QuVa Pharma

Facility & Manufacturing Engineer

QuVa Pharma • $70K — $95K *
Sugar Land, TX 77479In-Person
Pharmaceuticals & Biotech
Less than 5 years of experience
Today
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Job Overview by Ladders

Qualifications

  • Bachelor's in Mechanical Engineering or equivalent with 2+ years in manufacturing; or Associate's with 5+ years experience.
  • Ability to pass drug and background checks.
  • Understanding of equipment/instrument calibration principles.
  • Direct experience with large scale MEP systems.
  • Familiarity with Honeywell EBI building management systems.
  • Experience in cleanroom design, operation, and maintenance.
  • Knowledge of pharmaceutical-grade compressed air systems.

Responsibilities

  • Provide technical support for operations and ensure mechanical elements are designed and functioning.
  • Generate and execute validation project plans and related protocols and reports.
  • Develop and write specifications for production equipment across various stages of manufacturing.
  • Support design, commissioning, and qualification of production equipment.
  • Maintain and revise site-level facility drawings as necessary.
  • Develop site and departmental metrics to assess performance and identify improvement opportunities.

Benefits

  • Comprehensive health and wellness benefits including medical, dental, and vision.
  • 401k retirement program with company match.
  • 17 paid days off plus 8 paid holidays annually.
  • Opportunities for future career advancement in a high-growth industry.
Full Job Description
Our Facility / Manufacturing Engineer plays a vital role in ensuring the highest quality and safety standards of our pharmaceutical products. Once you complete our training, your responsibilities will include providing MEP support around the design, building and implementation of new facility projects and production equipment. Your attention to detail and adherence to precise procedures will guarantee that our medications meet the highest standards of safety, efficacy, and quality, providing patients with the best possible care and outcomes. Turn your passion for precision and your commitment to quality into a meaningful impact on healthcare across the US.

What the Facility/Manufacturing Engineer Does Each Day:

  • Provides technical skills and expertise to support operations and ensure mechanical elements for manufacturing are designed and operating as required
  • Generates and executes (as applicable) Validation Project Plans, Validation protocols -Installation Qualifications/Operational Qualifications/Performance Qualifications (IQ/OQ/PQ) and summary reports and Standard Operating Procedures (SOPs) as required for pharmaceutical manufacturing
  • Develop and write specifications for production equipment from aseptic processing to labeling and packaging
  • Support design of production equipment and responsible for commissioning/qualification
  • Maintaining site level facility drawings including revising where required
  • Supports development of site and departmental metrics to gauge ongoing performance of organization and identification of opportunities for continual process improvement


Our Most Successful Facility/Manufacturing Engineers:

  • Are team players
  • Have strong technical writing skills and verbal/written communication skills, including presentation skills
  • Utilize analytical, critical thinking and structured root cause analysis techniques for problem solving
  • Demonstrate expertise in project management
  • Creatively meet challenges and develop innovative approaches


Minimum Requirements for this Role:

  • Bachelor of Science in Mechanical Engineering or equivalent engineering degree with 2+ years' experience in a manufacturing environment or Associated degree in Mechanical Engineering or equivalent engineering degree with 5+ years' experience in a manufacturing environment
  • Able to successfully complete a drug and background check
  • Equipment/Instrument Calibration Principals
  • Direct experience working on large scale MEP systems
  • Honeywell EBI BMS
  • Cleanroom Design, Operation and Maintenance
  • Experience with pharmaceutical grade compressed air systems
  • Knowledge with local and state regulatory requirements
  • Must be currently authorized to work in the United States on a full-time basis; Quva will not sponsor applicants for work visas


Any of the Following Will Give You an Edge:

  • PC literate with a working knowledge of MS Project, Visio, AutoCAD and SolidWorks
  • 2 years of experience in a regulated industry


Benefits of Working at Quva:

  • Comprehensive health and wellness benefits including medical, dental and vision
  • 401k retirement program with company match
  • 17 paid days off plus 8 paid holidays per year
  • National, industry-leading high growth company with future career advancement opportunities


About QuVa Pharma

QuVa Pharma is a pharmaceutical company that specializes in the production and distribution of sterile injectable drugs. The company's products are used in hospitals, clinics, and other healthcare facilities to treat a variety of conditions, including pain, infections, and cancer. QuVa Pharma's facilities are located in Texas and North Carolina, and the company has distribution centers throughout the United States. The company was founded in 2015 and is headquartered in Sugar Land, Texas.
Learn more about QuVa Pharma
Size
500 employees
Industry
Pharmaceuticals & Biotech
Founded
2015
* Ladders Estimates

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