Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing. The incumbent ... Administer the electronic document review and approval process. All work is to be done in a ...
Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing. The incumbent ... Administer the electronic document review and approval process. All work is to be done in a ...
... processes and AABB Standards for cellular therapy. * Knowledge of FDA regulations governing human ... Demonstrate prior leadership experience in program development, with knowledge of cellular therapy ...
... processes and AABB Standards for cellular therapy. * Knowledge of FDA regulations governing human ... Demonstrate prior leadership experience in program development, with knowledge of cellular therapy ...
Stem Cell Transplant Physician
Roanoke, VA · On-site
$200K - $250K/yr
... processes and AABB Standards for cellular therapy. * Knowledge of FDA regulations governing human ... Demonstrate prior leadership experience in program development, with knowledge of cellular therapy ...
Stem Cell Transplant Physician
Roanoke, VA · On-site
$200K - $250K/yr
... processes and AABB Standards for cellular therapy. * Knowledge of FDA regulations governing human ... Demonstrate prior leadership experience in program development, with knowledge of cellular therapy ...
... processes and AABB Standards for cellular therapy. * Knowledge of FDA regulations governing human ... Demonstrate prior leadership experience in program development, with knowledge of cellular therapy ...
... processes and AABB Standards for cellular therapy. * Knowledge of FDA regulations governing human ... Demonstrate prior leadership experience in program development, with knowledge of cellular therapy ...
... processes and AABB Standards for cellular therapy. * Knowledge of FDA regulations governing human ... Demonstrate prior leadership experience in program development, with knowledge of cellular therapy ...
... processes and AABB Standards for cellular therapy. * Knowledge of FDA regulations governing human ... Demonstrate prior leadership experience in program development, with knowledge of cellular therapy ...
... processes and AABB Standards for cellular therapy. * Knowledge of FDA regulations governing human ... Demonstrate prior leadership experience in program development, with knowledge of cellular therapy ...
... processes and AABB Standards for cellular therapy. * Knowledge of FDA regulations governing human ... Demonstrate prior leadership experience in program development, with knowledge of cellular therapy ...
... processes and AABB Standards for cellular therapy. * Knowledge of FDA regulations governing human ... Demonstrate prior leadership experience in program development, with knowledge of cellular therapy ...
... processes and AABB Standards for cellular therapy. * Knowledge of FDA regulations governing human ... Demonstrate prior leadership experience in program development, with knowledge of cellular therapy ...
Stem Cell Transplant Physician
Virginia Beach, VA · On-site
$200K - $250K/yr
... processes and AABB Standards for cellular therapy. * Knowledge of FDA regulations governing human ... Demonstrate prior leadership experience in program development, with knowledge of cellular therapy ...
Stem Cell Transplant Physician
Virginia Beach, VA · On-site
$200K - $250K/yr
... processes and AABB Standards for cellular therapy. * Knowledge of FDA regulations governing human ... Demonstrate prior leadership experience in program development, with knowledge of cellular therapy ...
... processes and AABB Standards for cellular therapy. * Knowledge of FDA regulations governing human ... Demonstrate prior leadership experience in program development, with knowledge of cellular therapy ...
... processes and AABB Standards for cellular therapy. * Knowledge of FDA regulations governing human ... Demonstrate prior leadership experience in program development, with knowledge of cellular therapy ...
Stem Cell Transplant Physician
Richmond, VA · On-site
$200K - $250K/yr
... processes and AABB Standards for cellular therapy. * Knowledge of FDA regulations governing human ... Demonstrate prior leadership experience in program development, with knowledge of cellular therapy ...
Stem Cell Transplant Physician
Richmond, VA · On-site
$200K - $250K/yr
... processes and AABB Standards for cellular therapy. * Knowledge of FDA regulations governing human ... Demonstrate prior leadership experience in program development, with knowledge of cellular therapy ...
... processes and AABB Standards for cellular therapy. * Knowledge of FDA regulations governing human ... Demonstrate prior leadership experience in program development, with knowledge of cellular therapy ...
... processes and AABB Standards for cellular therapy. * Knowledge of FDA regulations governing human ... Demonstrate prior leadership experience in program development, with knowledge of cellular therapy ...
Hematopoietic Stem Cell Transplant Physician
Richmond, VA · On-site
$200K - $250K/yr
... processes and AABB Standards for cellular therapy. * Knowledge of FDA regulations governing human ... Demonstrate prior leadership experience in program development, with knowledge of cellular therapy ...
Hematopoietic Stem Cell Transplant Physician
Richmond, VA · On-site
$200K - $250K/yr
... processes and AABB Standards for cellular therapy. * Knowledge of FDA regulations governing human ... Demonstrate prior leadership experience in program development, with knowledge of cellular therapy ...
... processes and AABB Standards for cellular therapy. * Knowledge of FDA regulations governing human ... Demonstrate prior leadership experience in program development, with knowledge of cellular therapy ...
... processes and AABB Standards for cellular therapy. * Knowledge of FDA regulations governing human ... Demonstrate prior leadership experience in program development, with knowledge of cellular therapy ...
... processes and AABB Standards for cellular therapy. * Knowledge of FDA regulations governing human ... Demonstrate prior leadership experience in program development, with knowledge of cellular therapy ...
... processes and AABB Standards for cellular therapy. * Knowledge of FDA regulations governing human ... Demonstrate prior leadership experience in program development, with knowledge of cellular therapy ...
Hematopoietic Stem Cell Transplant Physician
Roanoke, VA · On-site
$200K - $250K/yr
... processes and AABB Standards for cellular therapy. * Knowledge of FDA regulations governing human ... Demonstrate prior leadership experience in program development, with knowledge of cellular therapy ...
Hematopoietic Stem Cell Transplant Physician
Roanoke, VA · On-site
$200K - $250K/yr
... processes and AABB Standards for cellular therapy. * Knowledge of FDA regulations governing human ... Demonstrate prior leadership experience in program development, with knowledge of cellular therapy ...
... processes and AABB Standards for cellular therapy. * Knowledge of FDA regulations governing human ... Demonstrate prior leadership experience in program development, with knowledge of cellular therapy ...
... processes and AABB Standards for cellular therapy. * Knowledge of FDA regulations governing human ... Demonstrate prior leadership experience in program development, with knowledge of cellular therapy ...
Hematopoietic Stem Cell Transplant Physician
Virginia Beach, VA · On-site
$200K - $250K/yr
... processes and AABB Standards for cellular therapy. * Knowledge of FDA regulations governing human ... Demonstrate prior leadership experience in program development, with knowledge of cellular therapy ...
Hematopoietic Stem Cell Transplant Physician
Virginia Beach, VA · On-site
$200K - $250K/yr
... processes and AABB Standards for cellular therapy. * Knowledge of FDA regulations governing human ... Demonstrate prior leadership experience in program development, with knowledge of cellular therapy ...
... processes and AABB Standards for cellular therapy. * Knowledge of FDA regulations governing human ... Demonstrate prior leadership experience in program development, with knowledge of cellular therapy ...
... processes and AABB Standards for cellular therapy. * Knowledge of FDA regulations governing human ... Demonstrate prior leadership experience in program development, with knowledge of cellular therapy ...
... processes and AABB Standards for cellular therapy. * Knowledge of FDA regulations governing human ... Demonstrate prior leadership experience in program development, with knowledge of cellular therapy ...
... processes and AABB Standards for cellular therapy. * Knowledge of FDA regulations governing human ... Demonstrate prior leadership experience in program development, with knowledge of cellular therapy ...
Senior Manager, Manufacturing Aseptic Process Leader
Hopewell, VA · On-site
$133 - $178/hr
Master's degree and 5+ years of sterile pharmaceutical, biologics, vaccine, or cell therapy ... With a broad portfolio, we are expediting development of our diverse pipeline of novel therapeutics ...
Senior Manager, Manufacturing Aseptic Process Leader
Hopewell, VA · On-site
$133 - $178/hr
Master's degree and 5+ years of sterile pharmaceutical, biologics, vaccine, or cell therapy ... With a broad portfolio, we are expediting development of our diverse pipeline of novel therapeutics ...
Cell Therapy Process Development information
What is cell therapy process development?
Cell Therapy Process Development refers to the design, optimization, and scaling up of manufacturing processes for cell-based therapies, such as CAR-T cells or stem cell products. Professionals in this field work on translating laboratory research into reproducible, efficient, and safe production methods that meet regulatory standards. This involves working with cell culture techniques, bioreactors, quality control, and process validation to ensure that therapies can be produced consistently for clinical and commercial use. The goal is to develop robust processes that deliver safe and effective cell therapies to patients.
What are the key skills and qualifications needed to thrive as a cell therapy process development professional?
To thrive in Cell Therapy Process Development, you need a solid background in cell biology, biotechnology, or a related field, often supported by a relevant degree and experience with cell culture techniques. Familiarity with bioprocessing equipment, Good Manufacturing Practice (GMP) regulations, and analytical tools such as flow cytometry and PCR is typically required. Strong problem-solving skills, attention to detail, and effective teamwork enhance performance in this collaborative and innovative environment. These competencies ensure the safe and efficient development of cell therapies, meeting rigorous quality standards and advancing clinical applications.
What are some typical challenges faced by professionals in cell therapy process development, and how are they addressed?
Professionals in Cell Therapy Process Development often encounter challenges such as scaling up production processes from laboratory to clinical or commercial scale while maintaining product quality and consistency. Additional hurdles include adhering to strict regulatory requirements and managing complex collaborations across cross-functional teams, like quality assurance, regulatory affairs, and manufacturing. These challenges are typically addressed through rigorous process optimization, thorough documentation, and ongoing communication with stakeholders to ensure that all aspects of the process meet industry standards and regulatory expectations.
What is the difference between Cell Therapy Process Development vs Cell Therapy Manufacturing Specialist?
| Aspect | Cell Therapy Process Development | Cell Therapy Manufacturing Specialist |
|---|---|---|
| Credentials | Typically requires a degree in biology, biochemistry, or biomedical engineering; certifications in GMP or cell therapy are common | Similar credentials; often holds degrees in related fields and GMP certifications |
| Work Environment | Research labs, development facilities, early-stage process optimization | Manufacturing plants, production floors, quality control labs |
| Industry Usage | Focuses on developing and optimizing cell therapy processes | Involved in large-scale production and process execution |
Cell Therapy Process Development professionals focus on designing and refining cell therapy procedures, while Cell Therapy Manufacturing Specialists handle the production and quality assurance in manufacturing settings. Both roles require similar educational backgrounds and certifications but differ mainly in their work environment and specific responsibilities.
What are popular job titles related to Cell Therapy Process Development jobs in Virginia?
For Cell Therapy Process Development jobs in Virginia, the most frequently searched job titles are:
- Respiratory Therapist Manager
- Transport Respiratory Therapist
- Overnight Telehealth Therapist
- Certified Respiratory Therapist
- Neonatal Physical Therapist
- Per Diem Respiratory Therapy Technician
- Per Diem Remote Mental Health Therapist
- Respiratory Therapist
- Remote Respiratory Therapist
- Respiratory Therapist Director
What job categories do people searching Cell Therapy Process Development jobs in Virginia look for?
The top searched job categories for Cell Therapy Process Development jobs in Virginia are:
What cities in Virginia are hiring for Cell Therapy Process Development jobs?
Cities in Virginia with the most Cell Therapy Process Development job openings:
Contractor
Re-posted 21 days ago
Job description
Company Description
A Few Words About Us Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing.
Job Description
The incumbent will prepare analytical, formulation, stability, manufacturing, operating procedures and other technical and GMP related documentation.
Use Electronic Document Management System (EDMS) for the preparation and maintenance of electronic (documents) records.
Administer the electronic document review and approval process.
All work is to be done in a compliant manner according to SOP guidelines and cGMPs.
The incumbent will review for accuracy, readability and format ensuring that all documents are in compliance with company policies/guidelines and meet the required timelines.
This position will also maintain hard copy files, electronic data, and records for Consumer Global R&D and enter data in electronic database for data tracking purposes in support of Training department.
Responsible for performing essential functions of record operations, such as indexing, filing, retrieving, distributing (via copying or check-out), and ensuring the integrity of records housed in the PR&D site repository.
The individual also participates in various operations, such as annual file review, relocation of records, inventory control, etc., as required.
The individual assists with other QC&C clerical activities, as required
Qualifications
Position requires excellent writing, communication, and organizational skills, and attention to detail.
Technical writing experience in the pharmaceutical industry is preferred.
Advanced knowledge of Microsoft tool suite (Word, Excel, PowerPoint, and Access) is required.
BS Degree in Scientific field plus 1-3 years of direct experience preferred (Pharmaceutical experience a plus).
Additional Information
Warm Regards
Ricky Bansal
732-429-1925
About Integrated Resources
Sourced by ZipRecruiter
Integrated Resources Inc (IRI), based in Edison, NJ, US, is an esteemed player in the staffing solutions industry with a credible presence on their official website irionline.com. Notably, IRI provides a range of professional staffing services including contract, contract-to-hire, and direct hire solutions to a wide spectrum of industries such as healthcare, life sciences, manufacturing, financial, insurance, and others. Since its inception, IRI has been committed to delivering top-talent and optimum solutions to meet its clients' diverse needs.
Industry
Recruiting and staffing services
Company size
51 - 200 Employees
Headquarters location
Edison, NJ, US
Year founded
1996