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Associate Downstream Process Development Scientist Jobs in Missouri

Eurofins

Scientist - Analytical Assay

Chesterfield, MO · On-site

We are seeking a highly motivated Analytical Scientist to support biotherapeutic process development programs, with a primary focus on large molecule characterization (proteins, polysaccharides ...

kindeva

Sr. MS&T Process Engineer II

Maryland Heights, MO

$100K - $130K/yr

The position leads cross-functional initiatives including process development, process ... S. in Science or Engineering * 7+ years of equivalent job experience. * Strong leadership skills ...

kindeva

Sr. MS&T Process Engineer II

Maryland Heights, MO · On-site

$100K - $130K/yr

The position leads cross-functional initiatives including process development, process ... S. in Science or Engineering * 7+ years of equivalent job experience. * Strong leadership skills ...

kindeva

Sr. MS&T Process Engineer II

Maryland Heights, MO · On-site

$100K - $130K/yr

The position leads cross-functional initiatives including process development, process ... S. in Science or Engineering * 7+ years of equivalent job experience. * Strong leadership skills ...

kindeva

Sr. MS&T Process Engineer II

Maryland Heights, MO · On-site

$100K - $130K/yr

The position leads cross-functional initiatives including process development, process ... S. in Science or Engineering * 7+ years of equivalent job experience. * Strong leadership skills ...

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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 Missouri? The most popular types of Downstream Process Development Scientist jobs in Missouri are:
What cities in Missouri are hiring for Associate Downstream Process Development Scientist jobs? Cities in Missouri with the most Associate Downstream Process Development Scientist job openings:
Associate Downstream Process Development Scientist jobs near you
Pharmaceutical Development Senior Associate Scientist II

Pharmaceutical Development Senior Associate Scientist II

Catalent Pharma Solutions

Kansas City, MO

Full-time

Medical, Life, Retirement, PTO

Posted 9 days ago

Catalent rating

7.4

Company rating: 7.4 out of 10

Based on 51 frontline employees who took The Breakroom Quiz

52nd of 72 rated pharmaceutical

Job description

Pharmaceutical Development Senior Associate Scientist II

Position Summary

  • Shift: Tuesday - Friday 12pm-10pm
  • 100% on-site

Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, manufacture, and supply products that help people live better and healthier lives. Catalent is dedicated to delivering unparalleled service to pharma, biotech, and consumer health customers, supporting product development, launch, and full life-cycle supply. With time-tested experience in development sciences, delivery technologies, and multi-modality manufacturing, Catalent supports the acceleration of development programs and the launch of more than a hundred new products every year. Powered by thousands of scientists and technicians and the latest technology platforms at more than 40 global sites, Catalent supplies billions of doses of life-enhancing and life-saving treatments for patients annually.

The Senior Associate Scientist II supports formulation design and development of oral solid drug products. Trains others in clinical trial manufacturing operations using sound pharmaceutical principles. Ensures that all work is carried out is in compliance with regulatory requirements, good manufacturing practices (cGMP) and standard operating procedures (SOPs).

The role:

  • Maintain high quality laboratory documentation in accordance with applicable regulatory guidance and Site SOPs
  • Draft technical documents such as laboratory notebook writeups, protocols and batch records.
  • Trains others on procedures and laboratory techniques
  • Executes efficiency improvement project with guidance
  • Has applied knowledge of the principles and concepts of a discipline.
  • Applies technical and functional knowledge to job related duties on most projects/ assignments within own group/project team.
  • Performs parallel review of GMP documents and laboratory notebooks and may become qualified to conduct compliance technical reviews.
  • Develop and executes procedures, methods, manufacturing processes with minimal complexity, with high quality.
  • Demonstrated ability to lead small team projects

The candidate:

  • Bachelor's degree in related life science or physical science field required with 4+ years related work experience
  • Master's degree in related life science or physical science field required with 2+ years related work experience
  • Ability to interpret a variety of instructions furnished in written, oral, diagram, or schedule form
  • Individual may be required to sit, stand, walk regularly and occasionally lift 0-15 pounds;

Why you should join Catalent:

  • Competitive medical benefits and 401K
  • 152 hours PTO + 8 Paid Holidays
  • Dynamic, fast-paced work environment
  • Opportunity to work on Continuous Improvement Processes

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.

What Catalent employees say

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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

Social media

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