Would you like to work at Anika? Our current open positions are listed below. In addition, we are always accepting resumes from candidates of all types with expertise in a variety of areas. Submit your resume to our active database today.
What Moves Us?
- We’re engaged in the business – not just the job.
- Seeing the impact of our work – helping people makes us happy.
- Achieving results and sharing success – teamwork.
What Moves You?
If you are ready to get moving and start doing work that will improve the lives of others, then we are ready to meet you.
Explore Open Positions
Clinical Specialist/Senior Clinical Project Manager
The Clinical Specialist/Senior Clinical Project Manager is responsible for the design, execution, and results of clinical studies and for providing hands-on technical support to the study, including supporting clinical cases in the Operating Room (OR) and training Investigators through cadaver labs or animal models. This role is a key interface for Anika in developing relationships with investigators and KOLs and requires a thorough knowledge of anatomy and physiology, as well as the mechanism of action of Anika’s products and competitive products. The role includes developing the protocol, building the project plan, initiating and executing the clinical study, working with Regulatory to use study results for product approvals, and working with the Commercial team for potential publications and abstracts. The position ensures all studies are conducted in compliance with GCP and all applicable standards and regulations.
Senior Product Development Scientist/Engineer
Under the supervision of Principal R&D Scientist, the Sr. Product Development Scientist/Engineer is responsible for contributing technical expertise in support of developing and commercializing new products to support Anika’s commercial growth. An expert in the field, the Sr. Scientist/Engineer reviews, generates and executes design activities associated with new product and technology development projects.
QC Incoming Inspector II
The QC Incoming Inspector II completes all activities required to approve raw materials for use in product manufacture. The position also performs inspection activities during in-process manufacturing performs inspection and testing of components. The position revises and updates standard operating procedures as needed.
Process Development Manager
The Process Development Manager will lead the process development function within the Engineering department responsible for developing and transferring processes for the manufacture of new products The candidate will represent the department on process development project teams and will also be expected to interact on a routine basis with colleagues in research and development, QC methods development and commercial manufacturing as well as regulatory compliance groups. The candidate and the team will also be responsible for authoring and reviewing technical reports, protocols, technology transfer documents and CMC sections in regulatory filings; and will lead and participate in on-going technology development efforts within the Department. These efforts include developing of new formulation, product transfer, filling and sterilization technologies aimed to improving the efficiency, productivity and capacity of existing processes. The Process Development Manager will make presentations to management providing periodic progress updates on projects and proposals for new technology development initiatives and advanced data analytics.
QC Microbiologist II
Responsible for microbiological and some analytical testing of production materials under GMP conditions. Responsible for process and equipment validation (autoclave and depyrognenation oven) in cooperation with Engineering and R&D (New Product Sterility and LAL validation.)
Supplier Quality Engineer
The Supplier Quality Engineer (SQE) is responsible for the establishment and implementation of disciplines/processes that enable realization of a zero-defect philosophy to our patients/customers for supplied material as well as complaints by overseeing and owning the supplier program.
Senior Regulatory Affairs Specialist
The role of the Senior Regulatory Affairs Specialist is to execute on the global regulatory programs in accordance with current global regulations. The individual will coordinate the collection of information and documentation and compile into submissions, license renewals, periodic updates and registrations to regulatory agencies and partners worldwide. The individual will be responsible for the review of labeling, protocols, product development and manufacturing documents for compliance with regulatory requirements.
The Accounting Manager is primarily responsible for various aspects of the monthly financial close including close management, consolidations, and review of journal entries prepared by Staff and Senior Accountants. In addition, the Accounting Manager will work closely with the Finance Director to prepare various financial schedules for quarterly SEC reporting purposes including Form 10-Q and 10-K based on understanding of US GAAP.
Quality Control Analyst II
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. The position follows established procedures in the execution of daily activities and completes required documentation.