We have other current jobs related to this field that you can find below


  • Thousand Oaks, United States EPITEC Full time

    Summary:This engineering position supports manufacturing activities associated with cGMP equipment and facilities for a leading pharmaceutical company. The senior engineer works in partnership with the automation, maintenance, project management, corporate engineering, and manufacturing to develop and oversee the operation and reliability of equipment while...


  • Thousand Oaks, United States BioPharma Consulting JAD Group Full time

    Job DescriptionJob DescriptionJoin the team at BioPharma Consulting JAD Group as a Maintenance Technician Senior. In this role, you will be responsible for overseeing the maintenance and repair of equipment and systems used in the biopharmaceutical industry. You will work closely with the Facilities & Engineering Department to ensure equipment reliability...


  • Thousand Oaks, United States BioPharma Consulting JAD Group Full time

    Job DescriptionJob DescriptionJoin the team at BioPharma Consulting JAD Group as a Maintenance Technician Senior. In this role, you will be responsible for overseeing the maintenance and repair of equipment and systems used in the biopharmaceutical industry. You will work closely with the Facilities & Engineering Department to ensure equipment reliability...


  • Thousand Oaks, United States BioPharma Consulting JAD Group Full time

    Join the team at BioPharma Consulting JAD Group as a Maintenance Technician Senior. In this role, you will be responsible for overseeing the maintenance and repair of equipment and systems used in the biopharmaceutical industry. You will work closely with the Facilities & Engineering Department to ensure equipment reliability and compliance with regulatory...


  • Thousand Oaks, United States BioPharma Consulting JAD Group Full time

    Job DescriptionJob DescriptionJoin the team at BioPharma Consulting JAD Group as a Maintenance Technician Senior. In this role, you will be responsible for overseeing the maintenance and repair of equipment and systems used in the biopharmaceutical industry. You will work closely with the Facilities & Engineering Department to ensure equipment reliability...


  • Thousand Oaks, United States Quality Consulting Group Full time

    Job DescriptionJob DescriptionQUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and enthusiastic to join our team. In this role, you’ll work with a highly enthusiastic team, contributing in a world-class manufacturing industry in Puerto Rico &...


  • Thousand Oaks, United States Quality Consulting Group Full time

    Job DescriptionJob DescriptionQUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and enthusiastic to join our team. In this role, you’ll work with a highly enthusiastic team, contributing in a world-class manufacturing industry in Puerto Rico &...


  • Thousand Oaks, United States The Steely Group Full time

    Job DescriptionJob DescriptionResponsibilities:Maintain and repair all production mechanical equipmentSupport the maintenance, operation, and repair of all systems, subsystems, and equipment within the Fill / Finish facilityProvide support to engineering and operations in the design, installation, testing, operation, and maintenance of Fill Finish...


  • Thousand Oaks, California, United States Aequor Full time

    Senior Maintenance Technician (Onsite Job potential for 2nd or 3rd shift most likely will be night shift 4 nights on, 3 off / etc)Onsite at Thousand Oaks, CA - potential for 2nd or 3rd shift most likely will be night shift 4 nights on, 3 off / etc.Mechanically inclined - person that has experience working with hands/ hands onPrecision machinery experience...


  • Thousand Oaks, United States Aequor Full time

    Senior Maintenance Technician (Onsite Job potential for 2nd or 3rd shift most likely will be night shift 4 nights on, 3 off / etc)Onsite at Thousand Oaks, CA - potential for 2nd or 3rd shift most likely will be night shift 4 nights on, 3 off / etc.Mechanically inclined - person that has experience working with hands/ hands onPrecision machinery experience...

  • Engineer

    1 month ago


    Thousand Oaks, United States EPITEC Full time

    Position Overview:Seeking a highly skilled and practical Senior Engineer to support manufacturing activities associated with cGMP equipment and facilities at our Thousand Oaks location. The ideal candidate will have a strong background in technical engineering and mathematics, with hands-on experience in industries such as drug substance, pharmaceuticals,...

  • Process Engineer

    3 months ago


    Thousand Oaks, United States ACL Digital Full time

    Title: EngineerLocation: Thousand Oaks, CADuration: 12 + months contractThis engineering position supports manufacturing activities associated with cGMP equipment and facilities at Amgen Thousand Oaks (ATO). The engineer works in partnership with the automation, maintenance, project management, corporate engineering, and manufacturing to develop and oversee...


  • Thousand Oaks, United States The International Society for Pharmaceutical Engineering Inc Full time

    Job Title: Senior Engineer Location: Thousand Oaks, CA Duration: 12 Months Description: FULLY ONSITE AT USTO NOTES FROM HIRING MANAGER: Resumes must have strong detail that significantly demonstrates their senior level experience. Needs to be mechanical in nature, must have engineering degree, works directly with mechanics and maintenance teams. Looking for...

  • Process Engineer

    1 month ago


    Thousand Oaks, United States EPITEC Full time

    *Looking for Engineer experience in a pharma manufacturing setting*Not looking for quality lab/ bench top/ science work. This engineering position supports manufacturing activities associated with cGMP equipment and facilities. The senior engineer works in partnership with the automation, maintenance, project management, corporate engineering, and...

  • Process Engineer

    1 month ago


    Thousand Oaks, United States EPITEC Full time

    *Looking for Engineer experience in a pharma manufacturing setting*Not looking for quality lab/ bench top/ science work. This engineering position supports manufacturing activities associated with cGMP equipment and facilities. The senior engineer works in partnership with the automation, maintenance, project management, corporate engineering, and...


  • Thousand Oaks, United States Anansys Staffing LLC Full time

    Job DescriptionJob DescriptionJob Description: The Maintenance Director (internally called Plant Operations Director) is responsible for overseeing the care and maintenance of all aspects of the campus; the hiring, training and supervising of all plant personnel; the coordinating of life safety, transportation, and landscaping programs; and the procuring of...


  • Thousand Oaks, United States Amgen Full time

    HOW MIGHT YOU DEFY IMAGINATION? You’ve worked hard to become the professional you are today and are now ready to take the next step in your career. How will you put your skills, experience and passion to work toward your goals? At Amgen, our shared mission—to serve patients—drives all that we do. It is key to our becoming one of the world’s leading...

  • Sr Engineer

    2 months ago


    Thousand Oaks, United States Amgen Full time

    HOW MIGHT YOU DEFY IMAGINATION? Youve worked hard to become the professional you are today and are now ready to take the next step in your career. How will you put your skills, experience and passion to work toward your goals? At Amgen, our shared missionto serve patientsdrives all that we do. It is key to our becoming one of the worlds leading...

  • Sr Engineer

    3 months ago


    Thousand Oaks, United States Amgen Full time

    HOW MIGHT YOU DEFY IMAGINATION?Youve worked hard to become the professional you are today and are now ready to take the next step in your career. How will you put your skills, experience and passion to work toward your goals? At Amgen, our shared missionto serve patientsdrives all that we do. It is key to our becoming one of the worlds leading biotechnology...


  • Thousand Oaks, United States ACL Digital Full time

    Job Title: Senior Engineer Location: Thousand Oaks, CADuration: 12 Months Description:FULLY ONSITE AT USTO NOTES FROM HIRING MANAGER:Resumes must have strong detail that significantly demonstrates their senior level experience. Needs to be mechanical in nature, must have engineering degree, works directly with mechanics and maintenance teams) Looking for...

Maintenance Engineer

2 months ago


Thousand Oaks, United States ACL Digital Full time

Engineer Thousand Oaks, CA 12 months contract This engineering position supports manufacturing activities associated with cGMP equipment and facilities at Amgen Thousand Oaks (ATO). The senior engineer works in partnership with the automation, maintenance, project management, corporate engineering, and manufacturing to develop and oversee the operation and reliability of equipment while driving safety and quality compliance. The engineer will support the department and capital projects and provide data to support business cases and long term strategy. The Senior Engineer role will provide direct engineering technical support as follows: Demonstrating role modeling of leadership behaviors and positive values to create a positive working environment. Be individually accountable for manufacturing equipment reliability and deliverables on key capital projects to deliver business targets and deliverables Assist in the identification of critical quality parameters and process attributes for new equipment or facility modifications. Suggest design modifications to address risks and design in quality and safety. Develop the commissioning strategy based on the URS and Quality Risk Assessment for Automation and Equipment Systems (QRAES) to validate equipment design while minimizing project cost and schedule impact (risk-based approach). Oversee development of validation protocols in line with CQP, Automation Systems Delivery SOPs, and cGMP standards. Recommend, evaluate, and manage performance of contract resources Provide oversight for verification deliverables developed by outsourced/contract verification staff. Act as a liaison between engineering and quality assurance during project planning, execution, and closeout Ensure that work executed with safety compliant practices and documented in accordance with cGMP good documentation Review and approve the commissioning reports, maintenance practices and parts, and drive productivity improvement Related Activities: Participate or lead, when required, multidisciplinary site teams, e.g. cross functional team, root cause analysis lead. Support Lean Transformation and Excellence in Operations process improvement by leading, supporting, and documenting improvement opportunities to reduce cost, improve safety/quality, or improve speed. Provide ad hoc technical support and guidance for manufacturing and maintenance Provide coaching and guidance to project teams and engineers using risk-based approaches Defend the equipment-specific calibration, maintenance, & validation as required during regulatory inspections Participate in internal audits and assess in conjunction with quality assurance Assist in developing and maintaining business metric performance Basic Qualifications: Doctorate degree OR Master’s degree & 3 years of engineering and/or manufacturing experience OR Bachelor’s degree & 5 years of engineering and/or manufacturing experience OR Associate’s degree & 10 years of engineering and/or manufacturing experience OR High school diploma / GED & 12 years of engineering and/or manufacturing experience Preferred Qualifications / Skills / Experience: Bachelor's degree in engineering or another science-related field 7+ years of relevant work experience with 5+ years’ experience in operations/manufacturing environment Direct experience with regulated environments (FDA, OSHA, EPA, etc.) Working knowledge and experience with cGMP procedures and engineering practices on pharmaceutical/biotech production processes, clean utilities, facilities, instruments, and equipment Experience implementing risk-based verification on major GMP process equipment / automation projects, including validation protocol development and execution Understanding and awareness of industry/regulatory trends for verification/validation Experience with combination product / medical device quality systems verification Strong process equipment knowledge – cell culture, fermentation, purification, filling, and packaging Strong process automation knowledge – understanding of automation infrastructure, current technologies, and automation project execution / verification. Knowledge of Delta V, Rockwell, and Plant Information Systems is a plus Demonstrated strong communication and technical writing skills Strengths in facilitation and collaboration / networking Experience in developing SOPs and delivering training Individual must be a team player prepared to work in and embrace a team-based culture that relies on collaboration for effective decision-making Proven track record of applying process improvement methodologies to mature and improve business processes (e.g. PDCA, LEAN, Six Sigma, and fundamental understanding of statistics, etc.)

#J-18808-Ljbffr