for cultures. The position requires self-motivation and the capacity to work independently. Must have excellent communication abilities and basic computer skills. The position often requires a great deal of walking around client sites, may include climbing stairs or ladders, and may require lifting up to 25 pounds.
This is a part-time position with no company benefits. High School Diploma or GED required. Some college courses in Chemistry or Biology are a plus. A valid driver's license and an acceptable driving record for at least the last two years are required. If interested, please submit your resume highlighting your experience and how it directly applies to the above requirements.
Phigenics LLC is an Equal Opportunity Employer that does not discriminate on the basis of actual or perceived race, creed, color, religion, alienage or national origin, ancestry, citizenship status, age, disability or handicap, interaction, marital status, veteran status, interactionual orientation, arrest record, or any other characteristic protected by applicable federal, state or local laws.
In compliance with federal law, all persons hired will be required to verify identity and eligibility to work in the United States and to complete the required employment eligibility verification form upon hire. Job Posted by Applicant Pro
Health Information (PHI) and Personally Identifiable Information (PII) by Job Description/Role. " Key Duties and Responsibilities Provides quality check of scheduled print jobs prior to production; validates layout, imaging, and print quality. Notifies printers of any errors or corrections needed.
Reviews files for accuracy; ensures print jobs adhere to Plan guidelines and schedule. Reconciles size of print job to billing information. Facilitates progression of print job tickets through queue when needed. Maintains knowledge of Plans and regulations to ensure compliance of print jobs. Acts as primary contact for print job schedule changes and new client set up or offboarding. Maintains
print job schedules for assigned area. Facilitates receipt and distribution of mail and packages. Performs other duties as assigned. Minimum Qualifications High school diploma or GED.
Two years of experience in a mail and print production environment. The ability to follow standard operating procedures. Good organizational and time-management skills. Computer proficiency including Microsoft Office tools and applications. Preferred Qualifications Experience working in healthcare or third-party administrator environment. Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee
of this job. Duties, responsibilities, and activities may change at any time with or without notice.
Zenith American Solutions Real People. Real Solutions. National Reach. Local Expertise. We are currently seeking an experienced Print Quality Coordinator with the necessary skills, initiative, and personality, along with the desire to get the most out of their working life, to help us be our best every day. Zenith American Solutions is the largest independent Third Party Administrator in the United States and currently operates over 40 offices nationwide. The original entity of Zenith American has been in business since 1944. Our company was formed as the result of a merger between Zenith Administrators and American Benefit Plan Administrators in 2011.
By combining resources, best practices and scale, the new organization is even stronger and better than before We realize the importance a comprehensive benefits program to our employees and their families. As part of our total compensation package, we offer an array of benefits including health, vision, and dental coverage, a retirement savings 401(k) plan with company match, paid time off (PTO), great opportunities for growth, and much, much more! Internals to Apply: If you meet the minimum qualifications and are interested in applying for the above position, please submit an application.
All applications must be received by 5:00 pm on the Internal Posting Deadline listed above in order to be considered prior Job Posted by Applicant Pro
focus areas in translational multi-omics technologies, biomarkers identification, imaging, prediction, screening, detection and diagnosis, informatics and more. With more than $3 billion in revenue and over 11,000 employees, Revvity serves customers across medical and biotech, diagnostic labs, academia, and governments.
It is part of the S&P 500 index and has customer in more than 190 countries. JOB SUMMARYOur team is seeking a Senior Manager Quality Assurance to join us in our efforts to serve patients and families around the world. As the Senior Manager Quality Assurance, you will join the exciting area of genomic laboratory and companion diagnostics (CDx) solutions and services. You
will serve as the strategic project regulatory leader to provide strategic and tactical support with cross-functional development and laboratory service teams. You will act as a steward for Regulatory Affairs and have the opportunity to work with a team of professionals while collaborating with external medical company leaders to revolutionize the healthcare industry.
You will work closely with our Chief Scientific Officer to establish and execute regulatory strategies, negotiate with the FDA, lead FDA pre-submission packages, and author final product submission: IDE, 510(k), De Novo, PMA, and PMA supplements. In addition, you will work with cross functional team and Revvity Global Quality
Regulatory, Clinical Affairs (QRC) department throughout the entire product lifecycle from innovation concept, development, product launch, and post commercialization within the appropriate time guidelines.
Join our team to utilize your expertise to revolutionize what's possible in healthcare, with specialized focus in translational multi-omics technologies, biomarker identification, prediction, screening, detection, and diagnosis, informatics and more. DUTIES AND RESPONSIBILITIESEstablish Quality Management System (QMS) for Omics Companion Diagnostics (CDx) / In Vitro Diagnostics (IVD) business. Understand and communicate industry standards, regulatory requirements and feedback from healthcare authorities.
Provide quality input and direction for the Omics business. Partner with Omics business leaders to develop and implement compliant regulatory and quality assurance strategies. Implement and maintain an agile QMS with a risk-based approach. Develop KPIs and report on performance. Identify opportunities for improvement. Interface with Revvity business partners to ensure best utilization of QMS and internal partnerships. Provide Design Control guidance to ensure products comply with regulatory requirements, customer expectations, and Revvity standards.
Serve as Omics primary point of contact for Quality aspects with healthcare authorities and medical customers. Partner with customers and development teams to ensure successful completion of projects. Collaborate with technical and clinical team members to develop documentation required for regulatory submissions. Manage post market surveillance including customer complaint management. Manage audits and inspections to achieve proper ISO certificates for QMS per master plan. Maintain up-to-date knowledge of CDx and IVD regulations and applicable guidance; monitor development of regulations, and communicate impact to the business.
BASIC QUALIFICATIONSBachelors degree in life sciences.12 or more years of experience in quality, regulatory or clinical studies within the medical device or medical industry. In Vitro Diagnostics experience. Experience with US FDA clinical trials and regulatory submissions (IDE, 510(k), PMA). Familiarity with operation of laboratory instruments and applicable computer software. Ability to take direction and multi-task in a demanding environment. Ability to work independently and proactively with minimal supervision. Exceptional negotiation and critical thinking skills.
Superior interpersonal, verbal, and written communication skills. PREFERRED QUALIFICATIONSCompanion Diagnostics experience. Advanced degree or equivalent work experience. Successful experience collaborating with global cross-functional teams across multiple work locations. DIRECT REPORTS There are no direct reports in this role. WORKING CONDITIONSMinor exposure to clinical and research lab environment; exposure to blood borne pathogens; must wear personal protective equipment including lab coat, gloves and completely closed footwear while in the Laboratory. Ability to travel up to 25%, both domestic and international.
BENEFITSWe provide competitive and comprehensive benefits to our employees. Below are some highlights of our benefits: Medical, Dental, and Vision Insurance OptionsLife and Disability Insurance Paid Time-Off Parental Benefits401k with Company Match Employee Stock Purchase Plan Learn more about Revvity's benefits by visiting our Why Revvity page. PDN-9a854c78-ec67-43f7-a88c-18e8d0f0cb86
