Microbiology Analyst I

RXinsider LTD.; Columbia (SC); Hybrid; USD 45,000 - 65,000; Full time

Job summary

RXinsider LTD. is seeking a QC Microbiology Analyst I to perform microbiology testing of raw materials, in-process and finished products per USP methods and cGMP guidelines. You will also train staff, review results, and assist investigations to support product release.

The role requires 1+ year of pharma microbiology experience, aseptic technique know-how, and strong documentation skills in a fast-paced laboratory environment.

Qualifications

• Regionally accredited Bachelor's Degree in Biology, Microbiology, or Life Sciences; Master’s preferred.
• At least 1-year experience working directly with Pharmaceutical Microbiology methods.
• 1–2 years of experience in general laboratory skills and aseptic technique.

Responsibilities

• Perform microbiology testing of raw materials, in-process and finished product samples per USP methods and approved procedures.
• Notify Microbiology management of all OOS and OAL results.
• Provide feedback on SOPs, forms, logbooks, etc., to improve procedures.
• Perform routine testing to support release and company needs.
• Train fellow QC lab personnel on QC test methods.
• Interpret test results relative to acceptance of tested lots.
• Generate data for investigations and trend reports; data entry for systems.
• Document and communicate OOS/OOT results and investigations; assist Sample Management with receiving and waste destruction.
• Perform method validation testing when requested.
• Maintain housekeeping and station upkeep in the lab.
• Communicate observations and issues to QC leadership.

Skills

Microsoft Office

cGMP documentation

Interpersonal communication

Multitasking

Problem solving

Regulatory quality systems

Written communication

Willingness to training

Education

Bachelor’s Degree in Biology/Microbiology/Life Sciences

Master’s degree (preferred)

Job description

Job Purpose

The QC Microbiology Analyst I performs microbiology department related raw material, in-process, and finished product testing according to USP methods and established procedures that follow cGMP guidelines and demonstrate outstanding aseptic techniques. Must demonstrate a high level of proficiency in Microbiology testing.

Essential Duties And Responsibilities

• Applies quality scientific techniques in the microbiological analysis of raw materials; in-process & finished product samples to include: sterility, bioburden, identification, environmental monitoring, growth promotion, microbial recovery and media fill tests following approved procedures.
• Notifies Microbiology management of all OOS and OAL testing results.
• Provides feedback on SOPs, forms, logbooks, etc., as necessary, to facility ever-changing expectations for operating procedures and testing-related information.
• Performs routine testing of products to support release and company needs.
• Trains fellow QC laboratory personnel on QC test methods.
• Demonstrates ability to understand and interpret test results in relation to acceptance or rejection of lot tested.
• Generates data, as needed, for investigations; performs data entry for various systems and processes, and understands the necessity of trending reports
• Reports and initiates documentation and communication of OOS and OOT results and investigation reports.Assists the Sample Management team with sample receiving and waste destruction, as needed.
• Performs method validation testing if requested by supervisor.
• Performs general laboratory housekeeping and upkeep of various testing stations.
• Communicates all Microbiology-related observations, issues, problems, discrepancies, and any violation of company policies or procedures to QC Microbiology Shift Lead, QC Microbiology Supervisor, QC Microbiology Operations Manager, Director of Microbiology, or designee.

Supplemental Functions

• Performs other duties as assigned.

Job Specifications And Qualifications

Knowledge & Skills

• 2 – 4 years of experience with Microsoft Office programs, as well as the ability to learn new systems and computer software programs effectively and efficiently required.
• Experience with cGMP documentation systems and with implementation of quality control systems.
• Strong interpersonal, verbal, and written communication skills; effectively multi-tasking and problem solving skills.
• Must maintain flexibility in the assignments of tasks, and be open to receive and provide training in multiple areas.
• Knowledge of FDA manufacturing/regulatory quality systems regulations, qualifications, facilities, and requirements.
• Accepting of new changes in order to achieve department demands.
• Must possess effective written and oral communication skills and be able to handle multiple tasks within limited time frames.
• Aseptic technique and familiarity with cGMPs and regulatory requirements is required.
• Specific expertise, skills and knowledge within microbiology gained through education and experience.
• A broad perspective that aligns decisions to organizational objectives and long term consequences of day-to-day activities.
• The ability to take strategic objectives and accept accountability to drive results through effective actions.
• The ability and willingness to change direction and focus to meet shifting organizational and business demands.The ability to effectively manage one self, demonstrates integrity, be productive under pressure, and achieve development goals.
• Position requires bending, typing, lifting, reaching, vision, standing (50%), sitting (10%), walking (20%), and hearing.
• Incumbents required to wear safety glasses, gloves, laboratory coats and other non-specified protective equipment as necessary.

Education/Experience

• Regionally accredited Bachelor’s Degree in Biology, Microbiology, or Life Sciences, required; Master’s degree, preferred.
• At least 1-year experience working directly with Pharmaceutical Microbiology methods.
• 1 – 2 years of experience in general laboratory skills and a knowledge of aseptic technique.

Working Conditions / Physical Requirements

• This position requires bending, typing, lifting (up to 40 1bs.), standing, sitting and walking throughout the facility.
• Hours of work: 12-hour rotating shifts.
• Salary range: Based on experience.