status as a protected veteran or spouse/family member of a protected veteran; or disability. We will consider for employment all qualified applicants in a manner consistent with the requirements of all applicable laws, including but not limited to, the California Fair Chance Act, the Los Angeles County Fair Chance Ordinance for Employers, and the City of Los Angeles&rsquo; Fair Chance Initiative for Hiring Ordinance.

California Personnel Privacy Policy and Notice at Collection

Location: NORTH AMERICA : USA : CA-Los Angeles:US403 - LA CA-QC Building

Learn more about Grifols</div>

Intern - Quality Control Data Analyst 1

Clene Nanomedicine, Inc.

<div>Description:

The Micro Quality Control (Q/C) &amp; Biology Analyst I or II position will organize and perform testing activities with accuracy and precision while minimizing workloads. This position provides support for the team through hands-on training, activity oversight (when needed), preparation of media, cleaning lab areas, technician qualification, and product validation. 
Excellent benefits package, including, but not limited to:<ul><li>Up to 4 weeks paid leave.</li><li>Paid holidays.</li><li>Eligible for medical, dental, vision, and prescription coverage (employee &amp; family).</li><li>401(k) retirement plan with employer match.</li></ul>
Requirements:

Essential Duties and Responsibilities
This position is required to follow all Standard Operating Procedures (SOPs), Test Methods (TSMs), Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and internal processes.
Duties will include, but not limited to:<ul><li>Perform and monitor testing activities.</li><li>Review and update work schedules to effectively maintain the testing schedule.</li><li>Review testing results to ensure report accuracy.</li><li>Coordinate testing plans to ensure materials are testing according to schedule.</li><li>Plan usage of laboratory materials to ensure optimal testing levels.</li><li>Work with management to address issues regarding testing, quality, and production.</li><li>Manage deadlines based on project expectations.</li><li>Track production and research to help predict future scheduling needs.</li><li>Gather, process, analyze, and share research and product test data.</li><li>Work with management to establish SOPs for testing, equipment, and laboratory procedures.</li><li>Work with management to establish test methods, validate products, and qualify technicians.</li><li>Ensure GMP/GLP equipment calibration and IOPQ (mapping) are current.</li><li>Assist in the acquisition and/or production, if required, of research-related materials.</li><li>Work with management to design and enact research procedures.</li><li>Participate in research and/or microbiology testing.</li><li>Analyze and present research data.</li><li>Perform other duties as assigned.</li></ul> 
Education and/or Experience
This position requires the following:<ul><li>Bachelor's degree in microbiology/biology, or related science field.</li><li>One (1) to four (4) years' experience in a related field.</li><li>Exceptional analytical skill set and attention to detail.</li><li>Knowledge of USP testing procedures and FDS regulations.</li><li>Excellent computer skills, including, but not limited to, MS Office.</li><li>Excellent verbal and written communication skills with all levels.</li></ul>
Physical Demands
The physical demands described are representative of those that must be met by an employee to successfully perform the essential functions of this position. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.<ul><li>Required to stand, walk, and talk or hear.</li><li>Ability to lift up to 50 pounds.</li><li>Ability to read and interpret documents such as, operating, maintenance, and procedure manuals.</li></ul>
Work is normally performed Monday through Friday during normal business hours.
Resume must accompany online application to be considered to this position.</div>

Micro Quality Control (Q/C) & Biology Analyst I or II (based on experience)

<div>Description:

The Quality Control (Q/C) P-Chem Analyst II position will assist in the analysis of bioanalytical specimens obtained from animal and clinical studies conducted at contract research organizations. In addition, this position performs the analysis of production samples received from the manufacturing plant or research and development laboratory.
Excellent benefits package, including, but not limited to:<ul><li>Up to 4 weeks paid leave.</li><li>Paid holidays.</li><li>Eligible for medical, dental, vision, and prescription coverage (employee &amp; family).</li><li>401(k) retirement plan with employer match.</li></ul>
Requirements:

Essential Duties and Responsibilities
This position is required to follow all Standard Operating Procedures (SOPs), Test Methods (TSMs), Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and internal processes. 
Duties will include, but not limited to:<ul><li>Assist in the analysis of bioanalytical specimens (e.g., blood, urine, tissues).</li><li>Support development of validation protocols and reports.</li><li>Create and edit test methods and other quality documents.</li><li>Perform analytical characterization using all lab equipment, including, but not limited to:</li><li>oCEM Discover SPD Microwave Digester</li><li>Agilent ICP-MS 7700x/7900</li><li>Malvern Zetasizer ZS90</li><li>ThermoFisher UV-Vis</li><li>pH/Conductivity Meter</li><li>Shimadzu TOC-Vwp</li><li>Follow cGMP and cGLP standards, SOPs, and TSMs.</li><li>Execute and lead lab equipment validation and qualifications, when necessary.</li><li>Calibrate analytical instrumentation.</li><li>Maintain supply inventory and MSDS, including requesting purchase orders.</li><li>Attend as required, and successfully complete training on analytical instrumentation and procedures.</li><li>Report any issues that may affect the identity, strength, quality, and purity of the product.</li><li>Report any improvements to lab performance.</li><li>Assist in research and development experiments and all activities related to development.</li><li>Perform lab equipment verification.</li><li>Lead research and development experiments.</li><li>Troubleshoot lab equipment.</li><li>Assist in the shipping of samples for outsource testing.</li><li>Perform other duties as assigned.</li></ul>
Education and/or Experience
This position requires the following:<ul><li>Bachelor's Degree in a related science field.</li><li>One (1) to two (2) years' experience in a laboratory environment.</li><li>Proficient computer skills, including, but not limited to, MS Office.</li><li>Excellent verbal and written communication skills with all levels.</li></ul>
Physical Demands
The physical demands described are representative of those that must be met by an employee to successfully perform the essential functions of this position. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.<ul><li>Ability to lift up to 20 pounds.</li><li>Ability to read and interpret documents such as, operating, maintenance, and procedure manuals.</li></ul>
Work is normally performed Monday through Friday during normal business hours.
Resume must accompany online application to be considered to this position</div>

Quality Control (Q/C) P-Chem Analyst II

AMS SUPPLIES

ISO Certified, Exporting Company. Required Lab Analyst/Chemist , for material testing &amp; quality control.Minimum Graduate degree and past experience in this field .Maintain laboratory instruments, troubleshoot malfunctions.Maintain data of tests conducted, and results achieved.Evaluate and ensure compliance with laboratory safetyGulshan-e-Hadeed or near-by area preferred to applyPay: From Rs45,000.00 per monthEducation:<ul><li>Bachelor's (Preferred)</li></ul>Work Location: In person

Lab Assistant

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