Innovate to solve the world's most important challenges

The future is what you make it.

When you join Honeywell, you become a member of our global team of thinkers, innovators, dreamers and doers who make the things that make the future.

That means changing the way we fly, fueling jets in an eco-friendly way, keeping buildings smart and safe and even making it possible to breathe on Mars.

Be a part of a cross-functional team working with process development, toller management, customer interaction, and regulatory requirement at the Pottsville, PA site. This role will apply expertise and knowledge in finding innovative, cost-effective means to improve quality output and continuous improvements. You will drive process initiatives that ensures compliance with customer requirements, regulatory agencies, government regulations and engineering specifications while instilling accountability for governance of the Quality System, product acceptance and, product quality from development through day-to-day production.

Key Responsibilities

• Process Development
• Develop specifications for all SKUs
• Develop and validate test methods
• Specify testing and validation protocol for new SKUs
• Toller Management
• Assess quality systems of potential tolling partners
• Develop toller quality management processes
• Monitor ongoing Cpks at tollers
• Lead continuous improvement efforts
• Cost improvement analysis
• Drive technical solutions for quality improvements
• Customer Interaction
• Assist/Lead projects to improve product quality
• Lead customer audits
• Work with customers and tollers to resolve customer complaints
• Generate certificate of analysis for customers
• Regulatory
• Perform regulatory reviews
• Work with Product Stewardship for regulatory needs
• Perform risk analyses
• Analytical Equipment service and calibration
• Perform analytical equipment maintenance and calibration
• FT-IR Validations
• Analytical Balances
• Agilent GC CTFE standards
• Minolta Meter
• Die Line Camera
• WaveScan Dual
• HazeGard
• ZST timers and temperature checks
• Oven temperature checks
• Pycnometers
• Emveco micrometer
• Tape Rules
• Steel Rules
• Analytical Testing
• WVTR
• Film Surface Energy
• Film Properties

BENEFITS

In addition to a competitive salary, leading-edge work, and developing solutions side-by-side with dedicated experts in their fields, Honeywell employees are eligible for a comprehensive benefits package. This package includes employer subsidized Medical, Dental, Vision, and Life Insurance; Short-Term and Long-Term Disability; 401(k) match, Flexible Spending Accounts, Health Savings Accounts, EAP, and Educational Assistance; Parental Leave, Paid Time Off (for vacation, personal business, sick time, and parental leave), and 12 Paid Holidays.

The application period for the job is estimated to be 40 days from the job posting date; however, this may be shortened or extended depending on business needs and the availability of qualified candidates.

U.S. PERSON REQUIREMENTS
Due to compliance with U.S. export control laws and regulations, candidate must be a U.S. Person, which is defined as, a U.S. citizen, a U.S. permanent resident, or have protected status in the U.S. under asylum or refugee status.

In October 2024 Honeywell announced the spin-off of our Advanced Materials business to become a stand-alone publicly traded company, independent of Honeywell. Our intention is that this role, dedicated to the Advanced Materials business, will be a part of this future transaction when the separation occurs.

YOU MUST HAVE

• Minimum 2 years working in cGMP environment
• Six Sigma certification
• Proficient computer skills
• Statistical analysis skills (Excel, Minitab, and other statistical tools)

WE VALUE

• Bachelor's degree in engineering
• Process Development skills and experience
• Lab testing skills or familiarity with the testing equipment currently using
• Experience with testing, validations, Customer CAPA process, Process Capability
• Compliance Knowledge in Pharma
• Proficiency in regulatory investigations
• Knowledge of pharma regulatory compliance guidelines, international regulation familiarity FDA, EMA, ANVISA, CFDA, Japan Ministry of Health
• Hands on work ethic
• Provide clear and concise communications
• Ability to work independently
• Ability to partner with others on projects
• Ability to travel 25% of time, both domestic and international
• Understanding of quality processes
• Film manufacturing experience
• Lead Quality Auditor skills

Additional Information

• JOB ID: HRD245420
• Category: Integrated Supply Chain
• Location: 98 Westwood Rd,Pottsville,Pennsylvania,17901,United States
• Exempt

Honeywell is an equal opportunity employer. Qualified applicants will be considered without regard to age, race, creed, color, national origin, ancestry, marital status, affectional or sexual orientation, gender identity or expression, disability, nationality, sex, religion, or veteran status.