6,308 Biotech jobs in the United States

Biotech Research Assistant

89101 Sunrise Manor, Nevada $55000 Annually WhatJobs

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contractor
Our client, a cutting-edge biotechnology research firm, is seeking a dedicated Biotech Research Assistant to join their innovative laboratory in Las Vegas, Nevada, US . This role is pivotal in supporting ongoing scientific research and development projects, focusing on (mention a specific fictional biotech field, e.g., gene editing, cellular therapies, drug discovery). The Research Assistant will work closely with scientists and principal investigators, contributing to critical experiments and data analysis. Key responsibilities include preparing laboratory reagents and solutions, performing a variety of molecular and cellular assays, maintaining cell cultures, operating and maintaining laboratory equipment, and meticulously recording experimental data. You will also be involved in troubleshooting experimental protocols and contributing to the interpretation of results. The ideal candidate possesses a Bachelor's degree in Biology, Biotechnology, Molecular Biology, or a related life science field, coupled with hands-on laboratory experience. Proficiency in standard laboratory techniques such as PCR, Western blotting, cell culture, and sterile techniques is essential. Strong analytical skills, meticulous attention to detail, and a commitment to scientific rigor are paramount. We are looking for individuals who are eager to learn, highly organized, and capable of working both independently and as part of a collaborative research team. This is an excellent opportunity for individuals looking to build a career in scientific research and development, contributing to groundbreaking advancements in biotechnology.

Key Responsibilities:
  • Perform laboratory experiments and assays according to established protocols.
  • Prepare reagents, media, and solutions for experiments.
  • Maintain sterile cell cultures and perform related techniques.
  • Operate and maintain laboratory equipment, ensuring proper calibration.
  • Collect, record, and analyze experimental data accurately.
  • Assist in troubleshooting experimental procedures and optimizing protocols.
  • Contribute to the preparation of research reports and presentations.
  • Maintain a clean and organized laboratory environment.

Qualifications:
  • Bachelor's degree in Biology, Biotechnology, or a related life science field.
  • Hands-on experience with molecular and cellular biology techniques.
  • Proficiency in aseptic techniques and cell culture.
  • Familiarity with laboratory equipment operation and maintenance.
  • Strong analytical skills and attention to detail.
  • Excellent data recording and documentation abilities.
  • Ability to work collaboratively in a scientific research setting.
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Microbiology/ Nanotech/ Biotech Research Scientist

94039 Mountainview, California US Tech Solutions

Posted 4 days ago

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**Job Description:**
+ You'll be responsible for carrying out experimentation and data logging/aggregation/management that will enable deep cross-disciplinary technical projects spanning technology spaces ranging from: Microbiology, Chemistry, Microbiology, Electronics, Metallurgy, Micro and Nano Technology, and more.
+ You will need to work independently and change direction quickly and often. You'll be a key part of accelerating very early-stage projects to the next level.
+ The experiments you'll perform, the tests you'll run, and the data you'll collect, documentation you'll create will provide much of the evidence to make decisions about the future of projects and their potential to impact the world.
**Responsibilities:**
+ Execute experimental splits efficiently and effectively
+ Suggest the next step in an experimental process
+ Come to every interaction with a solution not a problem
+ Apply your cross-disciplinary knowledge to novel concepts
**Experience:**
+ You should be comfortable with instruments and technologies including:
+ Electronic test and measurement - Potentiometers, potentiostat, etc.
+ Liquid handling and biological sample prep - both manual and automated
+ Laboratory Environmental Chambers - Glove Boxes, Fume hoods
+ Analytical techniques - Microscopes, Spectrometers,
+ Chemical and Materials handling experience.
+ Debugging complex systems comprising hardware and custom software
+ You have an obsessive drive to get to the bottom of every problem you're presented with.
+ You are meticulous, detail oriented, data driven, able to prioritize responsibilities, multi-task, work under deadlines, and stay agile.
+ You thrive in a dynamic hands-on environment.
+ Highly proficient in data analysis
US Tech Solutions is a global staff augmentation firm providing a wide range of talent on-demand and total workforce solutions. To know more about US Tech Solutions, please visit ( .
US Tech Solutions is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.
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Senior Research Scientist - Biotech

80201 Denver, Colorado $130000 Annually WhatJobs

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Job Description

full-time
Our client, a leader in biotechnological innovation, is seeking a highly skilled Senior Research Scientist to join their pioneering team. This is a fully remote position, focused on advancing cutting-edge research and development in the field of (Specify area, e.g., gene therapy, immunology, diagnostics). As a Senior Research Scientist, you will design and execute complex experiments, analyze biological data, and contribute to the discovery and development of novel therapeutic or diagnostic solutions. You will play a pivotal role in hypothesis generation, experimental design, data interpretation, and the preparation of research findings for publication and presentation. This role requires a deep understanding of molecular biology, cell biology, biochemistry, or a related life science discipline, along with expertise in (mention specific techniques/assays, e.g., CRISPR, Next-Generation Sequencing, flow cytometry). You will collaborate with a multidisciplinary team of scientists, clinicians, and engineers to drive research projects from conceptualization to preclinical stages. Exceptional analytical, problem-solving, and communication skills are essential, as is the ability to interpret complex scientific data and communicate findings effectively. This remote position offers an exciting opportunity to contribute to groundbreaking scientific advancements in a flexible work environment.

Key responsibilities:
  • 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.

Qualifications:
  • 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.
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Principal Research Scientist - Biotech

10001 New York, New York $170000 Annually WhatJobs

Posted today

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Job Description

full-time
Our client, a world-renowned research institution, is looking for an exceptional Principal Research Scientist to lead groundbreaking studies in biotechnology at their state-of-the-art facility in New York City, New York, US . This senior leadership role is dedicated to advancing scientific discovery and developing innovative solutions in the biotech field. The Principal Research Scientist will be responsible for designing and conducting complex research projects, analyzing experimental data, and interpreting results to contribute to novel advancements. You will lead a team of researchers, mentor junior scientists, and collaborate with internal and external partners on interdisciplinary projects. Key responsibilities include developing research methodologies, securing grant funding, publishing findings in peer-reviewed journals, and presenting research at international conferences. The ideal candidate will hold a Ph.D. in Biotechnology, Molecular Biology, Biochemistry, or a closely related scientific discipline, with a minimum of 10 years of post-doctoral research experience. A strong publication record and a history of successful grant acquisition are essential. Proven experience in leading research teams and managing laboratory operations is required. Expertise in specific areas such as gene editing, protein engineering, cell-based assays, or bioinformatics is highly desirable. Exceptional analytical, critical thinking, and communication skills are paramount for success in this role. This is a unique opportunity to drive cutting-edge research and make significant contributions to the field of biotechnology. Our client offers a highly competitive compensation package, comprehensive benefits, and an intellectually stimulating environment with access to advanced technologies and resources.
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Senior Biotech

Newington, New Hampshire Lonza

Posted 1 day ago

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Job Description

Posted Job Advert

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.

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Senior Biotech

03825 Barrington, New Hampshire Lonza

Posted 1 day ago

Job Viewed

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Job Description

Posted Job Advert

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.

View Now

Senior Biotech

03858 Newton, New Hampshire Lonza

Posted 1 day ago

Job Viewed

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Job Description

Posted Job Advert

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.

View Now
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Senior Biotech

03824 Durham, New Hampshire Lonza

Posted 1 day ago

Job Viewed

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Job Description

Posted Job Advert

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.

View Now

Senior Biotech

03862 North Hampton, New Hampshire Lonza

Posted 1 day ago

Job Viewed

Tap Again To Close

Job Description

Posted Job Advert

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.

View Now

Senior Biotech

03891 Danville, New Hampshire Lonza

Posted 1 day ago

Job Viewed

Tap Again To Close

Job Description

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.

View Now
 

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