Regulatory Affairs Algeria & EFA
Share
Job Location:
Monthly Salary:
Posted on:
2 days ago
Vacancies:
1 Vacancy
Job Summary
JOB DESCRIPTION:
About Abbott
Abbott is a global healthcare leader who is creating breakthrough science to improve peoples health. We always look towards the future anticipating medical science and technology changes. We are dedicated to expanding access to our trusted medicines in some of the worlds fastest-growing countries. Our extensive portfolio includes high-quality differentiated branded generic medicines that cover various therapeutic areas such as gastroenterology womens health cardiometabolic health pain management/central nervous system disorders and respiratory diseases.
Working at Abbott
At Abbott you can do work that matters grow and learn care for yourself and your family be your true self and live a whole life. You will have access to:
- Career development with an international company where you can grow your dream career.
- A company recognized as a great place to work in dozens of countries worldwide and named one of the most admired companies by Fortune.
- A company recognized as one of the best big companies to work for and the best place for diverse working mothers female executives and scientists.
The Opportunity:
Key Responsibilities
Regulatory Strategy & Business Support
- Define and implement short medium and longterm regulatory strategies aligned with business objectives
- Provide strategic regulatory guidance to internal teams distributors health authorities and industry associations
- Lead product registrations new indications line extensions renewals and variations
- Monitor healthcare policy pricing and reimbursement trends and develop effective response strategies
- Translate regulatory strategy into actionable plans while proactively managing risks and issues
Operational Excellence
- Oversee country Regulatory Affairs teams across the cluster
- Ensure execution of regulatory activities including submissions labeling clinical trial support licenses and postmarketing lifecycle management
- Prepare and deliver regulatory plans that support sales market share and profitability goals
- Manage pricing strategies reference pricing reviews and authority submissions in collaboration with Finance
Market Intelligence & Business Development
- Partner with Business Development and Marketing on product portfolio expansion
- Provide regulatory input across all stages of product development and lifecycle planning
- Track market competitor and marketaccess trends to identify risks and opportunities
- Anticipate regulatory obstacles and develop crossfunctional solutions
People Leadership
- Lead and develop Regulatory Affairs teams in a matrixed multicultural environment
- Drive performance management talent development succession planning and coaching
- Foster a highperformance culture focused on collaboration accountability and growth
Business Partnering & External Engagement
- Build and maintain strong relationships with Ministries of Health payers and key stakeholders
- Act as area label coordinator working closely with QA manufacturing and global teams
- Support value proposition development and partnership initiatives
Compliance & Quality
- Ensure compliance with regulatory quality and corporate SOPs
- Support continuous improvement initiatives and training compliance
- Champion Abbotts values and ethical standards
Key Success Factors
- Strong influencing communication and stakeholdermanagement skills
- Deep understanding of local regulatory and healthcare environments
- Proven ability to translate strategy into execution and results
- Collaborative leadership style with a track record of building highperforming teams
Qualifications & Experience
- Pharmacy degree required
- Minimum 5 years experience in Regulatory Affairs within the pharmaceutical industry
- Experience in multinational or regional roles preferred
- Strong knowledge of regulatory requirements across multiple countries
- Fluent in French and English (Arabic is an advantage)
The base pay for this position is
N/AIn specific locations the pay range may vary from the range posted.
JOB FAMILY:
Regulatory Operations
DIVISION:
EPD Established Pharma
LOCATION:
Algeria > Algiers : Micro-Zone dactivité Hydra
ADDITIONAL LOCATIONS:
WORK SHIFT:
Standard
TRAVEL:
Yes 20 % of the Time
MEDICAL SURVEILLANCE:
No
SIGNIFICANT WORK ACTIVITIES:
Not Applicable
Key Skills
- Proofreading
- Adobe Acrobat
- FDA Regulations
- Manufacturing & Controls
- Biotechnology
- Clinical Trials
- Research & Development
- GLP
- cGMP
- Product Development
- Chemistry
- Writing Skills
About Company
WHO WE ARE CREATING LIFE-CHANGING TECHNOLOGY From removing the regular pain of fingersticks as people manage their diabetes to connecting patients to doctors with real-time information monitoring their hearts, from easing chronic pain and movement disorders to testing half the world’s ... View more
