Thursday, September 22, 2011

[CNG] Digest Number 2409[1 Attachment]

Messages In This Digest (9 Messages)

Messages

1.

JOB: Government Reporting Analyst - Wayne, NJ (Job & Career Network

Posted by: "Eric Nilsson" ericnilsson@earthlink.net   norsemantechnology

Wed Sep 21, 2011 6:55 pm (PDT)




Government Reporting Analyst - Wayne, NJ - (Negotiable Annual Base
Compensation w/full benefits and annual bonus eligibility)

The Government Reporting Analyst will be responsible for the following:

Responsibilities
* Prepare and analyze on a quarterly basis the "Best Price" (BP) to ensure
that our client is compliant with government regulations in determining
Medicaid Rebate Amounts.
* Prepare and analyze on a quarterly basis the "Average Manufacturing Price"
(AMP) to ensure that our client is compliant with government regulations in
determining Medicaid Rebate Amounts.
* Prepare and analyze on a quarterly basis the "Non-Federal Average
Manufacturers Price" (NFAMP) to ensure that our client's government pricing
is compliant with the Veterans Health Care Act.
* Responsible for calculating the "Federal Supply Schedule" (FSS) pricing.
Assist with negotiations in finalizing prices to be submitted to the
Government.
* Responsible for the quarterly calculation of the "Public Health Service"
(PHS) prices.
* Perform all Medicaid Impact amounts as requested by Finance.
* Responsible for obtaining the approvals of all Pharmaceutical and
Biological price change requests and updating the pricing in SAP/CARS.
* Perform as requested all profitability analysis for all State and PHS
contracts.

BEST INDUSTRY - Pharmaceutical
BEST DEPARTMENT - Government

Qualifications
BS or a BA degree is required.
7+ years business experience, preferably in a pharmaceutical contracting or
equivalent background is required.
The chosen candidate will possess an overall understanding of wholesale
activities, marketing management, trade development, pricing and company
operations which are imperative in performing adequately.
Candidates must have experience working with pharmaceutical pricing data and
economic analysis.
Understanding of legal and financial principles due to the strict government
pricing regulations is critical in this position.
The incumbent must have a broad knowledge of managed health care issues,
regulatory and governmental legislation in both federal and state areas.
Knowledge of all aspects of inclusion/exclusion criteria for government
calculations and experience with Federal Contract Law is essential.
The position requires a thorough understanding of financial analysis, legal
terminology, and contract procedures.
Highly developed communication skills are important and sensitivity to
people with varying backgrounds is necessary to maintain contact with all
levels of internal and external customers.
A thorough understanding of computer operations and capabilities is
necessary to direct the implementation and utilization of internal tracking
systems.
CARS IS, SAP, and MicroStrategy skills are essential.
The incumbent must be able to work independently and with no routine
supervision.

Compensation
Negotiable

If interested, please forward a word-formatted softcopy of your resume, as
an attachment to resumes@eConsultAmerica.com

Posted by Ronald Parks, Senior Managing Partner, eConsultAmerica at:

http://www.linkedin.com/groupAnswers?viewQuestionAndAnswers=
<http://www.linkedin.com/groupAnswers?viewQuestionAndAnswers=&discussionID=7
1381110&gid=23209&trk=eml-anet_dig-b_jb-ttl-cn&ut=1aI7bqxV0KPQU1>
&discussionID=71381110&gid=23209&trk=eml-anet_dig-b_jb-ttl-cn&ut=1aI7bqxV0KP
QU1

2a.

FW: Project Manager / NYC

Posted by: "Tom Bley" tombley@hotmail.com   tom.bley

Wed Sep 21, 2011 6:55 pm (PDT)




Please contact the recruiter directly. Good luck.

Best Wishes,

Tom Bley, PMP

Project / Program Manager
Cell (973) 919-1252

Date: Mon, 19 Sep 2011 18:06:38 -0400
From: jhart@bluewolfgroup.com
To: tombley@hotmail.com
Subject: Project Manager
























































Hi Thomas!




My name is Jessica and I'm an IT recruiter at Bluewolf, the nation's leading technology consulting firm and premiere IT resourcing agency. Our position in the industry gives us the ability to match top Media, Finance, and Retail companies with the best and brightest...YOU!

There is immediate need for your expertise! One of our clients has an open position we think you could be great fit for.




JOB TITLE: Project Manager




JOB DESCRIPTION:






Title: Project Manager

Location: NYC

Pay rate: $80-110K

Duration: PERM (US. Citizen, Greencard, EAD)

Start date: ASAP

University degree or college diploma in the field of Computer Science.

3+ years direct work experience in a project management capacity, including all aspects of process development and execution.

Training in Agile/SCRUM SDLC Methodology

Strong familiarity with project management software, such as MS Project, Visio

Familiar with programming languages, including PHP and Java

Database and operating systems experience with mySQL

Can conform to shifting priorities, demands and timelines through analytical and problem-solving capabilities.



Ability to read communication styles of team members and contractors who come from a broad spectrum of disciplines

Persuasive, encouraging, and motivating.

Ability to elicit cooperation from a wide variety of sources, including upper management, clients, and other departments.

Ability to defuse tension among project team, should it arise.

Ability to bring project to successful completion through political sensitivity

Strong written and oral communication skills.

Strong interpersonal skills.



Notes

Must have strong PM Skills

Must be able to scope the job, and then get the job done.

A good balance of Business/Technical Abilities

Knowledgeable within SCRUM and Agile



Please send your resumes to: Jhart@bluewolfgroup.com





Interested? Want to refer a friend? Send an email to jhart@bluewolfgroup.com with an updated resume and your availability.







Thanks!





Jessica Hart

Technical Recruiter, Bluewolf

P: 646.230.0876

220 5th Ave 15th Floor, New York, NY 10001<

jhart@bluewolfgroup.com

bluewolf.com














Bluewolf's Candidate Commitment:


We are contacting you for a real job requirement

We do not conduct fake interviews

We will not ask you for references unless you are being considered for a job

We will give you feedback the moment we get it from our customer

We NEVER subcontract. All of our customers are the end user




















If you would like to unsubscribe, please click here.

3.

E-Commerce, Search Engine Optimization, Web Marketing for Verizon Wi

Posted by: "Jonoronha1990" jonoronha1990@aol.com   onoronha2002

Wed Sep 21, 2011 6:55 pm (PDT)




I received the job spec below from a recruiter. If you fit the spec, please contact her direct and mention my name.

J. Oscar Noronha

Sarah Tonkin
Prestige Staffing | Recruiter
105 W Adams Street, Suite 1410 | Chicago, IL 60603
T: 312.443.6154 | F: 312.345.1941

stonkin@prestigestaffing.com

Buyer Reference











Site



NJ-One Verizon Way-Basking Ridge





Location



NJ-One Verizon Way-Basking Ridge





Work Location





One Verizon Way
Basking Ridge
NJ
USA
07920





Business Unit



2720 - MKT-Internet-Marketing (2720 (HQ - OH))





Labor Type



Technical





Positions Requested



1





Respond by Date



09/26/2011





Travel Time



0.000 %





Hours per Day



8





Hours per Week



40





Total Hours



1040





Estimated Additional Spend



10.000 %





Estimated Expenses



0.000 %





Flat Adjustments



0.00





Description





Senior ECommerce Merchandising Manager
----------------------------------------------------------
Looking for a senior ecommerce merchandiser with demonstrated experience in increasing online sales for retail products. Duties include creating online promotions and managing the online presentation of mobile phone products to maximize sales. Although telecommunications experience can be helpful, it is not required so long as the candidate has strong retail ecommerce experience. Proven production/project management skills, a creative eye, and effective collaboration are essential to successfully drive the execution of marketing campaigns.

Responsibilities also include:
- Working with product managers to place new products and track changes.
- Writing product description pages.
- Writing landing pages.
- Ensure integrity of existing user interfaces by continually reviewing and coming up with solutions for concerns.
- Maintain clear lines of communication with design, usability, IT, and test teams to ensure clear scope and project progress.
- Own webpage lifecycle through requirements gathering, design, development, launch, and success metrics.
- Development of sitemaps, conceptual mockups, and flow diagrams to illustrate requirements.
- Development of Powerpoint documents to report on assigned projects.
- Work with large, geographically dispersed teams.
- Take accountability for resulting performance of assigned projects.
- Perform site audits on a weekly basis to ensure content is up-to-date and accurate.
-Travel twice a quarter to Alpharetta GA site is required.

Required Skills & Experience
- Bachelor's Degree in Marketing, Sales, Technical Writing, Information Technology, or a related field.
- 5+ years of experience in retail ecommerce merchandising with a very firm grasp of website fundamentals, including HTML, CSS, content management, dynamic page generation, personalization, and Web 2.0. (Although coding will not be part of the job, thorough understanding of how the technology works is required.)
- Excellent copywriting skills.
- Fully up-to-date on current ecommerce sales tools and optimization techniques.
- Excellent command of current website optimization techniques, including A/B/n and multivariant testing.
- Able to make timely decisions, anticipate problems and provide creative solution.
- Ability to draw conclusions from sales reports and re-merchandise as appropriate for the business and brand.
- Must be extremely detail oriented and thorough.
- Passion for accuracy.
- Strong organization and time management skills.
- Ability to work well within a team environment and under pressure of deadlines.
- Demonstrated ability to work on multiple projects simultaneously.


A portfolio of websites and examples of written work is required - please ensure candidates have this available and it is submitted within FG.











Primary Skill Requirement







5+ years exp in retail ecommerce merchandising with a very firm grasp of website fundamentals








CM Work Order #







Coordinator Use Only



4.

Friends - Please Vote for ME

Posted by: "Bob Ketterer" bob@bobket.net   bobket

Wed Sep 21, 2011 6:55 pm (PDT)



My Friends,

*http://www.TotalCareerMakeover.org/vote* for me!! Vote another email
too.*Bob Ketterer
* - Please ask your friends to vote too.

*Here's why I need to win a Total Career Makeover!*

In December 2009, during my 10th year and late in my career, my former
employer off-shored my position along with three other mainframe network
systems programmers. The current reduction in force of US employees from my
group has grown to about fifteen, almost half the team. Although I had good
bi-annual reviews, I failed to aggressively network outside of my sphere.
Settling for status quo and �out of loyalty�, I failed to bid on new
opportunities to move into growing corporate areas. Afterwards, applying for
many opportunities based on my extensive institution expertise, I had only
two interviews for positions that were filled internally.

My aggressive search, especially through LinkedIn, in the North-East, finds
at most one opening as mainframe network systems programmer per month.
Weekly, I find one or two somewhat related opportunities. I average about
two hiring manager phone screens/interviews per month.

My plan B is to consult for companies on Internet marketing strategy
planning and social media because I have honed my skills by taking classes.
I had one major assignment so far from 8/2010-3/2011.

Your consideration is appreciated and please connect with me. Check out my
G+ with some new interesting photos.
Thanks for your support,
Bob Ketterer | 845-475-8698 | bobket@gmail.com
G+ http://GPlus.to/bobket | BOBKET.NET, LLC
http://www.linkedin.com/in/bobket
http://www.finbox.com/pub/BobKetterer%20LION/14309
5.

Article: Job Hunting for the Rusty (Net-Temps)

Posted by: "Eric Nilsson" ericnilsson@earthlink.net   norsemantechnology

Wed Sep 21, 2011 6:56 pm (PDT)



Job Hunting for the Rusty

The job market is the most competitive it's been since the early 80's. So
it's no surprise that I've seen an increase in emails from people who
haven't had to think about job hunting in a long time. Times have changed
when it comes to searching for a job, since the Internet has changed the
rules. Here are a few letters:

Dear Joan: What form is generally accepted for sending a resume to a
mid-sized company by e-mail? I think pdf would preserve all my MS Word
formatting and pdf is quite widely used.

Dear Joan: I am beginning a job search after several years and am looking
for guidance as to modern etiquette. First, when asked to email a resume, is
a person supposed to attach a cover letter to a blank email, or put the text
of the cover letter into the body of the email? And also, if sending hard
copies through the mail, is it a good idea to use colored paper? The
thinking years ago was that colored paper made you stand out and also had
some sort of subliminal effect on the reader that made him more likely to
read your resume.

Answer:

See the answer and more here:

http://www.net-temps.com/careerdev/crossroads/index.htm?op=view
<http://www.net-temps.com/careerdev/crossroads/index.htm?op=view&id=4485&new
sletter_id=1005> &id=4485&newsletter_id=1005

6.

Article: How to Read a Job Ad (WSJ)

Posted by: "Eric Nilsson" ericnilsson@earthlink.net   norsemantechnology

Wed Sep 21, 2011 6:56 pm (PDT)




How to Read a Job Ad

By
<http://online.wsj.com/search/term.html?KEYWORDS=DENNIS+NISHI&bylinesearch=t
rue> DENNIS NISHI

Seth Rabinowitz was puzzled by a series of job ads that were sent to him for
review by a client. He's a partner at Silicon Associates, a Tel Aviv,
Israel-based management consulting firm that occasionally helps clients to
fill job openings.

One ad: "Wanted: Sales agents who are able to stare intently into client
eyes while describing what they are looking for."

See what to look for here:

http://online.wsj.com/article/SB10001424053111903927204576577230493495482.ht
ml

7.

IT Manager - Inwood NY  - MFR/Dist Firm

Posted by: "Brian Mecca" Brian.Mecca@yahoo.com   bd_mecca

Wed Sep 21, 2011 7:46 pm (PDT)

[Attachment(s) from Brian Mecca included below]

If you have difficulty viewing this, please click on the link to go to the Yahoo Group or open the attachment 

Please self screen and contact Ralph Clark if interested.

 
For further info call or e-mail –ralph clark –732-446-7227 –rclark@ralphclarkassociates.com

Job Req Form
 
Priority: high                                                                                                                                               
 
Title: IT manger
 
Experience –10+ yrs exp
 
Company Name:   confidential
 
 
Company Description: mfr/dist firm                                                                                                               
 
 
Location:  Inwood NY [near jfk airport]  
 
 
 Perm position  
 
Salary:     100-130k range
 
Shift/Billable hours p-day:
 
Technical Skills Desired:       
 
Technical Skills Desired:
 
Job Description:  10 + yrs exp
with 5 yrs exp with mfr/or dist applications ---would like someone with some
ERP exp [ co is installing epicor ]—small it staff [ 2 ]—50 user's ---some pc
skills ---will also be dealing with several outside vendors [ hosted e-mail ,
epicor etc ]----will report into an outside consultant [ MB ]----
 
 
Interview Times/Process:-asap
 
Start Date: oct 2011
 
 
For further info call or e-mail
–ralph clark –732-446-7227
rclark@ralphclarkassociates.com

Attachment(s) from Brian Mecca

1 of 1 File(s)

8.

Career Hub - Teamwork Works -- In the Workplace and In Your Job Sear

Posted by: "Brian Mecca" Brian.Mecca@yahoo.com   bd_mecca

Thu Sep 22, 2011 7:42 am (PDT)





 If you have trouble reading this, please click on the subject line to go to the Yahoo Group or click the link below.

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"Career Hub" - 1 new article
1. Teamwork Works -- In the Workplace and In Your Job Search
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4. Prior Mailing Archive
Teamwork Works -- In the Workplace and In Your Job Search
We must all hang together or most assuredly we shall hang separately. ~ Benjamin Franklin Today my client and I were going through a PowerPoint presentation on Networking and Job Search. As we came to the slide about 'solo' versus...

 
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9.

FW: Rx positions open ray 811ip

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

Thu Sep 22, 2011 7:57 am (PDT)





-----Original Message-----
From: Windsor Southfield [mailto:wssc82@att.net]
Sent: Wednesday, September 21, 2011 2:07 PM
To: 'Windsor Southfield'
Subject: FW: Rx positions open ray 811ip

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.

Business Analyst

One of the largest Medicare contractors in the country, serving over 20
million customers with Medicare in 20 states seeks a Sr. Business
Development Research Analyst to be responsible for assisting with
development of new business for National Government Services which
complement existing offerings. Support meetings with customers,
consultants, and industry partners in support of market research, with
travel as required. Experience in understanding Federal budget and financial
data regarding Government programs or initiatives is desired. Market
research assignments will support strategic aspects at the market level as
well as detailed research and analysis of specific programs or opportunities
and perform analysis of market segment opportunities, identify and analyze
potential new business opportunities. Acquire and maintain data/information
on market, industry, economic, consumer and competitive conditions and
trends pertaining to identified market segments and related services. 5
years related experience with in-depth knowledge of the Federal Acquisition
Regulations and process based on having worked with customer and
marketing segmentation, customer analysis, competitive analysis,
positioning, etc. Indiana and/or Maryland. $55,000 - $75,000

Clinical Research Manager

Growing biotech wants 8 to 10 years of experience in medical, pharmaceutical
or device/diagnostic industry, with at least 4 years of clinical research
experience to manage the clinical trials/research and data collection
activities for products in development to ensure compliance with SOPs, FDA
regulations, and ICH/GCP guidelines. Will select sites; revise protocol and
CRF; revise procedures, as needed, and develop plan for data compliance;
develop monitoring plan; assist in hiring and training new CRA and CRO. West
Coast $90-130K

Group Product Marketing Manager

Major $billion global leader whose product marketing focus has been to
physicians is switching the focus to consumers and is seeking a candidate
who can lead a new $20-30M consumer marketing campaign to drive a $200-300M
brand. Highly interested in candidates with deep consumer package goods
marketing experience, especially candidates who have experience with cold &
flu products, Tylenol, or Motrin, etc. Last season was predominantly
online,but now will do print, radio, outdoor space, and TV in future
seasons. West Coast $150,000 - $175,000

International Regulatory Affairs

The U.S. Division of a world-wide manufacturer of Medical Equipment /
Devices is seeking an International Product Registrations specialist
responsible for coordinating the registrations of products in international
markets reporting to the Director of Regulatory Affairs. Will plan, compile,
prepare, and submit applications to register new, and re-register existing,
company products with foreign regulatory agencies. Requires 2 -5 years of
relevant international medical product registrations experience, preferably
with Asian, Middle Eastern, and Latin American registration requirements.
North Carolina $50,000 - $75,000

Sr. Principle Engineer

A global leader engaged in the design, manufacture and worldwide sales and
marketing of medical devices wants 8-15 years experience managing
cross-functional projects in regulated environments to lead in the
development, integration, test and implementation to manufacturing, of
high-reliability, cost effective, disposable products, separation chambers
and electro mechanical devices which can be used by customers world-wide.
Manages activities and staff responsible for Manufacturing Engineering and
technical support. Responsible for the identification and support of
significant automation projects for cost savings. Responsible for
supporting product engineering / modification/ development, and defect
analysis and corrective action. BS in mechanical, plastics, industrial or
other engineering. Northeast $100-150K

Financial Manager Government Contracts

Pharmaceutical company wants Financial Manager to be a part of the senior
management team for two large government contracts to help lead cost and
control activities to meet contractual requirements. Will be responsible
for cost/schedule preparation, internal and external reporting
(CPR/Corporate efforts, etc) and analysis of variances, as well as monthly
project business management reviews, data and cost trends analysis, and
assist in risk analysis as applicable. Assist in establishing and
maintaining approved Earned Value Management System, to include Program
Operational Directives (PODs) and Overall Desktop Procedures related to
assigned programs. Extensive experience in previous government EVMS
reporting with experience in Biotech or Pharmaceutical Industry highly
desired. Maryland $90-110K

Sr. Manager Manufacturing Engineering- Disposables

A manufacturer of Medical Equipment is looking for 8+ years of experience
in medical devices to help design manufacturing processes, procedures and
production layouts for assemblies, equipment installation, processing,
machining and material handling. Will be responsible for leadership and
effective management of a group of manufacturing engineers and technicians
to provide manufacturing insight and project deliverables to new or
modified product projects and insure timely transition into manufacturing,
with consideration to design, cost effectiveness and process validation. BS
Engineering or technical discipline. Northeast $95,000 - $115,000.

Manager- Developmental Products Global Strategic Marketing

The BioSciences Division of a growing biotech wants experience in new
product planning in the pharmaceutical/biotech industry to be responsible
for commercial analysis, directing and interpreting supporting market
research, and development of commercial strategy for pre-clinical and
clinical candidates. Provides commercial assessment of all indications for
pre-IND and IND products and determines commercial strategy and oversees
market sizing, segmentation, and other pre-launch studies. Knowledge of
oncology, autoimmune diseases, and infectious diseases desired. Mid-Atlantic

Manager RA/RC

An independent division of a global healthcare company wants significant
experience with US submissions for class II devices having direct
responsibility and participation in their completion. The Manager RA/RC is
to develop and execute sound regulatory strategies for complex Regulatory
Affairs and regulatory compliance programs, with emphasis on FDA and
worldwide regulatory submissions. Will Coordinate and prepare complex
regulatory submissions, including 510(k) premarket notifications,
pre-submission documentation, Investigational Device Exemption (IDE)
applications, Premarket Approval Applications (PMA), Biologic Licensure
Application (BLA). Midwest $110,000 - $120,000

Manager, Sales Operations

A growing biotech manufacturer wants at least two years of experience in the
pharmaceutical or biotechnology industry to be primarily responsible for
managing Sales Operations for global sales, performing Market Analytics to
identify opportunities for current and future products and managing US
Government and International Sales Contracts. Would like experience in
planning and conducting Market Research efforts; familiar with primary and
secondary market data, analyses and application, an experienced account
manager, with working knowledge of roles of various departments within a
biotechnology, drug development organization. Should be familiar with
government contracting policies and regulations, including Federal
Acquisition Regulations. Maryland $100-130,000

Project Manager

A leading developer and manufacturer of precision Medical Equipment and
Devices has an excellent opportunity for a Systems Project Manager to join
the R&D Team. Provides project management expertise for small to medium
sized projects. Leads a multi-functional core team from Concept through
Commercialization; establishes project plans and objectives, develops cost
analysis, creates and manages the project schedule and budget; tracks
progress and updates key stakeholders on project status. Requires 2-5 years
project management experience in an FDA-regulated and/or ISO 14971 certified
industry, managing 20-30 team members with 5+ years experience in the
medical device industry, prefer intravascular medical devices. BS in
Electronics Engineering. Calif. - $75,000 - $105,000

Director, BioStatistics

Pharmaceutical company wants Post graduate (PhD preferred) in Biostatistics
with a minimum of 10 years experience gained within a Pharmaceutical
company/CRO, with a minimum of 5 years management experience. Professional
Statistical certification (e.g., CStat) an advantage, but not mandatory.
Will provide statistical oversight and guidance for clinical research
activities for all phases of Research and Development activities; liaises
with various internal and external groups (Clinical, Non-clinical, Data
Management, Regulatory, Medical Writing, Drug Safety and Risk Management,
and external vendors including CROs and regulatory bodies) to take
responsibility for the implementation of effective, scientifically sound and
regulatory compliant statistical methodology and to maintain a high level of
quality and consistency across the clinical and non-clinical programs.
Mid-Atlantic $120-150K

Director, Quality Control

Commercial biologicals manufacturer wants experienced QC/QA professional to
provide strong leadership for a cGMP Quality Control organization to include
BioAnalytical, Chemical, Microbiological, and Bioassay testing of raw
materials, in process materials and finished products. Method validations
and transfers, Animal Resources, Laboratory Data Management and Stability
programs are also managed by the Quality Control Organization. At least 10
years experience in management in Vaccine, Biologics or Pharmaceutical
testing facility. Knowledgeable of FDA/ICH regulations and guidance's and
USP and other Pharmacopeia standards of testing. Experience in FDA,
corporate and third party audits. Strong management skills coupled with
strong technical knowledge in Chemical, Biochemical, and Microbiological
theory and methods such as HPLC, GC, SDS-PAGE, Protein Analysis,
Animal-Based and Cell-Based Bioassays, and Sterility testing. Midwest
$110-140K

PRODUCT/BRAND MANAGER - Ethical OTC

A leading manufacturer and marketer of branded healthcare and wellness
products for the rehabilitation, therapy, and professional wellness markets
wants a minimum of 3-5 years of Healthcare product or brand management
experience with business to business and/or consumer products. The company
provides products, tools, exercises, treatments, and research to physical
therapists, occupational therapists, athletic trainers, chiropractors,
podiatrists, licensed massage therapists, and other clinical professionals.
Ohio $75,000 - $90,000 plus

Scientist, Purification Process development

Global Biotech manufacturer wants 8 years of experience with protein
purification process development, technology transfer, and pilot or
industrial scale up, including specific experience with recombinant
therapeutic proteins by mammalian cultures; Would like participation in the
creation of a Biological License Application (BLA); and writing SOPs, batch
records, production protocols, deviation assessments, and technical reports
for GMPs. Some experience managing technical staff. PhD in Chemical or
Biochemical Engineering or Biochemistry. West Coast $80-120K

Sr Manager, Regulatory Affairs

Pharmaceutical company wants Regulatory affairs experience with direct
interaction with FDA to lead preparation of regulatory submissions including
pre-IND and formal meetings with FDA, INDs, Annual Reports, BLAs and BLA
supplements, and routine correspondence. Advanced Degree (MS or PhD
preferred) in a Biological Science with 6+ years of industry experience in
Regulatory Affairs. Mid-Atlantic $70-130K

Sr Manager, Technical Support

Manufacturer wants experience performing scientific evaluation and diligence
in support of M&A and product licensing activities with an understanding of
the different stages and requirements in product development. Should have
5-10 years industrial R&D experience developing new products for oncology
or autoimmune indications with strong communication, interpersonal,
analytical and problem-solving skills. Industrial R&D experience in a mid-
to large pharma environment preferred. Experienced and accomplished
biological scientist in two or more of the following disciplines/disease
areas: infectious diseases, autoimmunity, oncology, immunology. MS with 8
years experience in the biotech industry or PhD (or MD) degree in
biopharmaceutical sciences (immunology, cell biology, rheumatology,
autoimmune disorders, clinical oncology, tumor biology) with 5 years
biotech industry experience. Maryland $80-120K

Sr. Marketing Manager

A global leader engaged in the design, manufacture and worldwide sales and
marketing of blood management solutions needs a Sr. Marketing Manager with
experience within the medical device industry along with having experience
launching a software product/application within the healthcare industry.
Will create innovative products, design information technology platforms
and provide consulting services to advance the safety, quality and
availability of the world's blood supply. Will be responsible for the
development of the marketing portfolio including business plan, business
case, global marketing plan, positioning, identification of solutions for
new technology platforms, lifecycle plan for existing platforms and
products. Need 7+ years progressive sales, marketing, management experience
with a minimum of 5 years in a healthcare related industry. International
and domestic market experience including branding, mergers & acquisitions
beneficial with successful experience with launching a software application
within the Healthcare industry strongly preferred. Northeast $110-140K.

Manager, Project Engineering

A manufacturer of Medical Equipment wants 10 years experience in the
medical device or pharmaceutical industry with experience in process and new
product development. Reporting to the Director of Engineering, this position
is responsible for the management of the Sustaining Engineering group in
support of all manufacturing operations and Corporate PD activities. Manage
activities of planning and development of strategic projects and initiatives
aimed at current and future developments in manufacturing, processes, and
new product introduction. Manage group of Engineers to assess feasibility of
and develop new manufacturing processes for new and existing products, lead
development, review, and implementation of new manufacturing processes and
equipment for new and existing products, lead and coordinate development of
specifications for new manufacturing and testing equipment, coordinate
verification and validation of new and existing equipment and processes.
Will manage development and execution of engineering studies and validation
protocols for new equipment / processes / cleaning validations, as well as
for periodic re-validations of existing equipment / processes and utilities
to include Lyophilizers, Autoclaves, CCA, DIUF, RO/DI, WFI, Pure Steam, SIP
Systems, HEPA Filters, Class 100 and 10,000 clean rooms, controlled
temperature units, and lab equipment. MS in Mechanical Engineering,
Pharmaceutical Engineering, Chemical Engineering, Material Science or
equivalent, MBA preferred. New Jersey $105,000 - $115,000

Medical Science Liaison

Pharmaceutical company wants expertise in effectively communicating
educational, medical/scientific and clinical information to the medical
community to cover the Western third of the U.S. Should have knowledge of
Acute Care facilities/Health Care Systems and therapeutic areas plus
represent the company to key opinion leaders (KOL's) in a professional and
ethical manor. A clinical background is a must. Identify requests for
speakers for Continuing Education (CE) events/programs as well as
representing company at specific CE events/programs, medical meetings and
conventions. Can live in a city with easy access to direct flights within
the specified territory (i.e. Los Angeles, San Francisco, Phoenix and
Seattle) with up to 60% travel. Master's degree or higher in the sciences
(prefer MBA, BSN, PhD) Minimum of two - three years experience in the
healthcare industry. $100-130K.

Engineering Manager-Sample Preparation Products

A supplier of instrumentation to the biotech industry needs a Technical
degree with 5 years of experience to manage a team of engineers and
technicians, focused on the improvement of manufacturing design, improving
cost, quality and profitability in a high throughput environment. Management
experience within a Manufacturing environment required along with experience
working with production automation equipment. West Coast $80- $105K.

Senior Quality Engineer

Manufacturer of Intravascular Ultrasound imaging systems needs a Sr.
Quality Engineer for Systems to work with the Operations group, supporting
the manufacturing lines that assemble imaging systems and accessories.
Will include Risk Assessment, writing and reviewing Design Verification and
Validation protocols and reports, working with Manufacturing for Process
Validation or performing statistical analysis as required in verifications
and validations. Demonstrated knowledge and understanding of FDA
regulations, Quality System Regulations (QSR), ISO 13485 requirements.
Requires 8+ years experience in quality assurance in the medical device
industry with demonstrated experience of supporting Manufacturing lines.
Bachelor's degree in Engineering, Electrical Engineering preferred.
California $90,000 - $105,000.

Sr. Manager Manufacturing

A High Volume Custom Automation Manufacturing Environment needs experience
in all aspects of the manufacturing process in a pharmaceutical or
biotechnology environment. Manages the activities of two or more sections
or departments through subordinate managers who exercise full supervision in
terms of costs, methods and employees. Pennsylvania $110,000 - $130,000.

Sr Engineer, Manufacturing Development

Manufacturing Engineer reports to the leader of the Manufacturing
Development at Manufacturing Operations and is responsible for leading
process and technology transfer of one or more pipeline processes. This
includes creating process budgets, managing internal and external resources,
participating in project team meetings, reporting project schedule status
and providing in-suite support for GMP manufacturing campaigns. Need 4-yr
engineering degree with 8-10 years of process experience OR related
engineering masters degree with 6-10 years industry experience. Process
technology transfer experience in two or more of the following: Downstream
or upstream GMP manufacturing experience Viral or non-viral process
experience Microbial or mammalian process experience Technology transfer
experience required Subcontractor managing experience Knowledge of cGMPs and
experience working in a GMP environment. Maryland $90-130K.

Sr Engineer

Growing biotech wants Ph.D with 3-5, MS with 5-10 or BS with 10 to 15 years
in biochemical engineering or equivalent. Extensive knowledge of bioprocess
unit operations specifically with upstream fermentation/recovery as well as
protein biochemistry and protein purification required. Hands on experience
using bioreactors, centrifuges, cross flow filtration as well as protein
purification process equipment such AKTA Explorers, AKTA Pilot, and AKTA
Crossflow and Uniflux TFF as well as centrifugation and other cross flow
filtration systems. Responsibilities will include design and execution of
experimental protocols for developing/optimizing manufacturing processes,
identifying appropriate equipment and process scale and technology transfer
to manufacturing for candidate proteins to be used as vaccines and/or
therapeutics. Focus will be primarily on protein and viral expression
through bacterial and /or eukaryotic platforms as well as protein
recovery/purification utilizing standard methods including
centrifugation/cross flow filtration chromatography and tangential flow
diafiltration. Preparation of experimental protocols, including other forms
of documentation such as Technology Development Reports, Technology Transfer
Protocols, and generating Operational and Maintenance Equipment SOPs and
Manufacturing Batch Records. Maryland $90-130K.

Sr Project Engineer

Pharmaceutical company seeks 8 years of project engineering experience in an
industrial setting. -Detailed knowledge of facilities, systems, and
infrastructure with experience in a pharmaceutical, biopharmaceutical, and
consumer products process company or food industry. Experience in a
federally regulated industry. Bachelors of Science degree in an Engineering
discipline -Engineering degree in civil, mechanical, chemical, or electrical
disciplines -Training or exposure to project management. Midwest $60-85K.

Validation Engineer

Pharmaceutical manufacturer wants B.S. Engineering or closely related
scientific field with experience, in GMP procedures and guidelines. - Good
Documentation Practices. - Authoring, reviewing, and approving qualification
protocols. Skills: - Must have strong technical writing skills. Midwest $50
-70K.

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1 comment:

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