Aktuelle Jobs im Zusammenhang mit Regulatory Compliance Analyst - Biberach an der Riß, Baden-Württemberg - GULP – experts united
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Compliance Specialist
vor 3 Wochen
Biberach an der Riß, Baden-Württemberg, Deutschland GULP – experts united VollzeitAt GULP – experts united, we are seeking a highly skilled Compliance Specialist to join our team. As a key member of our compliance team, you will play a crucial role in ensuring that our pharmaceutical client in Biberach meets all regulatory requirements.Key Responsibilities:Develop and implement compliance structures within our newly created compliance...
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Compliance Specialist
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Biberach an der Riß, Baden-Württemberg, Deutschland GULP – experts united VollzeitAt GULP – experts united, we are seeking a highly skilled Compliance Specialist to join our team. As a key member of our compliance team, you will play a crucial role in ensuring that our pharmaceutical client in Biberach meets all regulatory requirements.Key Responsibilities:Develop and implement compliance structures within our newly created compliance...
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vor 4 Wochen
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Clinical Research Manager for Regulatory Affairs
vor 1 Monat
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vor 1 Monat
Heidenheim an der Brenz, Baden-Württemberg, Deutschland PAUL HARTMANN AG VollzeitJob Title: Clinical Research Manager for Regulatory AffairsWe are seeking a highly skilled Clinical Research Manager for Regulatory Affairs to join our team at PAUL HARTMANN AG. As a key member of our regulatory affairs team, you will be responsible for ensuring the proper execution of procedures demonstrating medical device compliance with relevant clinical...
Regulatory Compliance Analyst
vor 3 Monaten
Your Career Journey Starts Here
At GULP – experts united, we are currently seeking a Compliance Specialist to join our dynamic team. This role is pivotal for those who are passionate about ensuring adherence to regulations within the pharmaceutical sector.
What We Offer
- Competitive salary with long-term employment stability
- Comprehensive social benefits, including holiday and seasonal bonuses
- Generous vacation allowance of up to 30 days annually
- Company pension contributions post-probation
- A diverse array of employee perks
Your Responsibilities
- Engage actively in the formation and implementation of frameworks within a newly established compliance unit
- Oversee the planning, coordination, and follow-up of compliance-related initiatives
- Contribute to projects aimed at harmonizing, optimizing, and standardizing standard operating procedures (SOPs) in Clinical Supply
- Draft, revise, and structurally reorganize SOPs as necessary
- Ensure alignment of the SOP framework in Clinical Supply with other departments and global standards
- Develop tailored and comprehensive training programs for Clinical Supply personnel
- Proactively address discrepancies in quality-related incidents and processes
- Prepare for, participate in, and follow up on internal and interdepartmental meetings regarding compliance matters
Your Profile
- Master's degree in biotechnology, chemistry, or pharmacy, complemented by substantial professional experience or relevant training in biopharmaceutical development and production
- Strong technical insight into production processes and areas
- Excellent proficiency in both German and English
- Exceptional communication abilities, collaborative spirit, and organizational skills
- Self-motivated and responsible work ethic, characterized by initiative and proactive problem-solving
