Amneal-posted 8 days ago
$80,000 - $95,000/Yr
Full-time • Mid Level
5,001-10,000 employees

Description: Process Engineer reports to the Manager of Technical Services and plans, executes and functionally directs Process/Cleaning Validation/Study assignments and projects, which require sound pharmaceutical/engineering skills and independent judgment. Works as a team member, educates internal partners on the projects, monitors and executes. Maintains effective and cooperative relationships with all departments within and outside the organization. Managing the post approval projects. Essential Functions: Prepare validation protocols & reports for manufacturing process and cleaning process qualification, data analysisand prepare reports; execute the manufacturing process and cleaning process qualification/validation/study. Managing the post approval projects. coordinating with cross functional Teams and ensuring the timely completion of projects. Analyzes statistical data, products or functional specifications to determine conformance with standards andestablished quality requirements Coordinate/oversee the development of new processes or troubleshoot existing ones Assist in deviation/investigations to identify root causes and define corrective and/or preventative actions (CAPA) & assist in various audits Additional Responsibilities: Initiation of Change Controls and Planned Deviations when required

  • Prepare validation protocols & reports for manufacturing process and cleaning process qualification, data analysisand prepare reports
  • execute the manufacturing process and cleaning process qualification/validation/study
  • Managing the post approval projects
  • coordinating with cross functional Teams and ensuring the timely completion of projects
  • Analyzes statistical data, products or functional specifications to determine conformance with standards andestablished quality requirements
  • Coordinate/oversee the development of new processes or troubleshoot existing ones
  • Assist in deviation/investigations to identify root causes and define corrective and/or preventative actions (CAPA) & assist in various audits
  • Initiation of Change Controls and Planned Deviations when required
  • Bachelors Degree (BA/BS) Pharmaceutical/Biomedical Engineering - Required
  • 2 years or more in Pharmaceutical/Manufacturing Industry
  • Excellent verbal and written communication skills - Advanced
  • Proficiency in MS Word/Excel/ PowerPoint/MS project - Advanced
  • Basic Analytical Knowledge desirable
  • In-depth knowledge of manufacturing equipment and processes for Solid Oral, Medical Device, Transdermal, Topical and Liquid Orals
  • Master Degree (MS/MA) Pharmaceutical/Biomedical Engineering - Preferred
  • In addition, Amneal offers a short-term incentive opportunity, such as a bonus or performance-based award, as well as a long-term incentive award, such as restricted stock units, with this position within the first 12 months.
  • At the heart of our Total Rewards commitment is a comprehensive, flexible and competitive benefits program for eligible positions that enables you to choose the plans and coverage that meet your personal needs.
  • This includes above-market, diverse and robust health and insurance benefits to meet the varied needs of our employees as well as a significant 401(k) matching contribution to help our employees save for retirement.
  • We also promote employee well-being with programs that help you enjoy your career alongside life’s many other commitments and opportunities.
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