At Amaris, we strive to provide our candidates with the best possible recruitment experience. We like to get to know our candidates, challenge them, and be able to give them proper feedback as quickly as possible. Here's what our recruitment process looks like:
Brief Call: Our process typically begins with a brief virtual/phone conversation to get to know you! The objective? Learn about you, understand your motivations, and make sure we have the right job for you!
Interviews (the average number of interviews is 3 - the number may vary depending on the level of seniority required for the position). During the interviews, you will meet people from our team: your line manager of course, but also other people related to your future role. We will talk in depth about you, your experience, and skills, but also about the position and what will be expected of you. Of course, you will also get to know Amaris: our culture, our roots, our teams, and your career opportunities!
Case study: Depending on the position, we may ask you to take a test. This could be a role play, a technical assessment, a problem-solving scenario, etc.
As you know, every person is different and so is every role in a company. That is why we have to adapt accordingly, and the process may differ slightly at times. However, please know that we always put ourselves in the candidate's shoes to ensure they have the best possible experience.
We look forward to meeting you!
Job description ABOUT THE JOB
As a Senior Process Engineer, you will play a critical role in supporting day-to-day manufacturing operations and driving continuous improvement in a regulated biopharmaceutical environment. You will:
Support new product introduction (NPI) and technology transfer activities. Lead and support process validation and characterization studies. Develop validation and characterization protocols/reports in line with cGMP, policies, standards, and project timelines. Manage execution of validation and characterization studies, ensuring deviation root cause analysis (RCA) and investigations are completed. Collaborate with cross-functional teams to arrange, plan and ensure smooth execution of process validation activities. Lead or support process and technical change management and change implementation activities. Ensure day-to-day upkeep and final clean-up of the areas where activities are performed, in compliance with cGMP and safety regulations. Support any other validation-related tasks assigned by your manager. ABOUT YOU Academic Background: Degree or Diploma in Chemical, Bioprocess, Process, or Mechanical Engineering. 8–10 years of relevant working experience in the pharmaceutical or biologics manufacturing industry. Strong expertise in process validation and characterization. Knowledge of cGMP requirements and safety regulations. Experience with deviation management, root cause analysis and investigations. Ability to collaborate with cross-functional teams and stakeholders. You demonstrate strong problem-solving skills, rigor, and a proactive mindset.WHY AMARIS?
At Amaris Consulting, we believe in creating a thriving, positive workplace where every team member can grow, connect, and make a real impact. Here’s what you can expect when you join our dynamic community:
Global Diversity: Be part of an international team of 110+ nationalities, celebrating diverse perspectives and collaboration. Trust and Growth: With 70% of our leaders starting at entry-level, we’re committed to nurturing talent and empowering you to reach new heights. Continuous Learning: Unlock your full potential with our internal Academy and over 250 training modules designed for your professional growth. Vibrant Culture: Enjoy a workplace where energy, fun, and camaraderie come together through afterworks, networking events, and more. Meaningful Impact: Join us in making a difference through our CSR initiatives, including the WeCare Together program, and be part of something bigger.Equal Opportunity
Amaris Consulting is proud to be an equal opportunity workplace. We are committed to promoting diversity within the workforce and creating an inclusive working environment. For this purpose, we welcome applications from all qualified candidates regardless of gender, sexual orientation, race, ethnicity, beliefs, age, marital status, disability, or other characteristics.