Senior GXP Facilities Specialist

Job Description: Company Overview Founded over a decade ago, CRISPR Therapeutics is a leading biopharmaceutical company focused on developing transformative gene-based medicines for serious human diseases. The Company has evolved from a pioneering research-stage organization into an industry leader, marking a historic milestone with the approval of CASGEVY® (exagamglogene autotemcel [exa-cel]), the world's first CRISPR-based therapy, approved for eligible patients with sickle cell disease and transfusion-dependent beta thalassemia. CRISPR Therapeutics is advancing a broad and diversified pipeline across hemoglobinopathies, cardiovascular, autoimmune, oncology, regenerative medicine and rare diseases. The Company continues to expand its leadership in gene editing through the development of SyNTase™ editing, a novel and proprietary gene-editing platform designed to enable precise, efficient, and scalable gene correction. To accelerate and expand its impact, CRISPR Therapeutics has established strategic collaborations with leading biopharmaceutical partners, including Vertex Pharmaceuticals. CRISPR Therapeutics AG is headquartered in Zug, Switzerland, with its wholly-owned U.S. subsidiary, CRISPR Therapeutics, Inc., and R&D operations based in Boston, Massachusetts and San Francisco, California. Position Summary The role will be responsible for the day-to-day work of building and utility operations and repair, maintenance program execution, technician training and emergency response. Prior experience in the operation, shutdown support and execution, maintenance and repair of cGMP manufacturing facilities utility systems and process equipment, as well as proven leadership skills. Responsibilities Perform preventative and corrective maintenance activities to support process equipment and systems, in accordance with established procedures and/or approved practices. Support efforts in developing remediation for follow-up and emergency work. Responsible for performing all work using all prescribed safety procedures. Troubleshoot equipment and systems and repair malfunctioning equipment. Work with equipment owners/engineers and direct the performance of work by equipment vendors. Responsible for periodic inspections of equipment to ensure they are operating properly and safely. Assist with installation of equipment and write safety and maintenance procedures for new equipment. Must be able to effectively train equipment technicians. Must be able to lead troubleshooting activities to identify root cause and take immediate and appropriate action to implement the repair. Must be able to work with maintenance scheduling software to initiate, execute, and reconcile maintenance work orders. Respond to alarms and document activities in accordance with cGMP requirements. Working with equipment owners and develop remediation activities for alarms. Proficient performing Quality Management System tasks such as deviation, change control and CAPA deliverables. Must be able to assume a leadership role and effectively communication to Management when deemed necessary. Other duties as required. Provide "on-call" support on a rotating basis. Support regular 24-7 operation of facility and respond to facilities issues as needed. Minimum Qualifications 12+ years of experience performing process support equipment and plant utility maintenance, troubleshooting and repair required. 10+ years of experience working in a cGMP environment is required. Proven ability to effectively lead, influence and course correct as needed. Experience in installation of new equipment and systems, as well as, developing their maintenance SOPs. Experience interfacing with multiple external vendors. Ability to effectively communicate and collaborate with internal and external stakeholders. Ability to work effectively in a collaborative team environment. Strong knowledge, troubleshooting skills and maintenance competence on GMP utilities and equipment. Proficient knowledge of controls and automation. Self-driven, independently motivated, data driven and excellent problem-solving ability. Proficient in use of CMMS and BMS systems. Experience with Blue Mountain and/or Alberio systems a plus BS, Certificate or Associate's Degree Preferred Preferred Qualifications Bachelor's degree in industrial engineering or related technical field Competencies 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. Due to the nature of their work, our manufacturing and lab-based positions are located fully on-site. Senior GXP Facilities Specialist: Base pay range of $95,000 to $105,000+ bonus, equity and benefits The range provided is CRISPR Therapeutics' reasonable estimate of the base compensation for this role. The actual amount will be based on job-related and non-discriminatory factors such as experience, training, skills, and abilities. CRISPR Therapeutics, Inc. is committed to equal employment opportunity and non-discrimination 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. To view our Privacy Statement, please click the following link: http://www.crisprtx.com/about-us/privacy-policy Since its inception over a decade ago, CRISPR Therapeutics has transformed from a research-stage company advancing programs in the field of gene editing, to a company with a diverse portfolio of product candidates across a broad range of disease areas including hemoglobinopathies, oncology, regenerative medicine, cardiovascular and rare diseases. The Nobel Prize-winning CRISPR science has revolutionized biomedical research and represents a powerful, clinically validated approach with the potential to create a new class of potentially transformative medicines. To accelerate and expand its efforts, CRISPR Therapeutics has established strategic partnerships with leading companies including Vertex Pharmaceuticals. CRISPR Therapeutics AG is headquartered in Zug, Switzerland, with its wholly-owned U.S. subsidiary, CRISPR Therapeutics, Inc., and R&D operations based in Boston, Massachusetts and San Francisco, California, and business offices in London, United Kingdom. CRISPR Therapeutics, Inc. is committed to equal employment opportunity and non-discrimination 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. To view our Privacy Statement, please click the following link: http://www.crisprtx.com/about-us/privacy-policy