Microbiology Department Project Lead

ABBVIE; Waco (TX); On-site; USD 97,000 - 184,000; Full time

Benefits offered by this job

401(k) plan

Paid time off

Medical/dental/vision insurance

Job summary

AbbVie is seeking a Microbiology Department Project Lead to act as the technical leader for a sterile pharmaceutical manufacturing site. You will oversee microbiological testing, environmental monitoring, contamination control, laboratory operations, and GMP documentation, while coordinating with cross-functional partners.

You will drive method qualification, investigations, deviations, CAPAs, and continuous improvement, mentor personnel, and ensure regulatory readiness for inspections and

Qualifications

• Bachelor's degree in a relevant field and technical experience in GMP environments.
• Strong knowledge of cGxPs and regulatory inspections.
• Experience leading cross-functional project teams in global or matrixed setups.
• Excellent written and spoken communication and problem-solving skills.
• Proficiency with standard Office applications.

Responsibilities

• Lead microbiology projects and provide scientific oversight for testing and environmental monitoring.
• Manage change controls, investigations, deviations, CAPAs, and quality records.
• Author, review, and approve microbiology procedures and validation activities.
• Coordinate with QA, Manufacturing, Engineering, Validation, and Regulatory Affairs.
• Mentor staff and drive continuous improvement in laboratory operations.

Skills

Communication

Interpersonal skills

Project Management

Cross-functional leadership

Regulatory knowledge

Education

Bachelor's degree in Science/Engineering/Business Management or equivalent technical work experience

Tools

Office 365

Job description

• Compensation: USD 96500 - USD 183500 - yearly

Company Description

About AbbVie

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us atwww.abbvie.com . Follow @abbvie onLinkedIn, Facebook ,Instagram ,X andYouTube.

Job Description

The Microbiology Department Project Lead serves as the technical leader for a sterile pharmaceutical manufacturing site, overseeing microbiological testing, environmental monitoring, contamination control, laboratory operations, projects, change controls, GMP documentation, method qualification and validation, investigations, deviations, and CAPAs. The role also coordinates with cross-functional partners, assesses microbiological risks, drives continuous improvement, monitors regulatory and scientific developments, supports inspections and audits, analyzes data and trends, manages project resources, and mentors personnel while championing scientific excellence, compliance, and operational effectiveness.

For a Microbiology Department Project Lead role supporting a sterile pharmaceutical manufacturing site, you can position the role as the technical leader responsible for microbiology program governance, laboratory projects, and quality system improvements.

Key Responsibilities

• Serve as the technical lead for the Microbiology department, providing scientific oversight and guidance for microbiological testing, environmental monitoring, contamination control, and laboratory operations.
• Lead and manage microbiology-related projects from initiation through implementation, ensuring alignment with business objectives, regulatory requirements, and site priorities.
• Own and coordinate microbiology change controls, assessing technical impact, defining implementation strategies, and ensuring timely closure of quality records.
• Author, review, approve, and implement microbiology procedures, specifications, protocols, and technical documents to maintain compliance with current GMP requirements.
• Lead method qualification, verification, validation, and transfer activities for microbiological and rapid microbiological methods.
• Provide technical review and approval of investigations, deviations, laboratory events, and CAPAs related to microbiological processes and testing.
• Partner with Quality Assurance, Manufacturing, Engineering, Validation, and Regulatory Affairs to support product and process changes, new product introductions, and operational improvements.
• Assess microbiological risks associated with process changes, equipment modifications, facility upgrades, and contamination control strategies.
• Drive continuous improvement initiatives to enhance laboratory efficiency, data integrity, compliance, and contamination control effectiveness.
• Monitor and interpret emerging regulatory expectations, industry standards, and scientific advancements to ensure microbiology programs remain compliant and inspection-ready.
• Support regulatory inspections and customer audits by serving as the microbiology subject matter expert and presenting technical justifications, data, and program strategies.
• Analyze microbiological data and trends to identify risks, improve process understanding, and recommend actions that strengthen product quality and patient safety.
• Coordinate cross-functional teams to ensure successful execution of microbiology projects, timelines, deliverables, and resource planning.

Preferred Leadership Responsibilities

• Act as the primary microbiology SME for technical decision-making and strategic laboratory initiatives.
• Mentor microbiologists and laboratory personnel on scientific principles, regulatory expectations, and best practices.
• Champion a culture of scientific excellence, compliance, continuous improvement, and operational effectiveness within the Microbiology organization.

Qualifications

• Bachelor’s degree in Science/Engineering/Business Management or equivalent technical work experience
• 5+ years of relevant Quality experience in a GMP pharmaceutical, biologics, and/or medical device manufacturing environment
• Strong understanding of cGxPs, regulatory inspections, regulatory documents, global regulations, and standards
• Experience in Project Management and leading cross-functional project teams with technical professionals in a global and/or complex, matrixed organization
• Strong oral and written communication, interpersonal, time management, influence, and problem-solving skills
• Proficient in the use of standard software applications including Office 365

Additional Information

Applicable only to applicants applying to a position in any location with pay disclosure requirements under state orlocal law:

The compensation range described below is the range of possible base pay compensation that the Companybelieves ingood faith it will pay for this role at thetimeofthis posting based on the job grade for this position.Individualcompensation paid within this range will depend on many factors including geographiclocation,andwemay ultimately pay more or less than the posted range. This range may bemodified in thefuture.

We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick),medical/dental/visioninsurance and 401(k) to eligibleemployees.

This job is eligible toparticipate in our short-term incentiveprograms.

Note: No amount of payis considered to bewages or compensation until such amount is earned, vested, anddeterminable.Theamountandavailabilityof anybonus,commission, incentive, benefits, or any other form ofcompensation and benefitsthat are allocable to a particular employeeremains in the Company'ssole andabsolutediscretion unless and until paid andmay bemodified at the Company’s sole and absolute discretion, consistent withapplicable law.

AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.

US & Puerto Rico applicants seeking a reasonable accommodation,