Process/Validation Engineer

Branchburg, NJ, US • Posted 60+ days ago • Updated 1 hour ago

Full Time

On-site

Fitment

Dice Job Match Score™

🔗 Matching skills to job...

Job Details

Skills

PQ
Veeva
Regulatory Compliance
Pharmaceutics
Statistics
Production Support
Reporting
Change Control
Science
Process Engineering
Medical Devices
Pharmaceutical Industry
Microsoft Excel
Microsoft Outlook
Data Analysis
Technical Writing
21 CFR Part 11
ISO 9000
Six Sigma
Value Stream Mapping
Lean Manufacturing
Design For Manufacturability
Design Of Experiments
Manufacturing
Root Cause Analysis
Minitab
Microsoft PowerPoint
Microsoft Visio
Management
Strategic Thinking
Organizational Skills
Communication

Summary

Responsibilities:

Process and Cleaning Validation Experience.
Equipment Qualification (IOQ/PQ).
Quality System Experience (Veeva, Track wise, Compliance Wire).
Medical Device or Pharmaceutical Experience Required. Preferred Medical Device with 3-5 Years.
Statistical Analysis (Minitab or JUMP).
The Process/Validation Engineer is responsible for providing engineering production support including:
Implementing process and technology improvements.
Process and Cleaning Validation.
Equipment Qualification.
Collecting, monitoring, analysing, troubleshooting, and reporting manufacturing data related to performance in the areas of quality, cost, and speed/service to market.
Investigating non-conformances, CAPAs, process performance drifts and implementing corrective and preventative actions.
Responsible for the initiation and follow-through of the change control processes.

Requirements:

Bachelor's degree in engineering, science or closely related discipline is desired, or equivalent technical experience plus demonstrated competence, with a desired 3-5 years of significant process engineering and/or operational experience in Medical Device or Pharmaceutical industry. Additional post-graduate education may contribute towards the desired years of experience.
Experience with MS Office applications including Word, Excel & Outlook.
Demonstrated understanding and use of statistical methods in experiment design and data analysis.
ble to work independently and proactively in conjunction with all levels of the organization.
Excellent Technical writing skills and attention to fine detail.
Understanding of AATB, FDA, ISO, ISPE, and other regulatory guidelines including understanding of the various regulations and guidelines such as FDA 21 CFR 11, 820 and 1270, ISO 11737, 13485 and 14644, and others, as required.
Six Sigma, Value Stream Mapping, Lean Manufacturing, Design for Manufacturability, DOE.
Biological Products and aseptic processes.
Development of robust manufacturing processes, validation, and process monitoring.
Experience with root cause analysis methods.
Experience with applications including Minitab or other statistical software, Client PowerPoint, Project, and Visio.
Time management skills and follow-through skills with the ability to work on and manage multiple tasks with tight deadlines.
Strategic thinking and planning.
Excellent organizational skills.
Excellent oral and written communication skills.

Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.

Dice Id: 91116760
Position Id: d96ed89263cf4cb48125a0d60f8b0c05
Posted 30+ days ago

Create job alert

Never miss an opportunity! Create an alert based on the job you applied for.

Process/Validation Engineer

Dice Job Match Score™

Job Details

Skills

Summary

Similar Jobs