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| Manufacturing Engineer International Paper Hialeah The Job You Will Perform: Pulp & Paper Mill-based role interacting with engineers, hourly employees, contractors, and managers Safety leadership—awareness of safety hazards, courage to stop a job if notice something unsafe, wears appropriate PPE, etc. Specific responsibilities vary by location & role. Examples may include: Manufacturing process optimization, Data analysis, Machine reliability Coordinate aspects of shutdowns and start-ups for mill Cost-reduction efforts for procedures, processes, etc. in mill setting Sample collection—e.g., pulp, samples from the reel or the winder, Project coordination / management Training development for operators Working collaboratively with engineers, operators, contractors, interns/co-ops, managers, etc. Assist with capital project management Coordinate contractors’ work The Skills You Will Bring: College degree (B.S.) by August 2023 in engineering major, chemical, electrical, environmental, mechanical, paper science engineering preferred Manufacturing internship or co-op preferred Strong desire to work in heavy manufacturing setting High regard for safety in the workplace Able to learn on the fly, adapt in a highly dynamic environment, and effectively cope with and manage change Highly motivated, self-starter, results-driven individual who can also perform well in a team setting Excellent communication and interpersonal skills, including active listening Strong analytical and problem-solving skills Demonstrated leadership skills & experience (e.g., internships/co-ops, jobs, supervisory roles, student associations, projects, etc.) Comfort with all levels of employees, including peers, engineers, contractors, hourly operators, and management Cumulative GPA 2.8 Open to relocation now and in the future Must have access to reliable transportation Physical Location : Pine Hill (AL) Prattville (AL) Selma (AL) Pensacola (FL) Oglethorpe (GA) Rome (GA) Savannah (GA) Cedar Rapids (IA) Cayuga (IN) Henderson (KY) Maysville (KY) Bogalusa (LA) Campti (LA) Mansfield (LA) Columbus (MS) Vicksburg (MS) New Bern (NC) Riegelwood (NC) Valliant (OK) Springfield (OR) Georgetown (SC) Orange (TX) Franklin (VA) The Benefits You Will Enjoy: Paid time off including Vacation and Holidays Retirement and 401k Matching Program Medical & Dental Education & Development (including Student Loan Assistance & Tuition Reimbursement) Life & Disability Insurance The Career You Will Build: Development opportunities for a career in manufacturing Promotional opportunities Networking/relationship building across the organization The Impact You Will Make: We continue to build a better future for people, the plant, and our company IP has been a good steward of sustainable practices across communities around the world for more than 120 years. Join our team and you’ll see why our team members say they’re Proud to be IP . The Culture You Will Experience: International Paper promotes employee well-being by providing safe, caring and inclusive workplaces. You will learn Safety Leadership Principles and have the opportunity to opt into Employee Networking Circles such as IPVets, IPride, Women in IP, and the African American ENC. We invite you to bring your uniqueness, creativity, talents, experiences, and safety mindset to be a part of our increasingly diverse culture. The Company You Will Join: International Paper (NYSE: IP) is a leading global supplier of renewable fiber-based products. We produce corrugated packaging products that protect and promote goods, and enable worldwide commerce, and pulp for diapers, tissue and other personal care products that promote health and wellness. Headquartered in Memphis, Tenn., we employ approximately 38,000 colleagues globally. We serve customers worldwide, with manufacturing operations in North America, Latin America, North Africa and Europe. Net sales for 2021 were $19.4 billion. Additional information can be found by visiting InternationalPaper.com. Immigration sponsorship is not available for this position. As a general rule, International Paper does not sponsor candidates for nonimmigrant visas or permanent residency. International Paper may make exceptions on a discretionary basis depending on factors such as the Company's specific business needs, place of recruitment, unique skills needed for certain jobs, and/or particular qualifications of the individual. International Paper is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected veteran status, age, or any other characteristic protected by law. Memphis TN 38197 2023-01-03T00:13:03Z | |
| Manufacturing Engineer International Paper Miami The Job You Will Perform: Pulp & Paper Mill-based role interacting with engineers, hourly employees, contractors, and managers Safety leadership—awareness of safety hazards, courage to stop a job if notice something unsafe, wears appropriate PPE, etc. Specific responsibilities vary by location & role. Examples may include: Manufacturing process optimization, Data analysis, Machine reliability Coordinate aspects of shutdowns and start-ups for mill Cost-reduction efforts for procedures, processes, etc. in mill setting Sample collection—e.g., pulp, samples from the reel or the winder, Project coordination / management Training development for operators Working collaboratively with engineers, operators, contractors, interns/co-ops, managers, etc. Assist with capital project management Coordinate contractors’ work The Skills You Will Bring: College degree (B.S.) by August 2023 in engineering major, chemical, electrical, environmental, mechanical, paper science engineering preferred Manufacturing internship or co-op preferred Strong desire to work in heavy manufacturing setting High regard for safety in the workplace Able to learn on the fly, adapt in a highly dynamic environment, and effectively cope with and manage change Highly motivated, self-starter, results-driven individual who can also perform well in a team setting Excellent communication and interpersonal skills, including active listening Strong analytical and problem-solving skills Demonstrated leadership skills & experience (e.g., internships/co-ops, jobs, supervisory roles, student associations, projects, etc.) Comfort with all levels of employees, including peers, engineers, contractors, hourly operators, and management Cumulative GPA 2.8 Open to relocation now and in the future Must have access to reliable transportation Physical Location : Pine Hill (AL) Prattville (AL) Selma (AL) Pensacola (FL) Oglethorpe (GA) Rome (GA) Savannah (GA) Cedar Rapids (IA) Cayuga (IN) Henderson (KY) Maysville (KY) Bogalusa (LA) Campti (LA) Mansfield (LA) Columbus (MS) Vicksburg (MS) New Bern (NC) Riegelwood (NC) Valliant (OK) Springfield (OR) Georgetown (SC) Orange (TX) Franklin (VA) The Benefits You Will Enjoy: Paid time off including Vacation and Holidays Retirement and 401k Matching Program Medical & Dental Education & Development (including Student Loan Assistance & Tuition Reimbursement) Life & Disability Insurance The Career You Will Build: Development opportunities for a career in manufacturing Promotional opportunities Networking/relationship building across the organization The Impact You Will Make: We continue to build a better future for people, the plant, and our company IP has been a good steward of sustainable practices across communities around the world for more than 120 years. Join our team and you’ll see why our team members say they’re Proud to be IP . The Culture You Will Experience: International Paper promotes employee well-being by providing safe, caring and inclusive workplaces. You will learn Safety Leadership Principles and have the opportunity to opt into Employee Networking Circles such as IPVets, IPride, Women in IP, and the African American ENC. We invite you to bring your uniqueness, creativity, talents, experiences, and safety mindset to be a part of our increasingly diverse culture. The Company You Will Join: International Paper (NYSE: IP) is a leading global supplier of renewable fiber-based products. We produce corrugated packaging products that protect and promote goods, and enable worldwide commerce, and pulp for diapers, tissue and other personal care products that promote health and wellness. Headquartered in Memphis, Tenn., we employ approximately 38,000 colleagues globally. We serve customers worldwide, with manufacturing operations in North America, Latin America, North Africa and Europe. Net sales for 2021 were $19.4 billion. Additional information can be found by visiting InternationalPaper.com. Immigration sponsorship is not available for this position. As a general rule, International Paper does not sponsor candidates for nonimmigrant visas or permanent residency. International Paper may make exceptions on a discretionary basis depending on factors such as the Company's specific business needs, place of recruitment, unique skills needed for certain jobs, and/or particular qualifications of the individual. International Paper is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected veteran status, age, or any other characteristic protected by law. Memphis TN 38197 2023-01-03T00:13:55Z | |
| Manager, Manufacturing myGwork Westchester As part of the Thermo Fisher Scientific team, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world's toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer Location/Division Specific Information Miami, FL / Biologicals and Chemicals Division How will you make an impact? The Manufacturing Manager shall lead and supervise the manufacturing team and process for Power and Liquid products. Reporting directly to the Site Leader / Operations Manager and responsible for quality, production, financial targets as well as establishing operational objectives and priorities to meet short / long term business goals. Follow the Thermo Fisher Scientific corporate standards, and best management practice. What will you do? Lead the manufacturing team to meet or exceed operational goals in safety, quality, availability, cost, efficiency, and inventory. Plans, schedules, and leads manufacturing processes. Leads manufacturing staff in the day-to-day performance of their jobs. Ensures manufacturing performance, volume and quality goals are met by efficient methods and maintaining appropriate staffing levels. Management responsibilities such as hires, job assignments, terminations, transfers, promotions, salary actions, and performance reviews. Directly interact with cross-functional team members and customers while carrying out business processes associated with the support, development and execution of warehouse operations. Provides guidance to Partners with appropriate functions and sites to help prepare for new product launches in alignment with Operational and Commercial goals. Proactivelywith their team, internal customers and peers to implement opportunities for continuous improvement / Practical Process Improvement, using Lean and Six Sigma principles. Effectively use of resources to increase operational efficiency. Develop, track, report, and make management decisions using relevant operational metrics. Establish / sustain strong culture of accountability and data driven decision making process. Lead and promote process improvement initiatives to drive improvements in product quality, cost, and process efficiency. Achieves financial objectives by preparing an annual budget; scheduling expenditures; analyzing variances; initiating corrective actions. Ensures manufacturing budgets, schedules, and performance requirements are met. Perform all job duties within regulatory or statutory requirements. How will you get here? Education and Experience Bachelor's Degree in science or engineering and/or management, with 6 years of validated experience in relevant industry such as biopharmaceutical, pharmaceutical, media, chemical manufacturing or other technical manufacturing. Or experience of 8 years of biopharmaceutical, pharmaceutical, media, chemical manufacturing or other technical manufacturing. Knowledge Skills and Abilities Strong leadership abilities with capability to demonstrate diverse resources, respond quickly, understand impact of changes and decisions, facilitate agreement, build collaborative relationships and understand customer's needs Acts as an advisor to direct reports to meet schedules and/or resolve problems. Strong written and verbal communication skills with ability to relate across all levels of the organization. Effective skills in analytical thinking and problem solving. Ability to perform multiple tasks and ability to effectively manage conflict. Ability to work in teams to obtain results, self-motivated/directed, ability to organize activities, minimal direction required. Ability to apply the requirements from standards, regulations, and industry best practices to the work environment. Good technical and project management skills with the ability to successfully manage multiple projects and daily responsibilities. Self-motivated with the ability to develop and champion creative and innovative solutions. Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one global team of 100,000 colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. StartYourStory at Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued. Apply today http://jobs.thermofisher.com Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status. Accessibility/Disability Access Job Seekers with a Disability: Thermo Fisher Scientific offers accessibility service for job seekers requiring accommodations in the job application process. For example, this may include individuals requiring assistance because of hearing, vision, mobility, or cognitive impairments. If you are a job seeker with a disability, or assisting a person with a disability, and require accessibility assistance or an accommodation to apply for one of our jobs, please submit a request by telephone at 1-855-471-2255. Please include your contact information and specific details about your required accommodation to support you during the job application process. This telephone line is reserved solely for job seekers with disabilities requiring accessibility assistance or an accommodation in the job application process. Messages left for other purposes, such as not being able to get into the career website, following up on an application, or other non-disability related technical issues will not receive a response. This employer is a corporate member of myGwork - LGBTQ professionals, the business community for LGBTQ professionals, students, inclusive employers & anyone who believes in workplace equality. 2023-01-21T14:22:49Z | |
| Project Manager (Manufacturing) Rise Technical Recruitment Project Manager (Manufacturing) $85,000 - $110,000 Great Company Benefits Progression Opportunities Healthcare PTO 401(k) Miami, Florida Are you a Project / Program Manager with a background in manufacturing, looking to work in a fully autonomous position where you will play a crucial role have a significant impact on the business? On offer is a diverse and exciting role where you will take ownership of important projects from cradle to grave, you will be highly influential in developing relationships with both new and existing clients that are key to the success of the business. This industry leading, specialist company design and manufacture high-quality plastic molded parts for a wide range of industries and applications. This highly innovative business have been established for over 50 years and are experiencing a high period of growth, which has now seen them require an ambitious Project Manager to join the team. In this position, you will work collaboratively across multiple departments within the business, you will be responsible for maintaining and developing a good customer relationship with both new and existing clients, you will manage projects from beginning to end, implement APQP processes, ensure projects are completed on time and provide regular updates and reports on the performance of projects on a monthly basis. This position would suit a Project / Program Manager from a manufacturing background looking to play a key role and contribute to continuing success of an innovative, industry leading business. The Role: Lead crucial projects / programs from cradle to grave Maintain and develop relationships with new and existing clients Working to ensure APQP processes are implemented $85,000 - $110,000 Great Company Benefits Progression Opportunities Healthcare PTO 401(k) The Candidate: High level of knowledge and experience in the manufacturing industry Strong working knowledge of APQP, PFMEA and TS16949 Experience managing projects in a customer facing role Ability to interpret engineering drawings Reference Number: BB173187 To apply for this role or to be considered for further roles, please click "Apply Now" or contact Lucas Spindler at Rise Technical Recruitment. Rise Technical Recruitment Ltd acts an employment agency for permanent roles and an employment business for temporary roles. The salary advertised is the bracket available for this position. The actual salary paid will be dependent on your level of experience, qualifications and skill set. We are an equal opportunities employer and welcome applications from all suitable candidates. Job type [] 2023-02-02T10:17:14Z | |
| Senior Manufacturing Scientist myGwork Hialeah Wondering what's within Beckman Coulter Diagnostics? Take a closer look. At first glance, you'll see that for more than 80 years we've been dedicated to advancing and optimizing the laboratory to move science and healthcare forward. Join a team where you can be heard, be supported, and always be yourself. We're building a culture that celebrates backgrounds, experiences, and perspectives of all our associates. Look again and you'll see we are invested in you, providing the opportunity to build a meaningful career, be creative, and try new things with the support you need to be successful. Beckman Coulter Diagnostics is proud to work alongside a community of six fellow Diagnostics Companies at Danaher. Together, we're working at the pace of change to improve patient lives with diagnostic tools that address the world's biggest health challenges. The Senior Manufacturing Scientist identifies and resolves complex technical issues with current products and qualifies enhancements to existing product configurations. The role supports day-to-day manufacturing operations with scientific expertise to ensure robust manufacturing processes, drive failure investigations of commercialized products, and support processes to ensure performance within the expected parameters. They also support the validation activities for process improvements and the successful transfer of new products from development to manufacturing at commercialization. This position is part of the Manufacturing Science and Engineering team located in Hialeah, FL, and will be on-site. At Beckman Coulter, our vision is to relentlessly reimagine healthcare, one diagnosis at a time. You will be a part of the Manufacturing Sciences team and report to the Manufacturing Science Manager responsible for supporting day-to-day manufacturing operations with scientific expertise to ensure robust manufacturing processes, drive failure investigations of commercialized products, and support processes to ensure performance within the expected parameters. If you thrive in a fast-paced, multifunctional role and want to work to build a world-class Manufacturing organization—read on. In this role, you will have the opportunity to: Perform comprehensive tests using sophisticated experimental design, Analyze results using statistical data analysis Optimally resolves sophisticated technical problems and utilizes the scientific method as the foundation for problem-solving Work with multi-functional teams addressing non-conformances and projects Test and troubleshoot the manufacturing process and assay assignment of hematology and flow cytometry blood controls Troubleshoot manufacture and dye conjugation of antibodies, as well as the manufacture and dye loading of fine particles for use in the life science product line Use strong written and oral communication skills to promote and debate key issues and lead and participate in problem-solving efforts. The essential requirements of the job include: 5 years of industrial experience with a bachelor's degree, 3 years of experience with a master's degree, or a Ph.D. degree Degree in Chemistry, Biochemistry, Cytometry, Cellular Sciences, Molecular Biology, or Chemical Engineering It would be a plus if you also possess: Experience leading teams Experience with standard work and daily management Industrial experience When you join us, you'll also be joining Danaher's global organization, where 80,000 people wake up every day determined to help our customers win. As an associate, you'll try new things, work hard, and advance your skills with guidance from dedicated leaders, all with the support of powerful Danaher Business System tools and the stability of a tested organization. Danaher Corporation and all Danaher Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. We value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes. The EEO posters are available here . We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform crucial job functions, and to receive other benefits and privileges of employment. Please contact us at applyassistancedanaher.com to request accommodation. If you've ever wondered what's within you, there's no better time to find out. This employer is a corporate member of myGwork - LGBTQ professionals, the business community for LGBTQ professionals, students, inclusive employers & anyone who believes in workplace equality. 2022-12-21T17:29:57Z | |
| Supervisor Reagents Manufacturing myGwork Miami Wondering what's within Beckman Coulter Diagnostics? Take a closer look. At first glance, you'll see that for more than 80 years we've been dedicated to advancing and optimizing the laboratory to move science and healthcare forward. Join a team where you can be heard, be supported, and always be yourself. We're building a culture that celebrates backgrounds, experiences, and perspectives of all our associates. Look again and you'll see we are invested in you, providing the opportunity to build a significant career, be creative, and try new things with the support you need to be successful. Beckman Coulter Diagnostics is proud to work alongside a community of six fellow Diagnostics Companies at Danaher. Together, we're working at the pace of change to improve patient lives with diagnostic tools that address the world's biggest health challenges. The Reagent Manufacturing Supervisor will support the Hematology Controls and Calibrators Production Controlled Area. This role will own the day-to-day operations of the Manufacturing group, including identifying and implementing improvement opportunities. This role requires working in a controlled environment that requires the donning of PPE (aseptic gowning). You will have the opportunity to work with your team in a hands-on capacity mentoring and troubleshooting within the controlled areas. This position is an integral part of the manufacturing and operations team located in Miami, FL and will be onsite. A t Beckman Coulter, our vision is to relentlessly reimagine healthcare, one diagnosis at a time. You will report to the Manager, Reagents Manufacturing. If you thrive in a result-oriented, fast-paced role and want to work to build a world-class manufacturing organization—read on. In this role, you will have the opportunity to: Ensure that manufacturing schedule is generated and adhered to, mitigating issues as needed. Support departmental and site KPI's, including associate/team Engagement, Safety, On Time Delivery, and Productivity. Empower associate performance to include staffing and crafting goal/development objectives. Utilize problem solving techniques to implement both containment, root cause analysis, and countermeasure determination and implementation. Take ownership for quality in area by utilizing quality guidelines, including documentation, internal quality improvement, & scrap reduction. Supports Kanban process for material needs and owns inventory reduction initiatives. Manages both direct & indirect costs in the value streams. Requirements for this role: Bachelor's degree with 5 years' experience OR Master Degree with 3 years of experience highly preferred, or High School Diploma with 8 years' experience Experience working in an FDA-controlled production environment using cGMP's. 3 years experience in a people-leading role Strong data analysis ability (Excel experience at a minimum) The following is considered a plus: Experience with DBS (Danaher Business Tools), i.e. Lean, Six-Sigma, Kaizen, DVM When you join us, you'll also be joining Danaher's global organization, where 80,000 people wake up every day determined to help our customers win. As an associate, you'll try new things, work hard, and advance your skills with guidance from dedicated leaders, all with the support of powerful Danaher Business System tools and the stability of a tested organization. Given the essential job duties of this position, the employee is required to be fully vaccinated against COVID-19 as a condition of employment, subject to reasonable accommodation and applicable law. Danaher Corporation and all Danaher Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. We value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes. The EEO posters are available here . We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform crucial job functions, and to receive other benefits and privileges of employment. Please contact us at applyassistancedanaher.com to request accommodation. If you've ever wondered what's within you, there's no better time to find out. This employer is a corporate member of myGwork - LGBTQ professionals, the business community for LGBTQ professionals, students, inclusive employers & anyone who believes in workplace equality. 2022-11-30T20:27:57Z | |
| Manufacturing Manager-Reagents myGwork Hialeah Wondering what's within Beckman Coulter Diagnostics? Take a closer look. At first glance, you'll see that for more than 80 years we've been dedicated to advancing and optimizing the laboratory to move science and healthcare forward. Join a team where you can be heard, be supported, and always be yourself. We're building a culture that celebrates backgrounds, experiences, and perspectives of all our associates. Look again and you'll see we are invested in you, providing the opportunity to build a significant career, be creative, and try new things with the support you need to be successful. Beckman Coulter Diagnostics is proud to work alongside a community of six fellow Diagnostics Companies at Danaher. Together, we're working at the pace of change to improve patient lives with diagnostic tools that address the world's biggest health challenges. The Reagent Manufacturing Supervisor/Manager will support the Hematology Controls and Calibrators Production Controlled Area. This role will own the day-to-day operations of the Manufacturing group, including identifying and implementing improvement opportunities. This role requires working in a controlled environment that requires the donning of PPE (aseptic gowning). You will have the opportunity to work with your team in a hands-on capacity mentoring and troubleshooting within the controlled areas. This position is an integral part of the manufacturing and operations team located in Miami, FL, and will be onsite. A t Beckman Coulter, our vision is to relentlessly reimagine healthcare, one diagnosis at a time. You will report to the Manager, Reagents Manufacturing. If you thrive in a result-oriented, fast-paced role and want to work to build a world-class manufacturing organization—read on. In this role, you will have the opportunity to: Ensure that manufacturing schedule is generated and adhered to, mitigating issues as needed. Support departmental and site KPI's, including associate/team Engagement, Safety, On Time Delivery, and Productivity. Empower associate performance to include staffing and crafting goal/development objectives. Utilize problem solving techniques to implement both containment, root cause analysis, and countermeasure determination and implementation. Take ownership for quality in area by utilizing quality guidelines, including documentation, internal quality improvement, & scrap reduction. Supports Kanban process for material needs and owns inventory reduction initiatives. Manages both direct & indirect costs in the value streams. Requirements for this role: Bachelor's degree with 5 years' experience OR Master Degree with 3 years of experience highly preferred, or High School Diploma with 8 years' experience Experience working in an FDA-controlled production environment using cGMP's. 3 years experience in a people-leading role Strong data analysis ability (Excel experience at a minimum) The following is considered a plus: Experience with DBS (Danaher Business Tools), i.e. Lean, Six-Sigma, Kaizen, DV When you join us, you'll also be joining Danaher's global organization, where 80,000 people wake up every day determined to help our customers win. As an associate, you'll try new things, work hard, and advance your skills with guidance from dedicated leaders, all with the support of powerful Danaher Business System tools and the stability of a tested organization. Danaher Corporation and all Danaher Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. We value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes. The EEO posters are available here . We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform crucial job functions, and to receive other benefits and privileges of employment. Please contact us at applyassistancedanaher.com to request accommodation. If you've ever wondered what's within you, there's no better time to find out. This employer is a corporate member of myGwork - LGBTQ professionals, the business community for LGBTQ professionals, students, inclusive employers & anyone who believes in workplace equality. 2023-01-31T20:06:54Z | |
| VP Quality, Biologics Manufacturing Jobot Fort Lauderdale Established but growing Biologic CDMO seeks tenured Quality VP to join the team This Jobot Job is hosted by: Hunter Prater Are you a fit? Easy Apply now by clicking the "Apply" button and sending us your resume. Salary: $180,000 - $250,000 per hour A bit about us: Our client is a CDMO with a full range of mammalian cell culture development and manufacturing services ranging from the creation of up and downstream processes sufficient for the manufacturing of proof of concept or toxicology product material to processes for licensed manufacturing. Why join us? Competitive Salary Annual Bonus Equity Great benefits and perks Opportunity to help sculpt a changing organization Relocation assistance available for the right candidate Job Details JOB SUMMARY The VP of Quality is responsible for leading all CDMO-related quality activities at the facility in Plantation, FL. Quality personnel at the site will have direct and/or indirect reporting structure to the VP of Quality, in total 15-20 reports. The VP, CDMO Quality is a key member of the leadership team responsible for building, leading and executing a quality strategy that supports the following: Contract partner relationships; Quality process design and development; Product and facility approval; Sustainable manufacturing; Supply through in-house capabilities and well as third-party development; and External manufacturing partners. ESSENTIAL FUNCTIONS Develop and maintain quality processes and competencies to drive a culture of compliance and collaboration Lead the development and consistent application of quality processes aligning policies and procedures with internal and outsourced activities Document review and approval New Product Introduction Investigations Changeover Change control Promote quality awareness and continuous improvement at the site Develop the required site processes and competencies to ensure that quality standards are implemented in accordance with corporate goals Develop quality management systems in conformance with ISO, FDA, and EU regulatory standards Enable formal risk assessments processes to identify compliance risks and appropriate mitigation strategies Provide quality standards for product lifecycle management Ensure the proper interface of the quality function to contract partners, product development, manufacturing, engineering/maintenance, regulatory affairs, and other areas as required Collaborate with all departments and functions to ensure that quality standards and ISO/GxP compliance are met and maintained Other duties may be assigned MINIMUM EDUCATION, EXPERIENCE, SKILLS BS degree in Engineering, Science, or Operations Management; Advanced Degree (s) preferred Position requires a seasoned Quality Assurance professional with a minimum of 10 years of experience at biopharmaceutical/biotechnology companies Must have large molecule experience Prior CDMO experience is preferred Interested in hearing more? Easy Apply now by clicking the "Apply" button. 2023-02-06T22:56:57Z | |
| Manufacturing/Process Engineer II myGwork Miami Wondering what's within Beckman Coulter Diagnostics? Take a closer look. At first glance, you'll see that for more than 80 years we've been dedicated to advancing and optimizing the laboratory to move science and healthcare forward. Join a team where you can be heard, be supported, and always be yourself. We're building a culture that celebrates backgrounds, experiences, and perspectives of all our associates. Look again and you'll see we are invested in you, providing the opportunity to build a meaningful career, be creative, and try new things with the support you need to be successful. Beckman Coulter Diagnostics is proud to work alongside a community of six fellow Diagnostics Companies at Danaher. Together, we're working at the pace of change to improve patient lives with diagnostic tools that address the world's biggest health challenges. The Manufacturing/Process Engineer II for Beckman Coulter Diagnostics is responsible for being a key support role for production to verify equipment and processes are being followed to engineering standards in addition to identifying and implementing continuous improvement opportunities for the site. This position is part of the Manufacturing Technical Operations (MTO) - Engineering Department located in Hialeah, Florida, and will be onsite. A 75% Traveling requirement will occur in the first 1½ years to support Relocation Project. At Beckman Coulter, our vision is to relentlessly reimagine healthcare, one diagnosis at a time. You will be a part of the Engineering Team and report to the Supervisor Manufacturing/Process Engineering, responsible for working with fellow engineers and technicians to support production line associates, equipment, and processes. If you thrive in a fast-paced multifunctional support role and want to work to build a world-class Manufacturing Engineering organization—read on In this role, you will have the opportunity to: Specifically support an Internal Relocation project of one of our manufacturing sites to be a lead contributor and decision stakeholder for the equipment and processes to be transferred. Will make critical decisions based on Water Purification systems, Pooling, Filling, and Packaging studies for production operations. Advocate/Implement DBS training and tools for the manufacturing site and support Kaizen's and sustainment initiatives. Design/implement and Print 3D Drawings to conceptualize improving new or existing equipment or processes. Assist with management of the AMMS PM system, generation of work orders and completion of PMs to remain within compliance across multiple sites and departments. Working closely with Technicians to identify PM opportunities to streamline equipment maintenance and maintain equipment uptime. Collaborate with multiple departments to create/update quality control documents to standardize SOP's, Work instructions or improvement opportunities for production operations working in FDA-controlled environment using cGMP's. The essential requirements of the job include: Engineer may work in Blood exposure/Biohazard areas and must follow all PPE/OSHA guidelines. Bachelor's degree in field with 2 years of experience OR Master's Degree in the field with 0-2 years of experience. Preferred Experience with following software's: AutoCAD, Solid works, Ladder Logic, Microsoft Excel (macro/VBA coding), and Microsoft Word (Document Redlining) Experience with Project Management tools and independently driven to reach project timeline deliverables. When you join us, you'll also be joining Danaher's global organization, where 80,000 people wake up every day determined to help our customers win. As an associate, you'll try new things, work hard, and advance your skills with guidance from dedicated leaders, all with the support of powerful Danaher Business System tools and the stability of a tested organization. Danaher Corporation and all Danaher Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. We value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes. The EEO posters are available here . We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform crucial job functions, and to receive other benefits and privileges of employment. Please contact us at applyassistancedanaher.com to request accommodation. If you've ever wondered what's within you, there's no better time to find out. This employer is a corporate member of myGwork - LGBTQ professionals, the business community for LGBTQ professionals, students, inclusive employers & anyone who believes in workplace equality. 2022-12-06T17:02:45Z | |
| Aerospace Manufacturing QA Engineer CyberCoders Miami If you are a Aerospace Quality Engineer with experience, please read on Top Reasons to Work with Us This Role reports to Phoenix, AZ RELOCATION ASSISTANCE AVAILABLE Great salaries & benefits Annual bonuses 2-3 weeks PTO What You Will Be Doing Interfacing with all internal organizational groups as well as with vendors and customers. Maintain strong communication with Customers, internal management team, and Vendors to ensure quality level is meeting expectations. Integrate new parts into the quality system, working with customers, engineering, manufacturing, and the quality department. Execute activities related to the development, application, and maintenance of quality standards for processing materials into finished materials or product. Develop and analyze statistical data and specifications to indicate present product and process standards and establish proposed quality reliability expectancy of finished product. Investigate and provide solutions to problems for process and product non-conformance and MRB. Perform and support AS/ISO/Nadcap/customer/supplier quality audits of process and products. What You Need for this Position Knowledge of Quality Control and Quality Assurance systems, processes and techniques. Capable of maintaining, auditing and improving and established Quality Management System in Aerospace or other regulated industry. Strong ability for root cause analysis, corrective and preventive action. Familiar with measurement and test equipment operation and calibration in a manufacturing environment. Computer skills in Microsoft Word, Excel, Power-point, and Access. History of good judgment, decision making, and planning skills. Candidate must be able to work well in a team environment and work well across various departmental functions within the company. Candidate must possess the ability to prepare and make technical presentations as required. - AS 9100 - Quality - Manufacturing - RCCA - Root Cause Analysis - Green Belt - Black Belt - Internal Audits - AS9100 - Aerospace Quality Engineer So, if you are a Aerospace Quality Engineer with experience, please apply today Applicants must be authorized to work in the U.S. Additional ways to apply We’ll share your profile. The job poster may use it for jobs with other companies. Learn More Salt Lake City, UT Full-time $145,000.00 - $165,000.00 Houston, TX Full-time $180,000.00 - $200,000.00 Job ID: MR7-1707147 CyberCoders, Inc is proud to be an Equal Opportunity Employer All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, protected veteran status, or any other characteristic protected by law. Your Right to Work – In compliance with federal law, all persons hired will be required to verify identity and eligibility to work in the United States and to complete the required employment eligibility verification document form upon hire. Copyright 1999 - 2023. CyberCoders, Inc. All rights reserved. CyberCoders is an Equal Employment Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, breastfeeding, or related medical conditions), age, sexual orientation, gender identity or expression, national origin, ancestry, citizenship, genetic information, registered domestic partner status, marital status, status as a crime victim, disability, protected veteran status, or any other characteristic protected by law. CyberCoders will consider qualified applicants with criminal histories in a manner consistent with the requirements of applicable law. CyberCoders is committed to working with and providing reasonable accommodation to individuals with physical and mental disabilities. If you need special assistance or an accommodation while seeking employment, please email Benefitscybercoders.com. We will make a determination on your request for reasonable accommodation on a case-by-case basis. UnitedHealthcare creates and publishes the Transparency in Coverage Machine-Readable Files on behalf of CyberCoders. 2023-02-06T14:42:23Z |
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