Senior Manager Regulatory Affairs (m / w / d) - Medicinal Products

OmniVision GmbH; Rimini; In loco; EUR 70.000 - 90.000; Tempo pieno

Descrizione del lavoro

OmniVision GmbH is seeking a Senior Manager for Regulatory Affairs to join their expanding team in Rimini. This role involves regulatory submissions, compliance with EU standards, and management of product information within a mid-sized pharmaceutical setting. The ideal candidate will possess a strong background in regulatory affairs, natural sciences education, and expertise in eCTD sequences. Employees can expect competitive compensation, flexible working arrangements, and numerous benefits including a company pension plan and wellness initiatives.

Servizi

30 days of annual vacation

Flexible working hours

Subsidized company pension plan

Financial support for job bikes

Coverage of public transportation ticket

Subsidized lunch

Seasonal fruit basket

Company events

Online employee discount portal

Competenze

• At least 5 years of experience in regulatory affairs (medicinal products) in the EU.
• Fluent in German and English with excellent communication skills.

Mansioni

• Plan and submit regulatory change notifications and variations.
• Create and manage eCTD sequences for regulatory submissions.
• Coordinate regulatory lifecycle management across subsidiaries.

Conoscenze

Analytical thinking

Communication skills

Team leadership

Service-orientation

Flexibility

Proactivity

Formazione

University degree in natural sciences

Strumenti

eCTD

Regulatory Information Management Systems (RIMS)

Microsoft Office Suite

Descrizione del lavoro

Senior Manager Regulatory Affairs (m / w / d) - Medicinal Products

OmniVision GmbH is an expanding medium-sized ophthalmology company with its headquarters in Germany and locations in Austria, Italy, Spain and Switzerland. In Germany, OmniVision GmbH is one of the leading non-corporate ophthalmology companies. Our product portfolio includes pharmaceuticals, medical devices and nutritional supplements.

In the course of our strong growth, we are looking for a committed and motivated person to join our headquarters in Puchheim near Munich as soon as possible :

Your Profile :

• University degree in natural sciences, preferably Pharmacy, Biology or Chemistry
• At least 5 years of professional and practical experience in regulatory affairs (medicinal products) within the EU
• Experience in creating eCTD sequences
• Open-minded personality
• Ability to lead a team
• Service-orientation
• Ability to grasp things quickly, analytical thinking in combination with an independent, structured and goal-oriented way of working
• Proactive thinking and acting, assertiveness, flexibility and strong communication skills
• Fluent in German and English with excellent oral and written communication skills
• IT affinity : eCTD, databases, Regulatory Information Management Systems (RIMS), Microsoft Office suite

Your contribution :

• Planning and submission of national change notifications and EU-variations to competent authorities
• Compilation of variation packages regarding quality (CMC) and product information aspects
• Planning and submission of renewal applications
• Management of national and European variation and renewal procedures
• Communication with European competent authorities (EU and Switzerland)
• Answering letters of deficiency (List of Questions (LoQs))
• Procurement and assessment of documents from international suppliers (Contract Manufacturing Organizations (CMOs))
• Creation and revision of product information texts (SmPC, PIL, labelling) for the implementation of officially requested text amendments and / or for text adaptations to the current state of knowledge
• Coordination of all regulatory lifecycle management activities in the OmniVision subsidiaries (Austria, Italy, Spain and Switzerland)
• Creation of eCTD sequences for the submission of variation and renewal applications
• Maintaining and updating the company's internal marketing authorization database
• Collaboration in the company's internal change control process
• Monitoring, interpretation and implementation of new regulatory requirements

We offer you :

• Permanent, long-term employment in a successful, owner-operated medium-sized pharmaceutical company
• An attractive compensation package
• 30 days of annual vacation
• Flexible working hours including remote work options
• Modern IT infrastructure
• Modern and air-conditioned offices
• Ergonomic workstations
• Subsidized company pension plan
• Financial support for job bikes (company bicycle program)
• Coverage of the "Deutschlandticket" (nationwide public transportation ticket)
• Subsidized lunch including free beverages
• Seasonal fruit basket
• Company events
• EGYM Wellpass
• Online employee discount portal via Corporate Benefits

Does this sound interesting to you?

We look forward to receiving your application (cover letter stating your salary expectations and earliest possible starting date, CV and references) to the attention of Francisco Lopez, HR Manager.

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