Manufacturing Technician (Aseptic), 1st Shift: 6:00am-2:30pm

Job Description\n \nWhat You'll Do\n \nThe Aseptic Manufacturing Technician II has primary responsibility for the activities and procedures required for the manufacture and filling of aseptic products. This role follows established procedures in the execution of daily activities and receives instruction on new assignments.\n \nHow You'll Contribute\n\n Operates production equipment according to Standard Operating Procedures (SOPs), Batch Records, Manufacturing Directions (MD), and Manufacturing Operating Procedures (OPM).\n Executes all procedures associated with aseptic fills (transfer, set-up, sanitization, autoclaving, process simulation, etc.).\n Performs scheduled cleaning and sterilization of equipment.\n Supports changeover activities.\n Troubleshoots and resolves process-related issues.\n Records data into Batch Records, log books, and OPMs.\n Reviews log books and forms.\n Documents all work activities according to Good Documentation Practices.\n Reports procedural deviations and nonconformance to management.\n Maintains current training on all assigned procedures, including read-and-understood, skills development, and classroom training activities as required.\n \nWhat It Takes\n \nThe position works on assignments that are routine in nature where cGMP experience is required to perform work activities. The Aseptic Manufacturing Technician II normally follows procedures on routine work and requires instruction and training on new assignments.\n \nWhat You Bring\n\n High school diploma or GED, or equivalent experience.\n 2\u20134 years of related experience in a cGMP manufacturing environment.\n Ability to work flexible hours to complete work activities.\n Strong written and verbal communication skills.\n Ability to gown and gain entry to biotechnology/pharmaceutical manufacturing areas and wear personal protective equipment such as safety glasses/goggles, gloves, and safety shoes.\n Ability to lift, pull, or push equipment requiring up to 25\u201350 lbs. and stand for up to 6 hours in a production suite.\n Ability to climb ladders and work platforms.\n Ability to work around chemicals including alcohols, acids, and bases.\n Ability to work flexible hours to complete work activities.\n \nNice to Have\n\n Manufacturing experience in the medical device industry.\n Experience working in a clean room or using aseptic technique.\n Experience using commercial-scale automated equipment.\n Ability to perform computerized transactions and maintain spreadsheets.\n \nThe salary range provided is based on the Company's reasonable estimate of the base salary pay range for this position at the time of posting. Actual base pay is determined by several factors relevant to the position, including skills, competencies, experience, education, and geographic location. Anika also offers a discretionary bonus program for all full-time employees, comprehensive healthcare benefits, health savings account, 401(k) plan with up to 5% company match which includes immediate vesting, employee stock purchase plan at a 15% discount, accrued paid time off, additional long-term incentives including stock awards, and much more. At Anika, we take pride in offering robust Total Rewards, inclusive of market-leading benefits to meet our employees where they are in their career and in life.\n \nThe compensation and benefits information is provided as of the date of this posting. Anika reserves the right to modify compensation and benefits at any time, subject to applicable law.\n \n1st Shift: 6:00am-2:30pm\n \nPowered by\n \nPosition Details\n \nNow Hiring\n \nLocationBedford, MA\n \nEmployment TypeFull-Time\n \nSalary Range$47,000 \u2013 $60,000\n \nApply Now\n \nShare This Career\n\n \n \n \n \n \nReady to Apply?\n \nClick the button below to submit your application for this position.\n \nApply Now\n \nOther Open Positions\n \nCareer\n \nSenior Quality Assurance Specialist (CMC)\n \nFull-Time\u2022Bedford, MA\n \nWhat You'll Do The Senior Quality Assurance Specialist provides quality assurance oversight across CMC development, Quality Control, Analytical Development, manufacturing, and supply chain activities, ensuring\u2026\n \nView Position\n \nCareer\n \nEnd User Support Specialist\n \nFull-Time\u2022Bedford, MA\n \nEnd User Support Specialist What You'll Do The End User Support Specialist delivers high-quality technical support and ensures a seamless technology experience for employees across\u2026\n \nView Position\n \nCareer\n \nSenior QC Incoming Inspector\n \nFull-Time\u2022Bedford, MA\n \nWhat You'll Do The Senior QC Incoming Inspector supports quality control activities related to the inspection, approval, and release of raw materials and components used\u2026\n \nView Position\n \nProducts Navigation" data-detect-dark-bg="true">Products\n\n Regenerative Solutions\n OA Pain Management\n Our Technology\n \nResources Navigation" data-detect-dark-bg="true">Resources\n\n Literature & Videos\n News & Blog\n Just For Patients\n Events\n Certifications\n Form 1095-C\n Instructions for Use\n Find a Doctor\n \nCompany Navigation" data-detect-dark-bg="true">Company\n\n About Anika\n Meet Our Team\n Our Story\n Join Us\n \nConnect Navigation" data-detect-dark-bg="true">Connect\n\n Investor Relations\n Contact Us\n Find a Rep\n \nFollow Us\n\n LinkedIn\n Instagram\n Facebook\n X\n YouTube\n \n3 Media Web Solutions, Inc\n \n2026 Anika Therapeutics, Inc. 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