Microbiology Technical Specialist – Contract
- Tampa, FL, United States
$30 USD / hour · Contract · Temporary
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Job details
- Pay
- $30 USD / hour
- Job type
- Contract · Temporary
- Apply by
- Experience
- Minimum of 5 years of relevant microbiology experience, preferably within pharmaceutical, biotechnology, medical device, or contract manufacturing (CDMO) environments.
- Posting language
- English
- Posted
Original job description
Microbiology Technical Specialist – Contract
Kelly Science & Clinical | Pharmaceutical Manufacturing
Location: Tampa, FL Area | Local Candidates Only
Job Type: Temporary / Contract
Start Date: ASAP
Schedule: Monday–Friday, with occasional weekend work and flexibility required
Compensation: Competitive, based on experience
Position Overview
Kelly Science & Clinical is seeking an experienced Microbiology Technical Specialist for a contract opportunity supporting a pharmaceutical manufacturing facility in the Tampa, FL area.
This position is ideal for a former Microbiology Supervisor, Microbiology Manager, or senior-level Microbiology professional with extensive hands-on laboratory experience who is looking to transition into a technical leadership and compliance-focused role.
The selected candidate will provide technical oversight and support for microbiology laboratory operations, regulatory compliance activities, investigations, qualifications, and continuous improvement initiatives.
This is a non-testing, non-people-management role. Candidates must possess a strong foundation in hands-on microbiology testing and be comfortable independently managing technical responsibilities, troubleshooting laboratory challenges, and driving projects to completion.
Key Responsibilities
- Provide technical support and subject matter expertise for microbiology laboratory operations, with an emphasis on bioburden testing and pharmaceutical microbiology.
- Support regulatory inspections, audit readiness, and laboratory compliance activities in accordance with applicable GMP and pharmacopeial requirements.
- Lead and support laboratory investigations, deviations, root cause analyses, corrective and preventive actions (CAPAs), and change controls.
- Author, review, and execute technical protocols, qualification documentation, investigation reports, and other GMP documentation.
- Support media qualifications, equipment qualifications, performance qualifications (PQ), and sterilization-related activities.
- Collaborate with cross-functional teams on laboratory automation initiatives, including automated plate-reading systems and updated microbial identification technology.
- Provide technical input and execution support for equipment implementation, validation, and qualification projects.
- Troubleshoot microbiological testing processes, laboratory equipment, and technical issues to ensure timely resolution.
- Participate in project meetings, technical discussions, and cross-functional initiatives involving microbiology and sterilization processes.
- Coordinate technical deliverables, track project progress, and proactively address challenges to maintain established timelines.
- Utilize electronic quality and laboratory systems to manage documentation, investigations, change controls, and laboratory records.
- Maintain compliance with GMP, applicable regulatory requirements, internal procedures, and laboratory quality standards.
Qualifications
Required Qualifications
- Bachelor’s degree in Microbiology, Biology, or a related scientific discipline preferred.
- Minimum of 5 years of relevant microbiology experience, preferably within pharmaceutical, biotechnology, medical device, or contract manufacturing (CDMO) environments.
- Previous hands-on microbiology laboratory testing experience, particularly bioburden testing.
- Strong working knowledge of pharmaceutical microbiology, GMP requirements, and applicable USP/pharmacopeial standards.
- Demonstrated experience supporting laboratory investigations, CAPAs, deviations, change controls, and technical documentation.
- Experience authoring or reviewing protocols, technical reports, and qualification documentation.
- Ability to independently troubleshoot complex technical issues and coordinate multiple projects.
- Excellent written and verbal communication skills, with the ability to collaborate effectively across departments.
- Strong organizational skills, attention to detail, and a proactive, solutions-oriented approach.
- Must be local to the area or within a reasonable commuting distance.
Preferred Qualifications
- Previous experience as a Microbiology Supervisor, Senior Microbiologist, or Senior Microbiology Technician.
- Experience in sterile pharmaceutical manufacturing, particularly injectable products, aseptic processing, and classified manufacturing environments.
- Knowledge of environmental monitoring, contamination control, and microbiological requirements for controlled environments.
- Experience with media qualifications, equipment qualifications, performance qualifications, and sterilization processes.
- Experience supporting laboratory automation, microbial identification systems, or automated plate-reading technologies.
- Familiarity with endotoxin testing.
- Experience using electronic quality and laboratory systems such as Documentum, CATSWeb, TrackWise, GLIMS, or comparable platforms.
- Background in pharmaceutical manufacturing, sterile injectables, medical devices, or CDMO operations.
Ideal Candidate Profile
The ideal candidate is a technically strong microbiology professional who can quickly step into a laboratory technical support role and contribute with minimal oversight.
This individual will bring a combination of hands-on microbiology expertise, regulatory compliance knowledge, investigation experience, and strong project execution skills.
Success in this position requires someone who is confident, self-directed, detail-oriented, and comfortable taking ownership of technical activities while collaborating with laboratory leadership and cross-functional stakeholders.
This opportunity is particularly well suited for an experienced Microbiology Supervisor or senior-level laboratory professional who enjoys solving technical problems, improving processes, and supporting regulatory compliance without direct personnel management responsibilities.
Why Join Kelly Science & Clinical?
At Kelly Science & Clinical, we connect talented scientific professionals with opportunities to make a meaningful impact in the pharmaceutical, biotechnology, and life sciences industries.
This contract opportunity offers the chance to contribute to critical microbiology compliance activities, laboratory modernization projects, and technical initiatives within a regulated manufacturing environment.
Apply today to learn more about this exciting opportunity with Kelly Science & Clinical!
Kelly is an equal opportunity employer committed to providing employment opportunities to qualified candidates.
10444074
More about this job
Skills
- Pharmaceutical processes
- Leadership
- Regulatory compliance
- Process improvement
- Troubleshooting
- Technical support
- Inspection
- Good manufacturing practices
- Documentation
- Troubleshoot
- Laboratory equipment
- Attend design meetings
- Biotechnology
- Perform laboratory tests
- Communication skills
- Organizational skills
- Attention to detail
- EMC Documentum
- Medical devices
- Personnel management