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# Google IT Automation with Python

- **Company:** CareerCircle
- **Location:** Rahway, NJ, United States
- **Salary:** $117,000.0 - $184,200.0
- **Contract:** Permanent contract
- **Skills:** Microsoft Excel, Artificial Intelligence, Data Analysis, Microsoft Outlook, Spreadsheets, Data Security, Data Warehousing, Document Management Systems, Microsoft Office, Microsoft PowerPoint, Web Application Security, GXP, Custom Reports
- **Published:** July 8, 2026
- **Apply:** https://www.careercircle.com/jobs/all/all/usa/nj/rahway/0d2ce1ea-2fbb-4b42-b25a-a5b34ba3e20c

## About the Role

Automation
Mentorship
Innovation
Autoclaves
Compassion
Supply Chain
Communication
Self-Motivation
Problem Solving
Small Molecules
Scope Management
Telephone Skills
Technical Acumen
Critical Thinking
Change Management
Growth Mindedness
Biopharmaceuticals
Project Management
Strategic Thinking
Analytical Testing
Process Simulation
Sterile Processing
Automation Systems
Root Cause Analysis
Process Improvement
Process Development
Cycle Time Variation
Contingent Workforce
Process Optimization
Willingness To Learn
Chemical Engineering
Six Sigma Green Belt
Production Equipment
Six Sigma Black Belt
Deviation Management
Six Sigma Methodology
Organizational Skills
Mechanical Engineering
Project Implementation
Biomedical Engineering
New Product Development
Process Hazard Analysis
Deviation Investigations
Distributed Control Systems
Standard Operating Procedure
Good Manufacturing Practices
Continuous Improvement Process
Troubleshooting (Problem Solving), * BS or MS in Chemical Engineering, Mechanical Engineering, Biomedical Engineering or related engineering field with a minimum of 5 years of relevant experience., * Subject Matter Expertise in various sterile processing equipment such as automated filling lines, lyophilizers, autoclaves, part washers, isolators and etc.

 * Knowledge of automation systems such as PLC, DCS, and MES.
 * Knowledge of Drug Product aseptic processing techniques.
 * Experience in leading and supporting quality deviation investigations and change management.
 * Familiarity with United States and European Union GMP and Safety compliance regulations.
 * Ability to prepare Standard Operating Procedures (SOP) and current GXP documents.
 * Strong technical aptitude and critical thinking skills to effectively troubleshoot and resolve issues on the production floor.
 * Demonstrated project management experience leading cross-functional initiatives from planning through execution, with a proven ability to manage scope, timelines, risks, and stakeholder expectations.
 * Possess and leverages strong working knowledge of theories, practices, and procedures to train others efficiently. Applies knowledge to improve processes.
 * Familiarity with common Drug Product processing unit operations such as mixing, filtration, temperature control and etc.
 * Lean Six Sigma Green Belt certification.
 * Effective interpersonal and communication skills, both verbal and written.
 * Excellent organizational skills to multi-task.
 * Desire and willingness to learn, contribute and lead.
 * Track-record of independent problem-solving.

Preferred Experience and Skills:

 * Experience providing technical mentorship to engineers and cross-functional team members, including guidance on problem-solving, project execution, and professional development.
 * Experience with Commissioning, Qualification and Validation of equipment.
 * Understanding of ISA88 and ISA95 principles.
 * Knowledge of Investigational drug regulatory requirements.
 * Understanding of Clinical Supply Chain Operations.
 * Lean Six Sigma Black Belt certification.

#eligibleforERP, Analytical Testing, Change Management, Chemical Engineering, Chemical Technology, Deviation Management, Equipment Qualification, GMP Compliance, Good Manufacturing Practices (GMP), Process Hazard Analysis (PHA), Process Improvements, Process Optimization, Root Cause Analysis (RCA), Six Sigma, Strategic Thinking, Technical Problem-Solving, Data Analysis
Data Security
Detail Oriented
Microsoft Excel
Risk Management
Compliance Risk
Microsoft Office
Ad Hoc Reporting
Data Warehousing
Analytical Skills
Quality Assurance
Loan Documentation
Workflow Management
Microsoft PowerPoint
Credit Risk Management
Business Administration
Web Application Security
Document Management Systems
Standard Operating Procedure
Ethical Standards And Conduct
Customer Relationship Management
+0

## Description

The Formulation, Laboratory, and Experimentation (FLEx) Center in Rahway, New Jersey, features a cutting-edge sterile drug product cGMP clinical supply manufacturing facility, known as FLEx Sterile. The FLEx Sterile facility is poised to play a pivotal role in the long-term success of delivering our clinical pipeline to patients worldwide, encompassing a diverse range of product modalities, including sterile small molecules, biologics, vaccines, and antibody-drug conjugates (ADCs). The FLEx organization has a mission to enable development of our Company's pipeline products with speed, agility, and rigor. This mission will be accomplished by: 1) Enabling robust formulation and process development with flexible physical and digital infrastructure; 2) Delivering compliant, high quality clinical supplies; 3) Developing talents with a new operating model and promoting a growth mindset. As the facility just completed its Process Simulation execution and is officially released for clinical
manufacturing, this presents an exciting opportunity for individuals eager to learn, demonstrate themselves, and grow with a rapidly expanding team., The FLEx organization is seeking a highly motivated individual to serve the role of Senior Specialist, Technical Operations Engineer, reporting to the Technical Operations Engineering Lead. The successful candidate will support routine operations through timely troubleshooting and resolution of production equipment issues, establishment of new processes and implementation of continuous improvement projects with goals to reduce operation cycle time, errors, and costs. This individual will collaborate closely with the Production, New Product Introduction, Facilities, Equipment, Automation and Quality teams to ensure compliant, right first-time execution and timely delivery of business goals. The role is on-site, based in Rahway, NJ and will support our first shift operations. To ensure continuity of operations, occasional second-shift coverage may be required to support the second-shift team during periods of absence. Occasional weekend support may also be necessary based on business and
operational needs., Union Beach, NJ*On-Site
Research
Chemistry
Visionary
Innovation
Collections
Scale (Map)
Food Science
Distillation
Wet Chemistry
Detail Oriented
Beverage Products
Technical Management
Laboratory Equipment
Artificial Intelligence
Engineering Design Process
Good Laboratory Practice (GLP)
Gas Chromatography Mass Spectrometry
High-Performance Liquid Chromatography
+0
Rental Agent
Aston Carter
Woodbridge, NJ*On-Site
Filing
Finance
Operations
Data Entry
Accounting
Procurement
Real Estate
Spreadsheets
Supply Chain
Communication
Certified Mail
Detail Oriented
Microsoft Excel
Lease Contracts
Customer Service
Microsoft Outlook
Property Management
Administrative Support
Artificial Intelligence
Administrative Functions


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