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
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 Marketing Assistant is responsible for providing project and administrative support for the Marketing and Sales Team. The position coordinates and completes time-sensitive and confidential work of both a routine nature and project basis.
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.
Executive Director of Quality
This position is responsible for leading the Quality Operations organization inclusive of Quality Assurance, Quality Control Chemistry, Microbiology, and Raw Material, and Quality Systems according to Food and Drug Administration (FDA) guidelines, current Good manufacturing Practices (cGMP), and current ISO requirements. Reporting to the Chief Operations Officer, this position works internally across the Anika organization to provide the vision, results-oriented leadership and creativity required to build a world-class organization and establish a robust and efficient Quality System. As the company’s head of quality, the incumbent will engage in proactive relationships with FDA and other U.S. and International regulatory authorities and when required, present and defend strategies and approaches to facilitate the advancement of the Company’s objectives.
Manager Talent Acquisition
The Manager Talent Acquisition has primary responsibility for managing full cycle talent acquisition for Anika Inc. In collaboration with the VP Human Resources, this person will have responsibility for identifying needs, designing and implementing all programs to meet the human capital requirements of the Company. The Manager Talent Acquisition will be responsible for developing and implementing programs and processes that attract and retain top level, quality talent. This person will also be responsible for the development and management of metrics and processes to define and determine the success of hires within the organization and ensure top talent is identified, hired and on boarded appropriately. This role will also works cross functionally as assigned on projects key to the growth and success of the Company. Most importantly, this key position will focus on sourcing, attracting, assessing and the hiring of top talent for all roles within Anika from entry level to senior management.
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.
The Senior Microbiologist is responsible for all microbiological testing of production materials; raw, in-process and finished goods; environmental monitoring under static and dynamic conditions and personnel monitoring 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).
Senior Clinical Project Manager (2 Openings)
The Senior Clinical Project Manager is responsible for the design, execution, and results of significant clinical studies. This includes 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.