or university and/or graduate of an accredited school of medical technology, or equivalent such as military training as defined by 42 CFR 493.1489. Personnel who, prior to 2/28/92 have qualified at the Medical Technologist level by achieving a satisfactory grade on a HHS examination.
The above meets required criteria as defined by CLIA regulations for High Complexity testing (42 CFR 493.1489, Jan. 24, 2003). PREFERRED EXPERIENCE: 6 months to 1-year Medical Lab Scientist experience in acute care facility PREFERRED CERTIFICATIONS/LICENSURE: Certified (registered) or registry-eligible in accordance with an approved certifying agency, e. g. ASCP, HHS, AMT. Registry eligible should obtain
certification within 1 year from date of hire. Once certified, no annual renewals are required. #LI-JH5Tenet complies with federal, state, and/or local laws regarding mandatory vaccination of its workforce.
If you are offered this position and must be vaccinated under any applicable law, you will be required to show proof of full vaccination or obtain an approval of a religious or medical exemption prior to your start date. If you receive an exemption from the vaccination requirement, you will be required to submit to regular testing in accordance with the law.230#######Employment practices will not be influenced or affected by an applicant s or employee s race, color, religion, interaction
(including pregnancy), national origin, age, disability, genetic information, interactionual orientation, gender identity or expression, veteran status or any other legally protected status.
Tenet will make reasonable accommodations for qualified individuals with disabilities unless doing so would result in an undue hardship. Associated topics: blood collection, lab, laboratory, medical, pathology, scientist, technician i, technician iii, technologist, testing
Johnson & Johnson, and you can count on us to keep working tirelessly to make that future a reality for patients everywhere, by fighting sickness with science, improving access with ingenuity, and healing hopelessness with heart. We focus on areas of medicine where we can make the biggest difference: Cardiovascular & Metabolism, Immunology, Infectious Diseases & Vaccines, Neuroscience, Oncology, and Pulmonary Arterial Hypertension.
Visit us: Janssen Research & Development, L. L. C. develops treatments that improve the health and lifestyles of people worldwide. Research and development areas encompass novel targets in neurologic disorders, gastroenterology, oncology, infectious disease,
diabetes, hematology, metabolic disorders, immunologic disorders, and reproductive medicine. The Lead Regulatory Scientist provides support for regulatory activities for products in the assigned portfolio, including ensuring that content and intent of regulatory filings support the global regulatory strategy.
Key Responsibilities: Participate in global and regional regulatory team meetings and advise the regulatory team on applicable regulatory requirements, project-specific regulatory issues as assigned Develop an understanding of the regional regulatory environment, competitor intelligence, and therapeutic area Assist in the preparation of meetings and act as backup for contact with
Regulatory Agencies as needed Ensure responses to Regulatory Agency queries are made in a timely manner, and that content is consistent with the regulatory strategy Work cross-functionally and lead team meetings as appropriate Review clinical trial plans, protocols and submission plans ensuring alignment with regulatory requirements Advise team in required documents and submission strategies Support the development and improvement of processes related to regulatory submissions Provide regulatory input for and appropriate follow-up to inspections, audits, litigation support, and product complaints Keep abreast of current and pending approvals in specific therapeutic areas and is knowledgeable of laws, guidances and requirements related to those areas Interact with Health Authorities (HA) regarding program-specific issues and serve as secondary HA point-of-contact May have interaction with internal and external colleagues with coordination between departments May represent J&J or company externally with some degree of supervision Proactively anticipates issues; exercises judgment in developing new approaches/solutions and resolving issues Influences or persuades others within area of immediate responsibility, scope and level to accept new ideas, practices and approaches Qualifications Education: One of the following combinations of education and experience is required: A Bachelor's Degree with a minimum of 6 years of relevant experience An Advanced/Master's Degree with a minimum of 4 years of relevant experience A Pharm D/Ph D with a minimum 2 years of relevant experience Experience and Skills: Required: Previous health regulatory industry experience and understanding of the drug development process is required Skilled at effectively prioritizing assignments for multiple projects simultaneously is required Experience within a cross-functional team environment as an individual contributor and decision maker within a matrix organization is required Strong interpersonal and communication skills is required Preferred: Understanding of regulatory submission and approval process and applicable US and EMA regulatory guidelines is preferred Relevant regulatory affairs experience in medical/biotech is preferred Experience responding to Healthy Authority (HA) requests, managing HA interactions and life cycle management of IND/CTA/NDA/MAA applications is preferred Project management experience and ability to manage multiple priorities is preferred Diverse therapeutic area experience is preferred Direct experience in regulatory affairs is preferred Regulatory, Clinical or R&D experience with products in early and late development stages is preferred Experience responding to FDA requests, leading FDA interactions, and lifecycle management of IND/NDA applications is preferred Immunology Drug Development experience is preferred Other: 10% domestic travel and potential international travel may be required for this position Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer.
All qualified applicants will receive consideration for employment without regard to race, color, religion, interaction, interactionual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.
For more information on how we support the whole health of our employees throughout their wellness, career and life journey, please visit www. careers.
most complex problems for a safer, healthier world. About the role: The Sample Receiving Supervisor directs the daily operations of the sample administration group. This includes oversight of sample receiving, and bottle orders. The Sample Receiving Supervisor must possess a strong working knowledge of laboratory information management systems as well as have a technical background in laboratory analysis and operations.
The position requires a combination of superior client services skills, technical knowledge, system/process management, and supervisory experience. Responsibilities About you: Establish a cohesive integrated group that is responsive to both customer and laboratory needs.
Services of the group include all aspects of sample management. Develop standardized procedures within the group for sample management. Review incoming work to ensure work requests are properly specified according to project requirements.
Track projects through the laboratory to allow real time communication of pertinent issues with the client. Manage costs associated with operation of sample management, and bottle order. Develop formal cross training procedures in conjunction with QA to ensure backup in all aspects of the sample receiving department. Required Qualifications: A bachelor's degree in chemistry is preferred with a proven track record of experience that demonstrates
the ability to fulfill the position requirements. An advanced degree in chemistry or a related science is a plus.
Physical Demands: Able to speak and hear clearly while communicating with staff, management, and clients. Able to sit and /or stand for 100% of an 8 hour day. Dexterity in hands and fingers to operate computer and other equipment. Must have average vision and able to see to read reports and operate equipment. Qualifications Working at ALS: Our people are our most valuable asset and drive our success at ALS. We are a diverse community of dedicated professionals united by our passion to make a difference in the world. We reward excellence and uphold our values in our work and how we treat each other.
At ALS, you'll be supported to expand your skills and develop new ones so you can reach your full potential. We invest in our people with a range of programs and provide opportunities across the company, giving our people scope to grow diverse careers and develop as leaders. We want everyone to have a safe, flexible and rewarding career that makes a positive impact on our people, the planet and the communities where we work. Our benefits include: Structured wage increases Comprehensive benefit package (including: medical, dental, and vision coverage, life and disability insurance, retirement plan with company match, employee assistance and wellness programs, access to company perks) Additional vacation days for years of service Business support for education or training after 9 months with the company Learning & development opportunities (unlimited access to e-learnings and more)About ALS: ALS is a global leader in scientific testing, providing comprehensive testing solutions to clients in more than 60 countries across a wide range of industries, including environment, food and beverage, mining, personal care, medical, healthcare and equipment reliability.
Using state-of-the-art technologies and innovative methodologies, our dedicated international teams deliver the highest-quality testing services and personalised solutions supported by local expertise. We help our clients leverage the power of data-driven insights for a safer and healthier world. Everyone matters: ALS is proud to be an equal opportunity employer committed to achieving and maintaining a workforce which reflects and affirms the diversity of our society ALS is a VEVRAA Federal Contractor. EOE AA Minority, Female, Veteran, Individuals with Disabilities Click Here to view the EEO is the Law poster Click Here to view the FMLA Law poster Click Here to view the EPPA Law Poster Click Here to view the Pay Transparency Provision Click Here to view company E-Verify Participation Poster ALS also welcomes applications from people with all levels of ability.
Accommodation is available on request for candidates taking part in all aspects of the selection process.
nursing. Makes appropriate assignments and delegates to other care providers as a means to help manage the clinical situation. Requirements: Education/Skills Bachelor of Science Degree in Nursing, preferred. Experience 1 year of experience in the related nursing specialty preferred.
Licenses, Registrations, or Certifications BLS within 2 weeks of hire RN License in state of Texas or compact Work Type: Full Time We now have RECRUITER ON DEMAND to enhance your candidate experience. If you want to talk to a recruiter NOW and it’s Monday-Thursday 9:00am to 3:00pm, please click the link below! We would love to tell you more about this position. Microsoft Teams meeting Join on your computer,
mobile app or room device Click here to join the meeting Meeting ID: 548 Passcode: KZCaf Q Download Teams Join on the web EEO is the law - click below for more information: www.
eeoc. gov/sites/default/files/2023-06/22-088_EEOC_Know Your Rights6.12 Screen Rdr. pdf We endeavor to make this site accessible to any and all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process, please contact us at (844) 257-xyz X. For more details: jobs-search. org/sciences_tyler-c448626/rn-registered-nurse-observation-full-time-tyler_i1976183110
nursing. Makes appropriate assignments and delegates to other care providers as a means to help manage the clinical situation. Requirements: Bachelor of Science Degree in Nursing, preferred. 1 year of experience in the related nursing specialty preferred. BLS within 2 weeks of hire RN License in state of employment or compact Work Type: Per Diem As Needed We now have RECRUITER ON DEMAND to enhance your candidate experience.
If you want to talk to a recruiter NOW and it’s Monday-Thursday 9:00am to 3:00pm, please click the link below! We would love to tell you more about this position. Microsoft Teams meeting Join on your computer, mobile app or room device Click here to join the meeting
Meeting ID: 548 Passcode: KZCaf Q Download Teams Join on the web EEO is the law - click below for more information: www. eeoc. gov/sites/default/files/2023-06/22-088_EEOC_Know Your Rights6.12 Screen Rdr.
pdf We endeavor to make this site accessible to any and all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process, please contact us at (844) 257-xyz X. For more details: jobs-search. org/sciences_tyler-c448626/rn-registered-nurse-infusion-services-tyler_i1976331126
