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
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.
The Shipper Receiver II is responsible for activities related to the receiving of raw materials, control of inventory and shipment finished goods. The position follows established procedures in the execution of daily activities.
Senior Clinical Project Manager
The Senior Clinical Project Manager is responsible for the design, execution, and results of clinical studies including complex, multi-center pivotal trials. This includes developing strategic approach, building the project plan, developing the protocol, initiating and executing the clinical study, and working with Regulatory to use study results for product approvals. Studies must be conducted meeting enrollment timelines and budgets. The position ensures all studies are conducted in compliance with GCP and all applicable standards and regulations.
Regulatory Affairs Specialist II
The Regulatory Affairs Specialist II is responsible for filing necessary submissions and handling all regulatory authority interactions pertaining to the regulation process for product submissions. Supports necessary regulatory activities required for product market approval, and post-approval requirements.
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.
Director of Regulatory Affairs
The Director of Regulatory Affairs is responsible for defining and implementing regulatory strategies to obtain global approvals of new/modified devices and combination products to support meeting Anika’s business objectives. This role requires the ability to analyze complex technical and medical information and formulate strong regulatory arguments that can be defended with regulatory agencies such as the FDA and international Health Authorities. The Director of Regulatory Affairs must also ensure compliance with global regulations for design controls, cGMP, facility registration, device listing, licenses, safety reporting, complaints, clinical trial requirements, post-market surveillance, labeling, and permissible marketing communication. This position reports to the VP of Regulatory/ Clinical Affairs. The Director of Regulatory Affairs manages a staff of Regulatory Affairs professionals in the U.S and Europe. The Director of Regulatory Affairs provides the Regulatory Affairs department interface to executive management and is one of the top leaders in Anika.
Clinical Research Associate II
The Clinical Research Associate (CRA) II will assist the Clinical Project Manager in the conduct of clinical trials.
Process Engineer III
Leads diverse process improvement and new manufacturing and packaging process development projects. Acts as technical lead in multi-disciplined project teams. Works on problems of diverse scope where analysis of data is utilized to make timely and effective decisions. Performs design, purchase, validation and implementation of equipment and system used in manufacturing and packaging of medical devices and drug products.
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.
Senior Manager, Planning & Distribution
The Senior Manager is responsible for ensuring continuous supply of product in a compliant and cost-efficient manner. The Senior Manager ensures effective planning and storage of raw materials, APIs, components, intermediates and finished goods. This position is responsible for overseeing master planning for the entire company finished-goods inventory encompassing internal manufacturing and external third-party services. The senior manager is responsible for leading S&OP with commercial counterparts, analyzing variability in demand and leadtime, working with relevant stakeholders to determine the optimal stocking policy and level using statistical techniques.