12 Manufacturing jobs in Stroudsburg

Immediate need for a talented Quality Control Analyst I (Manufacturing/Quality) 1st Shift . This is a 12+ Months Contract opportunity with long-term potential and is located in Swiftwater, PA (Onsite) . Please review the job description below and contact me ASAP if you are interested.

Employee benefits include, but are not limited to, health insurance (medical, dental, vision), 401(k) plan, and paid sick leave (depending on work location).



Perform operations necessary for quality testing and plays a role in implementing new technology within quality control.

At more senior levels, provide an investigative or technological orientation in designing, executing, interpreting and validating quality procedures and test methods.

Complete routine inspection (i.e. visual and dimension inspection/testing) and sampling of raw materials, in accordance with SOPs for material release and validation.

Conduct data review and preliminary evaluation of results.

Solve problems using limited predetermined options such as repeating the inspections when parameters are not met to determine the cause, etc.

Contacts are primarily with immediate supervisor and other personnel in the section or group.

Skills- Quality control/quality testing

Inspection

raw materials

Pharma/ biotech experience

High level overview, perform incoming inspections, raw materials, packaging, etc.

Local candidates only --Heavy lifting, up to 50 pounds

Ability to pass a visual/ eye exam at health center .

MS Office, Word, Excel, Power Point --Exposure to chemicals: Nice to Have/ Preferred:GMP experience, CAPA, deviations seen as a plus --Pharma/ biotech experience SAP



Our client is a leading Healthcare Industry and we are currently interviewing to fill this and other similar contract positions. If you are interested in this position, please apply online for immediate consideration.



Pyramid Consulting, Inc. provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.



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Immediate need for a talented Quality Control Analyst I (Manufacturing/Quality) 1st Shift . This is a 12+ Months Contract opportunity with long-term potential and is located in Swiftwater, PA (Onsite) . Please review the job description below and contact me ASAP if you are interested.

Job ID:

Pay Range: $25 - $30/hour. Employee benefits include, but are not limited to, health insurance (medical, dental, vision), 401(k) plan, and paid sick leave (depending on work location).

Key Responsibilities:

• Perform operations necessary for quality testing and plays a role in implementing new technology within quality control.
• At more senior levels, provide an investigative or technological orientation in designing, executing, interpreting and validating quality procedures and test methods.
• Complete routine inspection (i.e. visual and dimension inspection/testing) and sampling of raw materials, in accordance with SOPs for material release and validation.
• Aid in the development of test methods.
• Conduct data review and preliminary evaluation of results.
• Solve problems using limited predetermined options such as repeating the inspections when parameters are not met to determine the cause, etc.
• Provide input to the technical composition of operating documentation. Work is closely supervised.
• Follows standard practices to obtain solutions.
• Contribute to the completion of routine technical tasks.
• Failure to achieve results can normally be overcome without serious effect on schedules and programs.
• Contacts are primarily with immediate supervisor and other personnel in the section or group.
• Years of Experience: 1 - 3

Key Requirements and Technology Experience:

• Skills- Quality control/quality testing
• GMP
• SOP
• Inspection
• raw materials
• CAPA, deviations
• Pharma/ biotech experience
• High level overview, perform incoming inspections, raw materials, packaging, etc.
• Fully onsite, potential OT --Possibility of extension --Free parking onsite .
• Minimum Education: AA Degree or higher (strongly preferred)
• Local candidates only --Heavy lifting, up to 50 pounds
• Ability to pass a visual/ eye exam at health center .
• Possible exposure to refrigerated area Must have Skills: --1-3 years of experience in related role .
• Certifications a plus related to: GMP related a plus, or pharm related .
• MS Office, Word, Excel, Power Point --Exposure to chemicals: Isopropyl Alcohol, bleach, disinfectant.
• Nice to Have/ Preferred:GMP experience, CAPA, deviations seen as a plus --Pharma/ biotech experience SAP

Our client is a leading Healthcare Industry and we are currently interviewing to fill this and other similar contract positions. If you are interested in this position, please apply online for immediate consideration.

Pyramid Consulting, Inc. provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.

By applying to our jobs you agree to receive calls, AI-generated calls, text messages, or emails from Pyramid Consulting, Inc. and its affiliates, and contracted partners. Frequency varies for text messages. Message and data rates may apply. Carriers are not liable for delayed or undelivered messages. You can reply STOP to cancel and HELP for help. You can access our privacy policy here .

Primary Duties & Responsibilities

• Performs Epitaxial growth and related technological processes in accordance with instructions from the engineering team. Responsibilities include, but not limited to prepare lot travelers, inspect substrates prior to use, prepare SiC substrates for epi growth, operate reactors and characterization tools, unload wafers (cassettes) on reactors and characterization tools, wafer inspections, enter observations and process records into Database.
• Monitors and adjusts temperature, time, gas flow, power and other process parameters working with engineering. Maintains accurate records of process parameters.
• Supports the development and evolution of operating procedures.
• Supports engineering in other areas such as wafer cleaning and characterization as needed.
• Participates in FMEA activities.
• Participates in troubleshooting of Epitaxial growth equipment when malfunctions occur and perform maintenance on and/or replace Epi growth chamber components.
• Keep epi reactor and characterization areas clean. Actively participates in housekeeping initiatives.
• Follows all health, safety, environmental, ergonomic, and clean room requirements, regulations, and procedures.

Education & Experience

• High School Diploma with 3 years experiences in related technical field.
• Experience in Epi and or Characterization preferred.
• Experience in testing and data analysis, process improvement and equipment maintenance preferred.
• Computer literate. Experience with Microsoft Word, Excel, Outlook, PowerPoint, Email, and Internet.

Skills

• Must be technically inclined with good written, attention to details and mechanical skills.
• Must be well organized and able to perform several tasks in parallel.
• Must be computer-literate to operate computer-controlled equipment and make data entry.
• ITAR compliance requirement: Individual must be a U.S. Citizen, Permanent Resident Alien, or Protected Individual per 8 U.S.C. 1324b(a)(3).
• Strong interpersonal, teamwork skills, and work with our engineering team.

Working Conditions

• 100% on site; day shift 6am to 6pm or night shift 6pm to 6am 3 days on 4 days off, 4 days on 3 days off with swing day on Wednesday.

Physical Requirements

• Ability to work at computer.
• Must be able to lift 40lb parts.

Safety Requirements

All employees are required to follow the site EHS procedures and Coherent Corp. Corporate EHS standards.

Quality and Environmental Responsibilities

Depending on location, this position may be responsible for the execution and maintenance of the ISO 9000, 9001, 14001 and/or other applicable standards that may apply to the relevant roles and responsibilities within the Quality Management System and Environmental Management System.

Culture Commitment

Ensure adherence to company's values (ICARE) in all aspects of your position at Coherent Corp.:

I ntegrity - Create an Environment of Trust

C ollaboration - Innovate Through the Sharing of Ideas

A ccountability - Own the Process and the Outcome

R espect - Recognize the Value in Everyone

E nthusiasm - Find a Sense of Purpose in Work

Coherent Corp. is an equal opportunity/affirmative action employer. All qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected Veteran status, age, or any other characteristic protected by law.

If you need assistance or an accommodation due to a disability, you may contact us at .Coherent is a global leader in lasers, engineered materials and networking components. We are a vertically integrated manufacturing company that develops innovative products for diversified applications in the industrial, optical communications, military, life sciences, semiconductor equipment, and consumer markets. Coherent provides a comprehensive career development platform within an environment that challenges employees to perform at their best, while rewarding excellence and hard-work through a competitive compensation program. It's an exciting opportunity to work for a company that offers stability, longevity and growth. Come Join Us!

Note to recruiters and employment agencies: We will not pay for unsolicited resumes from recruiters and employment agencies unless we have a signed agreement and have required assistance, in writing, for a specific opening.The successful applicant will work with the engineering team with focus on epitaxial growth technology for wide bandgap semiconductors and characterization measurements tools. Will work under the guidance of the epi engineering team and will closely follow the engineering guidelines and written technological procedures/work instructions. Loading substrates (cassettes) into reactors and characterization tools and operating the equipment for epitaxial growth and test measurements. Techs need to follow procedures, work instructions, and SOP's. Perform visual inspections on grown wafers and generate Maps on Characterization tools. Logs process data into run sheets and Epi reactor software. Maintains order and cleanliness in the clean room work areas.

**Job Title:** Summer 2026 Intern - Biologics Manufacturing
**Location:** Swiftwater, PA
**Grade:** Co-op Intern LL
**Hiring manager:** Rhonda Williams
**About the Job**
We deliver 4.3 billion healthcare solutions to people every year, thanks to the flawless planning and meticulous eye for detail of our Manufacturing & Supply teams. With your talent and ambition, we can do even more to protect people from infectious diseases and bring hope to patients and their families.
The intern candidate will be a member of the Manufacturing & Supply team and will participate in a variety of small-scale projects and support activities across Biologics Manufacturing.
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:**
_Tasks may include_
+ Assisting with manufacturing support and troubleshooting,
+ Data integrity
+ Process monitoring
+ Technical writing of protocols/reports
+ Documentation updates
+ Assisting with execution of validations, test scripts, and/or notebook studies.
**About You**
**Basic Qualifications:**
+ Currently enrolled and pursuing a bachelor's degree in engineering, health sciences, or other STEM related field at an accredited college or university with the expectation that you will complete your current degree by the Spring of 2027.
+ Candidate must be currently enrolled the semester after the Internship/Co-Op with Sanofi.
+ **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.**
+ Advanced knowledge of MS Office including Excel, PowerPoint and Word.
+ Must be able to relocate to the office location and work 40hrs/week, Monday-Friday, for the full duration of the co-op/internship.
**Preferred Qualifications:**
+ Demonstrated leadership skills and the desire and ability to work effectively in a team environment
+ Excellent communication and interpersonal skills
+ Adaptability in a changing and challenging environment
+ Strong organizational skills, attention to detail and analytical skills
+ Desire to learn about Pharmaceutical and Vaccine production
+ Major: Life Sciences, Engineering or similar technical field
**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.
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-SP
#LI-SP
#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 ( 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 ( 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 (

Job Title: Quality Control Technician I

Location: Swiftwater, PA- 18370

Duration: 12-month contract

1st Shift: 8 AM – 4:30 PM, M-F

We are looking for someone hands-on with incoming inspection and quality control of raw materials and packaging . The ideal candidate is reliable, detail-oriented, and physically able to handle the demands (lifting up to 50 lbs, working around chemicals, and refrigerated areas). The focus is on entry-level to early-career candidates (1–3 years of experience) with GMP exposure being highly preferred but not strictly mandatory.

They’re looking for someone who can:

• Perform routine inspections (visual/dimensional) of raw materials.
• Work independently but under supervision .
• Follow SOPs and compliance guidelines.
• Support project-related tasks and help with documentation .
• Be local and available onsite , with flexibility for overtime.

Responsibilities / Day-to-Day Tasks (Simplified)

• Inspect raw materials and packaging upon arrival (visual & dimensional checks).
• Perform sampling and testing following SOPs.
• Document inspection results and support technical documentation.
• Conduct data review and initial troubleshooting when results don’t meet standards.
• Assist in method development and validation under supervision.
• Work with supervisors and team members to maintain compliance and quality.
• Handle lifting of materials , possible work in refrigerated areas, and exposure to cleaning chemicals.

Must-Have Keywords / Skills

• Incoming inspection / Raw material inspection
• Quality Control (QC) / Quality Assurance (QA)
• GMP (Good Manufacturing Practices)
• Raw materials, packaging inspection
• Visual inspection / Dimensional testing
• Sampling & data review
• SOP compliance
• MS Office (Word, Excel, PowerPoint)
• Able to lift 50 lbs / work in refrigerated areas
• Eye/visual exam clearance

Nice-to-Have Skills

• GMP certifications
• Pharma / biotech industry experience
• SAP exposure
• CAPA, Deviations handling
• Familiarity with chemicals: isopropyl alcohol, bleach, disinfectants

Job Title: Quality Control Technician I

Location: Swiftwater, PA- 18370

Duration: 12-month contract

1st Shift: 8 AM – 4:30 PM, M-F

We are looking for someone hands-on with incoming inspection and quality control of raw materials and packaging. The ideal candidate is reliable, detail-oriented, and physically able to handle the demands (lifting up to 50 lbs, working around chemicals, and refrigerated areas). The focus is on entry-level to early-career candidates (1–3 years of experience) with GMP exposure being highly preferred but not strictly mandatory.

They’re looking for someone who can:

• Perform routine inspections (visual/dimensional) of raw materials.
• Work independently but under supervision.
• Follow SOPs and compliance guidelines.
• Support project-related tasks and help with documentation.
• Be local and available onsite, with flexibility for overtime.

Responsibilities / Day-to-Day Tasks (Simplified)

• Inspect raw materials and packaging upon arrival (visual & dimensional checks).
• Perform sampling and testing following SOPs.
• Document inspection results and support technical documentation.
• Conduct data review and initial troubleshooting when results don’t meet standards.
• Assist in method development and validation under supervision.
• Work with supervisors and team members to maintain compliance and quality.
• Handle lifting of materials, possible work in refrigerated areas, and exposure to cleaning chemicals.

Must-Have Keywords / Skills

• Incoming inspection / Raw material inspection
• Quality Control (QC) / Quality Assurance (QA)
• GMP (Good Manufacturing Practices)
• Raw materials, packaging inspection
• Visual inspection / Dimensional testing
• Sampling & data review
• SOP compliance
• MS Office (Word, Excel, PowerPoint)
• Able to lift 50 lbs / work in refrigerated areas
• Eye/visual exam clearance

Nice-to-Have Skills

• GMP certifications
• Pharma / biotech industry experience
• SAP exposure
• CAPA, Deviations handling
• Familiarity with chemicals: isopropyl alcohol, bleach, disinfectants

Job Title: Quality Control Technician I

Location: Swiftwater, PA- 18370

Duration: 12-month contract

1st Shift: 8 AM 4:30 PM, M-F

We are looking for someone hands-on with incoming inspection and quality control of raw materials and packaging . The ideal candidate is reliable, detail-oriented, and physically able to handle the demands (lifting up to 50 lbs, working around chemicals, and refrigerated areas). The focus is on entry-level to early-career candidates (13 years of experience) with GMP exposure being highly preferred but not strictly mandatory.

Theyre looking for someone who can:

• Perform routine inspections (visual/dimensional) of raw materials.
• Work independently but under supervision .
• Follow SOPs and compliance guidelines.
• Support project-related tasks and help with documentation .
• Be local and available onsite , with flexibility for overtime.

Responsibilities / Day-to-Day Tasks (Simplified)

• Inspect raw materials and packaging upon arrival (visual & dimensional checks).
• Perform sampling and testing following SOPs.
• Document inspection results and support technical documentation.
• Conduct data review and initial troubleshooting when results dont meet standards.
• Assist in method development and validation under supervision.
• Work with supervisors and team members to maintain compliance and quality.
• Handle lifting of materials , possible work in refrigerated areas, and exposure to cleaning chemicals.

Must-Have Keywords / Skills

• Incoming inspection / Raw material inspection
• Quality Control (QC) / Quality Assurance (QA)
• GMP (Good Manufacturing Practices)
• Raw materials, packaging inspection
• Visual inspection / Dimensional testing
• Sampling & data review
• SOP compliance
• MS Office (Word, Excel, PowerPoint)
• Able to lift 50 lbs / work in refrigerated areas
• Eye/visual exam clearance

Nice-to-Have Skills

• GMP certifications
• Pharma / biotech industry experience
• SAP exposure
• CAPA, Deviations handling
• Familiarity with chemicals: isopropyl alcohol, bleach, disinfectants

**Job Title:** Summer 2026 Intern - Manufacturing & Supply, Smart Process
**Location:** Morristown, NJ / Framingham, MA / Swiftwater, PA
**About the Job**
We deliver 4.3 billion healthcare solutions to people every year, thanks to the flawless planning and meticulous eye for detail of our Manufacturing & Supply teams. With your talent and ambition, we can do even more to protect people from infectious diseases and bring hope to patients and their families.
The Global Process Intern will support the Manufacturing and Supply Business Process Owners team in the implementation of the "In Use" metrics for M&S ERP solutions, internal communication of business process advancements, and restructuring and optimization of the Business Process website which includes trainings and documentations. There is a great opportunity to understand and gain experience in business process optimization for pharmaceutical manufacturing and supply processes.
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:**
+ Support the implementation of the "In-Use" MySUA (Solution Usage Adherence) measures
+ Own and publish monthly business process newsletter
+ Restructure and optimize internal training and documentation repository website
**About You**
**Basic Qualifications:**
+ Currently pursuing a bachelor's or master's degree in engineering, information technology, computer science, or related field at an accredited college or university with the expectation that you will complete your current degree by the Spring of 2027
+ 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:**
+ English Speaker, French or other languages a plus
+ Accountability and Reliability
+ Target orientated with an agreeable character and can-do attitude
+ Able to lead / animate networks, teams, experts
+ Analytical, process-oriented with drive for continuous improvements and simplification
+ Strong communication skills with ability to train and teach/coach others
+ Tenacity and energy in leading change
+ Ability to work out of comfort zone
**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.
+ 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.
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 ( 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 ( 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 (

**Job Title:** Vaccine Process Development Intern, Manufacturing Technology -Summer 2026 Intern
**Location:** Swiftwater, PA
**About the Job**
We deliver 4.3 billion healthcare solutions to people every year, thanks to the flawless planning and meticulous eye for detail of our Manufacturing & Supply teams. With your talent and ambition, we can do even more to protect people from infectious diseases and bring hope to patients and their families.
Sanofi, a global healthcare leader, discovers, develops, and distributes therapeutic solutions focused on patients' needs. Sanofi Pasteur, the vaccines division of Sanofi, is the largest company in the world devoted entirely to human vaccines. Our driving goal is to protect people from infectious diseases by creating safe and effective vaccines. Our company distributes more than 1 billion doses of vaccine each year, making it possible to vaccinate more than 500 million people across the globe. Sanofi Pasteur offers the broadest range of vaccines in the world, providing protection against 20 bacterial and viral diseases.
The Swiftwater, PA site is an end-to-end vaccine manufacturing site which includes both upstream drug substance manufacturing (seed and vaccine antigen manufacturing), as well as downstream drug product manufacturing (formulation, filling, inspection, and packaging). The site is located on over 500 acres in the Poconos mountains.
Manufacturing Sciences, Analytics and Technology department (MSAT) drives the vaccines industrialization and improvement of processes and products. It embarks new technologies and digital trends and is the keeper of manufacturing process knowledge. MSAT is at the crossroads of R&D and production as the team is spread over nine production sites. The successful candidate will join the Bacterial Process Development group of MSAT supporting manufacturing and development of vaccines.
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:**
+ Conduct scientific experiments (e.g., process development or manufacturing troubleshooting studies) in a safe manner within the regulations of a chemistry lab
+ Literature search and data analysis
+ Maintain proper records (lab notebook, files, etc.)
**About You**
**Basic Qualifications:**
+ Currently working towards a bachelor's degree in Chemistry, Biological Sciences, Life Sciences, Chemical Engineering or similar at an accredited university with GPA >3.0
+ Advanced knowledge of MS Office including Excel, PowerPoint, and Word
+ 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:**
+ Prior laboratory research experience in organic chemistry or biochemistry strongly preferred
+ Passionate about research, organized, detail and results oriented
+ Excellent record-keeping skills, excellent verbal and written communication skills
+ Analytical thinking, integrity, persistence, and energy
**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-SP
#LI-SP
#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 ( 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 ( 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 (