1. 林智聰 Lam Chi Chung (Brian) - Curriculum Vitae
Date of birth: 15th November 1990 Marital Status: Single
Address: Flat 1, 1st Floor, Block K, Beverly Hill, 6 Broadwood Road, Happy Valley, HK
Tel: +85267523686 Email: brianlam88@gmail.com
Career Objective
QA officer with a proven track record of quick delivery, making key decisions, prioritising and have
demonstrated great teamwork ability in order to improve quality management systems dynamically in
pharmaceutical industries.
Working Experience
Feb 2014 – May 2015: Bristol Laboratories, Luton, United Kingdom - Quality Assurance
Officer
Working under QA manager and a group of QA members in the implementation of quality systems at
the site. Key responsibility includes:
 Sampling and testing of incoming packaging materials, testing and release of packing
materials via SAP and LIMS (Laboratory information management system)
 Approve the artwork in co-ordination with Quality Control Department,Packaging
Department and Production.
 Artwork and shade cards control, making sure that all the materials are within MHRA
specifications
 To review and control MBR for each batch product and fill in necessary documents for the
bulk products to packaging.
 Controlled drug issuance
 Filing, archiving and control of all documents.
 Ensure all operations in Production / QC / WAREHOUSE are performed in accordance with
the relevant cGMP guidelines
 To approve all master documents BMR, PBR,Specifications, SOP, Validation Protocols and
reports
 To accompany External audit personnel during inspections and prepare corrective action plan
in conjunction with Production / QC / WAREHOUSE and ensure implementation of
corrective actions
 Drafting and executing process validation protocols and report
 Drafting, editing and reviewing Standard Operating Procedures (SOP)
 Reconciliation for batch release
 To register all customer complaint and co-ordinate investigation activities with QC /
Production and to prepare final report.
 Ensuring environmental monitoring is in place and they are conducted on a regular basis.
 To prepare schedule and perform internal audits to ensure GMP compliance. Corrective
Action Plan to be put in place for the observation and shall be filed.
 To co-ordinate all validation activities associated with production and QC i.e. process,
equipment, utility, analytical method

2. July – Aug 2011: Watsons Ltd., Hong Kong - Pharmacy Clerkship
Working under a qualified pharmacist in the store - duties including:
 Developed strong interpersonal and communication skills by helping different customers in
the store. Giving helpful advices to customers.
 Gained a better understanding of different brands of Paracetamoland anti-histamines in terms
of their indication and which one should be used under different situations, produced an excel
table to compare the ingredients
Education
2012 -2013: University ofBradford, United Kingdom, MSc Pharmaceutical Technology - Merit
70%Taught 30%Research
 Gained experience in the production/process methods of pharmaceutical products in industry
(spray drying, hot melt extrusion and coating)
 Learnt the new concept of Quality by Design (QbD) and Process Analytical Technology
(PAT) through researching papers and giving out presentations
 Acquired basic analytical skills (Raman, TGA, DMA,DSC, PXRD, IR and SEM)
 Obtained skills for analysis for molecular mechanics simulation, geometry optimisation,
compartment modelling through Material Studio and J Sim software
 Gained skills and experience in coating pharmaceutical products during dissertation, produced
pellets and also tested them (e.g. during the coating process the parameters needs to keep on
changing as the pellets will get wet or its static force,so to counteract these issues, I will need
to reduce the pump rate as well as increasing the flow rate,or increasing the pump rate)
2009 -2012: University ofManchester, United Kingdom, BSc Pharmaceutical Science - 2nd Class
2nd Honour
2005 - 2009: Oundle School, Peterborough, United Kingdom - GCSE and A levels
Personal Qualities
 Fast learner
 Positive Attitude
 Good interpersonal and team skills
 Good communication skills
 Able to multitask
Technical Skills
 Proficient in Microsoft Word, Excel, Power Point
 SAP and Caliber LIMS (Laboratory information management system)
 Good report writing skills
 Good time management and organisation skills