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# Google IT Support Drafter

- **Company:** CareerCircle
- **Location:** Rahway, NJ, United States (Remote available)
- **Experience:** Expert
- **Salary:** $117,000.0 - $184,200.0
- **Contract:** Permanent contract
- **Skills:** 3d Models, Computer-Aided Design, AutoCAD, Artificial Intelligence, Data Analysis, Computer Literacy, SolidWorks (CAD), Rhinoceros 3D, GXP
- **Published:** August 19, 2026
- **Apply:** https://www.careercircle.com/jobs/all/all/usa/all/all/dc8876a5-af72-433c-8619-87c2d64271dd

## About the Role

Chemistry
Operations
Leadership
Innovation
Compassion
Scale (Map)
Supply Chain
Adaptability
Communication
Data Analysis
Investigation
Process Design
Pharmaceuticals
Detail Oriented
Clinical Trials
Problem Solving
Small Molecules
Telephone Skills
Change Management
Biopharmaceuticals
Strategic Thinking
Analytical Testing
Sterile Processing
Root Cause Analysis
Process Development
Medicinal Chemistry
Contingent Workforce
Process Optimization
Technical Leadership
Willingness To Learn
Chemical Engineering
Deviation Management
Organizational Skills
New Product Development
Pharmaceutical Sciences
Process Hazard Analysis
Medical Supply Management
Standard Operating Procedure
Good Manufacturing Practices
Sterile Techniques And Procedures, + Bachelor's degree in Chemical Engineering, Chemistry, Pharmaceutical Sciences or related scientific field with a minimum of 5 years relevant experience

 + Master's degree in Chemical Engineering, Chemistry, Pharmaceutical Sciences or related scientific field with a minimum of 3 years of relevant experience, or a
 + PhD degree in Chemical Engineering, Chemistry, Pharmaceutical Sciences or related scientific field with a minimum of years of relevant experience.

Required Experience and Skills:
*

 + Excellent enterprise leadership skill demonstration
 + Excellent interpersonal and communication skills, both verbal and written.
 + Experience in leading quality investigations and change management.
 + Familiarity with United States and European Union GMP and Safety compliance regulations.
 + Ability to convert new drug product attributes and process needs to an executable series of steps and procedures to enable acceptable product manufacture.
 + Ability to prepare Standard Operating Procedures (SOP) and current GXP documents.
 + Experience with quality systems.
 + Excellent organizational skills.
 + Desire and willingness to learn, contribute and lead.
 + Track-record of independent problem-solving.

Preferred Experience and Skills:
*

 + Experience with sterile GMP facility startup.
 + Knowledge of Investigational drug regulatory requirements.
 + Understanding of Clinical Supply Chain Operations.
 + Expertise in drug product aseptic processing, equipment, and sterile technique.

#eligibleforERP, Adaptability, Adaptability, Analytical Testing, Change Management, Chemical Engineering, Clinical Trials Operations, Data Analysis, Detail-Oriented, Deviation Management, Equipment Qualification, GMP Compliance, Good Manufacturing Practices (GMP), Medical Supply Management, Medicinal Chemistry, Pharmaceutical Sciences, Process Design, Process Hazard Analysis (PHA), Process Optimization, Root Cause Analysis (RCA), Standard Operating Procedure (SOP), Standard Operating Procedure (SOP) Development, Sterile Procedures, Strategic Thinking, Technical Leadership, Technical Problem-Solving {+ 1 more}, Asepsis
Visionary
Operations
Innovation
Punctuality
Disinfecting
Biotechnology
Sterilization
Pharmaceuticals
Detail Oriented
Medical Devices
Computer Literacy
Strong Work Ethic
Aseptic Processing
Sterile Processing
Workflow Management
Process Architecture
Artificial Intelligence
Engineering Design Process
Standard Operating Procedure
Good Manufacturing Practices

## Description

The Formulation, Laboratory, and Experimentation (FLEx) Center is a new multi-modality (small molecule, biologics, vaccine) Drug Product development and Good Manufacturing Practice (GMP) clinical supply manufacturing facility in Rahway, New Jersey.

The Sterile Process Engineer role at the Senior Specialist level will leverage the individual's leadership, technical, and communication skillsets to drive the success of our clinical manufacturing facility and organization.

This role will directly support the pipeline's most technically complex formulations and process development through process tech transfers, scale-up activities, quality investigations, change management, and authoring GMP standard operating procedures and protocols in support of sterile clinical drug product operations. This individual will collaborate closely with the development scientists, engineers, operations, quality representatives, and other team members to ensure the quality of the clinical supplies, the scientific rigor of the processes, and ultimately to enable the flexibility and speed of our Company's pipeline. The role is, on-site, based in New Jersey and reports to the Sterile Process Engineering Lead of the FLEx GMP facility within Pharmaceutical Operations and Device Development (PSDD)., AutoCAD
Visionary
Innovation
3D Modeling
Shop Drawing
Communication
Rhinoceros 3D
Exhibit Design
SolidWorks (CAD)
Technical Drawing
Parametric Modeling
Artificial Intelligence
Technical Documentation
Engineering Documentation
Fusion 360 (CAD Software)
Engineering Design Process
+0
Aseptic Technician- 2nd Shift
Actalent

Fairfield, NJ*On-Site


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