PharmEng Technology

Sr Automation Engineer

PharmEng Technology  •  Houston, TX (Onsite)  •  8 days ago
Apply
AI can make mistakes so check important info. Chat history is never stored.
58
AI Success™

Job Description

We are seeking a Sr. Process Automation Engineer for a contract-to-hire position with our client, located in Houston. This role offers an exciting opportunity to support manufacturing operations through technical expertise in automation systems and instrumentation, ensuring optimal production efficiency and compliance.

Key Responsibilities:

Operations Support

  • Provide 24x7 automation support to manufacturing by troubleshooting equipment, systems, and processes.
  • Support ongoing production operations and the introduction of new equipment and processes.
  • Participate in off-shift and on-call rotation as needed.
  • Offer operational support on the manufacturing floor.
  • Assist in evaluating historical process and equipment data.
  • Act as a subject matter expert (SME) for cross-functional groups such as QA, QC, PD, and engineering teams.

Leadership

  • Mentor and train junior team members, including technicians, analysts, and engineers.
  • Develop and support training plans for site personnel.
  • Communicate progress, opportunities, and roadblocks to leadership and stakeholders effectively.

Equipment/Systems Ownership

  • Serve as the owner and administrator for manufacturing equipment and systems.
  • Conduct periodic reviews and manage training and access for automation systems.
  • Oversee regulatory aspects of data collection, monitoring, and SCADA systems, including CMS, BMS, and OSI Pi.
  • Manage backups and restoration of automation configurations.
  • Support and maintain OT networks and control systems.

Continuous Improvement

  • Enhance process control through advanced automation concepts.
  • Develop and implement automation standards, SOPs, and design documents.
  • Author and review specifications for projects and process changes.
  • Ensure adherence to site automation standards in project implementation.

Quality Assurance

  • Develop and support change controls, deviations, investigations, and CAPAs.
  • Review and approve validation protocols and related documentation.
  • Support audits and regulatory inspections.
  • Ensure compliance with IT/OT security policies, data integrity, and regulatory requirements.

New Equipment and Process Introductions

  • Incorporate innovative technologies into equipment and process designs.
  • Develop automation requirements and specifications for new systems and process improvements.

Preferred Technical Expertise:

  • Hands-on experience with:
    • OSIsoft PI (DHS)
    • Vaisala viewLinc (CMS)
    • Rockwell Software Suite
    • Automated Logic WebCTRL
    • Wonderware System Platform
    • Windows OS
    • DCS systems
    • Industrial communication networks

Qualifications:

  • Extensive experience in process automation and manufacturing environments.
  • Proven ability to manage projects involving complex equipment and significant process improvements.
  • Strong knowledge of FDA 21 CFR Part 11, Annex 11, and data integrity requirements.
  • Excellent troubleshooting, communication, and leadership skills.

Join us to drive innovation and excellence in process automation for our clients state-of-the-art manufacturing facility. Apply now to become an integral part of this dynamic team!

#ProcessAutomation #AutomationJobs #HoustonJobs #ContractToHire

PharmEng Technology

About PharmEng Technology

PharmEng Technology, now part of Efor Group, leader in Compliance Engineering, is a leading provider of technical services and solutions to the pharmaceutical, biotechnology, and healthcare industries. With over 25 years of experience, we specialize in Commissioning, Qualification, and Validation (CQV) services for facilities, utilities, equipment, and processes.

As part of Efor’s global network of 3,000 experts across 12 countries, we are better equipped than ever to deliver innovative and comprehensive solutions tailored to the unique needs of clients worldwide. This integration strengthens our ability to combine global expertise with local proximity, positioning PharmEng as a strategic partner for the industry’s most prominent players.

Our team of highly skilled professionals brings a wealth of industry expertise and knowledge to every project, ensuring that our clients receive the highest quality services and solutions. We pride ourselves on our ability to provide flexible, innovative, and cost-effective solutions that meet our clients' unique challenges.

At PharmEng Technology by Efor, we are committed to delivering excellence in everything we do. We work closely with our clients to understand their goals and objectives, developing customized solutions that deliver measurable results. Our focus on quality, safety, and compliance ensures that our clients can trust us to meet their most critical needs.

Specialties: PharmEng Technology specializes in the planning, design, construction, and validation of Health Care, Laboratory, API Pharmaceutical, and Biotechnology facilities and equipment, including computer systems. We provide professional services that meet both regulatory and business demands, following current Good Manufacturing Practices (cGMP), Good Engineering Practices (GEP), and Good Laboratory Practices (GLP).

Industry
Chemicals & Materials
Company Size
201-500 employees
Headquarters
Toronto, CA
Year Founded
Unknown
Social Media