medtech quality professional course · harry wong is also an asq certified quality engineer and...
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50% funded under the HRDF Industry Certification (INDCERT) Scheme
MEDTECH QUALITY PROFESSIONAL COURSE
Course Outline• ISO13485:2016 Quality Management System• ISO13485 Internal Audit• 21 CFR Part 820 and QSIT• EN ISO14971 Risk Management• Failure Mode Effects Analysis• Process Validation• Sterilization• NCR / CAPA / Complaint Handling• Design Control / Quality Function Deployment• Medical Device Classification, Labelling, EUMDR and CE Marking• Acceptance Sampling Methods• Statistical Process Control• Medical Device Single Audit Programme (MDSAP)• MDA Regulations
Target ParticipantsThis training aims to train quality assurance professionals.
Medtech Quality Professional Course
FRANK RIEDDirector, Ried Q&C Consulting
Frank Ried is a German national living and working for more than 20 years inMalaysia. He holds a Mechanical Engineering Degree (Dipl. Ing.) fromUniversity of Kassel/Hessen (Germany). Frank is a Quality Engineer andQuality Auditor certified by EOQ (European Organisation of Quality),respectively by DGQ (Deutsche Gesellschaft fuer Qualitaet). He is alsotrained as Lead Auditor for ISO 9001, ISO 13485 and USFDA 21 CFR Part 820requirements and has vast experience auditing and setting up compliancesystems in these areas.
Frank has over 30 years of professional work experience in the MedicalDevice manufacturing, pharmaceutical, personal protection and condomindustry. He worked in two companies (B. Braun and Ansell) and in variousdepartments during this time. End of 2016 Frank left Ansell to concentratemore on his own company Ried Q&C Consulting Sdn. Bhd. Frank is nowconsulting in the compliance area of ISO 9001, ISO 13485 and QSR (FDA) -by conducting training course as well as internal audits (incl. Mock-FDAInspections) and supplier audits.
CHOO BENG BOONQA Manager, Mira Medsource
Beng Boon, Choo possesses Bachelor of Science degree fromCampbell University, N. Carolina, USA and MBA from NorthernUniversity of Malaysia. He has more than twenty five years of workingexperience with wide knowledge and experience in QualityOperations especially in Medical Devices industries.
He also acquire good teaching skills and has been lecturing part-timefor more than 12 years in private colleges and universities in TQM,Operations Management, Strategic Management and BusinessStatistic. He is currently the QA Manager in Mira Medsource (M) SdnBhd an Owens & Minor Company.
GOBU DEVARAJANAssociate Director, QA/RA,APAC Quality AssuranceMedical Global Business Unit, Ansell Melaka.
Mr Gobu possesses Master Degree in Electrical and ElectronicEngineering and Certified Manager of Quality/OrganizationalExcellence (CMQ/OE, Certified Quality Auditor (CQA) fromAmerican Society of Quality (ASQ). Certified Six Sigma Green Belt.He has more than twenty five years of working experience withextensive knowledge in the field of Quality Engineering, StatisticalAnalysis and Quality System Requirements.
He possesses excellent communication and presentation skills. He iscapable of designing, conducting training programs and performgap analysis according to QSR (21 CFR Part 820), ISO 13485, ISO9001, ISO 16949 and ISO 14971. MDD 93/42/EEC, CMDCAS andJPAL.
He was Quality Technical Manager at Teleflex Medical beforeassuming his current position at Ansell.
Harry Wong has over 18 years’ of professional work experience in
Quality Assurance of medical device, Ceramic Former and Metal
Stamping for Electrical, Electronics and Automotive industries. He
currently holds the position of Senior Manager, Global Complaint and
Risk Management, Global Quality Assurance in one of the global leaders
in protection solutions.
As the subject matter expert of risk management, he provides advice,
direction and training for Risk Management personnel across global sites
and facilities; ensuring their risk management process complies with all
necessary regulatory standards including QSR (FDA), MDD and ISO
requirements. He is responsible for developing the global harmonized
risk management SOP and tools which are implemented in the global
organization facilities and sites.
Harry Wong is also an ASQ Certified Quality Engineer and Lead Auditor
for ISO 9001 and ISO 13485 and has extensive involvement in mock
audits for global sites preparing for CCC, ANVISA, SEI and FDA.
HARRY WONG HON MENGSenior Manager, Complaint and Risk Management,Global QA at Ansell
Lim is a Certified Six Sigma Master Black Belt. He has a Bachelor ofScience in mechanical Engineering and a Master in BusinessAdministration. He has over 20 years of working experience in Process,Quality System and Business Process Improvement in variety ofindustries including medical device industry. He has worked with and atsenior management level to improve process efficiency, implementeffective Lean manufacturing systems and improve profitability. He hascoached and consulted for Motorola University’s clients which haveembarked on the Lean Six Sigma Business Improvement Campaign.
In addition to consulting, he has trained Six Sigma and Lean Green andBlack Belts candidates in Australia, New Zealand, People Republic ofChina, India, Malaysia, Singapore, Indonesia and Thailand. He is currentlyalso serving as advisor to senior leadership for companies in variety ofindustries, some of which are multinationals (MNC) and medical devicemanufacturing company.
L.K. LIMDirector, NexMU
Course Exam & Certificate
AMMI Medtech Examination Committee
Company Committee Members Position
Abbott Ms Kek Soo Ling Director, Quality
Ambu Ms Koh Seok Ling Sr QA/RA Manager
Ansell Mr Khor Siek Meng Sr Director, QA
Ansell Ms Seow Lan Hoon RA Director, EMEA/ APAC
Haemonetics Ms Gan Poh Siew Director, QA/RA, APAC
Course Exam
Certificate of Competency
Certificate of Attendance
Passing Mark: 60/100
Less than or 59/100
Training Venue
Address: Plaza WCOE, 41A, Jalan Cassia Selatan 3/3, Batu Kawan Industrial Park, 14110 Bandar Cassia, Penang
The selected employee should have at least 80% training attendance to
complete the course.
AttendanceCommitment
Company shall pay back 100% of the training course fee to AMMI
if the selected employee’s attendance is less than 80%.
<80%
>80%
Penalty
Attendance commitment letter from the AMMI member companies and trainees
Agreement betweenCompany & AMMI
Attendance Commitment
Terms and Conditions
Eligibility • All HRDF registered employers (AMMI members and non-members) are eligible to participate under the INDCERT scheme.
• Each employer can only train a maximum of 25 employees for the approved courses under INDCERT scheme.
Employee • Each employee is only entitled to attend one approved course under the INDCERT scheme.
ReplacementReplacement of trainee before the training • Replacement of trainees is allowed with 5 working days
notification before the training commences.
WithdrawalWithdrawal or replacement of trainee after the training commences • Replacement of trainees is not allowed if the trainees withdraw
after the training commences.
Timeline and Registration Process Flow
1) Pre-registration for Medtech Courses • Submit registration via AMMI Medtech website• https://ammi.com.my/medtech-2020/
2) Confirmation of registration• Successful registration will receive a confirmation from
AMMI.
4) Successful Application• Upon approval by HRDF, successful application will receive
a notification from HRDF.
5) Submission of Commitment Letter• Company shall submit signed Letter of Commitment to
AMMI before commencement of training.
3) Online Application via HRDF portal • Upon receiving the required documents from AMMI,
company can submit the application via HRDF portal (www.hrdf.com.my).
Registration Process:
Process Flow
www.ammi.com.my
Association of Malaysian Medical Industries (AMMI) Tel : +6010 4040 662Fax : +603 2178 4347
Email : [email protected]
Contact: Ms Heng Ee Ling : 010 4040 662Ms Melissa Khoo : 016 4224 818Mr CS Ching : 012 4766 558