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Form of workJob Description
Ultimate Staffing is partnering with a pharmaceutical company in Round Rock whose seeking a Facilities & Maintenance Technician with HVAC experience to join their growing team! This role will be responsible for supporting the manufacturing and process development initiatives for a cGMP pharmaceutical facility. Continuous running operations are expected and will require this position to be flexible to after-hours support roles as assigned.
Overview:
This position will report to the Senior Manager, Facilities and Maintenance Engineering and will have interactions with members of other departments including Quality Control, Analytical/Stability, Manufacturing, Quality Assurance, Validation, R&D, and outside customers.
- Round Rock, Texas - Direct Hire
- Payrate: $25-$42/HR+ DOE | FLSA Status: Hourly, Non-Exempt
- Competitive Benefits Package
- Schedule: Monday-Friday 8AM-5PM with occasional on call, as needed
Responsibilities:
- Electrical installation, troubleshooting, and repair from 24VDC up to 3 phase 480VAC.
- Mechanical installation, troubleshooting, and repair.
- Ability to troubleshoot automation systems to include PLC's, HMI's, Vision Systems, Robotics, Servo's, etc.
- Maintain and Support Production Processes.
- Keep current on all required training and SOPs
- Assist in maintaining a clean laboratory.
- Adhere to safety protocols and policies.
- Ensure cGMP documentation is followed.
- Assist in developing maintenance and calibration procedures for assigned area(s).
- Track and trend production data, identify and implement process and/or equipment improvements that will improve business measures and/or increase overall equipment reliability.
- Draft and Perform qualifications on cGMP equipment/processes as necessary.
- Proactively ensure equipment is maintained to minimize disruption to production schedules.
- Provide Mechanical, Electrical, and Control System troubleshooting and Maintenance support to assigned area(s).
- Plan and execute new or existing equipment projects as assigned.
- Assist in investigating both in-process and field product complaints as well as the development and implementation of appropriate corrective actions as assigned.
- Keep Engineering and Operations informed of process issues and plans to resolve these issues.
- Provide support for Deviations and CAPA's for assigned area(s).
Qualifications:
- Relevant Work Experience or a Two -year Associates Degree in Industrial Maintenance, Industrial Systems, Instrumentation, Electrical Systems, Electronics, or similar field preferred.
- Minimum of 3 years work experience, in a cGMP pharmaceutical/medical device environment and FDA regulated experience preferred.
- Have in-depth knowledge of electrical hydraulics, mechanical, and automation control systems.
- Strong HVAC and/or PLC experience a plus.
- Ability to read and interpret electrical/mechanical schematics.
- Have in-depth knowledge of EHS (Environmental, Health and Safety).
- Must be able to create and follow written procedures relevant to assigned tasks.
- Work hours must be flexible to meet production timelines.
Core Competencies:
- Strong planning skills and project management skills.
- Must have effective written and verbal English communication skills.
-Detail oriented, self-motivated, and able to multitask in a production environment.
If you would like to be immediately considered, please apply or email your resume to Megan at:
All qualified applicants will receive consideration for employment without regard torace, color, national origin, age, ancestry, religion, sex, sexual orientation, gender identity, gender expression, marital status, disability, medical condition, genetic information, pregnancy, or military or veteran status.We consider all qualified applicants, including those with criminal histories, in a manner consistent with state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance.
