Lead sanitation team in food manufacturing facilities, ensuring compliance with GMP, HACCP, FDA, and OSHA standards.
Locations (6)
Carthage, Missouri, United States
North Carolina, United States
Arkansas, United States
Missouri, United States
Kansas, United States
Illinois, United States
Responsibilities
Provides leadership to team members to execute cleaning and sanitizing to an effective level as instructed by Sanitation Management.
Partners with sanitation management to troubleshoot sanitation problems; recommending changes to improve sanitation policies, procedures, and cleaning effectiveness.
Ensures the necessary sanitation oversight and resources are available to fully support the operation.
Implements and promotes chemical/sanitation safety programs and safe work practices through active participation in safety meetings.
Supporting the development of sanitation workers through effective training.
Requirements
High School Diploma or equivalent
Nice to have: Bilingual in English and Spanish
Nice to have: Ability to read, write, and/or speak English
Responsible for performing numerous repetitive tasks, manual and/or machine-assisted, to produce turkey products and parts such as processing, cutting, and packaging products, while adhering to strict safety, quality, and sanitation standards, to support the daily production and company goals in their assigned department.
The Clinical Research Associate II (CRA II) will be a key contributor to AtriCure’s clinical affairs department and primarily responsible for the site management of assigned clinical investigative sites.
Locations (2)
Mason, Ohio, United States
Minnetonka, Minnesota, United States
Compensation
US Pay Range
$85,000—$105,000 USD
Responsibilities
Assist Clinical Project Managers and Sr. CRAs in the study development and start-up process
Verify that the investigator and research staff follow the approved protocol and all GCP procedures
Conduct weekly maintenance and management of study sites to ensure site compliance with study protocol, GCP/ICH, and applicable regulations
Conduct initial and ongoing study training of site personnel throughout the clinical study
Monitor and report to ATRC site enrollment activities
Lead sanitation operations at the Abilene, TX facility, overseeing daily cleaning, GMP compliance, and employee training.
Compensation
$20 per hour
Responsibilities
Comply with GMPs, HACCP and other Food Safety, quality and security guidelines
Maintain regular processes and paperwork required for continued SQF compliance
Effectively train personnel in safety awareness, use of personal protection equipment, departmental procedures, and proper operation of relevant equipment
Oversee daily cleaning of raw and finished goods processing and packaging departments
Provide scientific leadership and technical support to the Executive Director of NAMs across a diverse portfolio of initiatives.
Responsibilities
Assist the Executive Director of NAMs in providing scientific direction, technical review, and execution support across the NAMs portfolio and NAMs Developer Coalition workstreams.
Support NAMs-DC working groups and member activities, including scientific priorities, technology-specific development plans, evidence gaps, milestones, and deliverables.
Provide scientific support for the ARPA-H CATALYST project and participating CATALYST teams, including technical assessment, regulatory science input, advisor engagement, and coordination of scientific deliverables.
Support NCAC initiatives, including the development, scientific review, harmonization, regulatory science input on validation studies, and maintenance of a NAMs Glossary and related terminology or standards activities.
Contribute scientific expertise to collaborative initiatives.
Requirements
PhD
PharmD
MD
or equivalent doctoral degree in a relevant scientific or clinical discipline
Nice to have: experience with NAMs applications in toxicology
Opportunity to take autonomous ownership of Interactive Response Technology (IRT) systems supporting Moderna’s growing clinical portfolio, translating complex clinical development and supply requirements into robust, timely system solutions.
Compensation
The salary range for this role is $121,600 - $194,000.
Responsibilities
Autonomously manage IRT systems for assigned program(s) and studies
Lead IRT implementation project management activities, including requirements gathering, system design, configuration-related coordination, user acceptance testing, implementation, maintenance and ongoing system lifecycle support
Work closely with external IRT vendors on day-to-day operational delivery
Collaborate cross-functionally to gather relevant requirements and translate clinical development, supply and operational needs into detailed and effective IRT system designs
Apply deep subject matter expertise in IRT systems and IRT-related integrations
Performs on-going Planned Maintenance (PM) and Corrective Maintenance (CM) of high-level diagnostic and therapeutic imaging equipment used throughout the healthcare facility. Assists in the planning and installation of diagnostic and therapeutic imaging equipment.
Responsibilities
Perform on-going Planned Maintenance (PM) and Corrective Maintenance (CM) of high-level diagnostic and therapeutic imaging equipment
Assists in the planning and installation of diagnostic and therapeutic imaging equipment
Maintain, repair, and service specialized equipment in nuclear medicine, ultrasound, angiography, and radiation therapy
Order parts and supplies required for emergency service and repair
Coordinate repairs with vendors and users
Requirements
Associates of Applied Sciences Degree in related field of medical electronics, electronic technology, imaging service technology or equivalent related military training and experience
Nice to have: Certified Radiology Equipment Service (CRES)
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