AS&T Expert
Novartis is hiring an AS&T Expert. It pays €67k-€105k a year and Level rates it ; you can apply on Novartis.
Level's read on this job
- Level rates this role Little AI ●○○○: aI is not part of the work.
- The posting mentions MS Office, analytical chemistry and gmp among its tools and skills.
- Level classes it as a senior role.
- Novartis has 890 other open roles on Level.
- Posted within the past two weeks.
AI in this role
Coordinate and manage analytical activities, method transfers, and stability studies as an AS&T Expert in a GMP environment.
Salary Range:
€66,918.00 - €105,200.00
Job Description Summary
#LiHybridLocation: Kundl - Austria.
This role is based in Kundl, Austria. Novartis is unable to offer
relocation support for this role: please only apply if this location is accessible for you.
The Analytical Science and Technology (AS&T) Expert is responsible for coordinating and managing analytical activities across products, including both customer-related projects and innovative Novartis initiatives, and for providing scientific analytical expertise and support.
Job Description
Major Accountabilities
- Management and oversight of all analytical activities related within responsible projects.
- Coordination and management of analytical method transfers and stability studies.
- Presentation and discussion of analytical data in local and international project teams. Life-cycle management of analytical methods, including control of method performance, analytical method validation, pharmacopoeia and health authority compliance and definition of method improvements.
- Handling of deviations, investigation, OOS/OOE/OOT cases as well as changes and complaints.
- Person of contact for analytical questions from health authorities and analytical subject matter expert during audits and inspections.
- Cross-functional interface with Manufacturing Science & Technology team, analytical development, production, quality assurance and regulatory department.
- Implementation of GMP requirements. Compilation and Review of documents (analytical protocols and reports, annual performance quality reports, ongoing process verification reports, registration documents).
- Budgeting and cost control of external analytical activities.
- Management of reference substances and control samples.
Essential Requirements:
- University degree or FH with natural science/technical background (e.g. chemistry, pharmacy, biology) or equivalent education.
- Approx. 3 to 5 years in pharmaceutical industry and/or analytical laboratory in GMP environment. MS Office- and other standard IT applications.
- Fluent in English and German.
We offer a 2-year temporary contract for this role.
Rewards
You can find everything you need to know about our benefits and rewards in the Novartis Life Handbook. https://www.novartis.com/careers/benefits-rewards
In addition to a market-competitive base salary, we offer an attractive incentive program, a modern company pension scheme, childcare facilities, learning and development opportunities as well as worldwide career possibilities within the Novartis group
In accordance with Austrian law, we are obliged to disclose the minimum salary as stated in the collective bargaining agreement. For this position the minimum salary is € 66,918.00
/year (on a full time basis). We also offer a potential market oriented excess payment in line with your experience and qualifications.
The salary offered is determined based on gender-neutral objectives, such as relevant skills, competencies and experience in accordance with the Novartis pay setting policy and upon joining Novartis will be reviewed periodically.
In addition to your base salary, you may be eligible for a performance-based bonus depending on certain performance parameters. Further details will be provided during the application process.
Pay equity is a fundamental principle of our employment policy and reflects our commitment to create a diverse, equitable and inclusive environment that treats all employees with dignity and respect, as outlined in our Code of Ethics.
Note: Benefits and compensation may vary by country and are subject to local legal requirements, including provisions of collective bargaining agreements where applicable. A full overview of your compensation package, including any relevant collective bargaining agreement details applicable to your role based on your employment location and Novartis employer entity, will be communicated separately to you during the application process.
Commitment to Diversity and Inclusion / EEO paragraph:
Novartis is committed to building an outstanding, inclusive work environment and diverse teams’ representative of the patients and communities we serve.
Skills Desired
Collaboration, Communication, Data Integrity, Decision Making, Digital Fluency, Good Manufacturing Practices (GMP), Health Safety Regulations, Intelligent Risk Taking, Laboratory Testing, Leadership, Managing Ambiguity, Operational Excellence, Organizational Savvy, Problem Solving, Quality Assurance (QA), Quality Compliance, Quality Control (QC), Quality Inspections, Quality Management Systems (QMS), Regulatory Compliance, Statistical Process Control (SPC)How we rate this
AS&T Expert at Novartis rates 0 out of 100 for how much of the daily work is AI. That makes it Little AI (AI Level 1 of 4). The level is about AI in the job, not seniority.
Little AI. AI is not part of the work.
- ●●●● Builds AI80 to 100
- ●●●○ Works on AI60 to 79
- ●●○○ Uses AI40 to 59
- ●○○○ Little AI0 to 39
Levels come from how often the tools, models and workflows of the role are named in the posting itself. Read the description and count the AI tools, models and workflows it names.
Prepare for this job
Built from this posting and from similar jobs on Level.
Skills and AI tools this role asks for
Questions you could be asked
- Tell me about a project where analytical chemistry was part of your work. What did you do?
- Tell me about a project where gmp was part of your work. What did you do?
- Tell me about a project where lifecycle management was part of your work. What did you do?
- Tell me about a project where method validation was part of your work. What did you do?
- Tell me about a project where pharmaceuticals was part of your work. What did you do?
Adapt your resume
- List these exact terms on your resume: Analytical Chemistry, Gmp, Lifecycle Management, Method Validation, and Pharmaceuticals. An applicant tracking system matches the wording, not the idea.
- Attach one line of real, concrete experience to at least one of them. A tool named with nothing behind it rarely survives a human read.
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