Project Analyst NPI (all genders) | Fixed-term contract for 2 years | Full-time

Company Description

AbbVie’s mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube.

Job Description

At our production site in Ludwigshafen am Rhein, we are looking for a Project Analyst NPI (all genders) to start as soon as possible.

Responsibilities

As Project Analyst NPI, you will be responsible for ensuring and carrying out the proper, GMP-compliant testing of intermediates, bulk and finished medicinal products, stability samples, and, where applicable, other samples such as validation batches, based on valid test instructions.

• Independently and fully perform established methods, testing assignments, and techniques in accordance with test instructions.
• Largely independently select and perform non-routine analytical testing and specialized techniques.
• Independently plan, report, and perform validations and method transfers, and independently support the introduction of new techniques.
• Independently evaluate, document, and assess the activities performed in accordance with the applicable departmental procedures, ensuring the traceability, plausibility, and accuracy of the results obtained.
• Comply with and optimize all GMP, EHS, and 5S guidelines.
• Plan and procure the chemicals, reagents, and consumables required to carry out the investigations.
• Proactively resolve analytical problems.

Qualifications

• Successfully completed training as a chemical or biological laboratory technician, CTA, PTA, or BTA; a bachelor’s degree in a natural science with at least five years of professional experience; or a comparable master’s degree with at least two years of professional experience.
• Depending on the area of assignment, knowledge of and experience in high-performance liquid chromatography (HPLC), UV/VIS spectrometry, and bioanalytics, including ELISA and reporter gene assays.
• Good knowledge of good documentation practices and confidence working in a GMP-regulated environment.
• A structured and independent way of working, as well as experience working in a fast-paced environment.
• Very good German and good English language skills.
• Reliability and a high degree of accuracy at work.
• Very good communication and teamwork skills.

What We Offer

• A varied area of responsibility where you can truly make a difference.
• An open corporate culture.
• Attractive compensation.
• Comprehensive onboarding supported by a mentor.
• Flexible working-time models to support a healthy work-life balance.
• Company health management, including comprehensive health and sports programs.
• Company social benefits.
• Diverse career opportunities within an internationally operating company.
• Attractive professional development opportunities at a high level.
• A strong international network.

We have been recognized worldwide several times as a "Great Place to Work," and we are proud to offer our employees the flexibility to maintain a healthy work-life balance. We take our impact on the environment and our communities seriously and therefore focus on regularly giving back. We are committed to equality, equal opportunities, diversity, and inclusion (EED&I)—a commitment that is fundamental to us. This includes valuing different perspectives, creating an inclusive culture, and treating all employees with dignity and respect.

Additional Information

AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.

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