drjobs HCG Process Engineer - Pharmaceutical Manufacturing

HCG Process Engineer - Pharmaceutical Manufacturing

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الوصف الوظيفي

We are seeking a highly skilled and motivated Process Engineer to join our pharmaceutical manufacturing team. The Process Engineer will play a crucial role in optimizing manufacturing processes ensuring product quality and improving operational efficiency. This position requires a deep understanding of pharmaceutical manufacturing principles process engineering and regulatory compliance.



Key Responsibilities


Process Optimization:

  • Develop evaluate and optimize manufacturing processes to enhance efficiency quality and costeffectiveness.
  • Identify and implement process improvements to reduce waste increase yield and improve overall production performance.


Quality Assurance:

  • Ensure all manufacturing processes comply with Good Manufacturing Practices (GMP) regulatory standards and company quality policies.
  • Conduct root cause analysis and corrective actions for process deviations and nonconformances.


Technical Support:

  • Provide technical support to production teams troubleshoot processrelated issues and recommend solutions.
  • Collaborate with R&D Quality Control and other departments to ensure smooth technology transfer and process validation.


Documentation and Compliance:

  • Prepare and maintain detailed documentation including Standard Operating Procedures (SOPs) process flow diagrams and validation protocols.
  • Ensure compliance with all regulatory requirements including FDA EMA and other relevant agencies.


Project Management:

  • Lead or participate in crossfunctional project teams to develop and implement new processes equipment and technologies.
  • Manage project timelines budgets and resources effectively to ensure successful project completion.


Continuous Improvement:

  • Drive continuous improvement initiatives by implementing Lean Manufacturing Six Sigma and other methodologies.
  • Conduct regular process audits and reviews to identify areas for improvement and implement best practices.


Requirements

Education: Bachelor s or Master s degree in Chemical Engineering Biochemical Engineering Pharmaceutical Engineering or a related field.


Experience:
  • Minimum of 5 years of experience in process engineering within a pharmaceutical manufacturing environment.
  • Experience with process optimization scaleup and validation in a GMPregulated setting.
  • Strong background working with Emerson DCS SCADA Siemens or Allen Bradley PLCs MES LIMS BMS ERPs
  • Excellent communication and interpersonal skills to collaborate effectively with crossfunctional teams.
  • Knowledge of regulatory requirements and quality systems in the pharmaceutical industry.
  • Ability to manage multiple projects and prioritize tasks in a fastpaced environment.


Preferred Qualifications
  • Certified Lean Six Sigma Green Belt or Black Belt.


BS Engineering (or equivalent experience) 2+ years working Automation experience in the Pharmaceutical Industry (preferable in API/bulk manufacturing) Previous Pharmaceutical Automation Project experience including: Deriving S88 physical model from P&IDs Deriving software control strategies from PFDs and related process documents DeltaV DCS implementation exposure/experience Exceptional teamwork abilities Strong knowledge of GMP s, regulatory requirements and computer system validation principles Excellent written and verbal communication skills for both technical and non-technical audiences

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