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Vaccine Manufacturing Jobs (NOW HIRING)

Technician, Operations

Durham, NC · On-site

$57K - $91K/yr

The individual in this position will support the vaccine manufacturing process through hands on processing activities. Key responsibilities for the Production Associate include the execution of ...

The individual in this position will support the vaccine manufacturing process through hands on processing activities. Key responsibilities for the Production Associate include the execution of ...

$57K - $91K/yr

The individual in this position will support the vaccine manufacturing process through hands on processing activities. • Key responsibilities for the Production Associate include the execution of ...

... vaccine, pharmaceutical, or biotechnology manufacturing Demonstrated experience leading large teams in regulated environments (cGMP, USDA, FDA, or similar) Experience implementing LEAN manufacturing ...

This is a hybrid role, focused on the startup and future routine operation of the vaccine manufacturing facility.- Utilizing a team concept, this role will spend a portion of time working in a Bio ...

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Vaccine Manufacturing information

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$13

$24

$34

How much do vaccine manufacturing jobs pay per hour?

As of Jun 12, 2026, the average hourly pay for vaccine manufacturing in the United States is $24.95, according to ZipRecruiter salary data. Most workers in this role earn between $20.19 and $28.85 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in the Vaccine Manufacturing position, and why are they important?

To excel in Vaccine Manufacturing, you need a solid background in biology, chemistry, or related sciences, often supported by a relevant degree or technical training. Familiarity with Good Manufacturing Practices (GMP), aseptic processing, and laboratory equipment is crucial, and certifications such as Six Sigma or lean manufacturing can be beneficial. Attention to detail, teamwork, and strong problem-solving abilities help you excel in fast-paced, highly regulated environments. These skills ensure vaccine safety, process efficiency, and compliance with strict industry standards.

What are the typical daily responsibilities in a Vaccine Manufacturing role?

In a Vaccine Manufacturing position, your daily responsibilities may include preparing and operating equipment, monitoring production processes, conducting quality control tests, and maintaining a sterile environment. You'll document each step carefully to meet regulatory requirements and may troubleshoot issues as they arise. Collaboration with quality assurance, engineering, and supply chain teams is common to ensure smooth and compliant production. This role is ideal for detail-oriented individuals who enjoy working as part of a mission-driven team to deliver high-impact healthcare solutions.

What is a Vaccine Manufacturing job?

A Vaccine Manufacturing job involves overseeing the production of vaccines, ensuring they are safely and efficiently manufactured. Professionals in this field work in specialized facilities, following strict regulatory guidelines to maintain quality and safety. Their responsibilities may include managing raw materials, operating production equipment, conducting quality control checks, and ensuring compliance with government health regulations. This role is critical in producing vaccines that protect public health and prevent the spread of infectious diseases.

More about Vaccine Manufacturing jobs
What are the most commonly searched types of Vaccine Manufacturing jobs? The most popular types of Vaccine Manufacturing jobs are:
What states have the most Vaccine Manufacturing jobs? States with the most job openings for Vaccine Manufacturing jobs include:
Infographic showing various Vaccine Manufacturing job openings in the United States as of June 2026, with employment types broken down into 92% Full Time, 6% Part Time, and 2% Nights. Highlights an 96% Physical, 2% Hybrid, and 2% Remote job distribution, with an average salary of $51,890 per year, or $24.9 per hour.
Vaccine Manufacturing Technician

Vaccine Manufacturing Technician

Sanofi EU

Scranton, PA

Full-time

Posted 2 days ago


Job description

Job Title: Production Technician

Location: Swiftwater, PA

This is either 1st, 2nd or 3rd shift position. Must be able to work weekends and holidays as needed.

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. Your job, as a Production Technician - Vaccine within our Biologics Team, will have the potential to transform the practice of medicine, turning the impossible into possible for millions of people.

 

We are an innovative global healthcare company that helps the world stay ahead of infectious diseases by delivering more than 500 million vaccine doses a year. Across different countries, our talented teams are exploring new technologies to protect people and promote healthy communities. We chase the miracles of science every single day, pursuing Progress to make a real impact on millions of patients around the world.

Sanofi is seeking a motivated professional candidate to operate within Biologics production and perform manufacturing activities. This is an exciting opportunity for a candidate to develop technical skills and learn about the biopharmaceutical industry.   The production technician will operate in a cGMP manufacturing area performing equipment set up and operations tasks to meet all standards for safety, quality, and efficiency.  The candidate will perform production in accordance with volume fluctuation, business need, and effective procedures. 

Job Duties and Responsibilities:

  • Ensuring that processes are always compliant with FDA regulations.

  • Works to become trained in all assigned training modules.

  • Identifying and preventing deviations and assisting in investigation and root cause analysis.

  • Helping with deviation investigations, Corrective and Preventive Actions (CAPA), Change Control Requests (CCR), and other assigned projects.

  • Ensuring that quality documents like Batch Production Records (BPRs) and logbooks are completed accurately and on time.  

  • Ensuring documentation is completed accurately and in real-time is crucial for compliance and quality control.

  • Preparing areas for the next shift helping to maintain smooth operations and efficiency.

  • Responsibly use material in an efficient manner to reduce waste.

  • Sharing improvement ideas, issues, and concerns with team members along with providing solutions.

  • Proactive in identifying and solving production issues to ensure smooth operations.

  • Model and uphold HSEEn standards, ensuring compliance with all safety procedures.

  • Report safety concerns, near misses, equipment issues, and environmental incidents promptly.

  • Participate in safety meetings, walkthroughs, and improvement initiatives.

  • Maintain a clean, organized, and safe work environment, performing necessary checks and inspections.

  • Support continuous improvement by providing input on corrective and preventive actions.

  • All other duties as assigned.

About You

Required Qualifications

  • High School Diploma with 0-6 months of experience.

  • Good mechanical skills, computer skills and detail oriented.

  • Must have basic mechanical aptitude, computer skills, good comprehension skills, retention skills, troubleshooting and manual dexterity.

  • Proficiency in at least not limited to one area of operation or product line.

Preferred Qualifications

  • Bachelor’s degree

  • 6-month experience in a cGMP environment or pharmaceutical experience.

*For Manufacturing & Supply Only*

Special Working Conditions

  • Ability to lift up to 50 lbs.

  • Ability to stand on average 8 hours per shift.

  • Ability to gown and gain entry to manufacturing areas.

  • Ability to work a twelve-hour rotating shift and every other weekend, including holidays as scheduled.

  • May require personnel to flex into another platform within MTech and/or another M&S department, as well as the possibility to work weekends, holidays or off shift hours based on business need.

  • May also include working in an aseptic processing area.

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.​

THE FINE PRINT 

  • For influenza production roles (excluding FFIP roles): candidate must be able to be receive influenza vaccine which is required for building access

  • For aseptic area production roles (excluding Flu production tech roles): candidate must be able to obtain and maintain current aseptic gowning qualification

  • This position may be required to be moved or temporarily flexed to another department or building within the FFIP operation due to business needs. Additionally, candidates should expect to work in multiple buildings. Some over-time/off-shift work hours may be required based on business needs. We will attempt to provide as much advance notice as possible, two weeks where applicable if any such change is needed.

  • Must be able to lift up to 25 lbs., and bend/lift/move objects as part of the job.

  • Able to stand for up to 8 hours a day (with occasional breaks)

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.

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All compensation will be determined commensurate with demonstrated experience. Employees may be eligible to participate in Company employee benefit programs, and additional benefits information can be found here.