... processing staff and nursing * Respond to unsolicited requests for scientific and product ... Experience supporting the development and/or launch of a new pharmaceutical product in the U.S.
New
... processing staff and nursing * Respond to unsolicited requests for scientific and product ... Experience supporting the development and/or launch of a new pharmaceutical product in the U.S.
New
... processing staff and nursing * Respond to unsolicited requests for scientific and product ... Experience supporting the development and/or launch of a new pharmaceutical product in the U.S.
New
... processing staff and nursing * Respond to unsolicited requests for scientific and product ... Experience supporting the development and/or launch of a new pharmaceutical product in the U.S.
New
... cell processing staff and nursing Respond to unsolicited requests for scientific and product ... Development (R&D) Support and represent Medical Affairs at relevant congresses and scientific ...
New
... cell processing staff and nursing Respond to unsolicited requests for scientific and product ... Development (R&D) Support and represent Medical Affairs at relevant congresses and scientific ...
New
Maintain current knowledge of advances in stem cell transplantation and cellular therapy through ongoing professional development Qualifications * Board certification in Internal Medicine
Maintain current knowledge of advances in stem cell transplantation and cellular therapy through ongoing professional development Qualifications * Board certification in Internal Medicine
Manager, Process Development
Brighton, MI · On-site
$100K - $120K/yr
Opportunity to lead technical transfer and process development activities supporting commercialization of innovative therapies. * High visibility and cross-functional leadership exposure across ...
Manager, Process Development
Brighton, MI · On-site
$100K - $120K/yr
Opportunity to lead technical transfer and process development activities supporting commercialization of innovative therapies. * High visibility and cross-functional leadership exposure across ...
Manager, Process Development
Brighton, MI · On-site
Opportunity to lead technical transfer and process development activities supporting commercialization of innovative therapies. * High visibility and cross-functional leadership exposure across ...
Manager, Process Development
Brighton, MI · On-site
Opportunity to lead technical transfer and process development activities supporting commercialization of innovative therapies. * High visibility and cross-functional leadership exposure across ...
Manager, Process Development
Brighton, MI · On-site
Why Join BiovireOpportunity to lead technical transfer and process development activities supporting commercialization of innovative therapies.High visibility and cross-functional leadership exposure ...
Quick apply
Manager, Process Development
Brighton, MI · On-site
Why Join BiovireOpportunity to lead technical transfer and process development activities supporting commercialization of innovative therapies.High visibility and cross-functional leadership exposure ...
... Cell Therapy Clinical Development. In this role, you will provide clinical leadership and ... As part of the recruitment process, certain background checks may be conducted in accordance with ...
... Cell Therapy Clinical Development. In this role, you will provide clinical leadership and ... As part of the recruitment process, certain background checks may be conducted in accordance with ...
... included, developed and empowered to fulfil their aspirations. Join Kite and help create more ... Support ATC readiness and comfort with CAR T processes to enable demand generation Cross Functional ...
... included, developed and empowered to fulfil their aspirations. Join Kite and help create more ... Support ATC readiness and comfort with CAR T processes to enable demand generation Cross Functional ...
Executive Medical Director, Clinical Program Lead, Hematology Oncology Cell Therapy
Warren, MI · On-site
In this role, you will shape clinical development strategy and drive execution of clinical trials ... As part of the recruitment process, certain background checks may be conducted in accordance with ...
Executive Medical Director, Clinical Program Lead, Hematology Oncology Cell Therapy
Warren, MI · On-site
In this role, you will shape clinical development strategy and drive execution of clinical trials ... As part of the recruitment process, certain background checks may be conducted in accordance with ...
... 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
Grand Rapids, MI · 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
Grand Rapids, MI · 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
Detroit, MI · 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
Detroit, MI · 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
Ann Arbor, MI · 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
Ann Arbor, MI · 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 ...
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 Michigan?
For Cell Therapy Process Development jobs in Michigan, the most frequently searched job titles are:
- Respiratory Therapy Associate
- Respiratory Therapist Volunteer
- Respiratory Therapist Director
- Respiratory Therapist Manager
- Pulmonary Rehabilitation Coordinator
- Weekend Certified Respiratory Therapist
- Respiratory Therapist
- Life Flight Respiratory Therapist
- Weekend Contract Respiratory Therapist
- Weekend Remote Respiratory Therapist
What job categories do people searching Cell Therapy Process Development jobs in Michigan look for?
The top searched job categories for Cell Therapy Process Development jobs in Michigan are:
What cities in Michigan are hiring for Cell Therapy Process Development jobs?
Cities in Michigan with the most Cell Therapy Process Development job openings:
Full-time
Medical, Dental, Vision, Retirement, PTO
Posted 3 days ago
New
AstraZeneca rating
8.4
Based on 45 frontline employees who took The Breakroom Quiz
24th of 86 rated pharmaceutical
Job description
Senior Medical Science Liaison - Cell Therapy (Great Lakes)
Do you have expertise in, and passion for Medical Affairs in Cell Therapy? Are you ready to make a significant impact in the field of Multiple Myeloma? AstraZeneca's vision in Cell Therapy is to boldly transform the CAR-T experience with unwavering commitment to cure and access for every patient in need. Help to advance our pipeline by applying expertise and accelerating our pathway to finding a cure.
We are seeking a Senior Medical Science Liaison (MSL) to join our Cell Therapy team in the territory of Great Lakes! This role serves as the local medical voice of AZ in cell therapy and myeloma and will build a local medical strategy to improve patient care and outcomes in their territory.
The MSL is an established field-based professional with extensive scientific, clinical, and therapeutic area expertise responsible for providing medical and scientific support for AstraZeneca's cell therapy assets.
What you'll do
Minimum Qualifications
Preferred Qualifications
The territory includes Detroit You should live within this territory.
Why AstraZeneca?
At AstraZeneca when we see an opportunity for change, we seize it and make it happen, because any opportunity no matter how small, can be the start of something big. Delivering life-changing medicines is about being entrepreneurial - finding those moments and recognizing their potential. Join us on our journey of building a new kind of organization to reset expectations of what a bio-pharmaceutical company can be. This means we're opening new ways to work, pioneering groundbreaking methods, and bringing unexpected teams together. Interested? Come and join our journey.
Are you ready to bring new insights and fresh thinking to the table? Brilliant! We have one seat available, and we hope it's yours. Apply today.
AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We follow all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements.
The annual base salary for this position ranges from $174,455.20 - $261,682.80 USD. Our positions offer eligibility for various incentives-an opportunity to receive short-term incentive bonuses, equity-based awards for salaried roles and commissions for sales roles. Benefits offered include qualified retirement programs, paid time off (i.e., vacation, holiday, and leaves), as well as health, dental, and vision coverage in accordance with the terms of the applicable plans.
Date Posted
28-Aug-2026
Closing Date
10-Sept-2026
Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.
Do you have expertise in, and passion for Medical Affairs in Cell Therapy? Are you ready to make a significant impact in the field of Multiple Myeloma? AstraZeneca's vision in Cell Therapy is to boldly transform the CAR-T experience with unwavering commitment to cure and access for every patient in need. Help to advance our pipeline by applying expertise and accelerating our pathway to finding a cure.
We are seeking a Senior Medical Science Liaison (MSL) to join our Cell Therapy team in the territory of Great Lakes! This role serves as the local medical voice of AZ in cell therapy and myeloma and will build a local medical strategy to improve patient care and outcomes in their territory.
The MSL is an established field-based professional with extensive scientific, clinical, and therapeutic area expertise responsible for providing medical and scientific support for AstraZeneca's cell therapy assets.
What you'll do
- Develop and maintain scientific relationships with hematology/cell therapy thought leaders, investigators and appropriate HCPs across academic and community centers within an assigned territory
- Engage in scientific exchanges with the multidisciplinary team, including treating hematologists/oncologists, cell therapy physicians, APPs, pharmacists, apheresis and cell processing staff and nursing
- Respond to unsolicited requests for scientific and product information in accordance with company policy
- Establish oneself as a trusted scientific advisor, peer and expert to both internal stakeholders and external HCPs (e.g. functions as an expert in response to scientific questions)
- Educate cell therapy provider teams on disease state, CAR-T mechanism of action, multiple myeloma therapeutic landscape, safety and clinical management, manufacturing processes and data pertaining to the infusion center and patient management, guided by compliance considerations
- Support the implementation of cell therapy infusions in cell therapy infusion centers by timely support of health care providers in navigating the complexity of cell therapy and diverse stakeholder groups
- Gather and synthesize site-level insights from site physician leadership, multiple HCP segments within the region and communicate with medical leadership and relevant internal partners
- Identify data and educational gaps through discussion with External Scientific Experts (ESE) to inform medical affairs strategy and address unmet patient needs
- Identify opportunities to partner with HCPs on disease state initiatives, collaborative research projects, and investigator sponsored research (ISR) of interest and in alignment with areas of scientific interest
- Collaborate with key stakeholders across Medical Affairs, Commercial, and Research and Development (R&D)
- Support and represent Medical Affairs at relevant congresses and scientific meetings through scientific exchange with ESEs, medical booth coverage and sharing scientific and competitive insights
Minimum Qualifications
- Advanced scientific degree required (i.e. PharmD, MD/DO, PhD, PA or NP) in a relevant health science or clinical discipline
- 5+ years of experience in hematology/oncology with at least 2 years in a field medical or equivalent scientific engagement role, preferably in cell therapy and/or multiple myeloma
- Ability to express ideas clearly in written documentation, one-on-one conversations and in small group dialogues with the ability to distill complexity down to key messages and scientific narrative for internal/external stakeholders
- Experience supporting the development and/or launch of a new pharmaceutical product in the U.S.
- Experience operating in a matrixed environment with cross-functional partners in Medical Affairs, Commercial and R&D
- Ability to travel (40-60% by car, train and plane domestic)
Preferred Qualifications
- Doctorate degree (e.g. MD or equivalent, PharmD or PhD) with oncology/hematology specialization preferred
- Direct knowledge, experience and expertise in Hematology/Oncology Cell Therapy
- Experience of working with headquarters and implementing HQ plans in field
- Collaborative matrix management skills within diverse groups to achieve excellent results in shared goals
- A track record of building and maintaining a deep continued connection to medical practice/healthcare delivery
- Working knowledge of FDA and GMP requirements, industry rules and regulations governing cell therapy quality manufacturing and field based medical roles
The territory includes Detroit You should live within this territory.
Why AstraZeneca?
At AstraZeneca when we see an opportunity for change, we seize it and make it happen, because any opportunity no matter how small, can be the start of something big. Delivering life-changing medicines is about being entrepreneurial - finding those moments and recognizing their potential. Join us on our journey of building a new kind of organization to reset expectations of what a bio-pharmaceutical company can be. This means we're opening new ways to work, pioneering groundbreaking methods, and bringing unexpected teams together. Interested? Come and join our journey.
Are you ready to bring new insights and fresh thinking to the table? Brilliant! We have one seat available, and we hope it's yours. Apply today.
AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We follow all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements.
The annual base salary for this position ranges from $174,455.20 - $261,682.80 USD. Our positions offer eligibility for various incentives-an opportunity to receive short-term incentive bonuses, equity-based awards for salaried roles and commissions for sales roles. Benefits offered include qualified retirement programs, paid time off (i.e., vacation, holiday, and leaves), as well as health, dental, and vision coverage in accordance with the terms of the applicable plans.
Date Posted
28-Aug-2026
Closing Date
10-Sept-2026
Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.
What AstraZeneca employees say
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About AstraZeneca
Sourced by ZipRecruiter
AstraZeneca is a global, science-led, patient-focused biopharmaceutical company that focuses on the discovery, development and commercialization of prescription medicines for some of the world's most serious diseases. But we're more than one of the world's leading pharmaceutical companies. A place built on courage, curiosity and collaboration - we make bold decisions driven by patient outcomes. Empowered to lead at every level, free to ask questions and take smart risks that write the next chapter for our pipeline and Oncology team. Make a meaningful impact that brings real benefits to society. By applying your knowledge of data, you will help to redefine our industry and ultimately save lives. Work with experts who share a common goal: to accelerate the potential of medicines and the science of tomorrow.
Industry
Pharmaceutical product wholesalers and pharmaceutical and medicine manufacturing
Company size
10,000+ Employees
Headquarters location
Cambridge, Cambridgeshire, GB