Internal Audit Salary at Roofexpro Llc BETA

The ideal candidate is a critical thinker who will proactively improve the quality systems of the company through internal audits, participation in process improvement programs, and interaction with key partners to obtain constructive feedback. Qualifications BA or BS in the life sciences or a related degree program Experience with commercial-stage medical devices and/or drug-device combination products. This must be clearly demonstrated in your resume. 5+ years in a role with extensive quality experience in an FDA-regulated environment Experience successfully interfacing with accreditation and regulatory agencies (ISO,FDA), writing responses and other documents required in a regulated environment. Responsibilities Review and approve applicable document change orders. Assist management in developing strategic regulatory approaches for new product/business development. Oversee the day-to-day activities related to the quality and safety of the Company’s medical device manufacturing. Esta

The Quality Control Inspector ensures compliance with quality standards for electronic components, sheet metal fabrications, printed circuit boards, and hardware. This role is essential in maintaining product integrity through inspections, testing, and collaboration with internal teams. Responsibilities: - Inspect first article, incoming, in-process, and final products for compliance with IPC-A-610, IPC/WHMA-A-620, IPC J-STD-001 standards, customer specifications, assembly drawings, and BOM requirements. - Conduct Automated Optical Inspection (AOI) to detect SMT paste, component placement, and solder joint defects accurately. - Perform visual and measurement tests to verify product quality. - Document and communicate non-conforming items through corrective action, scrap, and non-conformance reports promptly. - Maintain accurate inspection records and generate required quality documentation. - Conduct internal audits of manufacturing processes under the guidance of the Quality Manager.

Supernus Pharmaceuticals is an award-winning biopharmaceutical company with more than 30 years of experience in developing and commercializing products that treat central nervous system (CNS) diseases. At Supernus, we develop innovative products that help treat neurological and psychiatric conditions. We currently have 8 products in the market that are making a real impact on patient outcomes. Job Summary: Responsible for supporting the Company's Quality Assurance and quality management systems by initiating & reviewing documentation, including executed batch records for Commercial products, deviations, and change controls. Essential Duties & Responsibilities: Review of GMP documentation from commercial contract manufacturing organizations (CMO); including line clearances, control of raw materials and equipment cleaning processes. Communicating with external CMOs and internal stakeholders to ensure the timely release of material. Performing review of deviations and change controls from

Xometry (NASDAQ: XMTR) powers the industries of today and tomorrow by connecting the people with big ideas to the manufacturers who can bring them to life. Xometry's digital marketplace gives manufacturers the critical resources they need to grow their business while also making it easy for buyers at Fortune 1000 companies to tap into global manufacturing capacity. We are seeking a highly motivated and experienced Director/Senior Manager, SEC Reporting to lead our SEC reporting function. This role is critical in ensuring the timely and accurate preparation and filing of all periodic SEC reports and supporting technical accounting matters. The ideal candidate will possess a strong understanding of U.S. GAAP, SEC regulations, and have a proven track record of managing the SEC reporting process within a publicly traded company. You will be a key liaison with external auditors, internal audit, and various stakeholders across the organization. Responsibilities: SEC Reporting Leadership: Dir

POSITION SUMMARY: The Financial Reporting/Accounting, Investor Relations, & Governance + Compliance Intern will support the following teams with investor relations, finance, and audit related tasks. ESSENTIAL FUNCTIONS: Financial Reporting/Accounting: Support the accounting and SEC reporting for areas that may include interest rate derivatives, debt, joint ventures and other investments. Perform activities to support external and internal audit requirements, including schedule preparation and workflow management. Assist with the compilation of reporting packages to joint venture partners and lenders. Investor Relations: Primary Responsibility - complete an assigned project and present findings to senior management. Secondary Responsibility - Assist the Investor Relations team with the following - Stakeholder Relationships Manage relationships with Analysts and Investors. Internal Communications Generate value added information for senior management. External Communications Communicate

Job Type Full-time Description This role is an exciting opportunity to be a part of the Quality Assurance team at Granules Pharmaceuticals, Inc. in Chantilly, VA. As a member of a growing team, you'll play an important role maintaining, tracking and closure of all Quality events. Requirements Key Responsibilities Improve and maintain Quality Management System at site in line with current regulations, including change management, deviation and CAPA management. Responsible to adhere to data integrity requirements and ensure the same are implemented in Quality management Systems. Partner with cross-functional leads in timely initiation, implementation and closure of Quality Management System elements. Support in Implementation of TrackWise Digital at site. Responsible for initiation of Deviations, initial impact assessment and investigations relating to Quality Assurance functions. Participate in organization and execution of Internal Audit Program for site. Responsible for data analysis/

As a Regulatory Compliance Risk Experienced Associate, you will get the opportunity to grow and contribute to our clients' business needs by providing in-depth technical knowledge on emerging regulations and help organizations leverage efficiencies within the Risk Advisory Practice – all with the resources, environment, and support to help you excel. You’ll collaborate with teams to provide comprehensive compliance optimization strategies, to help clients remediate regulatory gaps, streamline operations and limit risk exposure. From day one, you’ll be empowered by the greater Risk team to help clients make strategic decisions that will help them achieve their vision and help you achieve more, confidently. Your day-to-day may include: Conduct engagement activities including transactional testing, policy, and procedure review, meet preparation, walkthroughs, etc. Conduct testing activities for Consent Order Validation, Issue Validation, and independent monitoring engagements, responsible

Overview: We are seeking a highly skilled and experienced Corporate Accountant to join our finance team. The Corporate Accountant will play a crucial role in overseeing the financial operations of our organization, ensuring accuracy, compliance, and efficiency in all accounting processes. This position offers an exciting opportunity for a talented professional to contribute to the financial success and growth of our company in the dynamic real estate industry. Responsibilities: Financial Reporting: Prepare and analyze monthly, quarterly, and annual financial statements in accordance with GAAP standards. Budgeting and Forecasting: Assist in the development of annual budgets and long-term financial forecasts, providing insights and recommendations to support strategic decision-making. General Ledger Management: Maintain the integrity of the general ledger, overseeing journal entries, account reconciliations, and accruals to ensure accuracy and completeness of financial data. Financial An