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Associate Process Development Scientist Jobs in Houston, TX

Lead product and process developments of chemical and petrochemical compounds. Possesses a full ... S. in Chemistry, Chemical Engineering, Material Science, Biochemistry, or Polymer Chemistry ...

Lead product and process developments of chemical and petrochemical compounds. Possesses a full ... S. in Chemistry, Chemical Engineering, Material Science, Biochemistry, or Polymer Chemistry ...

Senior R and D Scientist

Katy, TX · On-site

$90K - $115K/yr

SINOPEC Employee Position Overview The Senior R&D Scientist is responsible for advancing catalyst and catalytic process research at the SINOPEC-UOP Joint Research Center. This position independently ...

FORMULATION SCIENTIST

Rosenberg, TX · On-site

$87K - $105K/yr

Design, execute, analyze, and document formulation and process development studies using scientific and risk-based approaches. * Apply Quality by Design (QbD) and Design of Experiments (DoE ...

Senior Associate - Process Risk and Controls

Houston, TX · On-site

$77K - $95K/yr

... associates on foundational industry policies, procedures, and work-programs * Owns process level ... Commit to self-development in response to constructive feedback received. * Provide assistance ...

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Associate Process Development Scientist information

See Houston, TX salary details

$17

$34

$54

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

As of Aug 17, 2026, the average hourly pay for associate process development scientist in Houston, TX is $34.31, according to ZipRecruiter salary data. Most workers in this role earn between $26.63 and $39.04 per hour, depending on experience, location, and employer.

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

AspectAssociate Process Development ScientistProcess Development Scientist
Required CredentialsBachelor's or Master's in Life Sciences or Chemical EngineeringBachelor's or Master's, often with more experience or specialization
Work EnvironmentEntry-level, supporting process optimization in labs or manufacturingMore independent, leading process improvements and validations
Employer & Industry UsagePharmaceutical, biotech, or biotech manufacturing companiesSame industries, with increased responsibilities

The Associate Process Development Scientist typically supports process development tasks under supervision, focusing on experimental execution. In contrast, the Process Development Scientist takes on more independent roles, leading projects and process improvements. Both roles are common in biotech and pharmaceutical industries, with the main difference being experience level and scope of responsibilities.

What are popular job titles related to Associate Process Development Scientist jobs in Houston, TX?

For Associate Process Development Scientist jobs in Houston, TX, the most frequently searched job titles are:

What job categories do people searching Associate Process Development Scientist jobs in Houston, TX look for?

The top searched job categories for Associate Process Development Scientist jobs in Houston, TX are:

Infographic showing various Associate Process Development Scientist job openings in Houston, TX as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 15% Part Time, and 3% Contract. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $71,359 per year, or $34.3 per hour.

Manufacturing and Process Development Manager

CEDENT

Houston, TX

Full-time

Re-posted 19 days ago


Job description

Client is seeking a passionate and dedicated Manufacturing and Process Development Manager to be part of our dynamic team at the forefront of regenerative medicine. As a Manufacturing and Process Development Manager, you will oversee the GMP manufacturing facility and lead the Manufacturing and Process Development team, providing expert technical guidance for the development, scale-up, and transfer of stem cell-derived exosome manufacturing processes tailored for the wellness industry. The ideal candidate will excel in a collaborative, cross-functional team setting, driving key decisions to ensure the successful creation of innovative wellness products. You will work alongside leading experts in the field, contributing to groundbreaking research that can revolutionize the future of health and wellness. This is an exciting opportunity to be part of a visionary company dedicated to pushing the boundaries of science and improving lives on a global scale.
Responsibilities:
· Facility Management: Oversee the establishment and operation of a state-of-the-art GMP manufacturing suite designed for the production of stem cell-derived exosomes, incorporating a diverse array of processing technologies and capabilities initially tailored to wellness applications.
· Technical Expertise: Serve as a Subject Matter Expert on the operation of specialized equipment for exosome isolation, purification, and characterization, rapidly adopting new technologies and providing comprehensive guidance, training, and technical direction to the team.
· Experimentation: Design and conduct experiments to deepen process understanding and produce GMP-compliant batches of exosomes at multiple scales, ensuring consistency and quality for wellness applications.
· Systems Management: Accountable for developing, managing, and maintaining robust systems and procedures, including batch records, change controls, and SOPs, with a keen emphasis on operational efficiency and ongoing process enhancement in exosome manufacturing.
· Process Development Leadership: Lead process development initiatives to create scientifically grounded, well-characterized exosome products and manufacturing processes that are scalable, robust, and reproducible. Determine optimal parameters for prototype and final product manufacturing to guarantee consistent quality and efficacy for wellness applications.
· Technology Transfer: Implement a structured approach to Process Development and Technology Transfer to maintain consistency and uphold the highest quality standards in exosome manufacturing processes.
· Documentation: Prepare, review, and approve critical documentation, including protocols, reports, and regulatory submission sections, ensuring compliance with industry standards for wellness products.
· Compliance: Ensure full compliance with cGMP, safety, environmental regulations, and company policies, integrating these considerations into daily operations.
· Communication: Effectively communicate technical data and process insights to cross-functional teams and senior management, highlighting critical issues and proposing solutions as a recognized expert in exosome process development.
· Team Leadership: Lead, mentor, and develop junior team members in Manufacturing and Process Development, fostering a culture of excellence and continuous learning.
· Additional Duties: Undertake additional responsibilities as needed to support the team’s objectives.
Basic Requirements:
· Education & Experience: Bachelor’s Degree in bioengineering, biotechnology, or a related scientific discipline, with 5-10+ years of experience in the biopharmaceutical or biotechnology industry, preferably with a focus on exosome or nanoparticle manufacturing, including 2-3 years of team leadership.
Preferred Requirements:
· Technical Proficiency: Deep expertise in key processing techniques relevant to exosome manufacturing, including cell culture, exosome isolation and purification, aseptic processing, and formulation.
· Process Expertise: Proven track record in process development, scale-up, and technical transfer, specifically for exosome or similar nanoparticle-based products.
· Analytical Skills: Advanced skills in experimental design, data analysis, and interpretation, particularly for optimizing exosome yield, purity, and functionality.
· Problem-Solving: Strong technical problem-solving skills, leveraging the latest research and technologies in exosome science and manufacturing.
· Industry Knowledge: Comprehensive understanding of the product development lifecycle for wellness applications, with a focus on the critical role of process development in bringing exosome-based products to market.
· Leadership & Communication: Exceptional leadership abilities, with a collaborative approach, strong interpersonal skills, and outstanding communication capabilities, both verbal and written.
· Regulatory Expertise: In-depth knowledge of relevant regulatory guidelines (e.g., FDA, USP) for wellness products, with the ability to apply these standards appropriately throughout the development process.

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About Cedent

Sourced by ZipRecruiter

CEDENT strives to attract and retain the best people and provide an environment where they can all develop professionally and build a rewarding career. As a result, we create an inclusive environment that is rich in diversity, acknowledges each individual's uniqueness and promotes respect, personal achievement and stewardship. Our clients are global and so is CEDENT. We build and maintain a global workforce that includes people from different backgrounds, with a vast range of skills and experience all united by a common culture and commitment to help our clients achieve high performance. Cultivating a diverse workforce and inclusive work environment makes business sense. Our peoples varied skills are the talent engine that powers CEDENT, enabling it in turn to deliver the innovative solutions that help our clients outperform competitors.

Industry

It services

Company size

11 - 50 Employees

Headquarters location

Plano, TX, US

Year founded

2008