Job details
Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams rich in diversity. Take your career farther than you thought possible. Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us . Excited to grow your career? At Bristol Myers Squibb, we are inspired by a single vision – transforming patients’ lives through science. In oncology, haematology, immunology and cardiovascular disease – and one of the most diverse and promising pipelines in the industry – each of our passionate colleagues contribute to innovations that drive meaningful change. We bring a human touch to every treatment we pioneer. Join us and make a difference. Bristol Myers Squibb Ireland Bristol Myers Squibb has been in operation in Ireland since 1964, employing over 650 people across a range of activities and business units. Located in Dublin, Cruiserath Biologics Campus, a one billion Multi-Product Cell Culture Biologics Manufacturing facility plays a central role in the Global Product Development and Supply (GPS) network as the company’s first European biologics manufacturing facility.This state of the art facility will produce multiple therapies for the company’s growing biologics portfolio. Global Biologics Laboratory (GBL) responsible for the release testing of Biologics Drug product for the network, is also based on the Cruiserath Biologics Campus. BMS Cruiserath has been awarded“Biopharma Company of the Year 2019” in the Irish Pharma Industry Awards and is certified as a Great Place to Work since 2017, including as a Great Place to Work for Women in 2020, 2021 and 2022. The Role BMS Cruiserath Biologics are seeking to recruit a QC Site Operations QC Manager (Training) to Lead & Support training and training related project initiatives at its Multi-Product Cell Culture Drug Substance Facility. Reporting to the QC Site Operations Projects Senior Manager, they will support training activities as defined below in this job description. Key Duties and Responsibilities
- Coordination and scheduling of training to ensure a robust training programme is maintained.
- Lead/Support for the QC Induction Programme “Door to Floor”.
- Lead Continuous Improvement projects as part of the QC Projects team portfolio related to Training.
- Trainer for some “Door to Floor” modules and relevant laboratory techniques
- Generation and approval of forms for curricula amendment, removal, and creation.
- Generation and approval of Training waivers for QC personnel.
- Assignment of curricula for new starts as part of the QC Induction Programme “Door to Floor”.
- Support organization of external training across QC.
- Support generation and socialisation of Training Metrics across QC.
- Compliance with Standard Operating Procedures and Registered Specifications.
- Ensure the laboratory is operated in a safe manner and a Safety culture is embedded within the team.
- Keeps abreast of current corporate and industry requirements and compliance trends as they pertain to laboratory operations.
- Participate in regulatory agency inspections as required.
- Strategically plan and implement procedures and systems to maximise operating efficiency through the use of Operational Excellence tools.
- The successful candidate must demonstrate excellent written and verbal communication skills and experience.
- Minimum of a third level qualification (Degree) in Science or related discipline along with years of experience in a pharmaceutical / healthcare laboratory or related technical function with at least 2 years in a training related function.
- A Strong background in Lab Operations and knowledge of training programs is required.
- You will help patients in their fight against serious diseases
- You willbe part ofa company that encourages excellence and innovation, respects diversity, develops leaders and values its employees
- You’ll get a competitive salary and a great benefits package including an annual bonus, pension contribution, family medical assurance, 27 day annual leave,life assurance and on-site gym
- This role is to cover maternity leave for a minimum of 1 year
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Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams rich in diversity. Take your career farther than you thought possible. </p><p> Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us . </p><p><b> Excited to grow your career?</b></p><p><p> At Bristol Myers Squibb, we are inspired by a single vision – transforming patients’ lives through science. In oncology, haematology, immunology and cardiovascular disease – and one of the most diverse and promising pipelines in the industry – each of our passionate colleagues contribute to innovations that drive meaningful change. We bring a human touch to every treatment we pioneer. Join us and make a difference. </p><p><b> Bristol Myers Squibb Ireland </b></p><p> Bristol Myers Squibb has been in operation in Ireland since 1964, employing over 650 people across a range of activities and business units. </p><p> Located in Dublin, Cruiserath Biologics Campus, a one billion Multi-Product Cell Culture Biologics Manufacturing facility plays a central role in the Global Product Development and Supply (GPS) network as the company’s first European biologics manufacturing facility.This state of the art facility will produce multiple therapies for the company’s growing biologics portfolio. </p><p> Global Biologics Laboratory (GBL) responsible for the release testing of Biologics Drug product for the network, is also based on the Cruiserath Biologics Campus. </p><p> BMS Cruiserath has been awarded“Biopharma Company of the Year 2019” in the Irish Pharma Industry Awards and is certified as a Great Place to Work since 2017, including as a Great Place to Work for Women in 2020, 2021 and 2022. </p><p><b> The Role </b></p><p> BMS Cruiserath Biologics are seeking to recruit a QC Site Operations QC Manager (Training) to Lead & Support training and training related project initiatives at its Multi-Product Cell Culture Drug Substance Facility. Reporting to the QC Site Operations Projects Senior Manager, they will support training activities as defined below in this job description. </p><p><b> Key Duties and Responsibilities </b></p><ul><li><p> Coordination and scheduling of training to ensure a robust training programme is maintained. </p></li><li><p> Lead/Support for the QC Induction Programme “Door to Floor”. </p></li><li><p> Lead Continuous Improvement projects as part of the QC Projects team portfolio related to Training. </p></li><li><p> Trainer for some “Door to Floor” modules and relevant laboratory techniques </p></li><li><p> Generation and approval of forms for curricula amendment, removal, and creation. </p></li><li><p> Generation and approval of Training waivers for QC personnel. </p></li><li><p> Assignment of curricula for new starts as part of the QC Induction Programme “Door to Floor”. </p></li><li><p> Support organization of external training across QC. </p></li><li><p> Support generation and socialisation of Training Metrics across QC. </p></li><li><p> Compliance with Standard Operating Procedures and Registered Specifications. </p></li><li><p> Ensure the laboratory is operated in a safe manner and a Safety culture is embedded within the team. </p></li><li><p> Keeps abreast of current corporate and industry requirements and compliance trends as they pertain to laboratory operations. </p></li><li><p> Participate in regulatory agency inspections as required. </p></li><li><p> Strategically plan and implement procedures and systems to maximise operating efficiency through the use of Operational Excellence tools. </p></li><li><p> The successful candidate must demonstrate excellent written and verbal communication skills and experience. </p></li></ul><p><b> Qualifications, Knowledge and Skills Required </b></p><ul><li><p> Minimum of a third level qualification (Degree) in Science or related discipline along with years of experience in a pharmaceutical / healthcare laboratory or related technical function with at least 2 years in a training related function. </p></li><li><p> A Strong background in Lab Operations and knowledge of training programs is required. </p></li></ul><p><b> Why you should apply </b></p><ul><li><p> You will help patients in their fight against serious diseases </p></li><li><p> You willbe part ofa company that encourages excellence and innovation, respects diversity, develops leaders and values its employees </p></li><li><p> You’ll get a competitive salary and a great benefits package including an annual bonus, pension contribution, family medical assurance, 27 day annual leave,life assurance and on-site gym </p></li></ul><p><b> Additional information </b></p><ul><li><p> This role is to cover maternity leave for a minimum of 1 year </p></li></ul><p> BMSBL </p><p><b>#LI-Hybrid </b></p><p><i> If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career. </i></p><p><b> Uniquely Interesting Work, Life-changing Careers </b><br> With a single vision as inspiring as “Transforming patients’ lives through science ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues. </p><p><b> On-site Protocol </b></p><p> BMS has a diverse occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. 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If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to adastaffingsupport@bms.com . Visit to access our complete Equal Employment Opportunity statement. </p><p> BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. 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'title' => 'QC Training Manager, QC Projects', 'vacancies' => null, 'job_type_id' => null, 'description' => null, 'pay_status' => 'Free', 'external_job_description' => '<p><p><b> Working with Us </b><br> Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams rich in diversity. Take your career farther than you thought possible. </p><p> Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us . </p><p><b> Excited to grow your career?</b></p><p><p> At Bristol Myers Squibb, we are inspired by a single vision – transforming patients’ lives through science. In oncology, haematology, immunology and cardiovascular disease – and one of the most diverse and promising pipelines in the industry – each of our passionate colleagues contribute to innovations that drive meaningful change. We bring a human touch to every treatment we pioneer. Join us and make a difference. </p><p><b> Bristol Myers Squibb Ireland </b></p><p> Bristol Myers Squibb has been in operation in Ireland since 1964, employing over 650 people across a range of activities and business units. </p><p> Located in Dublin, Cruiserath Biologics Campus, a one billion Multi-Product Cell Culture Biologics Manufacturing facility plays a central role in the Global Product Development and Supply (GPS) network as the company’s first European biologics manufacturing facility.This state of the art facility will produce multiple therapies for the company’s growing biologics portfolio. </p><p> Global Biologics Laboratory (GBL) responsible for the release testing of Biologics Drug product for the network, is also based on the Cruiserath Biologics Campus. </p><p> BMS Cruiserath has been awarded“Biopharma Company of the Year 2019” in the Irish Pharma Industry Awards and is certified as a Great Place to Work since 2017, including as a Great Place to Work for Women in 2020, 2021 and 2022. </p><p><b> The Role </b></p><p> BMS Cruiserath Biologics are seeking to recruit a QC Site Operations QC Manager (Training) to Lead & Support training and training related project initiatives at its Multi-Product Cell Culture Drug Substance Facility. Reporting to the QC Site Operations Projects Senior Manager, they will support training activities as defined below in this job description. </p><p><b> Key Duties and Responsibilities </b></p><ul><li><p> Coordination and scheduling of training to ensure a robust training programme is maintained. </p></li><li><p> Lead/Support for the QC Induction Programme “Door to Floor”. </p></li><li><p> Lead Continuous Improvement projects as part of the QC Projects team portfolio related to Training. </p></li><li><p> Trainer for some “Door to Floor” modules and relevant laboratory techniques </p></li><li><p> Generation and approval of forms for curricula amendment, removal, and creation. </p></li><li><p> Generation and approval of Training waivers for QC personnel. </p></li><li><p> Assignment of curricula for new starts as part of the QC Induction Programme “Door to Floor”. </p></li><li><p> Support organization of external training across QC. </p></li><li><p> Support generation and socialisation of Training Metrics across QC. </p></li><li><p> Compliance with Standard Operating Procedures and Registered Specifications. </p></li><li><p> Ensure the laboratory is operated in a safe manner and a Safety culture is embedded within the team. </p></li><li><p> Keeps abreast of current corporate and industry requirements and compliance trends as they pertain to laboratory operations. </p></li><li><p> Participate in regulatory agency inspections as required. </p></li><li><p> Strategically plan and implement procedures and systems to maximise operating efficiency through the use of Operational Excellence tools. </p></li><li><p> The successful candidate must demonstrate excellent written and verbal communication skills and experience. </p></li></ul><p><b> Qualifications, Knowledge and Skills Required </b></p><ul><li><p> Minimum of a third level qualification (Degree) in Science or related discipline along with years of experience in a pharmaceutical / healthcare laboratory or related technical function with at least 2 years in a training related function. </p></li><li><p> A Strong background in Lab Operations and knowledge of training programs is required. </p></li></ul><p><b> Why you should apply </b></p><ul><li><p> You will help patients in their fight against serious diseases </p></li><li><p> You willbe part ofa company that encourages excellence and innovation, respects diversity, develops leaders and values its employees </p></li><li><p> You’ll get a competitive salary and a great benefits package including an annual bonus, pension contribution, family medical assurance, 27 day annual leave,life assurance and on-site gym </p></li></ul><p><b> Additional information </b></p><ul><li><p> This role is to cover maternity leave for a minimum of 1 year </p></li></ul><p> BMSBL </p><p><b>#LI-Hybrid </b></p><p><i> If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career. </i></p><p><b> Uniquely Interesting Work, Life-changing Careers </b><br> With a single vision as inspiring as “Transforming patients’ lives through science ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues. </p><p><b> On-site Protocol </b></p><p> BMS has a diverse occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role: </p><p> Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function. </p><p> BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to adastaffingsupport@bms.com . Visit to access our complete Equal Employment Opportunity statement. </p><p> BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. 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Hiring company
Bristol-Myers Squibb
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