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Associate Downstream Process Development Scientist Jobs in Virginia

As a Scientist I on our Analytical R&D team, you would be responsible for testing the product ... Support the R&D team by testing the process development sample for content uniformity, blend ...

... and support downstream analytics and search solutions. * Collaborate with data engineers to ... Support development of analytics, reporting, and dashboards to drive operational insights and ...

AI/ML Data Scientist

Arlington, VA · On-site

$113K - $188K/yr

... and support downstream analytics and search solutions. * Collaborate with data engineers to ... Support development of analytics, reporting, and dashboards to drive operational insights and ...

Data Scientist, Associate

Mclean, VA · On-site

$59K - $60K/yr

... development processes • Experience with econometric/economic modeling and analysis • Working knowledge of federal budgeting and spending mechanics, processes, and data. • Planning, Programming ...

Associate Scientist I

Sterling, VA · On-site

$45K - $48K/yr

... development * Perform laboratory housekeeping duties to include autoclaving and glassware processing * Prepare necessary standards, solutions, reagents, media, etc., required for sample analyses

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Associate Downstream Process Development Scientist information

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 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 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 most commonly searched types of Downstream Process Development Scientist jobs in Virginia? The most popular types of Downstream Process Development Scientist jobs in Virginia are:

Other

Posted 26 days ago


Job description

Description

**US Based CANDIDATES ONLY**


Job Summary:


As a Scientist I on our Analytical R&D team, you would be responsible for testing the product development samples and supporting R&D team on timely manner with analytical sample testing. This includes performing the Assay Dissolution, analytical method development, and method validation including preparing analytical method validation and verification protocols . Additionally, you would be responsible for the testing and release of in-process, finished product, and Stability samples including process evaluation samples.

Following SOPs to complete tasks, while ensuring safe and efficient execution of job duties is crucial in this role.


Job Duties and responsibilities inclue but not limited to:

  • Proficient in operating the laboratory instrumentation/equipment, including but not limited to: FTIR, HPLC, UPLC, Dissolution apparatus, ICP-MS, GC, UV-Vis, Karl fisher (KF), Ion chromatography (IC), Malvern Master sizer, etc.
  • Support the R&D team by testing the process development sample for content uniformity, blend uniformity, Assay, particle size distribution, density, water determination by KF, viscosity, and other tests as required.
  • Conduct analytical method development, method optimization, method validation, method verification and method transfer for finish products.
  • Draft test methods, method validation protocols and reports as per the Company SOPs and regulatory guidelines
  • Perform additional analytical testing (multimedia dissolution, photo stability, Dose dumping etc.) for ANDA submission
  • Timely execution and completion of assigned tasks
  • Document experiments accurately and complete all associated documents (Instrument, Standard and Column usage logbooks) in compliance with internal SOPs and FDA guidelines
  • Maintain work area and laboratory with good housekeeping practices and in compliant with cGMP.
  • Identify and communicate continuous improvement opportunities to the Analytical Manager and Director
  • Monitor and ensure availability of chemicals, columns, standards, and other consumable for sample testing.
  • Other duties assigned by management based on requirements


Management responsibilities include:

  • Assign daily work schedule in timely manner
  • Provide guidance in method Development and validation.
  • Interpret and review generated results
  • Provide assistance in professional development.

Requirements

Minimum Education & Experience:

  • Bachelor's degree in Pharmaceutical Chemistry, Analytical Chemistry, Pharmaceutical Sciences, or related area with 5+ years of directly related expereince in pharmaceutical industry OR
  • Master's degree in Pharmaceutical Chemistry, Analytical Chemistry, Pharmaceutical Sciences, or related area with 2+ years of directly related expereince in pharmaceutical industry
  • Knowledge of Good Manufacturing Practices (cGMP)
  • Experience with software and information systems (e.g. Empower, Microsoft word and Excel)

Required Knowledge, Skills, & Abilities

  • Proven Knowledge of the major analytical techniques and operation of instruments such as HPLC, GC, dissolution, FT-IR, UV-VIS Spectrophotometer, Particle size analysis (Malvern Mastersizer, Sonic sifting and Sieve shaker), Karl Fisher Instrument, Potentiometric Titration, Density meter, pH meter, Melting point apparatus, Analytical Balances, Viscometer
  • Expereince with HPLC Method development & validation
  • Proficient in documentation as per Good Documentation Practice
  • Computer skills including Microsoft and Excel
  • Excellent verbal and written communication and skills

Physical Requirements/Working Environment:

  • Must be able to stand for long periods of time (up to 12-hour shifts), maneuver at least 40 pounds, wear a respirator and pass associated respirator tests and/or requirements, and be able to wear all required PPE.
  • Vision - ability to see details at close range (within a few feet of the observer).


Disclaimer

The above information on this description has been designed to indicate the general nature and level of work performed by employees within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities, and qualifications required of employees assigned to this job.