Site Digital Manager

Ology Bioservices, Inc.
Job Description

Summary: The Site Digital Manager is responsible for daily oversight of Digital infrastructure and operations and ensuring key SLA's are met. The position leverages people, processes, and technology to execute business strategies in a way that bolsters product quality, maintains regulatory compliance, and exhibits a high degree of ethics and integrity.

Key Responsibilities:

  • Lead, manage, direct, and coordinate the activities of the site Digital Operations and Digital Infrastructure teams, and associated quality objectives of the business to meet corporate objectives.
  • Build and nurture effective working relationships throughout the business to maximize inter-departmental synergy and collaboration.
  • Set and execute tactical objectives for the site Digital Team to achieve company goals.
  • Drive customer satisfaction by identifying and improving key operational metrics.
  • Drive continuous improvement through standardization, process automation, and operational efficiencies.
  • Execute and test site disaster recovery & business continuity plans.
  • Create and continuously update site SOP's to ensure accuracy.
  • Know, apply, and contribute to the quality system and relevant regulations / standards.
  • Develop and monitor the operating, capital, project budgets, and make periodic reforecasts as needed.
  • Manage appropriate staffing of the IT department.
  • Continuously strive to improve department and corporate processes.
  • Ensure the Confidentiality, Integrity, and Availability of information in accordance with SLA's.
  • Develop innovative solutions to complex and abstract problems.
  • Assist with implementation of corporate policies and procedures.
  • Facilitate site inspections, audits, and incident response teams as needed.

*All employees are expected to adhere to the Quality Management System established in the Quality Manual, Quality Policy, Standard Operating Procedures, Current Good Manufacturing Practices, and any other applicable regulations and standards to the duties within their role.

  • 3+ years of experience in a highly regulated manufacturing environment.
  • Extensive knowledge of information systems technology systems.
  • Strong and demonstrated strategic thinking and critical thinking skills.
  • Experience working with Quality Systems in GMP regulated operations such as Change Control, Deviation / Investigation, CAPA’s and other quality systems.
  • Ability to coordinate multiple projects and personnel.
  • Ability to develop data-driven solutions to dynamic and complex challenges.
  • Firm understanding of on-premise datacenter technologies, end-user computing, and cloud computing.
EOE STATEMENT Ology Bioservices,is an equal opportunity employer. Employment decisions are made without regard to race, color, religion, national origin, gender,sexual orientation, gender identity, age, physical or mental disability, genetic factors, or military/veteran status or any other characteristics protected by law.

EEO Minorities/Women/Disabled/Veterans  
ABOUT THE ORGANIZATION Thank you for your interest in joining the Ology Bioservices team! We believe we have the most talented and committed employees in the industry with decades of combined experience in manufacturing, developing and licensing vaccines and protein/antibody therapeutics.
Ology Bioservices is a full-service Contract Development Manufacturing Organization specializing in biologic drug substance manufacturing from early stage through commercial product. The company has 183,000 square feet of manufacturing, process development and QA/QC space in our state of the art Advanced Development and Manufacturing ADM) facility in Florida. Ology Bio has 20 years of experience developing and manufacturing drugs and biologics for the US Government, and over $500M in government contracts awarded over that time.
The company expanded to Commercial Manufacturing upon the move into the new facility in early 2017. Our infrastructure provides unique services to our clients, including full regulatory support from preclinical through licensure, clinical trial operational support and bioanalytical testing, as well as cGMP manufacturing up to Biosafety Level 3 (BSL3).
We offer outstanding career growth opportunities, excellent fringe benefits, and competitive pay.
We are an Equal opportunity Employer
AA/EEO Minorities/Women/Disabled/Veterans  
POSITION Site Digital Manager  
LOCATION Alachua  
Contact Information