6,308 Biotech jobs in the United States

• Design, conduct, and optimize complex experiments to address specific research questions.
• Analyze and interpret large datasets using advanced statistical and bioinformatics tools.
• Develop and validate novel assays and experimental methodologies.
• Contribute to the development of new therapeutic candidates or diagnostic tools.
• Stay abreast of the latest scientific literature and technological advancements in the field.
• Collaborate with cross-functional teams to integrate research findings into broader project goals.
• Prepare scientific manuscripts for publication in peer-reviewed journals.
• Present research findings at internal meetings and external scientific conferences.
• Mentor junior scientists and research associates.
• Ensure compliance with laboratory safety protocols and regulatory guidelines.

• Ph.D. in Molecular Biology, Cell Biology, Biochemistry, Immunology, Genetics, or a related life science discipline.
• Minimum of 5 years of postdoctoral research experience or equivalent industry experience in R&D.
• Proven track record of successfully designing and executing complex research projects.
• Extensive hands-on experience with (mention key techniques/methodologies relevant to the field).
• Proficiency in data analysis software (e.g., R, Python, GraphPad Prism) and bioinformatics tools.
• Strong understanding of scientific principles and research methodologies.
• Excellent written and verbal communication skills, with experience in scientific writing and presentation.
• Demonstrated ability to think critically, solve problems, and work independently.
• Ability to collaborate effectively in a remote, team-oriented environment.
• A strong publication record in reputable scientific journals is highly desirable.

Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is dedicated people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that’s the kind of work we want you to be part of!

We are seeking a motivated and detail-oriented Biotechnologist I to join our production team in Portsmouth, NH. This full-time, on-site role supports day shift operations (7 AM – 7 PM) on a rotational schedule. The Biotechnologist I is responsible for the manufacture of therapeutic proteins (API) under current Good Manufacturing Practices (cGMP). Working under close supervision, associates will execute process recipes, follow written procedures (SOPs), monitor equipment and processes, and perform basic laboratory tasks such as pH and conductivity testing and sampling.

This role also includes routine sanitization tasks to maintain facility and equipment standards, and requires the demonstration of aseptic technique in handling products and materials. The ideal candidate will be eager to learn, comfortable asking questions, and committed to maintaining compliance with cGMP and GDP standards.

Schedule

Rotational: 2 on, 2 off, 3 on, 2 off, 2 on, 3 off (repeat)
Day Shift: 7:00 AM – 7:00 PM
Weekend shifts include additional pay.

Key Responsibilities

• Set up, operate, and monitor production equipment and processes, including Clean-in-Place (CIP) and Steam-in-Place (SIP) operations.

• Document production activities in accordance with Good Manufacturing Practices (GMPs) and Good Documentation Practices (GDPs).

• Attain and maintain qualifications for assigned tasks and keep individual training plans up to date.

• Perform basic laboratory tasks such as monitoring pH, conductivity, and testing product samples.

• Transfer raw materials and chemicals across production areas.

• Maintain the cleanliness and organization of facilities and equipment; support 6S programs.

• Participate in administrative tasks, including shift exchanges, meetings, emails, and project involvement.

• Perform other duties as assigned.

Required Qualifications

High school diploma or equivalent.

Experience in GMP, biotech, or pharmaceutical environments is a plus but not required.

Preferred Skills

Strong attention to detail.

Comfortable asking questions and following Standard Operating Procedures (SOPs).

Reporting Structure

Reports to a Shift Supervisor.

Every day, Lonza’s products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically.

People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference!

Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law.

Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is dedicated people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that’s the kind of work we want you to be part of!

We are seeking a motivated and detail-oriented Biotechnologist I to join our production team in Portsmouth, NH. This full-time, on-site role supports day shift operations (7 AM – 7 PM) on a rotational schedule. The Biotechnologist I is responsible for the manufacture of therapeutic proteins (API) under current Good Manufacturing Practices (cGMP). Working under close supervision, associates will execute process recipes, follow written procedures (SOPs), monitor equipment and processes, and perform basic laboratory tasks such as pH and conductivity testing and sampling.

This role also includes routine sanitization tasks to maintain facility and equipment standards, and requires the demonstration of aseptic technique in handling products and materials. The ideal candidate will be eager to learn, comfortable asking questions, and committed to maintaining compliance with cGMP and GDP standards.

Schedule

Rotational: 2 on, 2 off, 3 on, 2 off, 2 on, 3 off (repeat)
Day Shift: 7:00 AM – 7:00 PM
Weekend shifts include additional pay.

Key Responsibilities

• Set up, operate, and monitor production equipment and processes, including Clean-in-Place (CIP) and Steam-in-Place (SIP) operations.

• Document production activities in accordance with Good Manufacturing Practices (GMPs) and Good Documentation Practices (GDPs).

• Attain and maintain qualifications for assigned tasks and keep individual training plans up to date.

• Perform basic laboratory tasks such as monitoring pH, conductivity, and testing product samples.

• Transfer raw materials and chemicals across production areas.

• Maintain the cleanliness and organization of facilities and equipment; support 6S programs.

• Participate in administrative tasks, including shift exchanges, meetings, emails, and project involvement.

• Perform other duties as assigned.

Required Qualifications

High school diploma or equivalent.

Experience in GMP, biotech, or pharmaceutical environments is a plus but not required.

Preferred Skills

Strong attention to detail.

Comfortable asking questions and following Standard Operating Procedures (SOPs).

Reporting Structure

Reports to a Shift Supervisor.

Every day, Lonza’s products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically.

People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference!

Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law.

Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is dedicated people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that’s the kind of work we want you to be part of!

We are seeking a motivated and detail-oriented Biotechnologist I to join our production team in Portsmouth, NH. This full-time, on-site role supports day shift operations (7 AM – 7 PM) on a rotational schedule. The Biotechnologist I is responsible for the manufacture of therapeutic proteins (API) under current Good Manufacturing Practices (cGMP). Working under close supervision, associates will execute process recipes, follow written procedures (SOPs), monitor equipment and processes, and perform basic laboratory tasks such as pH and conductivity testing and sampling.

This role also includes routine sanitization tasks to maintain facility and equipment standards, and requires the demonstration of aseptic technique in handling products and materials. The ideal candidate will be eager to learn, comfortable asking questions, and committed to maintaining compliance with cGMP and GDP standards.

Schedule

Rotational: 2 on, 2 off, 3 on, 2 off, 2 on, 3 off (repeat)
Day Shift: 7:00 AM – 7:00 PM
Weekend shifts include additional pay.

Key Responsibilities

• Set up, operate, and monitor production equipment and processes, including Clean-in-Place (CIP) and Steam-in-Place (SIP) operations.

• Document production activities in accordance with Good Manufacturing Practices (GMPs) and Good Documentation Practices (GDPs).

• Attain and maintain qualifications for assigned tasks and keep individual training plans up to date.

• Perform basic laboratory tasks such as monitoring pH, conductivity, and testing product samples.

• Transfer raw materials and chemicals across production areas.

• Maintain the cleanliness and organization of facilities and equipment; support 6S programs.

• Participate in administrative tasks, including shift exchanges, meetings, emails, and project involvement.

• Perform other duties as assigned.

Required Qualifications

High school diploma or equivalent.

Experience in GMP, biotech, or pharmaceutical environments is a plus but not required.

Preferred Skills

Strong attention to detail.

Comfortable asking questions and following Standard Operating Procedures (SOPs).

Reporting Structure

Reports to a Shift Supervisor.

Every day, Lonza’s products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically.

People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference!

Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law.

Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is dedicated people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that’s the kind of work we want you to be part of!

We are seeking a motivated and detail-oriented Biotechnologist I to join our production team in Portsmouth, NH. This full-time, on-site role supports day shift operations (7 AM – 7 PM) on a rotational schedule. The Biotechnologist I is responsible for the manufacture of therapeutic proteins (API) under current Good Manufacturing Practices (cGMP). Working under close supervision, associates will execute process recipes, follow written procedures (SOPs), monitor equipment and processes, and perform basic laboratory tasks such as pH and conductivity testing and sampling.

This role also includes routine sanitization tasks to maintain facility and equipment standards, and requires the demonstration of aseptic technique in handling products and materials. The ideal candidate will be eager to learn, comfortable asking questions, and committed to maintaining compliance with cGMP and GDP standards.

Schedule

Rotational: 2 on, 2 off, 3 on, 2 off, 2 on, 3 off (repeat)
Day Shift: 7:00 AM – 7:00 PM
Weekend shifts include additional pay.

Key Responsibilities

• Set up, operate, and monitor production equipment and processes, including Clean-in-Place (CIP) and Steam-in-Place (SIP) operations.

• Document production activities in accordance with Good Manufacturing Practices (GMPs) and Good Documentation Practices (GDPs).

• Attain and maintain qualifications for assigned tasks and keep individual training plans up to date.

• Perform basic laboratory tasks such as monitoring pH, conductivity, and testing product samples.

• Transfer raw materials and chemicals across production areas.

• Maintain the cleanliness and organization of facilities and equipment; support 6S programs.

• Participate in administrative tasks, including shift exchanges, meetings, emails, and project involvement.

• Perform other duties as assigned.

Required Qualifications

High school diploma or equivalent.

Experience in GMP, biotech, or pharmaceutical environments is a plus but not required.

Preferred Skills

Strong attention to detail.

Comfortable asking questions and following Standard Operating Procedures (SOPs).

Reporting Structure

Reports to a Shift Supervisor.

Every day, Lonza’s products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically.

People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference!

Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law.

Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is dedicated people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that’s the kind of work we want you to be part of!

We are seeking a motivated and detail-oriented Biotechnologist I to join our production team in Portsmouth, NH. This full-time, on-site role supports day shift operations (7 AM – 7 PM) on a rotational schedule. The Biotechnologist I is responsible for the manufacture of therapeutic proteins (API) under current Good Manufacturing Practices (cGMP). Working under close supervision, associates will execute process recipes, follow written procedures (SOPs), monitor equipment and processes, and perform basic laboratory tasks such as pH and conductivity testing and sampling.

This role also includes routine sanitization tasks to maintain facility and equipment standards, and requires the demonstration of aseptic technique in handling products and materials. The ideal candidate will be eager to learn, comfortable asking questions, and committed to maintaining compliance with cGMP and GDP standards.

Schedule

Rotational: 2 on, 2 off, 3 on, 2 off, 2 on, 3 off (repeat)
Day Shift: 7:00 AM – 7:00 PM
Weekend shifts include additional pay.

Key Responsibilities

• Set up, operate, and monitor production equipment and processes, including Clean-in-Place (CIP) and Steam-in-Place (SIP) operations.

• Document production activities in accordance with Good Manufacturing Practices (GMPs) and Good Documentation Practices (GDPs).

• Attain and maintain qualifications for assigned tasks and keep individual training plans up to date.

• Perform basic laboratory tasks such as monitoring pH, conductivity, and testing product samples.

• Transfer raw materials and chemicals across production areas.

• Maintain the cleanliness and organization of facilities and equipment; support 6S programs.

• Participate in administrative tasks, including shift exchanges, meetings, emails, and project involvement.

• Perform other duties as assigned.

Required Qualifications

High school diploma or equivalent.

Experience in GMP, biotech, or pharmaceutical environments is a plus but not required.

Preferred Skills

Strong attention to detail.

Comfortable asking questions and following Standard Operating Procedures (SOPs).

Reporting Structure

Reports to a Shift Supervisor.

Every day, Lonza’s products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically.

People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference!

Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law.

Today, Lonza is a global leader in life sciences operating across three continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that’s the kind of work we want to be part of.

Level I associates have the remarkable opportunity to be part of a high-reaching team at Lonza, where premier biotechnological solutions come to life! Our Biotechnologist I role is critical to our manufacturing operations in New Hampshire. This position is ideal for those who strive to deliver outstanding performance and are passionate about making a difference in the life sciences field!

This position is for the day shift from 7 AM-7 PM, on a rotational schedule every other week:

• Week 1: M/T - F/SAT/SUN

• Week 2: W/TH

• Shift differentials are included for weekends worked
  

Key Responsibilities:

• Operate and maintain equipment, supervise production processes, and meticulously report production in both written and electronic formats. Follow GMPs and GDPs, troubleshoot issues, and review documentation to ensure strict compliance.

• Exhibit expertise in suite-specific production activities and laboratory tasks such as bioreactor inoculation and chromatography column operation. Understand and apply the scientific theories behind these processes. You may also be responsible for training other associates on these tasks and theories.

• Run administrative tasks, including attending shift exchanges, participating in meetings, sending and receiving emails, and engaging in projects. In addition, you will be involved in technical writing, such as documenting deviations and completing document change forms.

• Attain and maintain qualification for all assigned tasks and adhere to an individual training plan to ensure continuous improvement and compliance.

• Perform material movements, including the transfer of raw materials and chemicals into, out of, and across production areas. Other duties may be assigned as needed.
  

Key Requirements:

• Confirmed working experience in manufacturing, preferably in a cGMP setting, or some experience as an Associate Level I in the bio-pharma industry.

• Proven logical decision-making abilities, critical thinking skills, and strong written and verbal communication skills.

• Flexibility to adapt to changing business priorities, live the cultural beliefs, and actively seek and implement feedback to improve performance.
  

Every day, Lonza’s products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically.

People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference.

Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law.