Manufacturing Technology Investigator - Bristol-Myers Squibb - Ireland
Other Citiy, , GB
6d ago

Bristol-Myers Squibb has built a new state-of-the-art Multi-Product Cell Culture biologics manufacturing facility in Cruiserath, Dublin 15, approximately a $1 billion investment.

Once commissioned, the new facility will significantly increase Bristol-Myers Squibb?s biologics manufacturing capacity and play a central role in its global manufacturing network.

BMS Cruiserath Biologics is seeking to recruit a permanent Manufacturing Technology Investigator. Reporting to the MT Manager & Site Lead Investigator within MS&T, the Manufacturing Technology Investigator supports a large-

scale highly-automated cell culture facility on a growing campus with many career development opportunities. The successful candidate will be a key contributor in a dynamic and highly collaborative team environment.

The candidate will set appropriate objectives and priorities, overcome obstacles, and deliver results within project timelines.

Key Responsibilities : Conducts and manages resolution of deviations, root cause investigations, impact assessments and CAPAs as a Lead Investigator Liaises with many different groups / organizations as a Lead Investigator Proactively identifies and facilitates resolution of obstacles to timely completion Leads and participates in cross-

functional investigation teams Presents investigation findings to key stakeholders and site management Uses Quality Risk Management and Operational Excellence principles to facilitate risk-

based decision-making, drive continuous improvement, and eliminate waste Addresses at risk quality metrics by identifying unit operation improvement opportunities and collaborating with process experts and Quality Assurance to implement solutions Liaises with Manufacturing Sciences & Technology Organization for investigations and other project work Key Requirements : Minimum BS or equivalent in the biological sciences or chemical / biochemical engineering or a related discipline, with a minimum 4-

8 years relevant experience, MS or equivalent with minimum of 2-6 years relevant experience, Ph.D. in upstream and / or downstream manufacturing technical support or upstream / downstream process development in the biopharmaceutical industry.

Experience in writing investigations, and demonstrated effectiveness in quality systems in a FDA and EMA regulated environment.

The candidate must have strong interpersonal, communication and presentation skills for this position as well as good time management, multi-

tasking and organizational skills. Employees are expected to display the BMS Biopharma Behaviours, which enable them to be successful and perform at their highest level.

The BMS Behaviours are : Passion, Innovation, Accountability and Speed . Why should you apply : You will help patients in their fight against serious diseases and you will increase the survival of more people with cancer 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, 23.

5 days annual leave plus 3 Company days, life assurance, on-site gym and gain-sharing bonus.

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