IT Laboratory Operations Onsite Specialist

Who we are Together, we're on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It's a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds. Working here means working with the world's leading manufacturer of generic medicines, and the proud producer of many of the products on the World Health Organization's Essential Medicines List. Today, at least 200 million people around the world take one of our medicines every single day. An amazing number, but we're always looking for new ways to continue making a difference, and new people to make a difference with. Purpose of Role

-    Provides support in the process of creating the documentation specific to computerized systems: validation plan, user requirements, software and hardware configuration design documents.

-    Creation of documentation associated with establishing the qualification status of production and laboratory equipment. This includes installation qualification (IQ), operational qualification (OQ), performance qualification (PQ) documents.

-    Be the site responsible for delivering, supporting and managing Quality systems and solutions in the laboratories and production area. These systems maybe standalone or interfaced with other systems.

-    To be the site expert on all laboratory computer systems – LIMS (Labware), CDS (Empower), standard-alone computer driven instrumentation and other applications identified by laboratory management.

-    To manage and support standalone Laboratory / Quality systems, maintaining support for Interfaces and troubleshooting as and where required.

-    Maintain the integrity of these systems and ensuring backup up solutions are in place by the global or local ITMU's using standardised solutions.

-    To ensure sufficient consideration is paid to all regulatory compliance requirements for system implementation and maintenance including cGMP, computer systems validation, security and risk. Assist in the generation and execution of validation deliverables.

-    To ensure appropriate service levels are developed and monitored, for support of laboratory IS systems working with the global team, external partners and providers of specific software related to the labs. Ensure support partners perform to the defined SLA and provide resolutions within the agreed timescales.

-    Exchange and fix infrastructure compoments in the respective area 

-    Coordinate between business / IT stakeholder management and global ITO teams

-    Contribute to a continous documentation of the system landscape in the respective area

-    Provide technical support as point of contact for IT for the site.

-    New users onboarding preparing IT assets and tools.

-    End-user desktop, laptops, office IT support. Installation support for various software on end user systems and equipments when required.

-    Onboarding and mentoring of external IT Operations onsite engineers

-    Offboarding support, collecting IT assets and sanitizing IT assets and keep in stock.

-    Handling tickets on the internal Ticketing system (ServiceNow) platform.

-    IT Asset Management.  Manage Hardware rollouts.

-    Perform troubleshooting, parts replacement, system upgrades, and basic deployments and repair on sites where required. 

-    IP phone, Video conference support, Printers support.

-    Basic installation and maintenance of technical products.

-    Installs, maintains, and optimizes desktop /notebook configurations. Reviews, troubleshoots, and approves operational quality desktops, notebooks, printers, and associated peripherals. 

-    Ensure that all work carried out is in compliance with the required standards conforming to company cGMP, cGLP, SOP, Health & Safety Specifications, Environmental and Regulatory requirements.

Knowledge, Skills and Abilities 

-    IT Business experience with desktop, mobile computing and/or network, including problem analysis/resolution, and installation. 

-    Experience across a broad range of Quality / Laboratories systems and applications in the Pharmaceutical Industry.

-    Knowledge of Microsoft Windows OS, Network equipments, Internet connectivity and knowledge of computer networking / server and compute environments.

-    Knowledge of PC Hardware configurations and troubleshooting

-    Strong written, numerical and verbal communications skills.  Compliance, Validation GxP experience.

Qualifications and Accreditations

-    High School diploma in Computer Science, Management Information Systems, Engineering or related field

-    Bachelor's Degree in computing, science or a related subject / equivalent field experience - preferable

-    Minimum 2 years experience across various IT systems 

-    Pharma Validation experience – GXP / GMP – preferrable.  Experience in the pharmaceutical, chemical or food industry is an advantage

-    Very good command of English 

Competencies

•    Collaboration - The ability to work effectively with peers, partners and others, to positively impact performance

•    Planning & Organizing - Adopts a structured approach, establishes plans, priorities and goals that are clear and logical; Organizes resources.

•    Drive & Resilience - Demonstrates drive and persistence to meet and exceed objectives; remains positive in challenging situations and recovers quickly from setbacks.

•    Effective Communication - Communicates clearly to others and ensures understanding.  Adjusts style of communication appropriately to the audience.

•    Leading Others - The ability to empower, grow, develop and inspire high performing teams and individuals.

•    Change & Adaptability - The ability to recognize and act upon change as a necessity to achieve goals. 

•    Analytical Thinking & Problem Solving - Analyses information effectively; identifies the causes of problems and provides realistic and practical solutions to address them.

•    Customer Focus - Identifies and understands the customer's needs.  Focuses on meeting their needs, ensuring both satisfaction and a continuing business relationship.

•    Integrity - Maintains high standards of honesty and trustworthiness.  Considers ethical implications of issues and decisions.

 

Already Working @TEVA?

If you are a current Teva employee, please apply using the internal career site available on "Employee Central". By doing so, your application will be treated with priority. You will also be able to see opportunities that are open exclusively to Teva employees. Use the following link to search and apply: Internal Career Site

The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner.

Teva's Equal Employment Opportunity Commitment Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience.

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