Senior Manufacturing Technician, 1st Shift (Aseptic)

If you are unable to complete this application due to a disability, contact this employer to ask for an accommodation or an alternative application process. Regular Full-Time Bedford, MA, Bedford, MA, US 30+ days ago Requisition ID: 1685 Salary Range: $58,000.00 To $73,000.00 Annually What You’ll Do The Sr. Aseptic Technician performs routine and non-routine activities and procedures required for the manufacture and filling of aseptic products. This role follows established procedures in the execution of daily activities and uses judgment in resolving basic issues or making recommendations. How You’ll Contribute Operates production equipment according to Standard Operating Procedures (SOPs), Batch Records, Manufacturing Directions (MD), and Manufacturing Operating Procedures (OPM). Executes all procedures associated with aseptic fills (transfer, set‑up, sanitization, autoclaving, process simulation, etc.). Performs scheduled cleaning and sterilization of equipment. Supports changeover activities. Troubleshoots and resolves process‑related issues. Initiates work orders. Reviews manufacturing documentation for compliance. Coordinates sample preparation and testing. Records data into Batch Records, log books, and OPMs. Documents all work activities according to Good Documentation Practices and recommends document revisions. Reports procedural deviations and nonconformance to management. Assists Lead Technician in quality system generation, reviewing log books and non‑critical forms, and maintaining floor metrics. Maintains current training on all assigned procedures, including read‑and‑understood, skills development, and classroom training activities as required. What It Takes The position works on assignments that are moderately difficult, requiring judgment in resolving issues or making recommendations. The Sr. Aseptic Technician normally receives little instruction on daily work and general instructions on newly introduced assignments. What You Bring High school diploma or GED, or equivalent experience. 4–6 years of related experience in a cGMP manufacturing environment. Ability to work flexible hours to complete work activities. Strong written and verbal communication skills. Proficiency in computer skills and Microsoft Office applications. 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. Ability to lift, pull, or push equipment requiring up to 25–50 lbs. and stand for up to 6 hours in a production suite. Ability to climb ladders and work platforms. Ability to work around chemicals including alcohols, acids, and bases. Nice to Have Manufacturing experience in the medical device industry. Experience working in a clean room or using aseptic technique. Experience with ERP systems, preferably SAP. The 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. The 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. #J-18808-Ljbffr Anika Therapeutics