KINETIC BUSINESS SOLUTIONS (KBS) JOBS Latest Jobs

HealthcareWorldNigeria
RC:4907 Login Registration English | French | Dutch

HWN....browse for free, get verified to super communicate!
HWN....No.1 E-platform for Healthcare professionals and the public!
HWN....uniting and empowering healthcare professionals and the entire populace
..in a unique and systematic manner, through networking, couching and funding!
HWN....empowering healthcare professionals and the entire populace!
HWN....enlightening the general populace on health issues!

HWN Blogs

View All Blogs

Job Catagory

+add Job

job - KINETIC BUSINESS SOLUTIONS (KBS) JOBS back to all Jobs

KINETIC BUSINESS SOLUTIONS (KBS) JOBS

Kinetic Business Solutions (KBS) was founded in 2012 and has enjoyed dramatic growth, becoming one of the leading recruiters to the pharmaceutical, medical device, healthcare, FMCG and consumer industries. Our business approach is to constantly strengthen our service delivery to achieve quality results.

Kinetic Business Solutions (KBS) on behalf of its client, is currently recruiting to fill the following position:

Position: Regulatory Professional

Location: Nigeria

Job Type: Direct

Hours: Full Time

Travel: No

Relocation: No

Job Description:

A top tier Multi National Pharmaceutical company and Global leader are now looking to hire a Regulatory Professional to be based in Nigeria, and report directly to the Regulatory Lead for SubSaharan Africa.

The Regulatory Professional will support submissions, approvals and maintenance of Marketing Authorization Application (MAA) for projects in Nigeria.

Other responsibilities will include:

Participate in project meetings with appropriate members of the EMEA Regulatory Affairs team.

with the EMEA Regulatory Leader provide both strategic and tactical regulatory support to Projects.

Act as primary point of contact with regulatory health authority and/or company appointed legal trade representative.

Assist with timely MAA availability, ensure that all document components are in place on time, identify and track critical path activities

regulatory support throughout the registration process and the life-cycle of the product, including support to the company Distributor to ensure the timely follow up of approval applications. As well as acting as liaison between the Distributor and Internal Teams

Lead the transfer of Market Authorisation Holder Transfers in a timely and effective manner

Ensure appropriate and timely responses and follow-up to Health Authority comments and/or questions received.

Develop and ensure effective implementation of national regulatory strategies and tactics in support of the global development and life-cycle management plans.

Provide input for the PI based on an understanding of the implications of the regional regulatory strategy for labelling; Manages artwork; Ensure labelling * compliance in the region and document it in the appropriate system.

Ensure appropriate electronic archiving of all communications from or to the Regulatory Agencies

Maintain planned and actual regulatory submission dates (including dossier submissions and Regulatory Agency responses) in the appropriate systems (eg SPS, MPD/PKB)

Contribute to standardisation/new systems and processes to ensure efficiency gains and to support continuity

Contribute to compliance with all regulatory requirements (e.g. timely submission of dossiers, post-marketing commitments, renewals, timely implementation of new national and international legislation, timely implementation and training of SOP’s & supporting systems).

Develop a deep understanding of the regional regulatory environment, competitor intelligence and disease area.

Act as the designated quality assurance pharmacist and provide, inter alia, effective management of product complaints, recalls, compliance (including artwork).

Qualifications/Requirements:

University Degree - Medical or Paramedical (Pharmacy, Biology, Veterinary etc.), or equivalent by experience 6-8 years related experience in pharmaceutical industry in Sub Saharan Africa, particularly in the Nigerian environment

Experience in some or all of the following pharmaceutical functions would be an advantage, particularly in Nigerian environment : regulatory, PV and quality.

Experience in managing third parties intermediaries or significant experience in working with third party regulatory intermediaries

Strong knowledge of general regulatory requirements and guidelines

Project teamwork and/or matrix organisation experience

Knowledge of and relationships with the Nigerian regulator

Skills:

Ability to manage multiple tasks, projects, priorities,and complex systems simultaneouslybility to work in a matrix organization and participate effectively both independently and as part of multiple teams

Project management skills

Strong Interpersonal and communication skills, supervisory skills, and presentation skills are a must

Fluency in English. Knowledge of French is highly preferred

Ability to work under strict timelines, combined with flexibility when emergency situations require this.

Knowledge of company standardised computer software

Ability for decision making, working under pressure, and exercising good judgment on special situations.

Capacity to be aware, abstract, analyze, calculate, catalogue, classify, compare, coordinate, copy, detect, diagnose, edit, estimate, evaluate, influence, inspect, instruct, interpret, read, measure, negotiate, observe, plan, group, organize, supervise, synthesise, and select.

Method of Application:

All potential job applicants should copy link attached below and paste on a browser to Apply:

https://www.linkedin.com/jobs2/view/141705318?refId=2728797341465208281679&trk=vsrp_jobs_res_name&trkInfo=VSRPsearchId%3A2728797341465208281679%2CVSRPtargetId%3A141705318%2CVSRPcmpt%3Aprimary

Application Deadline: Not Specified [Apply Speedily].

HWN.......a division of Tripple World Africa Network!

: 2016-06-30 | : 2472