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Associate Downstream Process Development Scientist Jobs in Silver Spring, MD

As a Development Support Process Engineer, you will support a customer Program Management Office ... Bachelor's degree in Computer Science, Information Systems, Engineering, Business, or Education ...

As a Development Support Process Engineer, you will support a customer Program Management Office ... Bachelor's degree in Computer Science, Information Systems, Engineering, Business, or Education ...

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Associate Downstream Process Development Scientist information

See Silver Spring, MD salary details

$19

$34

$51

How much do associate downstream process development scientist jobs pay per hour?

As of Aug 22, 2026, the average hourly pay for associate downstream process development scientist in Silver Spring, MD is $34.82, according to ZipRecruiter salary data. Most workers in this role earn between $28.56 and $42.74 per hour, depending on experience, location, and employer.

What is an associate downstream process development scientist?

An Associate Downstream Process Development Scientist is a professional who works in the biotechnology or pharmaceutical industry, focusing on developing and optimizing processes that purify biological products, such as proteins or antibodies, after they have been produced by cells. Their work is crucial for ensuring the final product meets quality and safety standards before it is used in research or clinical applications. They typically perform laboratory experiments, analyze data, and collaborate with other scientists and engineers to improve yield and efficiency. This role is often entry-level or early-career, providing hands-on experience in process development and technical troubleshooting.

What are some typical challenges faced by an associate downstream process development scientist, and how can they be addressed?

Associate Downstream Process Development Scientists often encounter challenges such as optimizing purification processes, troubleshooting equipment performance, and ensuring batch-to-batch consistency. These challenges can be addressed by maintaining meticulous documentation, collaborating closely with upstream and analytical teams, and staying current with best practices in chromatography and filtration. Proactively seeking feedback from experienced colleagues and participating in cross-functional meetings can also help in identifying solutions and improving process efficiency.

What are the key skills and qualifications needed to thrive as an associate downstream process development scientist, and why are they important?

To excel as an Associate Downstream Process Development Scientist, you need a solid understanding of biochemistry, chemical engineering, and downstream purification techniques, often supported by a bachelor's or master's degree in a life science or engineering discipline. Familiarity with chromatographic systems (such as AKTA), filtration equipment, and analytical tools, as well as knowledge of GMP/GLP regulations, is typically required. Strong problem-solving, attention to detail, and effective teamwork and communication skills help you navigate complex experiments and collaborate with cross-functional teams. These skills ensure efficient process optimization, compliance with regulatory standards, and successful development of biopharmaceutical products.

What is the difference between Associate Downstream Process Development Scientist vs Associate Upstream Process Development Scientist?

AspectAssociate Downstream Process Development ScientistAssociate Upstream Process Development Scientist
Primary FocusPurification and recovery of bioproductsCell culture and fermentation processes
Required SkillsProtein purification, chromatography, filtrationCell culture, bioreactor operation, media preparation
Work EnvironmentLaboratories, manufacturing facilitiesLaboratories, bioreactor labs
Common CertificationsBiotech or bioprocessing certificationsBiotech or bioprocessing certifications

Both roles are essential in biopharmaceutical development, focusing on different stages of the production process. The Associate Downstream Process Development Scientist specializes in purification techniques, while the Associate Upstream Process Development Scientist concentrates on cell growth and fermentation. Understanding these distinctions helps candidates target their skills and career paths effectively.

What are the most commonly searched types of Downstream Process Development Scientist jobs in Silver Spring, MD?

The most popular types of Downstream Process Development Scientist jobs in Silver Spring, MD are:

What cities near Silver Spring, MD are hiring for Associate Downstream Process Development Scientist jobs?

Cities near Silver Spring, MD with the most Associate Downstream Process Development Scientist job openings:

Senior Scientist, Fermentation - IR&D, Product Development

Catalent, Inc.

Baltimore, MD • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 26 days ago


Catalent rating

7.6

Company rating: 7.6 out of 10

Based on 55 frontline employees who took The Breakroom Quiz

60th of 86 rated pharmaceutical


Job description

Senior Scientist, Fermentation - IR&D, Product Development
About Site
Catalent's Baltimore site is a leading facility specializing in biologics development and manufacturing, offering state-of-the-art capabilities to support advanced therapies. The campus provides a collaborative environment where teams work on innovative solutions for clinical and commercial supply, including cell and gene therapies. With modern laboratories and manufacturing suites, the site is designed to foster scientific excellence and operational efficiency. Employees here are part of a dynamic setting that emphasizes quality, innovation, and patient-focused outcomes, making it an exciting place to contribute to life-changing medicines.
Position Summary
We have an opportunity for a Senior Scientist, Fermentation - IR&D, Product Development to join our team. This role supports process and product innovation to keep Catalent at the forefront of leading CDMOs. You will work on upstream fermentation development, clone selection, and technology improvements for novel vectors. The position involves collaboration with internal teams and clients, contributing to innovative solutions for advanced therapies.
Shift: Monday - Friday 8AM - 5PM
Location: Baltimore, MD - BioPark
100% Onsite
The Role
  • Lead platform fit assessment for novel vectors (IR&D) and optimize upstream fermentation conditions.
  • Execute clone selection using DASGIP (4x1L) and Eppendorf BioFlo systems to identify candidates for RCB and eventual GMP MCB generation.
  • Perform strain selection across E. coli hosts to ensure plasmid stability, integrity, and high yield.
  • Evaluate novel plasmid vectors for AAV/lentiviral production via shake-flask transfection studies.
  • Conduct transfection, cloning, and high-throughput screening (ambr15 48-bioreactor system) to identify top-performing clones.
  • Tech transfer clone-specific fermentation processes to Process Development and GMP manufacturing (UpTempo and custom client vectors).
  • Drive innovation by improving strain selection, fermentation processes, media, and lysis strategies.
  • Maintain plasmid inventory, oversee fermentation lab operations, and support critical equipment ownership.
  • Troubleshoot technical challenges while collaborating cross-functionally, communicating with stakeholders/clients, and mentoring junior team members.
  • Other duties as assigned.

The Candidate
Minimum Requirements
  • PhD degree with 4+ years of upstream process development/R&D, or Master's degree with 8+ years, or BA/BS with 10+ years in upstream process development/R&D. Education must be in a biological, scientific, or engineering discipline (biology, biochemistry, chemical engineering, or equivalent).
  • Experience with a wide array of E. coli strains including Dh5, DH10b, NEB, Stbl.
  • Excellent problem-solving and written/verbal communication skills.
  • Strong interpersonal skills and ability to work effectively within a team.
  • Ability to execute detailed experimental plans, record procedures, analyze data, and present results.
  • Proficient in MS Office, specifically Excel and Word, and programs for laboratory equipment.
  • Ability to sit at a desk or computer for periods of time to prepare documentation, reports, and data analyses.
  • Ability to work in a laboratory environment for extended periods, including standing, walking, or sitting.
  • Manual dexterity to safely and accurately handle laboratory instruments, pipettes, chromatography equipment, and various tubing and fittings.
  • Occasional lifting of containers or lab equipment weighing up to 30 pounds.
  • Good vision and hand-eye coordination for detailed work.
  • Use of personal protective equipment (PPE) including lab coats, gloves, safety goggles, and, when required, respiratory protection.

Preferred Skills & Background
  • Experience with mammalian cell types including HEK293, CHO, and others is a plus.
  • Scale-up of fermentation or cell-culture processes to 50L+ bioreactor scale is a plus.
  • Experience with preparation of regulatory documents is a plus.
  • Experience with various cell lines for recombinant protein and gene therapy vector expression, process development, and/or bioprocess manufacturing is a plus.

Pay
The anticipated salary range for this position in MD is $120,000 - $150,000 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
  • Biologics services include process development, analytical development, quality systems, stability studies, fill/finish, and cell and virus banks.
  • Featured technologies include adeno-associated virus (AAV), vaccines, and oncolytic virus.
  • 152 hours PTO plus 8 paid holidays.
  • Medical, dental, and vision coverage options.
  • Generous 401(k) match.
  • 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.

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About Catalent

Sourced by ZipRecruiter

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.Catalent is committed to the health and safety of its employees, visitors and the customers and patients we serve.

Industry

Pharmaceutical product wholesalers

Company size

10,000+ Employees

Headquarters location

Somerset, NJ, US

Year founded

2007

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