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Pilot Plant Operations Specialist, Small Scale Organics (3rd shift)

USA - New Jersey - Rahway, United States

Job Description

The Small Scale Organics Pilot Plant is a (Good Manufacturing Practices) manufacturing facility in the Small Molecule Process Research and Development (SM PR&D) organization. The SSO pilot plant enables gain of critical internal experience with scale-up of manufacturing Good Manufacturing Practices steps, demonstration of new manufacturing technology/processes, training opportunities for improved manufacturing process development, and seamless technology transfer to commercial sites.

The SSO Operations Specialist will provide hands on assistance for daily production activities while ensuring compliance with Safety & Environmental (S&E) and current Good Manufacturing Practices (cGMPs) requirements to meet SSO objectives and customer requirements. The position is responsible for implementing actions to meet S&E and GMP requirements. This position is also responsible for ensuring facility readiness for batch processing and shares accountability for the building performance. Ultimately, this position is expected to work cooperatively with the SSO leadership team and SSO partners to drive overall success and performance of the building, and ultimately strong support for the overall SM PR&D pipeline.

Responsibilities:

  • Under the scientific direction of a facility lead, the Operations Specialist will participate in equipment setups, raw material sampling and subdivisions, solution preparations, batch processing planning and execution at a pilot scale, process knowledge capture, and troubleshooting equipment with the aim of advancing process development, aiding technology development, and supplying Active Pharmaceutical Ingredient (API) for clinical use and drug product development. This will involve handling of a variety of reagents, solvents, and active pharmaceutical ingredients during “wet chemistry” operations (performing chemical reactions, extractions, distillations, crystallizations, filtration, drying, etc.) as well as dry powder processing (e.g., dry milling).

  • Ensure processes are run within the capability constraints of the facility.

  • Ensure facility readiness with respect to cleaning (including documentation and execution), dummy run and batch execution, building housekeeping, and consumable inventory.

  • Provide input for incident root cause analysis, reporting, and action items.

  • Facilitate and drive building improvement projects and corrective/preventative action closures.

  • Provide input on process setups.

  • Provide regular feedback to peers to promote a continuous improvement mindset.

  • Collaborate with all building staff to share and align on best practices.

  • Actively investigate problem statements and safety observation reports (SORs) to promote fast and efficient closure.

  • As needed, safely perform High Risk Work involving hazardous energy control.

  • Identify and follow through on opportunities to improve building flexibility, efficiency, compliance, and safety.

  • Author lessons learnt and summary reports to capture knowledge gained.

  • Mentor and help train rotational and …

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Job Profile

Regions

North America

Countries

United States

Restrictions

Hybrid Hybrid work Hybrid work model On-site Onsite Puerto Rico residents only Travel required US and Puerto Rico residents only

Benefits/Perks

Bonus eligibility Diverse workplace Equal opportunity Equal opportunity employer Flexibility Flexible work Flexible work arrangements Health Care Hybrid work Hybrid work model Inclusion Inclusive environment Insurance Paid holidays Retirement benefits Sick Days Training opportunities Vacation

Tasks
  • Communication
  • Compliance
  • Documentation
  • Execution
  • Innovation
  • Leadership
  • Planning
  • Presentation
  • Process development
  • Reporting
  • Technical writing
  • Technology Transfer
  • Troubleshooting
Skills

Accountability Analysis API Batch processing Best Practices Chemical Chemistry Cleaning Clinical Collaborative mindset Commercial Communication Compliance Continuous Improvement Coordination Cross-functional Teams Current good manufacturing practices Development Documentation Documentation Practices Drug product Drug product development Education Equipment Execution Filtration Flexibility GMP Good Documentation Practices Good Manufacturing Practices Inclusion Innovation IT Laboratory Leadership Lean Lean Six Sigma Manufacturing Manufacturing Practices Manufacturing Process Manufacturing process development Manufacturing technology Mechanical Mechanical aptitude Mentoring Operations Organization Pharmaceutical Pharmaceutical Development Planning Presentation Process Development Process research Product Development Reporting Research Research and development Root Cause Analysis Safety Safety Compliance Scale-Up Science Six Sigma Teams Technical Technical Writing Technology Technology development Technology Transfer Training Troubleshooting Word Word Processing Writing

Experience

6 years

Education

AS Associate Business Certification Chemistry Degree Development Diploma GED Health Care Higher Higher Degree High School High school diploma IT Relevant experience Science Technology

Certifications

Lean Six Sigma Six Sigma

Timezones

America/Anchorage America/Chicago America/Denver America/Los_Angeles America/New_York Pacific/Honolulu UTC-10 UTC-5 UTC-6 UTC-7 UTC-8 UTC-9