Alan Lin
** **** **, *****: 647-***-****
Scarborough, Ontario M1S2K3 E-mail: ***********@*****.***
PROFILE
Over 10 years consulting experiences in management of scope, schedule, budget and quality of e ngineering
projects related to GMP process equipment, piping, and controls.
Responsible for preparation and presentation of project status reports; piping & instrumentation diagrams(PID)
and other related drawings and documents; management of the design review, site acceptance, and installation
of equipment.
Familiar with management of project plans, budgets, and schedules.
Familiar with QA/Validation department relative duty of by preparation of design documents.
Familiar with relative policies and regulations of clean and safe working environment.
Good communication ability by enforcing compliance with local government and supervising section
regulations.
Good ability of supervision and coordination of different disciplines engineers (Design, Process, HVAC,
Mechanical, Electrical, Fire Safety, Water Supply and Drainage, Automation) and construction contractors.
Thorough knowledge of GMP and sanitary equipment design requirements; Substantial design understanding of
pharmaceutical GMP clean workshop, clean room and function equipment; advanced knowledge of engineering
documentation required for GMP process equipment.
Strong written and oral communication skills; strong computer and programming skills, proficient in
AUTOCAD, TARCH, PIDCAD, WORD and EXCEL.
Self-motivated and dependable, good team player; solid leadership and project management skills.
EDUCATION
B. Eng., Biochemical Engineering, Shanghai Jiao Tong University, China
REGISTRATION & PROFESSIONAL ASSOCIATIONS
Member of the International Society for Pharmaceutical Engineering (ISPE), 2013
Certified Bidding Evaluation Expert of Chongqing Development and Reform Commission, 2011
Certified Senior Engineer of Pharmaceutical Eng., SINOPHARM, 2004
PROFESSIONAL EXPERIENCE
SINOPHARM (China National Pharmaceutical Group Corporation)
Jun. 1991– Mar. 2013
Chongqing Pharmaceutical Industry Design Institute
Engineering Project Manager / Pharmaceutical Senior Engineer / Engineer
Worked at various roles, typical responsibilities include:
As a Engineering Project Manager
Creates and manages (initiate, plan, execute, control, close) proj ect plans based on project goals as stated in
the technical proposal and input from business development; coordinates assembly of project team; creates and
directs functional project sub-teams as needed; delegates project tasks appropriately among project team
members.
Responsible for initiating, defining, planning, schedu ling, and budgeting of assigned programs, also for meeting
the goals and objectives of the program within the approved budget and time schedule; management of
resources related for facilitating project execution.
Serves as the primary contact with client on project matters, interacts with client to advise and develop the
goals, scope and direction of current and future project activities; keeps client informed of project status,
timelines, milestones and any other crucial information that may affect the succ essful outcome of the project,
serves as the primary representative to lead technical project discussions during on -site and off-site meetings
with clients.
Leads the project team, motivates team members, plays a principal role in supervising and promoting team
members to accomplish assigned project tasks internally, prepares the internal project team for client
interactions, leads meetings between internal and client project teams, develops deep and broad relationships
within internal different disciplines resources to ensure success of the project with consideration of time and
budget schedules.
Participates in the development of agreements and contract terms related to project requireme nts, partners and
negotiates with clients to drive programs to milestones ; responsible for ensuring the project as executed adheres
to the terms of the project contract, translates contract terms to project execution; assists proprietors as
appropriate to advance project to obtaining production license.
As a Pharmaceutical Senior Engineer / Engineer
Responsible for scheme design of pharmaceutical GMP clean workshop, chemical process design, and
preliminary design & construction documents design in close cooperation with other disciplines and clients for
projects of pharmaceutical engineering, Chinese traditional medicine extraction, biotech engineering,
fermentation engineering and so on.
Responsible for compiling project feasibility study reports for the proprietors’ decision.
Responsible for proposing improvement suggestions for proprietors to solve the problems existing in
reconstructing projects, and redesigning new process flow which can meet the related standards and
requirements and is rational and easy for operation, so as to raise production efficiency.
REPRESENTATIVE PROJECTS
Chengdu Huashen Hi-Tech Industrial Park Pharmaceutical Plant Engineering, Chengdu, China, 2013
Chongqing Porton Fine Chemicals Ltd. Multi-Purpose API Workshop Project, Joint Design with Jacobs
Engineering Singapore Pte Ltd, Chongqing, China, 2012
Jiangzhong Pharmaceutical Co., Ltd. R & D Center Project, Nanchang, China, 2010
Yunnan Baiyao Group Co., Ltd. New Industrial Base Construction Project, Kunming, China, 2009
Guilin Tianhe Pharmaceutical Co., Ltd. Relocation and Expansion Project, Guilin, China, 2007
Jiangxi Guoyao Pharmaceutical Co., Ltd. Relocation Project, Nanchang, China, 2004
IHG Taiji Pharmaceutical (Macau) Limited Natural Medicine Industrial Park Project, Macau, China, 2003
Sichuan Pearl Pharmaceutical Plant GMP Reconstruction Project, Sichuan, China, 2002
Mudanjiang Lingtai Pharmaceutical Group Co., Ltd. Reconstruction Project, Mudanjiang, China, 2000
Qinghai Sanpu Pharmaceutical Plant GMP Reconstruction and Expansion Project, Xining, China, 1999