Entry Level Nurse Scientist Jobs
New grad nurse scientist jobs welcome recent graduates and entry level candidates with zero to two years of experience, where strong internship work or a research portfolio can matter more than a long resume. Most openings are on-site roles across Healthcare & Medical Services, Technology & Software, and Biotechnology & Pharmaceuticals, with employers like Quest Diagnostics, TikTok, and Amazon hiring at this level now.
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Associate Scientist II, Downstream
About Site
Our Gene Therapy facility, located at the University of Maryland (UMD) BioPark in the city of Baltimore, MD, specializes in upstream and downstream process development of viral vectors for clinical applications. Baltimore is a hub of national and international travel and communications and is also home to and near major universities and several federal agencies, including the FDA, USDA, NIH, Johns Hopkins University, and UMD Schools of Medicine. The facility houses process development labs and CGMP cleanroom suites for Phase 1 and 2 programs focused on a variety of transformative technologies, including AAV and other viral vectors, vaccines, and oncolytic immunotherapies.
Position Summary
We have an opportunity for an Associate Scientist II, Downstream to join our team in Baltimore, MD - BioPark. The role supports downstream process development, pilot scale execution, and technology transfer to GMP manufacturing. The position involves hands-on laboratory work, collaboration with cross-functional teams, and contribution to process development activities. The successful candidate will bring technical expertise, scientific curiosity, and a commitment to quality and continuous improvement.
Shift: Monday – Friday, 8:00 am – 5:00 pm.
Location: Baltimore, MD - BioPark
100% Onsite
The Role
- Perform downstream processing of macromolecules expressed in mammalian cell lines, insect cells, or microbes.
- Develop and execute purification protocols from bench scale to large scale.
- Collaborate with analytical and upstream teams for purification and analysis of target molecules.
- Execute laboratory procedures and methods with high quality and moderate guidance.
- Build credibility within the group by delivering high-quality work.
- Assist other members of the Downstream Process Development group as needed.
- Follow standard operating procedures, protocols, and maintain required training.
- Manage data, complete batch and experimental records according to Good Documentation Practices (GDP).
- Document and communicate results through presentations, discussions, and meetings.
- Manage samples and inventory related to experiments.
- Assist with lab maintenance, stocking, cleaning, and troubleshooting equipment.
- Participate in project team decision-making and scientific discussions.
- Accommodate occasional weekend and evening work.
- Perform other duties as assigned.
The Candidate
Minimum Requirements
- Degree in Engineering or Life Science discipline with relevant experience (Bachelor of Arts or Bachelor of Science – at least 1+ years; or Master of Science – 0+ years).
- At least 1 year of relevant experience in biologics purification including chromatography and aseptic processing.
- Ability to sit at a desk or computer for documentation and data analysis.
- Ability to work in a laboratory environment for extended periods, including standing, walking, or sitting.
- Manual dexterity to handle laboratory instruments, pipettes, chromatography equipment, and tubing.
- Occasional lifting of containers or lab equipment up to 30 pounds.
- Good vision and hand-eye coordination for detailed work.
- Use of personal protective equipment (PPE) such as lab coats, gloves, safety goggles, and respiratory protection when required.
Preferred Skills & Background
- Experience with centrifugation, normal and tangential flow filtration, depth filtration, virus removal, and inactivation steps.
- Experience operating AKTA chromatography systems, UNICORN software, and chromatography column packing.
- Downstream process development experience specific to AAV, virus, VLP, or protein production.
- Awareness of GMP operations and process technical transfer.
Pay
The anticipated salary range for this position in MD is $70,000 – $90,000 Plus Bonus. The final salary offered to a successful candidate may vary, and will be dependent on several factors that may include but are not limited to: the type and length of experience within the job, type and length of experience within the industry, skillset, education, business needs, etc. Catalent is a multi-state employer, and this salary range may not reflect positions that work in other states.
Why You Should Join Catalent
- Defined career path and annual performance review and feedback process.
- Diverse, inclusive culture.
- Potential for career growth on an expanding team within an organization dedicated to preserving and bettering lives.
- Competitive paid time off plus 8 paid holidays.
- Community engagement and green initiatives.
- Medical, dental, and vision benefits effective day one of employment.
- Tuition reimbursement.
Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.
personal initiative. dynamic pace. meaningful work.
Visit Catalent Careers to explore career opportunities.
Catalent is an Equal Opportunity Employer, including disability and veterans.
If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to DisabilityAccommodations@catalent.com. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.
Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.
Important Security Notice to U.S. Job Seekers:
Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond— it is a fraudulent request. Please forward such requests to spam@catalent.com for us to investigate with local authorities.
California Job Seekers can find our California Job Applicant Notice HERE.
Volunteer Work Disclosure: Applicants for employment in Massachusetts may include in their employment history any verified work performed on a volunteer basis.
Massachusetts Lie Detector Test Notice: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law may be subject to criminal penalties and civil liability. Consistent with Massachusetts law, Catalent does not require or administer lie detector tests as a condition of employment or continued employment.
Associate Scientist II, Downstream
About Site
Our Gene Therapy facility, located at the University of Maryland (UMD) BioPark in the city of Baltimore, MD, specializes in upstream and downstream process development of viral vectors for clinical applications. Baltimore is a hub of national and international travel and communications and is also home to and near major universities and several federal agencies, including the FDA, USDA, NIH, Johns Hopkins University, and UMD Schools of Medicine. The facility houses process development labs and CGMP cleanroom suites for Phase 1 and 2 programs focused on a variety of transformative technologies, including AAV and other viral vectors, vaccines, and oncolytic immunotherapies.
Position Summary
We have an opportunity for an Associate Scientist II, Downstream to join our team in Baltimore, MD - BioPark. The role supports downstream process development, pilot scale execution, and technology transfer to GMP manufacturing. The position involves hands-on laboratory work, collaboration with cross-functional teams, and contribution to process development activities. The successful candidate will bring technical expertise, scientific curiosity, and a commitment to quality and continuous improvement.
Shift: Monday – Friday, 8:00 am – 5:00 pm.
Location: Baltimore, MD - BioPark
100% Onsite
The Role
- Perform downstream processing of macromolecules expressed in mammalian cell lines, insect cells, or microbes.
- Develop and execute purification protocols from bench scale to large scale.
- Collaborate with analytical and upstream teams for purification and analysis of target molecules.
- Execute laboratory procedures and methods with high quality and moderate guidance.
- Build credibility within the group by delivering high-quality work.
- Assist other members of the Downstream Process Development group as needed.
- Follow standard operating procedures, protocols, and maintain required training.
- Manage data, complete batch and experimental records according to Good Documentation Practices (GDP).
- Document and communicate results through presentations, discussions, and meetings.
- Manage samples and inventory related to experiments.
- Assist with lab maintenance, stocking, cleaning, and troubleshooting equipment.
- Participate in project team decision-making and scientific discussions.
- Accommodate occasional weekend and evening work.
- Perform other duties as assigned.
The Candidate
Minimum Requirements
- Degree in Engineering or Life Science discipline with relevant experience (Bachelor of Arts or Bachelor of Science – at least 1+ years; or Master of Science – 0+ years).
- At least 1 year of relevant experience in biologics purification including chromatography and aseptic processing.
- Ability to sit at a desk or computer for documentation and data analysis.
- Ability to work in a laboratory environment for extended periods, including standing, walking, or sitting.
- Manual dexterity to handle laboratory instruments, pipettes, chromatography equipment, and tubing.
- Occasional lifting of containers or lab equipment up to 30 pounds.
- Good vision and hand-eye coordination for detailed work.
- Use of personal protective equipment (PPE) such as lab coats, gloves, safety goggles, and respiratory protection when required.
Preferred Skills & Background
- Experience with centrifugation, normal and tangential flow filtration, depth filtration, virus removal, and inactivation steps.
- Experience operating AKTA chromatography systems, UNICORN software, and chromatography column packing.
- Downstream process development experience specific to AAV, virus, VLP, or protein production.
- Awareness of GMP operations and process technical transfer.
Pay
The anticipated salary range for this position in MD is $70,000 – $90,000 Plus Bonus. The final salary offered to a successful candidate may vary, and will be dependent on several factors that may include but are not limited to: the type and length of experience within the job, type and length of experience within the industry, skillset, education, business needs, etc. Catalent is a multi-state employer, and this salary range may not reflect positions that work in other states.
Why You Should Join Catalent
- Defined career path and annual performance review and feedback process.
- Diverse, inclusive culture.
- Potential for career growth on an expanding team within an organization dedicated to preserving and bettering lives.
- Competitive paid time off plus 8 paid holidays.
- Community engagement and green initiatives.
- Medical, dental, and vision benefits effective day one of employment.
- Tuition reimbursement.
Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.
personal initiative. dynamic pace. meaningful work.
Visit Catalent Careers to explore career opportunities.
Catalent is an Equal Opportunity Employer, including disability and veterans.
If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to DisabilityAccommodations@catalent.com. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.
Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.
Important Security Notice to U.S. Job Seekers:
Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond— it is a fraudulent request. Please forward such requests to spam@catalent.com for us to investigate with local authorities.
California Job Seekers can find our California Job Applicant Notice HERE.
Volunteer Work Disclosure: Applicants for employment in Massachusetts may include in their employment history any verified work performed on a volunteer basis.
Massachusetts Lie Detector Test Notice: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law may be subject to criminal penalties and civil liability. Consistent with Massachusetts law, Catalent does not require or administer lie detector tests as a condition of employment or continued employment.
See All 874+ Entry Level Nurse Scientist Jobs
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Find JobsEntry Level Nurse Scientist Job Market
Who's Hiring
- Quest Diagnostics126
- TikTok67
- Amazon15
- University of Miami12
- DoorDash11
Top Industries Hiring
- Healthcare & Medical Services325
- Technology & Software145
- Biotechnology & Pharmaceuticals110
- Education95
- Science & Research61
Entry Level Nurse Scientist Jobs: Frequently Asked Questions
How do I get an entry level nurse scientist job?
Start by highlighting clinical rotations, research projects, or internships that show hands-on scientific thinking alongside your nursing background. Employers at this level look for candidates who can bridge bedside practice and research methodology, so tailor your resume to show both. A strong cover letter explaining your research interests and any relevant lab or quality-improvement experience gives you a clear edge over candidates with similar credentials.
Which companies hire entry level nurse scientists?
Companies hiring entry level nurse scientists right now include Quest Diagnostics, TikTok, and Amazon, based on current listings on Migrate Mate as of November 2026. At this level, hiring tends to come from academic medical centers, hospital systems, and health research organizations that run structured new graduate programs or dedicated research fellowships.
Are there remote entry level nurse scientist jobs?
Yes, though most entry level nurse scientist roles involve some on-site clinical or lab component. About 10% of entry level nurse scientist openings are remote or hybrid as of November 2026, with remote work most common in roles focused on data analysis, protocol development, or health outcomes research rather than direct patient-facing science.
Are these new grad nurse scientist jobs?
Yes, these listings include new grad, recent graduate, and junior roles. A posting is new-grad friendly when it welcomes zero to two years of experience, accepts internships or clinical rotations in place of full-time history, or explicitly invites a research portfolio. If the job description does not require previous professional employment, it is generally open to candidates entering the field for the first time.
Which industries hire the most entry level nurse scientists?
Entry Level nurse scientist roles concentrate in Healthcare & Medical Services, Technology & Software, and Biotechnology & Pharmaceuticals, based on current listings on Migrate Mate as of November 2026. These sectors drive entry level hiring because they run ongoing clinical trials, quality-improvement initiatives, and evidence-based practice programs that need junior researchers to support data collection, literature review, and protocol coordination.