Medivant Healthcare
Base pay range
$45,000.00/yr - $60,000.00/yr
About Medivant Healthcare Medivant Healthcare is a U.S.-based pharmaceutical manufacturer focused on producing high-quality, sterile injectable medications for hospitals and healthcare providers nationwide. With state-of-the-art, FDA-inspected facilities in Chandler and Deer Valley, Arizona, Medivant is committed to manufacturing excellence, regulatory compliance, and operational innovation.
Job Title - Engineering Associate Position Summary
The Engineering Associate – Entry Level will support the manufacturing engineering team in maintaining, troubleshooting, and improving pharmaceutical production systems and processes. This position is ideal for a recent engineering graduate or early-career professional interested in gaining hands‑on experience in a regulated pharmaceutical manufacturing environment.
Key Responsibilities
Assist in troubleshooting and resolving mechanical, electrical, or process issues on production equipment.
Support preventive maintenance, equipment qualification (IQ/OQ/PQ), and calibration programs.
Document engineering activities, changes, and test results in accordance with cGMP and FDA standards.
Participate in process improvement initiatives focused on efficiency, reliability, and compliance.
Collaborate with production, quality, and validation teams to support manufacturing operations.
Assist with data collection, analysis, and reporting to identify trends or potential process improvements.
Maintain accurate and timely records within engineering logs and databases.
Ensure safety standards and company policies are upheld in all operations.
Qualifications Required:
Bachelor’s degree in Mechanical, Electrical, Industrial, Chemical, or related Engineering discipline.
0–2 years of experience (internship or co-op experience in a manufacturing or regulated industry preferred).
Basic understanding of mechanical systems, instrumentation, and process equipment.
Strong analytical, problem‑solving, and technical documentation skills.
Ability to work collaboratively across departments and communicate effectively.
Proficiency in Microsoft Office and basic CAD tools (AutoCAD, SolidWorks, or similar).
Preferred:
Experience or coursework in pharmaceutical, biotech, or cleanroom environments.
Knowledge of cGMP, FDA, or ISO 9001 standards.
Familiarity with PLCs, control systems, or automated equipment.
Work Environment & Physical Requirements
This is a full-time, onsite role in Chandler or Deer Valley, AZ. The position involves working in a cleanroom and production environment. Must be able to stand for extended periods, occasionally lift up to 25 lbs, and wear appropriate PPE when required.
45K-60K annually plus company bonuses
Comprehensive medical, dental, and vision coverage.
401(k) with employer match.
Paid time off, holidays, and opportunities for career growth within a rapidly expanding company.
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About Medivant Healthcare Medivant Healthcare is a U.S.-based pharmaceutical manufacturer focused on producing high-quality, sterile injectable medications for hospitals and healthcare providers nationwide. With state-of-the-art, FDA-inspected facilities in Chandler and Deer Valley, Arizona, Medivant is committed to manufacturing excellence, regulatory compliance, and operational innovation.
Job Title - Engineering Associate Position Summary
The Engineering Associate – Entry Level will support the manufacturing engineering team in maintaining, troubleshooting, and improving pharmaceutical production systems and processes. This position is ideal for a recent engineering graduate or early-career professional interested in gaining hands‑on experience in a regulated pharmaceutical manufacturing environment.
Key Responsibilities
Assist in troubleshooting and resolving mechanical, electrical, or process issues on production equipment.
Support preventive maintenance, equipment qualification (IQ/OQ/PQ), and calibration programs.
Document engineering activities, changes, and test results in accordance with cGMP and FDA standards.
Participate in process improvement initiatives focused on efficiency, reliability, and compliance.
Collaborate with production, quality, and validation teams to support manufacturing operations.
Assist with data collection, analysis, and reporting to identify trends or potential process improvements.
Maintain accurate and timely records within engineering logs and databases.
Ensure safety standards and company policies are upheld in all operations.
Qualifications Required:
Bachelor’s degree in Mechanical, Electrical, Industrial, Chemical, or related Engineering discipline.
0–2 years of experience (internship or co-op experience in a manufacturing or regulated industry preferred).
Basic understanding of mechanical systems, instrumentation, and process equipment.
Strong analytical, problem‑solving, and technical documentation skills.
Ability to work collaboratively across departments and communicate effectively.
Proficiency in Microsoft Office and basic CAD tools (AutoCAD, SolidWorks, or similar).
Preferred:
Experience or coursework in pharmaceutical, biotech, or cleanroom environments.
Knowledge of cGMP, FDA, or ISO 9001 standards.
Familiarity with PLCs, control systems, or automated equipment.
Work Environment & Physical Requirements
This is a full-time, onsite role in Chandler or Deer Valley, AZ. The position involves working in a cleanroom and production environment. Must be able to stand for extended periods, occasionally lift up to 25 lbs, and wear appropriate PPE when required.
45K-60K annually plus company bonuses
Comprehensive medical, dental, and vision coverage.
401(k) with employer match.
Paid time off, holidays, and opportunities for career growth within a rapidly expanding company.
#J-18808-Ljbffr