Quality Assurance Associate Salary in the United States

Our client is a global, research-driven pharmaceutical focusing on treatment options for diseases and conditions for which there is no satisfactory treatment option to date. The company is looking for a QA Associate to join the team. This is an amazing opportunity to work on cutting edge treatments and make a difference! Schedule: 1st Shift Pay: $25-28/hr. 6 month development opportunity with the potential for this to turn into a direct hire with the company or extension As a QA Associate, you will be responsible for executing QA operations and overseeing junior team members as they assess, evaluate, and review operations on the floor (as defined) against cGMPs to assure real time observation of activities, issue identification/ resolution including proper and timely documentation. Responsibilities: Provides guidance to MFG, E&T, and/or QC to ensure compliance with all applicable regulations and assists in resolution of issues identified. Information must be proactively shared across Q

Job Description: Preferred: Bachelor’s degree in any life science, GMP, Pharma industry experience At least 1 year of experience 100% on-site Ideal candidate has reviewed docs in a GMP setting or worked in a quality role in a GMP setting. Energetic, quick learner, excellent attention to detail technical documentation for product design - PLUS Primary objective of position: The Associate Quality Systems Specialist will be part of the Quality team and responsible for providing quality support for the site quality management system. This position ensures compliance of the quality system with regulations relevant to the business, including but not limited to, ISO13485, MDSAP, IVDD/IVDR, CFR 21, GxP, and the quality manual. This position is multi-disciplinary with opportunities to work on future products and current product and process improvements. The position may represent Quality on cross-functional teams to support business needs driving a positive site quality culture. The position pr

Job Description: Preferred: Bachelors degree in any life science, GMP, Pharma industry experience At least 1 year of experience 100% on-site Ideal candidate has reviewed docs in a GMP setting or worked in a quality role in a GMP setting. Energetic, quick learner, excellent attention to detail technical documentation for product design - PLUS Primary objective of position: The Associate Quality Systems Specialist will be part of the Quality team and responsible for providing quality support for the site quality management system. This position ensures compliance of the quality system with regulations relevant to the business, including but not limited to, ISO13485, MDSAP, IVDD/IVDR, CFR 21, GxP, and the quality manual. This position is multi-disciplinary with opportunities to work on future products and current product and process improvements. The position may represent Quality on cross-functional teams to support business needs driving a positive site quality culture. The position pre

quality assurance associate. phoenix , arizona posted 3 days ago job details summary $17 - $18 per hour temporary category production occupations reference1015253-1 job details As a quality assurance associate, you will be responsible for inspecting materials and packaging to make sure they meet quality requirements. The job involves the completion of daily QA reports and documentation. Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com. Pay offered to a successful candidate will be based on several factors including the candidate's educatio

Medivant Healthcare is a new fully automated injectable manufacturing & outsourcing (503B) facility based in Phoenix, AZ. The company manufactures single dose liquid injectable vials for sales to hospitals around the country. Company focuses on molecules and products that are on FDA's shortage list. Current molecules being sold to hospitals are Sterile water, Sodium Chloride, Lidocaine, Bupivacaine and a few more. Company will be expanding its range to 15 molecules by end of the year. Schedule: F/T: Monday through Friday, more details upon interview Benefits: Health, Dental, Vision, LTD, STD, Accident, Life Salary: $45,000 to $70,000 The Quality Assurance Associate is responsible for management of routine quality assurance needs associated with manufacturing and testing of raw materials and finished pharmaceuticals, quality system maintenance and improvement initiatives, and compliance to GMP quality and regulatory standards. Serves as first responder for Manufacturing, Packaging, or L

Quality Assurance and Regulatory Compliance Associate Role Summary Our client seeks a quality assurance and regulatory compliance associate (QARC) to join their rapidly growing team. The QARC Associate oversees all Quality Assurance activities for their assigned Distribution Center. This position serves as an interface for the Food and Drug Administration (FDA) and ISO and other state and local regulatory inspections and communications related to client needs. The scope of the position includes ensuring that Quality Programs, systems for clients, and software meet all applicable regulatory requirements and are consistent with internal QA goals and initiatives. This role is Key Results Area Manage and maintain the Quality Management System at the distribution center Ensure the Quality Management System is maintained in support of the ISO Program for the client, including but not limited to an effective and compliant Corrective Action/Preventative Action Program (CAPA). Verifies that app