
Laboratory Manager - Microbiology
发布于 大约 2 个月前中层管理(经理/总监)
AI 估算 · 75k–115k
Base on US biotech lab manager median salary, adjusted for Burlington MA cost of living.
职位详情
关于这个职位
This role leads the Bacterial Retention team within the North American Validation Services group at MilliporeSigma, managing a team of scientists and specialists. You will oversee day-to-day microbiology and physical testing on pharmaceutical filtration devices, ensure compliance with cGMP, and drive continuous improvement. The position requires a mix of technical expertise in microbiology and laboratory management skills.
最低要求
Bachelor’s Degree in a life science field (e.g., Biology, Microbiology, Chemistry, etc.)
工作职责
Manage day to day operations focusing on microbiology and physical components testing on pharmaceutical filtration devices
优先资格
Experience leading with proven skills in managing diverse scientific teams
AI 洞察
优缺点分析
优点
- Work for a global leader in life science (MilliporeSigma) with strong brand and resources.
- Hands-on leadership role with direct impact on team performance and laboratory efficiency.
- Exposure to cGMP environment and regulatory compliance, which is highly valued in the industry.
- Competitive compensation and benefits, including performance-based bonuses.
- High responsibility for meeting aggressive timelines and managing multiple customer projects simultaneously.
- Requires balancing technical oversight with administrative tasks (performance reviews, hiring, etc.).
- Must stay current with evolving regulatory guidelines and ensure team compliance.
- This role is ideal for an experienced microbiologist or lab manager with a strong background in regulated biopharma, who enjoys leading a team and driving operational excellence.
缺点 / 挑战
暂无明显挑战项
角色解读
- Advance to senior laboratory manager or director roles within the Validation Services group or broader biopharma operations.
- Transition to global harmonization projects, gaining exposure to international regulatory standards and cross-site management.
- Develop expertise in advanced filtration technologies and regulatory strategy, potentially moving into R&D or quality assurance leadership.
- Lead and develop a team of scientists and specialists performing microbiology and physical testing on pharmaceutical filtration devices.
- Manage daily laboratory operations, including scheduling, resource allocation, and ensuring compliance with cGMP and regulatory standards.
- Drive continuous improvement initiatives to enhance cycle time, right-first-time rates, and rerun KPIs.
- Coordinate customer projects, prioritize high-visibility tasks, and maintain equipment calibration and validation programs.
- Strong background in microbiology and experience in regulated biopharma industry (cGMP).
- Proven laboratory management experience, including team leadership, performance management, and resource planning.
- Proficiency with laboratory electronic systems (LIMS, ELN) and data analysis to drive team performance.
- Excellent communication and collaboration skills, with ability to manage change and maintain composure under pressure.
申请策略
- Tailor your cover letter to express interest in leading a team at MilliporeSigma and your passion for validation services.
- Research the company's recent developments in life science and mention how your experience aligns with their mission.
- Emphasize your experience managing a laboratory in a cGMP environment, including specific metrics like cycle time reduction or right-first-time improvements.
- Highlight any team leadership roles, detailing the size of the team and your responsibilities like performance management and recruiting.
- Showcase your technical expertise in microbiology and familiarity with pharmaceutical filtration or validation testing.
- Include proficiency with LIMS, ELN, and other lab management software.
- If not already certified, consider taking a course on cGMP or regulatory affairs to demonstrate commitment.
- Enhance your data analysis skills (e.g., using Excel, Minitab, or statistical process control) to better manage KPIs.
面试指南
- Use the STAR method (Situation, Task, Action, Result) to structure your responses, focusing on specific examples from your experience.
- Highlight your leadership philosophy: balance between technical oversight and people management, and emphasize your proactive approach to compliance and improvement.
- How do you prioritize tasks when managing multiple customer projects with tight deadlines?
- Describe a time you implemented a continuous improvement initiative in a lab. What was the outcome?
- How do you ensure your team stays compliant with cGMP and regulatory guidelines?
- Tell me about your experience with laboratory electronic systems. How have you used data to manage team performance?
- How do you handle underperforming team members? Provide an example.
- Review the MilliporeSigma website and understand their validation services and filtration product lines.
职位点评
Competitive pay and benefits, impactful role in pharma validation, but limited WLB due to on-site requirements and tight deadlines.
薪资福利
The position offers a competitive salary range ($100,300-$155,900/year) plus performance bonuses and comprehensive benefits (health insurance, PTO, retirement). This is a solid compensatory package for a mid-level management role in the biotech industry.
成长发展
The role provides opportunities to lead a team, participate in global harmonization projects, and drive continuous improvement. However, there is no explicit mention of formal training or career advancement programs beyond the role itself.
工作生活
The role is on-site (Burlington, MA) with no mention of remote or flexible hours. The lab environment likely requires regular attendance, and the job description includes phrases like 'aggressive timelines' and 'meet aggressive timelines' which suggest potential overtime.
使命价值
MilliporeSigma's mission to 'enrich people's lives with solutions in Healthcare, Life Science, and Electronics' is clearly stated. The role contributes to validation testing for pharmaceutical filtration, which has direct impact on patient safety and product quality.