Vollzeit | Kundl I 60 % on site
Are you an expert in your field, ready to apply your know-how to exciting projects?
Join the Hamburger TECCON Group, a team of over 450 professionals specializing in IT, engineering, and business. We develop innovative solutions for prestigious clients, aiming to discover and nurture human potential by creating tailored connections between companies and talents. Bring your expertise to our projects and actively shape the future.
Deine Aufgaben
GMP Compliance & Quality Oversight: You ensure compliance with cGMP guidelines by supporting QA activities independently or within a cross-functional team.
Document Review & Release Management: You review, approve, and release GMP-relevant documents and tools to guarantee high-quality and compliant deliverables.
Project & Portfolio Management: You manage QA-related project activities such as TRD product portfolios, quality initiatives, and process improvements.
Cross-Functional Collaboration: You contribute as an active project team member, supporting project management and ensuring alignment with quality standards.
GMP Advisory & Support: You provide expert guidance to TRD line functions on GMP-related topics and quality requirements.
Quality Systems & Compliance: You ensure adherence to internal SOPs, Quality Manuals, regulatory guidelines, and health authority requirements.
Deviation & Change Control Management: You review and approve deviations and change controls to maintain compliance and continuous improvement.
Material Release & Systems Approval: You release raw materials and approve documents within systems such as ESOPS D2, CONDOR, and SUBWAY.
Dein Profil
Educational Background: You hold a Bachelor’s degree with at least 5 years or a Master’s degree with at least 3 years of experience in pharmaceutical quality or operations.
Language Skills: You communicate fluently in English (written and spoken) and ideally have good command of the local site language.
cGMP Expertise: You bring solid knowledge of cGMP and practical experience in technical development, production, or Quality Assurance.
Scientific & Regulatory Knowledge: You demonstrate strong scientific, technical, and regulatory understanding within the pharmaceutical environment.
Analytical & Compliance Skills: You analyze and evaluate cGMP compliance effectively and make sound quality decisions.
Organizational & Decision-Making Skills: You prioritize tasks efficiently and take ownership of quality-related decisions in a dynamic environment.
Deine Benefits
Exciting, self-organized and responsible tasks
Long-term employment relationship, pleasant working atmosphere in a young, dedicated team
Flexi time agreement, flexible working time model, work-life balance
Opportunities for specialization and subject-specific further education and training
Extremely collegial team with a friendly approach
Various development opportunities within the TECCON Group
The gross annual salary is at least EUR 70.000 but of course we offer overpayment in line with the market, depending on qualifications and professional experience.
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Are you an expert in your field, ready to apply your know-how to exciting projects?
Join the Hamburger TECCON Group, a team of over 450 professionals specializing in IT, engineering, and business. We develop innovative solutions for prestigious clients, aiming to discover and nurture human potential by creating tailored connections between companies and talents. Bring your expertise to our projects and actively shape the future.
Deine Aufgaben
GMP Compliance & Quality Oversight: You ensure compliance with cGMP guidelines by supporting QA activities independently or within a cross-functional team.
Document Review & Release Management: You review, approve, and release GMP-relevant documents and tools to guarantee high-quality and compliant deliverables.
Project & Portfolio Management: You manage QA-related project activities such as TRD product portfolios, quality initiatives, and process improvements.
Cross-Functional Collaboration: You contribute as an active project team member, supporting project management and ensuring alignment with quality standards.
GMP Advisory & Support: You provide expert guidance to TRD line functions on GMP-related topics and quality requirements.
Quality Systems & Compliance: You ensure adherence to internal SOPs, Quality Manuals, regulatory guidelines, and health authority requirements.
Deviation & Change Control Management: You review and approve deviations and change controls to maintain compliance and continuous improvement.
Material Release & Systems Approval: You release raw materials and approve documents within systems such as ESOPS D2, CONDOR, and SUBWAY.
Dein Profil
Educational Background: You hold a Bachelor’s degree with at least 5 years or a Master’s degree with at least 3 years of experience in pharmaceutical quality or operations.
Language Skills: You communicate fluently in English (written and spoken) and ideally have good command of the local site language.
cGMP Expertise: You bring solid knowledge of cGMP and practical experience in technical development, production, or Quality Assurance.
Scientific & Regulatory Knowledge: You demonstrate strong scientific, technical, and regulatory understanding within the pharmaceutical environment.
Analytical & Compliance Skills: You analyze and evaluate cGMP compliance effectively and make sound quality decisions.
Organizational & Decision-Making Skills: You prioritize tasks efficiently and take ownership of quality-related decisions in a dynamic environment.
Deine Benefits
Exciting, self-organized and responsible tasks
Long-term employment relationship, pleasant working atmosphere in a young, dedicated team
Flexi time agreement, flexible working time model, work-life balance
Opportunities for specialization and subject-specific further education and training
Extremely collegial team with a friendly approach
Various development opportunities within the TECCON Group
The gross annual salary is at least EUR 70.000 but of course we offer overpayment in line with the market, depending on qualifications and professional experience.
#J-18808-Ljbffr
