Careers

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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.

Group Of Happy And Positive Business People In Casual Dress

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.

Notice to Candidates

We were recently notified that individuals posing as Anika employees are contacting potential candidates and making job offers as a way of obtaining personal information that may be used for fraudulent activities. While Anika recruiters and authorized Agencies partnering with Anika on specific searches will proactively reach out to potential candidates about employment opportunities, they will not ask for personal information over the phone, by email or text/SMS. Offers of employment are not extended until a formal, multi-phase interview and screening process has been completed and a candidate has submitted an application through our secure online employment portal. If you believe that you have been the victim of a fraudulent employment offer, please contact the Federal Trade Commission or your local police department.

Explore Open Positions


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Validation Engineer II

Location: Bedford, MA

Performs start-up, commissioning, qualification, validation and revalidation for facility, equipment, critical utility, automation/computer system, cleaning, sterilization, medical device and drug product manufacturing processes.

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Executive Director of Investor Relations and Corporate Communications

Location: Bedford, MA

Working closely with Anika’s CEO and CFO, the Executive Director of Investor Relations and Corporate Communications will contribute to Anika’s mission by shaping and managing the Company’s investor relations message in a consistent and strategic manner. This role is responsible for collaborating with CEO and CFO in developing and executing the global investor relations program. Responsibilities include helping develop corporate messages, presentations and analyses in support of quarterly earnings, investor conferences, roadshows, and other investor events. This role will serve as a liaison for day-to-day inquiries from investors and sell-side analysts. This role will work with multiple functional areas in the Company, as well as across different fully owned subsidiaries.

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Packaging Technician II

Location: Bedford, MA

The Packaging Technician II will perform intermediate technical set-up and troubleshooting of labeling, sterilization and packaging equipment for proper operation including change-over.

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Investor Relations Associate

Location: Bedford, MA

The Investor Relations Associate is responsible for executing the company’s annual and long-term IR plans. The Investor Relations Associate will assist the Executive Director of Investor Relations and Corporate Communications to manage relationships with investors, analysts, and the company’s external IR and PR service providers. Additional responsibilities include maintenance of the company’s IR database, coordination of quarterly investor earnings calls, and investor outreach programs.

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Process Engineer III

Location: Bedford, MA

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.

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Packaging Operator II

Location: Bedford, MA

The Packaging Operator II will perform intermediate packaging, sterilization, and cartoning operations to meet commercial product demands. The position follows established procedures and documents work in batch records and forms.

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IT Support Specialist

Location: Sarasota, FL

The position is primarily responsible to provide local and remote hardware and software support for desktops, laptops, printers, and other peripherals. This position interacts with all levels of employees and candidates must be able to maintain a courteous, professional manner. Candidates must have an ability to work independently, research and resolve problems quickly and efficiently, and multitask well while maintaining deadlines. Candidate must be able to communicate technical items to non-technical employees. Duties will include local and remote troubleshooting and problem resolution. Candidate will be expected to remain current with standard industry services, programs, developments, and features throughout their employment.

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IT Support Specialist

Location: Bedford, MA

The position is primarily responsible to provide local and remote hardware and software support for desktops, laptops, printers, and other peripherals. This position interacts with all levels of employees and candidates must be able to maintain a courteous, professional manner. Candidates must have an ability to work independently, research and resolve problems quickly and efficiently, and multitask well while maintaining deadlines. Candidate must be able to communicate technical items to non-technical employees. Duties will include local and remote troubleshooting and problem resolution. Candidate will be expected to remain current with standard industry services, programs, developments, and features throughout their employment.

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Senior QA Compliance Specialist

Location: Franklin, MA

The Senior Quality Specialist works with a high degree of independence and is adept at troubleshooting problems to create and execute improved internal procedures, and to ensure compliance with applicable regulatory requirements. This position is a subject matter expert for Quality Management System Regulations and policies, batch records, validation protocols and resolving non-conformances.

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Product Manager/Sr Product Manager

Location: Sarasota, FL

The Product Manager/Senior Product Manager (Sr. PM) will work directly for the Executive Director of Americas Marketing to manage a broad range of upstream and downstream product responsibilities across the full life cycle of a product family or portfolio of products. Takes a lead role on new product development teams, providing marketing expertise throughout the development phases and fully preparing new products for successful commercialization. Internal subject matter expert on products, competitors, and market dynamics. Develops product level strategies and provides tactical content to Marketing Operations (sales education, medical education, marketing communications) for collaborative execution.

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Quality Engineer

Location: Sarasota, FL

This position works collaboratively with quality, manufacturing and engineering to ensure the quality management system is effectively implemented and maintained throughout product realization. The ideal candidate will be someone who has excellent interpersonal communication skills, is hands-on and eager to learn and grow with an innovative, medical device manufacturing company. They are a team player possessing initiative and self-motivation.

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Accounting Manager

Location: Sarasota, FL

The Accounting Manager is primarily responsible for all accounting, reporting, and controls at the Parcus Medical company in Sarasota, FL.

Parcus Medical designs, manufactures, and distributes implants and instrumentation used by orthopedic surgeons in sports medicine procedures to repair the shoulder, knee, hip, and distal extremities. Parcus offers over 400 innovative products, in over 60 countries around the world. Founded in 2007, Parcus Medical is headquartered in Sarasota, Florida.

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Senior Quality Engineer

Location: Bedford, MA

This position is responsible for providing support for new product development and manufacturing support for commercial products. This key technical role will support the development and manufacture of medical device and drug/device combination products by providing expertise on regulated standards processes such as design control, human factors/usability engineering, and risk management.. Working closely with Operations, Manufacturing Engineering and Research and Development Engineering, the Senior Quality Engineer ensures a high level of product quality and effective and efficient corrective and preventive action plans.

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QC Microbiologist II

Location: Bedford, MA

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.)

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Senior Regulatory Affairs Specialist

Location: Bedford, MA

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.

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Accounting Manager

Location: Bedford, MA

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.

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Quality Control Analyst II

Location: Bedford, MA

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.

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