Quality/Assurance/Control specialist
Resume:
AFEEZ ADENIYI MAKINDE
(AIMNM)
PROFILE
OBJECTIVE
As a Professional Microbiologist with close to 10 years of work experience my objective is to contribute my quota to the growth and development of any organization I found myself and the entire world as a whole.
SKILLS
Quality Department Skill: Good Laboratory Practice, c GMP, Validation, Good Documentation Practice, packaging material, Staining, Environmental Monitoring, Bioburden Test, Disinfectant efficacy Test, Finger Dab test, Chemical assay, Water analysis, Antimicrobial/Preservative Effectiveness Test, Slide Presentation skills, Aseptic technique, Skilled multi-tasker and result oriented, Packaging material analysis, Data trend analysis, Sensitivity test and sterility test.
Computer Knowledge: Very good Excel and Microsoft Word User
CONTACT
PHONE:
+234**-********, +234**********
Address:
12 Felicia Sipe Street, Alagbole Akute, Lagos.
WEBSITE:
LinkedIn: https://www.linkedin.com/in/makinde-afeez-749413a5/
EMAIL:
***********************@*****.***
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HOBBIES
1.Reading.
2.Networking
3.Brainstorming.
4.Slide presentation.
ASSOCIATION
AIMN Member
AIMN: Association of Industrial Microbiologist Nigeria
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EDUCATION
Olabisi Onabanjo University, Ago Iwoye, Ogun State.
2003 - 2007
[Second Class Honor)
Owu Community Comprehensive High School Elere Adubi, Ogun State
1994/95 – 2001
Phebean Nursery and Primary School, Ojota Lagos
84/85-1992/93
WORK EXPERIENCE
Company Name: Chris-Ejik Pharmaceuticals & Health Care Products Ltd,
Position Held: Microbiologist/Quality Analyst
NOV 14TH 2017–Till Date
Job Description:
Preparation of Standard Operating Procedure, Log and Worksheet etc.
Sampling and analysis of raw materials including water {(Both microbial and Chemical analysis e.g. Identification test, Sulphated Ash, L.O.D, Assay}, packaging materials (Primary and Secondary), intermediate and finished products based on c-GMP, GLP, Good analytical method with reference to B.P or U.S.P in other to ensure safe and high quality products output.
Supervision of laboratory assistants in other to ensure that tests are conducted in compliance with approved practices and procedures.
Conducting of Sensitivity test on raw material and finished product.
Carrying out Compressed Air Integrity test for production machines in other to microbially know the air quality.
Conducting of environmental monitoring of factory premises (including Laminar flow, Dispensing and Sampling Booth) as to ensure air quality is microbially safe for production and also to control the level of microorganisms.
Carrying of Finger dab/Glove print test on personnel in the production section so as to improve high personnel hygienic standard in other to prevent contamination of product during production.
Conducting of Disinfectant efficacy test on different disinfectant used in the factory to know the safest and effective concentration (MIC) to be used.
Carrying of Gelatine hydrolytic test [GHT] on the empty hard gelatine capsule shell to ensure and ascertained the quality if collagen base.
Carrying out of Growth Promotion Test on Media use for microbial enumeration test so as to validate the
media that it would yield a quality result when use for analysis.
Carrying out of an Antimicrobial/Preservative effectiveness test [AET].
Handling of reference test organism viable [both in slant or stock culture] for GHT, AET, used for media growth promotion test, MLT validation and AET.
In House training of staffs/Training of staff especially junior ones on basic personal hygiene.
Ensuring all work properly done and Documented.
Calibrating and monitoring performance of instruments for efficiency and effectiveness.
Trending of analytical report data’s, interpreting the results and making of a strong befitting conclusive suggestion to aid improve quality of product and plant process.
Conducting of swab test on packaging materials, machines used for production to ensure its safe for production.
Carrying out of cleaner’s supervision, development of a more effective cleaning method alongside with a well design cleaning log for a proper documentation for the cleaners all to ensure the factory is clean and safe for production
Chemiron International Ltd
Position Held: Acting Quality Manager/Microbiologist
Plot 12 Block B, Metal Box Road, Ogba – Ikeja, Lagos State Job Description:
2014–Nov, 13th 2017
Manage quality department team.
Release/reject of product.
Ensured that all request for quality where made on time and judiciously utilised.
Setting up of c-GMP team.
Training of staffs towards achieving quality in the overall production based system.
Ensured company targets is met I accordance to regulatory bodies rules and regulation
Carried out Sampling and analysis of raw materials, intermediate and finished products (chemical and microbial analysis).
Carried out Research and Development of new product, market feasibility studies i.e price survey, and working on improving of quality of the product compared to other products in the market.
Organization of workflow, ensuring staffs been handled understand their duties or delegated task.
Carried out Environmental monitoring of the production premises in other to have a safe and controlled environment for factory use and production.
Carried out water sampling and analysis in other to ensure water quality is satisfied for production.
Conducted cleaner’s supervision and developed effective cleaning method and cleaning logs for the cleaners all to ensure the factory is clean and safe for production.
Conducted preservative effectiveness test on the preservatives used in the production.
Carried out Finger Dab test on the personnel in contact with production in other to avoid contamination of product during production process.
Conducted Monitoring and documentation of ongoing production process in other to check and make
corrections if any irregularities occur during production process that might lead to product non-conformity.
Consistency approval/ reject (in-case of non-conformity) of raw material, packaging material and finished product meeting up with time.
Conducted analytical report data’s, interpreting the results and inducing from it a strong befitting conclusive suggestion to aid improve quality of product and plant process.
Spare headed and worked in R&D department
Also engaged in market feasibility studies part which is part of a new product development.
Nostrum Pharmaceuticals Ltd (A subsidiary of Nestor Pharmaceutical UK Limited).
Position Held: QA Officer (In-Process check)/QC Microbiologist
OCT 2010 to 2014
Job Description
Carried out Sensitivity Test on raw and finished products.
Carried out Microbial Limit Test on raw material, intermediate and finished product.
Carried out water sampling and analysis [microbial and chemical]
Carried out Handling of reference test strains(organism).
Carried out Swab Sampling and Test on machines.
Carried out Environmental Monitoring test.
Carried out Finger Dab Test on production personnel
Others:
Carried out In-process check during production process.
Carried out Chemical test/identification test on material.
Raising of cleaning log record and cleaning supervision
Federal Institute of Industrial Research Oshodi (FIIRO).
Position Held: Industrial Attachment/Internship
2005 to 2006
Department: Enzymology laboratory [under the supervision of Doctor A.K Lawal}
TRAINING/WORKSHOP (CERTIFICATION)
Organizer: Association of Industrial Microbiologist of Nigeria
1. Title: Laboratory Quality Management System (ISO.17025:2017)
Date: Sept 17th, 2019.
2. Title:The Roles of Microbiologists In Research and
Development for Effective Organization Performance.
Date: Nov 5th 2018.
3. Title: Industrial Effluent Treatment Options.
Date: Nov 5th 2015
4. Title: Validation of Microbiological Method
Date: Oct 22nd 2014.
5. Title: Quality Risk Management in Food, Beverage, Brewery
and Pharmaceuticals
Date: Oct 18th, 2013.
Organizer: West African Postgraduate College of
Pharmacists
[Faculty of Drug Production and Quality Assurance)
6. Title: Audit in the Pharmaceutical Manufacturing Industry.
Date: Nov 13 and14th 2018.
.
IN-HOUSE TRAINING(CERTIFICATION)
Organizer: Nostrum Pharmaceuticals Ltd (A subsidiary of
Nestor Pharmaceutical UK Limited).(No.7-9)
7. Title: cGMP on Basic GMP Principles, Handling of
Deviation and Quality Risk Management.
Date: March 6th – 8th 2013
8. Title: cGMP on Good Documentation Practice.
Date: Feb 27th, 2012.
9. Title: Training on cGMP
Date: Jan 4th, 2012
REFEREES
ROTIMI JACOB
QUALITY ASSURANCE MANAGER
FAMA ORGANICS LIMITED
Email: **********@*******.***
Phone: +234**********
GRACE OMISORE
QUALITY ASSURANCE MANAGER
CHEMO-PHARMALABORATORIES LIMITED
Email: ********@*****.***
Phone: +234**********
Contact this candidate