Senior Manager, Site Operations Lead
2 weeks ago
CRISPR Therapeutics is seeking a highly skilled and experienced Senior Manager, Site Operations to join our team. This role will be responsible for developing and managing the master site schedule, site projects, business process improvements, and short to long-range strategic planning for the site.
Key Responsibilities:- Develop and monitor site goals, manage short-term and long-range strategic planning for the site.
- Manage master site schedule, select site projects to ensure activities are completed on time and within budget while meeting quality and safety standards.
- Manage site risk register, work with site leadership to develop risk mitigation strategies, solutions as needed.
- Identify site business process gaps and improvement strategies to enhance operational efficiency and effectiveness.
- Lead cross-functional teams, and process improvement projects, including defining project scope, objectives, and timelines.
- Utilize continuous improvement methodologies and tools to analyze current processes, identify areas of improvement, and recommend solutions to streamline workflows.
- Work with site leadership and functional areas to track key performance indicators (KPIs) to measure the impact of process improvements and sustainable change.
- Consistently perform duties within established SOPs, and in accordance with GxP requirements, where applicable.
- Provide training and support to employees on project management, and process improvement methodology and tools.
- Stay current on industry best practices, trends, and process excellence to continuously improve processes.
- Bachelor's degree and 10+ years of relevant experience or advanced degree 8+ years relevant experience, including 3+ years of experience leading projects.
- Prior GMP experience required.
- Excellent project management skills with the ability to lead cross-functional teams and deliver results on time within budget.
- Experience working cross-functionally to manage interdisciplinary schedules and risk.
- Experience in process improvement methodologies such as Lean Six Sigma (e.g., Value Stream Mapping, Kaizen) or other continuous improvement frameworks.
- Strong leadership skills, including demonstrated ability to influence at all levels of an organization.
- Detail-oriented with a focus on continuous improvement and driving change.
- Excellent oral and written communication skills, including presentation and facilitation skills.
- Expertise in Microsoft suite.
- Proven ability to deliver sustained results.
- Ability to work independently and successfully in a matrix environment, prioritize and manage multiple tasks simultaneously, integrate cross-functional issues, and balance competing priorities effectively.
- PMP strongly preferred, Lean 6 Sigma Certification a plus.
- Knowledge of biotechnology/pharmaceutical product technical transfer, manufacturing, and quality control assays preferred.
- Experience in Smartsheet, process mapping, and process optimization tools/software.
- Strong problem-solving skills and a proactive approach to identifying opportunities for improvement.
- Ability to work independently and as part of a team in a fast-paced environment.
- Collaborative – Openness, One Team.
- Undaunted – Fearless, Can-do attitude.
- Results Orientation – Delivering progress toward our mission. Sense of urgency in solving problems.
- Entrepreneurial Spirit – Proactive. Ownership mindset.
CRISPR Therapeutics is an equal employment opportunity and non-discrimination employer for all employees and qualified applicants without regard to a person's race, color, gender, age, religion, national origin, ancestry, disability, veteran status, genetic information, sexual orientation, or any characteristic protected under applicable law.
For more information, please visit our website at http://www.crisprtx.com/about-us/privacy-policy.
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