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 Packaging Technician will perform technical and routine packaging operations using automated packaging and sterilization equipment. This position requires ownership in the area of traying/pouching, labeling, and VHP surface sterilization according to established cGMP procedures. This position has direct oversight for Packaging Operators that work within this area of the business.
Process Excellence Manager
The Process Excellence Manager leads a group within the Technical Operations function in close collaboration with Manufacturing, to recommend, develop, and implement process improvements and controls.
• Leads continuous improvement projects to cost effectively produce products which meet critical product attributes.
• Role includes managing multiple engineers, projects, technical floor support as well as coordinating process improvement activities and supporting transfer of new products/processes into manufacturing.
• Identifies new process and analytical 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.
The Manufacturing Crosslinking 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 Packaging Supervisor is responsible for ensuring the scheduling, execution, and completion of activities in an ISO 13485 packaging environment ensuring safety, quality, compliance, delivery and cost are maintained on the packaging floor.
Senior Business Analyst (SAP)
The Senior Business Analyst (BA) works collaboratively with the business users and the extended IT solution delivery team, and is responsible for executing the activities associated with the continuous improvement of business processes and systems. The BA must analyze current needs, anticipate future needs and provide solutions for our operations, finance and sales teams in integrating various business operations into one platform. Primary activities include the analysis, design and implementation of continuous improvement opportunities, enabled by SAP functionality and related integrated applications, as well as other business application opportunities.
The BA will engage a variety of stakeholders to understand their business needs and help identify and prioritize opportunities for improvement, aligning with the long-term business strategy. The BA should possess strong / broad SAP expertise along with good presentation and interpersonal skills. This position will be located in our Bedford, MA facility and may occasionally require travel.
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.
The Manufacturing Operator is responsible for performing manufacturing operations for the production of commercial medical device and drug products according to cGMP regulations.
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.
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.