Lead Process Engineer Responsibilities:

• Lead and execute Design of Experiments (DOE) studies to evaluate and optimize pharmaceutical manufacturing and packaging processes
• Provide technical leadership for process improvement initiatives, focusing on efficiency, reliability, and product quality
• Support and optimize liquid/gel filling and bottle/tube packaging operations within pharmaceutical manufacturing environments
• Conduct root cause investigations for process deviations or performance issues and implement sustainable corrective actions
• Collaborate with cross-functional teams including manufacturing, quality, and engineering to support process development and improvement efforts
• Serve as a client-facing technical expert, working directly on-site with customers and stakeholders to address process challenges
• Document process studies, experimental results, and improvement initiatives in accordance with industry and company standards

Job Requirements:

• Bachelor’s or Master’s degree in Chemical Engineering
• 5–10+ years of experience in the pharmaceutical industry supporting manufacturing or process engineering
• Minimum 5 years of hands-on experience designing and executing DOE (Design of Experiments) studies
• Demonstrated experience supporting liquid/gel filling and bottle/tube packaging processes
• Strong analytical and problem-solving skills with experience performing root cause analysis and implementing process improvements
• Ability to work on-site 75%+ of the time

The Opportunity:

We are seeking a motivated Manufacturing Engineer to support daily manufacturing operations for our cfDNA-based diagnostic assay platform. This entry-level position is ideal for a detail-oriented, hands-on individual eager to learn in a fast-paced, regulated biotech environment. You will play a vital role in executing production tasks, maintaining equipment, and ensuring quality and compliance across manufacturing workflows.

You will be part of a team that is passionate about developing novel diagnostic tests for the early detection of cancers. As part of the team, you will be in a Company that aims more than to become one of the leaders in the industry. We want to have a huge positive impact on society by achieving the ambitious purpose of “making cancer a curable disease by detecting it earlier”.

How you’ll contribute: 

• Execute routine manufacturing activities in compliance with established SOPs and batch records.
• Prepare reagents, buffers, and consumables according to specifications.
• Operate, clean, and maintain laboratory and production equipment per defined schedules.
• Record all data accurately and maintain complete, traceable documentation in accordance with GMP standards.
• Perform basic calibration checks and assist with preventive maintenance programs.
• Promptly report equipment issues or maintenance needs to supervisors.
• Complete all documentation following GDP (Good Documentation Practice) and GMP requirements.
• Ensure all entries are legible, dated, and verified where required.
• Support audit readiness and contribute to maintaining compliant laboratory environments.
• Adhere to biosafety, chemical safety, and PPE requirements at all times.
• Follow QMS procedures to maintain high product quality and data integrity.
• Immediately escalate deviations, non-conformances, or safety concerns for resolution with Quality and Operations.
• Communicate task progress, delays, or issues clearly to supervisors.
• Collaborate with peers to maintain smooth production flow and continuous improvement.
• Participate in departmental meetings, training, and improvement initiatives.
• Contribute to a respectful, inclusive, and team-oriented culture.

What you’ll bring:

• BS degree in Bioengineering, Chemical Engineering, Molecular Biology, or related field.
• 0–2 years of experience in manufacturing, laboratory, or process engineering.
• Familiarity with basic laboratory techniques, aseptic practices, and documentation standards.
• Strong attention to detail and ability to follow written procedures accurately.
• Exposure to reagent or diagnostic kit manufacturing, liquid handling, or scale-up operations.
• Reliable, organized, and committed to learning in a fast-paced environment.
• Positive and proactive attitude with strong teamwork skills.
• Effective communicator with solid problem-solving and time management abilities.

What we´ll offer:

We’re proud to offer exceptional corporate benefits which include:

• 22 days of PTO with the possibility to carry over 10 days to the following year. 
• Company Holidays, plus your Birthday off!  
• Company-sponsored benefit plans, including medical, dental, and vision insurance plus life, STD, and LTD coverage, and 401(k). 
• Flexible work schedule  
• And more to come!