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Health is seeking a Material Science and Technology Transfer Chemist for its Nuclear and Precision Health Solutions team. The role involves radiopharmaceutical product development and technology transfer across qualified manufacturing facilities, emphasizing cGMP and GDP compliance. Request deadline: April 12,2025.">
Health, Material science, Technology Transfer Chemist, Nuclear Manufacturing, Radiopharmaceutical, cGMP, GDP, Job Opportunity"> health-chemist-job"> Health Seeks Material Science and Technology Transfer Chemist">
Health's Nuclear and Precision Health Solutions team as a Material Science and Technology Transfer Chemist. apply by April 12, 2025.">
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Cardinal Health Seeks Material Science and Technology Transfer Chemist for Nuclear Manufacturing
Table of Contents
- Cardinal Health Seeks Material Science and Technology Transfer Chemist for Nuclear Manufacturing
- Key Responsibilities and Expectations
- Qualifications and Preferred Experience
- What to Expect at This Level
- Compensation and Benefits
- application Deadline
- Conclusion
- Cracking the Code: A Deep Dive into the World of Radiopharmaceutical Manufacturing and the Cardinal Health Chemist Role
- Cracking the Code: A Deep Dive into the World of Radiopharmaceutical Manufacturing and the Cardinal Health Chemist Role
Cardinal Health is actively recruiting a Material Science and Technology Transfer Chemist to join its Technical Operations team within the Nuclear and Precision Health Solutions division.This pivotal role centers on the development and technology transfer of radiopharmaceutical products across a network of qualified manufacturing facilities. The position demands strict adherence to current Good Manufacturing Practices (cGMP), Good Documentation Practices (GDP), environmental health and safety guidelines, and internal policies. The application window is anticipated to close on April 12, 2025, urging interested candidates to apply promptly.
The Material Science and Technology Transfer Chemist will be instrumental in adapting, setting up, transferring, training, and maintaining drug products. This position necessitates a combination of technical expertise, independence, and teamwork to meet program timelines and production demands.The role offers a unique opportunity to contribute to the advancement of nuclear medicine and patient care.
Key Responsibilities and Expectations
The core responsibilities of the position are multifaceted, encompassing both project-specific tasks and broader support for manufacturing operations. The primary focus is delivering on all operational timelines related to technical transfer projects. A secondary, but equally critically important, focus involves providing day-to-day support for the manufacturing site and other Nuclear and Precision Health Solutions (NPHS) projects.
Key responsibilities include:
- executing timelines and maintaining clear, accurate communications.
- maintaining all required qualifications.
- Completing equipment qualification, computer system validation, and cleaning verification protocols in partnership with validation personnel.
- Leading investigations and documenting deviations and exceptions during technology transfer.
- Training facility personnel on new manufacturing and testing procedures and providing routine production support.
- Facilitating the operation and maintenance of production equipment and testing instrumentation.
- Cleaning and maintaining all production, testing, and related laboratory equipment during technology transfer.
- Collaborating and partnering with cross-functional teams.
- Communicating all issues related to safety, quality, and compliance to leadership.
- Traveling as necessary based on business needs (approximately 35% travel).
Qualifications and Preferred Experience
Candidates for the Material Science and Technology Transfer Chemist position should possess a Bachelor of Science degree or equivalent experience, with a preference for a background in analytical chemistry or engineering. Strong written and verbal interaction skills are essential.
Additional qualifications include:
- Demonstrated experience in the operation, use, and maintenance of pharmaceutical production equipment and cleanroom facilities.
- Experience in the manufacture of radiopharmaceutical products.
- Foundational expertise in the setup,operation,and maintenance of conventional analytical instrumentation (HPLC/GC/TLC/etc.) and modern chromatography data systems.
- Ability to work in a controlled surroundings requiring special attention to environmental,health,and safety regulations.
- Commitment to maintaining data integrity through strict adherence to standardized procedures and relevant compliance requirements.
- Motivation to work effectively and cooperatively with others, and to establish and maintain good working relationships.
- Desire to create, develop, and mature manufacturing and testing processes, and facility and systems infrastructure, to streamline operational efficiency across a broad range of products.
- Adaptability to work periodic off-shift hours to accommodate routine production schedules among qualified facilities.
- Prior Authorized User certification is preferred; Nuclear Pharmacy Training can be provided.
- Ability to lift up to 55 pounds as needed.
The role also requires the ability to travel as necessary based on business needs, estimated at around 35%.
What to Expect at This Level
At this level, the accomplished candidate will be expected to apply working knowledge in the application of concepts, principles, and technical capabilities to perform varied tasks. Thay will work on projects of moderate scope and complexity, identifying possible solutions to a variety of technical problems and taking action to resolve them. Judgment will be applied within defined parameters, with general guidance provided, and more detailed instruction on new projects. Work will be reviewed for sound reasoning and accuracy.
Compensation and Benefits
The anticipated salary range for the position is $75,600 – $108,000. While the position is not bonus eligible, Cardinal Health offers a complete benefits package to support employee health and well-being.These benefits include:
- Medical, dental, and vision coverage
- Paid time off plan
- Health savings account (HSA)
- 401k savings plan
- Access to wages before payday with myFlexPay
- Flexible spending accounts (FSAs)
- Short- and long-term disability coverage
- work-Life resources
- Paid parental leave
- Healthy lifestyle programs
Cardinal Health emphasizes that the listed salary range is an estimate, and actual pay is determined by multiple factors, including geographical location, relevant education, experience, skills, and an evaluation of internal pay equity.
application Deadline
Interested candidates are encouraged to submit thier applications quickly, as the application window is anticipated to close on April 12, 2025.
Conclusion
The Material Science and Technology Transfer Chemist position at Cardinal Health offers a challenging and rewarding chance for qualified individuals to contribute to the development and manufacturing of radiopharmaceutical products. With a focus on technical expertise, collaboration, and adherence to strict quality standards, this role is ideal for those seeking to advance their careers in the pharmaceutical industry. The deadline for applications is approaching, so interested candidates should apply without delay.
Cracking the Code: A Deep Dive into the World of Radiopharmaceutical Manufacturing and the Cardinal Health Chemist Role
Did you know that the demand for skilled chemists in radiopharmaceutical manufacturing is exploding? This isn’t just about filling prescriptions; it’s about pushing the boundaries of medical science and improving lives through cutting-edge nuclear medicine. Let’s explore this burgeoning field with Dr. Anya Sharma, a leading expert in pharmaceutical technology transfer and nuclear medicine.
World-Today-News.com Senior Editor: Dr. Sharma, thank you for joining us. Cardinal Health’s new opening for a Material Science and Technology Transfer Chemist has sparked significant interest. What makes this role so crucial in today’s healthcare landscape?
It’s a critical role,indeed. The demand for radiopharmaceuticals—radioactive drugs used in diagnostics and therapy – is growing exponentially. This position focuses on the vital process of technology transfer within radiopharmaceutical manufacturing.It’s not just about making the drug; it’s about ensuring consistent, high-quality production across multiple facilities, adhering strictly to current Good Manufacturing Practices (cGMP) and Good Documentation practices (GDP). Think of it as the bridge between scientific innovation and safe, accessible patient care.Without seamless technology transfer, we can’t effectively scale up production to meet the increasing global demand for these life-saving medicines.
Dr. Anya Sharma, Pharmaceutical Technology Transfer Expert
World-Today-news.com Senior Editor: The job description highlights the importance of GMP and GDP compliance. Can you elaborate on why this is so critical, notably in the nuclear and precision health sector?
Absolutely. In radiopharmaceutical manufacturing, compliance isn’t just a box to tick; it’s basic to patient safety and the integrity of the entire process.cGMP ensures the product meets stringent quality standards, from raw materials to the final product. GDP ensures proper record-keeping, traceability, and audit trails, enabling regulators and stakeholders to verify the whole manufacturing process. Any deviation from these standards can have serious consequences,perhaps leading to inaccurate diagnoses,ineffective treatments,or even patient harm. These rigorous standards are non-negotiable in this field, especially considering the inherent risks associated with handling radioactive materials.
Dr. Anya Sharma, Pharmaceutical Technology Transfer Expert
World-Today-News.com Senior Editor: The role description mentions several key responsibilities, including equipment qualification, computer system validation, and cleaning verification. Why are these aspects so vital for a accomplished technology transfer?
These are all crucial pieces of the puzzle for successful technology transfer. Equipment qualification verifies that the equipment used in manufacturing performs as intended, consistently producing the desired quality. Computer system validation ensures the software and systems used in controlling and monitoring the processes are accurate and reliable. This is notably critically important in high-precision manufacturing processes like radiopharmaceutical production. Efficient cleaning verification protocols are essential to prevent cross-contamination, maintaining the purity and integrity of each batch. Without these validations, the entire process is at risk, negating the benefits of efficient transfer.
Dr. Anya Sharma, Pharmaceutical Technology Transfer Expert
World-Today-News.com Senior Editor: The ideal candidate needs a variety of technical skills, including proficiency in analytical chemistry and experience with specific instrumentation. What skills truly stand out for creating a successful candidate?
Beyond the required skills, the successful candidate will possess a blend of expertise:
- Strong analytical skills: Proficiency in techniques like HPLC, GC, and TLC is essential for ensuring product purity and quality control.
- Problem-solving acumen: The ability to troubleshoot technical issues independently and in a collaborative team setting is vital, especially during technology transfer.
- Effective dialog: Clearly conveying complex technical data is crucial for coordinating with manufacturing teams, regulatory bodies, and other stakeholders.
- Adaptability: A willingness to adapt to new processes and technologies and embrace continuous learning.
Dr. Anya Sharma, Pharmaceutical Technology Transfer Expert
World-Today-News.com Senior Editor: The position requires significant travel. How does this factor into the responsibilities and success in the role?
The travel aspect is a key element of the technology transfer process. The successful candidate must be comfortable traveling to different manufacturing facilities, providing on-site support, training staff, and troubleshooting any arising issues. This field requires adaptability and a proactive approach to overcoming challenges. the ability to work effectively in diverse environments and build strong working relationships is essential.
Dr. Anya Sharma, Pharmaceutical Technology Transfer Expert
World-today-News.com Senior Editor: What advice would you give to
Cracking the Code: A Deep Dive into the World of Radiopharmaceutical Manufacturing and the Cardinal Health Chemist Role
The demand for skilled chemists in radiopharmaceutical manufacturing is exploding, creating a critical need for experts who can bridge the gap between scientific breakthroughs and safe, accessible patient care.
World-Today-News.com Senior Editor: Dr. Sharma, thank you for joining us.Cardinal Health’s new opening for a Material Science and Technology Transfer Chemist has sparked significant interest. what makes this role so crucial in today’s healthcare landscape?
Dr. Anya Sharma, Pharmaceutical Technology Transfer Expert: It’s a critical role, indeed. the burgeoning field of nuclear medicine relies heavily on radiopharmaceuticals—radioactive drugs used in diagnostics and therapy.This Material Science and Technology Transfer Chemist position focuses on the vital process of technology transfer within radiopharmaceutical manufacturing. it’s not simply about synthesizing the drug; it’s about ensuring consistent, high-quality production across multiple facilities, adhering strictly to current Good Manufacturing Practices (cGMP) and Good Documentation Practices (GDP). Think of it as the bridge between scientific innovation and safe, accessible patient care. Without seamless technology transfer, we can’t effectively scale up production to meet the increasing global demand for thes life-saving medicines. The role directly impacts patient safety and the overall efficiency of the drug advancement and delivery pipeline.
World-today-News.com senior Editor: The job description highlights the importance of GMP and GDP compliance. Can you elaborate on why this is so critical, notably in the nuclear and precision health sector?
Dr. Anya Sharma: Absolutely. In radiopharmaceutical manufacturing, compliance isn’t merely a regulatory requirement; it’s essential to patient safety and the integrity of the entire process. cGMP ensures the product meets stringent quality standards, from raw material sourcing to final product formulation and release. GDP ensures proper record-keeping, comprehensive traceability, and meticulous audit trails, enabling regulators and stakeholders to verify every step of the manufacturing process. Any deviation from these standards can have serious consequences, potentially leading to inaccurate diagnoses, ineffective treatments, or even patient harm. These rigorous standards are non-negotiable in this field due to the inherent risks associated with handling radioactive materials and the critical role these pharmaceuticals play in patient care, thereby requiring high manufacturing quality standards.
World-Today-News.com Senior Editor: The role description mentions several key responsibilities, including equipment qualification, computer system validation, and cleaning verification. Why are these aspects so vital for a triumphant technology transfer?
Dr. Anya Sharma: These are all essential components of successful technology transfer and ensuring high-quality production. Equipment qualification verifies that manufacturing equipment consistently performs as intended, producing the desired quality. Computer system validation ensures that software and systems controlling and monitoring processes are accurate and reliable—especially crucial in the high-precision surroundings of radiopharmaceutical production.Rigorous cleaning verification protocols are vital to prevent cross-contamination, maintaining the purity and integrity of each batch. Without these validations, the entire process is at risk, hindering safe and efficient technology transfer to other facilities.
World-Today-News.com Senior Editor: The ideal candidate needs a variety of technical skills, including proficiency in analytical chemistry and experience with specific instrumentation. What skills truly stand out for creating a successful candidate?
Dr. Anya Sharma: Beyond the stated technical requirements, a successful candidate will possess a unique blend of essential capabilities:
Strong analytical skills: Proficiency in analytical techniques like High-Performance Liquid Chromatography (HPLC), Gas Chromatography (GC), and Thin-Layer Chromatography (TLC) is critical for quality control and product purity assurance.
Problem-solving acumen: the ability to effectively troubleshoot technical issues independently and collaboratively is vital, especially during technology transfers.
Effective dialog: Clearly communicating complex technical data is crucial for collaboration with manufacturing teams, regulatory bodies, and other stakeholders.
Adaptability: A willingness to adapt to new processes and technologies and a commitment to continuous learning are essential.
World-Today-News.com Senior Editor: The position requires significant travel. how does this factor into the responsibilities and success in the role?
dr. Anya sharma: The travel aspect is integral to the technology transfer process. The successful candidate must be pleasant traveling to various manufacturing facilities to provide on-site support, train staff, and troubleshoot issues.This necessitates adaptability and a proactive approach to problem-solving in diverse settings. The ability to work effectively in different environments and build strong working relationships is paramount for successful technology transfer and the ultimate success of this role.
World-Today-News.com Senior editor: What final thoughts would you offer to aspiring candidates?
Dr. Anya Sharma: This is a truly rewarding career prospect at the forefront of nuclear medicine. Individuals with a passion for pharmaceutical science, a commitment to quality, and a collaborative spirit will thrive in this role. The ability to contribute to the advancement of radiopharmaceutical production, ultimately improving patient care, is a highly impactful aspect of the position. If you possess the required expertise and are prepared for a challenging yet fulfilling career, I strongly encourage an application before the April 12th deadline.
We urge our readers to share their thoughts and insights on this critical role in the comments below. What other key skills and attributes would you consider essential for success in this rapidly expanding and crucial field?