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

Manufacturing Supervisor

The Manufacturing Supervisor is responsible for commercial manufacturing operations for film and fiber terminally sterilized medical device products. The position ensures the effective scheduling and utilization of materials, equipment and personnel in producing quality products meeting customer delivery requests and internal performance targets.

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Senior Buyer/Planner

The Senior Buyer Planner is responsible to perform all supply chain planning and buying activities for assigned product lines. Included are Materials Requirements Planning items that are contained on a BOM, purchasing, and inventory control. The position will interact with other departments to resolve issues and meet customer requirements. All activities will be conducted within cGMP requirements and corporate policy.

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Manufacturing Operator

The Manufacturing Operator is responsible for performing manufacturing operations for the production of commercial medical device and drug products according to cGMP regulations.

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Quality Control Manager

Responsible for managing all microbiological and chemical testing of production materials and incoming inspection of raw materials under GMP conditions in accordance with agreed upon timelines and schedules. In coordination with R&D and Technology Transfer, responsible for method development, method validation and testing for developmental products. Responsible for development, implementation and maintenance of Quality Control systems.

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Quality Compliance Specialist

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

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Process Engineer III

The Process Engineer in collaboration with Commercial Operations, recommends, develops and implements process improvements and controls:
• Designs and modifies processes to cost effectively produce products which meet critical product attributes. Performs experiments to screen critical process control factors. Uses experimental design techniques to develop robust processes.
• Through experiments, literature searches, and internal and external interactions, identifies new technologies aimed at improving manufacturing efficiencies, and product quality.
All Engineering activities must be in compliance with FDA, GMP, ISO and Corporate Quality System regulations.

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HSE Manager

Responsible for health, safety and environmental (HSE) compliance at all Anika facilities. This will include assessment and implementation of absent programs and the continued oversight and administration of existing HSE programs. This position will interface with all departments to ensure existing processes and special projects are in compliance with all Federal, State, and Local regulations. The HSE Manager implements and maintains an environmental health and safety program involving hazard identification evaluation and control, accident/injury prevention, hazardous material/waste management, emergency preparedness, fire/life safety, ergonomics, industrial hygiene, and environmental regulatory compliance.

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Senior Packaging Engineer

Responsible for the design, development, validation and implementation of optimized packaging materials, packaging equipment and systems. Interface with all departments to ensure materials and processes are compatible for technology transfer and consistent with established project plans and corporate goals.

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Clinical Research Associate

Position Scope: The Clinical Research Associate (CRA) will assist the Clinical Project Manager in the conduct of clinical trials. The position ensures the study is conducted in accordance with International Conference on Harmonization Good Clinical Practice (ICH GCP), US FDA and international regulations to ensure the safety and effectiveness of Anika products.  

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Senior Product Manager (Marketing)

The Senior Product Manager (Marketing) will work directly with the Executive Director of Global Marketing to prepare the commercial organization for the launch of CINGAL. The SPM will lead the conceptualization, development, and tactical execution of promotional strategy for the launch of CINGAL in the US.
Responsibilities for the CINGAL Brand include the analysis and incorporation of market research results, advisory board feedback, competitor activities, and current and future market events, such as new product launches. The SPM will manage and direct the creative Agency of Record (AOR) staff to ensure that all promotional materials align to the overall brand strategy, are relevant and impactful, and are launched in a timely manner. The PM will ensure that the allocated budget is managed appropriately. Additionally, the SPM will establish productive and fruitful working relationships with all internal and external stakeholders. This is an excellent opportunity to play a key role in developing the organizations commercial capabilities while planning for and eventually launching the organizations first managed injectable, CINGAL.

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Validation Manager

This position is responsible for leading the Bedford Site’s Validation program for new and existing cGXP systems including process equipment, utilities, and information systems according to current Good Manufacturing Practices (cGMP), ISO requirements, and ICH guidelines. Reporting to the Director of Engineering, this position works internally across the Anika organization to define, administer, and continuously improve the site’s validation system. The incumbent will manage master service agreements with multiple external validation service partners and also manage contract staff and project resources.

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Systems Administrator

The Systems Administrator will be responsible for the design, implementation, troubleshooting and maintenance of all Information Technology systems. Manage the IT system infrastructure and any processes related to these systems. Provide support to IT systems including day-to-day operations, monitoring and problem resolution for all of the client/server/storage/network/VoIP and mobile devices, etc. This includes installing, diagnosing, repairing, maintaining, and upgrading all hardware and software to ensure maximum availability and optimal computing and equipment performance. This position will also be responsible for proposing and implementing system and process enhancements that will improve the performance and reliability of the system.
The Systems Administrator will be located in our Bedford, MA facility and may occasionally require travel.

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