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Job Description Position Description: Seeking a motivated, intelligent and hard-working individual to Develop and maintain quality and regulatory compliance in Genadynes' processes. Individual will ensure compliance with ISO 13485 and MDSAP requirements are maintained. Specific Responsibilities : Ensure the quality and processes are practiced and maintained. Compile documents required for audits. Create and maintain product technical files. Initiate corrective and preventive actions for non-conformities. Maintain/calibrate the accuracy of all testing equipment. Conduct risk assessments of medical devices and processes. Maintaining the effectiveness of quality control system and non-conforming materials control system. Discuss and solve quality problems with vendors. Investigate problems and make improvement on current processes. Develop/design effective test methods. Facilitate software design and development for medical devices. Performance testing and reporting on software, hardware and the compatibility for all accessories. Perform risk assessments for medical devices and accessories. Development and prototyping of new products with existing or new vendors. Abilities: Familiar with FDA CFR 820, ISO 134850, SOPs regulations. Extreme attention to details. Ability to think outside the box with excellent problem solving abilities. Excellent interpersonal, communication, and writing skills. Highly organized. Excellent computational skills. Knowledge of European regulations is a plus. Knowledge of common medical materials (silicone, polyurethane, etc.) Knowledge of electrical circuits and basic programming. Knowledge of C/C++ is a plus. Maintain MDD/MDR EN ISO Experiences: Regulatory compliance. Quality management. Cross functional team management. Quality assurance Requirements: Bachelor degree in mechanical, electrical, material, biomedical engineering or relative field. (Master degree preferred.) Benefits: Medical, Dental, Vision, PTO, 401K, Legal Services, FSA, Life Insurance Salary Range: $68,000 - $72,000/Annual Powered by JazzHR oSPuR7OKHc

Job Description Nassau Candy is one of the largest US wholesale manufacturers of specialty and private label confections, supplying many of the national retailers and independent stores across the country. In addition to Nassau Candy-made creations, we import and distribute the most sought-after confectionery, soda, gourmet food, and natural brands, including health, beauty and household care. But Nassau Candy isn’t just candy! We are also parent company to NC Custom, the promotional arm of our business and home to the following industry-leading brands: Chocolate Inn/Taylor & Grant (edibles), Lanco (promotional hard goods), SPD Shoreline (apparel and soft goods), ACE (outdoor apparel and drinkware), and Fresh Beginnings (baked goods). We are currently hiring a well-rounded Senior Regulatory Affairs Manager to join our growing QC team. Position Responsibilities • Provide deep technical support for FDA and Labeling Compliance., • Review and assess Raw Material Specifications, Formulations, and Food Labels for Compliance with applicable Government Regulations, NC standards and Customer Requirements., • Develop nutritional panels, ingredients statements and product specifications for all new products as well as review and verify nutritional and ingredient information of existing products ensuring data is current and accurate meeting CFR Code of Federal Regulations- Title 21- FDA., • Respond to Technical requests from customers, portals, and questionnaires., • Support All NC company Art Dept. Initiatives and Requests. Review and verify nutritional and ingredient information of existing products ensuring data is current and accurate. Proofread final mechanicals received from the art department prior to print. Work closely with internal departments to ensure that all product labeling and packaging plans adhere to company policy and federal regulations., • Maintain electronic project folders and accounts details. Compile data and documents accordingly for the development of individual product specification sheets and raw material specifications as needed., • Support the ongoing development of FDA regulations and Customer requirements., • Work on other projects as assigned by the Operations Manager and VP. Other Competencies: • Expert knowledge of CFR Code of Federal Regulations- Title 21- FDA, • Expertise in laws and regulations governing product labeling., • Highly detail oriented with Superior proofreading, organizational, time management and analytical skills., • Assist Regulatory Affairs, Operations Manager with projects as assigned., • Work with TEAM on priority projects as needed., • Continual assessment of processes and recommend best practices., • Canadian Food Labeling (a plus)., • Self- Starter with the ability to multi-task in a very fast-paced environment., • Proficient in MS Excel, Word; nutrition software a plus., • Able to communicate technical and regulatory information to broad audiences. Minimum Requirements: • Bachelor’s degree in food science or related discipline, • Well-developed written and verbal communication skills and ability to translate (English/Spanish) a plus., • Minimum of 5 years of experience in a regulatory capacity, preferably in the food industry., • Expert knowledge of Food Regulatory. Knowledge of NON-GMO Project Verified a plus., • Numerical and analytical aptitude, • Highly detail oriented, • Well-developed organizational, follow up and discipline skills., • Self- Starter, • PC literacy – proficient in database and spreadsheet software, • Ability to multi-task and take charge of projects. We Offer: • Competitive Salary / Annual Reviews, • Medical / Dental / Vision / AFLAC / Pet Insurance!, • 401 (k), • Entrepreneurial culture…and more! We are an Equal Opportunity Employer

Job Description The START Center for Cancer Research (“START”) is the world’s largest early phase site network, fully dedicated to oncology clinical research. Throughout our history, START has provided hope to cancer patients in global community practices by offering "Hope Through Access” to cutting edge trials throughout the United States and Europe. We are seeking a Pharmacokinetic (PK) Lab Technician. The PK Lab Technician operates to support the investigation team in adherence to phase 1 research protocols within the Standard Operating Procedures of the department. Under general supervision, this position performs laboratory receiving, processing, handling, storage and shipping procedures, equipment maintenance and inventory control within the Pharmacokinetic Department. The hourly rate for this role is $25/hour-$28/hour. However, base pay may vary depending on multiple individualized factors including market location, job-related knowledge, skills, and experience. Work Schedule: Monday- Friday 8a.m - 5p.m with rotating on-call for after hours and weekend coverage. Location: START 119 W 124th St. New York, New York 10027 Essential Responsibilities: • Ensure compliance with all applicable Federal, State and local laws and regulations as they apply to biological sample processing, handling, and shipping., • Receive, process, handle, store, and ship biospecimens per study specifications., • Prepare research sample collection supplies per specific study specifications., • Adhere to the company SOP and GLPs., • Recognize inconsistencies in sample collection data and take appropriate corrective action as needed. Contact Nurse immediately to have situation corrected before patient leaves the building., • Record data in electronic data systems in compliance with SOPs and GLP., • Process and ship tissue specimens according to protocol requirements. Coordinate with other healthcare providers to receive patient tissue. Prepare tissue specimens as needed per study protocol., • Perform administrative functions associated with the Pharmacokinetic Department, to include but not limited to work tally records, scanning internal and study specific forms, filing, and sample management documentation., • Complete study forms to include but not limited to shipping logs, shipping documentation, sample requisition forms, flow sheets, and sample manifests., • Contribute to study specific and departmental inventory control and re-supply of reagents and supplies as needed. Replenish lab supplies daily., • Sanitize laboratory equipment daily, weekly, monthly, and yearly., • Perform and record daily/weekly/annual maintenance of equipment., • Participate in on-call rotation for emergency response for drug and specimen storage. Participate in on-call rotation for emergency management., • Other duties may be assigned at any time. Education & Experience: • High School Diploma., • General knowledge of medical terminology., • High attention to detail and strong organizational skills., • Excellent written and verbal communication skills., • Ability to work well independently., • Organizational skills to troubleshoot unplanned situations while still meeting established deadlines., • Proficient level of experience with Microsoft Office and the ability to learn new software., • Must maintain punctuality, good attendance and be flexible to work hours to accommodate clinic patient schedule. Preferred Education and Experience: • Associate or bachelor’s degree in a chemical, physical, biological or clinical laboratory science or medical technology., • Experience in a laboratory setting, with a solid understanding of laboratory techniques and safety protocols., • Experience in data management., • Experience in logistics and operations., • Experience with electronic medical record program(s) and laboratory information systems. Physical and Travel Requirements: • Able to perform manual tasks that require the use of fine muscle motor skills., • Able to lift 40 pounds., • Able to stand and / or sit for prolonged periods., • Able to freely bend/stretch. Able to access, input and retrieve information from computer., • Utilizing personal vehicle to transport specimens may be required on occasion. Best-in-Class Benefits and Perks We value the time, talent, and dedication our employees bring to START. Our commitment to your well-being and growth is reflected in a competitive compensation package—based on experience—along with comprehensive benefits designed to support you both personally and professionally: • 401(k) retirement savings plan with employer match, • Eligibility for an annual performance bonus, based on role and company results, • Generous paid time off and paid holidays, • Comprehensive medical, dental, and vision coverage and optional insurance options, • Company p‑aid life and disability insurance for added financial protection, • Employee Assistance Program (EAP) providing confidential, no ‑cost support for you and your family from day one, • Flexible FSA and HSA plans to support your financial wellness, • Commitment to a supportive environment that values balance, wellbeing, and flexibility, • We’re committed to fostering a collaborative, creative workplace where every team member is encouraged to contribute. At START, you’ll join a team that values continuous learning, professional growth, shared ideas, and a culture built on inclusivity and innovation. More About START START clinical trial sites have conducted more than 1,000 early-phase clinical trials, including dozens of therapies that were approved by the FDA or EMA. START represents the world’s largest roster of early-phase principal investigators across its Network of clinical trial sites. Learn more at STARTresearch.com. Ready to be part of a team changing the future of cancer treatment? Join us in our mission to conquer cancer, one clinical trial at a time. Your expertise and dedication can help us bring hope and healing to patients worldwide. Please submit your application online. We are an equal opportunity employer that welcomes and encourages diversity in the workplace. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law.

Job DescriptionPlant Manager – Promotional Products & Food Production ???? Hicksville, NY ???? Salary Range: $140,000 – $160,000 ???? About Nassau Candy Nassau Candy is a leading manufacturer and distributor of specialty confections, fine foods, and promotional products. Through divisions such as NC Custom, Chocolate Inn, AmuseMints®, and Lanco, we deliver high-quality, customized solutions with speed, precision, and scale. Our operations are built to support high-volume, high-mix production with rapid turnaround times, often within 24–72 hours, while maintaining the highest standards of food safety and quality. ???? Position Overview We are seeking a high-impact Plant Manager to lead day-to-day operations across a fast-paced promotional products environment, including food and chocolate production, fulfillment, and packaging. This is a hands-on leadership role focused on execution, accountability, and performance. The Plant Manager will own the floor, lead teams across shifts, and ensure the operation is set up for success from close to open every day. ⚙️ Key Responsibilities???? Operational Leadership • Lead all daily plant operations across production, fulfillment, and shipping, • Drive execution to meet aggressive ship dates in a high-volume, short lead-time environment, • Maintain full visibility across all orders and actively “order chase” to ensure nothing falls behind, • Ensure operational readiness from close to open, including staffing, materials, and priorities???? Throughput & Efficiency, • Improve output across all departments, with a strong focus on bottleneck identification and resolution, • Drive labor efficiency and manage payroll within budget expectations, • Implement process improvements to increase throughput without adding unnecessary cost, • Balance workload across departments to maintain consistent production flow???? Team Leadership & Accountability, • Lead, coach, and develop supervisors and production teams across the facility, • Establish and enforce clear performance expectations and daily metrics, • Hold teams accountable to productivity, quality, and safety standards, • Build a culture of urgency, ownership, and continuous improvement???? Scheduling & Execution Alignment, • Partner closely with Scheduling and Planning to ensure realistic, executable production plans, • Ensure alignment between production, packing, and shipping operations, • Monitor real-time performance and adjust labor and resources as needed???? Food Safety & Compliance, • Ensure full compliance with GMP, FDA, HACCP, and all food safety requirements, • Maintain a clean, organized, and audit-ready facility at all times, • Partner with QA/QC to uphold product integrity, consistency, and regulatory standards???? Cross-Functional Coordination, • Collaborate with Customer Service, Sales, and Operations Leadership, • Provide clear communication on order status, risks, and recovery plans, • Support new product launches and ensure operational readiness for new items✅ Qualifications, • 7–10+ years of plant or operations management experience, • Background in food production, packaging, or regulated manufacturing required, • Experience in high-mix, high-volume environments with short lead times Strong working knowledge of: • Throughput and capacity management, • Labor planning and payroll control, • Production scheduling and execution, • Proven leadership ability in fast-paced, execution-driven environments, • Strong problem-solving and decision-making skills, • Working knowledge of food safety standards (GMP, FDA, HACCP preferred)???? What We Offer, • Competitive base salary ($140,000 – $160,000) with performance-driven upside, • Comprehensive benefits package, • 401(k) with company match, • Opportunity to lead a mission-critical operation within a growing, family-owned business, • A culture focused on execution, accountability, and continuous improvement???? Join Nassau Candy If you are an operational leader who thrives in fast-paced environments, takes ownership of outcomes, and knows how to drive performance on the floor—this is an opportunity to make a significant impact.

Job DescriptionCustoms House Broker located in the JFK/ Five Towns area seeks the following candidates: Experienced entry writer with knowledge of HTS classification for FDA related merchandise in addition to knowledge of USDA/ Fish & Wildlife products. ISF Data entry clerk, duties include allocating all shipping documents, track & trace incoming ocean cargo and filing of ISF IMMEDIATE HIRE!!!!!

Job DescriptionJob Title: Regulatory Affairs Specialist Job Description As a Regulatory Affairs Specialist, you will play a critical role in supporting regulatory compliance and quality systems for medical devices. You will assist in preparing, compiling, formatting, and submitting regulatory filings and maintain regulatory records and product registrations. Responsibilities • Assist with the preparation, compilation, formatting, and submission of regulatory filings., • Maintain regulatory records, product registrations, declarations of conformity, and submission documentation., • Support regulatory agency correspondence and requests for additional information., • Participate in U.S. and international product registration and approval activities., • Support post-market regulatory requirements, including annual reports and regulatory updates., • Assess regulatory impact of product changes, manufacturing transfers, and process modifications., • Prepare regulatory documentation, certifications, authorization letters, technical dossiers, and customer compliance requests., • Collaborate with Quality Assurance to maintain compliance with applicable regulations and standards., • Support internal and external audit preparation activities., • Ensure document control and regulatory records are maintained accurately., • Assist with the development and maintenance of regulatory procedures and processes., • Monitor regulatory changes and communicate potential business impacts., • Partner with Engineering, Clinical, Manufacturing, and Quality teams to gather technical information for submissions., • Track regulatory deliverables and project timelines., • Support regulatory training and compliance awareness initiatives., • Contribute to continuous improvement projects within the Regulatory Affairs function., • Maintain regulatory databases and information management systems.Essential Skills, • Experience in regulatory affairs within the medical device industry., • Hands-on experience supporting 510(k) submissions., • Knowledge of FDA 21 CFR 820, ISO standards, and EU MDR 2017/745., • Proficiency in regulatory submission processes., • Strong written and verbal communication skills., • Excellent organizational and project management abilities., • Ability to work effectively with cross-functional teams., • Proficient with Microsoft Office and standard business systems.Additional Skills & Qualifications, • Bachelor's degree in Regulatory Affairs, Biomedical Sciences, Engineering, Life Sciences, or a related field., • 3–5 years of Regulatory Affairs experience within the medical device industry., • Experience working in an FDA-regulated environment., • Familiarity with quality systems and regulatory frameworks.Work Environment The work environment involves collaborating with cross-functional teams, including Engineering, Clinical, Manufacturing, and Quality. You will work with one other team member and report to the regulatory manager. This position requires proficiency in Microsoft Office and other standard business systems. Job Type & Location This is a Permanent position based out of Baldwin, NY. Pay and Benefits The pay range for this position is $75000.00 - $90000.00/yr. Currently in Baildwin and moving to Woodbury later this year. Workplace Type This is a fully onsite position in Baldwin,NY. Application Deadline This position is anticipated to close on Jul 29, 2026. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options. San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records. Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability. Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.

Job Description Translink CHB, Inc. – Brokerage division of Translink Shipping, Inc. – located in Great Neck, NY has current opening for an Entry Writer Responsibilities include but are not limited to: • HTS Classification of import goods including FDA, USDA, DOT, USFWS, etc., • Must have knowledge on ISF filing, • Possess knowledge of Customs clearance processes, regulations, and valuation, • Processing of US Customs entries in accordance with US Customs regulations and all other Government agencies., • Review entry documents for accuracy and provide feedback to appropriate parties if any information is missing or incomplete, • Communicate with CBP and PGAs as needed to facilitate the release of the shipment, • Maintain Customs compliance documentation, • Communicate with clients and colleagues consistently with accurate and detailed information to ensure effective customer service Qualifications: • Entry writing, ocean import experience minimum 2 Years, • Position requires working directly with Customs, other Government agencies, carriers, customers, vendors and all related parties concerning the import process., • Excellent communication and interpersonal skills (both verbal and written), • Highly organized and detail-oriented, • Ability to work independently and be a team player, working closely with teammates for a positive outcome. Salary: DOE Job Type: Full-time Benefits: • 401(k), • Dental insurance, • Health insurance, • Paid time off Schedule: • 8 hour shift, • Monday to Friday Experience: • Entry Writing, Ocean Import: 2 years (Required)Company DescriptionFirst, I express heartfelt gratitude to all of you who have extended the opportunity for Translink Shipping, Inc. to service your shipping needs and your ongoing support. TRANSLINK SHIPPING, INC. was established on September 2nd, 1987. For nearly twenty years, TRANSLINK has adhered to the operation philosophy of "integrity, diligence and innovation". Evolving towards "specialization, informational global system, and large-scale", we continue to provide a service level towards every client sincerely, managing every business aspect with high performance and superior quality. Our goal is to provide top notched global freight agency service to each and every client no matter how large our client base is. TRANSLINK continues to soar in developing service systems since its establishment. We currently have set up a global integrated service network consisting of subsidiaries in Hong Kong, Taiwan, Mainland China and Germany as well as whole Asia, Europe, Oceania, South America and Africa in addition to its American headquarters and six subsidiaries. We have ranked among first five positions in "Pan-Pacific Freight Volume Appraisal" by U.S. Customs Service for running years since 1995 and have become an American freight agency company in rapid yet stable development. Services we provide encompass a wide range but not limited to: access to agencies of shipping and air freight to all points, declaration and clearance of imported and exported goods, entry-exit inspection and quarantine of goods, goods warehousing, containerization, marine cargo insurance, domestic railway consignment and inland transportation of imported and exported goods. With the development of international trade and shipping industry, the shipping agency company is more than just a common carrier. It has evolved into a logistic specialist that masters international transportation, trade and insurance knowledge. With associated expertise it is capable of sending clients'' goods to destinations successfully. In order to make wise strategic decisions, TRANSLINK has implemented and pooled its resources and now has over 600 operating and business staffs with years of employment in shipping business in place to explore deep into the market to learn about market dynamics. This has lead to the developing and executing a complete and sophisticated computer network operating system for timely presentation and effective shipping information to clients. Through the accumulation of experiences in shipping industry for years combined with the unremitting efforts of entire colleagues, the business of TRANSLINK around the world is soaring in development; a complete and sound service network, and stable shipment volume. TRANSLINK has established and maintains a long-term sound cooperative relationship with many world known shipping lines, and accordingly is ensured the absolute advantage in shipping schedule and freight rate. In part due to excellent records of safe transportation, TRANSLINK enjoys a high reputation among a good many of shipping enterprises. We are confident and capable of providing you with more convenient and timely shipping information, more reasonable freight rates, more accurate and stable shipping schedules and more adequate spaces and enabling you to enjoy the most surpassing VIP services in respective ports. We pay close attention to and listen to varied requirements of clients sparing no efforts to meet these needs. We believe that TRANSLINK is your optimal choice, because your satisfaction is our primary target! Yours sincerely, Sam Chen President, TRANSLINK SHIPPING, INC.First, I express heartfelt gratitude to all of you who have extended the opportunity for Translink Shipping, Inc. to service your shipping needs and your ongoing support.\r\n\r\nTRANSLINK SHIPPING, INC. was established on September 2nd, 1987. For nearly twenty years, TRANSLINK has adhered to the operation philosophy of "integrity, diligence and innovation". Evolving towards "specialization, informational global system, and large-scale", we continue to provide a service level towards every client sincerely, managing every business aspect with high performance and superior quality. Our goal is to provide top notched global freight agency service to each and every client no matter how large our client base is.\r\n\r\nTRANSLINK continues to soar in developing service systems since its establishment. We currently have set up a global integrated service network consisting of subsidiaries in Hong Kong, Taiwan, Mainland China and Germany as well as whole Asia, Europe, Oceania, South America and Africa in addition to its American headquarters and six subsidiaries. We have ranked among first five positions in "Pan-Pacific Freight Volume Appraisal" by U.S. Customs Service for running years since 1995 and have become an American freight agency company in rapid yet stable development. Services we provide encompass a wide range but not limited to: access to agencies of shipping and air freight to all points, declaration and clearance of imported and exported goods, entry-exit inspection and quarantine of goods, goods warehousing, containerization, marine cargo insurance, domestic railway consignment and inland transportation of imported and exported goods.\r\n\r\nWith the development of international trade and shipping industry, the shipping agency company is more than just a common carrier. It has evolved into a logistic specialist that masters international transportation, trade and insurance knowledge. With associated expertise it is capable of sending clients'' goods to destinations successfully.\r\n\r\nIn order to make wise strategic decisions, TRANSLINK has implemented and pooled its resources and now has over 600 operating and business staffs with years of employment in shipping business in place to explore deep into the market to learn about market dynamics. This has lead to the developing and executing a complete and sophisticated computer network operating system for timely presentation and effective shipping information to clients.\r\n\r\nThrough the accumulation of experiences in shipping industry for years combined with the unremitting efforts of entire colleagues, the business of TRANSLINK around the world is soaring in development; a complete and sound service network, and stable shipment volume. TRANSLINK has established and maintains a long-term sound cooperative relationship with many world known shipping lines, and accordingly is ensured the absolute advantage in shipping schedule and freight rate. In part due to excellent records of safe transportation, TRANSLINK enjoys a high reputation among a good many of shipping enterprises. We are confident and capable of providing you with more convenient and timely shipping information, more reasonable freight rates, more accurate and stable shipping schedules and more adequate spaces and enabling you to enjoy the most surpassing VIP services in respective ports.\r\n\r\nWe pay close attention to and listen to varied requirements of clients sparing no efforts to meet these needs. We believe that TRANSLINK is your optimal choice, because your satisfaction is our primary target!\r\n\r\nYours sincerely,\r\nSam Chen\r\nPresident, TRANSLINK SHIPPING, INC.

Job DescriptionQuality Specialist & Internal Auditor Location: Hicksville, NY Company Overview Nassau Candy is a leading manufacturer and distributor of specialty confections, fine foods, and promotional products with a national footprint. As a family-owned business, we combine entrepreneurial agility with operational excellence—delivering high-quality products while investing in our people, processes, and facilities. Position Summary The Quality Specialist & Internal Auditor supports the Food Safety & Quality Manager in maintaining Nassau Candy's Food Safety Management System (FSQMS) and ensuring compliance with food safety, quality, regulatory, and customer requirements. This role is responsible for monitoring quality systems, conducting internal audits, supporting production operations, and promoting a strong food safety culture throughout the organization. The position partners cross-functionally to ensure products consistently meet Nassau Candy's quality and food safety standards while supporting continuous improvement initiatives. *This position will be on-site in our Hicksville, NY facility. Essential Functions • Support the maintenance and continuous improvement of the Food Safety Management System (FSQMS) and SQF Program., • Ensure compliance with HACCP, GMPs, GDPs, FDA regulations, SQF requirements, customer specifications, and other applicable food safety and quality standards., • Serve as Recall Coordinator and support mock recalls and traceability exercises., • Conduct GMP, GDP, and internal quality audits to verify compliance and identify improvement opportunities., • Support internal, customer, regulatory, and third-party audits, ensuring timely follow-up and corrective action completion., • Monitor production operations to verify product quality, food safety, and adherence to established procedures., • Review batch records, production documentation, quality records, and product release documentation for accuracy and compliance., • Investigate customer complaints, product deviations, and non-conformances, supporting root cause analysis and corrective actions., • Track, monitor, and verify the effectiveness of Corrective and Preventive Actions (CAPA)., • Develop, maintain, and update Standard Operating Procedures (SOPs), work instructions, forms, and quality documentation., • Deliver food safety, GMP, GDP, and quality training for employees and new hires while maintaining training records., • Analyze quality data and prepare reports to support management review and continuous improvement initiatives., • Partner with Production, Warehouse, Sanitation, Maintenance, Purchasing, and other departments to resolve quality issues and improve operational performance., • Promote a culture of food safety, quality, compliance, accountability, and continuous improvement throughout the facility., • Travel as required to support audits, inspections, or other business needs., • Perform other duties as assigned.Minimum Qualifications, • Associate degree in Food Science, Microbiology, Quality Assurance, Quality Management, or a related field., • Five (5) or more years of experience in food manufacturing, food safety, or quality assurance., • Working knowledge of HACCP, GMPs, GDPs, FDA regulations, and food safety systems., • Experience supporting SQF, BRCGS, ISO 22000, or other GFSI-recognized food safety programs preferred., • Strong understanding of Quality Management Systems (QMS), document control, and regulatory compliance., • Knowledge of FDA food labeling regulations (21 CFR); familiarity with Canadian labeling requirements (CFIA) is a plus., • Proficiency with Microsoft Office Suite, SharePoint, Microsoft Teams, and MRP/ERP systems., • Strong analytical, organizational, communication, and problem-solving skills., • Ability to manage multiple priorities in a fast-paced manufacturing environment., • What We Offer, • Medical, Dental, Vision, AFLAC, and Pet Insurance, • Paid Vacation, PTO, Annual Reviews, and Competitive Salary, • 401(k) with Company Match, • Employee Discounts and more Nassau Candy is an Equal Opportunity Employer.

Job Description At Precision Medicine, we are revolutionizing healthcare! Our mission is to empower the evolution of modern medicine by providing accessible, personalized, and efficient healthcare solutions. Join our dynamic team where your expertise matters, your ideas are valued, and your background helps shape the future of patient care. We celebrate diverse perspectives and foster an environment where you can thrive, innovate, and make a meaningful impact on patients' lives. Job Summary We are seeking a detail-oriented, compliance-focused Quality Inspector to support quality operations within our 503A compounding pharmacy and direct-to-consumer telehealth fulfillment operations. This role is responsible for inspecting compounded products, materials, packaging, and processes to ensure compliance with regulatory requirements, internal quality standards, and patient safety expectations. The Quality Inspector will support the company's Quality Management System by conducting audits and inspections across compounding, pharmacy verification, fulfillment, shipping, packaging validation, vendor qualification, third-party testing, and batch release activities. This position reports directly to the Director of Quality and will be located on-site in Bellmore/Farmingdale, NY. Key Responsibilities Perform inspections and reviews that support the company's Quality Management System, regulatory standards, and business objectives. Conduct routine and unannounced audits across compounding, pharmacy verification, fulfillment, shipping, and dispensing operations to confirm adherence to SOPs and regulatory requirements. Inspect compounded products for identity, labeling accuracy, container integrity, documentation accuracy, and overall product quality. Verify order-to-fulfillment accuracy, including patient information, prescription details, packing accuracy, and shipment readiness. Inspect compounding operations for compliance with USP <795>, <797>, <800>, <1163>, and applicable state board of pharmacy requirements. Support HIPAA, DEA, DSCSA, and pharmacy regulatory compliance within telehealth fulfillment workflows. Document, escalate, and support the resolution of nonconformances, deviations, and quality concerns. Design and conduct pack-out studies to confirm that products maintain required storage temperatures throughout transit. Analyze temperature-monitoring data from pack-out studies and document findings to support shipping configuration, carrier, packaging, insulation, and coolant qualification. Oversee in-process and finished product testing, including potency, sterility, and stability testing. Coordinate shipment of compounded product samples to third-party testing laboratories. Input third-party testing results into the quality software system and track outstanding results to closure. Review testing results, supporting documentation, and Certificates of Analysis to confirm compliance before batch release. Review batch records, compounding logs, fulfillment documentation, and quality records for accuracy, completeness, and adherence to SOPs. Monitor cleanroom gowning, aseptic practices, environmental monitoring, and related quality procedures. Support deviation, CAPA, and change control activities by providing inspection data and verification. Assist in qualifying new and existing vendors and suppliers, including raw material, packaging, and testing vendors. Collect and review vendor qualification documentation, including certifications, COAs, and quality agreements. Support periodic vendor requalification, maintain approved vendor records, and escalate concerns identified during review. Provide feedback to staff on observed deficiencies and reinforce best practices during inspections. Track inspection findings, pack-out study results, testing trends, and quality metrics to support continuous improvement initiatives. Recommend improvements to inspection methods, packaging validation processes, quality monitoring, and operational workflows. Help prevent rework, reshipments, product loss, temperature excursions, and compliance issues by identifying and resolving quality concerns early. Required Qualifications High school diploma or equivalent required. 1–3 years of experience in quality assurance, quality control, pharmacy, healthcare, or compounding operations required. Ability to review batch records, compounding logs, Certificates of Analysis, and fulfillment documentation for accuracy and compliance. Strong understanding of documentation practices, inspection readiness, and quality standards. Exceptional attention to detail with strong organizational and documentation skills. Effective written and verbal communication skills for inspection reporting and staff feedback. Analytical and problem-solving skills to support investigations, CAPA processes, and process improvements. Ability to work independently while collaborating across pharmacy, fulfillment, and quality teams. Commitment to patient safety, regulatory compliance, and continuous improvement. Preferred Qualifications Associate's or Bachelor's degree in Pharmacy, Pharmaceutical Sciences, Chemistry, Biology, Quality Management, or a related field. Pharmacy technician, pharmaceutical inspection, compounding, or fulfillment quality experience. Familiarity with USP <795>, <797>, <800>, <1163>, FDA 21 CFR Parts 210/211, HIPAA, DEA, DSCSA, and state board of pharmacy requirements. Experience using inspection and monitoring tools such as balances, pH meters, environmental monitoring devices, and temperature data loggers. Familiarity with cold-chain or temperature-controlled packaging and shipping validation, including pack-out studies. Strong computer skills, including Google Workspace. Familiarity with eQMS, EHRs, or pharmacy management systems. Experience working in a fast-paced compounding pharmacy, fulfillment, or direct-to-patient healthcare environment. Job Details Salary Competitive; commensurate with experience. Benefits 401(k) 401(k) Matching Dental Insurance Health Insurance Paid Time Off Vision Insurance Schedule Monday through Friday, 9:00 AM to 5:00 PM Location Bellmore/Farmingdale, NY Why Join Us As part of Precision Medicine, you'll be at the heart of an exciting transformation in the telemedicine landscape. Together, we're pioneering solutions that bridge technology and compassionate care, improving health outcomes for all. We're committed to your growth, providing you with the resources and support you need to build a meaningful career while exploring your creativity. Ready to be a part of something groundbreaking? Join us as we move healthcare forward, one innovation at a time! Learn more at: https://precisionmeds.com Equal Opportunity Statement Precision Medicine is 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 mailto:recruiting@mypcphealth.com to request accommodation.

Job DescriptionActalent is urgently hiring for a Packaging Lab Inspector! Please APPLY NOW for immediate consideration! Book a virtual interview NOW: https://talentassistant.actalentservices.com/assistant/bookings/fc055e71-ac0b-4839-90d3-fc9a1bb77750 Job Title: Packaging Lab Inspector Job Description The Packaging Lab Inspector supports the finishing department by performing laboratory-based processing, inspection, and documentation activities that ensure products meet quality and regulatory standards before release. This role involves hands-on work with raw materials and finished products, operating specialized laboratory and production equipment, and assisting across multiple areas of the finishing department as needed. The position requires strong attention to detail, adherence to procedures, and a willingness to work in a fast-paced, production-oriented environment. Responsibilities • Defat raw materials by handling ether and acetone, drying samples, and accurately weighing materials according to established procedures., • Set up and operate extraction processes for various products, ensuring correct configuration and safe handling of materials., • Perform gross filtration by setting up filtration equipment, monitoring operations, and completing thorough cleaning after use., • Set up and clean clarification equipment to support downstream processing and ensure product clarity and quality., • Perform aseptic processing activities, including equipment setup, operation, and cleaning, while maintaining strict aseptic techniques., • Carry out dialysis operations, including filling dialysis bags, monitoring processes, and emptying and cleaning dialysis tanks., • Operate the Bock centrifuge for molds and inhalants, following all safety and quality procedures., • Prepare laboratory solutions and reagents by following written instructions and ensuring accurate measurements and labeling., • Manage FTQ paperwork distribution and support inventory control requirements to maintain accurate documentation and stock levels., • Complete routine laboratory chores, including maintaining scales, freezers, pH meters, pass-through equipment, nitrogen systems, and lab room assignments., • Perform freeze drying activities such as loading materials, monitoring reconstitution, and cleaning freeze-drying equipment., • Operate the Amicon DC-10 (standard cat pelt use) according to standard operating procedures., • Operate the DPR-6000 centrifuge and related equipment safely and efficiently., • Use the ball mill for mite processing, ensuring proper setup, operation, and cleaning., • Perform dilution and compounding activities in accordance with laboratory and production protocols., • Complete SAP-related duties, including COR6N and goods movements, to record and track materials and production activities., • Cross-train into aseptic filling operations after successful PST media fills and completion of full training requirements., • Assist throughout the finishing department, including areas such as label review and blistering, based on operational needs., • Support warehouse activities as needed, including material handling and movement, to ensure smooth product flow., • Follow all FDA, quality assurance, and internal policies and procedures to maintain compliance and product quality., • Maintain a clean, organized, and safe work area, and promptly report any equipment issues or safety concerns., • Perform any other assigned duties that support laboratory, production, or finishing operations. Essential Skills • Foundational knowledge in biology, chemistry, biochemistry, pharmaceutical sciences, or related biological sciences, typically gained through a high school diploma with relevant coursework or equivalent experience through undergraduate studies., • Ability to understand and follow laboratory procedures related to defatting, extraction, filtration, clarification, dialysis, aseptic processing, and compounding., • Familiarity with laboratory and production environments, including handling chemicals, reagents, and biological materials., • Basic understanding of FDA-regulated environments and quality assurance principles., • Experience or strong aptitude for working in laboratory, pharmaceutical, biopharma, or production settings., • Ability to lift 25–50 lbs routinely throughout the day, multiple times per day., • Strong attention to detail with the ability to accurately measure, weigh, record, and document laboratory and production activities., • Comfort operating laboratory equipment such as centrifuges, freeze dryers, pH meters, and related devices after training., • Willingness and ability to work in both first and second shift schedules as needed., • Reliable transportation to and from the worksite., • Proactive, go‑getter mentality with a positive attitude and willingness to assist where needed., • Ability to work effectively in a production-oriented team environment and adapt to changing priorities. Additional Skills & Qualifications • Biopharma experience is preferred and considered a strong plus., • Experience in a laboratory-type setting for at least 1+ year is valued, particularly for candidates without a college degree., • Background in chemistry, biology, biochemistry, pharmaceutical, or biological science coursework is beneficial., • Experience with production, compounding, or finishing operations in a regulated environment is advantageous., • Familiarity with SAP, including goods movements and transaction codes such as COR6N, is a plus., • Comfort working with quality assurance documentation and following standard operating procedures., • Strong communication skills to work effectively with cross-functional teams in the finishing department and warehouse., • Demonstrated ability to learn new equipment and processes quickly and to follow detailed technical instructions. Work Environment This role is based in the finishing department, which is the final area products pass through before release. The finishing department includes multiple functions such as label review, blistering, and related packaging and inspection activities. The Packaging Lab Inspector works in a laboratory and production setting that involves operating equipment like centrifuges, freeze dryers, ball mills, dialysis tanks, and aseptic processing systems, as well as using pH meters, scales, freezers, and nitrogen systems. The environment is regulated and quality-focused, with procedures aligned to FDA and quality assurance standards. The position requires flexibility and a strong team mindset, as you will support various areas of the finishing department and assist in the warehouse as needed. Consistent willingness to help where needed in finishing or warehouse operations is expected. Typical hours are approximately 6:30 a.m. to 3:30 p.m., with additional hours often worked after the scheduled shift and potential overtime as required. The role offers strong medical benefits, paid time off, and opportunities for career progression based on performance and reliability. Dress and attire are consistent with a laboratory and production environment, requiring appropriate safety and protective clothing as defined by site policies. Please APPLY NOW for immediate consideration! Book a virtual interview NOW: https://talentassistant.actalentservices.com/assistant/bookings/fc055e71-ac0b-4839-90d3-fc9a1bb77750 Job Type & Location This is a Permanent position based out of PORT WASHINGTON, NY. Pay and Benefits The pay range for this position is $20.00 - $20.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in PORT WASHINGTON,NY. Application Deadline This position is anticipated to close on Aug 7, 2026. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options. San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records. Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability. Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.

Job Description The START Center for Cancer Research (“START”) is the world’s largest early phase site network, fully dedicated to oncology clinical research. Throughout our history, START has provided hope to cancer patients in global community practices by offering "Hope Through Access” to cutting edge trials throughout the United States and Europe. We are seeking a CTMS Entry Coordinator. This role will assist the Clinical Research Coordinators in all tasks to support their roles. It will require an understanding of research terminology and basic protocol interpretation. Work Schedule: Monday-Friday, 8am-5pm Location: START – New York-Long Island: 450 Lakeville Road, Entrance A, Lake Success, NY 11042 The annual base salary for this role is $24/hour-$26/hour. However, base pay may vary depending on multiple individualized factors including market location, job-related knowledge, skills, and experience. Essential Responsibilities • Collect, de-identify, enter/transcribe, and transmit/submit clinical data in paper and/or electronic case reports forms (CRFs), including correction and query resolution for assigned investigational drug studies. This includes but is not limited to images, lab results, and ECGs., • Collaborate with Clinical Research Coordinator to ensure data timepoints are accurate and provide query resolution., • Contact patients in follow-up as needed per protocol., • Review and utilize protocols as guides for study activities for assigned studies., • Assist with the setup and formatting of study-specific Eligibility, Study Schedules, and Flow Sheets documents per protocol., • Assist with CTMS upkeep, including but not limited to tracking patient visits, IRB re-consents, Serious Adverse Events (SAEs) and Deviations., • Ensure that data transmissions remain current for assigned studies., • Provide support and information to onsite and remote monitors as necessary., • Comply with all applicable regulations, guidelines, and procedures pertaining to data loading, EDC systems, and clinical research., • Share responsibility with Data Coordinators to identify lab facilities and normal lab values used for assigned studies so that lab certifications can be requested for the study file., • Attend meetings regarding assigned studies as needed, including site initiation visits, Roster meetings and Forms Committee., • Communicate as needed with accounts receivable staff regarding transmitted data. Required Education and Experience: • High School diploma or equivalent., • One year of research administrative experience within a healthcare, pharmaceutical, or research organization., • Knowledge and training in general office administration skills, including computer applications, filing systems, etc., • Familiarity with medical terminology., • Strong organizational skills and a sense of timeliness in completing projects., • Must be detail-oriented and able to understand instructions and work independently. Best-in-Class Benefits and Perks We value the time, talent, and dedication our employees bring to START. Our commitment to your well-being and growth is reflected in a competitive compensation package—based on experience—along with comprehensive benefits designed to support you both personally and professionally: • 401(k) retirement savings plan with employer match, • Eligibility for an annual performance bonus, based on role and company results, • Generous paid time off and paid holidays, • Comprehensive medical, dental, and vision coverage and optional insurance options, • Company‑paid life and disability insurance for added financial protection, • Employee Assistance Program (EAP) providing confidential, no‑cost support for you and your family from day one, • Flexible FSA and HSA plans to support your financial wellness, • Commitment to a supportive environment that values balance, wellbeing, and flexibility, • We’re committed to fostering a collaborative, creative workplace where every team member is encouraged to contribute. At START, you’ll join a team that values continuous learning, professional growth, shared ideas, and a culture built on inclusivity and innovation. More About START START clinical trial sites have conducted more than 1,000 early-phase clinical trials, including dozens of therapies that were approved by the FDA or EMA. START represents the world’s largest roster of early-phase principal investigators across its Network of clinical trial sites. Committed to accelerating passage from trials to treatments, START delivers hope to patients, families, and physicians around the world via our mission of “Hope Through Access”. As an example, in San Antonio, where START was founded, START treated the first patient ever with Keytruda – one of the most effective cancer drugs in medical history. Learn more at STARTresearch.com. Ready to be part of a team changing the future of cancer treatment? Join us in our mission to conquer cancer, one clinical trial at a time. Your expertise and dedication can help us bring hope and healing to patients worldwide. Please submit your application online. We are an equal opportunity employer that welcomes and encourages diversity in the workplace. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law.

Job DescriptionAbout the job This role collaborates cross-functionally with Quality, Engineering, Clinical, and Manufacturing teams to prepare, submit, and maintain regulatory filings with agencies such as the U.S. FDA, European Notified Bodies, and other international authorities. Key Responsibilities: Primary Responsibilities • Assist in the preparation, formatting, and collection of regulatory submissions, • Ensure the maintenance of regulatory files, declarations of conformity, and device listings/registrations are accurate and complete., • Oversee inquiries into regulatory agency requests for additional information for document submission., • Support U.S. and EU market approval processes and ensure compliance with regulatory standards, • Support post-market submissions (progress reports, annual reports, etc.), • Provide regulatory assessments for marketing, R&D, and manufacturing changes or product transfers., • Communicate with distributors in response to requests for information, regulatory inquiries or in support of regulatory filings.Compliance & Quality System Support, • Partner with Quality Assurance to ensure continued compliance with applicable regulatory standards, including FDA 21 CFR 820, ISO 13485, and EU MDR 2017/745., • Support in audits (internal and external) in document preparation as needed., • Support document control and recordkeeping to ensure regulatory documentation integrity and traceability., • Assist in preparing regulatory applications that are compliant with applicable regulatory requirements to achieve business objectives.Cross-Functional Collaboration, • Partner with Engineering and Clinical teams to gather information needed for submissions and documentation., • Assist in preparing summaries, tracking deliverables, and ensuring timely submission of regulatory documents., • Support training and awareness initiatives related to regulatory compliance., • Interpret new or existing regulations and ensure business practices align with compliance requirements., • Create documentation in response to customer regulatory requests which includes regulatory letters, authorization letters, certifications, attestations, technical packages, etc. for tenders and for pre-market clearance., • Clearly and effectively communicate team/project progress/status, decisions, timelines, etc. to other teams/departments and executive leadership., • Establish and maintain regulatory information systems., • Contribute in continuous improvement initiatives and process optimization within Regulatory Affairs.Qualifications:, • Bachelor's degree in biomedical, RA/QA or related scientific area for medical device industry (RAC certification preferred)., • Master’s degree in related field can count towards 1 year of relevant experience., • 3-5 years of experience in a regulated FDA environment (medical device industry experience required)., • Hands-on experience with 510(k) submissions (IDE and PMA knowledge a plus). Strong knowledge in regulatory strategy and approval approaches., • Working knowledge of FDA, EU MDR, or ISO regulatory environments preferred., • Audit experience as a contributor is preferred., • Ability to efficiently navigate through the regulatory process either individually or in a team setting ensuring a project’s success., • Strong organizational, communication (verbal and written), and planning skills., • Ability to interact cross functionally across multiple departments with various levels of the organization., • Detail oriented, practical and proactive problem solver., • Proficiency with PC systems and office applications., • Solid understanding of scientific principles applied to regulatory affairs., • Understanding of regulatory and business needs with ability to engage cross functional team members.Salary range is $75,000- $85,000/annual USD An employment offer is based on the candidate's professional experience, specialty, skillset, education, geography, related licenses or certifications, and other business needs. The compensation range indicated does not include other forms of compensation or benefits. We value the diversity of our team and inspire creativity in our innovation. elliquence proudly provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any kind without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state and local laws. We are committed to working with and providing reasonable accommodation to individuals with disabilities. If you need any reasonable accommodation due to a disability for any part of the application process, please email hr@elliquence.com. Powered by JazzHR KfrVHAUAmF

Job DescriptionCNC Programmer & Setup Technician (Swiss CNC) Medical Device Manufacturing | Plainview, NY Full-Time | On-Site About the Role: We are seeking an experienced CNC Programmer & Setup Technician to support precision manufacturing operations in a fast-paced medical device manufacturing environment. This role is responsible for programming, setting up, and optimizing Swiss-style CNC machines while developing efficient machining processes for new and existing products. The ideal candidate has extensive experience with Swiss CNC machines, particularly Tornos equipment, and is passionate about continuous improvement, precision machining, and delivering high-quality components that meet tight tolerances. This position works closely with Engineering, Quality, and Production teams to ensure new programs and setups are production-ready and optimized for efficiency. Responsibilities: • Develop, edit, and optimize CNC programs for Swiss-style CNC machines, with a strong emphasis on Tornos equipment., • Perform complete machine setups, including tooling, workholding, offsets, and program verification., • Develop machining processes for new product introductions while improving existing manufacturing methods., • Select appropriate cutting tools, fixtures, and workholding solutions to maximize productivity and quality., • Optimize cycle times, tooling strategies, and machining parameters to improve efficiency and reduce costs., • Troubleshoot machining, tooling, and program-related issues to minimize downtime., • Conduct first article inspections and validate machining processes prior to production release., • Train machine operators on new setups, tooling requirements, and production processes., • Update existing CNC programs using modern machining techniques and continuous improvement principles., • Maintain compliance with quality standards, engineering drawings, and manufacturing specifications., • Collaborate with Engineering, Quality, and Manufacturing teams to support production goals and new product development., • Support Lean Manufacturing and continuous improvement initiatives throughout the machining department. Qualifications:, • High school diploma, GED, or trade school certification in machining or a related field., • Minimum 5 years of experience operating Swiss CNC machines in a precision manufacturing environment., • Minimum 3 years of CNC setup experience., • Minimum 2 years of CNC programming experience, preferably with Swiss-style CNC machines., • Strong experience with Tornos Swiss screw machines is required., • Proficiency with CAD/CAM software, including SolidWorks and/or AutoCAD., • Ability to read and interpret blueprints, GD&T, engineering drawings, and technical specifications., • Experience selecting tooling, fixtures, and machining strategies for precision components., • Strong troubleshooting and problem-solving skills., • Excellent communication and teamwork abilities. Desired Qualifications:, • Experience in medical device, aerospace, or other highly regulated manufacturing environments., • Familiarity with Lean Manufacturing and continuous improvement methodologies., • Experience performing first article inspections and process validation., • Knowledge of precision inspection equipment and metrology., • Understanding of ISO 13485, FDA-regulated manufacturing, or other quality management systems., • Experience mentoring or training CNC operators on setup and machining best practices.

Job Description Job Title: Regulatory Affairs Technician (Food Labeling) Who We Are: Nassau Candy is a leading manufacturer and distributor in the confectionery, gourmet food, and private-label industries. With decades of expertise, we provide high-quality products to retailers across the nation. Our expansive portfolio includes a variety of confections, specialty foods, and customized solutions tailored to our customers’ needs. Position Overview: We are currently hiring a detail-oriented Regulatory Affairs Technician – Food Labeling with three + years of experience to join our Regulatory Affairs team. This role is responsible for reviewing, developing, and maintaining compliant product labels, specifications, and regulatory documentation for private label, branded, and bulk food products across the U.S. and Canada. This position is ideal for someone with a strong understanding of food labeling regulations, product specifications, and commercialization processes, who can effectively support cross-functional teams. Key Responsibilities: • Review and develop product labels to ensure compliance with FDA, USDA, and customer-specific requirements, • Create and verify ingredient statements, Nutrition Facts Panels, and allergen declarations across a variety of food products (e.g., candy, snacks, specialty foods), • Develop and maintain technical product specifications, including internal specs and customer-facing specifications through external portals (e.g., Oracle or similar systems), • Submit and manage product data for commercialization, ensuring accuracy and completeness across systems, • Evaluate and support product claims (e.g. kosher, non-GMO, RSPO, Fair Trade), • Collaborate with Product Development, Sales, QA, and the Art team throughout the label creation and approval process, • Review and proof packaging artwork prior to print to ensure accuracy and regulatory compliance, • Maintain organized regulatory documentation, project folders, and customer records, • Compile and manage raw material and finished product specifications in alignment with internal policies and customer requirements, • Monitor and interpret U.S. and Canadian labeling regulations, communicating updates to internal teams, • Manage supplier compliance documentation and support customer requests (e.g., allergen forms, spec sheets, COO documentation), • Support Regulatory Affairs and Operations with cross-functional projects and assignments Qualifications: • Bachelor’s degree in Food Science, Nutrition, or a related scientific field., • Minimum 3 years of experience in food industry regulatory affairs, labeling., • Strong knowledge of FDA labeling regulations (21 CFR); familiarity with CFIA requirements is a plus, • Familiarity with QMS systems, SOPs, and controlled documentation Systems & Software: • ESHA Genesis R&D / Trustwell (or similar nutrition analysis software), • Microsoft Excel & Word, • SharePoint, Microsoft Teams, or similar collaboration tools Skills & Competencies: • Exceptional attention to detail and accuracy, • Strong organizational and documentation skills, • Ability to manage multiple projects and meet deadlines, • Strong written and verbal communication skills, • Analytical mindset with strong numerical aptitude, • Self-starter with a proactive, can-do attitude, • Passion for regulatory compliance, food labeling, and product integrity, • Ability to work both independently and collaboratively, • Food manufacturing environment What We Offer: • Medical/ Dental/ Vision/ AFLAC / Pet Insurance, • 401(k), • Competitive Salaries / Annual Reviews, • Employee Discounts, • Entrepreneurial environment and more! Ready to Join Us? Be part of a company where your ideas matter, your impact is visible, and your passion drives success. Apply now to help shape the future of innovation at Nassau Candy. We are an Equal Opportunity Employer

Job DescriptionSalary: The START Center for Cancer Research (START) is the worlds largestearly phasesite network, fully dedicated tooncologyclinical research.Throughout ourhistory, START has provided hope to cancer patients inglobalcommunity practices by offering"Hope Through Accesstocutting edgetrials throughout the UnitedStatesand Europe. We are hiring aClinic Nurse. The Clinic Nurse is responsible for assisting the clinic providers with examination, evaluation and triage of individuals who are participants in research protocols that are conducted at START. The Clinic Nurse uses appropriate professional judgment and decision-making in planning and providing care. Nursing care is to be delivered in a manner consistent with the Standard Operating Procedures and standards of practice, and professional evidence-based standards. This position is offered at a pay range of $62/hr -$67/hr, based on experience, qualifications, and internal equity. In addition, employees in this role may be eligible for anannual bonus of up to 10%of base earnings. Work Schedule:8:00 am-5:00 pm EST, Monday-Friday Location:Lake Success, NY 11042 Essential Responsibilities: Patient Care • Perform telephone triage assessments of patients on trial when, • Provide patient education regarding participation in a clinical trial, chemotherapy/immunotherapy/investigational agent administration and potential side eects., • Enter patient history into the Electronic Medical Record based on records received and the patient provided history., • Perform basic patient assessment including physical exam, vital signs, ECGs and other patient assessments as, • Use nursing assessment skills to observe participants general well-being. Document and take appropriate action as, • Provide patients with visit, • Ensure that the dignity, health, safety, and welfare of participants are given the highest priority at all times., • Coordinate patient care with internal and external sta., • Respond to emergency situations based upon nursing, • Provide coverage for Infusion Nurse as directed by management. Planning and problem-solving tasks • Prepare for clinic day ensuring necessary supplies/results are, • Assist with prescription rells., • Assist with entry and completion of quality standards for EHR/PQRS. Communicating tasks • Provide telephone, • Assist with the training and mentorship of less tenured sta., • Complete preauthorization forms for medications and, • Assist in the referral process to, • Communicate and interact with peers and other departments in a manner that is viewed as having a positive eect on patient services and sta morale. Interact eectively with patients/family members and demonstrate sensitivity in regards to cultural diversity, age specic needs and condentiality. Protocol management tasks • Work with the physician to ensure that necessary labs and assessments are performed and results are, • Work with the physician to ensure that orders are Technical and quality tasks • Working knowledge of a variety of health care, • Serve as a team member by expanding his/her responsibilities as directed by management to facilitate optimal workow within the cancer center., • Time management and organizational skills. Eective written and verbal communication skills., • Other duties may be assigned at any Required Education and Experience: • High School Diploma or GED., • Licensed Registered Nurse in practicing state., • 1-year oncology experience., • Basic Life Support (BLS) Certification, an AHA (American Heart Association) certificate., • Experience working with Microsoft Office, including Teams, Excel, Outlook and Word. Preferred Education and Experience: • Bachelors degree of Nursing., • Oncology Certified Nurse (OCN)., • ONS/ONCC Chemotherapy Immunotherapy Certificate completed within the last 5 years or obtained within first year of employment., • Clinical Trials experience. Best-in-Class Benefits and Perks We value the time, talent, and dedication our employees bring to START. Our commitment to yourwell-beingand growth is reflected in a competitive compensation packagebased on experiencealong with comprehensive benefits designed to support you both personally and professionally: Plus, we work to maintain the best environment for our employees, where people can learn and grow with the company. We strive to provide a collaborative, creative environment where everyone feels encouraged to contribute to our processes, decisions, planning, and culture. • 401(k) retirement savings plan with employer match, • Eligibility for an annual performance bonus, based on role and company results, • Generous paid time off and paid holidays, • Comprehensive medical, dental, and vision coverageand optional insuranceoptions, • Company paid life and disability insurance for added financial protection, • Employee Assistance Program (EAP) providing confidential, nocost support for you and your family from day one, • Flexible FSA and HSA plans to support your financial wellness, • Commitment to a supportive environment that values balance, wellbeing, and flexibility, • Werecommitted to fostering a collaborative, creative workplace where every team member is encouraged to contribute. At START,youlljoin a team that values continuous learning, professional growth, shared ideas, and a culture built on inclusivity and innovation. More about The START Center for Cancer Research START clinical trial sites have conducted more than 1,000 early-phase clinical trials, including dozens of therapies that were approved by the FDA or EMA. STARTrepresentsthe worlds largest roster of early-phase principal investigators across its Network of clinical trial sites. Committed to accelerating passage from trials to treatments, START delivers hope to patients, families, and physicians around the world via our mission of Hope Through Access.As an example, in San Antonio, where START was founded, STARTtreated the first patient ever with Keytruda one ofthe most effective cancerdrugsin medical history. Learn more at STARTresearch.com. Ready to be part of a team changing the future of cancer treatment? Join us in our mission to conquer cancer, one clinical trial at a time. Yourexpertiseand dedication can help us bring hope and healing to patients worldwide.Pleasesubmityour application online. We are an equal opportunity employer that welcomes and encourages diversity in the workplace. We do not discriminateon the basis ofrace, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law.

Job Description The START Center for Cancer Research (“START”) is the world’s largest early phase site network, fully dedicated to oncology clinical research. Throughout our history, START has provided hope to cancer patients in global community practices by offering "Hope Through Access” to cutting edge trials throughout the United States and Europe. We are seeking an Advanced Practice Provider. The Advanced Practice Provider (APP) – Early Phase Clinical Research Program supports protocol-compliant patient care and clinical trial execution for Phase I and other early-phase oncology studies. Functioning as a sub-investigator under the supervision of the Principal Investigator (PI), the APP extends clinical capacity, supports screening and study visits, and enhances care coordination while preserving core investigator responsibilities specific to early-phase research Work Schedule: Monday-Friday 8:00am-5:00pm Location: 450 Lakeville Road, Entrance A, Lake Success, New York The annual base salary for this role is $190K-$205K. However, base pay may vary depending on multiple individualized factors including market location, job-related knowledge, skills, and experience. Essential Responsibilities: • Serve as a sub-investigator on assigned early-phase clinical trials following completion of required training and delegation documentation., • Conduct protocol-required physical examinations and study visits for patients in screening, on treatment, and in follow-up as delegated by the Principal Investigator., • Prepare comprehensive medical histories and clinical summaries in advance of new patient consults to support efficient PI evaluation., • Assist with screening activities prior to new patient visits, including preliminary chart review and protocol feasibility assessment., • Support post-consent screening by assisting with protocol-specific screening questions and required clarifications., • Assist with the identification, documentation, and follow-up of adverse events (AEs) and serious adverse events (SAEs) in collaboration with the Principal Investigator and research team. Attend sponsor or safety calls designated as low priority or routine, as delegated by the Principal Investigator., • Act as the first point of clinical contact for the research care team for day-to-day patient management questions and escalate issues to the Principal Investigator as appropriate., • Coordinate with nursing, pharmacy, clinical research coordinators, and data management to ensure safe, efficient, and protocol-adherent care delivery. Required Education and Experience: • Advanced practice degree (Nurse Practitioner or Physician Assistant) with current licensure in the applicable state(s)., • Minimum of 5 years of experience in oncology clinical care or oncology clinical research. Preferred Education and Experience: • Master’s degree or Doctoral degree in advanced practice nursing or physician assistant studies., • National certification as a Nurse Practitioner or Physician Assistant. Eligibility and willingness to serve as a sub-investigator on oncology clinical trials., • Prior experience in early-phase (Phase I) oncology clinical research. Physical & Travel Requirements: • Travel: Limited travel may be required during training and onboarding. More About START START clinical trial sites have conducted more than 1,000 early-phase clinical trials, including dozens of therapies that were approved by the FDA or EMA. START represents the world’s largest roster of early-phase principal investigators across its Network of clinical trial sites. Committed to accelerating passage from trials to treatments, START delivers hope to patients, families, and physicians around the world via our mission of “Hope Through Access”. As an example, in San Antonio, where START was founded, START treated the first patient ever with Keytruda – one of the most effective cancer drugs in medical history. Learn more at STARTresearch.com. Ready to be part of a team changing the future of cancer treatment? Join us in our mission to conquer cancer, one clinical trial at a time. Your expertise and dedication can help us bring hope and healing to patients worldwide. Please submit your application online. We are an equal opportunity employer that welcomes and encourages diversity in the workplace. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law.

Job Description Overview Amerita, Inc. is a leading provider in home Infusion therapy. We are looking for a Pharmacy Technician - Compounding to join our Pharmacy team as we grow to be one of the top home infusion providers in the country. The Pharmacy Technician will report to the Pharmacy Manager and work in our City, State branch. Amerita is an entrepreneurial-founded company and a wholly owned subsidiary of PharMerica. The home infusion market is positioned for rapid growth driven by the aging population, increase in chronic diseases, robust pipeline of infusible drugs coming to market, and an industry shift from hospital delivery settings to lower-cost, high-quality alternative providers such as Amerita. As a core member of the Pharmacy team, you will be expected to prepare technical and clerical tasks associated with the preparation, labeling and dispensing of pharmaceuticals. We will help you achieve your goals through continuous professional development and regular career progression discussions. Schedule: Monday - Friday between the hours 8:00am - 8:00pm and Saturday 9:00am - 5:00pm Availability must be flexible to accomodate any shift • Competitive Pay, • Health, Dental, Vision & Life Insurance, • Company-Paid Short & Long-Term Disability, • Flexible Schedules & Paid Time Off, • Tuition Reimbursement, • Employee Discount Program & DailyPay, • 401k, • Pet Insurance Responsibilities • Coordinates and schedules the preparation of sterile mixtures and home medical equipment orders with the assistance of the Pharmacist, • Completes all calculations on product preparation as necessary, • Compounds sterile mixtures and non-mixtures, including, but not limited to parenteral nutrition, antibiotics, chemotherapy, hydration and narcotic analgesics, using aseptic technique where state laws permit, • Ensures compounding/clean room areas and related equipment are cleaned, sanitized and maintained in compliance with company policies and procedures, and USP 797 and USP 800 standards, • Documents all activities on appropriate logs, • Participates in branch management, department and intra-departmental meetings and quality improvement activities, • Adheres to all accreditation, OSHA, FDA, state, local and federal regulations, and USP 797 and USP 800 standards relevant to infusion pharmacy and home medical equipment, • Documents all temperature logs, pressure and humidity monitors, records all sterility testing done in the clean room in compliance with company policies and procedures, and USP 797 and USP 800 standards, • Documents all activities on the appropriate logs, • Other duties as assigned Supervisory Responsibility: No Qualifications • Successful completion of an approved/accredited Pharmacy Technician training program; IV certification preferred, • Registered Pharmacy Technician license in state of practice per state regulations, • National Pharmacy Technician Certification as required by the state board of pharmacy in state of practice, • 1-3 years of related pharmacy experience in a home care setting, retail or pharmacy setting, preferred, • At least 1 year of aseptic preparation of infusion-related pharmaceuticals in a hospital or home infusion setting preferred, • General knowledge of drug terminology, pharmaceutical calculations, drug use and aseptic techniques, • Flexible schedule with the ability to work on-call evenings and weekends on an as-scheduled basis, • Effective mathematical and communication skills required, • Basic pharmacy knowledge of reading and interpreting prescriptions, • Ability to work independently, accurately and efficiently, • Valid driver's license Driving Position: Yes-Minimal driving for patient deliveries may be required To perform this role will require constant sitting and typing on a keyboard with fingers, and ocassionally standing and walking. The physical requirements will be the ability to push/pull and lift/carry 21-30 lbs

Perform entry clearance process through our ACE System for Customs, USDA, FDA, DEA, and Fish and Wildlife (FWS) regulated shipments.

Job DescriptionJob Title: QMS Supervisor - Medical Devices Job Description The Quality Management Systems (QMS) Supervisor oversees the development, implementation, and continuous improvement of the organization’s Quality Management System to ensure full compliance with applicable regulatory and industry standards. This role partners closely with cross-functional teams to foster a strong culture of quality, maintain audit readiness, and drive continuous improvement initiatives across the organization. Reporting into senior Quality leadership, the QMS Supervisor plays a hands-on role in audit management, CAPA oversight, document control, and QMS performance monitoring, while serving as a key resource for quality training and compliance guidance. Responsibilities • Own and maintain the Quality Management System structure, including policies, procedures, standard operating procedures (SOPs), and work instructions, ensuring alignment with regulatory requirements and organizational objectives., • Support and lead internal and external audits, including registrar, customer, supplier, and regulatory audits, covering audit preparation, hosting, and response execution., • Lead root cause investigations for nonconformances, deviations, and customer complaints, and develop, implement, and verify effective Corrective and Preventive Actions (CAPAs)., • Drive continuous improvement initiatives using Lean principles, statistical tools, and data analysis to enhance product quality and operational efficiency., • Oversee electronic Quality Management Systems (eQMS) and document control processes to ensure data accuracy, robust version control, and ongoing compliance., • Develop, track, and present quality metrics and key performance indicators (KPIs) to leadership to support informed decision-making and strategic planning., • Deliver QMS, Good Manufacturing Practice (GMP), and compliance training to cross-functional personnel to reinforce quality awareness and accountability throughout the organization., • Ensure alignment and consistency of quality programs and processes across all relevant departments and functions., • Regularly review, assess, and improve quality processes to enhance effectiveness, manage risk, and control costs within the quality system., • Collaborate closely with cross-functional teams, including manufacturing, R&D, and operations, to support compliance-driven activities and initiatives.Essential Skills, • Minimum of 5 years of experience in a Quality Management Systems or Quality Assurance leadership role within a regulated industry., • Strong working knowledge of quality management standards and audit processes, including ISO-based quality system frameworks., • Proven experience leading CAPA investigations, including root cause analysis, development of corrective and preventive actions, and verification of effectiveness., • Hands-on experience administering and maintaining an electronic Quality Management System (eQMS) platform., • Expertise in document control systems, including change management and training record management in a regulated environment., • Ability to analyze quality data, identify trends, and implement sustainable corrective and preventive actions based on data-driven insights., • Demonstrated experience in quality assurance for medical devices, including exposure to spine, neurology, or implantable device products., • Experience with internal and external audits within a quality-regulated environment., • Strong understanding of regulatory affairs and quality assurance practices in regulated industries., • Excellent written and verbal communication skills, with the ability to interface effectively with auditors, customers, and internal stakeholders at all levels., • Demonstrated ability to influence cross-functional teams and lead through collaboration without direct authority., • Strong organizational skills and high attention to detail, particularly in managing regulated documentation and records.Additional Skills & Qualifications, • Experience working in the medical device industry., • Knowledge of FDA Quality System Regulation (QSR) and Good Manufacturing Practice (GMP) requirements., • Certified Internal Auditor or equivalent certification in ISO-based quality management systems., • ASQ Certified Quality Auditor (CQA) or Certified Quality Engineer (CQE) credentials., • Lean Six Sigma Green Belt or Black Belt certification or training., • Experience supporting manufacturing, research and development (R&D), and operations teams within a compliance-driven environment., • Familiarity with quality management standards such as AS9100 and ISO 9001., • Background in quality management for specialized medical device areas such as spine, neurology, or implantable devices.Work Environment This role is 100% office-based in a cubicle work environment, providing a structured and professional setting focused on quality and compliance activities. The position centers on the use of electronic Quality Management Systems and other office-based tools to manage documentation, audits, metrics, and training. The work environment supports collaboration with cross-functional teams, including quality, manufacturing, R&D, and operations. Eligible employees may receive a discretionary year-end bonus, which is not tied to individual performance. Job Type & Location This is a Permanent position based out of Baldwin, NY. Pay and Benefits The pay range for this position is $95000.00 - $105000.00/yr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision, • Critical Illness, Accident, and Hospital, • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available - They match 25% of 1%, up to 4%., • Life Insurance (Voluntary Life & AD&D for the employee and dependents), • Short and long-term disability, • Health Spending Account (HSA), • Transportation benefits, • Employee Assistance Program, • Time Off/Leave (PTO, Vacation or Sick Leave) - 18 total days of PTO + 13 holidays Workplace Type This is a fully onsite position in Baldwin,NY. Application Deadline This position is anticipated to close on Jul 29, 2026. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options. San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records. Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability. Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.

Here at Optum, the largest network of medical groups in the nation, we are seeking a dedicated, patient-centric Hematology/Oncology APC to join our growing team in Lake Success, NY. At Optum, you'll have the clinical resources, data and support of a global organization behind you so you can help your patients live healthier lives. Experience the fulfillment of advancing the health of your community with the excitement of contributing new practice ideas and initiatives that could help improve care for millions of patients across the country. Because together, we have the power to make health care better for everyone. Join us and discover how rewarding medicine can be while Caring. Connecting. Growing together. • Comprehensive, community based, out-patient multispecialty practice that offers chemotherapy services in our on-site infusion center, • Established team of 7 physicians and 2 APC's, • Opportunity to participate in innovative clinical trials, many of which have already contributed to FDA approval of multiple lifesaving treatments, • No overnight or weekend call/hours required, • Patient visit hours in general will be from 8:30 AM - 4:00 PM but are flexible, • Exceptionally strong referral base, • In close coordination with our hematologists and oncologists, your responsibilities will include:, • Care for patients with a wide variety of both solid tumor and hematologic malignancies, • Supervising and evaluating patients receiving infusions in our infusion centers, • Visits with new patients to educate them on treatment side effects and schedules, • Providing survivorship visits to furnish patients with treatment summaries and educate them on their follow-up recommendations after completion of treatment, • Follow up office visits with patients on observation or receiving oral therapy, • Same day visits with patients who call with new complaints during treatment, • Quadruple Aim: Improving Patient Satisfaction; Lowering Costs; Delivery High-Quality Outcomes; Increasing Provider Satisfaction and Well-Being, • Clinicians are supported to practice at the peak of their license, • Clinician-centric and clinician focused, with shared EMR across businesses to support coordinated care, • The culture is one of clinical innovation and transformation, • Affiliations with prestigious organizations, • We are influencing change on a national scale while still maintaining the culture and community of our local care organizations, • Guaranteed, competitive compensation model based on quality, not quantity, with significant earning potential, annual increases, and bonus eligibility, • Financial stability and support of a Fortune 5 Company, • Robust retirement offerings including employer funded contributions and Employee Stock Purchase Plan (ESPP for UHG Stock), • APC Partnership opportunities and incentives, • Comprehensive benefits plan inclusive of medical, dental, vision, STD/LTD, CME and malpractice coverage The Optum Story in the Tri-State Region: Optum Tri-State was formed in 2022 by bringing together Riverside Medical Group, CareMount Medical and ProHealth Care. The regional alignment combines resources and services across the care continuum - from preventative medicine to diagnostics to treatment and beyond - and features 70 specialties, working in 360 medical practices and more than 55 urgent care locations across New York, New Jersey, and Southern Connecticut. As a Patient Centered Medical Home, Optum Tri-State can provide patient-focused medical care to the entire family. This dynamic position would afford you the opportunity to join a regional, inter-disciplinary care team of over 2,100 providers who serve nearly 2 million patients. Our doctors and clinicians have access to the latest medical information and technology, which lets them spend more time with patients, provide better care and realize better outcomes. With Optum, we've found that putting clinicians at the center of care is the best way to improve lives. Our physician-led organizations are some of the most dynamic and progressive health care organizations in the world. You will find our team working in local clinics, surgery centers and urgent care centers, within care models focused on managing risk, higher quality outcomes and driving change through collaboration and innovation. • Unrestricted licensure in the state of New York or has New York application in process, • Board Certification or board eligibility in Hematology/Oncology, • Active and unrestricted DEA License or ability to obtain prior to start Compensation for this specialty generally ranges from $113,000 - $173,500. Total cash compensation includes base pay and bonus and is based on several factors including but not limited to local labor markets, education, work experience and may increase over time based on productivity and performance in the role. We comply with all minimum wage laws as applicable. In addition to your salary, we offer benefits such as, a comprehensive benefits package, incentive and recognition programs, equity stock purchase and 401k contribution (all benefits are subject to eligibility requirements). UnitedHealth Group is an Equal Employment Opportunity employer under applicable law and qualified applicants will receive consideration for employment without regard to race, national origin, religion, age, color, sex, sexual orientation, gender identity, disability, or protected veteran status, or any other characteristic protected by local, state, or federal laws, rules, or regulations. UnitedHealth Group is a drug - free workplace. Candidates are required to pass a drug test before beginning employment.

PL Developments, also known as PLD, is a leading manufacturer, packager, and distributor of over-the-counter (OTC) pharmaceutical products and consumer healthcare goods. The QC Inspector is responsible for performing hourly quality checks on packaging, ensuring compliance with cGMP guidelines. Key duties include verifying lot numbers and expiration dates, maintaining accurate Batch Records, inspecting packaging components, and conducting equipment accuracy checks. The ideal candidate has knowledge of FDA/cGMP guidelines, basic math and writing skills, and strong communication abilities. The position requires the ability to lift 50 lbs. and stand for extended periods. Fluency in English is required. Work Schedule: Monday - Thursday 7 am - 5:30 pm JOB QUALIFICATIONS: • 0 - 2 years experience in related field, • Knowledge of FDA/cGMP guidelines, • Basic writing and math skills, • Strong verbal communication skills, • Fluent in English POSITION RESPONSIBILITIES: • Perform hourly quality checks of work-in-progress (WIP) and finished goods packaging according to company-defined attributes., • Maintain outgoing packaging quality levels and ensure compliance with cGMPs., • Verify lot numbers and expiration dates of finished packaging against the Certificate of Analysis and pick slip., • Confirm that packaging line clearance has been properly completed and release the line to Production., • Sign off on proper line preparation by initialing and dating the Equipment Use and Cleaning Log., • Ensure all pertinent information and required signatures are present on Batch Record forms., • Pull and record "beginning," "middle," and "end" packaging line retention samples., • Verify that all required documents are included in the Batch Record., • Inspect staged kit components awaiting packaging, as required., • Perform accuracy checks of weigh scales, in-line scales, and leak detection equipment as needed., • Conduct cap torque measurements as required., • Verify packaging specifications to meet customer requirements. PHYSICAL REQUIREMENTS: Employees must be able to lift up to 50 lbs and remain on their feet throughout the entire workday. This role requires consistent physical activity, including standing, walking, and performing manual tasks in a fast-paced production environment. The ability to carry out these duties safely and effectively is essential to maintaining quality control and compliance with FDA/cGMP standards Hourly Rate starting $19.00/hr BENEFITS: • Medical and Dental Benefits, • Vision, • 401K with employer match, • Group Life Insurance, • Flex Spending Accounts, • Paid Time Off and Paid Holidays, • Tuition Assistance, • Corporate Discount Program, • Opportunities to Flourish Within the Company PL Developments is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.

Assists the Team Leader in all aspects of daily operations including profitability, expense control, buying, merchandising, labor, regulatory compliance and special projects as assigned. Leads and develops Team Members. All Whole Foods Market Retail jobs require ensuring a positive company image by providing courteous, friendly, and efficient service to customers and Team Members at all times. All positions must be performed in accordance with team and store Standard Operating Procedures. Further, Team Members must be prepared and able to perform the duties inherent in other Team Member job descriptions. All positions must strive to support WFM core values and goals, promote national, regional, and store programs and initiatives, and ensure adherence to all applicable health and safety regulations including Food Safety and regulatory duties required in the department. Develops and maintains creative store layout and product merchandising. Works with Team Leader to achieve sales, purchasing, and labor targets. Assists Team Leader in analysis of sales, reports, and labor. Assists team leader in annual sales and expense projections and budget preparation. Assists team leader with ordering and inventory management. Works with Team Leader to resolve team concerns or issues. Functions as point person and departmental person in charge in absence of Team Leader. Sets and achieves the highest standards of retail execution. Fosters and encourages a positive environment of outstanding teamwork, mutual respect, and exceptional morale. Maintains awareness of customer flows and needs and directs Team Members as necessary to satisfy and delight customers; responds promptly to customer needs and questions. Selects, trains, develops, mentors, motivates, and counsels Team Members in a manner that sustains a high-performance team and minimizes turnover. Communicates and maintains Team Member safety and security standards. Provides timely, thorough, and thoughtful performance evaluations. Consistently communicates and models WFM vision and goals 18+ months retail Team Member experience and 6+ months of supervisory experience Must be able to lift 50 pounds. In an 8-hour work day: standing/walking 6-8 hours. Hand use: single grasping, fine manipulation, pushing and pulling. Work requires the following motions: bending, twisting, squatting and reaching. Exposure to FDA approved cleaning chemicals. Exposure to temperatures: <32 degrees Fahrenheit (freezing), 32-40 degrees Fahrenheit (refrigerators), >90 degrees Fahrenheit. Ability to work in a wet and cold environment. Ability to handle knives and other cutting equipment. Ability to work a flexible schedule including nights, weekends, and holidays as needed. Ability to use tools and equipment, including box cutters, electric pallet jacks, and other heavy machinery The wage range for this position is $20.05-$35.00 Hourly, commensurate with experience. Whole Foods Market offers "Whole Benefits". Whole Benefits offers a wide range of benefits for Full and Part-Time Team Members, including eligibility for a store discount, paid time off, financial wellness, health & wellness support programs, and access to other Team Member perks. Eligibility for Whole Benefits is determined under the terms of the applicable Whole Benefits plan at a person's date of hire and may vary based on work location, length of service, and job type (such as regular or seasonal).

GEODIS specializes in unlocking business value in a complex world, ensuring seamless movement of goods worldwide. As a global third-party logistics provider (3PL), we power A Better Way to Deliver for the world's top brands and manufacturers. Fuel your career with GEODIS and discover endless growth opportunities. Your role on the team: • Serves as the customer service liaison between the Company and the customer, • Processes Custom and OGA (other government agency) entries for clearance of goods into the United States, • Opens files, enters notes, information and document requests in Cargowise and/or AS400 system, • Classifies invoice based on HTS (Harmonized Tariff Schedule), • Sends information/document requests to company's employees, suppliers, service providers and/or U.S. Government agencies as needed, • Communicates with specified offices, departments, and teams on all issues affecting customs brokerage, • Files document requests, correspondence and documents in a file folder identified by the applicable shipping/reference number, • Ensures compliance with regard to U.S. Government regulatory agencies such as FDA, EPA, FCC, Fish & Wildlife, etc., • Coordinates shipping details with U.S. Forwarders, Steamship Lines, Airlines, Agents, etc., • Convert and verify shipment weight, volume and foreign currency, • Maintain communication with customers, carriers and vendors, • Coordinate pick-ups and invoice files, • Assist customers with questions, complaints, requests, tracking and tracing, • Handles accounting processes accurately and in a timely manner, • Coordination of shipments from airline, ocean piers and CFS (container freight station) to customer/consignee destination, • Review documentation or issue documents to meet government regulations and carrier regulations, • Must have knowledge of buying/selling rates to ensure profitability, • Ensure email and telephone calls are promptly and politely answered What you need: • Minimum 3 years experience in customs brokerage or an equivalent combination of both education and experience., • Knowledge of U.S. Government Agency requirements, • Knowledge of U.S. Customs and OGA clearance of freight, • PC literate with experience with Microsoft Outlook, Work, Access and Excel, • Excellent written and oral communication skills that demonstrate a proven ability to develop relationships with a range of internal and external customers, • Excellent planning and organizational skills, • Ability to read and interpret documents, • Ability to write routine reports and correspondence, • Ability to apply common sense understanding to carry out instructions furnished in written, oral, or diagram form, • Ability to multitask, • Mathematical skills essential to ensure accuracy in calculations What you gain from joining our team: • Access wages early with the Rain financial wellness app, • Free telemedical access to doctors and therapists through First Stop Health is available on the first day of employment, • Health, dental, and vision insurance after 30 days of employment, • 401k match, • Paid maternity and parental leave, • Access to career development, employee resource groups, and mentorship programs, • Employee discounts, • Access to employee perks like fitness class discounts and free access to a relaxation and meditation app, • Free financial wellness programs, • Daycare discount program, • Opportunities to volunteer and give back to your community, • + more! Join our Team! • Visit our website at workatGEODIS.com and chat with our virtual recruiter, Sophie, to fast-track your way to an interview!, • Text DELIVER to 88300 to apply! Equal Opportunity Employer This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor.

Are you ready to take your leadership skills to the next level in a fast-paced, dynamic environment where every day brings new challenges and opportunities? At Piping Rock Health Products, we're looking for a hands-on, solutions-driven supervisor to lead our production team with energy, confidence, and a passion for excellence. This is your chance to join a top workplace on Long Island (6 years running!) and a 2024 top supplement manufacturing company where innovation, quality, and people come first. As a supervisor, you'll be the driving force behind a motivated, efficient, and safety-focused team. Your mission is to ensure smooth operations, mentor associates, and spark continuous improvement. • Ensure compliance with GMPs, OSHA and/or all regulatory agencies, including company policies and procedures., • Oversee all manufacturing and packaging operations including pharmacy, blending, packaging, and warehouse to meet quality standards, efficiency and productivity in the workplace., • Allocate resources, assign tasks, and manage scheduling to optimize production output., • Lead, train, and coach associates to promote safety, consistent performance, and professional development., • Maintain workflow, foster team morale, and drive continuous improvement initiatives., • Facilitate effective communication and collaboration among associates, managers, and vendors., • Perform additional duties assigned to support overall departmental and company goals., • 5+ years of manufacturing or packaging leadership experience (FDA/GMP industries preferred)., • Solid supervisory skills with proven ability to organize, prioritize, and inspire teams., • Strong interpersonal, communication, and problem-solving abilities., • Flexibility to adapt, multitask, and support business needs with additional shifts when required., • Ability to lift up to 50 lbs, stand for long periods, and thrive in a physically active environment., • Bilingual in English/Spanish a plus! We proudly offer: Medical, dental, vision, 401K with company match, pet insurance and more! We reward the hard work of our team members with fun and exciting company events, summer picnic, festive packages, holiday celebrations, and associate referral bonuses! Founded in 2011, Piping Rock Health Products has gone on to win Long Island's top workplaces award 6 years in a row & securing the spot as top supplement manufacturing company 2024 by Food Business Review! Supported by a group of vitamin visionaries with over 40 years of industry experience and a carefully curated team of talented associates. Piping Rock is a global vitamin and supplement manufacturer with an unwavering commitment to creating quality wellness products. We believe that family always comes first, and that the dedication of our associates is the key ingredient to our success. We are a drug-free workplace, regulated by the FDA, required to follow federal guidelines; therefore in order to start as well as maintain employment, you must be able to successfully clear drug screening processes, which include testing for all illegal substances per federal guidelines. Piping Rock Health Products, INC is an equal opportunity employer.

We are a drug free workplace, regulated by the FDA, required to follow Federal Guidelines; therefore in order to start as well as maintain employment, you must be able to successfully clear drug screening processes, which include testing for all illegal substances per Federal Guidelines. Must be abl

Job Description We Offer Competitive Salary, Full Benefits Package, Paid time Off, Pension and Opportunities for Professional Growth South Shore Rehabilitation and Nursing, is currently looking to hire a Cook to join our dedicated team of professionals. We are looking for people who are passionate about their craft and bring professionalism to their work environment. Duties and Responsibilities: · Prepares food for meals, including modified textures for restricted and therapeutic diets. · Supervises dietary aides in the preparation and serving of foods and beverages. · Follows instructions of the Dining Services Director in the preparation of meals and maintains meal schedules. · Prepares food by methods that conserve nutritive value and flavor. Ensures foods are palatable, attractive and in the proper form to meet the individual needs of the residents. · Assures that all food items are handled properly to ensure safety and sanitation standards according to State and Federal regulations. Properly stores, covers, and refrigerates necessary items. Ensures that foods are cooked to the appropriate temperatures according to the FDA Food Code, latest edition. · Practices and supervises infection control policies. · Responsible for opening and closing the kitchen · Document temperatures of food prior to service, refrigeration and freezer · Assist with preparation and execution of special events and theme meals · Attends in-service education and dining services staff meetings as required. · Performs other duties as assigned by the Dining Services Director. REQUIREMENTS: • Certification in healthcare cooking (ServSafe or Sodexo), • Minimum one (1) year of experience in large-scale cooking, • Strong knowledge of large scale & therapeutic food prep, • Must be able to do some physical work, • Must be able to work as a team member, • High School Diploma or Equivalent, • Excellent customer service & communication skills, • Will manage Kitchen in absence of food service director, • Must be available for weekends and Holidays Who we are: We are an innovative skilled nursing facility that, specializes in caring for the elderly. Our successful reputation has been built by the efforts of our dedicated employees and is supported by Sapphire's future strategies, which reflect our appreciation for those who work in our organizations. Please join us and begin a successful and rewarding career. South Shore Rehabilitation and Nursing, considers the health and safety of its residents, family members, and team members as its highest priorities. All offers of employment with Sapphire Nursing at Meadow Hill are conditioned on completing and passing a background and drug test, participating in mandatory vaccine programs (e.g., Covid-19), participating in testing requirements (e.g. Covid-19, TB) and using designated PPE when required. EOE Statement WE ARE AN EQUAL OPPORTUNITY EMPLOYER. Applicants and employees are considered for positions and are evaluated without regard to mental or physical disability, race, color, religion, gender, national origin, age, genetic information, military or veteran status, sexual orientation, marital status or any other protected Federal, State/Province or Local status unrelated to the performance of the work involved.

Assists the Team Leader in all aspects of daily operations including profitability, expense control, buying, merchandising, labor, regulatory compliance and special projects as assigned. Leads and develops Team Members. All Whole Foods Market Retail jobs require ensuring a positive company image by providing courteous, friendly, and efficient service to customers and Team Members at all times. All positions must be performed in accordance with team and store Standard Operating Procedures. Further, Team Members must be prepared and able to perform the duties inherent in other Team Member job descriptions. All positions must strive to support WFM core values and goals, promote national, regional, and store programs and initiatives, and ensure adherence to all applicable health and safety regulations including Food Safety and regulatory duties required in the department. Develops and maintains creative store layout and product merchandising. Works with Team Leader to achieve sales, purchasing, and labor targets. Assists Team Leader in analysis of sales, reports and labor. Demonstrates advanced product knowledge and develops / maintains awareness of new products. Maintains good vendor relationships, develops new vendor relations, and ensures all paperwork is properly submitted for vendor processing. Works with Team Leader to resolve team concerns or issues. Functions as point person and departmental person in charge in absence of Team Leader. Sets and achieves the highest standards of retail execution. Fosters and encourages a positive environment of outstanding teamwork, mutual respect, and exceptional morale. Maintains awareness of customer flows and needs and directs Team Members as necessary to satisfy and delight customers; responds promptly to customer needs and questions. Selects, trains, develops, mentors, motivates, and counsels Team Members in a manner that sustains a high-performance team and minimizes turnover. Provides timely, thorough, and thoughtful performance evaluations. Consistently communicates and models WFM vision and goals High energy, enthusiastic, and displays an affinity for our products, core values, and company philosophy. Growth mindset towards greater responsibility and ownership. Desire to coach and mentor others for growth. Excellent interpersonal, motivational, team building, and customer relationship skills. Capable of teaching others in a positive and constructive manner. Thorough product knowledge. Advanced knowledge of regulatory and safety policies and procedures. Proficient mathematical skills for assessing financial performance, monitoring profitability, and managing inventory. Demonstrated decision-making ability, leadership skills, and ability to prioritize and delegate. Proficiency with email, Microsoft Office, and operations-related applications. 18+ months retail Team Member experience and 6+ months of supervisory experience. Must be able to lift 50 pounds. In an 8-hour work day: standing/walking 6-8 hours. Hand use: single grasping, fine manipulation, pushing and pulling. Work requires the following motions: bending, twisting, squatting and reaching. Exposure to FDA approved cleaning chemicals. Exposure to temperatures: <32 degrees Fahrenheit (freezing), 32-40 degrees Fahrenheit (refrigerators), >90 degrees Fahrenheit. Ability to work in wet and dry conditions. Ability to work a flexible schedule including nights, weekends, and holidays as needed. Ability to use tools and equipment, including knives, box cutters, electric pallet jacks, and other heavy machinery. May require use of ladders. The purpose of this document is to provide a general summary of essential responsibilities for the position and is not meant as an exhaustive list. This document does not reflect all job duties or requirements for every position. Requirements build as one progresses through the job levels, so any job duties required at a lower level may be required at the higher level in addition to the duties listed for that higher level. Duties, assignments, and other responsibilities may differ for similar positions based on business conditions, departmental or geographic location, and/or needs for the particular position. An individual must demonstrate successful performance in their current position before being considered for promotion. In addition, in order to promote into a higher-level position, a business need for the promotion must exist and the candidate must be considered the most qualified person for the new position. Completion of certain milestones such as obtaining an advanced degree or certification, time in current position, or developing skills to perform at the higher-level role do not guarantee a promotion. The wage range for this position is $20.05-$35.00 Hourly, commensurate with experience. Whole Foods Market offers "Whole Benefits". Whole Benefits offers a wide range of benefits for Full and Part-Time Team Members, including eligibility for a store discount, paid time off, financial wellness, health & wellness support programs, and access to other Team Member perks. Eligibility for Whole Benefits is determined under the terms of the applicable Whole Benefits plan at a person's date of hire and may vary based on work location, length of service, and job type (such as regular or seasonal).

Job DescriptionSalary: The START Center for Cancer Research (START) is the worlds largestearly phasesite network, fully dedicated tooncologyclinical research.Throughout ourhistory, START has provided hope to cancer patients inglobalcommunity practices by offering"Hope Through Accesstocutting edgetrials throughout the UnitedStatesand Europe. We areseekingaClinical Pharmacist, Investigational Drug Section.TheClinical Pharmacist, Investigational Drug Section(IDS)is responsible forallfacetsof medication order verification, dispensing and documentation process for investigational drugs, conventional chemotherapy and supportive care medications provided by the IDS. The pharmacistmay beinvolved in the provision of pharmaceutical care including assisting with patient interviews, maintenance of current medication lists, providing patient medication education, providing drug information to the healthcare team and patients. The pharmacist will practice with a high degree of autonomy, guided by IDS SOPs and quality assurance verification guidelines.This roleis responsible forthedaily supervision of staff assigned to medication preparation, dispensing, and operation of the IDSin accordance withall applicable rules and regulations. The salary range for this role is$165,000 - $175,000.However, base pay may vary depending on multiple individualized factors including market location, job-related knowledge, skills, and experience. Work Schedule:8 a.m.- 4:30 p.m. Monday - Friday Location: START- New York Long Island 450 Lakeville Road,Entrance A, Lake Success, NY 11042 Essential Responsibilities: • Verifymedication orders including accuracy of dosages and calculations, review of basic patient eligibility criteria, including but not limited to accurately signed / dated study consent form(s), laboratory values within treatment criteria, all appropriate tests have been completed, resolution of known toxicity from previous chemotherapy, and an absence of serious known drug interactions., • Overseethe preparation and dispensing of all medications from the IDS, including supervision of certified pharmacy technicians during preparation of IV admixtures and oral medication dosages,insuringcompliance with all steps of the double-check verification process prior to releasing dosages from the IDS., • Provide pharmaceutical care including patient medication and supportive carecounseling, anddrug information to the healthcare team and patients., • Oversee drug inventories including documentation of current inventory, projection of expected usage in concert with ordering, receiving, storage and dispensation tracking of Phase I and conventional medications., • Assistpharmacy technicians inmaintainingadequate investigational documentation, records, weekly inventory, and interactions with study personnel, • Review new protocol(s), protocolamendmentsand associated forms., • Maintain and generate reports using the IDS drug accountability program., • Contribute to the effective operation of the pharmacy department.Enteraccuratemedication computer order entries andaccuratemaintenance of reported patient home medications in the EMR., • Other duties may be assigned at any time. Education & Experience: • Graduate of an ACPE accredited School of Pharmacy., • Current State license., • Previoushospital/clinic pharmacy experience., • Familiarity with sterile compounding requirements for chemotherapy agents, USP<797>, USP<800>, laminar airflow hood(s) / biological safety cabinet(s); telephone and copier / scanner / facsimile machine., • Computer skills, includinguseMicrosoftOffice products, including Word, Excel, Power Point and Access., • Familiarity with the use of electronic medical record program(s), pharmacy softwareprogramsand study IRTsystems., • Knowledge of Good Clinical Practice (GCP) principles. PreferredEducationandExperience: • Sterile compounding & chemotherapy certification., • Intravenous sterile product training., • Prior experience in clinical trials and management of investigational drugs., • Specialty residency in oncology and/or current BPS Board Certified Oncology Pharmacist (BCOP)., • Bilingual. PhysicalandTravelRequirements: • 80% oftimespent standing and/or walking., • Ability tolift upto a25-pound weight load., • Some lifting and bending,pushingand/or pulling loads. Best-in-Class Benefits and Perks We value the time, talent, and dedication our employees bring to START. Our commitment to your well-being and growth is reflected in a competitive compensation packagebased on experiencealong with comprehensive benefits designed to support you both personally and professionally: • 401(k) retirement savings plan with employer match, • Eligibility for an annual performance bonus, based on role and company results, • Generous paid time off and paid holidays, • Comprehensive medical, dental, and vision coverageand optional insuranceoptions, • Company paid life and disability insurance for added financial protection, • Employee Assistance Program (EAP) providing confidential, no cost support for you and your family from day one, • Flexible FSA and HSA plans to support your financial wellness, • Commitment to a supportive environment that values balance, wellbeing, and flexibility, • Werecommitted to fostering a collaborative, creative workplace where every team member is encouraged to contribute. At START,youlljoin a team that values continuous learning, professional growth, shared ideas, and a culture built on inclusivity and innovation. More About START START clinical trial sites have conducted more than 1,000 early-phase clinical trials, including dozens of therapies that were approved by the FDA or EMA. STARTrepresentsthe worlds largest roster of early-phase principal investigators across its Network of clinical trial sites. Learn more atSTARTresearch.com. Ready to be part of a team changing the future of cancer treatment? Join us in our mission to conquer cancer, one clinical trial at a time. Yourexpertiseand dedication can help us bring hope and healing to patients worldwide.Pleasesubmityour application online. We are an equal opportunity employer that welcomes and encourages diversity in the workplace. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law.

Job Description Maintenance Technician – Food Manufacturing Location: [City, State] Job Type: Full-Time Industry: Food Manufacturing / Processing Position Overview We are seeking a skilled Maintenance Technician to support production and packaging operations in a food manufacturing facility. This role is responsible for preventive maintenance, troubleshooting, and repair of manufacturing and packaging equipment to ensure safe, efficient, and compliant production. The ideal candidate has hands-on mechanical and basic electrical experience, understands food-grade environments, and can respond quickly to minimize downtime. Key Responsibilities • Perform preventive and corrective maintenance on food processing and packaging equipment, • Troubleshoot mechanical, electrical, pneumatic, and hydraulic issues, • Maintain and repair conveyors, fillers, sealers, mixers, ovens, and packaging machinery, • Respond to equipment breakdowns and production support calls, • Perform machine setups, changeovers, and adjustments, • Conduct equipment inspections to ensure reliability and safety, • Read and interpret mechanical drawings and electrical schematics, • Document maintenance activities using CMMS or work order systems, • Follow GMP, HACCP, and food safety requirements, • Adhere to all safety policies, including lockout/tagout procedures Qualifications • 2–5+ years of maintenance experience in a food, beverage, or consumer goods manufacturing environment, • Strong mechanical troubleshooting skills, • Basic electrical knowledge (motors, sensors, wiring, controls), • Experience with conveyors and packaging machinery, • Ability to work independently and as part of a team, • Willingness to work off-shifts, weekends, or on-call as needed Preferred Experience • Experience with high-speed packaging lines, • Pneumatic and hydraulic system knowledge, • PLC troubleshooting exposure (not programming-heavy), • Familiarity with FDA-regulated or GMP environments, • Welding or fabrication experience

The Director Food Service is responsible for overseeing and optimizing food service retail operations at MMA. This role ensures contract compliance, operational excellence, food safety, financial performance, and customer satisfaction while aligning operations with DoD standards, military regulations, and company objectives. The Director of Food Service provides leadership to regional and installation-level managers, ensures consistent execution of DoD contract requirements, and serves as a primary liaison with government contracting officers, installation leadership, and inspection authorities. The Director will also drive standardization and modernization of operations through implementation of food service technologies, Food Information Management Systems (FIMS), cycle menu development, recipe standardization, and cost control systems to enhance operational efficiency, transparency, and performance. Key Responsibilities • Oversee daily food service retail operations., • Ensure full compliance with contract requirements, Performance Work Statements (PWS), and Service Level Agreements (SLAs)., • Interpret and execute DoD, DLA, and installation-specific policies and directives., • Serve as senior operational point of contact for Contracting Officers (CO), Contracting Officer's Representatives (COR), and installation leadership., • Lead and participate in performance reviews, inspections, audits., • Respond to Corrective Action Requests (CARs) and implement preventive measures., • Support proposal development and operational input for recompetes and new awards. Food Safety, Quality & Compliance • Ensure compliance with all food safety and sanitation standards, including:, • DoD Food Code, • FDA Food Code, • HACCP programs, • Army Veterinary Services / Public Health inspections, • Oversee sanitation, temperature control, allergen management, and food defense programs., • Ensure all facilities maintain inspection readiness and pass announced and unannounced audits. Financial & Retail Performance Management • Manage operational budgets, labor models, food costs, and margins across all sites., • Monitor retail KPIs including sales, labor productivity, shrink, inventory control, and customer throughput., • Ensure accurate forecasting, pricing compliance, and adherence to contract pricing structures., • Identify opportunities to improve profitability while maintaining contract compliance., • Implement and enforce food & beverage cost control systems and processes, including inventory management, waste reduction, yield tracking, and standardized reporting. Leadership & Workforce Management • Lead, mentor, and develop regional managers, project managers, and site leadership., • Ensure staffing levels meet contract requirements and service demands., • Oversee hiring, training, certification, and performance management of food service personnel., • Promote a culture of safety, accountability, professionalism, and customer service. Safety, Security & Risk Management • Ensure compliance with installation access requirements, background checks, and security protocols., • Oversee workplace safety programs and incident reporting., • Ensure emergency preparedness and continuity of operations plans are in place at all sites. Process Improvement & Innovation • Standardize operating procedures across installations while accommodating installation-specific requirements., • Implement technology solutions for scheduling, inventory, reporting, and compliance tracking., • Oversee deployment and utilization of Food Information Management Systems (FIMS) for menu management, allergen tracking, and nutritional transparency., • Drive development and execution of cycle menus aligned with DoD standards, customer demand, and operational efficiency., • Ensure recipe standardization across all locations to maintain consistency, portion control, and quality., • Drive continuous improvement in speed of service, food quality, and customer satisfaction. Qualifications Required • Bachelor's degree in Hospitality Management, Business Administration, Operations Management, or related field (or equivalent experience)., • 810+ years of progressive food service operations leadership experience., • Demonstrated experience managing DoD or federal food service contracts., • Strong understanding of PWS execution, COR interactions Physical Demands • Lift and carry up to 50 lbs, • Walks, stands and moves about the kitchen and dining facility to ensure compliance with SOP, • Some bending and stooping.

Job Description Overview PharMerica is hiring a full-time Pharmacist in Uniondale, NY ! Join our closed-door pharmacy team where you’ll work in a non-retail environment, dedicated to meeting the pharmaceutical needs of long-term care and senior living clients. If you’re passionate about delivering exceptional service and high-quality care, we want to hear from you. Apply today and become part of a team committed to making a difference! Schedule: Monday-Thursday: 1pm-11:30pm Sunday: 9:30am-6pm Benefits and perks for you! • Medical, Dental, Vision insurance, • Health Savings & Flexible Spending Accounts (up to $5,000 for childcare), • Tuition discounts & reimbursement, • 401(k), • Company Paid Time Off, • Shift Differential, • DailyPay, • Pet Insurance, • Employee wellness and discount programs *Benefits may vary by employment status Responsibilities How YOU will benefit: • Supportive team with room to work independently, • Ongoing training and career growth, • Advancement opportunities in a growing company, • Referral bonuses As a Pharmacist you will: • Evaluate physician medication orders for drug appropriateness, correct dosage, potential drug interactions, and proper route of administration., • Provide clinical recommendations to physicians and facility staff regarding medication therapy changes and optimizations., • Maintain up-to-date patient/resident profiles, including medical history, lab results, and current medications (prescription, OTC, and home remedies)., • Ensure laboratory tests required for monitoring high-risk medications are appropriately ordered, reviewed, and communicated to the healthcare team., • Collaborate with physicians, nurses, and other healthcare professionals to provide clinical and technical support., • Document all communications and clinical interventions in the patient’s medical record, including interactions with families and caregivers., • Implement and enforce policies and procedures for the safe procurement, storage, administration, and disposal of medications and biologicals., • Ensure compliance with all state and federal regulatory requirements related to pharmacy practice and medication management., • Report medication-related errors and adverse drug events to the Pharmacy Manager as required., • Educate and support facility/agency staff on safe and effective medication handling procedures., • Perform other pharmacy-related tasks and responsibilities as assigned. Qualifications Qualifications Required: • Bachelor’s Degree in Pharmacy, Pharm D preferred, • One year experience in long term care desired, • License/Certification(s): current and valid pharmacist license in the state of practice, • Knowledge of drug therapy guidelines, medication safety practices, and regulatory standards (CMS, DEA, FDA)., • Proficiency in electronic medical records and pharmacy information systems, • Strong clinical judgement, and effective written and verbal communication *Position will be posted for a minimum of 7 business day

Orders, replenishes and merchandises prepared foods products and participates in regional programs for purchasing and promotions. Monitors inventory control and replenishes product. Assists in organizing and developing promotional displays and maintaining OTS standards. All Whole Foods Market Retail jobs require ensuring a positive company image by providing courteous, friendly, and efficient service to customers and Team Members at all times. All positions must be performed in accordance with team and store Standard Operating Procedures. Further, Team Members must be prepared and able to perform the duties inherent in other Team Member job descriptions. All positions must strive to support WFM core values and goals, promote national, regional, and store programs and initiatives, and ensure adherence to all applicable health and safety regulations including Food Safety and regulatory duties required in the department. • Purchases and replenishes food for preparation through proper buying procedures., • Monitors and acts upon open PO reports for both purchases and credits in an accurate and timely manner., • Controls spoilage and shrink, achieves turn goals, participates in inventory., • Completes spoilage, sampling, temperature, and sweep worksheets as required., • Assists with counter service and cooks as scheduled or as necessary., • Communicates with Kitchen Manager / Chef and Team Leader on ordering needs and issues., • Maintains positive working relationship with vendors., • Works with Team Leader or Assistant Team Leader(s) to cost recipes., • Oversees customer special order procedure., • Supports leadership in conducting inventories., • Maintains financial profitability by meeting and exceeding purchasing and sales targets., • Arrives to work station on time, appropriately groomed, dressed and ready to work; works all scheduled shifts and attends required trainings and meetings., • Provides excellent customer service, addresses needs of customers in a timely and effective manner and models suggestive selling techniques; answers phones and pages promptly and courteously., • Maximizes sales potential through effective and proper procedures for prepping, storing, rotating, stocking, and merchandising product., • Follows and complies, or ensures compliance, with established procedures, including Weights and Measures, health and sanitation, and safe work practices., • Maintains, or ensures maintenance of, a clean and sanitary working and shopping environment; maintains equipment in accordance with WFM cleanliness and safety standards., • Performs opening, mid, and closing duties as assigned; ensures accuracy of signs and pricing., • Immediately reports safety hazards and violations., • Extensive product knowledge, including production, distribution, seasonal availability, advances, and trends., • Ability to create and negotiate price bids., • Familiarity and/or willingness to learn about products, nutritional information, and other areas of study., • Working knowledge and application of all Prepared Foods merchandising expectations., • Complete understanding of WFM margin program and profitability., • Ability to educate team on product knowledge and convey enthusiasm., • Strong basic math skills., • Knowledge and ability to use computer programs such as Microsoft Word, Excel, Outlook, and ordering systems., • Strong to excellent communication skills and willingness to work as part of a team., • Ability to deliver information in a clear and respectable manner to fellow Team Members, customers, and vendors., • Ability to meet customer service expectations and standards in all interactions with customers, vendors, and Team Members., • Ability to follow directions and procedures; effective time management and organization skills., • Passion for natural foods and the mission of Whole Foods Market., • Strong work ethic and ability to work in a fast-paced environment with a sense of urgency., • Understanding of and compliance with WFM quality goals., • 1+ years of Buying/Merchandising, • Must be able to lift 50 pounds., • In an 8-hour work day: standing/walking 6-8 hours., • Hand use: single grasping, fine manipulation, pushing and pulling., • Work requires the following motions: bending, twisting, squatting and reaching., • Exposure to FDA approved cleaning chemicals., • Exposure to temperatures: <32 degrees Fahrenheit (freezing), 32-40 degrees Fahrenheit (refrigerators), >90 degrees Fahrenheit., • Ability to work in wet and dry conditions., • Ability to work a flexible schedule including nights, weekends, and holidays as needed., • Ability to use tools and equipment, including knives, box cutters, electric pallet jacks, and other heavy machinery., • May require use of ladders. Note: The purpose of this document is to provide a general summary of essential responsibilities for the position and is not meant as an exhaustive list. This document does not reflect all job duties or requirements for every position. Requirements build as one progresses through the job levels, so any job duties required at a lower level may be required at the higher level in addition to the duties listed for that higher level in position. Duties, assignments, and other responsibilities may differ for similar positions based on business conditions, departmental or geographic location, and/or needs for the particular position. An individual must demonstrate successful performance in their current position before being considered for promotion. In addition, in order to promote into a higher-level position, a business need for the promotion must exist and the candidate must be considered the most qualified person for the new position. Completion of certain milestones such as obtaining an advanced degree or certification, time in current position, or developing skills to perform at the higher-level role do not guarantee a promotion. The wage range for this position is $18.00-$30.20 Hourly, commensurate with experience. Whole Foods Market offers "Whole Benefits". Whole Benefits offers a wide range of benefits for Full and Part-Time Team Members, including eligibility for a store discount, paid time off, financial wellness, health & wellness support programs, and access to other Team Member perks. Eligibility for Whole Benefits is determined under the terms of the applicable Whole Benefits plan at a person's date of hire and may vary based on work location, length of service, and job type (such as regular or seasonal). Whole Foods Market, we provide a fair and equal employment opportunity for all Team Members and candidates regardless of race, color, religion, national origin, gender, pregnancy, sexual orientation, gender identity/expression, age, marital status, disability, or any other legally protected characteristic. Whole Foods Market hires and promotes individuals solely based on qualifications for the position to be filled and business needs.

Syosset, NY is seeking an Order Fulfillment Associate to join their Direct-to-Consumer distribution center.The role involves handling fulfillment tasks from receiving to shipping products, ensuring customer satisfaction.Applicants should have order fulfillment experience, excellent communication ski

Part-Time Warehouse Load Coordinator.Come join our team as a Part-Time Warehouse Load Coordinator! We started with pastries handmade by Lois and Lloyd Martin produced inside of a garage and we have boomed into a multi-family company where our many products are produced by machines and shipped domest

Retail Warehouse & Production Associate.Position at Savers / Value Village.Pay Rate: Our starting pay ranges from $17.As one of the largest for-profit thrift operators in the United States, Canada and Australia for value priced pre-owned clothing, accessories and household goods, our mission is to c

Delivery Driver (CDL Class B) / Warehouse Associate.Location: Greenvale, NY Pay: $23.Schedule: Monday-Friday, 8:00 AM-4:30 PM.Rugby Architectural Building Products is a leading wholesale distributor of specialty building products with 26 locations across the United States.We supply architectural-gra

Opportunity, growth, and meaningful rewards! We offer: Health, dental and vision insurance Generous paid time off (vacation, flex or sick) Holiday pay 401(k) retirement plan Company paid life insurance Tuition reimbursement Employee discounts across all company brands Employee assistance program Tra

Warehouse Associate/Backup Driver.Job purpose: To maintain the warehouse and the product contained within, as well as performing related functions, such as loading, unloading, receiving, and additional branch support activities.This will contribute to ABCO's mission of exceeding customers' highest e

You care about making a positive impact in the world.A warehouse job at IKEA is so much more than moving things from A to B.It's the stuff in between that makes being a member of our logistics team unique.Together, we work to make a better everyday life for the many.It's the perfect fit if you want

For more than 80 years, Pioneer Industries, LLC, a subsidiary of HEICO Corporation has thrived by serving niche segments of the aviation, defense, space, and electronic industries by providing innovative and cost-saving products and services.HEICO's high energy culture focuses our Team Members' on p

OnTrac Hiring Package Handlers.OnTrac is hiring Package Handlers.Are you eager to join a dynamic and expanding company where you can both learn and make a meaningful impact? If you possess a strong sense of empathy, enjoy assisting others, thrive in a fast-paced environment, and excel at problem-sol

HW Staffing Solutions is currently seeking a warehouse associate for a 3rd party logistics company in Farmingdale, NY Monday-Friday 9:00 am 5:00 pm $18-$20 hourly DOE.Previous warehouse experience is necessary Excellent time management, communication, and troubleshooting skills.Move products to sto

Warehouse Associate | Home Depot.Warehouse associates are an essential part of The Home Depots distribution network.They load and unload trucks, move material within the facility and from the loading platform by carrying, pushing, rolling or operating hand trucks, forklifts, hoists, motorized convey

Maersk Warehousing and Distribution USA LLC handles end-to-end warehousing and distribution logistics needs utilizing our strategic network of storage facilities.Our facilities are capable of receiving, storing, processing and dispatching cargo, so we can build flexibility and resilience into the su

We have an incredible opportunity for a dynamic Equipment Packer to join our growing New York team!.We have a passion for hospitality culinary delights on every banquet floor and in the sky.With the three business segments of Airline Catering, International Event Catering, and Restaurants, Lounges &

Warehouse Associate / Backup Driver.Power-Flo Technologies is now hiring a full-time warehouse associate / backup driver to join our New Hyde Park team! Full-Time.This position involves warehouse responsibilities with driving duties (16 - 18 foot box trucks) as needed.Medical, dental and vision plan

Location: 140 Cooper Ave, Tonawanda, NY, 14150, United States.Relocation Expense Covered: No.

Warehouse Operator (Temporary) Pay: $22/hour Schedule: MondayFriday, 8:00 AM 4:30 PM (occasional weekends may be required based on business needs) Location Requirements: Steel-toe shoes required.Position Summary The Warehouse Operator is responsible for supporting daily warehouse operations, includ