Validation Technician

Unither Pharmaceuticals

Rochester, United StatesFull time
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Location
Rochester, United States
Job type
Full time
Posted
Oct 13
7 days ago
Career path

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About the company

Unither Pharmaceuticals

Pharmaceuticals · 1,001 to 5,000 employees

Unither Pharmaceuticals on LinkedIn

What you'll do

  • Execute and support equipment qualifications, cleaning and process validations, and recertifications.
  • Collect samples and data, maintain validation documentation and equipment, and assist with audits and calibration coordination.

Key skills

validation protocolsequipment qualificationsprocess validationscleaning validationsgood documentation practicesDT Pro softwaretemperature/humidity loggerscalibrated state

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Read the full posting here
JOB SUMMARY: Assists validation efforts in many ways including the following: executes/supports equipment qualifications, cleaning validations and recertifications, chamber (i.e., freezers, refrigerators, incubators) recertifications, and process validations, takes and delivers samples, collects and compiles data for validation reports, assists in maintaining the Validation Document Library, maintains test equipment and department documentation. ESSENTIAL FUNCTIONS / RESPONSIBILITIES: •Assists in the execution of validation protocols ( qualification, process validations, and recertifications) for facilities, chambers, manufacturing equipment, manufacturing processes, cleaning, and critical utilities. •Performs proper and timely post cleaning sampling from manufacturing equipment. Confirms there is an appropriate amount of required sampling materials and supplies available. Orders are to be placed as needed to ensure supplies are maintained. Responsible for organization of supplies and materials, FIFO is consistently followed.. •Maintains department documentation in an orderly library so that information can be provided to regulatory bodies in a timely manner. Participates in audits (i.e., customer and regulatory) and retrieves Validation documentation as requested. •Ensures good documentation practices are followed during protocol executions, verifications, validation plans and summary reports generated during validation/ qualification activities are maintained according to procedure. •Become proficient using temperature/humidity loggers along with the associated DT Pro software. Responsibilities will include, programing, reading, generating reports, as well as conducting routine maintenance per department procedure. •Reviews documentation executed during validation activities and ensures completeness is performed contemporaneously. All applicable documentation is scanned and transferred to the activity’s applicable project folder and all completed hardcopies are filed accurately within the site’s documentation room. •Ensures all department testing equipment is maintained in a current calibrated state. Communicates and works with outside vendors to schedule, ship, track, and receive testing equipment to be sent for calibration. Confirms a current calibration certificate is received with each piece of testing equipment. Inventory and calibration status is maintained within Blue Mountain Regulatory Asset Manager (BMRAM)..

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