Associate Director Regulatory Affairs at Johnson & Johnson
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- Company: Johnson & Johnson
- Location: Ghana
- State: Accra
- Job type: Full-Time
- Job category: Healthcare Jobs in Ghana
As one of the world’s largest healthcare companies, we are driven to foster better health for more
people in more places. While the world has made significant progress in providing improved
healthcare, major gaps remain, and bolder, smarter approaches are needed to overcome the drastic
inequity in access to care—now.
Through a dedicated global public health (GPH) organization that
combines research and development, global access strategies and programs, and local operations, we
are putting the world’s most vulnerable and underserved at the heart of everything we do—measuring
our success in lives improved.
As a team of innovators, we are committed to pioneering and sustainably
delivering meaningful and transformational products. Working with global and local partners, we will
ensure equitable access to these critical solutions that save lives, cure patients, and prevent disease
for those most in need. Upholding the rich heritage of Johnson & Johnson, we are taking on the
toughest challenges, and, ultimately, we hope to do our part to close the gap of inequity and pave the
way to a healthier future for the world’s most vulnerable and underserved populations.
Janssen/ GPH regulatory
Position Summary & Responsibilities
We are looking for an exceptional Associate Director Regulatory Affairs EMEA GPH Liaison (Vaccine
Programs) to support the JnJ Global Public Health Organization (GPH) who will drive the regulatory
strategy and execution plans for the GPH vaccines portfolio, including our COVID-19 and Ebola Vaccine
programs, across Africa. This role should prioritise and optimize the regulatory strategy to register
vaccines in Africa, identify policy issues to shape the Regulatory Affairs landscape in Africa and
effectively interact with relevant external stakeholders like the African Vaccines Regulatory Forum
(AVAREF), WHO AFRO and National Regulatory Authorities. The person will be responsible for working
with internal Global Regulatory Affairs (GRA) members and other functions at regional level and
working with LOC RA teams and LTRs in the in-scope markets to ensure timely submission and
regulatory compliance. May have indirect reports in markets
The Associate Director Regulatory Affairs EMEA GPH Liaison (Vaccine Programs) is a member of the
Global Regulatory Affairs organization. The position resides in the EMEA EM region and is responsible
for working with the local regulatory affairs teams, Global Regulatory Team and other teams (e.g.
Strategic Implementation Leader) to define, align and implement the regional regulatory strategy for
GPH Markets for assigned products. The position is accountable for leading and providing strategic
regional and local input into the global regulatory strategy (which includes identifying regional and
local regulatory requirements for efficient product registration, lifecycle management activities and
clinical trials within the region). Support to regional or local tender applications as appropriate.
This role will work closely and under the guidance with the WHO liaison (GRL) to discuss regional
regulatory affairs matters with the WHO Headquarters as appropriate. This position will be a full
member of the appropriate Access Strategy and Implementation team and a full member of the
regional launch team. It will liaise with the Head of Regulatory Affairs EM/ GPH and the WHO liaison
(GRL), and inter alia, with the LOCs and GRTs to develop and facilitate an efficient regulatory strategy
to achieve prompt submissions and earliest approvals for Janssen GPH products. The position is
responsible for the consolidation of the regional strategy and prioritisation of countries aligned with
The position will ensure regional and local affiliates (LOCs/ LTRs) are supplied with timely responses
to Health Authority enquiries; as well as regulatory support to GPH Africa Operations team. Position
will ensure adequate preparation for health authority meetings and may attend and provide
presentations to health authorities, if appropriate.
The Associate Director Regulatory Affairs EMEA GPH Liaison (Vaccine Programs) develops the
regulatory strategy for the in-scope GPH markets in Africa, aligning this with the overall GPH Access
Strategy and Implementation whilst liaising with regional Therapeutic Area (TA teams within GRA for
the respective programs as / if needed, hence will be required to participate as team members in the
various cross functional project teams within the global/ Africa GPH operations as the Regulatory
Affairs representative and also in GRA regional TA meetings.
Special focus on vaccine programs
• The Regulatory Affairs Liaison for GPH will support GPH vaccines portfolio and be responsible
o Providing internal engagement teams with vaccine specific regulatory support from
discovery to delivery for said portfolio as per direction of regional and global teams.
o Advising and working closely with the local engagement teams to align on efficient
and innovative regulatory strategies to facilitate and expedite vaccine development
and optimize the probability of success for regulatory approval at the originator and
destination countries and WHO Prequalification (PQ) for the markets in scope under
the guidance of the GRL WHO Liaison.
o Providing local team with support on strategy, tactics, and external resources (CROs,
consultants) as needed to facilitate timely clinical trial authorizations and vaccine
registrations as and if required.
o Advising local engagement teams on optimal strategies and tactics for in support of
GRL WHO liaison for timely WHO PQ and pathways for Low- and Middle-Income
Countries (LMIC) registration in EMEA region (focus Africa).
o Contribute to development of strategies for leveraging global health regulatory
systems initiatives aimed at facilitating registration and access in LMIC in EMEA region
(e.g. the WHO Collaborative Registration Procedure and regional regulatory
o Determine scope and nature of regulatory technical contribution to local engagement
teams, presentations to internal and external customers, leadership briefings, etc.
o Recommend regulatory strategic pathway for emergency and long-term filing to
ensure equitable access for Covid -19 vaccine across Africa with special focus on SSA.
o Work according to internal quality requirements and in line with established GRA
teams especially partnering with the WHO liaison.
•This role is responsible for high quality interactions and clear and consistent communications
with grantees and partners in the field, for example AVAREF and WHOAFRO.
Strategic and tactical input in development, post-approval and Life cycle management for
GPH Portfolio in Africa
- Work with the RA EM/GPH Head, WHO Liaison, GRL, relevant TA team, Access Strategy and
- Implementation Team, regional launch team and LOCs to develop the regulatory strategy for
EMEA GPH markets ensuring alignment with the overall global and regional GPH strategies.
- Advise the Project Team, EMEA lead and/or Regional Therapeutic Area Leader on applicable
regulatory issues, project-specific regulatory issues, and issues related to regional regulatory
- Drive understanding of regional guidance and national regulatory requirements, ensure
country specific requirements changes are adequately captured in relevant databases (e.g.
- CMC & RIACS)
- Develop and ensure effective implementation of regional and national regulatory strategy
and tactics in support of the global development and life-cycle management plan ensuring
utmost regulatory compliance.
- Develop a deep understanding of the regional regulatory environment, competitor
intelligence and therapeutic area
- Provide input to the Africa regulatory policy team to shape the regulatory environment in
- Develop and maintain the understanding of the external stakeholders and environment to
provide access to vaccines in the region
- Provide input for developing and updating the Target label(s) based on an understanding of
the implications of regional regulatory strategy for labelling
- Where appropriate ensure implementation of scientific advice / Regulatory Agency
comments into development and life-cycle management plan (e.g. WHO discussions,
regional EM HA discussions)
- Liaison with GPH teams to ensure GPH strategic business needs, and resource requirements
are understood, to aid building business in new markets in a complaint manner
Liaison with Regulatory Agencies and Local Operating Companies
- Work through LOC and/or CRO for National Regulatory Agencies contacts, as appropriate
- Ensure appropriate involvement and liaise with LOC regulatory affairs personnel to facilitate
local Regulatory Agency meetings
- Determine timing and strategy for Regulatory Agency meetings and scientific advice
- Liaise with LOC & RSI to ensure briefing books and documents available and aligned to
regional strategy and timelines
- Ensure that issues raised by Regulatory Agencies are promptly and adequately addressed
- Provide support for negotiations with Regulatory Agencies with respect to labelling, or other
activities, requiring global / regional alignment.
Input in document and process development
- Advise team on required documents and processes to support Regulatory Agency contacts
- Plan and develop briefing documents for meetings with Regulatory Agencies, including
determining content and review of documents
- Provide input to and review submission documents to ensure that they are fit for purpose
and support labelling statements as appropriate
- Define and facilitate the generation of appropriate data-driven (regional/local) responses to
- Regulatory Agency questions, enable LOC submission thereof.
Clinical Trial Applications (CTA)
- As needed, provide intel to ensure protocols are developed in alignment with regional
registration strategies to support registration, reimbursement and competitive labelling
- As needed, advise team on required documents and submission strategies in preparation of
- As needed, ensure CTA submission packages are complete and available according to agreed
Marketing Authorization Application (MAA)
- Provide regulatory support throughout registration process
- Provide regulatory support throughout life-cycle management and make sure this is done in
a complaint manner.
- Oversee RSI implementation of country-specific submission requirements are made available
to the LOCs according to the strategic implementation plan
Education and experience
- University degree – medical or paramedical (pharmacy, biology, veterinary etc.)
- At least 10 + years of experience in Regulatory Affairs of which at least 5+ years in Africa.
- Specific experience in vaccines and in working with Public Health stakeholders such as WHO, AVAREF is highly desirable.
- Experience with vaccine development, registration, and regulatory life-cycle management and tender business, ideally with experience in LMICs. Some experience with vaccines is key.
- Knowledge of major industrialized country regulatory processes and considerations, FDA, EMA, and WHO PQ. Experience with other developed and developing nations (e.g. national regulatory authorities in the EU, Canada, Australia, India, China, and South Africa) is a plus
- Experience in working in project teams and/or a matrix organization
- Experience in shaping regulatory environment via policy &/or trade associations is an advantage
Leadership & Culture
- We are guided by our Credo at the centre of everything we do. We believe that working with our leadership imperatives Connect, Shape and Grow is crucial for our success.
- Technical excellence, common appreciation of the problem at hand, humility, negotiation skills, listening, bottom up approach to collaboration, cultural sensitivity, firmness
- Able to navigate in a VUCA (volatility, uncertainty, complexity and ambiguity) environment.
- Can deal with highly complex situations; recommendations are made only after extensive research and consultation with others
- Demonstrated ability to lead people and teams to effectively achieve clear, yet complex goals and objectives.
- Strong experience in working effectively with senior decision makers as it pertains to strategy development and operations.
- Experience developing and handling strong partnerships and relationships both inside and outside the organization, handling conflicts, and building consensus.
- Ability to lead and influence data-driven strategy planning and implementation.
- Effective collaborator and experience working in a matrix environment (i.e., ability to influence without formal authority).
- Adept at project management; including critical path thinking, detail orientation, setting priorities, and planning.
- Broad knowledge of global health issues, vaccine development processes and regulatory requirements and procedures; at both global and national levels is helpful.
- High level of cultural competence
- Excellent knowledge of English
- Knowledge of the applicable therapeutic area
- In depth knowledge of the regulatory environment, guidelines and practice in Africa/ LMIC/Emerging Markets
Internal & External Contacts:
- Internally with GRA teams and Cross functional leadership/ project teams in the GPH space
- Externally with Heads and leadership of National Regulatory Agencies, WHO Advocacy Groups and Directors, Donor groups Directors, Pharma industry senior leadership, African Union agencies Director/Commissioner levels, etc.
Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.
Method of ApplicationSubmit your CV and Application on Company Website : Click Here
Closing Date : 22 Feb. 2021