LIMS Officer: QC Systems & Data Integrity

Hikma Pharmaceuticals

Sintra

On-site

EUR 38,000 - 54,000

Full time

28 hours ago
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Benefits offered by this job

Life insurance
Health insurance
Annual performance bonus
High career prospects

Job summary

Hikma Pharmaceuticals in Portugal is seeking an Officer, LIMS (m/f) to join the Quality Control Department on-site, reporting to the Sr. Supervisor, Quality Control. This role focuses on configuring and validating laboratory software to support accurate testing and compliant operations.

Key tasks include creating specifications in the software for raw materials and finished products, handling change controls in Ivanti, writing SOPs, and coordinating LIMS projects with the Columbus site.

Qualifications

  • Bachelor's degree in CS/Software Eng/IS or related field.
  • Experience with enterprise systems is required.
  • Experience with LIMS/CDS/ELN is beneficial.
  • Knowledge of GxP and Data Integrity desirable.
  • Ability to work in a highly structured regulated environment.

Responsibilities

  • Introduce/create effective software specifications for materials, packaging, finished products, and stability samples.
  • Create/update/validate analyses for laboratory use in the software.
  • Resolve daily software issues for labs/users.
  • Generate Change Control requests in Ivanti for new users.
  • Write/review SOPs when requested.
  • Manage LIMS projects in parallel with Columbus site.

Skills

English (High Level)
Teamwork
Attention to detail
Problem solving
Time management

Education

Bachelor's degree in Computer Science/Software Engineering/Information Systems

Tools

LIMS
CDS
ELN
Ivanti

Job description

Hikma Pharmaceuticals in Portugal is seeking an Officer, LIMS (m/f) to join the Quality Control Department on-site, reporting to the Sr. Supervisor, Quality Control. This role focuses on configuring and validating laboratory software to support accurate testing and compliant operations.

Key tasks include creating specifications in the software for raw materials and finished products, handling change controls in Ivanti, writing SOPs, and coordinating LIMS projects with the Columbus site.

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