QA Assistant Salary at Sanico BETA

Job Summary The Quality Assurance (QA) Engineer II will play a key role in the implementation of Onkos Surgical’s Quality Management System and have the opportunity to gain experience across a broad range of quality functions related ISO 13485 and 21 CFR Part 820 compliance. Specifically, the QA Engineer will champion complaint handling, product release procedures and approval, and support to both NCR and CAPA processes. This will require developing relationships and working closely with suppliers. This position will also work with cross-functional teams to provide quality engineering support in the development of technical files to ensure regulatory compliance during product development. Responsibilities Receive, document and process complaints related to product quality and patient safety. Conduct, coordinate and document complaint investigations. Review complaints for possible Adverse Events/MDRs and recommend regulatory reporting decisions. Prepare reports to regulatory agencies in

Summary See below for important information regarding this job. Additional vacancies may be filled from this announcement. Responsibilities Performs duties associated with the administration of the quality assurance provisions of contracts by designing, implementing, and maintaining a risk-based surveillance program and assessment plan. Identifies opportunities for process improvements through analysis of process measurement data. Serves as a member of a multi-functional or technical team. Responsible for implementing the overall Quality Program for a diversity of products and services in support of U.S. Government acquisition at one or more suppliers facilities. Ensures contractor compliance with all requirements related to the design, manufacturing, repair, overhaul, and modernization of a variety of items for contractor and customer activities throughout the world. Independently performs audits/surveillance of contractors processes to ensure customer and contractual requirements are

Job Description Job Description My client is a small business with over 35 years of expertise in manufacturing and engineering development services—is seeking an experienced Quality Assurance Manager to oversee and enhance operational standards at our state-of-the-art facility in Stirling, NJ. Reporting directly to the company president, this key leadership role will develop and implement quality control procedures, analyze performance metrics, and ensure compliance with all relevant standards (e.g., ISO 9001 / AS9100). You will collaborate closely with corporate leadership to uphold our QA system, maintain process integrity, and secure consistent, high-quality deliverables for our clients. Key Responsibilities ● Inspection & Compliance: Oversee all inspection activities (incoming, in-process, and final) to ensure parts, assemblies, and materials consistently meet customer specifications and quality standards. ● Equipment Calibration: Manage calibration of measuring and test equipment

Job Description Job Description ABOUT SANISURE SaniSure is a multinational manufacturer of single-use bioprocessing solutions (SUT) used in the production of biological drugs, including monoclonal antibodies, cell therapies, gene therapies, and vaccines. With operations in the U.S. and in Europe, SaniSure operates a leading platform of vertically integrated critical fluid management technologies and integrated solutions. Its single-use products and system solutions are sold to global pharma and biotech companies and are used from R&D through full-scale commercial cGMP manufacturing of among the most innovative large molecule therapeutics and vaccines. This role is expected to be on-site. We continue to be on a robust growth trajectory, via both organic and inorganic growth, as the company capitalizes on increasing global demand and continues its transition from a component manufacturer to an integrated systems and solutions provider. Our primary offering includes high-value assembly so

Job Description Job Description Summary Supervises and coordinates activities of workers engaged in inspecting and testing ingredients, raw materials, packaging supplies, products and finished goods, as they proceed through stages of the manufacturing process, applying knowledge of Company and regulatory quality assurance standards and procedures. Reviews quality and SQF instructions, product specifications and production schedules to determine methods of conducting inspections and tests, sequence of operations, SQF compliance standards, applications, and work assignments. Responsibilities Supervises and coordinates QA inspection activities. Review QA inspection and monitoring records and verify completion and accuracy. Communicate with other departments to solve quality issues. Assist in investigating customer/consumer complaints. Assist in developing QA procedures and forms. Assist in conducting plant audits. Assist in QA Training Programs. Monitor and enforce compliance with JFI SQF

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. Responsibilities Develop standardized production, quality, and customer-service standards Identify potential risks before they become a problem, focusing on root cause analysis and preventive action Perform internal and external quality audits and compile detailed reports of findings Build a strong team through coaching, mentoring, specific training and performance evaluations Qualifications Experience in FSC chain of custody and ISO 9000. Bachelor's degree or equivalent experience in Engineering 5+ years' relevant work experience Highly organized with excellent attention to detail

Before reading the job post, we encourage you to watch this video about our company. It gives you an inside look at how we started, the team and culture that made us successful, and where we're going. It's easy to read a job post and apply, but people often wonder about the culture and whether they would fit in. If you want to call Harrow your home and genuinely want to be part of a family and something big, then we encourage you to click this link and get to know us. Who is Harrow? Harrow (Nasdaq: HROW) is a leading North American ophthalmic-focused pharmaceutical company. Harrow is an incredible entrepreneurial company - where we celebrate the ability of every member of the Harrow Family to be the CEO of their job. Harrow's values have driven interest over the past decade in attracting high-performing professionals in a variety of disciplines. Members of our Harrow Family often express their pride in being a part of our commitment to (1) innovation, (2) patient access to affordable m

Quality Assurance Specialist || (Branchburg, NJ - Hybrid) (Must Have an experience with Pharmaceutical or Biotech Industry exp) Sharp Decisions Inc. is seeking a qualified Quality Assurance Specialist to support our client in Branchburg, NJ. This is an onsite position. The initial contract term is 03 years, with a strong possibility of extension based on performance and project needs. You will be responsible to … 1. Drive business results and customer value a. Responsible for performing activities as required to meet Q&R goals and objectives independently. Able to identify improvements and implement with collaboration from your manager. b. Be recognized internally as an expert in your own job discipline with in-depth knowledge/skill-set of related disciplines in the field. c. Act as a coach for colleagues with less experience and help them develop skills/expertise. d. Document authoring and review as required to support changes. Performs technical reviews, as applicable. May require co