1,151 Quality Control Chemist jobs in the United States

Cargill's size and scale allows us to make a positive impact in the world. Our purpose is to nourish the world in a safe, responsible and sustainable way.
Cargill is a family company providing food, ingredients, agricultural solutions and industrial products that are vital for living. We connect farmers with markets so they can prosper. We connect customers with ingredients so they can make meals people love. And we connect families with daily essentials - from eggs to edible oils, salt to skincare, feed to alternative fuel. Our 160,000 colleagues, operating in 70 countries, make essential products that touch billions of lives each day. Join us and reach your higher purpose at Cargill.
This position is in Cargill's food and bioindustrial business, where manufacturers, retailers, and foodservice companies rely on us to consistently deliver the products and services they need, and use our technical expertise and market knowledge to develop innovative products.
**Job Purpose and Impact**
The Quality Control Chemist will provide expertise with all daily operations in quality control laboratories. In this role, you will develop an in depth understanding of specific systems, ensure that products meet or exceed customer requirements for quality and food safety, and act as backup for FSQR roles including the FSQR Lab Technician. The Chemist I will support the buildup and maintenance of the instrumentation platform by providing reliable accurate analytical figures as well as perform validation and troubleshooting of analytical methods to ensure they meet the requirements. In this role, you will analyze malfunctions of instruments and control systems, determine necessary steps for repair, and work with scientific and analytic food safety and quality computer software, and data management systems.
**Key Accountabilities**
+ Provide ongoing technical support to stakeholders around food safety and quality performance instruments and control systems by investigating quality problems and deliver improvement actions with follow up.
+ Perform general maintenance on equipment and develop new and improved food safety and quality measuring and recording equipment.
+ Perform calibrations on various devices, documenting equipment inspection, testing and repair activities.
+ Perform method validation and verification to roll out new testing method in the lab.
+ Document standard operating procedures, identify possible trends in testing results with data analysis software and provide input to team members to improve quality control system.
+ Organize and maintain accurate and pertinent data, including spreadsheets, graphs, and reports.
+ Provide process improvement support, specialized testing, training, audit systems, analyze data, identify trends, troubleshoot, corrective action and communication regarding processing data and final product.
+ Assess quality parameters and systems including cross checks, raw materials, calibration, maintenance, procedures, food safety, training, auditing and oversight of analytical testing performed in control rooms.
+ PO's and ordering systems
+ Independently solve moderately complex issues with minimal supervision, while escalating more complex issues to appropriate staff, including internal resources and external suppliers.
+ Assist with customer audits, initiatives and follow ups.
+ Provide training, coaching, and mentoring to new team members.
+ Other duties as assigned
#LI-Onsite #LI-SM4
**Qualifications**
**Minimum Qualifications**
+ Bachelor's degree in a related field or equivalent experience.
**Preferred Qualifications**
+ Knowledge in calibrate, maintain and troubleshoot various analytical instruments.
+ Able to work independently and in a team environment, with high initiative level and communicate effectively
+ Proven ability to anticipate, recognize, solve process and laboratory problems.
+ Ability to handle multiple priorities with large projects.
+ Intermediate computer skills
+ Food safety, quality, and regulatory experience
Equal Opportunity Employer, including Disability/Vet

Job Title: Quality Control Chemist
Job Description
We are seeking a dedicated Quality Control Chemist to perform routine analytical testing of raw materials, in-process samples, and finished products, along with wastewater sampling and adjustments. The role requires strict adherence to standard operating procedures and conducting triplicate assessments on testing procedures to ensure accuracy and compliance.
Responsibilities
+ Ensure compliance with safety, health, and environmental protocols by wearing proper personal protective equipment.
+ Adhere to the company's Code of Conduct while conducting all business activities.
+ Perform in-process and finished product testing on various products.
+ Complete laboratory records and other documentation accurately following good documentation practices.
+ Communicate with the Shift Production Supervisor regarding in-process batch adjustments based on analytical test results.
+ Maintain cleanliness of the work area and notify colleagues when consumables need to be ordered.
+ Keep the workplace organized and orderly.
+ Facilitate effective communication within the Quality Control department and with other business units and customers.
Essential Skills
+ Understanding and adherence to safety, health, and environmental standards in the laboratory and facility.
+ Ability to communicate effectively and relate to employees at all levels within the company.
+ Ability to work independently while adjusting to the priorities of production.
+ Capability to walk and stand for extended periods.
Additional Skills & Qualifications
+ Bachelor's degree in a science discipline, with a preference for Chemistry.
+ Familiarity with basic laboratory equipment such as GC/LC/FTIR and techniques like titration and liquid-liquid partition.
+ Previous laboratory experience is preferred.
+ Basic computer skills, including familiarity with spreadsheet programs.
+ Strong math and analytical problem-solving skills.
+ At least 5 years of previous work experience.
+ Self-motivated and well-organized individual.
+ Proficient in speaking, reading, and writing English.
Pay and Benefits
The pay range for this position is $26.00 - $28.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
- Medical, dental & vision - Critical Illness, Accident, and Hospital - 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available - Life Insurance (Voluntary Life & AD&D for the employee and dependents) - Short and long-term disability - Health Spending Account (HSA) - Transportation benefits - Employee Assistance Program - Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in SALISBURY,NC.
Application Deadline
This position is anticipated to close on Oct 24, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email (% ) for other accommodation options.

Job Title: Quality Control Laboratory Chemist

Department: Quality Control
Reports To: Quality Control Manager
Employment Type: Full-Time | On-Site
Location: Gulfport, MS
Compensation: Median $23-$25/hour (commensurate with experience)

About the Role

Our client is seeking an experienced Quality Control Laboratory Chemist to join their Quality Control team. In this role, you will play a critical part in ensuring the quality and compliance of human and veterinary drug products by conducting a wide range of chemical analyses in a GMP-regulated laboratory environment . This position requires a strong background in chromatography and a proven track record of working within cGMP standards.

Please note that you must have experience beyond a university based laboratory setting to be considered for this position.

Key Responsibilities

• Perform chemical analyses on raw materials, in-process products, finished products, and stability samples.

• Operate, maintain, and calibrate analytical instruments (HPLC, GC, etc.).

• Prepare reagents and samples in compliance with SOPs and regulatory requirements.

• Accurately document and report test results according to GMP guidelines.

• Contribute to method development, validation, and transfer activities.

• Troubleshoot and investigate testing or equipment-related issues.

• Collaborate with QC team members and cross-functional departments.

• Mentor and support junior chemists when needed.

Qualifications & Requirements

• 3-5 years of direct hands-on experience in a GMP-regulated QC or manufacturing laboratory.

• Strong background in chromatography (HPLC, GC, UV/VIS, FTIR).

• Experience with analytical tools such as AA, IC, ICP-MS, and dissolution testing.

• Proficiency with Empower, Microsoft Office, and laboratory data systems.

• Solid understanding of cGMP , quality systems, and regulatory compliance (change control, deviations, CAPAs).

• Excellent attention to detail, communication, and organizational skills.

• Ability to multitask and prioritize in a fast-paced environment.

Note: Applicants with only academic or research lab experience will not be considered. A degree is not required. Relevant industry skills and experience are what matter most.

Physical Requirements

• Must be able to lift 50 lbs. or more daily.

• Ability to stand, walk, or sit for 8+ hours per day.

Stryker is hiring for a **QC Chemist I** located onsite in **Cary, IL.** The position of QC Chemist I is responsible for performing advanced analytical analysis of raw materials, in-process solutions, stability, finished goods, cleaning samples, as well as general laboratory support.
**What you will do:**
+ Performs routine and non-routine analysis for raw materials, in-process solutions, stability, and finished goods.
+ Responsible for conducting simple data review, including reagent review.
+ Performs laboratory maintenance activities including but not limited to equipment preventative maintenance, calibration etc.
+ Executes Phase I investigations for simple test methods. Supports problem solving, root cause analysis, identifies potential solutions, and evaluates them against requirements.
+ Follows regulatory requirements in their area of work.
+ With guidance, can create or approve records containing technical writing, including/not limited to NC/CAPA investigations and procedures. Be able to provide basic feedback to record owners when acting as an approver.
+ Basic knowledge and use of continuous improvement principles (e.g. 6S).
+ Participate in design/development of process/test methods.
**What you need**
+ Bachelor's degree in Chemistry or related field

**Preferred**
+ Experience working in a GxP laboratory environment and Good Manufacturing Practice (cGMP)
+ The ability to work independently with minimal supervision.
+ Strong written and oral communication skills (English).
+ Experience with common laboratory equipment such as balances, graduated cylinders, etc.
+ Experience with common analytical methods such as chromatography, spectroscopy, etc.
+ Must have experience with one or more of the following: HPLC (High Pressure Liquid Chromatography), UHPLC (Ultra High-Pressure Liquid Chromatography) or GC (Gas Chromatography)
+ Experience conducting compendial analytical testing.
+ Experience working with Laboratory Information Management System (LIMS).
+ Proficient in Microsoft Office applications.
+ $66,100.00 - $102,900.00 USsalary plus bonus eligible + benefits. Individual pay is based on skills, experience, and other relevant factors.
Health benefits include: Medical and prescription drug insurance, dental insurance, vision insurance, critical illness insurance, accident insurance, hospital indemnity insurance, personalized healthcare support, wellbeing program and tobacco cessation program. Financial benefits include: Health Savings Account (HSA), Flexible Spending Accounts (FSAs), 401(k) plan, Employee Stock Purchase Plan (ESPP), basic life and AD&D insurance, and short-term disability insurance. Stryker offers innovative products and services in MedSurg, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 150 million patients annually. Depending on customer requirements employees and new hires in sales and field roles that require access to customer accounts as a function of the job may be required to obtain various vaccinations as an essential function of their role.
Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer - M/F/Veteran/Disability.

** BR**
**Job Title:**
Quality Control Chemist - Kalamazoo, MI
**Department/Function:**
Operations: Manufacturing, Production, Maintenance, Utilities
**Job Description:**
**Quality Control Chemist - Kalamazoo, MI**
This is an exempt, salaried-level position
**Hours** :
+ Monday to Friday, 10:00 AM to 6:00 PM
+ Training to be conducted on 1st shift (approx. 8:00 AM to 4:00 PM)
**Position Summary:**
We are seeking a professional to contribute to all aspects of Quality for ADM's Mint Business Unit in Kalamazoo, MI. This role includes testing and inspecting products at various stages of the production process, as well as compiling and evaluating statistical data to ensure and maintain product quality and reliability. Additionally, the position involves performing Quality Assurance tasks at the Kalamazoo facility.
**Job Responsibilities:**
+ Selects products at specified stages of the production process and tests them for various qualities, including, but not limited to, physical and chemical characteristics
+ Records test data and applies statistical quality control procedures
+ Evaluates data and prepares reports to validate compliance or identify deviations from existing standards
+ Performs Quality Assurance responsibilities, including but not limited to, Good Manufacturing Practice (GMP) auditing
+ Complies with the food safety management system and actively participates, as required, to ensure food safety and maintain ISO/Food Safety certification
+ Performs other duties and assignments as needed
**Job Requirements:**
+ Bachelor's degree in chemistry or a related field; or one to two years of related experience and/or training; or an equivalent combination of education and experience
+ Knowledge of good laboratory practices
+ Experience with wet chemical methods
+ Proficiency in the operation and understanding of Gas Chromatography (GC) instrumentation
+ Proficiency in the operation and understanding of Gas Chromatography-Mass Spectrometry (GC/MS) instrumentation
+ Experience with analysis using ChemStation software
+ Proficiency in Microsoft Office applications
Excited about this role but don't think you meet every requirement listed? We encourage you to apply anyway. You may be just the right candidate for this role or another one of our openings.
ADM requires the successful completion of a background check.
REF: BR
"AJCIND"
**Req/Job ID:**
BR
**City:**
Kalamazoo
**State:**
MI - Michigan
**Ref ID:**
#LI-KR1
**:**
**About ADM**
At ADM, we unlock the power of nature to provide access to nutrition worldwide. With industry-advancing innovations, a complete portfolio of ingredients and solutions to meet any taste, and a commitment to sustainability, we give customers an edge in solving the nutritional challenges of today and tomorrow. We're a global leader in human and animal nutrition and the world's premier agricultural origination and processing company. Our breadth, depth, insights, facilities and logistical expertise give us unparalleled capabilities to meet needs for food, beverages, health and wellness, and more. From the seed of the idea to the outcome of the solution, we enrich the quality of life the world over. Learn more at equity, inclusion and belonging are cornerstones of ADM's efforts to continue innovating, driving growth, and delivering outstanding performance. We are committed to attracting and retaining a diverse workforce and create welcoming, truly inclusive work environments - environments that enable every ADM colleague to feel comfortable on the job, make meaningful contributions to our success, and grow their career. We respect and value the unique backgrounds and experiences that each person can bring to ADM because we know that diversity of perspectives makes us better, together.
We welcome everyone to apply. We are committed to ensuring all qualified applicants receive consideration for employment regardless of race, color, ethnicity, disability, religion, national origin, language, gender, gender identity, gender expression, marital status, sexual orientation, age, protected veteran status, or any other characteristic protected by law
**:**
**Benefits and Perks**
Enriching the quality of life for the world begins by taking care of our colleagues. In addition to competitive pay, we support your diverse needs with a comprehensive total rewards package to enhance your well-being, including:
+ **Physical wellness** - medical/Rx, dental, vision and on-site wellness center access or gym reimbursement (as applicable).
+ **Financial wellness** - flexible spending accounts, health savings account, 401(k) with matching contributions and cash balance plan, discounted employee stock purchasing program, life insurance, disability, workers' compensation, legal assistance, identity theft protection.
+ **Mental and social wellness** - Employee Assistance Program (EAP), Employee Resource Groups (ERGs) and Colleague Giving Programs (ADM Cares).
Additional benefits include:
+ Paid time off including paid holidays.
+ Adoption assistance and paid maternity and parental leave.
+ Tuition assistance.
+ Company-sponsored training and development resources, such as LinkedIn Learning, language training and mentoring programs.
*Benefits may vary for bargained locations, confirm benefit eligibility with your recruiter.
**:**
Base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience. Hourly and salaried non-exempt employees will also be paid overtime pay when working qualifying overtime hours.
If hired, employees will be in an "at-will position" and the Company reserves the right to modify base pay (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company or individual department/team performance, and market factors.
The pay range for this position is expected to be between:
**:**
$55,100.00 - $83,100.00

Our client is seeking a highly experienced Senior Pharmaceutical Quality Control Chemist to join their esteemed Quality Assurance department. This role requires dedicated on-site presence in **San Diego, California, US**, and is crucial for ensuring the quality, safety, and efficacy of pharmaceutical products. The Senior QC Chemist will be responsible for performing a wide range of analytical tests, developing and validating testing methods, and ensuring compliance with regulatory standards such as cGMP. The ideal candidate will possess a strong foundation in analytical chemistry, extensive experience with pharmaceutical testing equipment, and a meticulous approach to documentation and quality assurance. You will play a vital role in maintaining the highest standards of product integrity throughout the manufacturing process. Key Responsibilities:

• Perform a variety of analytical tests on raw materials, in-process samples, and finished pharmaceutical products using techniques such as HPLC, GC, UV-Vis, FTIR, and titration.
• Develop, validate, and transfer analytical methods in accordance with ICH guidelines and regulatory requirements.
• Troubleshoot and maintain analytical instrumentation, ensuring optimal performance and calibration.
• Analyze and interpret test data, preparing accurate and comprehensive reports.
• Ensure all laboratory activities are conducted in compliance with current Good Manufacturing Practices (cGMP) and relevant regulatory guidelines.
• Review and approve batch records, analytical test results, and method validation reports.
• Investigate Out-of-Specification (OOS) results and deviations, implementing corrective and preventive actions (CAPAs).
• Participate in internal and external audits as a subject matter expert.
• Train and mentor junior QC chemists, providing guidance on analytical techniques and procedures.
• Contribute to process improvement initiatives within the QC laboratory.
• Maintain laboratory equipment and inventory, ensuring adequate supplies.
• Stay current with advancements in pharmaceutical analysis and quality control technologies.

Qualifications:

• Master's degree or Ph.D. in Chemistry, Analytical Chemistry, Pharmaceutical Sciences, or a related field.
• 5+ years of experience in pharmaceutical quality control, with a strong emphasis on analytical testing.
• Extensive hands-on experience with analytical instrumentation, particularly HPLC, GC, and associated software.
• In-depth knowledge of cGMP, ICH guidelines, and other relevant regulatory requirements.
• Proven experience in method development and validation.
• Strong understanding of pharmaceutical manufacturing processes.
• Excellent analytical, problem-solving, and critical thinking skills.
• Meticulous attention to detail and strong organizational abilities.
• Exceptional written and verbal communication skills.
• Ability to work independently and as part of a collaborative team.
• Experience with LIMS (Laboratory Information Management System) is a plus.

This critical role is integral to our client's commitment to delivering high-quality pharmaceuticals and requires a dedicated professional on-site in **San Diego, California, US**.

**Schedule: Second Shift - Anticipated Monday- Friday 3:00 pm - 12:00 am**
At Cardinal Health, we're developing the innovative products and services that make healthcare safer and more productive. Join a growing, global company genuinely committed to making a difference for our customers and communities.
**What a Senior Specialist, Quality Control (Chemistry) contributes to Cardinal Health**
Quality Control is responsible for the analysis and inspection of products or processes for compliance with specifications and standards.
+ Performs visual assessment and analytical evaluation or testing of products/processes.
+ Demonstrates knowledge of testing methods, product usage, and applicable regulations and standards.
+ Adheres to established policies and procedures.
+ Establishes test methodology and may contribute to the development of policies and procedures.
+ May provide technical guidance and training to others on SOPs and quality guidelines.
**Responsibilities**
+ Performs analysis of incoming materials, in-process, and product samples.
+ Executes method verification, validation, and/or transfer protocols, analytical equipment qualification protocols, or computer system validation test scripts, as needed.
+ Performs stability testing in alignment with stability protocols at the prescribed cadence.
+ Performs laboratory investigations, change controls, deviations, and corrective/preventative actions as needed.
+ Authors and optimizes SOPs, analytical testing forms, and other documents as necessary.
+ Performs special projects or tasks as necessary based on skill set and/or development goals and business needs.
+ Champion Quality, cGMP compliance, and EHS/Radiation Safety practices.
+ Performs other job duties as assigned.
+ The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job.
+ While performing the duties of this job, the employee is regularly required to talk or hear. The employee is frequently required to stand; walk; use hands to finger, handle or feel; and reach with hands and arms; balance; stoop, kneel, crouch or crawl. The employee must occasionally lift or move up to 25 pounds. Specific vision abilities required by the job include close vision, distance vision, color vision, peripheral vision, depth perception and the ability to adjust focus.
+ The primary work environment consists of a professional office environment within a radiopharmaceutical manufacturing facility, the materials warehouse as well as the laboratory setting.
+ The facility is operated under well-controlled and closely monitored conditions that are regulated by both State and Federal agencies, and that are enforced by the corporate internal quality and regulatory groups. Each staff member will receive specific training in keeping radiation exposures within regulatory guidelines and he/she will be routinely monitored for their exposure to radiation. Noise levels are considered low to moderate.
**Qualifications**
+ Bachelor's degree or previous work experience in a similar role or related science field preferred.
+ 2+ years of relevant work experience working with 21 CFR 210, 211 in the FDA regulated industry (Pharmaceutical or Medical Device) preferred.
+ Has experience in authoring a variety of forms of documentation such as SOPs, Change Controls, CAPAs, Deviations and Laboratory Investigations preferred
+ Proficient in Microsoft Word and Microsoft Excel and possess strong technical writing skills preferred
**Schedule:**
+ 2nd Shift - Anticipated 3:00 pm - 12:00 am
+ Potential to work 1st shift, to cover PTO of other analysts
+ Initial training for this role will be provided on 1st shift.
**What is expected of you and others at this level**
+ Exhibits Cardinal Health's high ethical standards and code of conduct.
+ Approaches work situations with a positive and energizing style.
+ Possesses in-depth knowledge of work processes and tools within own area and can function as a Subject Matter Expert (SME) for processes, tools, and equipment.
+ Gain awareness of other departments at site. Seek to understand the functions of those departments and the points of interaction between QC and your role.
+ Exhibit professional conduct, respect for others, and understands how to be successful in a team environment.
+ Is detail oriented, organized, has the ability to multi-task, and is self-motivated. Is aware of internal/external business issues and adapts work priorities in own area.
+ Demonstrates strong communication skills. Effectively listens to and explains difficult issues to reach shared understanding and build alignment.
+ Takes actions to continually improve quality and safety in daily work. Actively participates in improving work processes to meet and exceed expectations. Identifies opportunities for improvement based on process observations, outcome measures, and feedback.
+ Reports errors in a timely and appropriate manner. Takes initiative and is accountable for areas of responsibility meeting regulatory requirements including but not limited to maintaining required trainings as appropriate to position requirements.
+ Has the ability to act calmly and patiently when working under pressure and/conditions of stress. Maintains integrity, composure, communicates with honesty, transparency, clarity and promotes alternative perspectives.
+ Actively builds relationships across functions/businesses that bring value to the company, encouraging the participation and perspectives of all team member, regardless of background.
+ Identifies quality events and aids in any associated investigations.
**Anticipated salary range:** $67,500- $96,400
**Bonus eligible:** No
**Benefits:** Cardinal Health offers a wide variety of benefits and programs to support health and well-being.
+ Medical, dental and vision coverage
+ Paid time off plan
+ Health savings account (HSA)
+ 401k savings plan
+ Access to wages before pay day with myFlexPay
+ Flexible spending accounts (FSAs)
+ Short- and long-term disability coverage
+ Work-Life resources
+ Paid parental leave
+ Healthy lifestyle programs
**Application window anticipated to close:** 11/11/2025
*if interested in opportunity, please submit application as soon as possible.
The salary range listed is an estimate. Pay at Cardinal Health is determined by multiple factors including, but not limited to, a candidate's geographical location, relevant education, experience and skills and an evaluation of internal pay equity.
_Candidates who are back-to-work, people with disabilities, without a college degree, and Veterans are encouraged to apply._
_Cardinal Health supports an inclusive workplace that values diversity of thought, experience and background. We celebrate the power of our differences to create better solutions for our customers by ensuring employees can be their authentic selves each day. Cardinal Health is an Equal_ _Opportunity/Affirmative_ _Action employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, ancestry, age, physical or mental disability, sex, sexual orientation, gender identity/expression, pregnancy, veteran status, marital status, creed, status with regard to public assistance, genetic status or any other status protected by federal, state or local law._
_To read and review this privacy notice click_ here (

At Elanco (NYSE: ELAN) – it all starts with animals!

As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets. At Elanco, we are driven by our vision of Food and Companionship Enriching Life and our purpose – all to Go Beyond for Animals, Customers, Society and Our People.

At Elanco, we pride ourselves on fostering a diverse and inclusive work environment. We believe that diversity is the driving force behind innovation, creativity, and overall business success. Here, you’ll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights.

Making animals’ lives better makes life better – join our team today!

Your Role:  Manufacturing Scientist/Quality Control Chemist Intern (Summer 2026)

As a Scientist Intern, you will be part of Animal Health Manufacturing (AHM) Lab team to deliver a practical solution to reducing analytical variability, a manufacturing technical project, or implementation of new lab methods. Interns will have exposure to many career path and diverse subject matter experts as many projects have site-wide impact.

Your Responsibilities:

• Understand the Animal Health Manufacturing process, document using GMP guidelines, and understand the importance of the Quality Unit

• Work within cross-functional teams to implement process or Quality Control lab improvements

• Learn about quality control, fermentation, product recovery, product finishing, or companion animal packaging

• Study design improvement processes

What You Need to Succeed (minimum qualifications):

• Education: Currently enrolled in a Microbiology, Biochemistry, Chemistry, Chemical engineering, or related engineering fields

• Experience with Microsoft Suites

• Demonstrate laboratory/manufacturing experience

• A willingness to learn

What will give you a competitive edge (preferred qualifications):

• Have an interest in animal health manufacturing, problem solving, scientific method, or cross-functional skill development

• Strong communication and interpersonal skills

• Thrive in cross-functional team settings

• Strong organizational and time management skills

• Must be able to work exceptionally well independently and with minimal supervision

Additional Information:

• Travel:  0%

• Location: Elanco Clinton Laboratories – Clinton, IN

Our Internship Program

Our internship program is designed to provide students with experiences! Internships are project based and comprised of business-critical needs. All interns have the opportunity to significantly impact Elanco’s success over the summer and kickstart a career that counts.

• Internship Dates: May 18th – August 7th (12 Weeks)

• Competitive salary: $20-$0/hour (dependent upon major and year in school)  

• Networking events

• Assigned mentors

• Professional development opportunities

• Optional all-inclusive housing for $ 50 per week or a 4000 housing stipend (ONLY for Sales and Kansas City/Elwood interns)

• Full time roles or additional internships for interns with outstanding performance

Don’t meet every single requirement? Studies have shown underrepresented groups are less likely to apply to jobs unless they meet every single qualification. At Elanco we are dedicated to building a diverse and inclusive work environment. If you think you might be a good fit for a role but don't necessarily meet every requirement, we encourage you to apply. You may be the right candidate for this role or other roles!

Elanco is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status