Expense Auditor Salary at Subway Ip Llc BETA

VARITE is looking for a qualified GLP Auditor in Ridgefield, CT. WHAT THE CLIENT DOES? A global, research-driven pharmaceutical company that focuses on developing innovative medicines in areas such as human pharmaceuticals, animal health, and biopharmaceutical contract manufacturing. WHAT WE DO? Established in the Year 2000, VARITE is an award-winning minority business enterprise providing global consulting & staffing services to Fortune 1000 companies and government agencies. With 850+ global consultants, VARITE is committed to delivering excellence to its customers by leveraging its global experience and expertise in providing comprehensive scientific, engineering, technical, and non-technical staff augmentation and talent acquisition services. Job Title: GLP Auditor Location: Ridgefield, CT Contract Duration: 7 months HERE'S WHAT YOU’LL DO: Summary: • To implement the BIPI Regulatory Compliance Program designed to assure the adherence of facilities, operations, studies, reports and

Job Description Job Description We are looking for GLP Auditor for our client in Ridgefield, CT Job Title: GLP Auditor Job Location: Ridgefield, CT Job Type: Contract Job Description: Pay Range: $30.92hr - $35.92hr Responsibilities: Review procedures for compliance to GxP requirements and Company standards. Conduct audits to support GLP studies (e.g. protocol, amendment, study data, Principal Investigator reports such as Toxicokinetic reports, etc.). Issue electronic audit reports and perform follow-up actions. Scan study records to facilitate audit requests. Monitor and update electronic system with new audit requests. Update the GLP Master Schedule as needed. Conduct internal facility audits as needed. Provide support during corporate audit and regulatory inspections as needed. Skills: GLP Auditing or comparable experience. Intermediate knowledge of relevant regulations and guidance. Works independently with moderate guidance. Excellent conflict resolution and negotiation skills. Goo

-6 month contract -Pay: $36.88/hr Duties: To implement the Regulatory Compliance Program designed to assure the adherence of facilities, operations, studies, reports and practices to regulations (e.g. FDA, EMEA, NRC, DEA USDA) as well as to Standard Operating Procedures (SOPs), internal policies, regulatory guidelines and good scientific and documentation practices. To inform Management of deviations from the cGMP, GLP, other Regulations observed during audits/inspections, to recommend appropriate corrective action when necessary and to verify that appropriate corrective actions have been implemented that adequately address any deviations reported during inspections. Duties & Responsibilities Review procedures for compliance to GxP requirements and Company standards Conduct audits to support GLP studies (e.g. protocol, amendment, study data, Principal Investigator reports such as Toxicokinetic reports, etc.) Issue electronic audit reports and perform follow-up actions Scan study record

Job Summary: The Regulatory Compliance Auditor is responsible for implementing and supporting the Regulatory Compliance Program to ensure facilities, operations, studies, and practices comply with applicable regulations (e.g., FDA, EMEA, NRC, DEA, USDA), internal SOPs, policies, and good documentation practices. This role includes conducting audits, issuing reports, monitoring corrective actions, and supporting inspections. Key Responsibilities: Review procedures for compliance with GxP and internal standards. Conduct audits related to GLP studies, including protocols, amendments, study data, and investigator reports (e.g., Toxicokinetic reports). Issue electronic audit reports and track follow-up actions. Maintain and update audit logs and the GLP Master Schedule. Scan and organize study records to support audit and inspection readiness. Conduct internal facility audits and support external inspections. Provide audit support during corporate and regulatory agency inspections. Requirem

Duration: 06 Months Contract Duties: To implement the *** Regulatory Compliance Program designed to assure the adherence of facilities, operations, studies, reports and practices to regulations (e.g. FDA, EMEA, NRC, DEA USDA) as well as to Standard Operating Procedures (SOPs), client policies, regulatory guidelines and good scientific and documentation practices. To inform client Management of deviations from the cGMP, GLP, other Regulations observed during audits/inspections, to recommend appropriate corrective action when necessary and to verify that appropriate corrective actions have been implemented that adequately address any deviations reported during inspections. As an employee of our pharmaceutical client, you will actively contribute to the discovery, development and delivery of our products to our patients and customers. Our global presence provides opportunity for all employees to collaborate internationally, offering visibility and opportunity to directly contribute to the

Job Description Job Description GLP Auditor External ID #385237 Ridgefield, CT- ONSITE 8 month W2 contract (with potential to extend or transition to perm) Pay rate: $30-37/hr - Depending on Education and Experience Shift: First Summary: As our team member of our client, you will actively contribute to the discovery, development and delivery of their products to their patients and customers. Their global presence provides opportunity for all employees to collaborate internationally, offering visibility and opportunity to directly contribute to the companies´ success. They realize that their strength and competitive advantage lie with their people. They support their employees in a number of ways to foster a healthy working environment, meaningful work, diversity and inclusion, mobility, networking and work-life balance. Review procedures for compliance to GxP requirements and Company standards Conduct audits to support GLP studies (e.g. protocol, amendment, study data, Principal Invest

Overview: Opportunity: Night Auditor Balance revenue and settle accounts nightly, maintain files, and reset the system for the next day of operations while performing Guest Service Agent tasks and duties. Your Growth Path Front Office Supervisor/Accounts Payable or Receivable Clerk Front Office Manager Your Focus Perform bookkeeping activities, such as balancing accounts and conducting nightly audits. Keep records of room availability and guests' accounts, manually or using computers. Prepare and distribute daily reports. Audit and reconcile cashiers. Audit, reconcile, consolidate, and transmit all credit cards on a timely basis. Input and update financial information into the BRAINS network. Check guests in/out and perform Guest Service Agents tasks. Respond to guest inquiries and resolve complaints. Be aware of guest satisfaction scores and work toward increasing departmental and overall guest satisfaction. Follow sustainability guidelines and practices related to HHMs EarthView prog

Job Title: GLP Auditor Location: Ridgefield CT 06877 Duration: 6 Months Summary: To implement the clients Regulatory Compliance Program designed to assure the adherence of facilities, operations, studies, reports and practices to regulations (e.g. FDA, EMEA, NRC, DEA USDA) as well as to their Standard Operating Procedures (SOPs), clients policies, regulatory guidelines and good scientific and documentation practices. To inform clients Management of deviations from the cGMP, GLP, other Regulations observed during audits/inspections, to recommend appropriate corrective action when necessary and to verify that appropriate corrective actions have been implemented that adequately address any deviations reported during inspections. You will actively contribute to the discovery, development and delivery of our products to our patients and customers. Our global presence provides opportunity for all employees to collaborate internationally, offering visibility and opportunity to directly contri