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Senior Associate, IT Systems Administrator

Billerica, Massachusetts
Category Information, Technology ID de l'offre R-38074
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Job Title:

Sr. Associate, IT Systems Administrator

Job Grade:

G10

Department:

Information Technology

FLSA Classification:

Exempt

Manager’s Job Title:

Senior Director, IT

Department Head Title:

CIO, Executive Vice President

Does This Position Have Any Direct Reports?

No

Job Description Approval Date:

May 2024

Job Summary

The Sr. Associate, IT Systems Administrator will manage day-to-day System Administration, user support and implementation of GxP Computerized Systems in QC Analytical Lab Manufacturing and other regulatory operations including, but not limited to, networked and non-networked standalone instruments, firmware based instruments, HMI’s, SCADA systems and any GxP application software at any manufacturing site across the North America region.

Area Of Responsibility

  • Collaborate with business partners in various functions, instrument vendors, and other IT team members to implement, perform applications administration and support GxP applications and systems in a controlled laboratory, manufacturing and other regulatory functions.
  • Maintain GxP Systems Inventory
  • User Access Management – activation, modification and deactivation
  • Manage user access privileges
  • Implementation and/or retirement of GxP systems
  • Ensure that Backup of all GxP systems is being taken
  • Recovery of GxP systems when required
  • Any other related activity assigned by IT Management through application of cGMP principles and following internal standard operating procedures (SOPs), work instructions (WIs), and regulatory requirements
  • Provide support during new systems implementation, overseeing design or configuration and validation (IQ / OQ/ PQ) to ensure the solutions will meet business needs while adhering to IT policies and procedures, compliance standards, and GxP requirements
  • Conduct Periodic Reviews such as but not limited to User Access Management, Systems Validation Reviews, SOP Reviews etc. to confirm computerized systems are compliant with company procedures and regulatory agency guidelines and requirements
  • Assist with QMS processes within IT, especially change control impact assessments, CAPA execution and managing deviations and incidents through root cause analysis for GxP systems changes
  • Propose alternate processes, procedures and process automation pathways to streamline and increase effectiveness and efficiency of IT operations
  • Collaborate with various stakeholders globally and/or across the sites within the region to understand and implement best GxP IT practices
  • Support regulatory, customer and other such audits from IT department.
  • Other duties as assigned

Work Conditions:

 Manufacturing/Production/Laboratory environment

Environmental related to manufacturing/production/laboratory environments:

  • Noise: Sufficient noise, either constant or intermittent, to cause marked distraction or possible injury to sense of hearing.
  • Fumes: Smoky or vaporous emissions, usually odorous, thrown off as the result of combustion or chemical reaction.
  • Odors: Unpleasant smells.
  • Gases: Examples include carbon monoxide and helium.
  • Dust: Airborne particles of any kind, such as textile dust, wood, and silica.
  • Hazards: Conditions where there is danger to life, health or bodily injury such as closeness to moving mechanical parts.

Physical Requirements:

  • Able to lift and carry up to 50 lbs.
  • While performing the duties of this job, the employee is frequently required to sit; use hands to finger, handle objects, or feel objects, tools, or controls; and reach with hands and arms. 
  • The employee is occasionally required to stand, stoop, kneel and crouch.
  • Specific vision abilities required of this job include close vision, distance vision, color vision and the ability to adjust focus.

The physical demands here are representative of those that must be met by an employee to successfully perform the essential functions of this job.  Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

Travel Estimate

Up to 25% to other sites within North American geography and sometimes for vendor audits

Education and Job Qualification

  • Minimum of a Bachelor's Degree, with preference being given to a candidate having a bachelor’s degree in Life Sciences, Pharmacy, Computer Science or Computer Information Systems (CIS) or related field.
  • Excellent understanding of GAMP 5, 21 CFR Part 11, Computer System Validation and Quality Management System.
  • Excellent collaboration and communication skills.
  • Ability to manage competing priorities and flexibility to shift workload when needed.
  • Excellent written and verbal communication skills and working knowledge of Microsoft Office Applications.
  • A team player with ability to work with people at all levels and diverse skill sets.
  • Requires travel for upto 25%-30% of the work hours.

Experience

  • Minimum 6-7 years of hands on experience maintaining, administering GxP systems, applications, instruments and shop floor machines in a manufacturing and/or quality function with detail orientation and strong problem solving, analytical, and critical thinking skills.

Disclaimer: The preceding job description has been designed to indicate the general nature and level of work performed by employee within this classification.  It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities, and qualifications required of employees as assigned to this job.  Nothing herein shall preclude the employer from changing these duties from time to time and assigning comparable duties or other duties commensurate with the experience and background of incumbent(s).

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À propos de nous

Au cours des vingt dernières années, Sun Pharma s'est affirmée comme un acteur majeur du marché des génériques aux États-Unis. Nous sommes la huitième plus grande entreprise pharmaceutique de génériques aux États-Unis et nous augmentons rapidement notre présence sur le marché des spécialités de marque, avec la dermatologie, l'ophtalmologie et l'oncologie comme segments cibles clés.

Nos valeurs

Sunology, une combinaison de Sun et d’idéologie, est le mode de vie chez Sun Pharma. Nous pratiquons l’humilité, l’intégrité, la passion et l’innovation.

Comment nous travaillons

Avec les gens au cœur de notre mission, Sun Pharma a créé une culture de travail inclusive et collaborative, où tous les employés sont encouragés à poursuivre leurs rêves et leurs aspirations professionnelles.

Avantages

  • Santé et bien-être

    Nous offrons des avantages complets, y compris une couverture médicale, dentaire et visuelle, ainsi que des programmes de santé et bien-être.

  • Financier

    Nous offrons un programme de contrepartie 401(k) compétitif ainsi que des programmes de bien-être financier pour soutenir les objectifs financiers à court et à long terme de nos employés.

  • Vie, travail et famille

    Nous offrons des avantages liés à la vie professionnelle qui soutiennent nos employés au-delà de leur journée de travail.

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