Quality Control Technician II

Job Description

Job Description

Job Description:
Sun-Wed and Wed-Sat, offsetting the two assignments. The first 6-12 weeks would be Monday-Friday because of training. 8:30 am to 430 pm.

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.
Should be willing to work on weekends and holidays.

Top Skills:
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.

MUST be flexible working weekends and holidays.
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

Nice to have:
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

EEO:
Mindlance is an Equal Opportunity Employer and does not discriminate in employment on the basis of Minority/Gender/Disability/Religion/LGBTQI/Age/Veterans.