Help protect product quality and patient safety by playing a vital role in environmental monitoring within a cutting-edge pharmaceutical environment.
Support manufacturing and validation activities by performing environmental monitoring, sampling, testing, and ensuring compliance with sterility assurance programs. Work collaboratively in a team environment to maintain high-quality standards and contribute to the success of operational goals.
Primary Responsibilities
- Collect environmental monitoring samples, including particulate, viable surface, air, and water samples.
- Perform laboratory and equipment cleanings.
- Read plates and interpret results of microbiological testing assays.
- Accurately complete laboratory data forms, logbooks, and other required documentation in compliance with cGMPs, CFR, and SOPs.
- Interact effectively with team members, supervisors, and lab customers.
- Meet established timelines and goals for delivering data.
- Follow all general and laboratory SOPs.
- Report observations of ongoing tests to management.
- Provide operational support for manufacturing activities.
- Contribute to departmental goals and overall operations.
Skills & Requirements
- Strong oral and written communication skills.
- Adaptability, flexibility, and ability to prioritize tasks effectively.
- Ability to manage individual responsibilities while collaborating as part of a team.
- Capability to work on multiple projects simultaneously.
- Bachelor's degree in Biology, Microbiology, or a related Life Science field.
- Familiarity with FDA and worldwide quality compliance regulations.
- Commitment to continuous training, skill development, and maintaining data integrity.