s*c
2 楼
有没有人对flow cytometry的工作有兴趣， BD在san jose有几个opening。一年
contract。虽然是合同工，但想进工业界的话，也许是个机会。PHD也行。会流式基本
操作就好，不一定要三年经验。
直接联系这个猎头， 9198876786 ext. 4135. [email protected]
/* */。 她挺靠
谱的，本人拿到过offer，但一些原因去不了。
Position Details:
Job Title: System Verification Specialist
Duration: 12 Months
Location: San Jose CA 95131
Job Description
· Participates in system verification testing for complex medical
diagnostic products and systems. The systems generally include a combination
of hardware, reagents and software components and can be part of an upgrade
or option to an existing system.
· Applies acquired job skills and company policies and procedures
to complete assigned tasks under supervision of the system verification lead
and system verification manager.
· Works on assignments that can be routine in nature and applies
judgment or decision making in agreement with the Supervisor or Team Lead.
· Normally follows established procedures on routine work, requires
instructions only on new assignments.
· Recognizes discrepancies in subsystem and system level results
during the execution of test protocols. Exercises judgment within generally-
defined practices and policies in selecting methods and techniques for
obtaining solutions.
· Understands individual impact to company work processes and
deliverables.
Duties and responsibilities
· Contributes to the system verification sub team as a member.
· Writes the test protocols and procedures and may participate in
the review and approval process for the protocols and procedures.
· Is involved in executing, analyzing and interpreting the results
of system verification studies; conducts basic data analysis using
statistical tools.
· Writes timely, detailed and accurate technical reports and
provides verbal feedback to program and project teams on product performance
, features and specifications.
· Enters defects, product incident reports or request for change
when they arise and manages the regression testing to improve the quality of
Client’s products.
· Clearly documents own work in a format useable and understandable
by others.
· Assists in preparing information for design documentation and
design reviews. Participates in technical and design reviews.
· Creates and maintains study binders of test execution notes,
protocols, addenda, deviations, amendments, statistical analysis, memos to
file, final reports, technical presentations and electronic media.
· Follows Quality Systems Regulations and ISO guidelines for design
control.
· Participates in developing and maintaining laboratory
infrastructure in the system verification labs, including laboratory quality
policy, QA and QC procedures, procedure manuals and daily record keeping
systems.
· Promotes a safe work environment. May provide recommendations on
maintaining the safety of the work environment. Participates in
Environmental Health and Safety programs. Addresses corrective actions
whenever a hazard is identified. Notifies supervisor of all observed
hazardous conditions or unsafe work practices.
· Updates personal training file continually and participates in
training assignments.
· Keeps abreast of the basic requirements for compliance in own
area of work and complies with those requirements. Participates as required
in training on regulatory issues affecting own area of work. Brings
regulatory compliance questions/issues to the attention of management.
Knowledge and skills
· Knowledge of immunology, hematology and/or clinical chemistry in
the clinical, research and pharmaceutical environment.
· Strong lab skills, with ability to perform detail-oriented work
with a high degree of accuracy.
· Basic hands on knowledge of flow cytometry, including instrument
platforms and software and assay applications.
· Ability to communicate technical ideas clearly, including
effective oral and written communication skills.
· Effective multi-tasking capabilities.
· Proficient with MS Word, MS Excel, MS PowerPoint, and MS
SharePoint.
· Knowledge of basic engineering principles, troubleshooting,
statistics and study design, including effective analytical and problem
solving skills.
· Demonstrated ability to keep neat, accurate and complete records
and logs.
· Understanding of basic statistic terms and concepts.
· Familiar with general GMP / GLP procedures with a strong focus on
quality.
Education and experience
· Typically requires a BS or MS degree in Immunology, Cell Biology,
and Biomedical Engineering or in a related scientific discipline.
· Requires a minimum of 3 years operational experience in flow
cytometry or analytical systems of similar complexity.
· In addition requires a minimum of 1 year experience in a GMP or
GLP environment with QSR (FDA) experience a plus.
contract。虽然是合同工，但想进工业界的话，也许是个机会。PHD也行。会流式基本
操作就好，不一定要三年经验。
直接联系这个猎头， 9198876786 ext. 4135. [email protected]
/* */。 她挺靠
谱的，本人拿到过offer，但一些原因去不了。
Position Details:
Job Title: System Verification Specialist
Duration: 12 Months
Location: San Jose CA 95131
Job Description
· Participates in system verification testing for complex medical
diagnostic products and systems. The systems generally include a combination
of hardware, reagents and software components and can be part of an upgrade
or option to an existing system.
· Applies acquired job skills and company policies and procedures
to complete assigned tasks under supervision of the system verification lead
and system verification manager.
· Works on assignments that can be routine in nature and applies
judgment or decision making in agreement with the Supervisor or Team Lead.
· Normally follows established procedures on routine work, requires
instructions only on new assignments.
· Recognizes discrepancies in subsystem and system level results
during the execution of test protocols. Exercises judgment within generally-
defined practices and policies in selecting methods and techniques for
obtaining solutions.
· Understands individual impact to company work processes and
deliverables.
Duties and responsibilities
· Contributes to the system verification sub team as a member.
· Writes the test protocols and procedures and may participate in
the review and approval process for the protocols and procedures.
· Is involved in executing, analyzing and interpreting the results
of system verification studies; conducts basic data analysis using
statistical tools.
· Writes timely, detailed and accurate technical reports and
provides verbal feedback to program and project teams on product performance
, features and specifications.
· Enters defects, product incident reports or request for change
when they arise and manages the regression testing to improve the quality of
Client’s products.
· Clearly documents own work in a format useable and understandable
by others.
· Assists in preparing information for design documentation and
design reviews. Participates in technical and design reviews.
· Creates and maintains study binders of test execution notes,
protocols, addenda, deviations, amendments, statistical analysis, memos to
file, final reports, technical presentations and electronic media.
· Follows Quality Systems Regulations and ISO guidelines for design
control.
· Participates in developing and maintaining laboratory
infrastructure in the system verification labs, including laboratory quality
policy, QA and QC procedures, procedure manuals and daily record keeping
systems.
· Promotes a safe work environment. May provide recommendations on
maintaining the safety of the work environment. Participates in
Environmental Health and Safety programs. Addresses corrective actions
whenever a hazard is identified. Notifies supervisor of all observed
hazardous conditions or unsafe work practices.
· Updates personal training file continually and participates in
training assignments.
· Keeps abreast of the basic requirements for compliance in own
area of work and complies with those requirements. Participates as required
in training on regulatory issues affecting own area of work. Brings
regulatory compliance questions/issues to the attention of management.
Knowledge and skills
· Knowledge of immunology, hematology and/or clinical chemistry in
the clinical, research and pharmaceutical environment.
· Strong lab skills, with ability to perform detail-oriented work
with a high degree of accuracy.
· Basic hands on knowledge of flow cytometry, including instrument
platforms and software and assay applications.
· Ability to communicate technical ideas clearly, including
effective oral and written communication skills.
· Effective multi-tasking capabilities.
· Proficient with MS Word, MS Excel, MS PowerPoint, and MS
SharePoint.
· Knowledge of basic engineering principles, troubleshooting,
statistics and study design, including effective analytical and problem
solving skills.
· Demonstrated ability to keep neat, accurate and complete records
and logs.
· Understanding of basic statistic terms and concepts.
· Familiar with general GMP / GLP procedures with a strong focus on
quality.
Education and experience
· Typically requires a BS or MS degree in Immunology, Cell Biology,
and Biomedical Engineering or in a related scientific discipline.
· Requires a minimum of 3 years operational experience in flow
cytometry or analytical systems of similar complexity.
· In addition requires a minimum of 1 year experience in a GMP or
GLP environment with QSR (FDA) experience a plus.
m*a
3 楼
信用卡把
g*e
4 楼
昨天刚去过。最新规定只收信用卡，cashier's check和money order，不收个人支票和
现金。
现金。
u*n
5 楼
国内的信用卡（双币卡）可以么？还是一定需要美国的？
【在 g***e 的大作中提到】
: 昨天刚去过。最新规定只收信用卡，cashier's check和money order，不收个人支票和
: 现金。
【在 g***e 的大作中提到】
: 昨天刚去过。最新规定只收信用卡，cashier's check和money order，不收个人支票和
: 现金。
c*2
6 楼
中领馆的网页上英文版的说可以用信用卡，中文版的没说。效率？
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