Consolidated Precision Products Corp.

Manufacturing and Process Development Manager (Houston, TX)

Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's Degree in bioengineering, biotechnology, or similar field.
  • 5-10+ years' experience in biopharmaceutical or biotechnology industry, particularly in exosome/nanoparticle manufacturing.
  • 2-3 years of leadership experience managing a team.
  • Deep expertise in exosome processing techniques like isolation, purification, and aseptic processing.
  • Proven track record in process development and technical transfer for exosome or similar products.

Responsibilities

  • Oversee and manage a state-of-the-art GMP manufacturing suite for stem cell-derived exosomes.
  • Act as a Subject Matter Expert on specialized equipment for exosome processes, providing guidance and training.
  • Design and conduct experiments to produce GMP-compliant exosome batches, ensuring quality and consistency.
  • Develop and maintain robust systems and procedures focusing on operational efficiency in exosome manufacturing.
  • Lead initiatives to create scientifically valid, scalable exosome products and manufacturing processes.
  • Implement structured Process Development and Technology Transfer for quality consistency in manufacturing.
  • Prepare, review, and approve documentation for regulatory compliance and operational excellence.
  • Communicate technical insights and data effectively to teams and senior management, identifying and solving critical issues.
  • Mentor junior staff in the team while fostering a culture of excellence and continuous learning.

Benefits

  • Opportunities for professional development and continuous learning.
  • Supportive work environment encouraging collaborative teamwork.
  • Flexible work arrangements to promote work-life balance.
  • Access to cutting-edge technology and state-of-the-art facilities.
  • Participation in innovative projects impacting wellness applications.
Full Job Description
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.

About Consolidated Precision Products Corp.

Consolidated Precision Products Corp. is a manufacturer of complex metal components and products for the aerospace and defense industries. The company was founded in 1991 and is headquartered in Carrollton, Texas. Consolidated Precision Products Corp. operates a network of manufacturing facilities across the United States, as well as in Mexico and Europe. The company's products include castings, forgings, and machined components, as well as assemblies and sub-assemblies. Consolidated Precision Products Corp. is committed to providing high-quality products and services to its customers.
Learn more about Consolidated Precision Products Corp.
Size
3,000 employees
Industry

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