Current jobs related to Regulatory Affairs Specialist Chemical and MoAO Compliance - Coralville, Iowa - Danaher
-
Chemical Process Specialist
4 weeks ago
Coralville, Iowa, United States Actalent Full timeJob SummaryActalent is seeking a skilled Chemical Technician 2 to join our team. As a key member of our production team, you will be responsible for ensuring the efficient and safe operation of our chemical manufacturing processes.Key ResponsibilitiesInventory Management: Monitor and manage inventory levels to ensure timely and effective production.Work...
-
Coralville, Iowa, United States Danaher Corporation Full timeAt Danaher Corporation, we are committed to accelerating the real-life impact of tomorrow's science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.This role is part of the Regulatory Affairs and Compliance Department and will be onsite...
-
Coralville, Iowa, United States Danaher Corporation Full timeAt Danaher Corporation, we are seeking a highly skilled Principal Quality Assurance and Risk Management Specialist to join our Regulatory Affairs and Compliance Department. This onsite position in Coralville, IA, will be part of our global team, celebrating our differences and inclusive in our approach.Key Responsibilities:Support all phases of product...
-
Chemical Process Specialist
2 weeks ago
Coralville, Iowa, United States Actalent Full timeJob DescriptionKey ResponsibilitiesMonitor and manage inventory levels to ensure efficient production processes.Utilize the ERP system to create work orders, transfer materials, and decrement inventory levels.Dispense materials for production as needed, adhering to established protocols.Participate in customer and regulatory audits, including OSHA and EPA...
-
Principal Quality Assurance Specialist
2 weeks ago
Coralville, Iowa, United States Integrated DNA Technologies Full timeJob Title: Principal Quality Assurance SpecialistIntegrated DNA Technologies (IDT) is a leading manufacturer of custom oligonucleotides and proprietary technologies for genomics applications. Our work is complex and cutting-edge, and our team members are curious, creative thinkers who understand that good data drives smart decisions. At IDT, we recognize...
-
Principal Quality Engineer
2 weeks ago
Coralville, Iowa, United States Danaher Corporation Full timeJob Title: Principal Quality Engineer - Design Assurance and Risk ManagementWe are seeking a highly skilled Principal Quality Engineer to join our Regulatory Affairs and Compliance Department. As a key member of our team, you will be responsible for ensuring the quality and compliance of our medical devices.Key Responsibilities:Support all phases of product...
-
Coralville, Iowa, United States Integrated DNA Technologies Full timeJob SummaryIntegrated DNA Technologies (IDT) is a leading manufacturer of custom oligonucleotides and proprietary technologies for genomics applications. We are seeking a highly skilled Principal Quality Engineer, Design Assurance and Risk Management to join our Regulatory Affairs and Compliance Department. This role will be based in Coralville, IA, and will...
-
Medical Support Specialist
2 weeks ago
Coralville, Iowa, United States Biolife Plasma Services Full timeAbout the RoleBioLife Plasma Services is seeking a Medical Support Specialist to join our team. As a Medical Support Specialist, you will play a critical role in ensuring the safety and well-being of our donors. Your primary responsibility will be to determine donor eligibility to donate plasma, manage donor adverse events, and review laboratory test...
-
Medical Support Specialist Plasma Center Nurse
2 weeks ago
Coralville, Iowa, United States Biolife Plasma Services Full timeAbout the RoleAs a Medical Support Specialist Plasma Center Nurse at BioLife Plasma Services, you will play a vital role in ensuring the quality and safety of plasma donations. Your primary responsibility will be to determine donor eligibility, manage donor adverse events, and review laboratory test results. You will work under the guidance of the Center...
-
Medical Support Specialist
2 weeks ago
Coralville, Iowa, United States BioLife Plasma Services Full timeAbout the RoleAs a Medical Support Specialist at BioLife Plasma Services, you will play a critical role in ensuring the safety and well-being of our donors. Your primary responsibility will be to determine donor eligibility to donate plasma, manage donor adverse events, and review laboratory test results. You will also be responsible for notifying donors of...
-
Medical Support Specialist
1 month ago
Coralville, Iowa, United States Biolife Plasma Services Full timeAbout the RoleWe are seeking a highly skilled Medical Support Specialist to join our team at BioLife Plasma Services. As a Medical Support Specialist, you will play a critical role in ensuring the safety and well-being of our donors and employees.Key ResponsibilitiesDetermine donor eligibility to donate plasma, including proper management of informed...
-
Medical Support Specialist
1 month ago
Coralville, Iowa, United States Biolife Plasma Services Full timeAbout the RoleWe are seeking a highly skilled and compassionate Medical Support Specialist to join our team at BioLife Plasma Services. As a Medical Support Specialist, you will play a critical role in ensuring the safety and well-being of our donors and employees.Key ResponsibilitiesDetermine donor eligibility to donate plasma, including proper management...
-
Medical Support Specialist Plasma Center Nurse
2 weeks ago
Coralville, Iowa, United States Biolife Plasma Services Full timeAbout the RoleAs a Medical Support Specialist Plasma Center Nurse at BioLife Plasma Services, you will play a vital role in supporting plasma center operations. Your primary responsibility will be to determine donor eligibility, manage donor adverse events, review laboratory test results, and notify donors of unsuitable test results. You will work under the...
-
Skilled Technician
1 week ago
Coralville, Iowa, United States Omni Inclusive Full timeJob Summary:The Chemical Production Specialist efficiently produces high-quality materials for use in Omni Inclusive's production labs. This role involves working a 12:00 noon to 9:00pm shift, 5 days a week (Monday to Friday).Key Responsibilities:Monitor inventory levels effectively, utilizing the ERP system.Participate in customer and regulatory audits as...
-
Licensed Practical Nurse LPN
2 weeks ago
Coralville, Iowa, United States BioLife Plasma Services Full timeAbout the RoleAs a Medical Support Specialist at BioLife Plasma Services, you will play a vital role in ensuring the highest quality plasma collection process. Your expertise will be instrumental in determining donor eligibility, managing donor adverse events, and reviewing laboratory test results. You will work closely with the Center Manager and Center...
-
Medical Support Specialist Plasma Center Nurse
2 weeks ago
Coralville, Iowa, United States Biolife Plasma Services Full timeAbout the Role:The Medical Support Specialist (Plasma Center Nurse) plays a vital role in supporting plasma center operations. This position requires a high level of customer service and quality commitment, ensuring a positive experience for donors.Key Responsibilities:Determine donor eligibility to donate plasma, including proper management of informed...
-
Medical Assessment Nurse LPN
2 weeks ago
Coralville, Iowa, United States Biolife Plasma Services Full timeAbout the Role:As a Medical Assessment Nurse LPN at BioLife Plasma Services, you will play a critical role in ensuring the safety and well-being of our donors. Your primary responsibility will be to determine donor eligibility to donate plasma, manage donor adverse events, review laboratory test results, and notify donors of unsuitable test results.Key...
-
Licensed Practical Nurse LPN
2 weeks ago
Coralville, Iowa, United States Biolife Plasma Services Full timeAbout the Role:As a Medical Support Specialist Plasma Center Nurse at BioLife Plasma Services, you will play a vital role in ensuring the safety and well-being of our donors. Your primary responsibility will be to determine donor eligibility to donate plasma, manage donor adverse events, review laboratory test results, and notify donors of unsuitable test...
-
Medical Support Specialist
1 month ago
Coralville, Iowa, United States Biolife Plasma Services Full timeAbout the RoleWe are seeking a highly skilled Medical Support Specialist to join our team at BioLife Plasma Services. As a Medical Support Specialist, you will play a critical role in ensuring the safety and well-being of our donors, while also contributing to the success of our plasma collection operations.Key ResponsibilitiesDetermine donor eligibility to...
-
Medical Support Specialist
1 month ago
Coralville, Iowa, United States Biolife Plasma Services Full timeAbout the RoleWe are seeking a highly skilled Medical Support Specialist to join our team at BioLife Plasma Services. As a Medical Support Specialist, you will play a critical role in ensuring the safety and well-being of our donors, while also contributing to the success of our plasma collection operations.Key ResponsibilitiesDetermine donor eligibility to...
Regulatory Affairs Specialist Chemical and MoAO Compliance
3 months ago
Integrated DNA Technologies (IDT) is the leading manufacturer of custom oligonucleotides and proprietary technologies for genomics applications. Our work is complex and cutting-edge, and our team members are curious, creative thinkers who understand that good data drives smart decisions. At IDT, we realize that although science may be uniform, people are unique. We promote a culture where engaged people are motivated and have opportunities to achieve their full potential, as part of one global team.
IDT is one of 10 Life Sciences companies of Danaher. Together, we accelerate the discovery, development and delivery of solutions that safeguard and improve human health.
This position is part of the Quality Assurance and Regulatory Affairs group located in Coralville, IA, USA and will be hybrid. At IDT, we are one global team. We celebrate our differences, engage in healthy debate, and are inclusive. Together, we accomplish great things.
In this role, you will have the opportunity to:
- Assist with maintaining SDS databases and authoring of GHS/CLP/OSHA compliant SDS and certifications for a diverse range of IDT's substances and mixtures globally for new and existing products.
- Interact and form constructive cross-functional relationships with stakeholders within Quality, Marketing, R&D, Systems Engineering and Operations
- Monitor and report status on existing and emerging global requirements with potential to impact IDT products, effectively communicate to management for consideration of impact to the business.
- Provide guidance applicable to labeling of products, which include hazardous chemical components, and completion of compliance questionnaires, as assigned.
- Assess product chemical composition and classify the products in line with applicable country regulations
The essential requirements of the job include:
- Bachelor's degree in a technical field such as chemistry, biochemistry, biology, or related work experience.
- 1-2 years of experience in regulatory/EHS/compliance role.
- Previous work experience in a regulated or standardized environment (i.e. ISO 9001/ISO
It would be a plus if you also possess previous experience in:
- Use or knowledge of SAP and/or UL WERCS
At IDT we believe in designing a better, more sustainable workforce. We recognize the benefits of flexible, hybrid working arrangements for eligible roles and are committed to providing enriching careers, no matter the work arrangement.
This position is eligible for a hybrid work arrangement in which you can work part-time at the Company location identified above and part-time remotely from your home. Additional information about this hybrid work arrangement will be provided by your interview team. Explore the flexibility and challenge that working for IDT can provide.
We offer a comprehensive package of benefits including paid time off, medical/dental/vision insurance and 401(k) to eligible employees.
Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole discretion unless and until paid and may be modified at the Company's sole discretion, consistent with the law.
#LI-AY1
At Danaher we bring together science, technology and operational capabilities to accelerate the real-life impact of tomorrow's science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. Our global teams are pioneering what's next across Life Sciences, Diagnostics, Biotechnology and beyond. For more information, visit
Danaher Corporation and all Danaher Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. We value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes.
The EEO posters are available here.
We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform crucial job functions, and to receive other benefits and privileges of employment. Please contact us at to request accommodation.
