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Senior Process Engineer; Pharmaceutical Manufacturing

Job in Glen, Alcorn County, Mississippi, 38846, USA
Listing for: Placements24
Full Time position
Listed on 2026-10-20
Job specializations:
  • Engineering
    Process Engineer, Manufacturing Engineer, Validation Engineer, Quality Engineering
  • Manufacturing / Production
    Manufacturing Engineer, Validation Engineer, Quality Engineering
Salary/Wage Range or Industry Benchmark: 67000 - 97000 USD Yearly USD 67000.00 97000.00 YEAR
Job Description & How to Apply Below
Position: Senior Process Engineer (Pharmaceutical Manufacturing)
Location: Glen

About the Role

Our client, a leading pharmaceutical company, is seeking a highly skilled Senior Process Engineer to enhance and optimize manufacturing processes at their facility in Welkom, Free State, ZA. This critical role involves designing, implementing, and validating new manufacturing technologies and processes to improve efficiency, yield, and product quality. The ideal candidate will possess a strong engineering background coupled with extensive experience in pharmaceutical manufacturing environments.

You will be instrumental in driving innovation and ensuring operational excellence within our client's production operations in Welkom, Free State, ZA.

Key Responsibilities
  • Lead process development and optimization initiatives for pharmaceutical manufacturing.
  • Design, specify, and implement new process equipment and technologies.
  • Develop and execute validation protocols (IQ/OQ/PQ) for manufacturing equipment and processes.
  • Analyze process data to identify areas for improvement and implement corrective actions.
  • Troubleshoot complex manufacturing process issues and provide technical solutions.
  • Ensure all processes comply with GMP, safety regulations, and environmental standards.
  • Collaborate with cross-functional teams including Production, Quality Assurance, R&D, and Maintenance.
  • Develop and deliver training to technical staff on new processes and equipment.
  • Stay abreast of industry best practices and emerging technologies in pharmaceutical manufacturing.
  • Prepare technical reports, process flow diagrams, and documentation for regulatory submissions.
Requirements
  • Bachelor's degree in Chemical Engineering, Mechanical Engineering, or a related field.
  • Master's degree preferred.
  • Minimum of 5-7 years of experience in process engineering within the pharmaceutical or biotechnology industry.
  • Proven experience in process design, scale-up, validation, and optimization of pharmaceutical manufacturing processes.
  • In-depth knowledge of GMP, FDA, and other relevant regulatory requirements.
  • Strong understanding of unit operations in pharmaceutical manufacturing (e.g., granulation, tablet compression, sterile filling).
  • Experience with process simulation and modeling software is a plus.
  • Excellent analytical, problem-solving, and project management skills.
  • Proficiency in technical writing and documentation.
  • Strong interpersonal and communication skills to effectively collaborate with diverse teams.
  • Must be willing to work full-time on-site in Welkom, Free State, ZA.
Benefits
  • Our client offers a competitive salary commensurate with experience.
  • A comprehensive benefits package including medical aid, retirement contributions, and performance bonuses.
  • Opportunities for professional growth through advanced training, workshops, and conference attendance.
  • The company fosters a collaborative and innovative work culture, prioritizing employee well‑being and a sustainable work‑life balance in Welkom, Free State, ZA.

This role provides a significant opportunity to impact pharmaceutical manufacturing advancements.

Position Requirements
10+ Years work experience
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