RCI-TEVA-9725 BioPharma Quality Auditor Associate (3rd Shift) cGMP/ FDA) - Salt Lake City, UT

+Job summaryA Quality Auditor Associate will be responsible for performing sampling and delivery of intermediate and finished products, conducting monthly GMP and batch-specific room audits. · +ResponsibilitiesPerform sampling and delivery of intermediate and finished products. · ...

Seeking a CSV Engineer with hands-on experience in Computer System Validation and Commissioning, Qualification, and Validation (CQV) to support GMP-regulated pharmaceutical or biotech operations. · ...

We are seeking a CSV Engineer with hands-on experience in Computer System Validation and Commissioning, Qualification, and Validation (CQV) to support GMP-regulated pharmaceutical or biotech operations across multiple sites. · ...

Perform visual, mechanical and functional inspections on medical device materials components and sub-assemblies. · ...

The sanitation supervisor owns the sanitation program in practice, not by delegation. · This role is responsible for executing, maintaining, and verifying sanitation systems across our facilities to meet cGMP, · FSMA, · and FDA food safety requirements—daily, · visibly, · and cre ...

This is a job description for an Analytical Chemist/ Scientist. The job involves performing laboratory analyses of Finished products and in-process materials. The candidate should have a Bachelor's Degree in Science or related science field from an accredited college or universit ...

We are seeking a proactive and detail-oriented Quality Assurance Supervisor to lead and improve our overall quality management system. This role ensures compliance with regulatory standards and customer expectations, contributing to our commitment to excellence. · Lead and develo ...

Welcome to DiscGenics, a pioneering biopharmaceutical company dedicated to advancing regenerative cell-based therapies for patients suffering from degenerative diseases of the spine. · ...

Develop validation strategies for FDA, EMA and ICH Q7 – Q10 compliance. Lead Process Validation Studies and draft PPQ protocols. Perform C&Q for GMP equipment and facilities. · ...

Able to perform entry level inspection repetitive tasks associated with visual inspections and basic functional testing knowledge.Responsible for ensuring company products are in compliance with internal and external specifications by performing a variety of routine and non routi ...

This is a full-time non-exempt position performing duties and assigned tasks under compliance of cGMP manufacturing guidelines in the bioreagents lab. · ...

The primary responsibilities of this position are to manage the daily operations of the two Cyclotron Radiochemistry Laboratories in a safe and compliant manner in support of clinical, · pre-clinical, and research activities.This position oversees staff radiochemists, · radiophar ...

+Imagine how your ideas and expertise can change a patient's life. · +Partner cross-functionally with manufacturing operations and sales teams, delivering thoughtful solutions to complex challenges all while developing your knowledge of the medical device industry. · The Director ...

The QC Lab Technician will perform routine operations of organoleptic testing and qc analytical instrumentation as well as maintain proper records according to appropriate FDA guidelines for Foods and Dietary Supplements. · Ensure compliance with established regulations and custo ...

Quality Inspector I · Able to perform entry level inspection repetitive tasks associated with visual inspections and basic functional testing knowledge · Responsible for ensuring company products are in compliance with internal specifications by performing routine inspections an ...

The Director of Quality is a people leader responsible for managing the Receiving Inspection team and ensuring the effective operation of the site's quality management system. · ...

A fast-growing biotechnology company is expanding their team in Salt Lake City and they are in immediate need of a Validation Engineer to support them fully onsite for 12 months. · ...

Perform entry level inspection and repetitive tasks associated with visual inspections and basic functional testing knowledge. · Minimum HS graduate or GED equivalent. · Must have basic computer skills to regularly access and document information in a computer. · ...

The Quality Systems Supervisor manages the QA functions that ensures the release and approval of the production work order according to internal and customer specifications. Also, oversee the duties of the QA Document Control Specialist, QA Specialist, Compliance Coordinator, and ...

We are Reckitt Home to the world's best loved and trusted hygiene health and nutrition brands.Join us in our fight to make access to the highest quality hygiene wellness and nourishment a right not a privilege. · Supply Our supply chain is the backbone of our business.It's how we ...