Microbiologist

TekWissen LLC; Greenville (NC); On-site; USD 55,000 - 90,000; Full time

Job summary

TekWissen Group has a temporary microbiology opportunity in Greenville, NC for a QC Microbiologist/Scientist II. The role focuses on performing moderately complex microbiological analyses in a pharmaceutical lab, testing raw materials, in-process and finished products, and supporting development and manufacturing operations with validated methods.

Candidates should have 3+ years of pharma microbiology experience, familiarity with GMP/GLP, and be able to document results and communicate findings

Qualifications

• Bachelor's degree in Biology or Chemistry preferred.
• 3+ years pharmaceutical microbiology experience.
• Experience with LIMS or document management systems.
• Knowledge of GMP/GLP compliance.

Responsibilities

• Conduct microbiological testing using validated methods.
• Identify and report OOS and non-routine results.
• Maintain and troubleshoot laboratory instruments.
• Prepare regulatory documentation and SOPs.
• Ensure GMP/GLP compliance and safety.

Skills

GMP/GLP knowledge

Analytical testing

Quality documentation

Lab teamwork

Education

Bachelor's degree in Biology or Chemistry

Associate degree in Biotechnology or related field

Tools

LIMS

SLIM

TrackWise

Documentum

Job description

Overview

TekWissen is a global workforce management provider headquartered in Ann Arbor, Michigan that offers strategic talent solutions to clients worldwide. The job opportunity below is with one of our clients specializing in biotechnology product development services. The client is dedicated to supplying laboratory equipment, chemicals, supplies, and services essential in healthcare, scientific research, safety, and education. As a global leader in serving the scientific community, the organization generates approximately $40 billion in annual revenue and is committed to making the world healthier, cleaner, and safer. Their global team delivers innovative technologies, convenient procurement solutions, and pharmaceutical services through industry-leading brands.

Position

Microbiologist

Location

Greenville NC 27834

Duration

12 Months

Job Type

Temporary Assignment

Work Type

Onsite

Shift

Monday To Friday from 08:00 AM to 05.00 PM

Summary

QC Scientist II / QC Microbiologist perform moderately complex microbiological analyses in a pharmaceutical microbiology laboratory. Test raw materials, in-process products, finished products, stability samples, and production intermediates. Support internal development and manufacturing operations through validated microbiological testing. Identify analytical issues, recommend solutions, and communicate accurate results. Ensure compliance with GMP, GLP, SOPs, and laboratory safety requirements.

Responsibilities

• Conduct microbiological testing using internally developed and compendial methods.
• Perform Bioburden, Bacterial Endotoxin, Particulate Matter, Sterility, and Water testing.
• Identify and report OOS, unexpected, and non-routine analytical/product results.
• Troubleshoot microbiological testing issues and recommend appropriate solutions.
• Maintain and troubleshoot analytical laboratory instruments.
• Document, review, and report test results in accordance with laboratory procedures.
• Communicate testing results with internal departments, clients, agencies, and external stakeholders.
• Prepare and support regulatory documentation.
• Develop and maintain SOPs, instructional documents, and method validation reports.
• Maintain laboratory equipment, supplies, and testing materials.
• Maintain clean, organized, and compliant laboratory work areas.
• Follow GMP, GLP, SOP, safety, and quality requirements.
• Support continuous improvement and PPI initiatives.

Required Skills

• Bachelor's degree in Biology or Chemistry preferred; Associate degree in Biotechnology or a related scientific field minimally required.
• 3+ years of pharmaceutical microbiology or related laboratory experience.
• Experience with LIMS, SLIM, TrackWise, or Documentum.
• Reviewer/approver or qualified checker experience.
• Experience supporting continuous improvement/PPI initiatives.
• Knowledge of microbiological method development and validation.
• Experience with qualitative and quantitative microbiological testing.
• Knowledge of chemistry and analytical instrumentation.
• Knowledge of pharmaceutical quality and regulatory requirements.
• Ability to interpret technical procedures and applicable governmental regulations.
• Strong analytical, mathematical, troubleshooting, and problem-solving skills.
• Strong written and verbal communication skills.
• Ability to prepare SOPs and method validation reports.
• Strong attention to detail, organization, and time management.
• Ability to work independently and collaboratively.
• Strong ownership, accountability, and customer focus.
• Ability to safely perform laboratory work while using required PPE.

TekWissen Group is an equal opportunity employer supporting workforce diversity.