Dear Sir/ Madam

I have more than 18 years of work experience in the pharmaceutical industry in different
positions. My experiences can be suitably fit for the position you require; I.e I have more than 11
years experience in managerial position, from which 5 years as plant and General manager, 4
years as production manager in pharmaceutical manufacturing sector requiring discipline,
maturity, knowledge, and high level of documentation. Besides I have the following core
competencies;
Educational background
MBA in industrial management
degree of business administration
The degree of bachelor of pharmacy
diploma in general mechanics
Work experiences
ØProven leadership skills (managing more than 200 employees); as plant manager
supervising and coaching production, QA-QC, finance, human resource, supply and
engineering departments.
ØProven knowledge and experience in ISO 9001:2015 implementation (working as task
force member and leader) and Kaizen philosophy.
ØProven skills in marketing strategy formulation, market analysis, and sales.
ØProven knowledge in product life cycle management (enhanced quality by design, life
cycle approach to process and cleaning validation)
Experience in coaching and training (conducting more than 50 structured training
sessions).
ØKnowledge in product registration and dossier preparation (registering of 26 products in
2 years, preparing 41 product registeration product dossier).
ØKnowledge in Quality By Design and applied statistics.
ØProven skills in strategy formulation and execution.
ØProven knowledge and experience in drug formulation and introduction of different
dosage forms (oral solid, oral liquid, small volume parenterals, large volume parenterals,
oral liquid, ophthalmic, ointment and creams).
ØOptimum knowledge in financial statement interpretation, resource mobilization and
cost management packages.
ØAdequate knowledge in organizational structure and staffing plan design.
ØIn-depth knowledge and experience in system level document preparation (quality
manual, SMF, validation and qualification protocols, standard operating procedures,
related forms etc).
ØIn-depth knowledge in current good manufacturing practice, good storage and
distribution practice.
ØKnowledge in productivity measurement and improvement packages.
I am highly enthusiastic to work, unleash and hence utilize my experience to the progress and
great achievement of your company.

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 Career Details
Experience Working Period
No Employer From To Position Major Responsibilities

1 Adigrat hospital 6 months October March Junior Responsible for advising on the selection and
2005G.C 2005 G.C pharmacist correct use of drugs, ensuring that drugs are
dispensed and administered safely, providing
advice on drug therapy and its effects,
assisting in improving patient care through
drug therapy and promoting the rational use of
medicines.
2 Addis 11 months March 2006 April Production Under the supervision of the section head,
pharmaceutical G.C 2007 G.C pharmacist coordinates and controls production activities.
factory Sc. Co Implements production plan/targets according
3 Faws 8 months April 2007 Decembe Production to cGMP. Supervises employees engage in
pharmaceutical G.C r2007G.C pharmacist manufacturing process and dispenses batches
factory PLC according to BMRs.
4 Ethiopian 3 years December May production Manage all aspects of
pharmaceuticals 2007G.C 2010 G.C pharmacist; Formulation/Manufacturing area, utilising
manufacturing section people, equipment and materials to meet or
sh.co head; exceed the production plan as efficiently as
research possible, with minimal wastage of resources.
and Organisation of daily tasks for Formulation
developmen team, run meetings and allocate work.
t senior Supervise and train Formulation staff .
pharmacist. Supervise and develop staff to create a
cohesive and highly skilled team through
effective training, mentoring, coaching,
performance management and
communication.
Monitor and inspire excellent performance of
personnel and record and report on Key
Performance Indicators.
Ensure that all products are manufactured in
accordance with GMP, company policies &
procedures, OHS and SOP's.
5 Addis 8 years April 31, Production Plans, organizes and manages all drug
pharmaceuticals 2018G.C and plant manufacturing activities in terms of quality
factory PLC, IV May 26, manager standards (cGMP), Cost & Manpower
solution 2010 G.C utilization for a successful achievement of
company objectives by coordinating other
supporting functions.
Guides instruct and manage Technical aspects
of overall production activities
Direct collaboration with planning &
warehouse, Production, QA/QC, MED, HR,
finance and supply division reports to General
Manager.
As a key member of the operations
management team he will co-ordinate
manufacturing activities interacting with
multi-disciplinary teams and leads a diverse

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 work force.
responsible for creating and evaluating the
product Quality Review in adequate periods.
6 CN Makris and Co 1 year and May 16, August General overseeing daily business activities, improving
plc medicine and 3 months 2018 G.C 2019 G.C manager overall business functions, training heads of
medical device departments, managing budgets, developing
importer strategic plans, creating policies, and
communicating business goals.
7 Humanwell 2 years November Novembe Technical Plans, organizes and manages all drug
pharmaceutical 01, 2019 r 30, manager manufacturing activities in terms of quality
Ethiopia plc 2021 standards (cGMP), Cost & Manpower
utilization for a successful achievement of
company objectives by coordinating other
supporting functions.
Guides, instruct and manage Technical aspects
of overall production activities
Direct collaboration with planning &
warehouse, Production, QA/QC, MED, HR,
finance and supply division reports to General
Manager.
As a key member of the operations
management team co-ordinate manufacturing
activities interacting with multi-disciplinary
teams and leads a diverse work force.
responsible for creating and evaluating the
product Quality Review in adequate periods.
8 Sansheng current December Till now R&D Plans, organizes and manages all drug
pharmaceutical plc 1,2021 Manager development, technology transfer,& product
registration activities in terms of quality
standards (cGMP), and cost for a successful
achievement of company objectives by
coordinating employees in the department.