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IT Lab Systems Analyst II - Hybrid 

Category Information Technology  

Why Join Societal CDMO?  

Mission and Culture:

Each day we Bring Science to Society as we work towards improving the quality of life for patients who benefit from the therapies that we manufacture. We strongly believe that every employee plays an impactful role in accomplishing our mission of improving patients’ lives through client partnerships. Whether you are working hands-on developing, manufacturing, or, testing the products or if you are utilizing your expertise in any other way, through your work here you will have an opportunity to positively affect countless lives.

We foster a culture that is diverse, inclusive, challenging, and supportive. At Societal, we are committed to continuous improvement both as individuals and as an organization and we encourage our employees to continue their personal and professional development in a variety of ways.


We offer a competitive total rewards package that includes health benefits, annual performance bonus, stock options, generous paid time off, holiday shutdowns, parental leave, matching 401k contributions and much more!

Your New Role At Societal:

We are looking for a IT Lab Systems Analyst II.  In this role you will provide support and administration for computer systems across all three sites. You may support the laboratory, manufacturing or business systems in this role. As an IT Systems Analyst II you will manage computer system implementation and validation projects including the development and execute of computer system validation (CSV) protocols and procedures.

This role will be hybrid with onsite work in San Diego, CA and will support IT at all sites.

How You Will Make An Impact:

  • Provide timely direct support and problem solving on the technical-based needs of end-users such as developing and revising operating procedures for system and performing system administration and maintenance activities, updates, and changes.
  • Develop and review computer validation strategies including the development and review of computer validation documents such as user requirements specifications, validation plans, function and design specifications, testing protocols, risk assessments, and validation summary reports.
  • Lead computer system implementation and validation projects with the ability to manage multiple projects varying in complexity from the creation of work plans, identifying resource and budget needs through managing the project schedules, budget and leading project teams.
  • Build relationships with system owners and communicates business requirements back to IT management. Make recommendations and implement improvements with customer involvement.
Position Requirements

Ideal Candidate Will Bring:

  • Bachelor’s degree (B. A.) in Computer Science or Information Systems from four-year college or university.
  • Generally a minimum of 4 years of related experience in similar role.
  • Experience with system implementation, including the design, validation and maintenance of computer systems in a GxP environment. 
  • Experience developing project plans, anticipating problems and proactively coming up with solutions.
  • Experience supporting business applications.
  • Experience with computer system development lifecycle and computer system validation.
  • Working and technical knowledge of related IT systems and administration including; Microsoft Windows Server and Active Directory technologies, Microsoft SQL and Oracle databases, Local and Wide Area Networks including their topologies, Microsoft Windows desktop and server operating systems, Windows Terminal Server, Citrix Metaframe, and data backup utilities.
  • Experience with Lab Systems is highly desirable, such as; LIMS, Waters Empower. Agilent Chemstation or OpenLab, Dissolution systems, HPLC, UPLC etc.
  • Experience with ERP systems, such as SAP or QAD and experience in a pharma or Life Science company highly desired.
About the Organization Societal is a bi-coastal contract development and manufacturing organization (CDMO) with expertise to deliver on our client's needs, regardless of complexity level. These projects span pre-Investigational New Drug (IND) development to commercial manufacturing and packaging for a wide range of therapeutic dosage forms. We provide industry leading support for small molecule therapeutic development, end-to-end regulatory support, clinical and commercial manufacturing, aseptic fill/finish, lyophilization, packaging and logistics services to the global pharmaceutical market. We do all of this in our best-in-class facilities in San Diego, California and Gainesville, Georgia.

If you would like to apply for this position, please visit our website at and click on the "Careers" section.

New hires will pass a background check, drug screen and will be required to show proof of COVID vaccination (subject to limited qualified exemptions) as a condition of employment.
EOE Statement We are an equal opportunity employer (EOE) dedicated to a diverse workforce and Drug Free work environment. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other characteristic protected by law.  
EmpID None Specified 

This position is currently not accepting applications.

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