Maintenance Technician - Metrology Focus
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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 at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube.
Job Description
At AbbVie, we are looking for a Maintenance Technician with a focus on Metrology to join our team.
In this role, you will help ensure the availability, reliability, and compliance of production, laboratory, and utility equipment across the site. You will be responsible for performing and documenting preventive and corrective maintenance, calibration, verification, troubleshooting, and repair activities on measurement and control instruments, while ensuring compliance with Good Manufacturing Practice (GMP) and Good Practice (GxP) requirements, internal procedures, Environment, Health & Safety (EHS) standards, and applicable metrology guidelines.
You will also play a key role in supporting investigations, continuous improvement initiatives, and the installation and qualification of new or modified equipment, contributing to the operational excellence and quality standards that support AbbVie's mission.
Key Responsibilities
Execute preventive, predictive, and corrective maintenance work orders on equipment, facilities, and utilities, ensuring their safe and reliable return to service.
Perform calibration, verification, adjustment, and functional testing of measurement and testing equipment, including temperature, pressure, flow, level, mass, humidity, conductivity, pH, and other relevant parameters.
Diagnose electrical, electronic, mechanical, and instrumentation failures; repair or replace defective components and accurately document all interventions.
Ensure metrological traceability of standards and instruments, verify calibration status and certificate validity, and report any situation that could impact quality or compliance.
In the event of out-of-tolerance results, secure the affected equipment, record all relevant data, contribute to impact assessments, and participate in investigations, root cause analyses, and Corrective and Preventive Actions (CAPA) activities.
Complete work orders, records, certificates, and documentation accurately and on time within the computerized maintenance and metrology management systems.
Coordinate external service providers when required; verify the quality of services delivered and the compliance of associated documentation.
Provide technical support to Production, Quality, and Laboratory teams, particularly during investigations, qualifications, equipment commissioning, and modification projects.
Contribute to the continuous improvement of maintenance and calibration plans, criticality assessments, equipment reliability programs, standardization initiatives, and optimization of intervention frequencies.
Comply with GMP/GxP procedures, data integrity requirements, health and safety regulations, and environmental standards; maintain tools, standards, and work areas in good condition and complete all required training.
Maintain work areas, tools, and spare parts in a condition consistent with cleanliness requirements, contamination prevention measures, and foreign matter control standards.
Ensure all required training is completed before performing GMP-related tasks and actively contribute to audits, inspections, and periodic reviews.
Qualifications
Qualifications & Experience
Technical secondary education diploma or Bachelor's degree in Electromechanics, Electrical Engineering, Electronics, Instrumentation, Automation, Industrial Maintenance, or an equivalent discipline.
Relevant experience in industrial maintenance and/or metrology; experience within pharmaceutical, biotechnology, chemical, food manufacturing, or other regulated environments is an asset.
Practical knowledge of calibration principles, measurement uncertainty, tolerances, traceability, and measurement and test equipment management.
Ability to read and interpret technical drawings, electrical schematics, process diagrams, technical manuals, specifications, and procedures.
Proficiency in troubleshooting techniques and the safe use of measuring instruments, calibration standards, and testing equipment.
Knowledge of GMP/GxP requirements, data integrity principles, and good documentation practices; familiarity with ISO 17025 is desirable.
Experience using Computerized Maintenance Management System (CMMS), such as Maximo, as well as Microsoft Office applications.
Fluent in French, with the ability to read and work with technical documentation in English.
Key Competencies
Strong attention to detail, accuracy, and commitment to documentation quality.
Analytical mindset, structured problem-solving skills, and a reliability-focused approach.
Ability to work independently, prioritize effectively, and manage workload according to operational impact and criticality.
Strong team spirit, collaborative attitude, and willingness to contribute to collective objectives.
Clear communication skills, active listening, and effective collaboration with multidisciplinary teams, end users, and external suppliers.
Adaptability to changing priorities, technical challenges, and operational constraints.
Flexibility and availability to participate in on-call rotations, shift work, or urgent interventions as required by site operations.
Continuous improvement mindset, knowledge-sharing attitude, and ability to train or mentor colleagues.
Strong safety culture and consistent adherence to procedures.
Additional Information
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 only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html
US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
https://www.abbvie.com/join-us/reasonable-accommodations.html
Job details
How this role compares
Computed from every other active Manufacturing & CMC role in our database, not just this employer's listings.
We currently track 2556 comparable Manufacturing & CMC roles across 173 biopharma companies.
Salary context
663 of 2556 peers report a salary range (USD, annualized)
Peers share this role's job function. This posting doesn't list a seniority level, so peers aren't narrowed by seniority either -- the range below may span more levels than usual.
Where these roles are based
Top locations among the 2556 comparable roles
+ 50 more countries
Seniority mix
1172 of 2556 peers have a known seniority level
Therapeutic area mix
12 of 2556 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden
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Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.
0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.