Avet Pharmaceuticals Jobs in United States

The QC Lab Assistant assists chemists and supervisors in the laboratory and follows established procedures and SOPs.HS diploma or GED · ...

The Senior Manager Supply Chain will lead end-to-end supply planning developing and managing supply plans across internal and external manufacturing partners. · This role drives the S&OP process translates demand forecasts into executable plans mitigates risks and implements scal ...

Packaging Operator I is an entry-level position in the packaging department. This position is responsible for performing packaging procedures and executing diverse tasks on various packaging equipment. · ...

An entry-level position in the Manufacturing department where the Production Helper I assists the Manufacturing Operators operating assigned manufacturing equipment. · ...

The Material Handler's primary duties will be to keep our warehouse clean and organized. · As well as assisting other departments by providing material in a timely manner.Withdraw Products from the in-process area as per paperwork/ procedure. · Prepare shipments final shipment. · ...

The Production Operator I is an entry-level role within our manufacturing department. · Executing manufacturing procedures and tasks on various manufacturing equipment. · Maintaining elevated compliance and quality standards throughout operations. · ...

The General Counsel oversees all legal matters for the organization. · J.D. from an accredited university · ...

The Lab Technician is an entry-level support position in the QC department. Reporting Relationships: Work is closely managed and supervised. · ...

The Procurement Manager leads procurement strategies to ensure reliable, cost-effective, and compliant sourcing of materials and services for generic pharmaceutical manufacturing and distribution. · Develop and execute sourcing strategies for raw materials, APIs, excipients, pack ...

This is a Temp onsite position based at our East Brunswick NJ facility. · Determine whether quality activities and related QC-QA audits and processes comply with the cGMP requirement. · Review of all the raw data including chromatograms certificate of analysis generated during va ...