.. . Closing date Thursday, 1 August 2024 Skills: HR Qualification, Hospital/Healthcare Experience desirable, Excellent communication and IT Skills Benefits: .. Strategy Work Scheduling Any other duties as required by Medical Manpower Manager Liaise with Consultants, MUH Liaise with Clinical Directorate Reporting .. read more
Position: Graduate Quality Control Analyst Start Date: September 2025 Location: Cork For more than 130 years, diversity, equity & inclusion (DEI) has been a part of our cultural fabric at Johnson & Johnson and woven into how we do business every day.
Rooted in Our Credo, the values of DEI fuel our pursuit to create a healthier, more equitable world.
Our diverse workforce and culture of belonging accelerate innovation to solve the world's most pressing healthcare challenges. We know that the success of our business - and our ability to deliver meaningful solutions - depends on how well we understand and meet the diverse needs of the communities we serve.
Which is why we foster a culture of inclusion and belonging where all perspectives, abilities and experiences are valued and our people can reach their potential. At Johnson & Johnson, we all belong. About the Johnson & Johnson Graduate Programme The Graduate Programme is a collaborative programme across the Johnson & Johnson Campus Ireland Sites.
It is aimed at high potential individuals who, when given the right tools, are empowered to proactively take responsibility, effect change and make a positive contribution to their teams and the business. The Successful Candidate will have the opportunity to: * Develop relevant technical skills within their area of expertise * Cross functional exposure both on site and within Campus Ireland * Regular one to ones and feedback to support your on-going development * Personal development and effectiveness training * Skills development in influencing & communication * Project and Project Management experience * Introduction to new and innovative technologies * Exposure to Senior Management Team * Continuous professional development program with a recognised qualification Johnson & Johnson Innovative Medicine (p.k.a.
Janssen Sciences Ireland) established its operation in Ringaskiddy in 2005 on a 100-acre site with an investment of 500 million.
For more than 25 years we have been a global leader in the field of biomedicines, particularly in groundbreaking monoclonal antibody technology, an approach to producing medicines that launched a new generation of products to treat immune related diseases such as rheumatoid arthritis and plaque psoriasis. The facility in Ringaskiddy is fully operational and currently expanding its operations to continue focusing on producing biomedicines for both the treatment of immune related diseases and new and creative cancer treatments. Job Purpose: We have an exciting opportunity for a QC Analyst on the Ireland Graduate Program.
This individual will be responsible for carrying out tasks and projects related to the analysis of biotechnology products as required by Good Manufacturing practice (GMP).
The individual will participate in the delivery of lab testing efforts by using both existing and new procedures or processes to independently interpret data and identify and correct issues.
Proposes ideas and next steps to supervisors and/or managers.
Receives intermittent, moderately detailed instructions from Quality leaders at various levels, in addition to other partners. What you're great at: * Analytical testing knowledge including an understanding of Biopharmaceutical manufacturing and batch release processes. * Knowledge of equipment qualification, analytical method transfers, root cause problem solving and continuous improvement desirable. * A strong teammate who is very customer focused, possesses leadership and testing skills and both stakeholder and project management experience. * Strong collaboration & interpersonal skills, both written and oral. As a QC Analyst, your typical day may include: * Supporting the QC Team Leader during day to day operations of area. * Testing for laboratory related projects e.g.
analytical method transfers, equipment qualification, invalid assay and NC reduction initiatives etc. * Performing IP/ Microbiology/ Bioassay/ Separations analysis. * Identifying and implementing laboratory process improvements leading to improved efficiency &/or compliance within area. * Authors and investigates internal investigations, participates in regulatory inspections & external technical discussions etc. * Keeping up to date with analytical technology and regulatory / compliance trends. * Participates in technical groups to implement laboratory activities while following local and global regulatory requirements as well as J&J standards. * Supports the roll-out of laboratory activities (for example, instrument life-cycle management). * Performs laboratory studies, projects, and processes/initiatives. * Assists in developing lab strategies, policies, and guidelines linked to area of expertise (for example, authoring Standard Operating Procedures). * Contributes to external and/or internal manuscripts, regulatory reports, and technical reports. * Supports equipment qualifications to ensure accuracy and consistency of results. Education and Experience: * Minimum Bachelors degree in Chemistry, Biochemistry or related Scientific discipline. * Recent graduate (2024 or due to graduate in 2025). * Technical troubleshooting and problem-solving skills. * Knowledgeable of FDA/EMEA regulatory requirements applicable to biologics and/or pharmaceuticals. * Be ambitious with excellent social, communication and partner management skills. * Acute attention to detail. * A focus on patients and customers at all times. Please note that the applic ation window is currently o pen until the 31st of August however, we may close early if we receive a high volume of applications. #JnJEMEAStudentCareers #JnJEMEAPharmaceuticals #JNJEMEAUndergraduate #JNJEMEAMasters #JNJEMEAQuality #JNJEMEAFullTime
Rooted in Our Credo, the values of DEI fuel our pursuit to create a healthier, more equitable world.
Our diverse workforce and culture of belonging accelerate innovation to solve the world's most pressing healthcare challenges. We know that the success of our business - and our ability to deliver meaningful solutions - depends on how well we understand and meet the diverse needs of the communities we serve.
Which is why we foster a culture of inclusion and belonging where all perspectives, abilities and experiences are valued and our people can reach their potential. At Johnson & Johnson, we all belong. About the Johnson & Johnson Graduate Programme The Graduate Programme is a collaborative programme across the Johnson & Johnson Campus Ireland Sites.
It is aimed at high potential individuals who, when given the right tools, are empowered to proactively take responsibility, effect change and make a positive contribution to their teams and the business. The Successful Candidate will have the opportunity to: * Develop relevant technical skills within their area of expertise * Cross functional exposure both on site and within Campus Ireland * Regular one to ones and feedback to support your on-going development * Personal development and effectiveness training * Skills development in influencing & communication * Project and Project Management experience * Introduction to new and innovative technologies * Exposure to Senior Management Team * Continuous professional development program with a recognised qualification Johnson & Johnson Innovative Medicine (p.k.a.
Janssen Sciences Ireland) established its operation in Ringaskiddy in 2005 on a 100-acre site with an investment of 500 million.
For more than 25 years we have been a global leader in the field of biomedicines, particularly in groundbreaking monoclonal antibody technology, an approach to producing medicines that launched a new generation of products to treat immune related diseases such as rheumatoid arthritis and plaque psoriasis. The facility in Ringaskiddy is fully operational and currently expanding its operations to continue focusing on producing biomedicines for both the treatment of immune related diseases and new and creative cancer treatments. Job Purpose: We have an exciting opportunity for a QC Analyst on the Ireland Graduate Program.
This individual will be responsible for carrying out tasks and projects related to the analysis of biotechnology products as required by Good Manufacturing practice (GMP).
The individual will participate in the delivery of lab testing efforts by using both existing and new procedures or processes to independently interpret data and identify and correct issues.
Proposes ideas and next steps to supervisors and/or managers.
Receives intermittent, moderately detailed instructions from Quality leaders at various levels, in addition to other partners. What you're great at: * Analytical testing knowledge including an understanding of Biopharmaceutical manufacturing and batch release processes. * Knowledge of equipment qualification, analytical method transfers, root cause problem solving and continuous improvement desirable. * A strong teammate who is very customer focused, possesses leadership and testing skills and both stakeholder and project management experience. * Strong collaboration & interpersonal skills, both written and oral. As a QC Analyst, your typical day may include: * Supporting the QC Team Leader during day to day operations of area. * Testing for laboratory related projects e.g.
analytical method transfers, equipment qualification, invalid assay and NC reduction initiatives etc. * Performing IP/ Microbiology/ Bioassay/ Separations analysis. * Identifying and implementing laboratory process improvements leading to improved efficiency &/or compliance within area. * Authors and investigates internal investigations, participates in regulatory inspections & external technical discussions etc. * Keeping up to date with analytical technology and regulatory / compliance trends. * Participates in technical groups to implement laboratory activities while following local and global regulatory requirements as well as J&J standards. * Supports the roll-out of laboratory activities (for example, instrument life-cycle management). * Performs laboratory studies, projects, and processes/initiatives. * Assists in developing lab strategies, policies, and guidelines linked to area of expertise (for example, authoring Standard Operating Procedures). * Contributes to external and/or internal manuscripts, regulatory reports, and technical reports. * Supports equipment qualifications to ensure accuracy and consistency of results. Education and Experience: * Minimum Bachelors degree in Chemistry, Biochemistry or related Scientific discipline. * Recent graduate (2024 or due to graduate in 2025). * Technical troubleshooting and problem-solving skills. * Knowledgeable of FDA/EMEA regulatory requirements applicable to biologics and/or pharmaceuticals. * Be ambitious with excellent social, communication and partner management skills. * Acute attention to detail. * A focus on patients and customers at all times. Please note that the applic ation window is currently o pen until the 31st of August however, we may close early if we receive a high volume of applications. #JnJEMEAStudentCareers #JnJEMEAPharmaceuticals #JNJEMEAUndergraduate #JNJEMEAMasters #JNJEMEAQuality #JNJEMEAFullTime