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 Maintenance/Calibration Scheduler is responsible for ensuring the efficient and effective work management of the facilities resources and external service providers performing work activities at the Anika Manufacturing Facility.
The role is responsible for the planning and scheduling of all maintenance and calibration work to be performed at the Anika Manufacturing Facility. The position will ensure that work management procedures are developed and adhered to and that performance metrics are established and reviewed on a regular basis.
The Packaging Technician will be responsible for the set up and adjustment of equipment within the department. All activities will be focused on optimization of equipment to maximize throughput. The Packaging Technician will also execute routine packaging and cartoning operations to meet commercial product demands.
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.
Director of Materials Management
This position is responsible for all supply chain related activities including strategic sourcing, production planning, inventory control, and distribution for Anika’s medical devices and drug products. The Director is focused on ensuring product is delivered on time and in full through both distributor and direct sale channels. The incumbent will define and implement business processes to support corporate objectives in the areas of safety, cost, quality, and delivery. The Director is a dynamic service orientated leader who manages complex tasks independently and also leads cross-functional teams in a fast-paced environment.
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.
The Product Manager (PM) will work directly with the Executive Director of Global Marketing to prepare the commercial organization for the launch of CINGAL. The PM 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 PM 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 PM 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.
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.
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.
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.
Director of Regulatory Affairs
The Director of Regulatory Affairs is responsible for defining and implementing regulatory strategies to obtain global approvals of new/modified devices and combination products in order to support meeting Anika’s business objectives.