Job Title: Intern - Supply Chain Job Type: Intern Compensation: $19.00/hour Internship will commence in May and end no later than August. About Us: As a developer, manufacturer, and supplier of essential medicines, Hikma Pharmaceuticals USA Inc. and its affiliates' purpose is to put better health within reach, every day for millions of patients around the world. We are a trusted, reliable partner and dependable source of over 760 high-quality generic, specialty and branded pharmaceutical products that hospitals, physicians and pharmacists need to treat their patients across North America, the Middle East, North Africa and Europe. Through our global footprint of 30+ manufacturing plants, 8+ R&D centers, and 9,000+ empowered employees, we are committed to making high-quality medicines accessible to the people who need them.
Description:
We are seeking a motivated and detail-oriented Supply Chain Intern to join our Materials Warehouse team. This internship offers a unique opportunity for hands-on experience supporting Warehouse Management System (WMS) activities, materials flow, and high‑volume handling system (HWS) design and efficiency initiatives. The intern will work on real-world materials management and inventory control projects with a focus on process optimization and Lean Six Sigma principles. The ideal candidate will be eager to learn, analyze, and interested in improving materials flow, system performance, and operational efficiency.
Responsibilities:
* The intern will work on various optimization projects.
* Assist with a variety of supply chain optimization activities, including work related to inventory settings, planning processes, reporting, and general operational improvements.
* Support cross-functional projects by gathering data, documenting processes, and contributing to updates that enhance efficiency, accuracy, and consistency within the supply chain function.
* Supply Chain department support
* Support WMS-related materials management activities, including inventory transactions, material movements, and process documentation
* Assist with HWS design, workstation layout, and efficiency analysis to improve materials flow, throughput, and labor productivity
* Participate in process optimization initiatives using Lean Six Sigma tools such as process mapping, root cause analysis, and standard work
* Collect, analyze, and organize data related to inventory accuracy, material availability, and operational efficiency
* Provide general support to the Materials Management function, including continuous improvement and system optimization efforts
* This internship provides an excellent platform for a supply chain student to develop practical skills in materials management, WMS functionality, system and workstation design, and Lean Six Sigma methodologies while contributing to impactful operational projects
* Other activities as assigned
Qualifications:
We value the skills and experiences candidates bring to the table. While we have listed some qualifications below, we encourage candidates to apply even if they do not meet all of them:
* Regular and predictable onsite attendance and punctuality.
* Completion of at least one year of college coursework toward a degree in Supply Chain Management, Operations Management, Industrial Engineering, Logistics, or a related field.
* Must be an Undergraduate, Graduate, or Professional Student in good academic standing.
* Completion of a minimum of 12 credit hours within a related major and/or relevant coursework such as materials management, inventory control, operations, or systems analysis.
* Demonstrated interest in materials management, WMS functionality, and process flow optimization.
* Preferred exposure to or interest in Lean Six Sigma concepts, continuous improvement, or process analysis methodologies.
* Strong analytical and problem-solving skills with the ability to interpret operational and system data.
* Ability to work independently and manage multiple tasks simultaneously in a hands-on operational environment.
* Strong organizational skills with a high level of attention to detail.
* Effective planning and time-management skills.
* Proficiency in Microsoft Office applications (Excel, Word, PowerPoint required; data analysis experience a plus).
* Strong verbal and written communication skills, with the ability to communicate clearly with cross-functional teams.
* Demonstrated initiative, positive attitude, and willingness to learn and support the Materials Management team.
* Ability to wear required personal protective equipment (PPE) and work in an operational environment as needed.
* Must be legally authorized to work in the United States without restriction; no sponsorship offered at this time.
* Must be willing to submit to a background investigation, including verification of employment, criminal history, and educational background.
* Must be willing to take a drug test.
* Must be 18 years of age or older.
Recruiters:
Please note that Hikma has a set roster of approved recruiters for specific roles agreed to in advance and does not accept unsolicited resumes or calls from third-party recruiters or employment agencies regarding open positions. In the absence of a signed agreement and approval from Hikma's Human Resources department to submit resumes for a specific position, Hikma will not approve, nor will be under an obligation to make, any payment to such non-approved third-parties in the event a candidate they refer is hired by Hikma.
Equal Opportunity Employer:
Hikma Pharmaceuticals USA Inc. is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status, or other characteristics protected by law.
#LI-KJ1
Location:
Columbus, OH, US, 43228
Nearest Major Market: Columbus
$19 hourly Auto-Apply 12d ago
Looking for a job?
Let Zippia find it for you.
Summer Internship - Regulatory Affairs, Labeling
Hikma Pharmaceuticals 4.9
Columbus, OH jobs
Job Title: Intern - Regulatory Affairs, Labeling Job Type: Intern Compensation: $19.00/hour Internship will commence in May and end no later than August. About Us: As a developer, manufacturer, and supplier of essential medicines, Hikma Pharmaceuticals USA Inc. and its affiliates' purpose is to put better health within reach, every day for millions of patients around the world. We are a trusted, reliable partner and dependable source of over 760 high-quality generic, specialty and branded pharmaceutical products that hospitals, physicians and pharmacists need to treat their patients across North America, the Middle East, North Africa and Europe. Through our global footprint of 30+ manufacturing plants, 8+ R&D centers, and 9,000+ empowered employees, we are committed to making high-quality medicines accessible to the people who need them.
Description:
We are committed to building a diverse and inclusive team and encourage applications from candidates of all backgrounds. We are seeking a talented and motivated College Summer Intern for our Regulatory Affairs team at our Columbus, Ohio site. As an Intern, you will earn practical experience as a fully integrated member of our team and participate in meaningful projects that will add value to our organization. In this role, you will provide support to the various Regulatory Affairs groups.
Responsibilities:
* Evaluates RLD updates and applies necessary revisions to company labeling.
* Works closely with regulatory team to provide regular updates on tasks.
* Assist in updating the comprehensive product list.
* Inputs meta data for products into the RIM system.
* Drafts annual reports for inactive products.
* Prepare redlines for artwork updates.
* Assist the Regulatory Affairs labeling team with daily tasks.
* Perform an audit of the current drug listings on DailyMed to ensure compliance.
* Other duties as assigned.
Qualifications:
We value the skills and experiences candidates bring to the table. While we have listed some qualifications below, we encourage candidates to apply even if they do not meet all of them:
* This internship will work 1st Shift hours.
* Regular and predictable onsite attendance and punctuality.
* Must be an Undergraduate, Graduate, or Professional Student in good academic standing.
* Must have completed 12 credit hours within a related major and/or other related coursework.
* Desired competencies include strong communication skills, taking initiative, detail oriented, and good teammate.
* Strong analytical and problem-solving skills (Business & Technical Knowledge)
* Ability to work independently and manage multiple tasks simultaneously.
* Highly motivated and inquisitive with a strong desire to learn.
* Organization skills to manage multiple tasks with strong attention to details.
* Planning and Organizational skills.
* Proficient usage of Microsoft Office applications.
* Strong mathematical, analytical, and problem-solving abilities.
* A positive, self-starting, can-do attitude, and a willingness to jump in to support the team.
* Excellent verbal and written communication skills, ability to communicate in a clear and persuasive manner, and attention to detail.
* Must be legally authorized to work in the United States without restriction, no sponsorship offered at this time.
* Must be willing to submit to a background investigation, including verification of your past employment, criminal history, and educational background.
* Must be willing to take a drug test.
* Must be 18 years of age or older.
Recruiters:
Please note that Hikma has a set roster of approved recruiters for specific roles agreed to in advance and does not accept unsolicited resumes or calls from third-party recruiters or employment agencies regarding open positions. In the absence of a signed agreement and approval from Hikma's Human Resources department to submit resumes for a specific position, Hikma will not approve, nor will be under an obligation to make, any payment to such non-approved third-parties in the event a candidate they refer is hired by Hikma.
Equal Opportunity Employer:
Hikma Pharmaceuticals USA Inc. is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status, or other characteristics protected by law.
#LI-KJ1
Location:
Columbus, OH, US, 43228
Nearest Major Market: Columbus
$19 hourly Auto-Apply 12d ago
2026 Future Talent Program - Research - Chemical Biology- Co-Op
MSD 4.6
Cambridge, MA jobs
The Future Talent Program features Cooperative (Co-op) education that lasts up to 6 months and will include one or more projects. These opportunities in our Research and Development Division can provide you with great development and a chance to see if we are the right company for your long-term goals.
We are Chemical Biology in the Quantitative Biosciences department at Our Company, where we leverage robust scientific methodology and state-of-the-art instrumentation to collaborate on driving the next medical breakthrough. Our mission is to advance the best drug candidates into the clinic by utilizing advanced capabilities that enable higher-resolution interrogations of novel biology and elucidation of mechanisms of action.
We are seeking a highly motivated Co-op scientist to contribute to our early drug discovery work. The successful candidate will focus on high-content imaging, morphological profiling, and multimodal data integration to study complex biological systems and support molecular mechanism-of-action studies.
Key Responsibilities:
• Aggregate, organize, and analyze high-content imaging data (e.g., cell painting, phenotypic profiling, live-cell imaging) to integrate multimodal datasets.
• Perform hands-on laboratory work including mammalian cell culture, perturbation experiments, and imaging-based assay execution.
• Analyze and interpret datasets and present findings to team.
Learning Opportunities:
• Gain hands-on experience in image-based profiling and multimodal data integration.
• Develop skills in experimental design, computational data analysis, and data-driven biological insight generation.
• Collaborate with experienced scientists in a fast-paced research environment.
Required Qualifications:
• Must be currently enrolled undergraduate or graduate student (BS, MS, or PhD) in biological sciences, bioengineering, computational biology, or related field.
• Must have experience with high-content imaging or microscopy-based data & analysis of multimodal biological datasets (examples: imaging data combined with RNA-Seq, small molecule/CRISPR-based high throughput screens, and / or proteomics data).
• Must possess proficiency with data analysis tools or programming languages (e.g., Python, R, MATLAB, or similar).
Preferred Qualifications:
• Prior hands-on experience with mammalian cell culture and imaging assays, including Cell Painting.
• Prior experience with multimodal data aggregation and visualization.
Co-Op Details:
• Location: Cambridge, MA
• Commitment: 6 months (start date flexible; by June 15th, 2026)
Please note that this position may be closed before the posted end date or may remain open longer, at the discretion of the company.
Salary range:
The salary range for this role is $39,600.00-$105,500.00 USD
FTP2026
RL2026
Required Skills:
Preferred Skills:
Current Employees apply HERE
Current Contingent Workers apply HERE
US and Puerto Rico Residents Only:
Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Please click here if you need an accommodation during the application or hiring process.
As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics. As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities. For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit:
EEOC Know Your Rights
EEOC GINA Supplement
We are proud to be a company that embraces the value of bringing together, talented, and committed people with diverse experiences, perspectives, skills and backgrounds. The fastest way to breakthrough innovation is when people with diverse ideas, broad experiences, backgrounds, and skills come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another's thinking and approach problems collectively.
Learn more about your rights, including under California, Colorado and other US State Acts
U.S. Hybrid Work Model
Effective September 5, 2023, employees in office-based positions in the U.S. will be working a Hybrid work consisting of three total days on-site per week, Monday - Thursday, although the specific days may vary by site or organization, with Friday designated as a remote-working day, unless business critical tasks require an on-site presence.This Hybrid work model does not apply to, and daily in-person attendance is required for, field-based positions; facility-based, manufacturing-based, or research-based positions where the work to be performed is located at a Company site; positions covered by a collective-bargaining agreement (unless the agreement provides for hybrid work); or any other position for which the Company has determined the job requirements cannot be reasonably met working remotely. Please note, this Hybrid work model guidance also does not apply to roles that have been designated as “remote”.
San Francisco Residents Only: We will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance
Los Angeles Residents Only: We will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance
Search Firm Representatives Please Read Carefully
Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.
Employee Status:
Intern/Co-op (Fixed Term)
Relocation:
No relocation
VISA Sponsorship:
No
Travel Requirements:
No Travel Required
Flexible Work Arrangements:
Not Applicable
Shift:
Not Indicated
Valid Driving License:
No
Hazardous Material(s):
Yes
Job Posting End Date:
02/6/2026
*A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.
$39.6k-105.5k yearly Auto-Apply 12d ago
Bachelor's-Level Internship - Pathway Caring for Children (Canton, OH)
Pathway Caring for Children 3.7
Canton, OH jobs
In-Person Flexible Schedule Supervised Learning Experience
Pathway Caring for Children, a nonprofit organization supporting children and families through foster care, adoption, and counseling services, is seeking Bachelor's-level interns in Social Work, Psychology, Human Development, or related fields for for-credit internships.
This placement offers meaningful, hands-on experience in community-based and mental health settings while learning from experienced professionals who are committed to your growth.
Why This Internship Is a Great Fit for Bachelor's Students
In-person or hybrid options available
Flexible scheduling to accommodate classes or work
Weekly supervision with experienced staff
Opportunities to observe counseling and supportive service roles
Exposure to child, family, and community mental health services
Supportive, mission-driven environment where learning is prioritized
What You'll Do
Learn how to complete documentation and intake procedures
Shadow staff in counseling, outreach, and supportive roles
Participate in group activities, team meetings, and program events
Assist with program development and school-based initiatives
Complete required university learning contract tasks
Engage in weekly supervision focused on skill-building, reflection, and professional development
Who Should Apply
Enrolled in a Bachelor's or Associate's degree program in Social Work, Psychology, Human Development, Counseling, or a related field
Internship must be for academic credit
Strong interpersonal and communication skills
Reliable, professional, and eager to learn
Able to meet university learning contract requirements
Background check required before placement
What You'll Gain
Real-world experience in child welfare and community mental health
Opportunities to observe counseling, case coordination, and team collaboration
Professional mentoring and weekly supervision
Skill development to strengthen your résumé and support future graduate school or career goals
Insight into nonprofit operations and multidisciplinary teamwork
How to Apply
Submit your resume and a brief cover letter including:
Your school and degree program
Internship dates and hour requirements
Any specific university requirements
Pathway is a smoke free and drug free organization. All applicants must be able to pass a background check.
About the Job Are you ready to shape the future of medicine? The race is on to speed up drug discovery and development to find answers for patients and their families. Your skills could be critical in helping our teams accelerate progress.
Join our B&P Neurology team as a Data Analyst and you'll lead one or several late phase studies, or lead an indication for a complex compound, under supervision of statistical project leader and/or team leader.
We are an innovative global healthcare company with one purpose: to chase the miracles of science to improve people's lives. We're also a company where you can flourish and grow your career, with countless opportunities to explore, make connections with people, and stretch the limits of what you thought was possible. Ready to get started?
Main Responsibilities:
* Contribute to the design and analysis of both early- and late-phase clinical trials by applying advanced statistical methods and data analysis techniques.
* Support the development, evaluation, and implementation of innovative statistical methodologies to address complex problems in clinical research.
* Work collaboratively under the guidance and mentorship of senior-level statisticians, gaining hands-on experience in study planning, data interpretation, and the preparation of statistical reports and publications.
About You
Basic Qualifications:
* Currently enrolled and pursuing PhD in Statistics or Biostatistics at an accredited college or university
* Candidates must have completed at least two years of graduate coursework and be working on a dissertation toward a PhD in Statistics or Biostatistics
* Experience with SAS and R
* Must be able to relocate to the office location and work 40hrs/week, Monday-Friday, for the full duration of the co-op/internship
* Must be permanently authorized to work in the U.S. and not require sponsorship of an employment visa (e.g., H-1B or green card) at the time of application or in the future. Students currently on CPT, OPT, or STEM OPT usually require future sponsorship for long term employment and do not meet the requirements for this program unless eligible for an alternative long-term status that does not require company sponsorship
Preferred Qualifications:
* Effective oral and written communication skills
* Experience with python is a plus
Why Choose Us?
* Bring the miracles of science to life alongside a supportive, future-focused team.
* Discover endless opportunities to grow your talent and drive your career, whether it's through a promotion or lateral move, at home or internationally.
* Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.
* Exposure to cutting-edge technologies and research methodologies
* Networking opportunities within Sanofi and the broader biotech community.
Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.
#GD-SA
#LI-SA
#LI-Onsite
#vhd
Pursue progress, discover extraordinary
Better is out there. Better medications, better outcomes, better science. But progress doesn't happen without people - people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let's be those people.
At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.
Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com!
US and Puerto Rico Residents Only
Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally inclusive and diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; natural or protective hairstyles; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.
$39k-46k yearly est. Auto-Apply 57d ago
Summer Intern - Analytical Data Analyst
Karyopharm Therapeutics 4.4
Newton, MA jobs
Role Overview & Key Functions:
If you want to do something that matters, this work matters. Patients drive our passion to pioneer novel cancer therapies. That's why we've built an environment centered around support, flexibility, and a shared mission. Creating and delivering medicine for cancer can only be done through focus, dedication, and heart. We hire exceptional people and trust each other to work in whatever way lets us, be us - whether that's onsite, from home, or anywhere in between.
Our summer intern program, which will run from May 26th - Aug 7th, allows students to gain real world work experience in a high energy, collaborative work culture.
Role Overview & Key functions:
We are seeking a motivated and detail-oriented Analytical Data Analyst Summer Intern to be part of our Analytical team. This internship offers hands-on experience in analytical data analysis, trending, and generating reports/dashboards to support business decision-making. This experience will enhance the Intern's career prospects in Analytical and related fields.
Transfer data between Smartsheet and excel worksheets/workbooks. Ensuring data integrity and correct formatting in the new destination file.
Develop complex spreadsheets including creating formulas, functions, PivotTables, Power Query, and data visualization tools to generate reports/dashboards for reporting metrics to be used for annual Quality Management Review (QMR) of XPOVIO products.
Improve filtering techniques for data queries.
Participate and collaborate in cross-functional meetings with Quality and Pharmaceutical Sciences to understand data requirements and deliver analytical support.
Perform administrative tasks related to documentation to standardize formats, ensuring version control and gap assessments for missing values or duplicates as needed.
Candidate Profile & Qualifications
Enrolled in a full-time pharmaceutical science, or statistical degree program
Proficiency with Microsoft Office including Word, Excel, PowerPoint, and Teams
Proficiency with PowerBI, JMP or excel statistical add-on packages a plus
Strong organization skills with the ability to handle multiple projects simultaneously and effectively
Strong communication and time management skills capable of working independently and cross-functionally in a remote work environment
Familiar with data analytics and trending including excel for graphing and hyperlinking source documents
Analytical or quality control experience in small or large molecules or oral drug products a plus for exposure to different types of data
Interest in understanding FDA regulatory commitments in commercial programs
Familiar with cGMP, USP, FDA, and ICH requirements a plus
You have a strong interest in life sciences and are passionate about giving patients with cancer a chance to enjoy more of life's precious moments.
You feel a strong connection with our ICARE values (Innovation, Courage, Alignment & Accountability, Resilience, and Energy)
You demonstrate enthusiasm for learnin
Candidate Profile & Requirements:
Must be able to complete the Karyopharm Internship Program 26 May - 07 Aug 2026
Currently enrolled high school or college (bachelor's program) student
Student must be returning to school in the Fall Term.
Must have a minimum GPA of 3.0
Must be highly organized and have the ability to work in independently and collaboratively as a team
Clear, concise verbal & written communication
Pay for internships ranges from $22 to $30 per hour, depending on the student's academic level (e.g., Bachelor's, Master's) and year in school.
Our Value Proposition:
At Karyopharm, we live and demonstrate our ICARE values every day! Check out our Culture Video!
$22-30 hourly Auto-Apply 36d ago
Summer 2026 Intern - Immunology New Product Launch Team
Sanofi Group 4.3
Cambridge, MA jobs
**Job Title:** Summer 2026 Intern - Immunology New Product Launch Team **About the Job** Sanofi is committed to becoming a leader in immunology with over 10 mid and late-stage clinical assets being studied across several immunological disease areas. The New Product Launch team was recently created to support the early commercial planning for this promising pipeline and to help prepare the company and the market for these new, potential treatment options for patients suffering from immunological diseases in the fields of dermatology, respiratory, rheumatology and gastroenterology.
We are an innovative global healthcare company, committed to transforming the lives of people with immune challenges, rare diseases and blood disorders, cancers, and neurological disorders. From R&D to sales, our talented teams work together, revolutionizing treatment, continually improving products, understanding unmet needs, and connecting communities. We chase the miracles of science every single day, pursuing progress to make a real impact on millions of patients around the world.
**Main Responsibilities:**
The New Product Launch (NPL) Summer Intern will report to a Senior Director within the NPL team to assist with one or more of the following projects:
+ Work with the global brand teams and NPL commercial team to support the development of a preliminary **US Brand Plan** for any of our late-stage clinical assets, including rilzabrutinib and duvakitug
+ Complete a **competitor analysis** within at least one of the following therapeutic areas: asthma / chronic spontaneous urticaria (CSU) / IgG4-related disease (IgG4-RD) / ulcerative colitis / Crohn's Disease to evaluate and summarize current treatments and existing competitors already in the space, therapies in development, and available resources and patient support programs
+ Support **market access assessment** and early forecasting efforts to scenario plan various launch strategies
+ Participate in **market research projects** and help identify any insights gaps for future planning
**About You**
**Basic Qualifications:**
+ Currently enrolled and pursuing an MBA at an accredited college or university with the expectation that you will complete your current degree in the Spring of 2027
+ Must have completed the first year of your MBAprogram prior to the summer internship
+ Must be enrolled in school the throughout the full duration of the internship with Sanofi
+ Must be able to relocate to the office location and work 40hrs/week, Monday-Friday, for the full duration of the co-op/internship
+ **Must be permanently authorized to work in the U.S. and not require sponsorship of an employment visa (e.g., H-1B or green card) at the time of application or in the future. Students currently on CPT, OPT, or STEM OPT usually require future sponsorship for long term employment and do not meet the requirements for this program unless eligible for an alternative long-term status that does not require company sponsorship**
**Preferred Qualifications:**
+ Desire to serve patients, passion for the patient
+ Excellent communication skills, interpersonally savvy, ability to collaborate across boundaries
+ Strong analytical skills, ability to package and present strategic insights and learning
+ Highly organized with the ability to effectively manage multiple projects and priorities
**Why Choose Us?**
+ Bring the miracles of science to life alongside a supportive, future-focused team.
+ Discover endless opportunities to grow your talent and drive your career, whether it's through a promotion or lateral move, at home or internationally.
+ Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.
+ Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks' gender-neutral parental leave.
+ Exposure to cutting-edge technologies and research methodologies.
+ Networking opportunities within Sanofi and the broader biotech community.
Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.
\#GD-SG
\#LI-GZ
\#LI-Onsite
\#vhd
**Pursue** **_progress_** **, discover** **_extraordinary_**
Better is out there. Better medications, better outcomes, better science. But progress doesn't happen without people - people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let's be those people.
At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.
Watch our ALL IN video (************************************************** and check out our Diversity Equity and Inclusion actions at sanofi.com (************************************************************************ !
_US and Puerto Rico Residents Only_
Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally inclusive and diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; natural or protective hairstyles; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.
Global Terms & Conditions and Data Privacy Statement (***************************************************************
Sanofi is dedicated to supporting people through their health challenges. We are a global biopharmaceutical company focused on human health. We prevent illness with vaccines, provide innovative treatments to fight pain and ease suffering. We stand by the few who suffer from rare diseases and the millions with long-term chronic conditions.
With more than 100,000 people in 100 countries, Sanofi is transforming scientific innovation into healthcare solutions around the globe. Discover more about us visiting ************** or via our movie We are Sanofi (*****************************
As an organization, we change the practice of medicine; reinvent the way we work; and enable people to be their best versions in career and life. We are constantly moving and growing, making sure our people grow with us. Our working environment helps us build a dynamic and inclusive workplace operating on trust and respect and allows employees to live the life they want to live.
All in for Diversity, Equity and Inclusion at Sanofi - YouTube (************************************************
Summer 2026 Intern: Application Lab, Health, Nutrition & Care Newark, NJ If you're looking to grow your network and gain new skills within a global company, an internship with dsm-firmenich could be the program for you. Our summer internships provide students opportunities to work on real business projects and gain invaluable professional experience. As an intern, you'll have exposure to many different areas of a global flavors, fragrances, and ingredients organization that works with some of the biggest brands in the world, along with opportunities to network with your peers and leadership. From engaging events to mentoring opportunities and valuable resume-building experiences, we're committed to preparing you for a fulfilling and enduring career, both at dsm-firmenich and beyond.
The 2026 dsm-firmenich Summer Internship Program will run from June 1, 2026 to August 14, 2026.
Working Hours: Monday - Friday, 8:00am - 5:00pm
Join our HNC Application team as an intern and gain invaluable professional experience. Enhance your skills and contribute to real projects that have visibility across the business through a Summer internship. Come discover all we have to offer!
Your Key Responsibilities:
* Operate dietary supplements and/or food process equipment with limited supervision.
* Generate reliable data during laboratory activity.
* Set-up, clean and maintain equipment for experiments by following the SOPs. Ensure all equipment is in a good condition to conduct product developments safely and effectively in a timely manner
* Organize raw materials, packaging materials, laboratory and supplies used in formulation development and maintain adequate inventory.
We Bring:
Opportunities for students to develop skills and expand their professional connections within a company where sustainability is not just a slogan but is at the core of our strategy and purpose. We strive to create inclusive communities within our organization where every employee is equally valued and respected, regardless of their background, beliefs, or identity. Additionally, we provide an environment that encourages curiosity and an open mindset, allowing for personal and professional growth. Together, we can learn from one another to drive progress and create a better future.
* Build Your Future Skills: Gain hands-on experience and develop practical skills that prepare you for a successful career.
* Expand Your Network: Connect with professionals and peers in a company where sustainability drives every decision and action.
* Thrive in an Inclusive Culture: Join a community that values and respects every individual-regardless of background, beliefs, or identity.
* Grow Through Curiosity: Work in an environment that encourages open-mindedness, learning, and collaboration to create a better future together.
You Bring:
* Current students pursuing an undergraduate or graduate degree in Food Science or related scientific major.
* The job requires lifting ~25 pounds. The job requires working in a highly regulated health and safety environment, which requires using gloves and safety glasses. The incumbent should not have health restrictions for these safety gears.
* Demonstrate ability to be self-motivated with an inherent winning can-do attitude. Ability to follow instructions from senior scientists, read and follow SOPs.
* Excellent communications and presentation skills - written and verbal; fluent in English. Knowledge of Microsoft word and excel is essential
The hourly rate for this position is $23.00 - $26.00 per hour. Compensation will be dependent on factors that include location, education, training, specific skills, and years of experience.
At the end of this internship, you will:
* Learn the complete process for formulating and manufacturing gummies, including ingredient selection and quality control.
* Gain experience in creating dietary supplement gummies that meet regulatory and nutritional requirements.
* Understand the steps involved in tablet formulation and compression, including active ingredient and excipient functionality.
About dsm-firmenich:
At dsm-firmenich, we don't just meet expectations - we go beyond them.
Join our global team powered by science, creativity, and a shared purpose: to bring progress to life.
From elevating health to making fortified food and sustainable skincare, the impact of your work here will be felt by millions - every single day. Whether it's fragrance that helps you focus, alternative meat that's better for the planet, or reducing sugar without losing flavor, this is where you help shape the future of nutrition, health, and beauty for everyone, everywhere.
And while you're making a difference, we'll make sure you're growing too. With learning that never stops, a culture that lifts you up and the freedom to move across businesses, teams, and borders. Your voice matters here. And your ideas? They're essential to our future.
Because real progress only happens when we go beyond, together.
Inclusion, belonging and equal opportunity statement:
At dsm-firmenich, we believe being a force for good starts with the way we treat each other. When people feel supported, included, and free to be themselves, they do their best work - and that's exactly the kind of culture we're building. A place where opportunity is truly equal, authenticity is celebrated, and everyone has the chance to grow, contribute, and feel they belong.
We're proud to be an equal opportunity employer, and we're serious about making our hiring process as fair and inclusive as possible. From inclusive language and diverse interview panels to thoughtful sourcing, we're committed to reflecting the world we serve.
We welcome candidates from all backgrounds - no matter your gender, ethnicity, sexual orientation, or anything else that makes you, you.
And if you have a disability or need any support through the application process, we're here to help - just let us know what you need, and we'll do everything we can to make it work.
Agency statement:
We're managing this search directly at dsm-firmenich. If you're applying as an individual, we'd love to hear from you. We're not accepting agency submissions or proposals involving fees or commissions for this role.
$23-26 hourly 23d ago
Dupixent Global Market Access and Pricing Dermatology Summer-Fall 2026 Co-op
Sanofi Us 4.3
Cambridge, MA jobs
About the Job
Join the team transforming care for people with immune challenges, rare diseases, cancers, and neurological conditions. In Specialty Care, you'll help deliver breakthrough treatments that bring hope to patients with some of the highest unmet needs.
Looking to launch your career at the cutting edge of healthcare? Join Sanofi for a chance to develop with mentoring and guidance from inspirational leaders while helping to make an impact on the lives of countless people worldwide. As a Dupixent Global Market Access & Pricing Dermatology Co-op in our Team, you'll support the global market access plan and operational excellence work streams including the coordination of key internal and external launch excellence events in collaboration with market access business partners (HEOR and pricing) and cross-functional brand team.
This position provides an excellent opportunity for students with an interest in developing market access foundational knowledge, access strategy development, tactical implementation and launch excellence execution capabilities by working with a team of market access experts on one of the most exciting products at Sanofi.
About Sanofi:
We're an R&D-driven, AI-powered biopharma company committed to improving people's lives and delivering compelling growth. Our deep understanding of the immune system - and innovative pipeline - enables us to invent medicines and vaccines that treat and protect millions of people around the world. Together, we chase the miracles of science to improve people's lives.
Main Responsibilities:
Coordinate project management activities related to payer interactions such as payer advisory boards, negotiation readiness workshops, and market access affiliate training events
Support market access launch excellence workstreams including project planning, dashboards, trackers, and reports
Assist Dermatology TA leads in the development of global market access strategy/plan and deliverables (e.g., payer value story, payer objection handler) for assigned Dupilumab indications based on business needs
Support Dupixent MAx launch execution and operations
Collaborate with cross-functional teams to ensure alignment on market access strategies and tactics
About You
Basic Qualifications:
Currently pursuing a bachelor's or advanced degree in Science, Engineering, Pharmacy, Business, Health Economics, Public Health, Policy/Government Affairs, or Marketing, or a related field at an accredited college or university with the expectation that you will complete your current degree by the Spring of 2028
Must be able to relocate to the office location and work 40hrs/week, Monday-Friday, for the full duration of the co-op/internship
Must be enrolled in an accredited college or university throughout the duration of the co-op/internship
Must be permanently authorized to work in the U.S. and not require sponsorship of an employment visa (e.g., H-1B or green card) at the time of application or in the future. Students currently on CPT, OPT, or STEM OPT usually require future sponsorship for long term employment and do not meet the requirements for this program unless eligible for an alternative long-term status that does not require company sponsorship
Preferred Qualifications:
Previous internship or coursework in pharmaceutical industry, healthcare, or related field
Experience with project management tools and methodologies
Knowledge of market access, health economics, or health technology assessment concepts
Interest in dermatology therapeutic area
Excellent written, verbal, and interpersonal communication skills
Strong organizational skills with attention to detail
Proficiency with Microsoft Office suite, particularly PowerPoint and Excel
Self-motivated with the ability to work both independently and as part of a team
Why Choose Us?
Bring the miracles of science to life alongside a supportive, future-focused team.
Discover endless opportunities to grow your talent and drive your career, whether it's through a promotion or lateral move, at home or internationally.
Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.
Exposure to cutting-edge technologies and research methodologies.
Networking opportunities within Sanofi and the broader biotech community.
Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.
#GD-SA
#LI-SA
#LI-Onsite
#vhd
Pursue
progress
, discover
extraordinary
Better is out there. Better medications, better outcomes, better science. But progress doesn't happen without people - people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let's be those people.
At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.
Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com!
US and Puerto Rico Residents Only
Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally inclusive and diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; natural or protective hairstyles; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.
$102k-136k yearly est. Auto-Apply 45d ago
Summer Internship - Process / Medical Device
Hikma Pharmaceuticals 4.9
Columbus, OH jobs
Job Title: Intern - Process / Medical Device Job Type: Intern Compensation: $19.00/hour Internship will commence in May and end no later than August. About Us: As a developer, manufacturer, and supplier of essential medicines, Hikma Pharmaceuticals USA Inc. and its affiliates' purpose is to put better health within reach, every day for millions of patients around the world. We are a trusted, reliable partner and dependable source of over 760 high-quality generic, specialty and branded pharmaceutical products that hospitals, physicians and pharmacists need to treat their patients across North America, the Middle East, North Africa and Europe. Through our global footprint of 30+ manufacturing plants, 8+ R&D centers, and 9,000+ empowered employees, we are committed to making high-quality medicines accessible to the people who need them.
Description:
We are committed to building a diverse and inclusive team and encourage applications from candidates of all backgrounds. Hikma Pharmaceuticals is currently seeking a talented College Intern to join the Technical Services group, you will have an opportunity to work on diverse pharmaceutical drug products and combination products (drug product & medical device) including nasal sprays, inhalation powders, tablets, capsules, solutions, suspensions etc. at various stages of their lifecycle ranging from early-development to scale-up/ commercial launch.
Your internship tenure will not only allow you to contribute towards Hikma's quality objectives and culture of putting "Better health. Within reach. Every day", but it will also directly impact lives of patients who rely on our products.
Responsibilities:
* Support Process Engineers with commercial batch production, cGMP documentation reviews, process optimization efforts, etc.
* Employ statistical methods (e.g. Cpk, ANOVA, Regression analysis etc.) and AI/ML models/ applications to analyze data and assist in driving quality/ regulatory decisions.
* Conduct physical properties, & performance testing of powders, tablets, capsules, etc. to support process validation activities. Support lifecycle review & continuous improvement of combination products by analyzing data from production, customer complaints, etc.
* Support Subject Matter Experts (SMEs) in performing risk analysis (e.g. FMEAs) following ISO 14971/13485 & CFR 820 principles.
* Support Tech Service department SMEs and management in other related duties and continuous improvement projects as assigned.
* Other activities as assigned.
Qualifications:
We value the skills and experiences candidates bring to the table. While we have listed some qualifications below, we encourage candidates to apply even if they do not meet all of them:
* Pursuant of undergraduate or graduate degrees/ programs in Engineering, Pharmacy, Chemistry, or related scientific disciplines.
* Prefer candidates with some prior work experience (at least 3 months) or academic research experience in the healthcare industry sector.
* Prefer for candidate to have knowledge of cGMP pharmaceutical production processes and combination products or medical devices.
* Prefer for candidate to have AI/ ML model development/ training, data analytics & programing skills with applications like MS- Excel, -Azure, -Power Apps, Minitab, SAS, etc.
* Require candidate to be a critical and analytical thinker with good situational leadership and communication skills.
* Candidates must meet cGMP, FDA, DEA, OSHA, and other applicable regulatory and Hikma guidelines.
* Regular and predictable onsite attendance and punctuality.
* Must be legally authorized to work in the United States without restriction, no sponsorship offered at this time.
* Must be willing to submit to a background investigation, including verification of your past employment, criminal history, and educational background.
* Must be willing to take a drug test.
* Must be 18 years of age or older.
* Must be an Undergraduate, Graduate, or Professional Student in good academic standing.
* Completion of a minimum of 12 credit hours within a related major and/or relevant coursework such as materials management, inventory control, operations, or systems analysis.
* Ability to work independently and manage multiple tasks simultaneously in a hands-on operational environment.
* Strong organizational skills with a high level of attention to detail.
* Effective planning and time-management skills.
* Strong verbal and written communication skills, with the ability to communicate clearly with cross-functional teams.
Recruiters:
Please note that Hikma has a set roster of approved recruiters for specific roles agreed to in advance and does not accept unsolicited resumes or calls from third-party recruiters or employment agencies regarding open positions. In the absence of a signed agreement and approval from Hikma's Human Resources department to submit resumes for a specific position, Hikma will not approve, nor will be under an obligation to make, any payment to such non-approved third-parties in the event a candidate they refer is hired by Hikma.
Equal Opportunity Employer:
Hikma Pharmaceuticals USA Inc. is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status, or other characteristics protected by law.
#LI-KJ1
Location:
Columbus, OH, US, 43228
Nearest Major Market: Columbus
$19 hourly Auto-Apply 12d ago
Master's Internship, CMHC or Social Work
Child Guidance & Family Solutions 3.6
Akron, OH jobs
CLINICAL MENTAL HEALTH INTERNSHIP - PAID
Child Guidance & Family Services is looking for Clinical Mental Health Interns to join our behavioral health team. Complete your internship and gain valuable experience while providing quality behavioral health care for children and families in need!
As an intern, you will receive extensive clinical supervision and a multitude of training opportunities in areas such as early childhood, play therapy, trauma, motivational interviewing, CBT and sandtray therapy. You'll also get opportunities to observe therapy groups in many different settings, including schools, clinical offices and the community.
Primary Responsibilities:
Conduct intake assessments
Provide diagnosis of mental health concerns under supervision
Develop an individualized treatment plan
Provide mental health counseling and CPST services such as individual, group and family counseling
Qualifications:
In the Practicum or Internship phase of an accredited Master's program for Clinical Mental Health Counseling or Social Work
Have, or be in the process of obtaining a CT (Counselor Trainee) or SWT (Social Work Trainee) license from the Ohio Board of Counselors, Social Workers and Marriage & Family Therapists
Benefits:
Paid Internships, $20 an hour
Flexible scheduling, Monday-Friday hours
Clinical supervision that meets licensure requirements
Experience with a variety of client ages and diagnoses
For more than 80 years, Child Guidance & Family Solutions has been a nationally recognized leader providing innovative and effective mental health services for children, teens, adults and families. Our therapists meet clients where they are - in our offices, in pediatricians' offices, in the home, at childcare centers, and on-site in elementary, middle and high schools.
Apply now to be part of a team that truly cares and Make a Difference!
Princeton, NJ If you're looking to grow your network and gain new skills within a global company, an internship with dsm-firmenich could be the program for you. Our summer internships provide students opportunities to work on real business projects and gain invaluable professional experience. As an intern, you'll have exposure to many different areas of a global flavors, fragrances, and ingredients organization that works with some of the biggest brands in the world, along with opportunities to network with your peers and leadership. From engaging events to mentoring opportunities and valuable resume-building experiences, we're committed to preparing you for a fulfilling and enduring career, both at dsm-firmenich and beyond. We are currently looking for a Creation Lab Technician Intern at our Plainsboro, NJ office.
The 2026 dsm-firmenich Summer Internship Program will begin June 1st, 2026 and run through August 14, 2026.
Working Hours: Monday - Friday, 8:00am - 5:00pm
Join our Taste Creation Lab team as an intern and gain invaluable professional experience. Enhance your skills and contribute to real projects that have visibility across the business through a Summer internship. Come discover all we have to offer!
Work side by side with Flavorists in compounding flavors used in newly developed foods, beverages, and supplements. Maintain your own laboratory space while compounding formulas for internal use and submission to clients. Work together with your colleagues as a critical part of the Creation team.
Your Key Responsibilities:
* Compound formula at a reliable and precise level, for flavorists and internal use and submission to clients.
* Maintain, manage and coordinate shipment of flavor samples.
* Keep daily compounding record, lab raw material record and other appropriate documentation on all laboratory work performed.
* Maintain and replenish laboratory supplies of stock raw materials, solutions, collection oil samples, glassware, and general laboratory equipment, ensuring the laboratory is well-stocked and resourced.
* Maintain a clean and well-organized laboratory/work place, and independently operate standard equipment/procedures to the required level. Assure compliance of HS&E procedures and proactively contribute to the improvement of lab safety.
* Identify common problems/issues encountered, report when an abnormal phenomenon happen: solubility, stability, color change, etc. Maintain awareness of technology and issues affecting own job.
We Bring:
* Build Your Future Skills: Gain hands-on experience and develop practical skills that prepare you for a successful career.
* Expand Your Network: Connect with professionals and peers in a company where sustainability drives every decision and action.
* Thrive in an Inclusive Culture: Join a community that values and respects every individual-regardless of background, beliefs, or identity.
* Grow Through Curiosity: Work in an environment that encourages open-mindedness, learning, and collaboration to create a better future together.
You Bring:
* Currently purusing a Bachelor's degree in Food Science, Chemistry, Biochemistry, Culinary, or related.
* Passion for technology.
* Self-motivated team player.
* Collaboration and team spirit.
* Candidates must be available to work full-time beginning on June 1, 2026 - August 14, 2026.
* Excellent communication and interpersonal skills.
The hourly rate for this position is $23.00 - $26.00 per hour. Compensation will be dependent on factors that include location, education, training, specific skills, and years of experience.
About dsm-firmenich:
At dsm-firmenich, we don't just meet expectations - we go beyond them.
Join our global team powered by science, creativity, and a shared purpose: to bring progress to life.
From elevating health to making fortified food and sustainable skincare, the impact of your work here will be felt by millions - every single day. Whether it's fragrance that helps you focus, alternative meat that's better for the planet, or reducing sugar without losing flavor, this is where you help shape the future of nutrition, health, and beauty for everyone, everywhere.
And while you're making a difference, we'll make sure you're growing too. With learning that never stops, a culture that lifts you up and the freedom to move across businesses, teams, and borders. Your voice matters here. And your ideas? They're essential to our future.
Because real progress only happens when we go beyond, together.
Inclusion, belonging and equal opportunity statement:
At dsm-firmenich, we believe being a force for good starts with the way we treat each other. When people feel supported, included, and free to be themselves, they do their best work - and that's exactly the kind of culture we're building. A place where opportunity is truly equal, authenticity is celebrated, and everyone has the chance to grow, contribute, and feel they belong.
We're proud to be an equal opportunity employer, and we're serious about making our hiring process as fair and inclusive as possible. From inclusive language and diverse interview panels to thoughtful sourcing, we're committed to reflecting the world we serve.
We welcome candidates from all backgrounds - no matter your gender, ethnicity, sexual orientation, or anything else that makes you, you.
And if you have a disability or need any support through the application process, we're here to help - just let us know what you need, and we'll do everything we can to make it work.
Agency statement:
We're managing this search directly at dsm-firmenich. If you're applying as an individual, we'd love to hear from you. We're not accepting agency submissions or proposals involving fees or commissions for this role.
$23-26 hourly 20d ago
Summer 2026 Intern - Immunology New Product Launch Team
Sanofi Us 4.3
Cambridge, MA jobs
About the Job
Sanofi is committed to becoming a leader in immunology with over 10 mid and late-stage clinical assets being studied across several immunological disease areas. The New Product Launch team was recently created to support the early commercial planning for this promising pipeline and to help prepare the company and the market for these new, potential treatment options for patients suffering from immunological diseases in the fields of dermatology, respiratory, rheumatology and gastroenterology.
We are an innovative global healthcare company, committed to transforming the lives of people with immune challenges, rare diseases and blood disorders, cancers, and neurological disorders. From R&D to sales, our talented teams work together, revolutionizing treatment, continually improving products, understanding unmet needs, and connecting communities. We chase the miracles of science every single day, pursuing progress to make a real impact on millions of patients around the world.
Main Responsibilities:
The New Product Launch (NPL) Summer Intern will report to a Senior Director within the NPL team to assist with one or more of the following projects:
Work with the global brand teams and NPL commercial team to support the development of a preliminary US Brand Plan for any of our late-stage clinical assets, including rilzabrutinib and duvakitug
Complete a competitor analysis within at least one of the following therapeutic areas: asthma / chronic spontaneous urticaria (CSU) / IgG4-related disease (IgG4-RD) / ulcerative colitis / Crohn's Disease to evaluate and summarize current treatments and existing competitors already in the space, therapies in development, and available resources and patient support programs
Support market access assessment and early forecasting efforts to scenario plan various launch strategies
Participate in market research projects and help identify any insights gaps for future planning
About You
Basic Qualifications:
Currently enrolled and pursuing an MBA at an accredited college or university with the expectation that you will complete your current degree in the Spring of 2027
Must have completed the first year of your MBA program prior to the summer internship
Must be enrolled in school the throughout the full duration of the internship with Sanofi
Must be able to relocate to the office location and work 40hrs/week, Monday-Friday, for the full duration of the co-op/internship
Must be permanently authorized to work in the U.S. and not require sponsorship of an employment visa (e.g., H-1B or green card) at the time of application or in the future. Students currently on CPT, OPT, or STEM OPT usually require future sponsorship for long term employment and do not meet the requirements for this program unless eligible for an alternative long-term status that does not require company sponsorship
Preferred Qualifications:
Desire to serve patients, passion for the patient
Excellent communication skills, interpersonally savvy, ability to collaborate across boundaries
Strong analytical skills, ability to package and present strategic insights and learning
Highly organized with the ability to effectively manage multiple projects and priorities
Why Choose Us?
Bring the miracles of science to life alongside a supportive, future-focused team.
Discover endless opportunities to grow your talent and drive your career, whether it's through a promotion or lateral move, at home or internationally.
Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.
Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks' gender-neutral parental leave.
Exposure to cutting-edge technologies and research methodologies.
Networking opportunities within Sanofi and the broader biotech community.
Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.
#GD-SG
#LI-GZ
#LI-Onsite
#vhd
Pursue
progress
, discover
extraordinary
Better is out there. Better medications, better outcomes, better science. But progress doesn't happen without people - people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let's be those people.
At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.
Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com!
US and Puerto Rico Residents Only
Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally inclusive and diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; natural or protective hairstyles; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.
$88k-125k yearly est. Auto-Apply 22d ago
Summer-Fall 2026 Co-Op - Media and Metabolic Profiling Development
Sanofi Group 4.3
Framingham, MA jobs
**Job title:** Summer-Fall 2026 Co-Op - Media and Metabolic Profiling Development **_Duration:_** _6-month Co-Op, July - December_ **About the Job** Are you ready to shape the future of medicine? The race is on to speed up drug discovery and development to find answers for patients and their families. Your skills could be critical in helping our teams accelerate progress.
We are seeking a highly motivated and talented Co-op to join the Cell Culture Platform (CCP) team within Cell Culture Development (CCD). CCP is globally responsible for providing solutions to process challenges through the development and application of platform cell culture media and innovative upstream process technologies throughout CCD. We are a dynamic team charged with identifying process pain points and resolving the underlying problems, generating compelling data from relevant proof of concept studies, and designing novel process platforms.
Our Co-op program offers the opportunity to learn cutting-edge bioanalytical industry techniques and develop cell culture subject matter expertise in an FDA-regulated setting.
We are an innovative global healthcare company with one purpose: to chase the miracles of science to improve people's lives. We're also a company where you can flourish and grow your career, with countless opportunities to explore, make connections with people, and stretch the limits of what you thought was possible. Ready to get started?
**Main Responsibilities:**
+ The successful candidate will collaborate with the modeling team to support and refine flux balance analysis (FBA) and metabolic flux analysis (MFA), providing high-quality experimental data to constrain and validate computational models
+ Design and execute isotopic labeling experiments, perform intracellular metabolite extraction, and analyze untargeted mass spectrometry data
+ The candidate should be comfortable interpreting experimental results such as growth rates, nutrient uptake/secretion, intracellular metabolite levels, and isotopologue distributions
+ Prepare samples for LC-MS analysis using automated liquid handling technology and process the results using a data automation platform
+ This candidate will have the opportunity to contribute to protocol and report writing, and present on findings in respective functional areas
**About You**
**Basic Qualifications:**
+ Currently enrolled and pursuing a master's degree or PhD in chemistry or engineering (biology, chemical, or biochemical) at an accredited college or university by Spring 2028
+ Must be able to relocate to the office location and work 40hrs/week, Monday-Friday, for the full duration of the co-op/internship
+ Experience with bioprocess analytical techniques
+ Experience with lab assays, high-throughput automation, and statistical analysis
+ **Must be authorized to work in the US for the full duration of the role**
**Preferred Qualifications:**
+ Strong interest in integrating experimental and computational approaches to study cell metabolism is essential
+ Experience in experimental investigation of mammalian cell metabolism, with a focus on metabolic profiling techniques
+ Experience using LC-MS instrumentation (preferably Thermo Q Exactive)
+ Experience with workflows in untargeted and targeted metabolomic
+ Minimum 3.0 GPA or equivalent
+ Ability to function independently and within a team environment
**Why Choose Us?**
+ Bring the miracles of science to life alongside a supportive, future-focused team.
+ Discover endless opportunities to grow your talent and drive your career, whether it's through a promotion or lateral move, at home or internationally.
+ Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.
+ Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks' gender-neutral parental leave.
+ Exposure to cutting-edge technologies and research methodologies.
+ Networking opportunities within Sanofi and the broader biotech community.
The salary range for this position is $45-$57 hourly . All compensation will be determined commensurate with demonstrated experience. Employees may be eligible to participate in Company employee benefit programs. Additional benefits information can be found through LINK (********************************************************************************************************* .
Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.
\#GD-SA
\#LI-SA
\#LI-Onsite
\#vhd
**Pursue** **_progress_** **, discover** **_extraordinary_**
Better is out there. Better medications, better outcomes, better science. But progress doesn't happen without people - people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let's be those people.
At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.
Watch our ALL IN video (************************************************** and check out our Diversity Equity and Inclusion actions at sanofi.com (************************************************************************ !
_US and Puerto Rico Residents Only_
Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally inclusive and diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; natural or protective hairstyles; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.
Global Terms & Conditions and Data Privacy Statement (***************************************************************
Sanofi is dedicated to supporting people through their health challenges. We are a global biopharmaceutical company focused on human health. We prevent illness with vaccines, provide innovative treatments to fight pain and ease suffering. We stand by the few who suffer from rare diseases and the millions with long-term chronic conditions.
With more than 100,000 people in 100 countries, Sanofi is transforming scientific innovation into healthcare solutions around the globe. Discover more about us visiting ************** or via our movie We are Sanofi (*****************************
As an organization, we change the practice of medicine; reinvent the way we work; and enable people to be their best versions in career and life. We are constantly moving and growing, making sure our people grow with us. Our working environment helps us build a dynamic and inclusive workplace operating on trust and respect and allows employees to live the life they want to live.
All in for Diversity, Equity and Inclusion at Sanofi - YouTube (************************************************
$45-57 hourly 13d ago
MSW Clinical Internship - Pathway Caring for Children (Canton, OH)
Pathway Caring for Children 3.7
Canton, OH jobs
In-Person Flexible Schedule Supervision by LISW-S Trauma-Informed Practice
Are you an MSW student looking for a meaningful, hands-on clinical internship with strong supervision and a supportive team? Pathway Caring for Children is currently accepting Master of Social Work interns seeking for-credit practicum or field placements for upcoming semesters.
This internship gives MSW students the opportunity to develop real-world clinical skills working with children, adolescents, and families in a mission-driven agency setting.
Why MSW Students Choose Pathway
Access to LISW-S supervisors who meet all Ohio CSWMFT Board supervision requirements
Opportunities to practice trauma-informed care, family systems work, and strengths-based interventions
Flexible scheduling that works with classes or employment
In-person or hybrid placement options
Exposure to both clinical counseling and child welfare programming
Real clinical experience that prepares you for LISW or LSW licensure and entry-level social work roles
A collaborative environment where interns are supported, encouraged, and treated as part of the team
Your Internship Experience Will Include
Orientation to agency programs, models, and trauma-informed practices
Shadowing individual and family sessions with licensed clinicians
Opportunities to co-facilitate therapy or psychoeducational groups
Learning intake, assessment, documentation, and case management steps
Supporting treatment planning and client goal development
Receiving weekly one-on-one supervision that aligns with your university requirements
Participation in staff meetings, case reviews, and professional development trainings
Providing supervised client sessions when approved by your supervisor
Who Should Apply
Currently enrolled in a Master of Social Work (MSW) program
Seeking an internship for academic credit
Interested in working with children, teens, and families
Professional, reliable, and committed to ethical practice
Strong communication, organization, and self-motivation
Comfortable working independently and within a multidisciplinary team
A background check is required before placement.
What You'll Gain
Direct clinical experience in child and family mental health
Hours that count toward Ohio LSW/LISW licensure requirements (when applicable)
Experience with documentation, treatment planning, and client engagement
Trauma-informed training and exposure to evidence-based practices
Networking and mentorship from licensed clinicians
A résumé that stands out for post-graduation job searches
How to Apply
Submit your resume and a short cover letter including:
Your university
Degree program (MSW)
Required internship dates/hours
Any specific placement requirements
Pathway is a smoke free and drug free organization. All applicants must be able to pass a background check.
$28k-35k yearly est. 48d ago
Intern, Assistant Project Manager
CN 2.9
Flint, MI jobs
At CN, we are committed to our pursuit of excellence. We take pride in delivering work of the highest standard, continually innovating to shape the railroad of the future. As responsible railroaders, we make the right decisions every time, putting safety first, acting with unwavering integrity, and holding ourselves accountable for our actions. We believe in succeeding together-by fostering inclusivity and collaboration, we sustainably deliver exceptional results for our customers.
We welcome students aboard to join our team and play a valuable role in the engine that keeps the North American economy on track. Expect an exciting environment where you'll be encouraged to learn, grow, and be recognized for your unique ideas and contributions. Work on pivotal projects with experienced collaborators who will encourage you to share your perspectives, and thrive in our close-knit, safety-focused culture. The careers we offer are meaningful because the work we do matters. Join us and get your career moving!
Starting hourly rate range : $19.05 - 29.95 Per hour
Please note that hourly rates for this position are based on type of degree and expected date of graduation.
In addition to exciting work projects and exposure to real-world challenges, CN interns benefit from a variety of activities specifically developed for them. These include train yard tours, intern game-hours, case competitions, speaker series, learning sessions, and opportunities to join intern-led committees. With a 93% satisfaction rating, CN's internship program successfully develops the leaders of tomorrow!
**Intern, Assistant Project Manager**
This is a full-time summer internship lasting from May 11, 2026, until August 28, 2026
**Job Summary**
The Intern, Assistant Project Manager is responsible for working within the Facility Management Project group. Mains tasks include researching baseline information such as drawings, specifications, and project objectives as well as supporting the day-to-day activities of the department. The CN Facility Management team provides its customers from Canada and the United States with unsurpassed facility maintenance and superior workplace management solutions by implementing the latest technologies and industry expertise.
**Major Responsibilities**
+ Participate and assist Project Managers in projects within CN yards and buildings
+ Set up and organize a database of existing drawings covering the buildings across the network in both Canada and the United States
+ Understand the process behind a project, from client request to completion
+ Coordinate and collaborate with staff across the network
**Requirements**
+ Fluently bilingual both written and verbal (English, French)
**Education**
+ Working towards a Bachelor's Degree in Civil, Mechanical or Building Engineering
**About CN**
CN is a premium railroad that sustainably generates value for our customers, shareholders, employees, and stakeholders with an unwavering commitment to safety and service. Essential to the economy, to the customers, and to the communities it serves, CN safely transports more than 300 million tons of natural resources, manufactured products, and finished goods throughout North America every year. CN's network connects Canada's Eastern and Western coasts with the U.S. South through a 20,000-mile rail network. CN and its affiliates have been contributing to community prosperity and sustainable trade since 1919. CN powers the North American economy and is committed to programs supporting social responsibility and environmental stewardship.
At CN, we are dedicated to building North America's safest (***************************** , most inclusive (*************************************** and sustainable (********************************************************* railroad, which includes reflecting the communities in which we operate. Research shows that candidates often don't apply unless they feel they fit the job posting at 100%. To all potential applicants, even if you don't meet every job requirement listed in a posting, we still encourage you to apply. If you require an accommodation for the recruitment process (including alternate formats of materials, accessible meeting rooms or other accommodations), please get in touch with our team at **cnrecruitment@cn.ca** .
As an equal opportunity employer, qualified candidates will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, and other protected status as required by applicable law.
Please monitor your email on a regular basis as communication to applicants is done via email.
$19.1-30 hourly 60d+ ago
Network Engineer Intern- Summer 2026
Medpace 4.5
Cincinnati, OH jobs
Our corporate activities are growing rapidly, and we are currently seeking an office-based Network Engineer Intern to join our Information Technology team. Responsibilities We have openings for entry level internships within the Core Infrastructure team at Medpace. The list below are samples of some of the technologies that we work with. While we desire candidates with experience in these specific technologies, we also understand that each of them has market alternatives, so the most important skillset a candidate can have is a good attitude and have a strong work ethic. Top candidates will have an aptitude to learn new technology and have a "do what it takes" attitude.
The ideal candidate will have some familiarity and exposure to network fundamentals, switching, wireless, and firewall. Scripting and demonstrated ability to automate tasks and processes is a plus.
* Cisco hardware
* Meraki wireless
* CheckPoint firewalls
* SD-WAN with SilverPeak
* zScaler ZIA and ZPA
* SolarWinds network monitoring
* Cisco DNA management
Qualifications
* Working towards bachelor's degree in computer science, Information Systems or a related field;
* Strong desire to learn and grow, with a solid foundation of technical background and experience;
* Ability to be self-directed with assigned tasks and ability to research solutions and come forward with recommendations for new and creative ideas to solve problems.
* Ability to communicate effectively with peers, end users, and management.
Medpace Overview
Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries.
Why Medpace?
People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.
The work we've done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.
Cincinnati Perks
* Cincinnati Campus Overview
* Flexible work environment
* Competitive PTO packages, starting at 20+ days
* Competitive compensation and benefits package
* Company-sponsored employee appreciation events
* Employee health and wellness initiatives
* Community involvement with local nonprofit organizations
* Discounts on local sports games, fitness gyms and attractions
* Modern, ecofriendly campus with an on-site fitness center
* Structured career paths with opportunities for professional growth
* Discounted tuition for UC online programs
Awards
* Named a Top Workplace in 2024 by The Cincinnati Enquirer
* Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024
* Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility
What to Expect Next
A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.
$59k-72k yearly est. Auto-Apply 29d ago
Summer Internship - Clinical Research & Development
Hikma Pharmaceuticals 4.9
Columbus, OH jobs
Job Title: Intern - Clinical Research & Development Job Type: Intern Compensation: $19.00/hour Internship will commence in May and end no later than August. About Us: As a developer, manufacturer, and supplier of essential medicines, Hikma Pharmaceuticals USA Inc. and its affiliates' purpose is to put better health within reach, every day for millions of patients around the world. We are a trusted, reliable partner and dependable source of over 760 high-quality generic, specialty and branded pharmaceutical products that hospitals, physicians and pharmacists need to treat their patients across North America, the Middle East, North Africa and Europe. Through our global footprint of 30+ manufacturing plants, 8+ R&D centers, and 9,000+ empowered employees, we are committed to making high-quality medicines accessible to the people who need them.
Description:
We are committed to building a diverse and inclusive team and encourage applications from candidates of all backgrounds. We are seeking a talented and motivated College Summer Intern for our Clinical Resarch and Development team at our Columbus, Ohio site. As an Intern, you will earn practical experience as a fully integrated member of our team and participate in meaningful projects that will add value to our organization. In this role, you will provide support to the various Research and Development groups, Participate in Clinical Research Trial Design and Implementation.
Responsibilities:
* Learn to conduct Clinical Trials developing experience in Phase I-IV, Bioequivalence, and Biosimilar studies/
* Review and Learn Good Clinical Practice.
* Review and Learn Good Manufacturing Practice.
* Participate in Regulatory Filings to support ANDA and IND submissions to FDA, Health Canada, and other regulatory agencies.
* Develop a working knowledge of Standard Operating Procedures (SOP's).
* Facilitate writing technical documents and presentations.
* Learn regulations for FDA Guidance, DEA Requirements, ICH Ethical Standards.
* Gain Project Management Experience.
Qualifications:
We value the skills and experiences candidates bring to the table. While we have listed some qualifications below, we encourage candidates to apply even if they do not meet all of them:
* Regular and predictable onsite attendance and punctuality.
* Must be an Undergraduate, Graduate, or Professional Student in good academic standing.
* Must have completed 12 credit hours within a related major and/or other related coursework.
* Overall, cumulative GPA must be at least 3.0 (on 4.0 scale) or better.
* Pursuing degree in a scientific discipline.
* Must be able to demonstrate effective communication skills.
* Strong mathematical, analytical, and problem-solving abilities.
* Highly motivated and inquisitive with a strong desire to learn.
* Organization skills to manage multiple tasks with strong attention to details.
* Proficiency in Microsoft Office applications (Excel, Word, PowerPoint required; data analysis experience a plus).
* Strong verbal and written communication skills, with the ability to communicate clearly with cross-functional teams.
* Demonstrated initiative, positive attitude, and willingness to learn and support the Materials Management team.
* Ability to wear required personal protective equipment (PPE) and work in an operational environment as needed.
* Must be legally authorized to work in the United States without restriction; no sponsorship offered at this time.
* Must be willing to submit to a background investigation, including verification of employment, criminal history, and educational background.
* Must be willing to take a drug test.
* Must be 18 years of age or older.
Recruiters:
Please note that Hikma has a set roster of approved recruiters for specific roles agreed to in advance and does not accept unsolicited resumes or calls from third-party recruiters or employment agencies regarding open positions. In the absence of a signed agreement and approval from Hikma's Human Resources department to submit resumes for a specific position, Hikma will not approve, nor will be under an obligation to make, any payment to such non-approved third-parties in the event a candidate they refer is hired by Hikma.
Equal Opportunity Employer:
Hikma Pharmaceuticals USA Inc. is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status, or other characteristics protected by law.
#LI-KJ1
Location:
Columbus, OH, US, 43228
Nearest Major Market: Columbus
$19 hourly Auto-Apply 7d ago
Bachelor's-Level Internship - Pathway Caring for Children (Canton, OH)
Pathway Caring for Children 3.7
Canton, OH jobs
Job DescriptionBachelor's-Level Internship - Pathway Caring for Children (Canton, OH)
In-Person • Flexible Schedule • Supervised Learning Experience
Pathway Caring for Children, a nonprofit organization supporting children and families through foster care, adoption, and counseling services, is seeking Bachelor's-level interns in Social Work, Psychology, Human Development, or related fields for for-credit internships.
This placement offers meaningful, hands-on experience in community-based and mental health settings while learning from experienced professionals who are committed to your growth.
Why This Internship Is a Great Fit for Bachelor's Students
In-person or hybrid options available
Flexible scheduling to accommodate classes or work
Weekly supervision with experienced staff
Opportunities to observe counseling and supportive service roles
Exposure to child, family, and community mental health services
Supportive, mission-driven environment where learning is prioritized
What You'll Do
Learn how to complete documentation and intake procedures
Shadow staff in counseling, outreach, and supportive roles
Participate in group activities, team meetings, and program events
Assist with program development and school-based initiatives
Complete required university learning contract tasks
Engage in weekly supervision focused on skill-building, reflection, and professional development
Who Should Apply
Enrolled in a Bachelor's or Associate's degree program in Social Work, Psychology, Human Development, Counseling, or a related field
Internship must be for academic credit
Strong interpersonal and communication skills
Reliable, professional, and eager to learn
Able to meet university learning contract requirements
Background check required before placement
What You'll Gain
Real-world experience in child welfare and community mental health
Opportunities to observe counseling, case coordination, and team collaboration
Professional mentoring and weekly supervision
Skill development to strengthen your résumé and support future graduate school or career goals
Insight into nonprofit operations and multidisciplinary teamwork
How to Apply
Submit your resume and a brief cover letter including:
Your school and degree program
Internship dates and hour requirements
Any specific university requirements
Pathway is a smoke free and drug free organization. All applicants must be able to pass a background check.
Job Posted by ApplicantPro
$27k-34k yearly est. 19d ago
Microbiology Laboratory Internship
PCI Pharma Services 4.1
Rockford, IL jobs
Life changing therapies. Global impact. Bridge to thousands of biopharma companies and their patients. **We are PCI.** Our investment is in People who make an impact, drive progress and create a better tomorrow. Our strategy includes building teams across our global network to pioneer and shape the future of PCI.
**JOB DESCRIPTION:**
Position Title: Microbiology Laboratory Intern
Location: Assembly Drive. Rockford, IL 61109
Department: Lab
Shift: 1st
Reporting To: _Director, Laboratory_
Responsible For (Staff): _None_
Brief Project Description: The Laboratory will have an intern to learn vital skills and assist in the Microbiology Department in day-to-day testing. This testing will include biological indicator testing, preparation of basic microbiology medium(s), collection of environmental monitoring samples from various packaging environments and water testing (total plate count and coliforms). The Microbiology Laboratory intern will work in conjunction with the Senior Microbiologist and Microbiologist to assist in the daily operations of the Microbiology Laboratory. This is a first shift, M-F position.
**ESSENTIAL DUTIES AND RESPONSIBILITIES:**
Learn day-to-day operations of the Microbiology Laboratory and assist Microbiologists in daily testing activities (biological indicator, total plate count, coliform testing, etc). Preparation of basic microbiological medium to be used in testing in addition to preparing poured plates for the Microbiologists to be used in testing. Perform environmental monitoring testing in various packaging environments with various testing equipment. Understanding technical writing requirements for working in a Laboratory/GMP environment. Assist in the day-to-day Laboratory activities such as washing dishes, operating the dishwasher, putting away supplies/reagents, operation of the autoclave, etc. Knowledge of and adherence to all PCI, cGMP, and GCP policies, procedures, and rules. Attendance to work is an essential function of this position Performs other duties as assigned by Manager/Supervisor.
Special Demands:
+ Stationary Position: None
+ Move, Traverse: 3/4 of the day and up.
+ Operate, activate, use, prepare, inspect, or place: 3/4 of the day and up.
+ Install, place, adjust, apply, measure, use, or signal: 3/4 of the day and up.
+ Ascend/Descend or Work Atop: 3/4 of the day and up.
+ Position self (to) or Move (about or to): 3/4 of the day and up.
+ Communicate or exchange information: 3/4 of the day and up.
+ Detect, distinguish, or determine: 3/4 of the day and up.
On an average day, the individual can expect to move and/or transport up to 25 pounds between 1/2 and 3/4 of the day.
**QUALIFICATIONS:**
**Required** :
+ Working toward Bachelor's Degree in related field.
+ College Level Math Skills
+ Advanced Computer Skills: Ability to perform the most complex computer tasks and operate various computer programs.
+ Full Professional Proficiency: Ability to speak, read, and write fluently and accurately on all levels pertinent to professional needs.
+ High Reasoning: Ability to solve practical problems and deal with a variety of concrete variables in situations where there is only limited standardization. Ability to interpret a variety of instructions that may be provided in various forms.
**Preferred** :
+ Ability to effectively present information to various people as the job requires.
+ Ability to work independently and/or part of a team.
+ Ability to display original thinking and creativity.
+ Ability to hold oneself in a professional manner.
_The hiring rate for this position is $20.00hour plus eligibility for an annual performance bonus. Final offer amounts are determined by multiple factors including but not limited to specific and relevant experience, education, credentials, geography, and subject matter expertise. PCI offers full-time employees a competitive benefits package that includes paid time off, health insurance coverage (including dental and vision), flexible spending account, and 401(k)._
Join us and be part of building the bridge between life changing therapies and patients. Let's talk future (*****************
**Equal Employment Opportunity (EEO) Statement:**
_PCI Pharma Services is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status._
_At PCI, Equity and Inclusion are at the core of our company's purpose: Together, delivering life-changing therapies. We are committed to cultivating an inclusive workplace by holding ourselves accountable to the highest standards of understanding, fairness, respect, and equal opportunity - at every level. We envision a PCI community where everyone can belong and grow, and we strive to bring this vision to reality by continuously and intentionally assessing our people practices, policies and programs, marketing approach, and workplace culture._
Why work for PCI Pharma Services?
At PCI, we have an uncompromising focus on providing quality and operational excellence and providing the industry leading customer experience. Our people make all of this happen, so providing an industry leading experience for our people is equally as important. By creating an authentic culture of purposeful work, we aspire to be an interesting and fulfilling place for talented individuals to grow careers. We live a philosophy of intentional learning combined with real-life experience supported by a fair and competitive rewards program. We are individuals, teams and a company that believes in our purpose and our approach is simple, the people who work at PCI fuel our business; we don't say no, we figure out how.
PCI Pharma Services is an Equal Opportunity Employer/Vet/Disabled