Anika Therapeutics Jobs in United States

We are seeking a highly organized and detail-oriented Maintenance & Calibration Planner with proven experience in the pharmaceutical and medical device industry. · Develop and manage preventive and corrective maintenance schedules for GMP-critical and non-GMP assets. · Plan and c ...

The Procurement Leader plays a key role in the Global Supply Chain team. · Manage procurement of raw materials, finished goods, · as well as outside service providers in alignment with · Demand, Supply and Manufacturing site needs and lead-times. ...

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. · Requires BS in Chemistry or other Physical Scienc ...

The Manufacturing Technician II has primary responsible for the activities and procedures required for the manufacturing of fiber and film based textile products. · ...

The Lead Calibration Technician will oversee and execute calibration activities for critical (and non-critical) instruments and equipment within a GMP manufacturing facility. · ...

The HYAFF Manufacturing Technician II has primary responsibility for the activities and procedures required for the manufacturing of fiber and film based textile products. · Operates production equipment according to Standard Operating Procedures (SOPs) · ...

Responsible for all microbiological and some analytical testing of production materials under GMP conditions. · ...

The Process Engineer II supports process improvement initiatives and process development projects for medical devices and drug products. This role designs, validates, · and implements equipment and systems that support cGMP-compliant manufacturing. · ...

The Crosslink Manufacturing Technician II position involves working on routine assignments in a cGMP manufacturing environment. The role follows established procedures and requires instruction and training for new tasks. · ...

The HYAFF Technician II has primary responsible for the activities and procedures required for the manufacturing of fiber and film based textile products. · Operates production equipment according to Standard Operating Procedures (SOPs), Batch Records, Manufacturing Directions (M ...

The Process Engineer II supports process improvement initiatives and process development projects for medical devices and drug products. · This role designs, validates, and implements equipment and systems that support cGMP-compliant manufacturing. · The engineer applies analytic ...

Senior Site Plumber · This role demands advanced technical proficiency in plumbing systems ability to interpret complex schematics and wiring diagrams sound judgment in high-risk environments. · Ensure all plumbing systems operate at peak performance efficiency and reliability · ...

The QC Incoming Inspector completes all activities required to approve raw materials for use in product manufacture. · ...

The Quality Assurance Documentation Specialist I is responsible for ensuring 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 the Quality Man ...

Position Scope · The Sr. Site Plumber will oversee plumbing operations and maintenance for a GMP manufacturing facility. This role ensures reliable operation of critical utility systems and supports manufacturing processes by performing and supervising plumbing-related tasks. The ...

· Position Scope: · The Packaging Operator I will perform routine packaging assembly and cartoning operations to meet commercial product demands. · Specific Tactical Responsibilities: · Performs routine cGMP functions associated with manual/automated packaging operations and car ...

+Job summary · Human Resources Generalist is responsible for providing day-to-day support of Anika's human resources programs, policies and objectives. Reporting to the Director of HR Operations & Shared Services. ...

+ Process Engineer II · Job summary: The Process Engineer II supports process improvement initiatives and process development projects for medical devices and drug products. This role designs, validates, and implements equipment and systems that support cGMP-compliant manufacturi ...

The Process Engineer II plays a key role in designing and implementing equipment systems that support cGMP-compliant manufacturing. · Key Responsibilities · Support design and specification of equipment systems aligned with cGMP standards. · Collaborate to identify cost reduction ...

The Process Engineer III leads diverse process improvement initiatives and process development projects for medical devices and drug products. Acting as a technical lead on multi-disciplinary teams this role designs purchases validates and implements equipment and systems that su ...