Operational Coach Lead Technician-2

Job description

Job Description For over 130 years, we have pioneered groundbreaking science. Today, we are driven by continuous innovation to develop breakthrough medicines, vaccines and technology. Rooted in direct experience on the farm and in the clinic, we work hand in hand with our customers every step of the way. Our singular focus is to empower those who care for animals, helping them manage their vital responsibility with confidence. Because when it comes to animal health, no one sees it like we do. Our Manufacturing Operations teams are the people that make our products. We work in the manufacturing plants with a “Safety First, Quality Always” mindset striving for continuous improvement. We work in the local plant connected to our global manufacturing network to ensure the highest quality of raw materials, intermediates and finished products. We are seeking an Lead Operations Technician within our Production Operations Team. The Lead Technician will primarily support the team by focusing on coaching at the team level, as well as productivity within the scope of their own team. Responsibilities: The duties within the department include large scale antigen production and processing in accordance with GMP (Good Manufacturing Practices). Primary daily tasks will include the following: Aseptic material handling and cell scale up Preparation/ operation of fermenters and stainless-steel vessels CIP and SIP of lines and tanks Employee Development & Leadership: Models Company leadership principles and inclusive behaviors Provides coaching and supports skills development and process capabilities within their team Supports effective feedback and coaching within the team during the Performance Management cycle Responsible for ensuring all operators receive appropriate training for all assigned tasks Supports the effective performance management of individuals in their team Safety & Quality Compliance: Demonstrates a strong compliance mind-set (EHS and Quality) and continuously sets a high standard for themselves and others Follows safe operating instructions for all tasks and equipment Ensures the right tools and equipment specified for the task are available and utilized Ensures the correct personal protective equipment required is available and utilized Follow up any reported defects or workplace hazards immediately Report all accidents, incidents and near misses within 24 hours and to participate in investigation and identification of effective corrective and preventative actions Supports the on-time completion of Quality compliance tasks in relation to Deviation, CAPA and Change Control management Responsible for all aspects of Quality Assurance including cGMP, RFT and good documentation practices and provides coaching to others Supports the update, review and approval of GMP documentation including SOP’s and MD’s Productivity: Responsible for the Daily, Weekly and Monthly schedule adherence of production activities within their department Build and maintain strong collaborations with different stakeholders throughout the Site Operations such as BTS, Engineering, Quality and R&D Supports the Manufacturing Operations Teams in creating a culture of continuous improvement and leads by example Supports initiatives for stabilizing and improving production processes Supports the effective application of Lean Six Sigma, Project Management and Change Management Tools Responsible for the facilitation of an effective Tier 1 Meeting:A visual status of training within the department A visual status of the completion of compliance tasks A visual status of schedule adherence Communication of key issues impacting the team Financial: Recognizes and investigates opportunities for financial savings Role Requirements: High School Diploma plus minimum five years working in a Pharmaceutical Manufacturing role OR BS Degree in a relevant scientific discipline plus minimum two years working in a Pharmaceutical Manufacturing role Strong attention to detail to achieve a consistent error-free execution of daily job tasks Good concurrent and complete documentation using Good Manufacturing Practices are essential Demonstrated ability to learn and effectively use a variety of software applications, databases, and digital tools Experience working in a shop floor supervisory or Team Lead role preferred #MSJR The salary range for this role is: $71,900 - $113,200 This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An employee’s position within the salary range will be based on several factors including, but not limited to relevant education, qualifications, certifications, experience, skills, geographic location, government requirements, and business or organizational needs. The successful candidate will be eligible for annual bonus and long-term incentive, if applicable. We offer a comprehensive package of benefits. Available benefits include medical, dental, vision healthcare and other insurance benefits (for employee and family), retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days. Required Skills: Adaptability, Adaptability, Autoclaving, Biopharmaceutical Industry, Cell Culture Process Development, Change Request Management, Data Analysis, Disease Prevention, Filtering Equipment, Global Manufacturing, GMP Compliance, Good Laboratory Practices (GLPs), Good Manufacturing Practices (GMP), Lean Six Sigma (LSS), Liquid Chromatography (LC), Manufacturing Documentation, Manufacturing Quality Control, Media Preparation, Organizational Performance Management, Pharmaceutical Manufacturing, Preventive Action, Process Control, Production Processes, Production Scheduling, Six Sigma {+ 1 more} Preferred Skills: Current Employees apply HERE Current Contingent Workers apply HERE US and Puerto Rico Residents Only: Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Please click here if you need an accommodation during the application or hiring process. As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics. As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities. For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit: EEOC Know Your Rights EEOC GINA Supplement​ We are proud to be a company that embraces the value of bringing together, talented, and committed people with diverse experiences, perspectives, skills and backgrounds. The fastest way to breakthrough innovation is when people with diverse ideas, broad experiences, backgrounds, and skills come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively. Learn more about your rights, including under California, Colorado and other US State Acts San Francisco Residents Only: We will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance Los Angeles Residents Only: We will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles’ Fair Chance Initiative for Hiring Ordinance Search Firm Representatives Please Read Carefully Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment oppo