The Boston Globe has repeatedly recognized Anika as one of Massachusetts best businesses. In fact, we’ve made the Boston Globe’s top “100 Ranking” list for best businesses in 8 of the last 9 years, which has cemented Anika Therapeutics’ status among the movers and shakers in the industry.
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
The Senior Scientist is responsible for providing support to R&D and Manufacturing teams under the supervision of the Director of R&D. We are seeking a candidate who is energetic and can carry out development projects with minimal supervision. A hands-on scientist that is a problem-solver, who can provide imaginative solutions to issues as they arise.
Corporate Legal Associate
The Corporate Legal Associate is responsible for providing various legal assistance and services to the organization under the supervision of the corporate legal counsel. The position coordinates and completes time-sensitive and confidential work of both an administrative and project-based nature to forward the business initiatives of the company.
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.
Senior Clinical Project Manager
The Clinical Project Manager is the primary person responsible for the planning and execution of assigned clinical trials. This encompasses all aspects that impact the completion of the trial and include development of study project plans, problem solving all trial related issues utilizing available resources, initiation and monitoring of trials in progress, completion, reporting and publication of study results. The position ensures all studies are executed within predefined timelines & budgets and are conducted in compliance with GCP and all applicable standards & regulations.
Senior Regulatory Affairs Associate
The role of the Senior Regulatory Affairs Associate 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.
Aseptic Manufacturing Supervisor
The Aseptic Manufacturing Supervisor is responsible for commercial manufacturing operations for drug and device products. The position ensures the effective scheduling and utilization of facilities, equipment and personnel in producing quality products meeting customer delivery requests and internal performance targets.
The Accounting Intern position will have access to a wide range of experience under the mentor ship of the Assistant Controller and other accounting and finance leaders. The position is an ideal opportunity to develop accounting skills in a real world work environment.
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.
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.
QA 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.