Regulatory Affair Specialist Salary at Vetoquinol Usa Inc BETA

Job Description Job Description Hours 8a-5p or 9a-6p Must be able to speak Chinese/Mandarin QC Technician/Inspector Conducts routine inspections, sampling, and testing on the production line to catch any deviations from quality specifications. They record and report data to support corrective actions. Quality Control Technician/Inspector (Quality Control (QC) / Quality and Regulatory Specialist) Key Responsibilities: In-Process Inspections: Perform routine inspections and sampling of raw materials, in-process products, and finished goods. Testing & Analysis: Conduct testing (e.g., weight, appearance, potency) according to established SOPs and GMP standards. Deviation Reporting: Document and report any deviations from quality standards, ensuring timely corrective actions. Regulatory Documentation: Maintain and update quality records and ensure all procedures meet regulatory requirements. Audit Support: Assist during internal and external audits by providing accurate QC records. Role Imp

The Clinical Research Associate position at Medpace offers the unique opportunity to have an exciting career in the research of drug and medical device development while making a difference in the lives of those around them. For those with a medical and/or health/life science background who want to explore the research field, travel the US, and be part of a team bringing pharmaceutical and medical devices to market - this could be the right opportunity for you! Our successful Clinical Research Associates possess various backgrounds in medical and other science-related healthcare fields. Backgrounds of individuals who have succeeded in the CRA role include: Nursing Dietetics Nutrition Science Pharmacist Pharmaceutical/Device Sales Representative Physical and Occupational Therapists Biomedical/Chemical Engineer PhD/Post-Doc Pharm.D Health and Wellness Education Coordinators Public Health Clinical Research Coordinators Research Assistants MEDPACE CRA TRAINING PROGRAM (PACE®) No research e

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

SR. Business Controls Specialist - GCAOO QC/QA Governance Fort Worth, Texas;Charlotte, North Carolina; Pennington, New Jersey; Plano, Texas **Job Description:** At Bank of America, we are guided by a common purpose to help make financial lives better through the power of every connection. Responsible Growth is how we run our company and how we deliver for our clients, teammates, communities and shareholders every day. One of the keys to driving Responsible Growth is being a great place to work for our teammates around the world. Were devoted to being a diverse and inclusive workplace for everyone. We hire individuals with a broad range of backgrounds and experiences and invest heavily in our teammates and their families by offering competitive benefits to support their physical, emotional, and financial well-being. Bank of America believes both in the importance of working together and offering flexibility to our employees. We use a multi-faceted approach for flexibility, depending on

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

GCAOO QC/QA Operations Controls Specialist Fort Worth, Texas **Job Description:** At Bank of America, we are guided by a common purpose to help make financial lives better through the power of every connection. Responsible Growth is how we run our company and how we deliver for our clients, teammates, communities and shareholders every day. One of the keys to driving Responsible Growth is being a great place to work for our teammates around the world. Were devoted to being a diverse and inclusive workplace for everyone. We hire individuals with a broad range of backgrounds and experiences and invest heavily in our teammates and their families by offering competitive benefits to support their physical, emotional, and financial well-being. Bank of America believes both in the importance of working together and offering flexibility to our employees. We use a multi-faceted approach for flexibility, depending on the various roles in our organization. Working at Bank of America will give you

Quality Operations Specialist (14 CFR Part 145 Repair Station) Location: Fort Worth, TX (76118) Job ID: #69560 Pay Range: $32-48 1st shift -- 9/80 Schedule - 700am - 230p Onsite job Position open to US Citizens Focus: Aviation Repair Station Experience: Previous work at 14 CFR Part 145 Repair Station THE COMPANY: An American Owned Aviation, Aerospace, Defense & Industrial Global Conglomerate. It is ranked in the top 300 of the Fortune 500 List. It's parent company's revenues are $13+bil and has 30k+ employees worldwide. The Quality Operations Specialist is responsible for developing conformity packages for the 525 program and to ensure the compliance of the Company's (QMS) Quality Management System to the regulatory requirements. The selected would be responsible for developing, revising and maintaining processes, procedures, and program plans in the QMS - Quality Management System. In addition, will also be responsible for developing, revising/maintaining the processes and procedures