Senior GMP Project Manager – 13530

Publiceringsdatum: 2025-10-07

Letar du efter möjligheter att arbeta inom data/it? Här är din möjlighet att bli en del av teamet hos Veritaz AB genom att arbeta som projektledare, it. Intresserade sökes för heltid-jobb hos Veritaz AB - är du intresserad? De letar efter någon som vill jobba 6 månader eller längre.

ospecificerad arbetsort är platsen där denna position är ledig. Om du är intresserad av en karriär inom projektledare, it, ta en titt på den lediga tjänsten som Veritaz AB erbjuder för att se om det är en matchning. Här är chansen att bli en del av Veritaz AB och jobba som projektledare, it! Ansök senast torsdag den sjätte november 2025.

Jobbannons

Veritaz is a leading IT staffing solutions provider in Sweden, committed to advancing individual careers and aiding employers in securing the perfect talent fit. With a proven track record of successful partnerships with top companies, we have rapidly grown our presence in the USA, Europe, and Sweden as a dependable and trusted resource within the IT industry.

Assignment Description

We are looking for a Senior GMP Project Manager to join our dynamic team.

What you will work on

• Interpret GMP requirements based on internal procedures and applicable regulations.
• Participate in the preparation and review of SOPs, handle referrals, and provide technical approvals.
• Support validation, change, and decommissioning projects by reviewing and technically approving related documentation.
• Write statements for deviation reports and investigations.
• Stay updated on developments in computerized systems and validation, and inform or train others accordingly.
• Participate in global information systems projects.
• Perform technical approval of validation documents, change requests, deviation reports, and related documentation.

What you bring

• Expertise in computerized systems with at least 5 years of relevant experience.
• University degree or equivalent experience in natural sciences, validation management, or process technology.
• Extensive experience in the pharmaceutical industry, particularly in GMP-regulated environments.
• Background in validation/QA, ideally as a CSV Engineer or QA-IT professional.
• Strong understanding of industrial IT/OT and automation systems.
• Excellent communication skills in Swedish and English, both written and spoken.