Find Manufacturing Automation Systems Engineer (DeltaV exp.|Biotech|Pharma industry|No C2C) Job in Hillsboro, Oregon | Snaprecruit

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Manufacturing Automation Systems Engineer (DeltaV exp.|Biotech|Pharma industry|No C2C)

  • ... Mindsource Inc
  • ... Hillsboro, Oregon, United States
  • ... Full time
  • ... Salary: 75 per hour
  • Posted on: Feb 02, 2024

Manufacturing Automation Systems Engineer (DeltaV exp.|Biotech|Pharma industry|No C2C)   

JOB TITLE:

Manufacturing Automation Systems Engineer (DeltaV exp.|Biotech|Pharma industry|No C2C)

JOB TYPE:

Contract

JOB LOCATION:

Hillsboro Oregon United States

No

JOB DESCRIPTION:

What you ll be working on:
Active involvement in the daily operations for all Manufacturing IT OT systems to support the system owners for all Manufacturing systems and supporting the team in manufacturing site projects and with various administrative tasks.

This include activities like:
Troubleshoot immediate DeltaV (DCS) issues, inquiries and Syncade MES inquiries as they arrive during normal business hours.
Update System lifecycle documentation, as the need arises, for both PCS and MES.
Help perform MILE (system maintenance) activities for PCS and MES.
Work with cross-functional team for thin client (P&F BTC22) requalification.
Perform System periodic reviews- This entails performing data collection from our deviations database on the past 3 year s worth of planned and unplanned events, review impact on system s validated state and draft reports.
Daily/weekly system monitoring for PCS and MES.
Attend coordination meetings with different groups within the organization to keep up with changes to global IT systems that may affect MES and PCS
(e.g. Single LIMS coordination meetings, ST300 Meetings).
Support System Owner squad in the overall procurement, development, integration, modification, operation, maintenance, and retirement of PCS and MES.
Support validation activities
Responsibility for the Periodic System Audit Trail Review.
Perform annual automation account review.
User account auditing, provisioning, resets and activation for all IT and OT systems.
Creating reports for various systems on demand.
Work with the System Owners and Business Process Owners for the upgrade/patching and changes to the system to ensure GMP compliance.
Review ServiceNow tickets and either address them or route them to the SME
Run monthly site termination report and updates to AD.
Support on documents management systems (Veeva, Condor, eVal Roche).
Support the team with administrative tasks.

Role Minimum Requirements
Education
Minimum Bachelor s degree in Computer Engineering, Automation Engineering or similar.
Minimum 5 years of experience in system and/or network administration.

Competencies
Management skills
Attention to details and good problem-solving skills
Demonstrated ability to think and solve problems at a system-level
Ability to work and interact productively with stakeholders from different technical domains
Ability to multi-task with a calm behavior and work under pressure in a fast-paced environment
Good team player, self-confident, motivated, and independent
Good communication skills

Technical skills
DeltaV (DCS) Administration
SQL Database Server proficiency. Knowledge with SQL Database Cluster (Always ON), is a plus.
Troubleshooting DCS (hardware and software), MES, web service issues.
MES (Syncade preferred) or other MES platforms.
Knowledge of ASP .net web services.
Network Administration.
Experience with industrial data and control interfaces, preferably OPC and OPC-UA.
System administration, supporting multiple platforms and applications.
Biopharmaceutical or similar Manufacturing domain knowledge.
Application Engineering experience with manufacturing control systems in a highly automated manufacturing environment, preferably Distributed Control Systems (e.g. DeltaV).
Keep abreast of key Manufacturing IT trends and be curious - Smart Buildings, Smart Manufacturing, Industrial IoT, Manufacturing Digital Plant Maturity, Cybersecurity, Pharma 4.0, Data Integrity principles, technology, and data standardization, etc.
Knowledge of Good Manufacturing Practices (GMP), Health Authority practices, 21 CFR Part 11,cGMP Annex 11, Data Integrity principles.
Entrepreneurial mindset e.g. \\\\\\\\\\\\\\\"automating automation\\\\\\\\\\\\\\\".

Position Details

POSTED:

Feb 02, 2024

EMPLOYMENT:

Full-time

SALARY:

75 per hour

SNAPRECRUIT ID:

S-1707363992-6498f85ed2c5bb59cd55f00a6c6fbb5c

LOCATION:

Oregon United States

CITY:

Hillsboro

Job Origin:

jpick2

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Manufacturing Automation Systems Engineer (DeltaV exp.|Biotech|Pharma industry|No C2C)    Apply

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What you ll be working on:
Active involvement in the daily operations for all Manufacturing IT OT systems to support the system owners for all Manufacturing systems and supporting the team in manufacturing site projects and with various administrative tasks.

This include activities like:
Troubleshoot immediate DeltaV (DCS) issues, inquiries and Syncade MES inquiries as they arrive during normal business hours.
Update System lifecycle documentation, as the need arises, for both PCS and MES.
Help perform MILE (system maintenance) activities for PCS and MES.
Work with cross-functional team for thin client (P&F BTC22) requalification.
Perform System periodic reviews- This entails performing data collection from our deviations database on the past 3 year s worth of planned and unplanned events, review impact on system s validated state and draft reports.
Daily/weekly system monitoring for PCS and MES.
Attend coordination meetings with different groups within the organization to keep up with changes to global IT systems that may affect MES and PCS
(e.g. Single LIMS coordination meetings, ST300 Meetings).
Support System Owner squad in the overall procurement, development, integration, modification, operation, maintenance, and retirement of PCS and MES.
Support validation activities
Responsibility for the Periodic System Audit Trail Review.
Perform annual automation account review.
User account auditing, provisioning, resets and activation for all IT and OT systems.
Creating reports for various systems on demand.
Work with the System Owners and Business Process Owners for the upgrade/patching and changes to the system to ensure GMP compliance.
Review ServiceNow tickets and either address them or route them to the SME
Run monthly site termination report and updates to AD.
Support on documents management systems (Veeva, Condor, eVal Roche).
Support the team with administrative tasks.

Role Minimum Requirements
Education
Minimum Bachelor s degree in Computer Engineering, Automation Engineering or similar.
Minimum 5 years of experience in system and/or network administration.

Competencies
Management skills
Attention to details and good problem-solving skills
Demonstrated ability to think and solve problems at a system-level
Ability to work and interact productively with stakeholders from different technical domains
Ability to multi-task with a calm behavior and work under pressure in a fast-paced environment
Good team player, self-confident, motivated, and independent
Good communication skills

Technical skills
DeltaV (DCS) Administration
SQL Database Server proficiency. Knowledge with SQL Database Cluster (Always ON), is a plus.
Troubleshooting DCS (hardware and software), MES, web service issues.
MES (Syncade preferred) or other MES platforms.
Knowledge of ASP .net web services.
Network Administration.
Experience with industrial data and control interfaces, preferably OPC and OPC-UA.
System administration, supporting multiple platforms and applications.
Biopharmaceutical or similar Manufacturing domain knowledge.
Application Engineering experience with manufacturing control systems in a highly automated manufacturing environment, preferably Distributed Control Systems (e.g. DeltaV).
Keep abreast of key Manufacturing IT trends and be curious - Smart Buildings, Smart Manufacturing, Industrial IoT, Manufacturing Digital Plant Maturity, Cybersecurity, Pharma 4.0, Data Integrity principles, technology, and data standardization, etc.
Knowledge of Good Manufacturing Practices (GMP), Health Authority practices, 21 CFR Part 11,cGMP Annex 11, Data Integrity principles.
Entrepreneurial mindset e.g. \\\\\\\\\\\\\\\"automating automation\\\\\\\\\\\\\\\".

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