Senior Process Engineer for Global Pharmaceutical Company

vor 1 Woche


Neuenburg, Neuenburg, Schweiz CK Group Vollzeit

Company Overview

CK Group is a leading pharmaceutical company with a global presence, committed to delivering high-quality products and services. Our team of experts works tirelessly to ensure the highest standards of quality and compliance in all aspects of our business.

Job Description

We are seeking an experienced Process Engineer to join our team in Neuchatel, Switzerland. As a Process Engineer, you will be responsible for manufacturing support activities, project management, and audit and regulatory questions related tasks.

Main Responsibilities:

  • Manufacturing support activities (deviation, process follow-up) 45% of the responsibilities.
  • Projects management represents 45% of the responsibilities.
  • Audit and Regulatory questions related activities represents 10% of the responsibilities.

Further Responsibilities:

  • Lead process improvement projects or activities.
  • Develop and optimize process parameters.
  • Ensure process performances through Quality by Design (QbD) and Continuous Process Verification (CPV) approaches.
  • Identify business opportunities.
  • Ensure communication and act proactively in case of performance trending.
  • Lead and/or support investigations related to deviation/CAPA process.
  • Perform product impact assessment for deviation.
  • Lead projects or activities related to FF process or equipment (from User Requirements Specifications to Process Performance Qualification).
  • Support validation activities.
  • Support or present topic during regulatory inspections.
  • Support technology transfer.

Salary: The estimated salary for this position is around $120,000 per annum, depending on experience.

Benefits:

  • Pension scheme
  • Life insurance
  • Holidays

Required Skills and Qualifications:

  • Minimum 3-5 years of experience in Fill and Finish area for recombinant protein.
  • Engineering or university degree in biotechnology.
  • Language skills: Fluent in English and French.
  • Knowledge of cGMP and quality requirements.
  • Able to deal with statistics.
  • Strong energetic team player with good communication skills.
  • Ability to lead effectively and efficiently process validation topics.
  • Ability to manage multiple priorities in a manufacturing plant setting.
  • Ability to analyze, review and interpret validation data.
  • Must have uncompromising dedication to quality and an excellent understanding of cGMPs and other regulatory guidelines.
  • Interpersonal skills that enables you to work with people at all levels.
  • Ability to plan, multitask, and manage time effectively.
  • Must display eagerness to learn, to innovate, drive for solutions and continuously improvement.


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