4,460 Biotechnology jobs in the United States

• Design, plan, and execute complex experiments in molecular biology, cell biology, or biochemistry.
• Develop and optimize new laboratory protocols and methodologies.
• Analyze experimental data using statistical software and present findings in internal meetings and scientific publications.
• Operate and maintain sophisticated laboratory equipment and instrumentation.
• Troubleshoot experimental issues and propose solutions.
• Collaborate with cross-functional teams, including R&D, clinical, and regulatory affairs.
• Contribute to the preparation of research proposals, grant applications, and reports.
• Maintain detailed and accurate laboratory notebooks and records.
• Mentor junior research staff and provide technical guidance.
• Stay current with scientific literature and emerging technologies in the field.

• Ph.D. in Molecular Biology, Cell Biology, Biochemistry, Genetics, or a related field.
• Minimum of 3-5 years of post-doctoral or industry research experience.
• Proven expertise in specific techniques relevant to biotechnology research (e.g., PCR, Western blotting, ELISA, cell culture, gene editing, protein expression and purification).
• Strong understanding of experimental design and statistical analysis.
• Proficiency in data analysis software (e.g., GraphPad Prism, R, Python).
• Excellent written and oral communication skills, with experience in scientific writing.
• Demonstrated ability to work independently and as part of a collaborative research team.
• Strong problem-solving skills and critical thinking abilities.
• Experience with bioinformatics tools and databases is a plus.
• A commitment to scientific rigor and ethical research practices.

• Designing and conducting complex experiments in molecular biology, cell biology, and/or biochemistry.
• Developing and optimizing new assays, protocols, and research methodologies.
• Performing data analysis using statistical software and interpreting experimental results.
• Troubleshooting experimental challenges and proposing solutions.
• Collaborating with a multidisciplinary team of scientists and engineers to achieve project goals.
• Maintaining meticulous laboratory notebooks and documentation of research activities.
• Presenting research findings at internal meetings and potentially at external scientific conferences.
• Staying current with the latest scientific literature and technological advancements in the field.
• Contributing to the intellectual property strategy through patent filings and publications.
• Ensuring compliance with laboratory safety standards and regulatory requirements.
• Mentoring junior researchers and technicians as needed.

• Design, conduct, and analyze complex experiments in the field of biotechnology.
• Develop and optimize novel experimental protocols and techniques.
• Perform advanced laboratory procedures, including cell culture, molecular cloning, PCR, Western blotting, and chromatography.
• Analyze experimental data using statistical methods and relevant software.
• Interpret results, draw conclusions, and contribute to scientific publications and presentations.
• Collaborate with team members to identify research objectives and develop project plans.
• Troubleshoot experimental issues and propose solutions.
• Maintain accurate and detailed laboratory notebooks and records.
• Stay abreast of the latest scientific literature and technological advancements in the field.
• Contribute to the preparation of grant proposals and research reports.

• PhD in Biotechnology, Molecular Biology, Biochemistry, Genetics, or a related life science discipline.
• 3+ years of post-doctoral or industry research experience in a relevant field.
• Proven expertise in experimental design, execution, and data analysis.
• Hands-on experience with a range of molecular and cell biology techniques.
• Proficiency in scientific data analysis software (e.g., GraphPad Prism, R, Python).
• Excellent written and verbal communication skills, with a strong publication record.
• Ability to work independently and collaboratively in a fast-paced research environment.
• Strong problem-solving skills and a creative approach to scientific challenges.
• Familiarity with regulatory requirements and quality standards in R&D is a plus.

• Designing, executing, and optimizing experiments to investigate therapeutic targets and pathways.
• Developing and validating new assays for screening compounds and evaluating drug efficacy.
• Utilizing a range of molecular biology techniques, including PCR, qPCR, Western blotting, ELISA, and cell-based assays.
• Conducting in vitro and ex vivo studies to assess drug candidates in relevant biological models.
• Analyzing experimental data using statistical software and drawing accurate conclusions.
• Troubleshooting experimental challenges and proposing solutions to maintain project momentum.
• Maintaining meticulous records of experimental procedures, results, and data in electronic lab notebooks.
• Collaborating closely with cross-functional teams, including chemists, pharmacologists, and clinical development personnel.
• Presenting research findings at internal meetings and external scientific conferences.
• Staying abreast of the latest scientific literature, technological advancements, and emerging trends in biotechnology and drug development.
• Contributing to the preparation of scientific publications and patent applications.
• Mentoring junior research staff and interns, providing technical guidance and support.
• Ensuring compliance with all laboratory safety protocols and regulatory guidelines.
• Managing laboratory inventory and ordering supplies as needed.

• Ph.D. in Molecular Biology, Cell Biology, Immunology, Biotechnology, or a related life science discipline.
• Postdoctoral research experience or 3+ years of relevant industry experience in drug discovery or development.
• Demonstrated expertise in a variety of molecular and cellular biology techniques.
• Strong experience with immunology, signal transduction pathways, or cellular metabolism.
• Proficiency in data analysis software (e.g., GraphPad Prism, R) and experience with bioinformatics tools.
• Excellent written and oral communication skills, with a strong publication record.
• Ability to think critically and creatively to solve complex scientific problems.
• Proven ability to work independently and collaboratively in a fast-paced research environment.
• Experience with mammalian cell culture and aseptic techniques.
• Knowledge of therapeutic areas such as oncology, infectious diseases, or autoimmune disorders is a plus.

• Design and conduct scientific experiments in the field of biotechnology.
• Analyze experimental data and interpret results using statistical methods.
• Develop and validate new experimental protocols and assays.
• Maintain detailed laboratory notebooks and records of experiments.
• Collaborate with team members on research projects and scientific discussions.
• Contribute to the writing of scientific publications and presentations.
• Ensure compliance with laboratory safety regulations.

• Ph.D. or Master's degree in Biotechnology, Molecular Biology, Biochemistry, or a related life science field.
• Proven experience in a research and development setting, preferably in the biotech industry.
• Expertise in relevant laboratory techniques and instrumentation.
• Strong analytical and problem-solving skills.
• Excellent written and verbal communication skills for scientific reporting.
• Ability to work independently and as part of a collaborative research team.

Aseptic Manufacturing Associates (Level I, II, III) Grand Rapids, MI

Join the Grand River Aseptic Manufacturing team!

Grand River Aseptic Manufacturing (GRAM) is a leading contract development and manufacturing organization (CDMO) specializing in sterile injectable fill-and-finish services for liquid and lyophilized vials, syringes, and cartridges. We are committed to advancing patient care by providing our clients with the experience, technology, and quality record necessary for effective clinical trials and successful commercialization.

We are currently hiring Level I, II, and III Aseptic Manufacturing Associates!

Quality, Service, Collaboration, Courage. Do you exhibit these values and wish to be around others that do too? Are you interested in making a difference in your community and the world? Are you looking for a place where you can grow and learn in a diverse, community-minded culture? If these statements resonate with you, Grand River Aseptic Manufacturing (GRAM) welcomes you to apply to join our community of dedicated individuals improving lives every day.

$23 to $29.44 per hour based on experience!

• 1st Shift: 6:00 am – 4:00 pm M-Th
• 2nd Shift: 2:00 pm – 12:00 am M-Th
• 3rd Shift: 10:00 pm – 8:00 am M-Th
• 4th Shift: 6:00 am – 6:00 pm F-Su

• Perform equipment preparation in a sterile environment, bulk drug formulation, and aseptic filling duties as needed.
• Accurately document data and complete batch records as needed.
• Perform cleaning and sanitization duties as instructed by the applicable procedure.
• Successfully complete facility’s aseptic gowning and manufacturing qualification program.
• Perform duties in ISO 5 (Grade A), and ISO 7 (Grade C) cleanrooms.

• Bachelor’s degree in Chemistry, Biology or related field is a +.
• Level I: HS Diploma or equivalent and 1+ years relevant work experience in a manufacturing, medical, and/or laboratory environment.
• Level II: HS Diploma or equivalent and 3+ years relevant experience, including sterile manufacturing.
• Level III: HS Diploma or equivalent and 4+ years relevant experience, including sterile manufacturing.
• The ability to become qualified for use of a full-face respirator is required when working with hazardous chemicals.
• Use of a Powered Air Purifying Respirator (PAPR) is required during chemical dispense and other activities.

• Medical, dental, vision, life insurance, and disability benefits available for you and your family on your first day of work.
• 401(k) program.
• Full-time employees accrue up to 13 days of time off per calendar year.
• 10 paid holidays per calendar year with immediate eligibility.
• Wellness time off: Earn 1 hour of time off for every 30 hours worked.
• Paid volunteerism from day 1: 16 hours of paid volunteer time per year!

Grand River Aseptic Manufacturing is an Equal Opportunity Employer. We embrace and encourage everyone’s differences in race, color, ancestry, national origin, gender, sexual orientation, marital status, height, weight, religion, age, disability, gender identity, genetic identity, military status, citizenship, or any other class legally protected by local, state, or federal law. We value the differences that make each and every one of you unique.

Grand River Aseptic Manufacturing only accepts employment applications through our Careers webpage. Please be mindful of fraudulent recruiting practices and job offers, and only discuss employment directly with Grand River Aseptic Manufacturing.