Wednesday, March 10, 2010

[CNG] Digest Number 1921

Messages In This Digest (10 Messages)

Messages

1a.

Great networking opportunity.

Posted by: "jordanwar" jordanwar@earthlink.net   jordanwar

Tue Mar 9, 2010 6:26 am (PST)




GPSEG Life Sciences Subgroup Meeting
BioStrategy Partners: A Regional Asset for Life Sciences Commercialization and Entrepreneurship

March 18, 2010

Cash Bar/Networking/Dinner:
5:30 - 9:00 p.m.

Held at Crowne Plaza Hotel, King of Prussia

Member & Alliance Partner Cost $40
Nonmember Cost $45

REGISTER NOW!

Ellen Derrico,
Life Sciences Chair

Irwin Darack,
Life Sciences Co-Chair

In 2009 Greater Philadelphia ranked 9th out of 11 regions in the Small Business Vitality Index while exhibiting a weaknesses in Innovation Output measures, trailing the 11-metro average in licenses/options executed, licensing income received, and patents issued (2009 Milken Report).

Our presenter, Dr. Karen J. Hanson, Executive Director of BioStrategy Partners, an anthropologist with twenty- nine years experience in creating and managing new initiatives, will describe a number of programs and partnerships to address the gaps that remain in our ability to support life sciences commercialization and entrepreneurship.

BioStrategy Partners is a non-profit capacity-building organization for idea-stage life sciences technologies and companies with a special focus on technology transfer, scientific founders and first-time entrepreneurs.

Prior to becoming Executive Director, Dr. Hansen created and ran the BioLaunch611+ KIZ (Keystone Innovation Zone) for the organization. She was a senior vice president at the Greater Philadelphia Chamber of Commerce where she developed the organizations economy-building agenda, which include Select Greater Philadelphia and the CEO Council for Growth. Karen holds a Bachelor of Arts degree in Political Science & Chinese Studies from Swarthmore College, a doctorate in Anthropology and a certificate in East Asian Studies from Columbia University.

About GPSEG
GPSEG is a non-profit professional association of senior-level executives committed to the exchange of business contacts and ideas and to the fostering of career fulfillment, business development, and professional and personal growth. The purpose of GPSEG is to provide meaningful senior-level networking contacts to our members; share knowledge, best practices, and resources; educate members on topics of interest to their professional and career development; and develop cooperative programs with other professional organizations in the Greater Philadelphia region.

Website: http://www.gpseg.org



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2.

FW: Senior Project Leader - contract in NYC with To Banking Company

Posted by: "Tom Bley" tombley@hotmail.com   pierres1010

Tue Mar 9, 2010 7:12 am (PST)



Please contact the recruiter directly. Good luck

Best Regards,

Tom Bley

Project / Program Manager

Cell (973) 919-1252

<http://www.linkedin.com/in/thomasbley> btn_myprofile_160x33

From: vetinger@diversant.com [mailto:vetinger@diversant.com]
Sent: Tuesday, March 09, 2010 9:54 AM
To: tombley@hotmail.com
Subject: Senior Project Leader - contract in NYC with To Banking Company

03/09/2010

Greetings,

My name is Vera Etinger and I'm a Recruiter at Info Technologies Inc.
You've received this email because the skills in your resume matched our
search criteria for a Senior Project Leader in our database. It is possible
that you may not be best suited for this particular position, but we have
multiple positions available in all areas and levels of IT where you may be
interested and better suited.

Please respond if you are qualified, available, interested, planning to make
a change, or know of a friend who might have the required qualifications and
interest in working with us as we have an excellent referral program.

Below is the job description to which I am referring for a current job
opening located in NYC, NY

Lead and manage various key programs/projects/initiatives for the business
group; ensure that projects are completed on time, on budget and within
scope. Coordinate technology, business, operation and other
internal/external resources from initiation through implementation. Manage
project-related vendors and contractors to ensure effective and
cost-efficient utilization. Work with the business leadership team to
identify, prioritize and plan the implementation of key strategic projects
critical for the success and growth of the businesses. Actively facilitate
senior management discussions on project progress including project timing,
budget tracking, issue resolution and risk mitigation.

The primary responsibilities include:

-Plan, organize, and implement project activities throughout its lifecycle.
-Provide direction, control and management of projects, including monitoring
the critical path, implementation of appropriate corrective actions and
proper escalation
-Provide overall project communication to stakeholders and management of
stakeholder expectations; including, preparation of presentations for the
various project and business leads.
-Facilitate communication between the business lines, operations, technical
areas
-Prepare various project artifacts such as project plans, status reports,
and business requirements.
-Manage agendas and meeting recaps/minutes to ensure all project tasks and
goals are being accomplished as expected.
-Develop and maintain strong working relationships with key personnel in
each functional area.
-Partner with business team members in the research and resolution of system
and process problems.

Qualifications

-8-12+ years progressive experience in the financial services industry
-Strong program & project planning, organizational and follow up skills
-Strong knowledge of financial services operations, information delivery,
change leadership/management, strategic planning, and project management
life cycle or system development life cycle
-Demonstrated strong collaborative partnership skills with internal and
external teams
-Ability to multi-task and maintain composure
-Excellent communication skills (verbal and written), Problem solving and
Analytical skills
-Computer skills (Microsoft Office: Word, Excel, Project, Visio,
PowerPoint).
-Bachelor's Degree; Masters, PMP or CFA preferred

Please reply with updated resume asap.

NO 3rd party candidates!!!

Thank you.

Sincerely yours,
Vera Etinger
(212) 710-5524
vetinger@diversant.com

If you would like to unsubscribe, please click here
<http://jobs.infotechnologiesinc.com/jobseekers/myjobs/emailmerge_optout.jsp
?d=33315f3132363736393332343739335f3630353630395f3130313837345f315f566572612
b4574696e676572&e=1af&t11=1268146465926> .

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3.

FW: #10-00(210)RR--Sr. Business Analyst--Perm Employee Only--Bergen

Posted by: "Tom Bley" tombley@hotmail.com   pierres1010

Tue Mar 9, 2010 7:15 am (PST)



Please contact the recruiter directly. Good luck.

Best Regards,

Tom Bley

Project / Program Manager

Cell (973) 919-1252

<http://www.linkedin.com/in/thomasbley> btn_myprofile_160x33

From: Tony.Bruno@itstaffinc.com [mailto:Tony.Bruno@itstaffinc.com]
Sent: Monday, March 08, 2010 5:24 PM
To: tombley@hotmail.com
Subject: #10-00(210)RR--Sr. Business Analyst--Perm Employee Only--Bergen
County, NJ

Contact: Tony Bruno - Sr. Staffing Specialist
IT Staffing, Inc. - 201-962-3563 (Direct)

Greetings Job Seeker,

We are a National Staffing Solutions Provider of IT, Mortgage and Financial
based jobs and your resume has been retrieved from one of our Career Job
Boards where you have posted your resume, and some key skills have been
identified that should match our client's Staffing needs.

I would welcome an opportunity to speak with you regarding your personal job
search, availability and location desired and to review if any of your job
needs or locations preferred or desired has changed from your previous needs
listed.

Please review the job specs to verify a match for this particular job.**To
expedite the screening and submittal process to the client, please call me
ASAP, along with emailing your current Word Doc resume to
tony.bruno@itstaffinc.com, so we can discuss your job skills more quickly
and efficiently.

Include your current personal job desires, availability, location and
rate/salary flexibility. Also include your status i.e.- Perm Resident,
Citizen or H1 Visa, in order to match the client's request..

**Please Note that a Criminal Background Check and Drug Screening Test will
be given for Fannie Mae contract jobs, once the offer is extended and the
contract is accepted.No open court cases will be honored..

Location: Bergen County, NJ--NO Telecommuting

Position: #10-00(210)RR--Sr. Business Analyst--Perm Employee Only--Bergen
County, NJ

*NO Visas, NO Third Parties

(Sr. BA) must have Heavy documentation exp. Also some exp working either in
a Hospital or Health Clinic environment.

Sr. Business Analyst needed with Healthcare exp.
Must have exp working either in a Hospital environment or Health Clinic.

Client wants people with exposure to Physician Workflow.
or Patient Medical Records type of technical environments.

Meaning if the B/Analyst worked at a hospital or health clinic...working on
patient medical records applications/projects.

I would appreciate a reply either way, even if you are Not currently
available, so I may note your future job needs.

Best Wishes and Success,

Tony Bruno - Sr. Staffing Specialist
IT Staffing, Inc.
5 Bliss Court, Suite 200
Woodcliff Lake, NJ 07677
201-962-3563 (Direct)
201-608-7100 (Corporate Fax);
<mailto:tony.bruno@itstaffinc.com> tony.bruno@itstaffinc.com
<http://www.itstaffinc.com/> www.itstaffinc.com
National Staffing Solutions for Information Technology

If you would like to unsubscribe, please click here
<http://jobs.itstaffinc.com/jobseekers/myjobs/emailmerge_optout.jsp?d=31335f
3132363736393332343739335f323335313738385f3130303633365f315f546f6e792b427275
6e6f&e=1bd&t11=1268087035706> .

Lookup
<http://jobs.itstaffinc.com/employers/open_candidate.jsp?canid=126769324793&
teamid=0&docids=-1> Candidate

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4.

FW: Business Analyst - Alternative Investments - Position with Major

Posted by: "Tom Bley" tombley@hotmail.com   pierres1010

Tue Mar 9, 2010 7:15 am (PST)



Please contact the recruiter directly. Good luck.

Best Regards,

Tom Bley

Project / Program Manager

Cell (973) 919-1252

<http://www.linkedin.com/in/thomasbley> btn_myprofile_160x33

From: yan@diversant.com [mailto:yan@diversant.com]
Sent: Monday, March 08, 2010 5:32 PM
To: tombley@hotmail.com
Subject: Business Analyst - Alternative Investments - Position with Major
Firm

03/08/2010

Hi! My name is Yan and I'm a Technical Recruiter at Diversant, Inc. a
national leader in the IT Staffing industry.

Our records show that you are an experienced IT professional with experience
as a NY - Business Analyst - Alternative Investments. This experience is
relevant to one of my current openings.

The opening is located in NEW YORK/Charlotte,NC .

Details are as follows:

Looking for a Business Analyst to interview clients, portfolio managers, and
other users and define requirements for alternative investment system.
Prefer candidates with background in Real Estate, Private Equity, or other
Alternative Investments.

Technology & Operations

Advanced

Excel , Caliber, Word, Experience with Investment management and accounting
system for Alternative investment a plus

. The individual performing the role of a Senior Business Analyst will be
required to analyze business and functional requirements provided from the
business. The individual must be able to partner with technology resources
to translate the requirements into technical requirements. The analyst must
have the ability to document functional and operational impacts to
associates and customers.
. Individual must have the ability to assist in the completion and
documentation of designs functional and technical. Must have the ability to
provide expert knowledge on assigned tasks, functionality and
associate/customer processes.
. Implement project management processes and methodologies to help ensure
that projects are delivered on time, within budget, adhere to high quality
standards, meet customer & client expectations, wherever applicable
. Manages project teams for complex business area initiatives, ensuring that
assigned areas are fully represented on corporate strategic projects,
wherever applicable

. The individual performing the role of a Senior Business Analyst will be
required to analyze business and functional requirements provided from the
business. The individual must be able to partner with technology resources
to translate the requirements into technical requirements. The analyst must
have the ability to document functional and operational impacts to
associates and customers.
. Individual must have the ability to assist in the completion and
documentation of designs functional and technical. Must have the ability to
provide expert knowledge on assigned tasks, functionality and
associate/customer processes.
. Implement project management processes and methodologies to help ensure
that projects are delivered on time, within budget, adhere to high quality
standards, meet customer & client expectations, wherever applicable
. Manages project teams for complex business area initiatives, ensuring that
assigned areas are fully represented on corporate strategic projects,
wherever applicable

. Must possess strong analytical skills and communication skills including
the ability to influence at the executive level
. Demonstrate the ability to facilitate meetings and drive a group to
consensus both in person and remotely
. Demonstrate the capacity to adapt to a rapidly changing environment and
shifting priorities as directives may change frequently
. Candidates must demonstrate a combination of business aptitude,
quantitative skills, strategic and creative thinking and distinguished
written and oral communications skills.
. Proficiency with Microsoft Excel, Project, PowerPoint and Word required

7

M-F

40

NONE

None

The following are a plus
1.Accounting background
2.Experience in developing Investment management and accounting systems for
Alternative investments
3.Good Communication skills

If you are qualified, available, interested, planning to make a change, or
know of a **friend who might have the required qualifications and interest,
please call me ASAP at (646) 794-8451, even if we have spoken recently about
a different position. If you do respond via e-mail please include a daytime
phone number so I can reach you. In considering candidates, time is of the
essence, so please respond ASAP.

If you have spoken to a Diversant Recruiter or Sales rep at an earlier time,
please feel free to contact them with the requirement information I am
sending, and they will be happy to assist you.

Thank you.

Best regards,
Yan Dekhtyar
Technical Recruiter
Diversant, Inc.
Tel: (646) 794-8451
yan@diversant.com

Go to www.diversantinc.com and click on Jobs to see all of our current
openings.

Note: Please allow me to reiterate that I chose to contact you either
because your resume had been posted to one of the internet job sites to
which we subscribe, or you had previously submitted your resume to
Diversant, Inc. I assumed that you are either looking for a new employment
opportunity, or you are interested in investigating the current job market.

If you are not currently seeking employment, or if you would prefer I
contact you at some later date, please indicate your date of availability so
that I may honor your request. In any event, I respectfully recommend you
continue to avail yourself to the employment options and job market
information we provide with our e-mail notices.

Thanks again.

**Diversant, Inc. Referral Policy: We will pay $10/day up to $2000 for
candidate referrals that are deployed successfully on an engagement with one
of our clients.

If you would like to unsubscribe, please click here
<http://jobs.infotechnologiesinc.com/jobseekers/myjobs/emailmerge_optout.jsp
?d=33315f3132363736393332343739335f3630343238365f3130333735385f315f59616e2b4
4656b6874796172&e=1ba&t11=1268087502135> .

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5.

FW: current Rx technical openings 310 ac

Posted by: "Ravi Chakravarthy" chakrar@hotmail.com   chakrar

Tue Mar 9, 2010 8:33 am (PST)





_____

From: Windsor Southfield [mailto:wssc82@att.net]
Sent: Saturday, March 06, 2010 12:27 PM
To: Sam Skeegan
Subject: current Rx technical openings 310 ac

Windsor Southfield

Service Co.

6400 Farmington Rd., Suite 105

West Bloomfield, MI 48322

Office: (248) 661-4174

Email: wssc82@att.net

We are executive recruiters nationwide and are recruiting for a number of
positions. Attached is a list of some of the positions currently available.
If you or someone you know is interested, please email, or call MR Tate or
Sam Skeegan.

General Manager.

A worldwide leader in manufacturing and marketing of dental, surgical and

medical devices needs a leader with experience with manufacturing
technologies used in the medical device or pharmaceutical industry. Will
direct the operation of a 500 employee optimized manufacturing facility that
fosters high quality and must have experience in an FDA-regulated industry
(medical device or pharmaceutical). BS degree engineering or business
discipline with 15+ years of progressive and extensive applicable work
experience in manufacturing, quality, or development engineering. MBA
preferred. Must be fluent in Spanish and English. Puerto Rico. $160-200K

Senior Formulations Scientist

Well established manufacturer of biological pharmaceuticals is seeking a
Sr. Formulations Scientist to develop formulations that ensure the stability
of biological molecules. Will study the chemical stability of proteins in
relation to excipient and storage conditions and develop final drug dosage
forms. Will develop and characterize stable parenteral formulations for
preclinical and early clinical studies as well as writing and reviewing
appropriate technical SOPs for use both internal and CMO and/or CROs
Communication. Experience in developing formulations of small molecules for
parenteral administration in both pre-clinical and clinical studies with
good understanding of excipient selection and limitations of use and 5 years
of pharmaceutical industry formulations experience in formulation
development for both liquid and solid dosage forms is required. PhD
Mid-Atlantic $70-90K

Sr. Director Engineering & Facilities

Expanding global pharmaceutical company wants a Sr. Director Engineering &
Facilites to lead all aspects of engineering, utilities, maintenance,
facilities services, construction management, facilities planning and
capital project management at a new manufacturing site. Need minimum of 10
years experience in a biopharmaceutical environment with at least 5 years
in a management role. Experience with cGMP operations in FDA regulated
facility required and experience with managing capital projects valued over
$5 M. Will write and approve Standard Operating Procedures, work closely
with Operations and Quality organizations during design, construction,
start-up commissioning/validation and operation of cGMP manufacturing
facility, write and approve deviation evaluations, CAPAs, and Change
Controls. BS in Engineering required. Masters degree in Engineering or
Business preferred. Licensed Professional Engineer (PE), Certified Facility
Manager (CFM) and/or Project Management Professional Certification (PMP)
preferred. mid-Atlantic $120-160K

Director Quality Assurance

Expanding pharmaceutical company needs 10-12 years of QA or Compliance
experience supporting GMP., GLP, and/or GCP operations in biologics
industry. Will direct the Quality compliance requirements and develop and
implement Quality Systems and infrastructure appropriate for product
development and in compliance with Good Laboratory Practice (GLP), Good
Manufacturing Practice (GMP) and Good Clinical Practice (GCP) regulatory
requirements. Will manage the Quality Assurance (QA) department to
effectively assure quality requirements for the supply and testing of
products from pre-clinical testing through BLA submission and monitor
compliance for the management and conduct of clinical trials. Requires
working knowledge of GMPs, GLPs, GCPs and ICH guidelines and the ability to
lead projects with minimal supervision. .Mid-Atlantic $120-150K

Project Analyst

A rapidly growing, publicly traded, biotech is looking for 3-5 years project
management experience to support complex cross-functional project teams
working on advancing the Company's products through the stages of product
development to licensure and commercialization. Certification in project
management (PMP, CAPM) preferred with a general understanding of the
pharmaceutical/biotechnology industry. Experience with regulatory. Quality,
clinical, non-clinical, process & analytical development or manufacturing is
a distinct advantage. Experience in working with government grants/contracts
and EVM. BS in biological sciences. Mid-Atlantic $50-70.

Senior Manager Regulatory Affairs

Pharmaceutical company wants 5+ years of experience in CMC regulatory
affairs, with experience in biological and vaccine products strongly
preferred. Will be an integral member of the Regulatory team, providing CMC
regulatory strategy development and implementation plans that incorporates
risk identification and contingency planning at a licensed manufacturing
facility. Will act as the main regulatory affairs contact for facility
personnel regarding implications of anticipated changes, such as process
scale up, technology transfer and other manufacturing process improvement
efforts. Will provide support to QA for Regulatory Agency inspections and
participate in communications with FDA or other Regulatory Agencies.
Mid-west.

Director Validation

Expanding biotech validating a new facility would like a minimum of 8
years experience in aseptic pharmaceutical manufacturing, with at least 5
years in a management role. Should also have experience with computerized
system validation and Part 11 compliance. Experience with new facility
commissioning and validation is critical. Will be responsible for
oversight of production, process control, and utility validation activities
in support of product manufacturing for both clinical and commercial
manufacturing operations. Will direct the Validation unit with regard to
ongoing development and implementation of the site Validation Master Plan
and, in conjunction with Quality Assurance, maintain the Validation program
in compliance with regulatory requirements, industry standards and industry
best practices. A working knowledge of SAP and DeltaV is desirable.
Mid-Atlantic $130-160K

SENIOR MANAGER PROCESS DEVELOPMENT

Premier marketer of plant-based health and beauty products seeks a senior
manager of process development to provide a high level of engineering
expertise. Will innovate, plan, and lead major process projects in all areas
of cosmetic manufactureing involving engineering design, development and/or
new processes or modification of existing processes. Will work with R&D
Director level personnel and Manufacturing/Production management to
implement projects, manage pilot manufacturing for on-site and off-site
pilots within the New Product Development Process. Bachelors degree in
Chemical Engineering or related technical discipline and 8+ years process
and supervisory experience in Cosmetic, Pharmaceutical, Food, or Fine
Chemical Manufacturing. Midwest $90-120K

Director Manufacturing Operations

Publicly traded growing biotech wants experience working in a biological
vaccine/therapeutic manufacturing environment in a management capacity.
Requires knowledge of cGMP and CFR requirements and FDA / CBER experience.
Mid-Atlantic $120-165K.

Director Regulatory Affairs

Growing manufacturer wants 8-15 years of experience in the Regulatory
Affairs of biologics to oversee all regulatory activities for the Company's
manufacturing facility. Will manage the Regulatory Affairs department to
effectively support international licensing activities and oversee
implementation of foreign registration requirements. Will plan and execute
key regulatory filings in support of various manufacturing changes to
enhance cGMP compliance, production capacity and product improvement and
serve as regulatory liaison to the FDA and other regulatory authorities for
assigned projects.

BS in a Biological Science. MS/PhD in a science preferred. Midwest
$120-160K

Biostatistician

Biopharmaceutical company is seeking a manager to lead Statistical
Operations for development projects within Clinical Development. Will
provide statistical input into clinical development plans,
protocols, statistical analysis, clinical study reports, summary
documents and clinical parts of Investigational Drug Brochures. BS in
Biostatistics with at least 7-10 years experience within a Pharmaceutical
company/CRO. Mid-Atlantic $80-110K.

Project Manager-Information Technology Projects

Pharmaceutical manufacturer needs 5 years experience managing multiple
technology application development projects using a software development
life cycle. Requires a strong background in using project scheduling tools
such as Microsoft Project and experience in biological or pharmaceutical
industry. PMI Certification desirable. Must possess strong management,
analytical and risk assessment skills, and the ability to manage multiple
projects with users at different sites (US and global) Midwest $60-70K

Director, Project Management

Pharmaceutical/biotech company that has recently gone public and is
introducing new products and building new facilities needs project
management experience for both clinical and process development projects.
Will be responsible for advancing projects through the various stages of
product development from R & D through clinical and licensure. Must direct
the overall process of plannning, scheduling, and managing the project team
from initiation to close out. Must also create, monitor, and update project
timelines, monitor budget and resource expenditures, track action items,
plan and document meetings, assist in the preparation of presentations, and
organize project documentation. Will also prepare project status reports and
utilize standardized project management tools. Additionally, these positions
will facilitate communication among all project-related parties including
Regulatory Affairs, QA, Clinical Development, Process Development,
Non-Clinical Research, Finance, Business Development, and the Scientific
Team Leaders. 2-4 years of professional experience in a biopharmaceutical
setting and experience with commercial biologics product development is a
plus. PMP, CAPM, or equivalent preferred. Experience working with government
contracts and/or biologics a plus. Ph.D/MS -Mid-Atlantic $120-150K

Engineering Supervisor

Pharmaceutical manufacturer wants 5 years experience in the pharmaceutical
industry or related technical field and 2-3 years of supervisory experience.
Will provide leadership in production/engineering issues, work with manager
to establish and manage department budget, goals, and staffing plans, assist
manager in determining and managing department priorities, lead engineering
teams to the successful completion of project goals and maintain and enhance
cross-functional relationships. Must ensure compliance with Good
Manufacturing Practice and Regulatory requirements. Associate's degree or
Bachelor's Degree in Engineering or technical field and experience with GMP
Manufacturing is preferred. Midwest $60-70K

Scientist -Assay Development

Will provide direction of Manufacturing Assay Development Unit staff in
collaboration with process engineers, pharmaceutical chemists to design and
conduct of scientific studies necessary to meet specific research project
goals. Constructs project timelines, identifies technical or resource
issues, and takes remedial action to prevent delays. Prepare reports,
proposals, patent application, publications, IND and NDA reports; Maintain
regulatory compliance and knowledge of safety, environmental and GMP issues;
Lead technology transfer projects from development sites, and to QC
laboratories for validation; Lead Troubleshooting and problem-solving
investigations; Resolves technical issues and drives the completion of
investigations that affect the technical scope; Provides input to the
development of internal systems and SOPs to ensure studies are carried out
in compliance with current regulations. Masters with 5-10 years, or PhD
with 2-5 years of pharmaceutical laboratory experience. .mid-west $70-90K

Immunologist

Product Development department of a major vaccine manufacturer seeks a
Ph.D. in Microbiology, Immunology, Biochemistry, or related discipline and 5
years of relevant experience (preferably industry). Wide knowledge and
experience with immunological assays including direct binding ELISA,
inhibition ELISA, capture ELISA, antibody neutralization assays, and other
cell- based immunoassays is required. Will design and develop novel and
critical serological assays, will oversee assay execution by subcontractors
performing assays, qualification and validation of serological assays- will
conduct analysis of data related to biodefense projects as well as
commercial vaccine projects, analysis of animal study data, design of animal
studies to evaluate vaccine candidates, review and approval of assay results
and study reports, assistance in the preparation of regulatory documents
(IND and FDA reports). Experience with ELISpot, immunoblots and cell culture
for cell-based assays is desired. In addition, general vaccine development
experience from R&D through licensure is desirable. Mid-Atlantic

Biochemical Engineer

The Technical Transfer & Manufacturing Support Division of a specialty
biologicals manufacturer is looking for 3-5 years of experience with a
broad knowledge of principles, practices and procedures of
biochemical/chemical engineering to apply them to the completion of
technical assignments related to manufacturing. BS Engineering . Midwest
$70-90K

Principal Scientist, In-Vivo Testing

Growing biotech wants experience in pre-clinical development of biological
products, particularly design and execution of animal studies, to support
non-clinical development of vaccines and immunotherapeutics. Will be
responsible for the design and implementation of non-clinical studies to
meet regulatory requirements for biologics and blood products and ensure
success of projects through interaction with scientists and CROs. Will
also participate in the evaluation of and response to Government RFPs, RFIs,
and RFAs in support of new and existing products. Must have strong
familiarity with GLP and requirements for demonstration of efficacy using
the FDA "Animal Rule". Ph.D. in Microbiology, Immunology, Biochemistry,
with 3+ years of post-doctoral training with 2+ years of directly related
experience. Mid-Atlantic $70-90K

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6a.

Telecommunications Billing Analysts - Cherry Hill NJ

Posted by: "bill_silberman" bsilberman@stsv.com   bill_silberman

Tue Mar 9, 2010 9:08 am (PST)



We have several openings for analysts with strong telecom experience with billing orders. Will be doing extensive data mapping / data entry. Any experience / knowledge with Amdocs, Kenon, ASR's, LSR's, CLEC is a strong plus. Will do data mapping of new phone orders. Consulting assignment will last 6-12 months.

Bill Silberman
Recruiting Executive
STS Consulting
620 Cranbury Road, Suite 202
East Brunswick, NJ 08816
www.stsv.com
bsilberman@stsv.com
Tel: (732) 257-9033 x 16

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6b.

Telecommunications Billing Analysts - Cherry Hill NJ

Posted by: "bill_silberman" bsilberman@stsv.com   bill_silberman

Tue Mar 9, 2010 9:14 am (PST)



Project Manager of Data Migration
Lead IBM resources for SAP Data Migration and act as Company Liason for client
transition.
- Significant Data Migration Leadership.
- Experience. SAP experience desirable.
- Pharmaceutical Validation and Sox
- Excellent communication, negotiation and leadership skills.
- Some international travel may be required.

Bill Silberman
Recruiting Executive
STS Consulting
620 Cranbury Road, Suite 202
East Brunswick, NJ 08816
www.stsv.com
bsilberman@stsv.com
Tel: (732) 257-9033 x 16

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7a.

Pharmaceutical Project Manager - Princeton NJ

Posted by: "bill_silberman" bsilberman@stsv.com   bill_silberman

Tue Mar 9, 2010 9:24 am (PST)



Project Manager of Data Migration
Lead IBM resources for SAP Data Migration and act as Company Liason for client
transition.
- Significant Data Migration Leadership.
- Experience. SAP experience desirable.
- Pharmaceutical Validation and Sox
- Excellent communication, negotiation and leadership skills.
- Some international travel may be required.

Bill Silberman
Recruiting Executive
STS Consulting
620 Cranbury Road, Suite 202
East Brunswick, NJ 08816
www.stsv.com
bsilberman@stsv.com
Tel: (732) 257-9033 x 16

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7b.

Pharmaceutical Project Manager - Princeton NJ

Posted by: "bill_silberman" bsilberman@stsv.com   bill_silberman

Tue Mar 9, 2010 12:39 pm (PST)



Project Manager of Data Migration
Lead IBM resources for SAP Data Migration and act as Company Liason for client transition.
- Significant Data Migration Leadership.
- Experience. SAP experience desirable.
- Pharmaceutical Validation and Sox
- Excellent communication, negotiation and leadership skills.
- Some international travel may be required.

Bill Silberman
Recruiting Executive
STS Consulting
620 Cranbury Road, Suite 202
East Brunswick, NJ 08816
www.stsv.com
bsilberman@stsv.com
Tel: (732) 257-9033 x 16

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8a.

Systems Engineer - SW Implementations - Energy - Reston/Richmond, VA

Posted by: "Gary Wright - Wright Associates" gary_wright@verizon.net   wrightassociates

Tue Mar 9, 2010 1:14 pm (PST)



Please feel free to refer this position to people you know who may be a good
fit. Referrals appreciated.

Still Looking for Suitable Candidates - 03-09-2010

Position Title - WRASSE012010

Systems Engineer - SW Implementations - Energy - Reston/Richmond, VA Area -
Up to $100K+ DOE

Local Candidates Only (VA) - No relocation - Sponsorship Possible for
Perfect Fit

$100K+ DOE + Bonus + Comprehensive Benefits

Company

Software Vendor - mid-sized, very successful, profitable, and fast growing
division of a $500m public company. Firm is the leader in providing energy
and utility companies worldwide with analytics-based software solutions that
unlocks the power of energy information.

Join a growing and successful firm that combines the excitement and energy
of a start-up with the stability of a mid-sized public company. Be part of a
team oriented, collaborative, dynamic, yet relaxed environment, and make a
difference. Great Company - Lots of Upside and growth possibilities.

Reports Into the Product Engineering organization.

Position Responsibilities - Summary:

My client is seeking a talented Systems Engineer to join their Professional
Services team. They looking for someone who takes great pride in delivering
high-quality system implementations to satisfied customers - and who really
knows their stuff.

As an experienced Systems Engineer you will play a lead role in the
technical implementation of sophisticated n-tier software products. You
will work collaboratively with a team of project managers, business
analysts, software developers and other systems engineers on system
installation, integration and configuration activities.

Detailed Responsibilities:

· Integrating applications with client enterprise systems
(developing input and output interfaces)

· Working with customers to establish system architecture to support
the applications

· Sizing databases and hardware to meet product performance

· Preparing technical specifications of product customizations and
features

· Delivering custom reports and other features

· Configuring systems to meet requirements

· Providing system support and troubleshooting

Required Technical Skills and Competencies:

· 3-5 years experience - Experience must be directly relevant to
systems engineering/software implementations.

· Strong development experience in PL/SQL, ASP.NET, VB.NET required.

· Solid experience with: Oracle 8i/9i/10g, SQL Server, SQL
performance tuning, Windows 2000/2003, & IIS.

· Familiarity with EAI environments and middleware products: e.g.
WebMethods, Tibco, MQ Series, Biz Talk

· Strong preference is given towards those with TIBCO integration
experience

· Experience working for a Software Vendor, Consulting Firm, or
Professional Services Organization

Pluses:

· Experience in C#, XML, & UNIX a plus

· Utility/Energy industry experience

Other Skills/Requirements;

· Strong analytical skills

· Strong communication skills and experience/comfort working in a
customer-facing environment

· Travel is required - Estimate of 30-40% Domestic Travel (Typically
1-2 days & 1 week on occasion)

· Bachelor's degree in Computer Science

Contact Information

Gary Wright - President - Wright Associates

Phone - (508) 761-6354

Email - replywrightassociates@verizon.net - WEB Site -
www.wrightassociates.org
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