Manufacturing Process Specialist

2 weeks ago


Bridgeton, New Jersey, United States Medvacon Life Sciences Full time
Job Overview

The Manufacturing Process Specialist at Medvacon Life Sciences will focus on the design, implementation, and enhancement of production processes aimed at ensuring the effective manufacture of pharmaceutical products. This position demands a solid grasp of process engineering concepts, exceptional analytical abilities, and a collaborative spirit in a dynamic setting. The ideal candidate will be pivotal in upholding the highest standards of quality and operational efficiency in manufacturing.

Key Responsibilities
  • Process Design and Development:
    • Craft and refine manufacturing processes for both new and established pharmaceutical products.
    • Perform process simulations and feasibility assessments to boost production efficiency and product integrity.
    • Establish and execute process control methodologies to guarantee uniform product quality.
  • Process Optimization:
    • Detect and implement enhancements to processes to elevate efficiency, lower expenses, and improve product quality.
    • Conduct thorough investigations into process anomalies and apply corrective measures.
    • Work alongside cross-functional teams to address and resolve process-related challenges.
  • Validation and Compliance:
    • Create and carry out process validation protocols in line with regulatory standards.
    • Ensure adherence to Good Manufacturing Practices (GMP) and other applicable regulatory guidelines.
    • Maintain comprehensive and precise documentation of all process-related activities.
  • Project Management:
    • Oversee and direct process engineering initiatives from inception to execution.
    • Formulate project timelines, budgets, and resource allocations to ensure successful outcomes.
    • Collaborate with suppliers and contractors to acquire necessary equipment and services.
  • Technical Support and Training:
    • Offer technical assistance and training to manufacturing personnel regarding new and existing processes.
    • Remain informed about industry trends and advancements in process engineering and pharmaceutical production.
Qualifications
  • Education:
    • Bachelor's degree in Chemical Engineering, Pharmaceutical Engineering, or a related discipline; a Master's degree is preferred.
  • Experience:
    • 3-5 years of experience in process engineering within the pharmaceutical sector.
    • Experience in process design, development, and optimization in a GMP-compliant environment.
  • Technical Skills:
    • Proficiency in process simulation and modeling tools (e.g., Aspen Plus, MATLAB).
    • Strong knowledge of process control principles and methodologies.
    • Familiarity with pharmaceutical manufacturing processes and equipment.
  • Soft Skills:
    • Outstanding problem-solving and analytical capabilities.
    • Strong project management and organizational skills.
    • Effective communication and interpersonal abilities.
    • Capacity to work autonomously and collaboratively in a fast-paced environment.

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