GMP Equipment Monitoring Technician, 3rd Shift

As the GMP Equipment Monitoring Technician at Forge Biologics, you'll be vital in overseeing and recording machinery performance, conducting regular maintenance, and managing compliance with regulatory standards. This role encompasses monitoring GMP and QC equipment to ensure all are in optimal working order, maintaining logbooks for performance data, addressing equipment issues promptly, and collaborating with various teams to improve operational processes.

To excel as a GMP Equipment Monitoring Technician at Forge Biologics, candidates should possess at least a high school diploma, though technical certification or relevant experience is preferred. Experience in laboratory settings, especially within regulated environments, strong problem-solving skills, and the ability to work independently during 3rd shift shifts are essential qualifications for this role.

Yes, Forge Biologics is committed to the professional development of its team members. As a GMP Equipment Monitoring Technician, you'll have access to various training opportunities, including in-house mentoring, leadership development coaching, and resources such as LinkedIn Learning. Our goal is to ensure you are well-equipped to handle your responsibilities and grow within the company.

The work environment for the GMP Equipment Monitoring Technician at Forge Biologics involves both laboratory and standard office settings. You’ll spend time in clean rooms and may need to wear personal protective equipment. The role requires precision and attention to detail, often standing or sitting for extended periods while monitoring equipment and conducting maintenance activities in a busy, team-oriented atmosphere.

Forge Biologics offers a comprehensive benefits package for the GMP Equipment Monitoring Technician role, which includes health, dental, and vision insurance starting on your first day, a flexible PTO policy, a 401(K) with company match, and wellness benefits. Additional perks include paid parental leave, an employee assistance program, and professional development resources to support your personal and career growth.

When answering this question, focus on specific experiences relevant to working with GMP and QC protocols. Detail any positions where you’ve monitored equipment and addressed issues, demonstrating your understanding of compliance and attention to detail in regulated environments.

Highlight your commitment to safety by discussing the steps you take to ensure compliance, such as following standard operating procedures, conducting regular checks, and maintaining accurate logs. Provide specific examples that demonstrate your proactive approach to anticipating and mitigating risks.

Use the STAR (Situation, Task, Action, Result) method to succinctly explain the context, your role, the necessary actions you took to resolve the issue, and the positive outcome. This showcases your problem-solving skills and ability to act decisively under pressure.

Effective communication is essential in a multi-shift environment. Discuss strategies you've implemented, such as maintaining detailed shift logbooks, utilizing communication tools, and fostering relationships with team members to ensure seamless information transfer.

Talk about the importance of regular preventive maintenance schedules, calibration checks, and thorough documentation. Mention any specific practices you believe keep equipment functioning optimally and compliant with laws and regulations.

Explain your methodology for addressing inconsistencies, which should involve investigating the root cause, consulting with team members, and adjusting the monitoring protocols if necessary. Emphasize your analytical mindset and focus on continuous improvement.

Articulate your understanding of how documentation supports compliance, quality assurance, and accountability in a regulated environment. Discuss your experience and practices in maintaining accurate and thorough records for audits and inspections.

Mention your commitment to ongoing education through workshops, webinars, and industry publications. Talk about how you keep updated on changes in regulatory standards and apply them to your practices at work to ensure compliance.

Share specific examples of collaborative projects where you’ve worked with teams from various departments. Focus on your role in facilitating communication, identifying shared goals, and solving problems collectively.

Discuss your passion for biotechnology and how it aligns with your values and career goals. Personal anecdotes or experiences that led you to this field can really showcase your enthusiasm and commitment to making a difference in patients’ lives.