Engineer II - MTS

As an Engineer II - MTS, you will play a pivotal role in our internal Manufacturing Technical Support team, where your main responsibilities include assisting in the execution of development experiments, conducting lab organization for operations, and performing various analytical tests on drug delivery devices. You will also help manage routine testing timelines, coordinate sample submissions, and contribute to the creation of essential technical documents.

To qualify for the Engineer II - MTS role, you should have a Bachelor’s degree in a relevant field such as biochemistry, chemistry, engineering, or related wet lab experience. Additionally, a minimum of two years of professional lab experience is required, along with familiarity in process development or investigations related to commercial manufacturing.

Success as an Engineer II - MTS hinges on strong teamwork and organizational skills, the ability to adapt to changing environments, and effective communication capabilities. You will also need to demonstrate the ability to independently handle multiple priorities while adhering to strict laboratory safety requirements.

The work schedule for the Engineer II - MTS role is set from Monday to Friday, typically from 9:00 AM to 5:00 PM. Importantly, no weekend work is required, allowing for a balanced work-life dynamic while you contribute to groundbreaking advancements in our labs.

Yes, as an Engineer II - MTS, you may be required to travel between our Alnylam sites, including Kendall, Alewife, and Norton as needed to perform your duties effectively. Flexibility and willingness to comply with this travel will be essential for this role.

In answering this question, highlight specific experiments you have conducted, the methods used, and the outcomes achieved. It’s important to emphasize your familiarity with techniques such as UPLC/HPLC and your ability to follow documented protocols.

Discuss your approach to managing multiple priorities by sharing examples from past experiences. Focus on your organizational strategies and how you effectively communicate with team members to ensure that deadlines are met without sacrificing quality.

Your answer should reflect your commitment to safety protocols. Mention specific safety procedures you follow, how you ensure proper lab equipment handling, and your familiarity with safety regulations relevant to laboratory environments.

Provide a concise example, focusing on the challenge, the steps you took to resolve it, and the outcome. This demonstrates your problem-solving skills and your ability to handle unexpected situations in the lab.

Discuss your methods for continuous learning, such as attending workshops, reading industry publications, or participating in relevant forums. This shows your initiative and commitment to professional development.

Identify specific instances where you have documented experiments or written technical documents such as SOPs or reports. Emphasize your attention to detail and ability to convey complex information clearly.

Talk about how you communicate with teammates, participate in group discussions, and share responsibilities. Highlight any collaborative projects you’ve contributed to and how teamwork enhanced the overall success of the work.

Explain your approach to identifying problems and implementing solutions based on analytical thinking. Include any practical examples where you successfully troubleshot issues during a lab process, which showcases your critical thinking abilities.

In your response, outline the differences between GMP and non-GMP operations. Highlight your understanding of the significance of compliance in laboratory work and how it translates to the quality of drug products.

Your answer should reflect genuine enthusiasm for the role and the company. Describe what excites you about contributing to the RNAi technology area, and how your skills align with the goals of the team and the company at large.