Explore Jobs

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.

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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

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.

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Administrative Assistant

The Administrative Assistant is responsible for providing administrative support for several senior level executives. The position coordinates and completes time-sensitive and confidential work of both a routine nature and project basis. The Administrative Assistant creates a positive image of Anika Therapeutics through communication and interaction with key stakeholders including employees, customers, partners, vendors, and appropriate government and regulatory authorities.

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QA Compliance Specialist II

The Quality Assurance Compliance Specialist II performs compliance activities in support of production, engineering and Research & Development ensuring all activities are performed according to internal Quality System requirements, cGMP, FDA and ISO 13485 standards. Areas of responsibilities include review of documents such as batch records, charts and logs review and approval of incoming materials for release. The position will provide floor support to production departments to include line clearances, in-process checks and assistance with investigations. The Compliance Specialist II also performs audits as assigned, and participates in customer and regulatory audits as part of the Audit Team.

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QC Microbiologist I

Responsible for all 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.)

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Regional Sales Director US

Anika Therapeutics is hiring 4 Regional Sales Directors in the US, responsible for commercial selling activity and distributor management in assigned geographic region to achieve financial goals.

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Principal Scientist/Engineer

Under the supervision of the Vice President, R&D , plans and conducts technical evaluations focused on the development of new product prototypes, new processes and analytical methods. Contributes significantly to new product concepts and their design.

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Senior QC Analyst

The Quality Control Analyst is primarily responsible for development, validation, and transfer of methods for new raw materials, intermediates, and finished products as well as 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. The position will also assist in optimization of existing analytical methods.

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Senior Maintenance Technician

The Senior Maintenance Technician performs preventative and corrective maintenance on a variety of complex utility systems within a GMP manufacturing facility. Equipment includes but is not limited to; HVAC-R, steam boilers, cold rooms, compressed air and gas systems, Reverse Osmosis (RO) and Water for Injection (WFI) systems, waste water treatment and clean steam generation.

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