quality control intern

Phibro Animal Health Corporation

<div><p><b>About Phibro Animal Health Corporation</b></p>
<p><b>
Phibro Animal Health Corporation</b> is a publicly traded, global organization with a rich history in animal health and nutrition as a manufacturer and marketer of medicated feed additives, vaccines, nutritional specialty products, and mineral nutrition. We strive to be a trusted partner with livestock producers, farmers, veterinarians, and consumers who raise or care for farm and companion animals by providing solutions to help them maintain and enhance the health of their animals.</p><br>
<p>
</p><p>Phibro is a diversified company in manufacturing and marketing products for ethanol performance, microbials for plants, home and industrial applications, and specialty chemicals for various industrial markets. In addition to, Phibro&rsquo;s revenues are in excess of $1 billion and are supported by over 2,400 employees worldwide.</p><br>
<p></p>
<p>
At Phibro, people are our greatest asset. We strive to develop a diverse workforce that fosters an environment where people feel supported in openly sharing their creativity and skills that allows them to be the most successful that they can be.</p><br>
<p>
</p><p>If you are interested in working for Phibro and feel that you do not meet all qualifications, we encourage you to apply as you might be the right candidate for this role or other positions.</p><br>
<p></p>
<p>
The Quality Control Intern is an integral part of our Quality team based out of our US - State College, PA site.</p><p></p><div><div><div><h2 class="jobSectionHeader"><b><br>
Position Details</b></h2>
</div><div><p>
This position is a Summer Internship. Interns at Phibro will get a great hands-on experience in a real work environment. Specific responsibilities include but are not limited to:</p></div></div><div><div><h2 class="jobSectionHeader"><b>
Key Responsibilities</b></h2>
</div><div><div>
Partner with the Quality team to support the day-to-day operations of the lab, including:<br>
<ul><li>Sample grinding</li><li>Solution Preparation</li><li>Labeling of samples and glassware</li><li>Feed lab administrative support</li><li>Cleaning and preparation of lab instruments and glassware</li><li>Non-release / stability sample preparation</li><li>Assist with metrology functions</li><li>Other general lab functions as needed</li></ul></div></div></div><div><div><h2 class="jobSectionHeader"><b>
Skills that will be developed:</b></h2>
</div><div><ul><li>General laboratory techniques</li>
<li>Glassware Preparation</li>
<li>Introduction to GMP environment</li>
<li>Multiple interactions with lab staff on a daily basis</li>
<li>Evaluate ability to learn new techniques and seek out information.</li>
</ul></div></div><div><div><h2 class="jobSectionHeader"><b>Education, Experience and Skills required</b></h2>
</div><div><ul><li>Rising Junior or senior pursuing a BS in a scientific field</li>
<li>Strong academic record</li>
<li>Strong analytical and interpersonal skills</li>
<li>Willingness to learn</li>
</ul></div></div></div><p><b>
Phibro is an Equal Opportunity Employer</b></p>
<p>
All qualified applicants will receive consideration for employment without regard to race, national origin, gender, age, religion, disability, sexual orientation, gender identity, veteran status, marital status or any other characteristics protected by law.</p>
<p><b>
Business Unit: Animal Health &amp; Mineral Nutrition
</b><br>
<b>Division: Animal Health &amp; Nutrition</b><br>
<b>Department: Quality</b><br>
<b>Location: US - State College, PA</b><br>
<b>Work Schedule: Monday - Friday (Standard Work hours)</b></p></div>

Quality Control Intern

Jubilant HollisterStier

<div></div><div><div><div><h4 class="jobSectionHeader"><b>JOB DESCRIPTION</b></h4></div></div><p></p><div><p>
Jubilant HollisterStier LLC, <b>Spokane&rsquo;s Largest Manufacturing Company,</b> and well-established member of the business community, provides a complete range of services to support the pharmaceutical and biopharmaceutical industries. Jubilant HollisterStier is a nationally recognized contract manufacturer of sterile injectable vials, and lyophilized products. The Allergy business is a worldwide leader in the manufacture of allergenic extracts, targeted primarily at treating allergies and asthma. Jubilant HollisterStier is a proud member of the Jubilant Pharma family.</p><p></p><p><b><i>
Our Promise: Caring, Sharing, Growing</i></b></p><p>
We will, with the utmost care for the environment and society, continue to enhance value for our customers and stakeholders by providing innovative products and economically efficient solutions&rsquo; through growth, cost effectiveness and wise investment of resources.</p><p><b><br>
Job Description:</b> <b>Analytical Quality Control Intern-</b>The Analytical Quality Control Intern will support routine laboratory operations within a pharmaceutical contract manufacturing quality control environment. This temporary position is designed to provide hands-on experience in a GMP laboratory while assisting with fundamental analytical and laboratory support activities. The intern will work under the supervision of experienced QC analysts and laboratory management. The internship will run for an estimated duration of 3&ndash;4 months, with a flexible schedule of 20&ndash;40 hours per week, depending on laboratory workload and business needs.</p><p><b>
Qualifications:</b></p><ul>
<li>Currently pursuing or recently completed coursework in chemistry, biology, biochemistry, pharmaceutical sciences, or a related scientific discipline required.</li>
<li>Ability to follow written procedures and instructions accurately.
</li><li>Basic understanding of laboratory safety practices.</li>
<li>Strong attention to detail and organizational skills.</li>
<li>Effective communication skills and the ability to work in a team environment</li>
<li>Previous coursework or exposure to: Analytical chemistry, Pharmaceutical or GMP environments required.</li>
<li>Familiarity with basic laboratory instrumentation (e.g., pH meters, balances) required.
</li><li>Interest in pharmaceutical quality control or analytical laboratories as a career path required.</li></ul><p><b>
Learning Outcomes:
</b></p><ul><li>Gain a foundational understanding of Good Manufacturing Practices (GMP) as applied to pharmaceutical quality control laboratories.
</li><li>Develop hands-on experience in: Reagent preparation and solution standardization.
</li><li>Use of basic analytical laboratory instruments (e.g., pH meters, balances, conductivity meters).</li>
<li>Learn proper laboratory safety practices, including the use of personal protective equipment (PPE) and chemical handling procedures.
</li><li>Understand the importance of data integrity and Good Documentation Practices (GDP) in a regulated laboratory environment.</li>
<li>Become familiar with routine QC laboratory workflows and expectations within a pharmaceutical contract manufacturing setting.
</li><li>Build professional skills such as attention to detail, time management, and effective communication in a team-based laboratory setting.</li></ul><p><b>
Shift: </b>Monday-Friday 8:00AM-5:00PM</p><p><b>
Compensation &amp; Benefits:</b></p><p>
This is an <b>on-site,</b> full-time position located in Spokane, WA.</p><ul>
<li>Hiring Wage: <b>$25.00</b> hr depending on experience, with opportunity for growth, promotion and annual raises. Midpoint and above is reserved for employees who have longevity with Jubilant HollisterStier and consistently exhibit outstanding performance over a period of time in the role</li>
<li>Medical, Dental, Vision, Flexible Spending and Health Savings Accounts</li>
<li>Life, AD&amp;D, Short and Long Term Disability</li>
<li>401(k) with company match</li>
<li>Generous paid time off plan</li>
<li>Employee Assistance Program</li></ul><p>
</p><p><i>Unlock your potential with Jubilant HollisterStier! If you&rsquo;re seeking a dynamic and rewarding career, we welcome your application today!</i></p><p></p><p><i>
https://jubilantcareer.jubl.com/</i><i>
</i></p><p><i>*Please click on the Spokane, Wa. Link*</i></p><p><i>
Jubilant HollisterStier is an EEO/AA Employer.</i></p><p><i>
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.</i></p><p><i>
If you require assistance applying for a position, please contact our HR Department at:</i>
</p><p><i>JHS-TalentAcquisition@jubl.com</i></p></div></div><p></p>

Intern Quality Contr

Forvia

<div><div><div><div><h2 class="jobSectionHeader"><b>Forvia, a sustainable mobility technology leader</b></h2>
</div><div><p>
New trends and expectations are reshaping the automotive industry. Inspired by the exciting new challenges associated with this revolution, FORVIA anticipates the future of mobility developing cutting-edge solutions for smart life on board and sustainable mobility. If you&rsquo;re willing to contribute and create value for tomorrow&rsquo;s cleaner and smarter mobility, FORVIA is the place to be.</p><p>
FORVIA is looking for a <b>year-round Quality Intern</b> for its location in <b>Columbus, Indiana</b>.</p></div></div><div><div><h2 class="jobSectionHeader"><b>
Your mission, roles and responsibilities</b></h2>
</div><div><p>
The Quality Intern will work with a Quality Engineer to manage the quality of the exhaust components being manufactured. This includes developing quality control processes, instructing factory workers on these processes, examining components and comparing against documentation, updating documentation, and presenting solutions to management. On the job training will be provided to ensure a successful experience.</p><p><b>
The main missions of the role are:</b></p><ul><li>
Ensure quality control processes are robust and being performed correctly</li><li>
Investigate complaints from customers</li><li>
Present to management on how to detect future quality issues</li><li>
Create instructions for factory workers to check for quality issues</li><li>
Interface with factory workers to understand and troubleshoot manufacturing processes</li><li>
Instruct factory workers on new quality procedures</li></ul></div></div><div><div><h2 class="jobSectionHeader"><b>
Your profile and competencies to succeed</b></h2>
</div><div><p><b>
Minimum education level:</b> Pursuing a Technical or Business Degree</p><p></p><p><b><br>
Skills and competencies:</b></p><ul><li>
Strong interpersonal and communication skills</li><li>
Proficient in Microsoft Office &ndash; strong excel, PowerPoint and word skills a plus</li><li>
Willingness to take ownership of problems and drive to resolution</li><li>
Commitment to the highest ethical standards and willingness to adhere to Faurecia&rsquo;s Code of Ethics and Code of Management</li><li>
Have a minimum of 2.8 GPA</li><li>
Can work year-round</li></ul></div></div><div><div><h2 class="jobSectionHeader"><b>
What we can do for you</b></h2>
</div><div><ul><li>At Forvia, you will find an engaging and dynamic environment where you can contribute to the development of sustainable mobility leading technologies.</li><li>
We are the seventh-largest global automotive supplier, employing more than 157,000 people in more than 40 countries which makes a lot of opportunity for career development.</li><li>
We welcome energetic and agile people who can thrive in a fast-changing environment. People who share our strong values. Team players with a collaborative mindset and a passion to deliver high standards for our clients. Lifelong learners. High performers. Globally minded people who aspire to work in a transforming industry, where excellence, speed, and quality count.</li><li>
We cultivate a learning environment, dedicating tools and resources to ensure we remain at the forefront of mobility. Our people enjoy an average of more than 22 hours of online and in-person training within FORVIA University (five campuses around the world)</li><li>
We offer a multicultural environment that values diversity and international collaboration. We believe that diversity is a strength. To create an inclusive culture where all forms of diversity create real value for the company, we have adopted gender diversity targets and inclusion action plans.</li><li>
Achieving CO2 Net Zero as a pioneer of the automotive industry is a priority: In June 2022, Forvia became the first global automotive group to be certified with the new SBTI Net-Zero Standard (the most ambitious standard of SBTi), aligned with the ambition of the 2015 Paris Agreement of limiting global warming to 1.5&deg;C. Three principles guide our action: use less, use better and use longer, with a focus on recyclability and circular economy.</li></ul></div></div><div><div><h2 class="jobSectionHeader"><b>
Why join us</b></h2>
</div><div><p>
FORVIA is an automotive technology group at the heart of smarter and more sustainable mobility. We bring together expertise in electronics, clean mobility, lighting, interiors, seating, and lifecycle solutions to drive change in the automotive industry.</p><p>
With a history stretching back more than a century, we are the 7th largest global automotive supplier, employing more than 157,000 people in 43 countries. You'll find our technology in around 1 out of 2 vehicles produced anywhere in the world.</p><p>
In June 2022, we became the 1st global automotive group to be certified with the SBTI Net-Zero Standard. We have committed to reach CO2 Net Zero by no later than 2045.</p><p>
As technological innovation and the need for sustainability transform the automotive industry, we are ideally positioned to deliver solutions that will enhance the lives of road-users everywhere.</p></div></div></div></div>

Quality Intern

Fairbanks Morse Defense

Mission-Driven. Honor-Bound. Fairbanks Morse Defense. What’s your calling? For the men and women of Fairbanks Morse Defense it’s the rapid and effective support of the fleets that entrust us to design, develop, and deliver the best naval power technology on the planet. We’re one of the nation’s leading marine defense contractors because of the highly trained and dedicated teams that provide reliable power systems, parts, and aftermarket services to the U.S. Navy, Coast Guard, Military Sealift Command, and Canadian Coast Guard. When you join Fairbanks Morse Defense, you join a legacy of commitment that spans 150 years. Fairbanks Morse Defense offers competitive benefits with a wide range of training and development opportunities. Our world-class teams are dedicated to helping every individual achieve their full potential. Discover what it’s like to be a part of the Fairbanks Morse Defense team here: https://www.fairbanksmorsedefense.com/careers
<br><br>
<b>Position Title:</b> Continuous Improvement Quality Engineering Intern
<br><br>
Fairbanks Morse Defense is seeking highly motivated Interns to join our team. As an Intern, you will be taking on impactful work, while engaging in dynamic learning experiences and working as a valued member of our team.
<br><br>
<b>General internship requirements:</b><br>
<ul>
<li>Legal authorization to work in the U.S. is required. Sponsorship for employment visas is not available for this job opening.</li>
<li>Must be willing to comply with pre-employment screening, including but not limited to, reference verification, post-offer drug testing, and background check</li>
<li>Proficient in Microsoft Office – Word, Excel, PowerPoint, Outlook</li>
<li>Must have access to reliable transportation</li>
</ul>
What projects will this intern work on?
<br>1. Certification Review – while performing incoming quality control activities, you will learn a great deal about the nature of parts used to construct a large diesel engine, metal grades and the specification that control them, and fundamentals of how to ensure purchased parts will perform as needed.
<br>2. Engine Birth Records – collect and assemble documents to form a cohesive record of the pedigree of parts used to assemble an engine. Improve, streamline, and automate birth record genesis. Maintain and update templates and data tools used to capture critical data throughout the build process.
<br>3. Nonconformance Disposition – learn how to respond to real world manufacturing variation scenarios. Where specification deviations occur, determine a technically sound course of action for the nonconforming items.
<br>What is expected from an intern?
<br><ul>
<li>Dedication to creating a safe workplace free of all injuries</li>
<li>Presentation to the leadership team at the conclusion of the internship</li>
<li>Completing work as assigned and meeting all deadlines</li>
<li>Routinely communicating with department staff and informing them of any difficulties in completing work</li>
<li>Willingness to work in a fast-paced, team environment</li>
<li>Desire to learn new things</li>
<li>Highly motivated approach to problem-solving</li>
<li>Working hours as agreed and giving advance notice of any necessary schedule changes</li>
<li>Adherence to dress code, which is casual but appropriate for an office environment</li>
</ul>
What can an intern expect from the company?
<br><ul>
<li>Competitive hourly wage</li>
<li>Housing/Transportation stipend of $1,000, paid during the second pay period after the start of the internship</li>
<li>The opportunity to receive a hands-on, professional work experience</li>
<li>Additional learning experiences outside of daily work, including training and workplace growth activities</li>
<li>Program support with regular progress updates, team-building activities, and professional guidance</li>
<li>Sufficient opportunity to build your professional portfolio, including interaction with professional work teams</li>
</ul>
Fairbanks Morse Defense offers a competitive benefits package including but not limited to, medical, dental, vision, life, and disability insurances, and 401k retirement plan with employer match. In addition, we offer paid time off, paid holidays, paid parental leave, and tuition reimbursement.
<br><br>
Equal Opportunity Employer/Veterans/Disabled

Continuous Improvement Quality Engineer

PepsiCo

<div>Overview:
<div>
At PepsiCo, you&rsquo;ll discover a place where our mission is to create smiles around the world. With a portfolio of more than 500 beloved brands including, Pepsi, Doritos and Lipton Ice Tea, our work touches millions of people every day.</div><div></div><div><br>
At the heart of the company is a team of thinkers, creators, and problem-solvers who collaborate to innovate and turn ideas into action. Driven by innovation and a focus on creating joyful moments through food and drinks, our decisions are guided by consumer centricity, creating opportunities for our associates to do meaningful work and make a lasting impact in the communities we serve.</div><div></div><div><br>
Whatever your role, you&rsquo;ll be part of a global community that values your ideas and empowers you to make an impact, on your career and on the world around you.</div><div></div><div><br>
First Gen is a two-month summer internship program, offering hands-on experience, dynamic learning and exciting networking opportunities.</div><div></div><div><br>
We are looking for a First Gen Summer Intern to join our Supply Chain team based in Manisa Plant.</div>
Responsibilities:
<ul><li>Ensure all products meet safety and quality standards</li><li>
Demonstrate strong collaboration and communication with the team</li><li>
Adapt to changes and manage unexpected challenges</li><li>
Identify and priotize tasks</li><li>
Handle a project for food safety and quality control and meeting deadlines</li></ul>
Qualifications:
<ul><li>3rd or 4th year undergraduate student who have completed at least their 2nd year</li><li>
Currently pursuing a degree in Engineering, preferably in Food or Chemical Engineering</li><li>
Fluent in both English and Turkish</li><li>
Available to work full-time in <b>Manisa Plant </b>between<b> July 1 &ndash; August 31</b></li><li>
Proficient in MS Office programs</li><li>
Highly motivated to learn, develop new skills, and grow in a dynamic environment</li><li>
Strong collaboration and communication skills</li></ul></div>

First Gen Summer Intern - Quality (Manisa Plant)

E.L.F. BEAUTY

<div>
 <strong>
  About The Company
  <br/>
  <br/>
 </strong>
 e.l.f. Beauty, Inc. stands with every eye, lip, face and paw. Our deep commitment to clean, cruelty free beauty at an incredible value has fueled the success of our flagship brand e.l.f. Cosmetics since 2004 and driven our portfolio expansion. Today, our multi-brand portfolio includes e.l.f. Cosmetics, e.l.f. SKIN, pioneering clean beauty brand Well People, Keys Soulcare, a groundbreaking lifestyle beauty brand created with Alicia Keys and Naturium, high-performance, biocompatible, clinically-effective and accessible skincare.
 <br/>
 <br/>
 In our Fiscal year 25, we had net sales of $1 Billion and our business performance has been nothing short of extraordinary with 26 consecutive quarters of net sales growth. We are the #2 mass cosmetics brand in the US and are the fastest growing mass cosmetics brand among the top 5. Our total compensation philosophy offers every full-time new hire competitive pay and benefits, bonus eligibility (200% of target over the last four fiscal years), equity, flexible time off, year-round half-day Fridays, and a hybrid 3 day in office, 2 day at home work environment. We believe the combination of our unique culture, total compensation, workplace flexibility and care for the team is unmatched across not just beauty but any industry.
 <br/>
 <br/>
 Visit our Career Page to learn more about our team: https://www.elfbeauty.com/work-with-us
 <br/>
 <br/>
 <strong>
  Position Summary
  <br/>
  <br/>
 </strong>
 The
 <strong>
  Quality Assurance e.l.f.tern
 </strong>
 will support critical quality operations tied to new product launches and ongoing standards management. This role offers hands-on exposure to cross-functional quality processes, manufacturing readiness, and investigation frameworks&mdash;while owning a meaningful project that strengthens consistency, traceability, and speed across the business.
 <br/>
 <br/>
 <strong>
  Responsibilities:
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Coordinate first production sample approvals across cross-functional partners (Quality Assurance, Product Development, Packaging, Supply Chain, and Regulatory) to support on-time shipments for new product launches
  </li>
  <li>
   Create and operationalize a centralized Product Standards Library (physical and digital), tracking standard ownership, storage location, and age/refresh cadence
  </li>
  <li>
   Audit and catalog existing product standards, ensuring accurate documentation
  </li>
  <li>
   Improve the OTC manufacturer list in partnership with Regulatory by incorporating quality certifications and key compliance indicators
  </li>
  <li>
   Participate in quality investigations training, including:
  </li>
  <li>
   Understanding how quality issues are identified (in-line checks, stability testing, consumer feedback, vendor reports)
  </li>
  <li>
   Learning structured investigation methodologies (5 Whys, Fishbone, containment and corrective actions)
  </li>
  <li>
   Supporting cross-functional collaboration to inform disposition decisions
  </li>
  <li>
   Build and maintain trackers, inventories, and documentation to support quality workflows and ongoing investigations
   <br/>
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Requirements:
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Must be a rising junior or senior at the time of the internship
  </li>
  <li>
   Must be available for the full internship period: June 1st - August 21st
  </li>
  <li>
   Currently pursuing a degree in Biology, Chemistry, Chemical Engineering, Materials Science, or a related engineering or science discipline
  </li>
  <li>
   Foundational understanding of laboratory practices, quality control principles, and data integrity; familiarity with cGMP concepts is a plus
  </li>
  <li>
   Exposure to manufacturing or process environments is helpful, but not required
  </li>
  <li>
   Proficient with spreadsheets and databases (Excel or Google Sheets); experience with Airtable or SharePoint is a plus
  </li>
  <li>
   Highly detail-oriented with strong organizational, documentation, and problem-solving skills
  </li>
  <li>
   Comfortable auditing inventories, reconciling discrepancies, and maintaining version-controlled documentation
  </li>
  <li>
   Clear written and verbal communication skills; able to coordinate effectively across QA, Regulatory, Product Development, Packaging, and Supply Chain
  </li>
  <li>
   Strong ownership mindset with the ability to identify gaps, propose process improvements, and follow through to implementation
  </li>
  <li>
   Collaborative, professional, and eager to learn in a fast-paced, launch-driven environment
   <br/>
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Business Rationale:
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   This summer, the Quality Assurance e.l.f.tern will lead the creation of a centralized Product Standards Library to enable faster, more reliable quality comparisons across SKUs. By auditing and organizing existing standards, defining ownership and refresh rules, and documenting the process through an SOP, the intern will help improve traceability, shorten investigation timelines, and strengthen consistency in product evaluations across the organization
   <br/>
   <br/>
   <br/>
  </li>
 </ul>
 We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.
</div>


Summer Intern, Quality Assurance

Bio-Rad Laboratories, Inc.

<div><div><p>As the <b>Quality Assurance Intern</b>, you will develop a structured process to identify, trend, and escalate repeat nonconformances (NCs) within the quality system. This project will involve analyzing historical NC data, defining objective criteria for repeat issues, and creating standardized tracking and response tools. The resulting process will be designed to be audit-ready and aligned with existing risk assessment and CAPA escalation procedures.</p><br>
<p></p>
<p><b>
Location: </b>This position must be based in <b>Irvine, California</b> and requires the employee to be located within commuting distance of the office.</p>
<p><b>
How You'll Make An Impact:</b></p><br>
<p></p>
<p>
This project will improve early detection of systemic quality issues, strengthen CAPA decision-making, and enhance inspection readiness while reducing the risk of recurring nonconformances.</p><br>
<p></p>
<p><b>
What You Bring:</b></p>
<ul>
<li>Currently pursuing a Bachelor&rsquo;s or Master&rsquo;s degree at an accredited university in Business, Project Management, Information Systems, Engineering, Analytics, or a related field.
</li><li>Work Experience: regulated device experience preferred but not required.</li>
<li>Detail oriented and ability to multitask.</li>
<li>Microsoft Office (word, excel, PPT).</li>
<li>Strong problem solving, decision making, time management, organization and communication skills.</li>
<li>3.0 Minimum GPA.</li>
<li>Rising Juniors, Seniors, and Masters Students.</li>
<li>Be willing to make a full-time commitment of 40 hours a week for 9 weeks from June 15 to August 14, 2026.</li>
</ul>
<p><b>Total Rewards Package: </b>At Bio-Rad, we&rsquo;re empowered by our purpose and recognize that our employees are as well. That&rsquo;s why we offer a competitive and comprehensive Total Rewards Program that provides value, quality, and inclusivity while satisfying the diverse needs of our evolving workforce. Bio-Rad's robust offerings serve to enrich the overall health, wealth, and wellbeing of our employees and their families through the various stages of an employee&rsquo;s work and life cycle.</p><br>
<p></p>
<p><b>
Benefits:</b> We&rsquo;re proud to offer a variety of options, including competitive medical plans for you and your family, free HSA funds, a new fertility offering with stipend, group life and disability, paid parental leave, 401k plus profit sharing, an employee stock purchase program, a new upgraded and streamlined mental health platform, extensive learning and development opportunities, education benefits, student debt relief program, pet insurance, wellness challenges and support, paid time off, Employee Resource Groups (ERG&rsquo;s), and more!</p><br>
<p></p>
<p><b>
Compensation: </b>The estimated hourly rate for this position is $25.00 at the time of posting. Actual compensation will be provided in writing at the time of offer, if applicable, and is based on several factors we believe fairly and accurately impact compensation, including geographic location, experience, knowledge, skills, abilities, and other job permitted factors. This position is eligible for a variable annual bonus, which is dependent upon achievement of your individual objectives and Company performance.</p><br>
<p></p>
<p><b>
Who We Are:</b> For 70 years, Bio-Rad has focused on advancing the discovery process and transforming the fields of science and healthcare. As one of the top five life science companies, we are a global leader in developing, manufacturing, and marketing a broad range of high-quality research and clinical diagnostic products. We help people everywhere live longer, healthier lives. Bio-Rad offers a unique employee experience with collaborative teams that span the globe. Here, you are supported by leadership to build your career and are empowered to drive change that makes an impact you can see.</p><br>
<p>
</p><p><b>EEO Statement: </b>Bio-Rad is an Equal Employment Opportunity/Affirmative Action employer, and we welcome candidates of all backgrounds. Veterans, people with physical or mental disabilities, and people of all race, color, sex, sexual orientation, gender identity, religion, national origin and citizenship status are encouraged to apply.</p><br>
<p></p>
<p><b>
Agency Non-Solicitation: </b>Bio-Rad does not accept agency resumes, unless the agency has been authorized by a Bio-Rad Recruiting Representative. Please do not submit resumes unless authorized to do so. Bio-Rad will not pay for any fees related to unsolicited resumes.</p><br>
<p></p>
<p><b>
Fraud Alert</b><b>:</b> Bio-Rad has received reports of individuals posing as Bio-Rad recruiters to obtain information, including personal and financial, from applicants. Beware of these fake &quot;recruiters&quot; and job scams. Click here for more information on this scam and how to avoid it. #LI-JS1</p>
</div>
<div>Legal Entity: (USA_1000)Bio-Rad Laboratories, Inc.</div></div>

Quality Assurance Intern

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