Laboratory System Administrator
MilliporeSigma

Job Info

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A career with MilliporeSigma is an ongoing journey of discovery: our 58,000 people are shaping how the world lives, works and plays through next generation advancements in Healthcare, Life Science and Electronics. For more than 350 years and across the world we have passionately pursued our curiosity to find novel and vibrant ways of enhancing the lives of others. MilliporeSigma is a business of Merck KGaA, Darmstadt, Germany.

Your Role:

The individual performs a variety of tasks within the Quality Assurance department including configuration and administration of laboratory systems and associated software. Will participate in and/or lead project teams across global operational departments to implement new laboratory systems.

Impacts the results of the Quality Assurance (QA) team and influences a range of customer, operational, project activities of Operations teams. Solves problems of varying complexity independently by identifying and selecting solutions and by analyzing information.

• Administrateavarietyoflaboratorysystems and associated software applicationsincluding defining, assigning and tracking user access permissions
• Responsiblefortroubleshooting,service,maintenance,orothersupport functions forsoftwareorfirmwareassociatedwithlaboratorysystems including OS upgrades, patch management and system security
• Acts as liaison with users, IT, system / software vendors in selection and implementation of laboratory systems
• Define requirements for and may perform validation activities related to system security and data integrity requirements for new or upgraded laboratory systems
• Responsible for timely communication of status of user requests and/or system outage reporting (e.g., helpdesk tickets)
• Lead and/or participate in laboratory system related investigations, corrective actions and change controls
• Continuously analyze data integrity controls to identify areas for improvement

Who You Are:

Minimum Qualifications:

• Bachelor's degree in a scientific (i.e. Biology, Chemistry, etc.) or technical (i.e. Engineering, Computer Science, etc.) field
• 3+ years of experience in a technical role supporting validation and/or administration of software applications or laboratory systems
• 2+ years of experience in regulated environment

Preferred Qualifications:

• Acts ethically and ensures quality of own work and that of others.
• Works with agilityand willing to embrace and implement change on a global scale.
• Applies technology to drive digitalization, improve quality and increase customer value
• Excellent communication and facilitation skills (ability to lead cross-functional meetings, demonstrated ability to bring consensus among diverse cross-functional teams)
• Proficient knowledge and application of FDA and EU regulations (cGMP, GLP)
• Advanced knowledge and application of data integrity regulatory guidance (e.g., FDA,MHRA, WHO)

RSRMS

What we offer: With us, there are always opportunities to break new ground. We empower you to fulfil your ambitions, and our diverse businesses offer various career moves to seek new horizons. We trust you with responsibility early on and support you to draw your own career map that is responsive to your aspirations and priorities in life. Join us and bring your curiosity to life!

Curious? Apply and find more information at https://jobs.vibrantm.com

The Company is an Equal Employment Opportunity employer. No employee or applicant for employment will be discriminated against on the basis of race, color, religion, age, sex, sexual orientation, national origin, ancestry, disability, military or veteran status, genetic information, gender identity, transgender status, marital status, or any other classification protected by applicable federal, state, or local law. This policy of Equal Employment Opportunity applies to all policies and programs relating to recruitment and hiring, promotion, compensation, benefits, discipline, termination, and all other terms and conditions of employment. Any applicant or employee who believes they have been discriminated against by the Company or anyone acting on behalf of the Company must report any concerns to their Human Resources Business Partner, Legal, or Compliance immediately. The Company will not retaliate against any individual because they made a good faith report of discrimination.

Job Requisition ID: 226130

Location: Rockville

Career Level: D - Professional (4-9 years)

Working time model: full-time

This job has expired.