Operational Technologies Specialist

Posted Yesterday
Be an Early Applicant
Bend, OR, USA
In-Office
Mid level
Biotech • Consulting • Pharmaceutical • Manufacturing
The Role
Manage, maintain, and deploy laboratory and manufacturing systems (CDS, LIMS, ELN, FTIR, Rockwell) across GMP and development environments. Serve as primary IT/OT contact, support lifecycle and qualification activities, ensure data integrity and compliance (21 CFR-11, GAMP5), draft SOPs/IOPs, coordinate vendors, reduce production downtime, and support cross-functional stakeholders.
Summary Generated by Built In
Serán is seeking an Operational Technologies Specialist who will be responsible for the management, maintenance, and deployment of laboratory and manufacturing systems across both GMP-regulated and development environments. This role partners closely with IT, Quality Assurance (QA), laboratory staff, and manufacturing teams to ensure seamless integration of technology solutions that enhance productivity, quality, data integrity, and operational efficiency.

Duties and Responsibilties

  • Administration and end user support for systems such as FTIR, Waters CDS, ELN, various manufacturing equipment, etc.
  • Primary point of contact between users, internal IT and vendors
  • Support lifecycle management of lab and manufacturing systems
  • Work with management and subject matter experts to improve, develop and test existing applications and systems
  • Identify and drive enhancements to existing systems and processes
  • Support qualifications activities such as drafting, executing and or reviewing IOP/Q documentation
  • Drafting SOP’s
  • Manage and or support system and data backups for all OT system
  • Ensure security, compliance and integrity of all data
  • Support vital commissioning and qualification of systems is completed in alignment with site cGMP requirements
  • May interact with regulatory and or client inspectors as necessary
  • Provide support to reduce production downtime
  • Adheres to Standard Operating Procedures, cGMPs, Quality Manual, and company policies
  • Participates in process improvement and other non-routine projects
  • Regularly interfaces with department stakeholders on technical and coordinative matters 
  • Demonstrates cross-functional support capabilities with other teams
  • Coordinate and oversee vendors and service providers

Required Skills and Abilities

  • Strong working knowledge of on-premises and cloud-based IT infrastructures and operations best practices
  • Excellent working knowledge of computer systems, network and systems administration, data storage systems, and security
  • Excellent verbal, written, and interpersonal communication skills
  • Ability to work independently or as a contributing team member
  • Strong analytical and problem-solving skills
  • Strong project management skills
  • Communicates effectively and maintains productive relationships with coworkers, clients, and other contacts outside the Company
  • Follow detailed written and oral instructions 
  • Demonstrated ability to collaborate and work in cross-functional teams
  • Excellent organizational skills and attention to detail
  • Strong time management skills with a proven ability to meet deadlines
  • Multitasks and adjusts priorities in a fast-paced environment, while maintaining focus and managing disruption and/or unexpected needs 
  • Accepts feedback from a variety of sources and constructively manages conflict  
  • Ability to prioritize tasks and to keep leadership apprised of performance to timelines
  • Proficient with Microsoft Office Suite

Education and Experience

    • Bachelor’s degree in information technology, Computer Science, Informatics, Chemistry or related field preferred
    • Combination of equivalent certification and experience accepted
    • Requires minimum 3 years of GMP experience
    • Extensive experience with CDS, LIMS, ELN, and related applications such as Empower, Tiamo, FTIR, Rockwell, etc. 
    • Experience leading and managing IT/OT projects such as infrastructure and or software deploymentsWorking knowledge of and experience with relational database systems such as Oracle, MS-SQL, MySQL, etc. preferred
    • Working experience with industry-related standards and regulations such as FDA 21 CFR-11, GAMP5, ALCOA+, etc

Physical Requirements

  • Prolonged periods of sitting or standing at a desk and working on a computer 
  • Must be able to demonstrate mobility throughout multiple campus buildings   
  • Must be able to lift up to 15 pounds at times routinely, 30 pounds occasionally.   
  • Installing and monitoring equipment requires reaching overhead, kneeling, and crouching

Skills Required

  • Minimum 3 years of GMP experience
  • Extensive experience with CDS, LIMS, ELN and related applications (e.g., Empower, Tiamo, FTIR, Rockwell)
  • Working knowledge of on-premises and cloud-based IT infrastructures and operations best practices
  • Experience with relational database systems (Oracle, MS-SQL, MySQL)
  • Working experience with FDA 21 CFR-11, GAMP5, ALCOA+ (industry standards/regulatory compliance)
  • Experience leading and managing IT/OT projects (infrastructure or software deployments)
  • Excellent knowledge of computer systems, network and systems administration, data storage systems, and security
  • Support for qualification activities (drafting/executing/reviewing IOP/Q documentation) and drafting SOPs
  • Strong project management, analytical, problem-solving, organizational, and time-management skills
  • Excellent verbal, written, and interpersonal communication skills and ability to work cross-functionally
  • Proficient with Microsoft Office Suite
  • Bachelor's degree in IT, Computer Science, Informatics, Chemistry or related field (or equivalent certification and experience)
  • Ability to lift up to 15 pounds routinely and 30 pounds occasionally; mobility across campus buildings
Am I A Good Fit?
beta
Get Personalized Job Insights.
Our AI-powered fit analysis compares your resume with a job listing so you know if your skills & experience align.

The Company
0 Employees
Year Founded: 2016

What We Do

Serán Bioscience is a contract development and manufacturing organization (CDMO) that provides comprehensive pharmaceutical support for small and large molecule drug development. They offer services ranging from discovery to clinical manufacturing, including formulation design, spray drying, and analytical quality control, with a science-first approach aimed at helping clients advance medicines to the clinic efficiently.

Similar Jobs

RigUp Logo RigUp

Senior Account Executive

Information Technology • Professional Services • Software • Energy
Remote or Hybrid
US
260 Employees

RigUp Logo RigUp

Senior Account Executive

Information Technology • Professional Services • Software • Energy
Remote or Hybrid
US
260 Employees

RigUp Logo RigUp

Recruiter

Information Technology • Professional Services • Software • Energy
Remote or Hybrid
USA
260 Employees

DraftKings Logo DraftKings

Non-Sports Manager, Predictions Operations

Digital Media • Gaming • Information Technology • Software • Sports • Esports • Big Data Analytics
Remote or Hybrid
United States
6400 Employees
112K-140K Annually

Similar Companies Hiring

Amplify Platform Thumbnail
Fintech • Financial Services • Consulting • Cloud • Business Intelligence • Big Data Analytics
Scottsdale, AZ
62 Employees
Fortune Brands Innovations Thumbnail
Manufacturing
Deerfield, IL
2450 Employees
Amalgamated Sugar Thumbnail
Food • Greentech • Agriculture • Industrial • Manufacturing
Boise, Idaho
768 Employees

Sign up now Access later

Create Free Account

Please log in or sign up to report this job.

Create Free Account