Anika Jobs in United States

The Crosslink Technician II has primary responsible for the activities and procedures required for cross linked hyaluronic acid product production. · ...

We are seeking a highly organized and detail-oriented Maintenance & Calibration Planner with proven experience in the pharmaceutical and medical device industry. · This role is responsible for planning, scheduling, and optimizing both maintenance and calibration activities to ens ...

The QC Incoming Inspector completes all activities required to approve raw materials for use in product manufacture. · Perform quality line clears and in process inspections during the inspection and packing processes according to specific SOP requirements · Issue lot numbers and ...

Process Engineer III leads diverse process improvement initiatives and process development projects for medical devices and drug products. · Key Responsibilities · Design, purchase, validate, and implement equipment and systems that support cGMP-compliant manufacturing. · Leverag ...

The Manufacturing Technician has primary responsible for the activities and procedures required for the cross linked hyaluronic acid and/or aseptic product production. · Operates production equipment according to Standard Operating Procedures (SOPs), Batch Records, Manufacturing ...

The Sr. Crosslink Technician performs routine and non-routine activities and procedures required forcross linked hyaluronic acid product production.The position follows established procedures in the execution of daily activities and uses judgement in resolving basic issues or mak ...

The Quality Assurance Documentation Specialist I is a quality focused individual who ensures documentation and record keeping processes conform to approved procedures and output documents are accurate. · This role will support the organization by maintaining documents required by ...

Facilities Manager Role Overview · This senior role leads the Facilities department in accordance with current Good Manufacturing Practices (cGMP), ISO requirements, and industry best practices. The incumbent manages a multi-million-dollar budget and engages in proactive relation ...

Human Resources Role Overview · This Human Resources Generalist plays a crucial day-to-day support role in managing Anika's human resources programs, policies, and objectives. · Key Responsibilities: · ...

The QC Incoming Inspector completes all activities required to approve raw materials for use in product manufacture on the second shift. · The position also performs inspection activities during in-process manufacturing for second shift.Perform quality line clears and in process ...

This position is responsible for leading the Facilities department in accordance with current Good Manufacturing Practices cGMP, ISO requirements and industry best practices. Reporting to the Director of Engineering this position provides results-oriented leadership and creativit ...

The Senior Process Engineer leads diverse process improvement initiatives and process development projects for medical devices and drug products. ...

The Crosslink Manufacturing Technician has primary responsible for the activities and procedures required for the cross linked hyaluronic acid product production. · ...

Job Description · The Manufacturing Technician II has primary responsibility for activities required for manufacturing of fiber and film based textile products. · Operating production equipment according to SOPs, Batch Records, MD, and OPM; · Fibers extrusion and packaging of wov ...

The Production Planner will set and oversee the production plans to align with the sales forecast while meeting business objectives of safety quality on-time delivery competitive customer lead times profitability and inventory. · Oversee the scheduling of production materials to ...

The Quality Control Analyst II is primarily responsible for the activities and procedures which are required to sample and test raw materials, work-in-process samples, finished goods, and stability samples under cGMP conditions. · Testing of incoming raw material according to USP ...

The Process Engineer III leads diverse process improvement initiatives and process development projects for medical devices and drug products.Key ResponsibilitiesLead the design and specification of equipment and systems in alignment with cGMP and other relevant standards. · Iden ...

This position is responsible for providing general support of R&D on various existing and new product development projects. · Supports EU MDR efforts for R&D including design control,bio-compatibility,and risk management. · Cultivates effective communication with departments such ...

Sr Site Plumber Overview · The Senior Site Plumber oversees plumbing operations and maintenance for a GMP manufacturing facility. · Ensure all plumbing systems operate at peak performance. · ...