Senior Manager, Manufacturing Engineering - Bristol Myers Squibb Irl
  • Dublin, Other, Ireland
  • via What Jobs
-
Job Description

Working with Us Challenging. Meaningful. Life-changing. Those arent 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. Youll 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: . The Role BMS Cruiserath Biologics is seeking to recruit a permanent Senior Manager, Manufacturing Engineering. Reporting to the Associate Director Manufacturing Engineering, the Senior Manager will lead a team of Manufacturing Engineers and act as a lead for Upstream Processes providing engineering support to Manufacturing systems and equipment. Key Duties and Responsibilities: Responsible for Manufacturing Equipment within the Multi-Product Cell Culture (MPCC) building, including but not limited to Inoculation, Single Use Bioreactors, Seed/Production Bioreactors, Centrifugation, Harvest and Process Support Systems (Media Preparation and Media Hold). Manage and develop a team of Manufacturing Engineers with focus on coaching, learning and career development. Provide support to Manufacturing with primary focus on troubleshooting equipment and automation issues. Supporting/leading manufacturing and process equipment investigations. Engineering owner for Upstream manufacturing areas and systems, focused on acquiring an in-depth knowledge of process operations and process equipment to support Manufacturing, Quality, Automation and Validation. Ensuring system compliance with all Regulatory requirements including Quality (cGDP/GMPs), and EHS requirements & procedures. Supporting internal and external audits as the Manufacturing Engineering Technical resource. Accountable for design and implementation of software changes to the Process Automation System (PAS). Manufacturing engineering equipment lead for new product introductions with input to equipment capability assessments, new equipment requirements and automated recipe design. Develop goals into appropriate scope and deliverables with demonstrated ability to meet agreed timelines. Plan and execute work assignments with ability to interpret results and report out to peers and stakeholders. Have a systematic approach to completing work activities, be willing to take on new activities, look to improve and contribute to building a sense of purpose within the team. Champion the use of continuous improvement. Qualifications, Knowledge and Skills Required: The successful candidate will have a BS in Engineering (Chemical or Mechanical preferred) with 5-6 years plus experience (or equivalent) with upstream manufacturing equipment support in the Biotechnology manufacturing industry. Knowledgeable and experienced in engineering principles related to typical biopharmaceutical upstream processing. The successful candidate will have demonstrated experience in leading a technical engineering team with minimum 2-3 years experience preferred. Candidates must be effective in both a team environment and an individual contributor role with minimal supervision. Ability to work extended hours or a modified work schedule as required for coverage of 24/7 manufacturing operation. The position is Monday through Friday, first shift, but requires on-call availability. The job requires high level of technical knowledge, and the candidate should have the ability to proactively troubleshoot. Knowledge of Delta V process automation software required; ability to use process historian, OSI PI, SEEQ and analyse data to assist troubleshooting. 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. Youll get a competitive salary and a great benefits package including, but not only, an annual bonus, pension contribution, family health insurance, 27 days annual leave, access to BMS Cruiserath on-site gym and life assurance. Skills: Upstream manufacturing process Delta-V, process automation systems management experience

;