Cipla USA
Overview
Job Title: IT Specialist Organization Name: InvaGen Pharmaceuticals, Inc (Cipla USA) Location: 927 Currant Rd. Employment Type: Exempt/Professional Salary Range: $78,000 - $101,920 Work Hours/Shift/Remote: General - 8:30 AM – 5:00 PM Mon. – Fri. (may require some weekends) Purpose : This role is responsible for partnering with the business for IT solutions following the Global, Regional and Country level set processes from the phase of IT solutioning to Go Live & support. The role interacts with Cipla support functions and vendors/partners. This role will perform IT Systems Support including Systems Implementation, Validation, Administration, etc., for Manufacturing, Packaging, Warehouse, Quality, etc.; IT project coordination and stakeholder management for systems implementation. Responsibilities / Accountabilities
Application Management : Build technical understanding of MES applications, Serialization Software’s, Quality Systems QC applications/software’s and end-to-end business processes to propose system changes and process transformations in line with evolving business requirements. SAP Support for Production, Warehouse and Quality Handling Audit Trails, CSV activities Network Administration, Software application management, Vendor management, User management with roles and profiles Define architecture of enterprise applications to engage internal employees, Vendors/Partners, Customers, etc. Evaluate new technologies, develop innovative solutions to deliver business objectives Engage with stakeholders : Multi-Functional teams across regions (e.g., Manufacturing, Packaging, WH, QC, QA, Engineering, Finance, HR) and IT Business Partners and other IT Verticals Strategy & Planning : Determine opportunities to implement/scale applications across regions with similar business processes Build business cases for the implementation of tactical solutions, keeping the future Roadmap in mind Project Management & Service Delivery : Track committed project timelines, milestones, budgets, scope deliverables and business outcomes Ensure KPIs and success criteria align with desired outcomes Propose, design and manage support models; ensure delivery of aligned SLAs for Incident, Change, and Request Management in collaboration with partners Education Qualifications
A bachelor’s degree in engineering, Information Technology or a related field Master’s or advanced programs/certifications in discipline (preferred) 3-5 years of work experience across various technology platforms Knowledge and experience in handling MES systems, Manufacturing, Packaging and WH machines Experience with Manufacturing, Packaging and WH IT solutions (MES/SCADA/LIMS, etc.), CSV activities with strong preference in pharmaceutical Knowledge and experience in handling QC systems, LIMS, QA/R&D/RA applications Experience with Quality, R&D, RA IT solutions (Waters/Master Control/LIMS, etc.), CSV activities with strong preference in pharmaceutical Knowledge, Skills And Abilities
Good oral and written communication skills; ability to work in a team environment Strong IT Manufacturing, Packaging and WH Systems support including IT administration, Systems Validation, PLC SAP Skills in Production, WH, Packaging and Quality modules Validation, Maintain Infrastructure & Security Demonstrated analytical skills Understanding MES solutions, Manufacturing software’s, SQL database, Application administration, and how to apply them to business scenarios Understanding Quality Systems solutions, Quality software’s, SQL/Oracle database, Application administration, and how to apply them to business scenarios Advanced Microsoft Suite, with emphasis on Excel Skills and Macros Experience supporting Manufacturing, Packaging, Serialization and WH solutions, IT infrastructure solutions Experience supporting Quality – QC/QA, R&D and RA software solutions, IT infrastructure solutions Strong interpersonal and collaboration skills for team-based work Proficiency in MS Suite including Excel, PowerPoint, Word, Outlook, Teams Excellent time management with a proven ability to meet deadlines Willingness to learn Physical Requirements
Able to lift 15 pounds with or without assistance Must be willing to work in a pharmaceutical manufacturing setting Must be willing to work some weekends based on business needs as required by management Prolonged periods of sitting at a desk and working on a computer Able to wear personal protective equipment (PPE) as required About Cipla & Equal Opportunity
Cipla is a leading global pharmaceutical company dedicated to high-quality, branded, and generic medicines. We are trusted by healthcare professionals and patients across geographies. Cipla’s purpose is to care for life and to make affordable, world-class medicines with uncompromising quality standards. InvaGen Pharmaceuticals, Inc. is a Cipla subsidiary engaged in the development, manufacture, marketing, and distribution of generic prescription medicines. EQUAL OPPORTUNITY EMPLOYER : Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. If reasonable accommodation is required for the application or interview process, please contact the recruiter.
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Job Title: IT Specialist Organization Name: InvaGen Pharmaceuticals, Inc (Cipla USA) Location: 927 Currant Rd. Employment Type: Exempt/Professional Salary Range: $78,000 - $101,920 Work Hours/Shift/Remote: General - 8:30 AM – 5:00 PM Mon. – Fri. (may require some weekends) Purpose : This role is responsible for partnering with the business for IT solutions following the Global, Regional and Country level set processes from the phase of IT solutioning to Go Live & support. The role interacts with Cipla support functions and vendors/partners. This role will perform IT Systems Support including Systems Implementation, Validation, Administration, etc., for Manufacturing, Packaging, Warehouse, Quality, etc.; IT project coordination and stakeholder management for systems implementation. Responsibilities / Accountabilities
Application Management : Build technical understanding of MES applications, Serialization Software’s, Quality Systems QC applications/software’s and end-to-end business processes to propose system changes and process transformations in line with evolving business requirements. SAP Support for Production, Warehouse and Quality Handling Audit Trails, CSV activities Network Administration, Software application management, Vendor management, User management with roles and profiles Define architecture of enterprise applications to engage internal employees, Vendors/Partners, Customers, etc. Evaluate new technologies, develop innovative solutions to deliver business objectives Engage with stakeholders : Multi-Functional teams across regions (e.g., Manufacturing, Packaging, WH, QC, QA, Engineering, Finance, HR) and IT Business Partners and other IT Verticals Strategy & Planning : Determine opportunities to implement/scale applications across regions with similar business processes Build business cases for the implementation of tactical solutions, keeping the future Roadmap in mind Project Management & Service Delivery : Track committed project timelines, milestones, budgets, scope deliverables and business outcomes Ensure KPIs and success criteria align with desired outcomes Propose, design and manage support models; ensure delivery of aligned SLAs for Incident, Change, and Request Management in collaboration with partners Education Qualifications
A bachelor’s degree in engineering, Information Technology or a related field Master’s or advanced programs/certifications in discipline (preferred) 3-5 years of work experience across various technology platforms Knowledge and experience in handling MES systems, Manufacturing, Packaging and WH machines Experience with Manufacturing, Packaging and WH IT solutions (MES/SCADA/LIMS, etc.), CSV activities with strong preference in pharmaceutical Knowledge and experience in handling QC systems, LIMS, QA/R&D/RA applications Experience with Quality, R&D, RA IT solutions (Waters/Master Control/LIMS, etc.), CSV activities with strong preference in pharmaceutical Knowledge, Skills And Abilities
Good oral and written communication skills; ability to work in a team environment Strong IT Manufacturing, Packaging and WH Systems support including IT administration, Systems Validation, PLC SAP Skills in Production, WH, Packaging and Quality modules Validation, Maintain Infrastructure & Security Demonstrated analytical skills Understanding MES solutions, Manufacturing software’s, SQL database, Application administration, and how to apply them to business scenarios Understanding Quality Systems solutions, Quality software’s, SQL/Oracle database, Application administration, and how to apply them to business scenarios Advanced Microsoft Suite, with emphasis on Excel Skills and Macros Experience supporting Manufacturing, Packaging, Serialization and WH solutions, IT infrastructure solutions Experience supporting Quality – QC/QA, R&D and RA software solutions, IT infrastructure solutions Strong interpersonal and collaboration skills for team-based work Proficiency in MS Suite including Excel, PowerPoint, Word, Outlook, Teams Excellent time management with a proven ability to meet deadlines Willingness to learn Physical Requirements
Able to lift 15 pounds with or without assistance Must be willing to work in a pharmaceutical manufacturing setting Must be willing to work some weekends based on business needs as required by management Prolonged periods of sitting at a desk and working on a computer Able to wear personal protective equipment (PPE) as required About Cipla & Equal Opportunity
Cipla is a leading global pharmaceutical company dedicated to high-quality, branded, and generic medicines. We are trusted by healthcare professionals and patients across geographies. Cipla’s purpose is to care for life and to make affordable, world-class medicines with uncompromising quality standards. InvaGen Pharmaceuticals, Inc. is a Cipla subsidiary engaged in the development, manufacture, marketing, and distribution of generic prescription medicines. EQUAL OPPORTUNITY EMPLOYER : Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. If reasonable accommodation is required for the application or interview process, please contact the recruiter.
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