Sr Data Engineer II-Manufacturing Systems bei Commercial
Commercial · Wilmington, Vereinigte Staaten Von Amerika · Onsite
- Senior
- Optionales Büro in Wilmington
Job Duties:
- Design, document, deploy, and verify data acquisition tags (alarms, events, time-series data) for manufacturing systems.
- Develop, deploy, and maintain SQL-based databases for ingesting raw manufacturing data.
- Create and manage metadata structures to contextualize manufacturing data.
- Administer manufacturing reporting applications and ensure their reliability and performance.
- Lead strategic vendor and partner engagements to support reporting, data acquisition, and database systems.
- Build and maintain visualization dashboards to enable data-driven decision-making for manufacturing teams.
- Manage all data-related projects within the IT Manufacturing Systems department, including during bi-annual facility shutdowns.
- Gather and translate user requirements into technical specifications and project deliverables.
- Collaborate with validation and quality teams to ensure compliance with regulatory standards (e.g., GxP).
Minimum Education & Experience Requirements:
- Bachelor’s Degree in Information Systems, Engineering, Computer Science, or a related field.
- Minimum of 8 years of professional experience in Data Engineering or Automation Systems.
- Experience in the pharmaceutical or biotech industry strongly preferred.
Knowledge/Skills Needed:
- Expertise in time-series data systems and SQL database development.
- Strong understanding of manufacturing systems and industrial data flows.
- Experience with data visualization tools and reporting platforms.
- Familiarity with pharmaceutical compliance standards (e.g., GxP, validation).
- Proven ability to lead cross-functional teams and manage complex projects.
- Strong communication, documentation, and stakeholder engagement skills.
Competencies:
- Technical Expertise
- Acts as a subject matter expert for assigned technical areas and has knowledge in other key business area(s)
- Understands the technology from a systematic, “big picture” view
- Manages multi-functional and multi-site teams and projects
- Facilitates knowledge sharing and creative problem solving with the affected business function
- Has a certified mastery of skills in areas such as project management and continuous/process improvement
- Knows and/or has experience with pharmaceutical concepts (e.g. GxP, validation)
- Collaboration and Communication
- Takes a leadership role in driving effective collaboration across IT and relevant business functions
- Uses effective communications to influence project stakeholders and adapt to each situation
- Mentors and motivates members of the project team, including cross-functional members
- Self-Awareness and Adaptability
- Serves as a leader and change agent across IT and cross-functional project teams
- Engages with others in IT and key business areas proactively to determine impacts of upcoming changes
- Drives continuous improvement and innovation within IT
- Sets the highest standards for personal performance regardless of project difficulty
- Grows knowledge in areas outside of IT
- Follows policies and procedures, identifies necessary changes and facilitates updates as required
- Decision Making
- Leads cross-functional project teams in problem solving
- Known as the trusted technical source for knowledge and advice on complex solutions and projects
- Applies innovative approaches and methods to complex projects and solutions
- Takes full accountability and responsibility for projects and decisions with minimal consultation
- Customer-Focus Results
- Anticipates major customers’ needs and is committed to developing value-added solutions that meet them successfully
- Builds broad network of relationships with customers and proactively seeks feedback on IT products and services
Company
Why join Team Alkermes?
Alkermes applies its deep neuroscience expertise to develop medicines designed to help people living with complex and difficult-to-treat psychiatric and neurological disorders. A fully-integrated, global biopharmaceutical company, headquartered in Ireland with U.S. locations in Massachusetts and Ohio, we are committed to pursuing great science, driven by deep compassion to make a real impact in the lives of patients. Alkermes has a portfolio of proprietary commercial products for the treatment of alcohol dependence, opioid dependence, schizophrenia and bipolar I disorder, and a pipeline of clinical and preclinical candidates in development for various neurological disorders, including narcolepsy.
Beyond our important mission of developing medicines to address unmet patient needs, we actively seek to foster a culture of diversity, inclusion and belonging throughout our business. We strive to ensure that all voices are respected and valued, recognizing that our diversity of thought, background and perspective makes us stronger. We are proud to have been recognized as an employer of choice by many national organizations, including being certified as a Great Place to Work in the U.S. in 2024, honored as a Healthiest Employer in both Ohio and Massachusetts in 2023, a Best Place for Working Parents in 2023, and to have received the Bell Seal at the Platinum level for Workplace Mental Health by Mental Health America for three consecutive years (2021-2023).
Alkermes, Inc. is an equal employment opportunity employer and does not discriminate against any qualified applicant or employee because of race, creed, color, age, national origin, ancestry, religion, gender, sexual orientation, gender expression and identity, disability, genetic information, veteran status, military status, application for military service or any other characteristic protected by local, state or federal law. Alkermes also complies with all work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA. Alkermes is an E-Verify employer.
