Crosslink Manufacturing Sr. Technician 2nd Shift 1:00pm-9:30pm

Anika Therapeutics; Bedford (MA); On-site; USD 28,000 - 35,000; Full time

Job summary

Anika Therapeutics in Bedford, MA is seeking a Crosslink Manufacturing Senior Technician for 2nd shift. The role involves operating production equipment, performing cleaning and sterilization, and coordinating sample testing to support cross-linked hyaluronic acid product production.

The position requires a strong background in cGMP manufacturing, ability to work 2nd shift, and aptitude for documenting processes and adhering to SOPs.

Qualifications

• High school diploma or GED is required.
• 4+ years of related experience in a cGMP manufacturing environment.
• Ability to work flexible hours to complete work activities.
• Proficiency in Microsoft Office.

Responsibilities

• Operate production equipment according to SOPs, Batch Records, MDs and OPMs.
• Execute all procedures for cross-linked hyaluronic acid product production.
• Perform COP/CIP cleaning of complex equipment and components.
• Conduct scheduled cleaning and sterilization of equipment.
• Support changeover activities and troubleshoot process issues.
• Initiate work orders and review manufacturing documentation for compliance.
• Coordinate sample preparation and testing; record data in Batch Records and log books.
• Maintain Good Documentation Practices and report deviations to management.

Skills

Strong communication

MS Office

PPE & GMP exposure

Manual handling

Education

High school diploma or GED

Job description

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.

Crosslink Manufacturing Sr. Technician 2nd Shift 1:00pm-9:30pm

Xlink Manufacturing Regular Full-Time Bedford, MA, Bedford, MA, US

2 days ago Requisition ID: 1776

Salary Range: $28.00 To $35.00 Annually

What You’ll Do

The Crosslink Manufacturing Senior Technician performs routine and non-routine activities and procedures required for cross-linked hyaluronic acid product production. 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 cross-linked hyaluronic acid product production.
• Adheres strictly to written work instructions to perform solvent recovery, clean out of place (COP), and clean in place (CIP) of complex equipment and components.
• 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; 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 Senior Crosslink Manufacturing 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+ 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 Microsoft Office.
• 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, push, or pull 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.