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Process Engineer Cell Therapy Jobs in Spring, TX

Cellipont Bioservices

Director MS&T

The Woodlands, TX · On-site

Stay current with advancements in process engineering, manufacturing technologies, and industry ... Gain experience in the cutting-edge cell therapy space "At Cellipont Bioservices, we look for ...

Skilled Capital Group

Be Seen First

Senior Technical Writer

Houston, TX · On-site

$50 - $65/hr

... cell therapy manufacturing facility. This role is central to ensuring compliant, accurate, and ... You will collaborate closely with Manufacturing, Quality, Process Development, Analytical ...

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All JobsProcess Engineer Cell Therapy JobsProcess Engineer Cell Therapy Jobs in Spring, TX

Process Engineer Cell Therapy information

See Spring, TX salary details

$44K

$81.9K

$126.8K

How much do process engineer cell therapy jobs pay per year?

As of Jul 14, 2026, the average yearly pay for process engineer cell therapy in Spring, TX is $81,886.00, according to ZipRecruiter salary data. Most workers in this role earn between $66,300.00 and $91,700.00 per year, depending on experience, location, and employer.

What does a Process Engineer in Cell Therapy do?

A Process Engineer in Cell Therapy is responsible for developing, optimizing, and overseeing the manufacturing processes used to produce cell-based therapies. They ensure that processes are efficient, scalable, and compliant with regulatory standards, while maintaining the quality and safety of the final product. Their work often involves collaborating with scientists, quality teams, and production staff to troubleshoot issues and implement improvements. Process Engineers in this field play a crucial role in bringing innovative cell therapies from the laboratory to clinical and commercial production.

What are the key skills and qualifications needed to thrive as a Process Engineer in Cell Therapy, and why are they important?

To thrive as a Process Engineer in Cell Therapy, you need a strong background in chemical or biomedical engineering, experience with cell culture processes, and often a relevant degree. Familiarity with GMP regulations, bioprocessing equipment, and quality control systems is typically required, along with experience using tools like bioreactors and analytical software. Excellent problem-solving, communication, and project management skills help you collaborate effectively and drive process improvements. These skills ensure the development and optimization of safe, scalable, and compliant cell therapy manufacturing processes.

What is the difference between Process Engineer Cell Therapy vs Process Engineer Bioprocess?

AspectProcess Engineer Cell TherapyProcess Engineer Bioprocess
CredentialsBachelor's/Master's in Bioengineering, Chemical Engineering, or related fieldsBachelor's/Master's in Bioengineering, Chemical Engineering, or related fields
Work EnvironmentCell therapy manufacturing facilities, GMP labsBiopharmaceutical production plants, GMP facilities
Industry UsageCell therapy companies, biotech firmsBiotech, pharmaceutical manufacturing
Common Search/ComparisonYesYes

Process Engineer Cell Therapy and Process Engineer Bioprocess roles share similar educational backgrounds and work environments, often within GMP manufacturing settings. The main difference lies in their focus: cell therapy engineers specialize in developing and scaling processes for cellular treatments, while bioprocess engineers work on broader biopharmaceutical production. Both roles are essential in biotech industries and often overlap in skills and certifications.

What are some typical challenges faced by Process Engineers in Cell Therapy manufacturing, and how are they addressed?

Process Engineers in Cell Therapy often encounter challenges such as scaling up production from clinical to commercial scale while maintaining stringent quality standards and regulatory compliance. Managing variability in biological materials and ensuring consistency across batches is another common hurdle. These challenges are typically addressed through robust process development, close collaboration with quality and manufacturing teams, and implementation of automation and data-driven process controls. Continuous training and adaptation to evolving regulatory guidelines also play a key role in overcoming these obstacles.
What are popular job titles related to Process Engineer Cell Therapy jobs in Spring, TX? For Process Engineer Cell Therapy jobs in Spring, TX, the most frequently searched job titles are:
Process Engineer Cell Therapy jobs near you
Infographic showing various Process Engineer Cell Therapy job openings in Spring, TX as of July 2026, with employment types broken down into 100% Contract. Highlights an 100% In-person job distribution, with an average salary of $81,886 per year, or $39.4 per hour.
QA Lead, Operations (Cell Therapy) (W)

QA Lead, Operations (Cell Therapy) (W)

Cellipont Bioservices

The Woodlands, TX • On-site

Full-time

Medical, Retirement, PTO

Posted 23 days ago

Job description

Job Summary
Cellipont Bioservices is growing, and we are looking for a QA Lead, Operations who believes in the potential of bridging client's discoveries to patient cures and who wants to challenge the status quo and take Cellipont and its clients to the next level.
The QA Lead, Operations will be the main point of contact for assigned client projects, supporting commercial readiness activities, managing relationships, and driving project deliverables. This individual will be responsible for preparing detailed project schedules, including the identification of major milestones for overseeing, controlling, communicating, and managing all activities required to complete client projects as they pertain to QA lot release and assigned commercial readiness activities.
The QA Lead, Operations will oversee batch record review, and lot release deliverables are client-focused, results-oriented, performance-driven, and in compliance with all applicable internal and external requirements and monitor projects and help resolve issues or escalate, appropriately to ensure on-time delivery of all client's projects with management of effective risk mitigation plans and stakeholder communication. This individual will provide QA support for new product introductions at the site. This role will also require the individual to demonstrate a strong ability to work cross-functionally and possess strong leadership skills.
The Role
  • Primary responsibility is to provide QA oversight and support to client projects while working closely with QA Management to ensure QA support for GMP operations for the manufacture of cellular therapies.
  • Represents QA in client interactions and meetings.
  • Works cross-functionally with Project Management, AD/PD, Supply Chain, Manufacturing, F&E, and Quality Control to execute client project activities timelines.
  • Identify compliance risks and escalate to management with remediation proposal and lead solution implementation.
  • Guides the successful completion of major programs and may function in a project leadership role.
  • Conducts review/approval of master batch records, executed batch records in real-time, and supporting documentation for accuracy, completeness, and compliance as required.
  • Act as the first responder for all manufacturing quality issues and interfaces with the client to gain resolution.
  • Supports GMP departments in performing and documenting deviations and failure investigations, including root cause analysis, evaluating product/facility impacts, and identifying/implementing effective corrective and preventive actions (CAPAs).
  • Provide training for new or revised quality processes.
  • Supports and/or leads client on-site audits and participates in on-site technical visits.
  • Support regulatory (i.e. FDA, EMA) inspections.
  • Maintains systems used for tracking various GMP manufacturing-associated support activities.
  • Generation and/or revise SOP documents following cGMPs.
  • Assists in managing the Quality programs and systems to ensure compliance with Quality requirements and provides advice on GMP-related issues.
  • Stay current, and be able to interpret, changes to current Good Manufacturing Practices, including FDA, EU, and other regulatory bodies (relevant to Cellipont Bioservices activities) and guidance bodies including ICH, ISPE, etc.

The Candidate
  • BS. in a Life Sciences discipline with a minimum 8 years of experience within the biopharmaceutical or regulated pharmaceutical industry (previous CDMO experience is a plus) and at least6 years of experience in Quality Assurance.
  • Strong technical and quality background related to biological manufacturing (preferably Cell Therapy)
  • Strong familiarity with commercial GMP processes within biologics. Experience with transitioning products from clinical to commercial processes and process validation is preferred.
  • Ability to apply basic scientific and regulatory principles utilized to solve operational, as well as routine quality tasks
  • Self-starter with the ability to produce results in a fast-paced environment to meet client deadlines under minimal supervision.
  • Strong knowledge base with Good Manufacturing Practices (GMPs), 21 CFR Parts 210, 211, biological regulations per 21 CFR Parts 600s, ICH Guidelines and EU GMPs.
  • Provides technical solutions to complex problems which require the regular use of ingenuity and creativity
  • Ability to quickly learn new and novel manufacturing processes supporting new clients
  • Able to work in a team setting and independently under minimum supervision
  • Familiarity with electronic systems, including developing and producing reports using Smartsheet and Excel
  • Requires the ability to produce quality results in a fast-paced environment to meet client deadlines
  • Able to communicate effectively orally and written with all levels of personnel and regulatory inspectors

Position Benefits
  • Opportunities for career growth within an expanding team
  • Defined career path and annual performance review & feedback process
  • Cross-functional exposure to other areas of within the organization
  • Robust benefit package designed for unique Health & Wellness needs, including coverage for your furry family members
  • 401K strong employer match
  • Tuition Reimbursement
  • Employee Referral Bonuses
  • Flexible work schedules and PTO based on role/level, increasing 1 PTO day each year and paid holidays
  • Gain experience in the cutting-edge cell therapy space

"At Cellipont Bioservices, we look for candidates with an innate desire to serve. Our "family" approach ensures you will get the mentorship you need to develop a satisfying career here!"
Notice to Agency and Search Firm Representatives
Cellipont Bioservices is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Cellipont Bioservices employee by a third-party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Cellipont Bioservices. No fee will be paid if a candidate is hired for this position because of an unsolicited agency or search firm referral. Thank you.

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