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Quality Control Microbiologist

Quality Control Microbiologist

Piramal Pharma SolutionsSellersville, PA, US
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Job Description

Job Overview

Under minimal direction from the manager, the QC Microbiologist I performs water testing, media preparation, and growth promotion of media. Additional opportunity for raw material testing, finished product testing, stability testing, antibiotic assay testing, gram staining, microbial enumeration suitability testing, antimicrobial effectiveness testing, and other microbial testing as needed. Work is completed with an overall quality and efficiency. Writes, updates, and evaluates new test methods and procedures. Attends team meetings and coordinates projects within the laboratory. This is a safety sensitive position.

Responsibilities

  • Perform routine water testing, media preparation, growth promotion of media, and environmental monitoring
  • Maintain cleanliness and organization of shared laboratory areas, ensuring a safe, tidy, and compliant working environment by taking ownership of general housekeeping duties.
  • Participate in stock inventory management, including placing orders as needed with minimal supervision.
  • Conduct routine Microbial Examination Testing (raw materials, finished products, stabilities).
  • Assist with Microbialsuitability testing, antimicrobial effectiveness testing, antibiotic assay testing, gram staining, and other microbial testing as needed.
  • Support other teams by performing routine testing when requested.
  • Adhere to Environmental, Health and Safety policies and procedures.
  • Flexibility to work overtime or weekends occasionally, as needed.

Education

  • B.S. in microbiology, biology or related life science.
  • Experience

  • B.S. with minimum 0-4 years related pharmaceutical microbiology experience.
  • Advanced degree in scientific field with 3 yrs. related experience.
  • Knowledge of autoclave usage, media preparation, aseptic technique, balance use, pH meter, environmental monitoring, and general plating practices.
  • Able to perform assigned task from start to finish independently without error. Including standard, sample, and reagent preparation through data processing and submission.
  • Specialized / Technical Knowledge

  • Working knowledge of aseptic technique, environmental monitoring, and microbial examination methods.
  • Knowledge of FDA, USP, ICH, cGMP, and cGLP requirements in a pharmaceutical quality control laboratory.
  • Proficient in LIMS, Microsoft Office Suite, and electronic data management systems.
  • Functional Skills

  • Strong organizational skills and attention to detail.
  • Excellent at multitasking, handling multiple projects at one time, and changing priorities based on business needs.
  • Takes ownership of tasks and working area.
  • Self-motivated with a proactive approach to problem-solving.
  • Excellent interpersonal and communication skills.
  • Effective time management skills.
  • Physical Requirements

  • Lift / move up to 10 lbs. and occasionally 25 lbs.
  • Individual may be required to handle hazardous and non-hazardous materials.
  • Individual may be required to wear Personal Protective Equipment.
  • Not allergic to chemicals or biosubstances found in the laboratory or production facilities.
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