Principal Regulatory Affairs Specialist

Permanent contract

Mirandola (MO)

06/29/2020

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Reference number

2020-14458

Category

Operations — Engineering/production

Business industry

Life sciences

Minimum level of experience required

3 to 5 years

Location

Modena, Italy, Emilia Romagna

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Job description

Founded in 1984, AKKA has a strong entrepreneurial culture and is pursuing fast-paced growth and international development in line with its strategic plan CLEAR 2022.
The Group continues to recruit at a steady pace to support its strong business growth.
As of 31 December 2019, the Group had 20.930 employees with an increase  of + 5.8% in France, + 1.6% in Germany and +5.0 on an international level.
Driven by its expertise in future mobility, digital and industry 4.0 technologies, the Group’s 2019 revenue rose by 20.8% to €1.801,5 million and has surpassed the €1.8B cap.

 


With a view to strengthening our team, we are looking for a

 



Principal Regulatory Affairs Specialist

 



The Resource is expected to perform with minimal supervision and is responsible for influencing department processes and procedures, developing strategies for worldwide regulatory approval, preparing US and EU submissions, and ensuring timely and high-quality execution of all regulatory deliverables. In addition, the Principal Specialist mentors’ other regulatory specialists, provides support for global regulatory approvals, and ensures compliance with company and government requirements.

Your focus will be:
• Prepare regulatory strategies/plans and worldwide regulatory requirements for both new and existing combination products/drug products.
• Writing and preparation of regulatory submissions coordinate the preparation of combination product/drug product filings.
• Respond to regulatory authorities on issues that during the review of submission dossiers.
• Interface internally with QA, R&D, Clinical and other affected departments to ensure timely availability of submission documents.
• Input, review, and approval of protocols, reports, labeling, promotional materials, training materials, and other documents used in submissions.
• Reviews, prepares and maintains regulatory files (administrative documents and technical documentation in format required by local laws, regulations, and standards) for new and/or changed products and submits to applicable authorities
• Maintenance of regulatory registration database.
• Implementation and distribution of information related to new worldwide regulations.
• Experience in define requirements WW and perform submission under Active Medical Device regulation, Pharma regulation, EUP-USP, GMP, API, Software life-cycle and cybersecurity, electrical equipment including systems, Human factors and usability, Risk management, Sterilization and biocompatibility, including reusable/re-sterilizable devices
• Pre- and post-market clinical studies support experience, CER review “Valid scientific evidence” and “substantial equivalence” topics, rationale redaction.
• Assist quality management system audits, including regulatory parts of MDSAP and EU MDR.
• Develop proficiency in worldwide regulatory requirements and establish and maintain good working relationships with agency personnel.

Profile

Education Required:

• Bach degree in pharmacy, pharmacology, chemistry, biomedical engineering or a related subject is required. MS/PhD is preferred; Ph. D. is highly preferred.

 

Desired/Preferred Qualifications:

• Minimum 5 years pharma or medical device industry experience, with at least 3 years in a regulatory role involving marketing authorization for medicinal product
• In-depth knowledge of preclinical and clinical study rules/regulations.
• Thorough knowledge of other regulations pertaining to the commercialization of medicinal product.
• Thorough/Working knowledge of EMA.
• Thorough understanding of drug development process and EU drug regulations is required.
• Preparation and review of CMC sections (IN PARTICOLAR eu Localised)
• Proven experience with navigating combination product regulatory filings including request for designations.
• Experience interacting with FDA OCP, CDER and CDRH and European Medicines Agency/Pharma Competent Authority
• Experience reviewing validation protocols for laboratory equipment, process equipment, and process validation.
• Excellent written and verbal communications skills (Mandatory Italian and English)
• Highly motivated and results-oriented leader.
• Project-management skills and experience.
• Ability to be flexible with changing priorities.
• Knowledge of GCP, cGMP, and Quality System Requirement and EU and/or International product approval process.
• Regulatory Compliance competency (Inspections, Audits, Field Actions)
• International Regulatory competency
• Clinical Trial experience
• Proficiency in PHARMA compliance

 

Location

The position is based in Mirandola, MO, Italy

 

Job Offer

Permanent Contract

 

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