Find & Apply For Production Worker Jobs in Walkersville, Maryland

Title

• Manufacturing Associate Level 1
  Location
• Walkersville MD
  Duration
• 6 Months (Possibility of extension)
  Supervisory Organization
• 
  Endotoxin Operations
  Reports to (position)
• 
  Supervisor
  Job Title
• 
  Manufacturing Associate I, Endotoxin
  Job Description Summary
  Provide a brief (3
• 4 sentence) description that states "why" the job exists and describes the nature and level of work.

Responsible for participating in upstream and/or downstream aseptic manufacturing of LAL products in a ISO 5 environment according to company and departmental SOPs. Performs set-up and operate production equipment in the LAL Filling and Finishing areas. Performs product inspections and final kit packaging of finished goods.

Key Accountabilities

Define all key accountabilities (5-10), which the role will be expected to perform in short to medium future. Make sure that you list the accountability on top, which the role will be doing most frequently and which has most impact on the the team/BU/Lonza. Begin each sentence with an action word, e.g. Provides appropriate coaching and performance feedback to all direct reports.

Operating in a safe work culture (safety chats, safety and EPS observations, 6S)

Completion of LAL Cleanroom General Training

Aseptic processing/gowning

Cleanroom Equipment Set-Up and Usage

Environmental Monitoring

Qualification of SAP Transactions (COR3, COR6, MIGO, LS26)

Completion of LAL Finishing General Training

Finishing Equipment Set-Up and Usage

Qualification of SAP Transactions (COR2, COR6, MIGO, MB1A, LB01, LS26)

GMP Documentation practices

Product Sample Submission

Inspection Proficiency Testing

Inspection Process

Component Kitting Process

Continuous Improvement Projects

Perform job functions with minimal operator related PRs

Perform aseptic processing with minimal operator related personnel excursions (EM)

Understand basic level of LAL process flow

Achieve yearly personnel utilization target

Maintain training compliance to meet yearly target

Must be able to demonstrate GMP documentation practices (minimal document errors)

Must be able to follow standard operating procedures and complete production records

Understand compliance in the execution of GMPs in a manufacturing environment

Comply with all safety policies and general regulations

Perform other duties as assigned.

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