Kinovate Life Sciences Inc
Process Engineering Manager
Kinovate Life Sciences Inc - Oceanside, California, United States, 92058
Work at Kinovate Life Sciences Inc
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Overview
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Kinovate Life Sciences, Inc. established in 2004 in Oceanside, California. A wholly owned subsidiary of Nitto Denko Corporation (www.nitto.com), Kinovate was spun-off from Oceanside, CA based R&D facility Nitto Denko Technical Corp (www.ndtcorp.com) with a mission to provide the highest quality materials to niche life science markets worldwide.
Since its inception, Kinovate has grown to become the market leader in solid support in the oligonucleotide synthesis field. We are bringing the most creative minds in science and technology to develop medical discoveries and breakthroughs. Our customers are well-known in the biotechnology industry. We are in a growth phase within ISO work environment and leading towards a GMP Certification. KLS is seeking extraordinary people to join the team. KLS is proud to be an equal employment opportunity employer.
Why Work Here:
Great place to work. Small subsidiary of large international company headquartered in Japan. Generous discretionary bonuses. Health, dental, vision, life, and disability insurance effective from date of hire. Additional benefits include 401(k), 3 weeks vacation in your first year, 12 paid yearly holidays, 5 paid sick days, tuition reimbursement and more. Basic Objective: The Process Engineering Manager is responsible for overseeing and optimizing manufacturing processes within KLS. Ensures that production systems run efficiently, cost-effectively, and meets the highest standards of quality and safety. This position involves leading a team of engineers, collaborating with various departments, and implementing innovative solutions to improve production methods. The Process Engineering Manager will develop and manage the Project Management methodologies and provide expert guidance to project leaders. Specific Duties and Responsibilities: Act as a Subject Matter Expert for KLS production processes and operations. Ensuring all processes are implemented to meet KLSs EHS, Quality and Production requirements. Design processes, systems and equipment meeting all applicable codes, regulations, and Engineering best practices. Working with other members of the project team, Production, EHS and Quality teams, external vendors, and contractors to deliver capital projects on time and within budget. Commissioning new plant and processes. Optimizing the operation of existing processes. Aiding and troubleshooting support to the site operating team to maintain plant production & quality. Providing specialist technical assistance to the site HSE department, including providing responses to questions from the regulatory authorities (California, USA and International). Training site staff in new processes & programs. Requirements: Bachelors or masters degree (preferred) in Engineering or a related field, with 7-10 years of experience, preferable in Industrial Pharmaceuticals and/or Chemical Manufacturing. Experience managing industrial projects from concept to startup. Experience applying Project Management methodologies and RAGAGEP. Experience with Six Sigma or other process improvement methodologies. Experience with cGMP and ISO standards. Experience participating and/or leading Process Hazard Analysis (PHA, HAZOP), implementing and supporting Process Safety Management. Experience sizing and selecting process equipment, such as CSTR reactors, agitation systems, heat exchangers, pumps, vacuum systems, process instruments, etc. Experience reading and commenting P&ID, PFD, and other technical drawings. Self-motivated with strong initiative and drive to succeed. With excellent interpersonal skills, will be able to work effectively in a team and on their own initiative, leading a team as required. Excellent problem solving and analytical skills. Must be proficient in IT (Office packages). Working knowledge of Autocad and other engineering tools. Physical Job Requirements: Lifting and carrying items weighing up to 50 pounds. Work with and around forklifts. The employee is regularly required to use their hands and fingers to operate a computer keyboard, mouse, and telephone keypad or to write, as well as talk and hear. Seniority level
Mid-Senior level Employment type
Full-time Job function
Engineering and Product Management Industries Pharmaceutical Manufacturing
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Great place to work. Small subsidiary of large international company headquartered in Japan. Generous discretionary bonuses. Health, dental, vision, life, and disability insurance effective from date of hire. Additional benefits include 401(k), 3 weeks vacation in your first year, 12 paid yearly holidays, 5 paid sick days, tuition reimbursement and more. Basic Objective: The Process Engineering Manager is responsible for overseeing and optimizing manufacturing processes within KLS. Ensures that production systems run efficiently, cost-effectively, and meets the highest standards of quality and safety. This position involves leading a team of engineers, collaborating with various departments, and implementing innovative solutions to improve production methods. The Process Engineering Manager will develop and manage the Project Management methodologies and provide expert guidance to project leaders. Specific Duties and Responsibilities: Act as a Subject Matter Expert for KLS production processes and operations. Ensuring all processes are implemented to meet KLSs EHS, Quality and Production requirements. Design processes, systems and equipment meeting all applicable codes, regulations, and Engineering best practices. Working with other members of the project team, Production, EHS and Quality teams, external vendors, and contractors to deliver capital projects on time and within budget. Commissioning new plant and processes. Optimizing the operation of existing processes. Aiding and troubleshooting support to the site operating team to maintain plant production & quality. Providing specialist technical assistance to the site HSE department, including providing responses to questions from the regulatory authorities (California, USA and International). Training site staff in new processes & programs. Requirements: Bachelors or masters degree (preferred) in Engineering or a related field, with 7-10 years of experience, preferable in Industrial Pharmaceuticals and/or Chemical Manufacturing. Experience managing industrial projects from concept to startup. Experience applying Project Management methodologies and RAGAGEP. Experience with Six Sigma or other process improvement methodologies. Experience with cGMP and ISO standards. Experience participating and/or leading Process Hazard Analysis (PHA, HAZOP), implementing and supporting Process Safety Management. Experience sizing and selecting process equipment, such as CSTR reactors, agitation systems, heat exchangers, pumps, vacuum systems, process instruments, etc. Experience reading and commenting P&ID, PFD, and other technical drawings. Self-motivated with strong initiative and drive to succeed. With excellent interpersonal skills, will be able to work effectively in a team and on their own initiative, leading a team as required. Excellent problem solving and analytical skills. Must be proficient in IT (Office packages). Working knowledge of Autocad and other engineering tools. Physical Job Requirements: Lifting and carrying items weighing up to 50 pounds. Work with and around forklifts. The employee is regularly required to use their hands and fingers to operate a computer keyboard, mouse, and telephone keypad or to write, as well as talk and hear. Seniority level
Mid-Senior level Employment type
Full-time Job function
Engineering and Product Management Industries Pharmaceutical Manufacturing
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