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Aseptic Manufacturing Technician
Job in
Cockeysville, Baltimore City, Maryland, 21030, USA
Listed on 2026-02-16
Listing for:
Jabil
Full Time
position Listed on 2026-02-16
Job specializations:
-
Manufacturing / Production
Pharmaceutical Manufacturing
Job Description & How to Apply Below
Overview
At Jabil we strive to make ANYTHING POSSIBLE and EVERYTHING BETTER. We are proud to be a trusted partner for the world's top brands, offering comprehensive engineering, manufacturing, and supply chain solutions. With over 50 years of experience across industries and a vast network of over 100 sites worldwide, Jabil combines global reach with local expertise to deliver both scalable and customized solutions.
Our commitment extends beyond business success as we strive to build sustainable processes that minimize environmental impact and foster vibrant and diverse communities around the globe.
- Complete and maintain aseptic qualification training.
- Obtain basic understanding of a task, unit operation and/or document (forms and/or SOPs) while aiding with oversight from Manufacturing Technician III and above.
- Attain and maintain gowning qualification per appropriate SOPs.
- Follow SOPs, product batch record instructions, logbooks and forms, and corresponding quality documentation in detail.
- Prepare and maintain accurate documentation following cGMP and GDP principles.
- Ensure documentations are completed in real-time in accordance to CGMP and GDP principles.
- Adhere to all environmental, health, and safety policies and procedures and proactively identify unsafe conditions.
- Support QC sampling, equipment calibration, equipment/utility validation, and preventive maintenance as needed.
- Work collaboratively with internal teams to meet site goals and objectives as part of a team.
- Initiate and foster a spirit of cooperation within and between departments.
- Review documentation for accuracy, make corrections and/or escalate to supervision/Manufacturing Quality Associate (MQA).
- Maintain all personal cGMP related training in a current state.
- Achieve and maintain cleaning and sanitization of cleanroom training.
- Participate in aseptic media qualification per the appropriate qualification protocol.
- Support manufacturing in the investigation of deviations and performs required risk assessments.
- Participate in personnel monitoring as requested.
- Work closely with Operational Excellence to identify and implement process improvements.
- Set up and breakdown the filling equipment per appropriate SOPs.
- Transport equipment and components as needed.
- Interact with filling machines at the validated speeds and volumes.
- Perform volume checks.
- Perform and document inherent and non-inherent interventions.
- Ensure slow and purposeful movements appropriate for a Grade A/B GMP aseptic environment.
- Work with R&D and tech transfer team for successful transfer of Programs into the GMP area.
- Perform all aseptic connections, respecting first air.
- Perform pre- and post-filter integrity testing as required.
- Aseptically sterile filter products into appropriate vessels.
- Complete routine and enhanced cleaning and sanitization of all controlled aseptic clean rooms, as needed.
- Attain and maintain ability to perform environmental tasks as required.
- Perform other duties as assigned.
- High school diploma or equivalent with 1-3 years’ experience, Bachelor’s degree with a minimum of 1 year of experience, or equivalent combination of education, training and professional experience that provides the individual with the required knowledge, skills, and abilities.
- Prior experience in related field, preferred.
- cGMP manufacturing knowledge, preferred.
- Aseptic filling and general production knowledge, preferred.
- Demonstrate basic math skills.
- Demonstrate the ability to establish good working relationships with other departments, including vendors, colleagues, and subordinates.
- Demonstrates the appropriate technical knowledge necessary to make sound decisions on development issues with minimal supervision.
- Demonstrate the ability to analyze data and information and assess and resolve complex problems/issues as required.
- Must be able to comprehend and follow all applicable SOPs.
- Demonstrate knowledge and experience with electronic Quality Management Systems such as Master Control and Trackwise.
- Demonstrate ability to acquire the appropriate knowledge from resources on the current federal, local, and international regulations regarding the production, testing, and…
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