20 beste Stellen als master data in mannheim, bw – aktuell auf Personalsuche

Validation Manager (all genders) | Fixed-term contract for 2 years | Full-time
AbbVie —Ludwigshafen am Rhein
- Vollzeit
- Englisch
- Master
- Produktion
6 Tage
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Validation Manager (all genders) | Fixed-term contract for 2 years | Full-time

AbbVie -
Ludwigshafen am Rhein

Jetzt bewerben

Details zur Stelle

Vollzeit
vor 6 Tagen

Qualifikationen

Englisch
Master
Verpackung
Produktion
Führungserfahrung

Vollständige Stellenbeschreibung

Company Description

About AbbVie

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 www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube.

Job Description

At our Ludwigshafen site, the Validation Manager plays a key role in the introduction of new manufacturing processes and the optimization of existing ones. The role has a particular focus on melt extrusion, secondary packaging, and the assembly of autoinjectors across the full product lifecycle, including development, validation, and manufacturing in a cGMP environment.

With your experience and passion, you will work closely with a cross-functional matrix team to support technology transfers and be responsible for introducing new products into production through to validation. You will also contribute to the development and optimization of processes and procedures for the manufacture and packaging of solid dosage forms, combination products, and medical devices.

Main Responsibilities

Support the introduction of new products through to validation.
Track and trend product and process data, perform statistical evaluation of data, and derive appropriate actions.
Independently prepare the annual validation master plan, including timelines, as well as templates for validation plans and reports.
Ensure compliance with internal requirements, cGMP, and current regulatory expectations, and support the implementation of these requirements within TechOps.
Present validation concepts and validation activities during regulatory inspections and internal audits, and represent the site in the CoE (Center of Excellence).
Independently lead investigations of potential deviations with impact on product quality.
Independently execute technical trials and update manufacturing and work instructions as needed.
Support and prepare the annual Product Quality Report for all existing and future products.

Qualifications

University degree (Master’s, Diploma) in Chemistry, Biochemistry, Pharmacy, or a similar scientific discipline.
Minimum 3 years of experience in the pharmaceutical industry, especially in secondary and primary packaging or the manufacture of solid dosage forms.
Experience in cGMP and validation environments in accordance with Annex 15, EU GMP Guide, and 21 CFR 210/211.
Strong experience in troubleshooting, process optimization, and scale-up of manufacturing processes.
Very good knowledge of the manufacture, packaging, testing, and evaluation of pharmaceutical dosage forms.
Excellent English language skills.
High level of initiative, self-motivation, and flexibility.
Strong leadership, communication, and teamwork skills, including in an international environment.

What we offer you

A varied role where you can truly make a difference.
An open corporate culture.
Attractive compensation.
Comprehensive onboarding supported by a mentor.
Flexible working models for a healthy work-life balance.
Corporate health management with extensive health and sports programs.
Company benefits.
Diverse career options within an international company.
Attractive, high-level professional development opportunities.
A strong international network.

At AbbVie, you will find a workplace where your individual contribution counts, enabling us to achieve great things together.

Join us and grow—and constantly surpass your own expectations!

Range E11T – E13T, depending on experience and qualifications.

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.

US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html

US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:

https://www.abbvie.com/join-us/reasonable-accommodations.html

Jetzt bewerben

Erweiterte Suche

master data Jobs in mannheim, bw

Validation Manager (all genders) | Fixed-term contract for 2 years | Full-time

Doctoral Researchers: up to 6 Fully Funded Positions in Data Science and Health

Intern Embellishment (all genders)

Working Student for HR Business Partner Grid Integration 40% (f/m/d)

Management Assistant to the Chief Technical Officer (f/m/d)

Bachelor/Master Thesis oder Praxissemester im Bereich Research & Development

Technician with focus on Product Development Beverage

Management Assistant to Board Member AMWA (f/m/d)

Mandatory Internship in Global Category Management (f/m/d)

Tender & Contract Specialist GSA

Internship Predictive Maintenance (m/f/d)

Lab-on-Chip Development Internship + Master Thesis at Near Patient Care (m/f/d)

Trainee SAP Business Intelligence (SAP BI) Consultant (m/w/d)

Transfer Pricing Senior Manager (m/f/d)

Team Lead Accounts Payable (f/m/d)

Internship (m/f/d) Electromechanical Energy harvesting

Electrical Designer / Hardware Planner (m/f/d)

Universitätsabsolventen als Management Associates (m/w/d)

External Lecturer on a fee basis Social Media Analytics & Generative AI for Creative Content f/m/d

Solution Consultant (m/w/d) - PIM / MDM

Ich möchte aktuelle Job-E-Mails für Stellen als master data in mannheim, bw erhalten

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