Careers

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.

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.

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Explore Open Positions


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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Manufacturing Technician

The HYAFF Technician has primary responsible for the activities and procedures required for the manufacturing of fiber and film based textile products. The position follows established procedures in the execution of daily activities.

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Senior Reliability Engineer

This Senior Reliability Engineer is responsible for developing, implementing, and maintaining reliability practices which ensure optimal levels of equipment reliability and availability. This position will develop and implement an asset lifecycle strategy for the site’s critical assets. The Reliability Engineer will be accountable for all maintenance and reliability engineering activities involving the design, installation, maintenance, and repair of utilities systems, manufacturing equipment, and facility support equipment. The Reliability Engineer will utilize tools such as Failure Modes and Effects Analysis (FMEA), equipment criticality analysis, and Root Cause Failure Analysis (RCFA) in order to identify, resolve, and prevent equipment/system failures.

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Director of Facilities

This position is responsible for leading the Facilities and HSE department in accordance with current Good Manufacturing Practices (cGMP), ISO requirements, and industry best practices.  Reporting to the CEO, this position provides the results-oriented leadership and creativity required to build a world-class organization and establish robust and efficient systems.  The Facilities group is responsible for the Maintenance and Calibration of all physical assets including process equipment, utilities, and site infrastructure as well as managing Capital Projects.  As the company’s head of Facilities, the incumbent will manage a multi-million dollar budget and engage in proactive relationships with local, state, and federal authorities.

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Receptionist

The Receptionist will create a positive image of Anika Therapeutics through communication and interaction with key stakeholders including employees, customers, partners, vendors, and visitors to the facility. This person is primarily responsible for the timely and professional handling of visitors and callers to Anika well as coordinating activities and events within the Company. This position will also provide general administrative support for Human Resources, Finance and other departments as needed.

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Senior QA Compliance Specialist

The Senior 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 Senior 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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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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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 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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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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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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