Position Title: Microbiology Technician
Work Location: Worcester, MA 01604
Assignment Duration: 12 Months (possible extension- performance based)
Work Schedule:
- Training: Monday–Friday for the first 6–12 weeks, 8:30 AM – 4:30 PM
- Post-Training: One position will work Sunday–Wednesday and the other will work Wednesday–Saturday, generally 8:30 AM – 4:30 PM
- Should be willing to work on weekends and holidays.
Position Summary:
- The Primary function would be to : Performs sample retain discard per GMP procedures. Performs routine Environmental Monitoring testing within a GMP environment.
Key Responsibilities:
- Performs sample retain discard per GMP procedures. Performs routine Environmental Monitoring testing within a GMP environment. Performs Environmental Monitoring (EM) during a fill operation.
- Supports other lab associated functions. Perform test methods as written to support product/material release. Effectively perform a multitude of laboratory techniques with minimal error for which they will be trained on.
- Understand, implement, and maintain GMP with respect to laboratory records, procedures, and systems in accordance with procedural requirements. Accept responsibility to complete assigned tasks as committed.
- Support investigation writers and approvers to gather data. effectively perform a multitude of laboratory techniques with minimal error for which they are or will be trained on. Writes or revises procedures with guidance.
- Works under the guidance of a supervisor but is able to manage their own time to ensure timely completion of assigned duties. Trends data to support trend reports.
Qualification & Experience:
- BS in Biology or other life science required
- QC Micro experience- -Hands- on experience with lab testing and EM.
- hands- on Aseptic Technique experience preferable.
- hands- on working experience in Biosafety hoods preferable.
- Attention to detail while running assays/ tasks in the lab and while performing EM is required
- Should have good organizational skills, ability to prioritize workload and extremely thorough with excellent attention to detail.
- Should perform tasks with supervision guidance, taking responsibility for complying with GMP requirements.
- Strong interpersonal / communication skills. Maintaining good working relationships within and outside the department.
- Adjusting quickly to new situations. Reprioritizing to meet schedule demands in continually changing work environment.
- Knowledge with the LIMS system, specifically entering results is preferred Knowledge of applicable regulations and standards affecting Pharmaceutical Products (e.g. USP, EP, JP pharmacopoeias, ICH guidelines, cGMP) is preferred.
- GMP and/or Clean-Room experience Clean-Room Gowning.
- Experience with cGMP documentation and record maintenance is required.
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