[Close] 

Facilities Manager

3002383 The world's most revolutionary biopharma companies are partnering with Agilent Technologies to advance the next frontier of medicine. Agilent continues to invest in capacity and expansion of its Colorado operations. Join our team of professionals dedicated to the development and commercialization of nucleic acid therapeutics for life changing, lifesaving medicines. Join a growing team with this exciting new opportunity for a Facilities Manager in our Engineering and Facilities group at our GMP facility in Frederick, Colorado. Work in our dynamic, fast-paced, API-Biopharma manufacturing environment with the ability to contribute to the growing industry of oligonucleotide (DNA-RNA) basedtherapeutics. Essential Duties Include: Supervision of Frederick Facilities process maintenance technicians / process mechanics, I&E / calibration technicians, and field service technicians. Oversees installation, troubleshooting, repair, preventive maintenance, calibration, and spare parts management of cGMP equipment and devices used in the manufacture of Active Pharmaceutical Ingredients (API) and implements policies todrive operational excellence in the areas of predictive maintenance. Supports utilization and design of cGMP production facilities including operational capacity, utility design, HVAC for controlled environments, control and monitoring along with design of equipment required for compliant safe manufacture of product. Oversees and manages troubleshooting of manufacturing equipment issues. Develops processes and implements solutions that drive continuous improvement. Responsible for management and support of QA related activities relevant to the Facilities team including electronic maintenance work records, calibration records, non-conformances / deviations, change controls, CAPAs, and participation in customer and agency audits. Responsible for management and support of EHS related activities relevant to the Facilities team including the hazardous area monitoring (LEL/O2) system, coordination of work in Class I Div I/II electrically classified areas, and Process Safety Management (PSM) compliance. Responsible for systems that are used for maintenance of cGMP equipment and instrumentation including the computerized maintenance management systems (CMMS) and all changes implemented. Managerial responsibilities include development of reports through coaching and training, responsible for scheduling, directing activities, budgeting, and hiring for department. Travel RequiredOccasionalSecondary LocationsDurationNot applicableRegionAmericasRequirements Qualifications Required: University degree or equivalent combination of education and or experience. 10+ years of equivalent experience in maintenance of equipment/facilities in a pharmaceutical and/or biologics area. 5+ years of equivalent experience in management within a cGMP production facility, including supervision and coordination of personnel responsible for process equipment troubleshooting, PMs, and calibration. Desired: Experience with maintenance and repairs of fluid handling and thermal control equipment (pumps, agitators, automated valves, piping systems, instruments, and temperature control module skids). Experience with electrical maintenance and troubleshooting of process and mechanical systems. Experience as owner of computerized maintenance management system (CMMS) software including Blue Mountain Regulatory Asset Manager (RAM), Maximo, SAP, or similar. Ability to read and interpret documents such as operating and maintenance instructions, Process and Instrumentation Diagrams (P&IDs), electrical and controls schematics, site drawings, equipment manuals, and safety procedures. Demonstrated communication skills, including verbal and written communication, in contact with vendors, internal customers, and employees. Knowledge of Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP). Knowledge of OSHA, PSM, Class I Div I/II electrically classified areas, lock-out tag-out, confined space, hot work permits, and standard EHS related workpractice requirements. Ability to work in a dynamic and progressive environment. Exceptional people skills, technical knowledge and influential leadership ability. Agilent Technologies, Inc. is an Equal Employment Opportunity and Affirmative Action employer. We value diversity at all levels. All individuals, regardless of personal characteristics, are encouraged to apply. All qualified applicants will receive consideration for employment without regard to sex, pregnancy, race, religion or religious creed, color, gender, gender identity, gender expression, national origin, ancestry, physical or mental disability, medical condition, genetic information, marital status, registered domestic partner status, age, sexual orientation, military or veteran status, protected veteran status, or any other basis protected by federal, state, local law, ordinance, or regulation and will not be discriminated against on these bases.
Salary Range: NA
Minimum Qualification
11 - 15 years

Don't Be Fooled

The fraudster will send a check to the victim who has accepted a job. The check can be for multiple reasons such as signing bonus, supplies, etc. The victim will be instructed to deposit the check and use the money for any of these reasons and then instructed to send the remaining funds to the fraudster. The check will bounce and the victim is left responsible.