QC Microbiologist

Staffing Resource Group, Inc; Tampa (FL); On-site; USD 88,828,000 - 97,424,000; Full time

Job summary

Staffing Resource Group, Inc. seeks a QC Microbiologist I to perform microbiological testing across raw materials, in-process and finished products, and environmental samples in a Tampa laboratory.

You will identify microorganisms, run sterility tests, and support investigations into deviations while contributing to continuous improvement. The role requires an associate degree (bachelor’s preferred), at least three years in a GMP/pharma setting, and proficiency with LIMS/eQMS and data tools.

Qualifications

• Associate degree in scientific discipline required; bachelor’s preferred.
• Minimum three years in pharma/GMP regulated environment.
• Knowledge of microbiological techniques and aseptic practices.
• Familiarity with USP <60>,<61>, and <62>, and environmental monitoring programs.

Responsibilities

• Perform microbiology testing of raw materials, in-process, utilities, water sampling/testing, finished products and environmental monitoring.
• Perform growth promotion and sterility testing of media.
• Investigate deviations and report findings.
• Maintain equipment and media; ensure lab supplies.
• Support audits and review SOPs/test methods related to microbiology.
• Travel between local Tampa worksites as needed.

Skills

Microbiology techniques

Aseptic practices

USP knowledge

LIMS

eQMS

Microsoft Office

Data analysis

Attention to detail

Problem solving

Communication

Education

Associate degree in scientific discipline (Microbiology, Biological Sciences)

Bachelor’s degree preferred

Tools

LIMS

eQMS

Microsoft Office

Job description

Title: QC Microbiologist ILocation: Tampa, FLIndustry: PharmaceuticalHours: M-F, 8am-5pm with possible OT and/or weekendsHourly Rate: $31/hr.-$34/hr. based on experienceEmployment Type: Contract positionSummary:The Quality Control (QC) Microbiologist I is responsible for performing microbiological testing of raw materials, utilities, in-process samples, water sampling/testing, finished products, and environmental monitoring samples to ensure compliance with regulatory requirements, company procedures, and quality standards. Perform microorganism identification. Perform growth promotion and sterility testing of media. This role supports manufacturing operations by providing accurate and timely microbiological data, investigating deviations, and contributing to continuous improvement initiativesKey Accountabilities:Performs, analyzes, and interprets QC and microbial limits testing according to USP and regulatory requirements for raw materials, finished products, and stability samples.Perform environmental monitoring, which includes water sampling and testing.Perform microbiology methods and sampling techniques.Perform microorganism identification.Report, investigate, and write deviations and investigations.Receive media. Perform growth promotion and sterility testing.Manages/supports microbiology projects.Execute validation protocols for test methods and equipment qualification.Provide support during audits.Review SOPs and test methods related to microbiology.Ensure the microbiological integrity of the environment, equipment, and facilities.Manage product testing based upon internal and customer specifications.Manage 3rd party laboratory testing and report results.Reports on testing results, including CoA s.Maintain equipment and media.Ensure the micro lab is adequately supplied and maintained.Perform other responsibilities to support the business as requested.Adhere to all defined Safety and Sustainability requirements and expectations and seek clarification whenever Safety and Sustainability requirements and expectations are either unknown or unclear.Promptly report identified Safety and Sustainability issues, problems, deficiencies, errors, incidents, and/or opportunities to management and correct where possible.Adhere to current Good Manufacturing Practices (cGMP), FDA, EMA, USP, and other applicable regulatory requirementsTrend environmental monitoring and utility data and identify potential issues.Recommend process improvements to enhance laboratory efficiency and compliance.Stop work where deemed necessary to maintain safety.Must be able to travel between local worksites in Tampa during the workday, as needed.Qualifications:Education and Experience:Minimum of associate s degree in scientific discipline (Microbiology, Biological Sciences, Biology), Bachelors Degree highly preferredMinimum of three years of pharmaceutical or relevant FDA/GMP regulated environmentTechnical SkillsKnowledge of microbiological techniques and aseptic practices.Familiarity with USP <60>,<61>, and <62>, and environmental monitoring programs.Experience with laboratory systems such as LIMS and electronic quality management systems.Understanding of cGMP requirements and microbiological investigations.Experience with data tools (Microsoft Office)CompetenciesAttention to detailAnalytical and problem-solving skillsStrong written and verbal communicationTime management and prioritizationAbility to work independently and within cross-functional teamsData analysis and trending capabilitiesWorking ConditionsLaboratory and manufacturing environment.May require weekend, holiday, or 12-hour shift coverage.Use of personal protective equipment (PPE) and adherence to safety procedures required.Success MetricsTimely completion of microbiological testing.Accuracy and integrity of laboratory data.Compliance with GMP and regulatory requirements.Effective investigation and resolution of laboratory deviations.Support of manufacturing schedules and product release timelines.EOE/ADAIND123