Specialist, QC Microbiology job opportunity at Bristol Myers Squibb.

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Bristol Myers Squibb Specialist, QC Microbiology
Experience: 1-years
Pattern: full-time
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QC Microbiology

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degreeAssociate
loacation Cruiserath - IE, Ireland
loacation Cruiserath - I..........Ireland

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. 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 .   The Role   BMS Cruiserath Biologics is seeking to recruit a QC Microbiology Analyst within the QC Microbiology Laboratory . Reporting to the QC Microbiology Manger, the QC Microbiology Analyst will be responsible for supporting site activities related to Product Testing and Environmental/Utility Monitoring, performing testing of samples and laboratory duties in accordance with cGMP regulations.   Responsibilities will include (but not limited to):   Performing Sterility testing on Drug Product samples. Performing Bacterial Endotoxin Testing on Drug Product, Drug Substance, Raw Material and Utility samples within required hold times.   Performing Bioburden testing on Drug Substance , Raw Materials and Utility samples within required hold times.    Performing Growth Promotion testing of media lots entering the laboratory.   Carrying out identifications of Microorganisms isolated post testing activities.   Performing QC Environmental Monitoring in classified areas including lot related monitoring.   Utility sampling including WFI, Clean Steam and Compressed Air/Gas.   Carrying out In-Process testing of critical lot related samples to support Manufacturing activities.   Carrying out the Minute Mouse Virus by PCR for in-process samples.   Performing compendial verification, method transfer/validation, and routine testing of in-process, drug substance and drug product samples in accordance with applicable procedures and cGMP requirements.   Completing all laboratory documentation in a timely and accurate manner.   Compliance with Standard Operating Procedures and Registered Specifications.   Assisting in authoring and reviewing documentation, including SOPs.   Providing support to other departments to ensure qualification and production schedules are adhered to.   Reviewing Batch paperwork, and reconciliation of analysis performed in the laboratory.   Ensuring that any alert/action limit excursions are investigated according to site procedures.   Ensuring a high standard of housekeeping and safety is maintained in the laboratory.   Performing any other activities as indicated by the Microbiology Manager.     Qualifications and Experience required :   The ideal candidate should hold a minimum of a Level 8 degree in Microbiology or related discipline.   At least 1 years’ experience in a pharmaceutical / healthcare laboratory or related technical function.   A strong background in Microbiology and aseptic manufacturing is desirable but not essential.   The successful candidate must demonstrate excellent written and verbal communication skills.   The ability to work in a team based collaborative environment is essential.   Sterility experience is desirable but not essential.   Note: This candidate may be required to work a 12/7 shift pattern.     Why you should apply :   You will help patients in their fight against serious diseases     You will be part of a 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 allowance, 27 days of annual leave, life assurance and on-site gym .     #LI-Onsite 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. Uniquely Interesting Work, Life-changing Careers 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 a supportive culture, promoting global participation 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. On-site Protocol BMS has an 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: 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. Supporting People with Disabilities 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 careers.bms.com/ eeo -accessibility to access our complete Equal Employment Opportunity statement. Candidate Rights BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area. If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information:  https://careers.bms.com/california-residents/ Data Protection We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at https://careers.bms.com/fraud-protection . Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations. If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at TAEnablement@bms.com . Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley. R1597350 : Specialist, QC Microbiology

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