Regulatory Specialist Salary at Nexius BETA

Senior QA/RA Specialist - CRO Experience Location: Dallas, Texas About Synergy Bioscience: Synergy Bioscience is a leading Contract Research Organization (CRO) specializing in pharmaceutical product development, analytical chemistry, and microbiology testing services across various industry sectors. We are committed to excellence and innovation, and we are looking for a proactive, detail-oriented, and experienced Quality Assurance Specialist to join our team at our Dallas facility. Position Summary: The Quality Assurance Specialist will play a critical role in maintaining and improving our quality management system to ensure compliance with regulatory standards, including 21 CFR Parts 11, 210, 211, 600s, and 820, as well as ISO 17025, EPA, and CLIA requirements. The ideal candidate will collaborate with cross-functional teams to establish, document, and enforce quality processes that meet regulatory and client expectations. Key Responsibilities: Quality Documentation: Develop, maintain

Location Designation: Fully Onsite When you join New York Life, you're joining a company that values development, career growth, collaboration, innovation, and diversity & inclusion. We want employees to feel proud about being part of a company that is committed to doing the right thing. Through various resources and programs, you can grow your career while developing personally and professionally. Business Unit Overview Join our Field Service Team, the driving force behind the delivery of exceptional experiences for New York Life's agents and clients. As part of our diverse team, you will have the opportunity to shape seamless customer experiences. Whether you're helping an agent meet their clients' life insurance needs, supporting strategic initiatives designed to enhance our operating environment, or educating our agents on innovative digital solutions, your work will have a direct and powerful impact on our success in fostering customer trust and loyalty. Role Overview Our General

Job Description Job Description Post Summary: S/he is an enterprise solution sales team member and executes sales to meet the revenue target. S/he has to have a strong background in selling enterprise software solutions within the healthcare industry, a deep understanding of the sales process, and the ability to build and maintain relationships with key decision-makers. The post holder requires excellent communication skills, strategic thinking, and a passion for driving sales growth. Main Duties: a) Sales Strategy and Planning - Develop and execute a strategic sales plan to achieve revenue targets and expand the customer base. - Identify and prioritize target accounts and sales opportunities within the healthcare sector. - Collaborate with the marketing team to develop and implement lead-generation strategies and sales campaigns. b) Prospecting and Lead Generation - Identify and qualify new business opportunities through various channels, including networking, industry events, and onl

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries. **_Senior Regulatory Affairs Specialist_** **Working at Abbott** At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. Youll also have access to: + Career development with an international company where you can grow the career you dream of. + Free medical coverage for employees* via the Health Investment Plan (HIP) PPO + An excellent retirement savings plan with high employer contribution + Tuition reimbursement, the Freedom 2 Save (https://www.abbott.com/corpnewsroom/strategy-and-strength/tackling-student-debt-for-our-employees.html) student debt program and FreeU (htt

Job Summary This is a highly visible role and will require extensive interaction with upper management as well as regulatory bodies. Main Duties: •Successful Global Regulatory Submissions and Approvals, including 510(k)s and Technical Documentation Review by Notified Body in EU. •Prepared product registrations for various countries and/or provided additional information to regulatory bodies for successful registration of products. •Reviewed design and labeling changes to assess regulatory impact, filed various submissions and updates with regulatory agencies. •Maintained up-to-date regulatory requirements for the business unit (Registrations/Regulatory Audits/Quality Manual/Quality System Certificates). •Prepared and submitted 510(k)'s, IDEs, and other applicable product submissions according to FDA guidelines. Job Responsibility: Regulatory specialist with proven ability in presenting, developing, and implementing pre and post-market regulatory strategies for medical device submission

Job Description Job Description This position provides critical support in ensuring compliance with regulatory standards for personal care and cosmetic formulations. The ideal candidate will assist with raw material data collection, compliance documentation, and serve as a liaison to the R&D team for onboarding new raw materials. This position reports to the Senior Manager of Regulatory Affairs. Essential duties and responsibilities Support or provide formula and raw material reviews. Collect, organize, and maintain raw material data and documentation. Ensure the accuracy of raw material certifications and specifications within product formulating systems and databases. Ensure correct INCI labeling for all raw materials Prepare and update regulatory statements, Ingredient Declarations (CIDs/ILs), and ingredient compliance documentation. Support formula compliance with customer and governing body requirements, including certifications (e.g., organic, ISO). Act as a liaison to the R&D te

Corporate Development Officer II The primary purpose of the role is to play a lead role in the development, refinement, and adherence to the Corporate Development governance process as it relates to all Corporate Development activitiesy throughout the Corporation. This position is responsible for executing the ongoing evaluation, modeling, analyzing, and formulating recommendations and presenting such recommendation to executive management which impact the Corporation. Including performing detailed market and strategic assessment, performing detailed financial studies that look to accurately measure the risks and rewards of a myriad of situations confronting the Corporation. This position interacts with senior and executive management on a regular basis as part of leading M&A and corporate initiatives, able to challenge assumptions and sponsor less popular views based on detailed rationale while serving as an independent party. Secondarily, the position manages the administrative aspec

This position is contingent on a contract award. Designs, develops, implements and evaluates program-wide learning solutions in support of Magellan's business objectives. Assists in developing learning paths and curriculum content that reflects sound instructional design based on adult learning principles and best practices. Facilitate training via live and recorded webinars and blended learning, using a mix of engaging instructional methods. Display demonstrated expertise in instructional design systems and software, learning technologies and adult learning best practices. Acts as technical expert and liaison with internal and external stakeholders to include MOS PMO, IT. Possesses and provides expertise in instructional design processes (ADDIE or other industry accepted models) to design, develop and implement effective instructional materials, learning resources and content. Creates design standards and templates and integrates technology-based tools into the development process. As