quality intern

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

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

dormakaba Americas

<div>
 <strong>
  Position Overview
  <br/>
  <br/>
 </strong>
 dormakaba is seeking a Quality Assurance Intern based in Lexington, KY. The Quality Assurance Intern is responsible for maintaining and improving product and process quality. This internship provides hands-on experience in testing, documentation, analysis, and continuous improvement initiatives while working alongside experienced professionals.
 <br/>
 <br/>
 Rising Talent Internship Program
 <br/>
 <br/>
 Looking to apply your skills to real-world business challenges alongside experienced professionals? dormakaba&rsquo;s Rising Talent Internship Program offers hands-on projects that make a real impact&mdash;from manufacturing and product design to customer engagement and innovation.
 <br/>
 <br/>
 Learn more about the program by watching this short video: https://www.youtube.com/watch?v=qD_8FLLdkOU
 <br/>
 <br/>
 HIRING SALARY RANGE: Base Salary $21.00 - $25.00 (Salary to be determined by the education, experience, knowledge, skills, and abilities of the applicant, internal equity, and alignment with market data.) Please visit our career site for more information on benefits.
 <br/>
 <br/>
 Applicants must be authorized to work for any employer in the U.S. We are unable to sponsor or take over sponsorship of an employment visa at this time.
 <br/>
 <br/>
 <strong>
  What You Will Do
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Assist in testing products, systems, or processes to ensure quality standards are met
  </li>
  <li>
   Document test cases, results, defects, and improvement recommendations
  </li>
  <li>
   Support quality audits and inspections
  </li>
  <li>
   Analyze data to identify trends, defects, or process gaps
  </li>
  <li>
   Help maintain QA documentation and reporting tools
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  What we require
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Pursuing a bachelor&rsquo;s or master&rsquo;s degree with anticipated graduation date in December 2026 through Spring 2029 in Computer Science, Computer Engineering or related field.
  </li>
  <li>
   Ability to work full-time, 40 hours per week for 10-12 weeks (May-August 2026)
  </li>
  <li>
   Basic understanding of quality assurance concepts
  </li>
  <li>
   Comfortable working with documentation and data
  </li>
  <li>
   Ability to work independently and as part of a team
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  What We Prefer
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Familiarity with QA methodologies, testing tools, or defect tracking systems
  </li>
  <li>
   Prior internship, project, or coursework related to QA or testing
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Who we are
  <br/>
  <br/>
 </strong>
 We are at the heart of every place that matters. From automatic doors to cloud-based access management &ndash; as a leading global provider in the access solutions market for schools, banks, airports, hospitals, hotels, and many more, we enable seamless movement within secure, safe, and sustainable places. With over 160 years of experience and a focus on excellence and innovation, we offer exciting opportunities to grow in an environment where you can make a real impact. At dormakaba, you are encouraged to take initiative, develop your skills, and build your career alongside 16,000 experts worldwide who are setting industry standards every day.
 <br/>
 <br/>
 Work in a place where you matter &ndash; apply now!
 <br/>
 <br/>
</div>


Quality Assurance Intern

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>

Takeda Pharmaceuticals

<div><p>By clicking the &ldquo;Apply&rdquo; button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda&rsquo;s Privacy Notice and Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge.</p><p></p><h2 class="jobSectionHeader"><b>
Job Description</b></h2><p></p><p>
The Quality Services and Improvement team, within Quality Assurance, partners with internal Data, Digital &amp; Technology (IT) &amp; Business Excellence teams to drive innovative initiatives. These initiatives, both digital and non-digital, continually enhance capabilities and improve overall operational efficiencies, and add value to our stakeholder functions.</p><p></p><p>
We are seeking a highly motivated and detail-oriented Quality Improvement Intern to join the Quality Services and Improvement team at our Libertyville office. This internship offers a unique opportunity to gain hands-on experience with a broad range of Quality initiatives in the pharmaceutical industry, including but not limited to digital transformation, process optimization, and continuous improvement projects.</p><p><b><br>
How You Will Contribute:</b></p><p>
In this role, you will:</p><ul><li><p>
Support activities that drive efficiency and value creation across site manufacturing and quality operations, including digital transformation (e.g., electronic batch records, eForms) and process improvement (e.g., streamlining workflows, updating specifications, supporting compliance initiatives)</p></li><li><p>
Create data visualizations and reports using tools like Power BI. You will help create clear, impactful visuals and dashboards that enable stakeholders to understand trends, patterns, and insights within the data</p></li><li><p>
Collaborate on cross-functional projects by engaging with multiple teams within the business unit, gaining experience with both digital and non-digital Quality initiatives</p></li><li><p>
Participate in general continuous improvement initiatives for the QA team, such as process mapping, deviation reduction, and implementation of best practices</p></li><li><p>
Contribute to the adoption and optimization of new technologies and methodologies, including AI tools, automation, and standard operating procedures (SOPs).</p></li></ul><p></p><p><b>
Internship Development Opportunities:</b></p><ul><li><p>
Direct Experience: Exposure to real-world Quality improvement projects, including digital transformation and process optimization</p></li><li><p>
Mentorship and Networking: Direct mentorship from a Quality Manager, along with opportunities to connect with other professionals in the pharmaceutical industry. Cross-functional collaboration with other departments at the site and global organization.</p></li><li><p>
Skill-Building: Develop technical skills in process mapping, data transformation, and visualization. Learning industry-standard tools and best practices.</p></li><li><p>
Project Ownership: Take responsibility for small Quality improvement projects, from design to implementation, providing practical project management experience.</p></li></ul><p></p><p><b>
Job Requirements:</b></p><ul><li><p>
This position will be onsite 5 days per week in the Libertyville office.</p></li><li><p>
Must be pursuing a Bachelor&rsquo;s Degree in Quality Management, Information Systems, Computer Science, Engineering, Science or related fields.</p></li><li><p>
Strong interest in Quality improvement, process optimization, and innovative technologies.</p></li><li><p>
Strong analytical and problem-solving skills.</p></li><li><p>
Knowledge of SQL or JavaScript a plus.</p></li><li><p>
Basic understanding of computer skills including MS Office (PowerPoint, Words, Excel).</p></li><li><p>
Highly reliable and a strong team player.</p></li><li><p>
Flexible with an attention to detail.</p></li><li><p>
Strong verbal and written communication skills.</p></li></ul><p></p><p><b>
Internship Eligibility</b></p><ul><li><p>
Must be authorized to work in the U.S. on a permanent basis without requiring sponsorship</p></li><li><p>
Must be currently enrolled in a degree program graduating December 2026 or later</p></li><li><p>
The internship program is 10-12 weeks depending on the two start dates (May 26th-August 14th or June 15th- August 21st)</p></li><li><p>
The intern must be able to commit to one of these time frames</p></li><li><p>
Able to work full time 40 hours a week during internship dates</p></li><li><p>
Takeda does not provide a housing stipend or relocation support for the U.S Summer Internship Program</p></li></ul><p></p><p><b>
Program Highlights:</b></p><ul><li><p>
Hands-on experience with real projects and responsibilities</p></li><li><p>
Dedicated mentorship program pairing interns with experienced professionals</p></li><li><p>
Networking opportunities with industry professionals and fellow interns</p></li><li><p>
Internship events focused on professional and skills development</p></li><li><p>
Exposure to multiple business areas or departments within a Pharmaceutical Organization</p></li></ul><p></p><div><p><b>
Takeda Compensation and Benefits </b><b>Summary</b></p></div><div><p>
We understand compensation may be an important factor as you consider an internship opportunity. We are committed to equitable pay for all employees, and we strive to be more transparent with our pay practices.</p></div><p></p><p><b>
For Location:</b></p>
USA - IL - Round Lake Innovation Park<p></p><p><b>
U.S. Hourly Wage Range:</b></p><p>
$21.00 - $46.00</p><p></p><div><div><div><p>
The estimated hourly range reflects an anticipated range for this position. The actual hourly wage offered will depend on the candidate&rsquo;s school year/level to be entered following completion of internship. The actual hourly wage offered will be in accordance with state or local minimum wage requirements for the job location.</p></div><p></p><div><p><br>
U.S. internship benefits vary by location and may include:</p></div><div><ul><li><p>
 Paid sick time</p></li></ul></div><div><ul><li><p>
Civic Duty paid time off</p></li></ul></div><div><ul><li><p>
Participation at company volunteer events</p></li></ul></div><div><ul><li><p>
Participation at company sponsored special events</p></li></ul></div><div><ul><li><p>
Access to on-site fitness center (where available)</p></li></ul></div><div><ul><li><p>
Commuter Benefit: To offset your work-commute expenses, Takeda provides U.S. employees with a fixed monthly subsidy to be used for either public transportation (transit) or parking.</p></li></ul></div></div></div><p></p><p><b>
EEO Statement</b></p><p><i>
Takeda is proud in its commitment to creating a diverse workforce and providing equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information or characteristics, marital status, status as a Vietnam era veteran, special disabled veteran, or other protected veteran in accordance with applicable federal, state and local laws, and any other characteristic protected by law.</i></p><p></p><h2 class="jobSectionHeader"><b>
Locations</b></h2>
USA - IL - Round Lake Innovation Park<p></p><h2 class="jobSectionHeader"><b>
Worker Type</b></h2>
Employee<p></p><h2 class="jobSectionHeader"><b>
Worker Sub-Type</b></h2>
Paid Intern (Fixed Term) (Trainee)<p></p><h2 class="jobSectionHeader"><b>
Time Type</b></h2>
Full time<p></p><p><b>
Job Exempt</b></p>
No</div><p></p>

2026 Summer Internship Program: Quality Improvement Intern

Easy Construction

<p><b>Company:</b><br/>Deeloops Private Limited<br/><b>Type:</b> Unpaid Internship<br/><b>Duration:</b> 3 Months<br/><b>Location:</b> Onsite (Office-Based)<br/><b>Timings:</b> Monday to Friday | 6:00 PM &ndash; 3:00 AM<br/><b>Opportunity:</b> Performance-Based Job Offer After Completion</p><p><b>Company Overview</b></p><p><b>Deeloops Private Limited</b> is a growing software development company specializing in WordPress and Laravel solutions. Based in Johar Town, Lahore, we provide scalable and high-quality web solutions to clients worldwide in a structured and growth-focused environment.</p><p><b>About the Role</b></p><p>We are looking for a detail-oriented <b>QA Intern</b> who wants to gain practical experience in website testing and quality assurance. You will work closely with developers to ensure projects meet quality standards before delivery.</p><p><b>Responsibilities</b></p><ul><li>Test websites before final delivery</li><li>Identify and report bugs clearly</li><li>Check responsiveness (mobile/tablet)</li><li>Verify forms, links, and overall functionality</li><li>Coordinate with developers for issue resolution</li></ul><p><b>Requirements</b></p><ul><li>Strong attention to detail</li><li>Basic understanding of websites</li><li>Good communication and reporting skills</li><li>Responsible and disciplined attitude</li><li>Personal laptop is mandatory</li><li>Commitment to complete full 3 months</li></ul><p><b>Important Notes</b></p><ul><li>This is a completely unpaid internship.</li><li>No certificate will be issued if the internship is left incomplete.</li><li>Timings must be strictly followed.</li></ul><p>Work Location: In person</p>

QA (Quality Assurance) 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

Search 10000+ Quality intern jobs near you this March. New roles added regularly across leading industries. Apply today.

10000 quality intern jobs Near Me

Quality Intern

Quality Control Intern

Quality Assurance Intern

Quality Assurance Intern

2026 Summer Internship Program: Quality Improvement Intern

QA (Quality Assurance) Intern

Intern Quality Contr