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        <title>BiotechPharmJobs.com</title>
        <link>http://www.biotechpharmjobs.com/</link>
        <description>BioTechPharmJobs.com is a recruitment job blog for jobs and video resume podcasts in the biotechnology, clinical, healthcare and pharmaceutical industries.
</description>
        <language>en</language>
        <copyright>Copyright 2012</copyright>
        <lastBuildDate>Tue, 13 Mar 2012 18:30:47 -0500</lastBuildDate>
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        <item>
            <title>Doe &amp; Ingalls: Sales Specialty Chemicals - MA/CT/NY, Springfield, MA</title>
            <description><![CDATA[<center><a href="http://www.doeingalls.com/" target="_blank"><img alt="Doe &amp; Ingalls" src="http://www.biotechpharmjobs.com/images/doe_ingalls.jpg" border="0" /></a></center><br /><br />
<b>Job Description:</b><br /><br />
<b>Job Title:</b> Sales Specialty Chemicals - MA/CT/NY  <br />
<b>Location:</b> Springfield, MA<br />
<b>Company:</b> Doe &amp; Ingalls<br />
<b>Job Industry:</b> Biotechnology <br />
<b>Job Industry:</b> Specialty Chemical Sales <br />
<b>Job Type:</b> Full-Time <br />
<b>Travel Required:</b> 25-50%
<br /><br />
<a href="http://www.doeingalls.com" target="_blank">Doe &amp; Ingalls</a> is looking for a <b>Sales Specialty Chemicals - MA/CT/NY </b> Account Manager for its <b>Springfield, MA</b> location.<br /><br />
The Account Manager is responsible for managing existing customers and developing new business for the life sciences product lines and/or chemical management services throughout central/western Massachusetts, parts of Connecticut and New York.
<br /> <br />
<b>Key duties and requirements:</b><br /><br />
• Manage and grow existing accounts with manufacturers and laboratories in the pharmaceutical, medical device and environmental industry offering process materials, laboratory chemicals, and associated chemical management services <br />
• A strong understanding of the pharmaceutical industry to be able to serve as a resource for our customers and effectively present information to engineers, managers and purchasing agents  <br />
• Bachelor's Degree or equivalent experience in appropriate specialty (preference for Chemistry, Biochemistry)  <br /> 
• 3 or more years of proven business development, sales and closing experience  <br /> 
• Willingness and availability to travel overnight up to 50% to visit customers, supplier facilities, and attend trade shows
<br /><br />
Apply Here: <a href="http://www.Click2Apply.net/zq5cykg" target="_blank">http://www.Click2Apply.net/zq5cykg</a>
<br /><br />
<a href="http://www.doeingalls.com" target="_blank">Doe &amp; Ingalls</a> is an Equal Opportunity and Affirmative Action Employer. Any application for employment will be considered active for 30 days or until the position is filled, whichever comes first.
<br /><br />
<em>Please reference BioTechPharmJobs.com when responding.</em>
]]></description>
            <link>http://www.biotechpharmjobs.com/2012/03/doe-ingalls-sales-specialty-ch.html</link>
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            <pubDate>Tue, 13 Mar 2012 18:30:47 -0500</pubDate>
        </item>
        
        <item>
            <title>Alliance Oncology: Physician Services Representative, Frederick, MD</title>
            <description><![CDATA[ <center><a href="http://www.alliancehealthcareservices-us.com/oncology" target="_blank"><img alt="Alliance Oncology" src="http://www.biotechpharmjobs.com/images/alliance_oncology.jpg" border="0" /></a></center><br /><br />
<b>Job Description:</b><br /><br />
<b>Job Title:</b> Physician Services Representative<br />
<b>Location:</b> Frederick, MD<br />
<b>Company:</b> Alliance Oncology<br />
<b>Job Industry:</b> Pharmaceutical <br />
<b>Job Type:</b> Part-Time <br />
<br />
<a href="http://www.alliancehealthcareservices-us.com/oncology" target="_blank">Alliance Oncology</a> is looking for a part-time <b>Physician Services Representative</b> for its <b>Frederick, MD</b> location.<br /><br />
<b>Responsibilities:</b><br />
• Increasing scan volume on a customer level to ensure that the territory and the Division will deliver on its budgeted same-store-growth, scan volume, target and revenue commitments<br />
• Analyzing physician referral patterns to develop customer-level marketing plans, identifying opportunities to increase scan volume with existing referrers and/or developing new referral channels<br />
• Works in conjunction with territory Marketing and Operations leadership to establish realistic customer and territory plans that will deliver on the territory's budgeted same-store-growth, scan volume, target and revenue commitments<br />
• Analyzes marketed account referral patterns; monitors variances/trends associated with existing referral base, works with operations management to determine possible causes for changes in referral patterns; provides accurate scan volume forecasts to the Senior Physician Services Representative<br />
• Cultivates strong relationships with top strategic referrers to increase scan volume; identifies key customer drivers (turnaround time, quality, etc); ensures that customer's needs are met and communicates any service deficiencies to the Operations Team to ensure existing scan volume is preserved<br />
• Targets new referrals based on market trends and conditions; uses consultative selling skills to engage new referrers and probes potential referrer to uncover competitive takeaways based on unmet needs<br />
• Identifies specific "high risk" demographics and implements targeted community outreach programs such as terrtiory-level educational campaigns (lunch and learns, etc), healthcare fairs, CME presentation and/or dinners and other events to promote consumer awareness<br />
• Working in conjunction with the Senior Physician Services Representative and Legal, develops collateral and education materials; uses a wide-range of media and advertising channels to attract additional referrals<br />
• Hosts Quarterly Business Reviews with existing customers and reviews action plans with Senior Physician Services Representative post-meeting. May participate in Quarterly Business Reviews with key strategic accounts<br />
• Uncovers potential sales leads; communicates leads to Sales and Operations leadership and may participate in customer sales presentations as appropriate
<br /><br />
<b>Requirements:</b><br />
• Bachelor's Degree from four-year college or university<br />
•  Candidate must possess at least one (1) year of physician sales and marketing experience in a healthcare environment<br />
•  Prior Oncology sales experience is preferred, but not required<br />
• Frequent travel is required<br />
• A valid driver's license is mandatory for this position
<br /><br />
Apply Here: <a href="http://www.Click2Apply.net/qkrdgwf" target="_blank">http://www.Click2Apply.net/qkrdgwf</a>
<br /><br />
An Equal Opportunity Employer, m/f/d/v.
<br /><br />
<em>Please reference BioTechPharmJobs.com when responding.</em>]]></description>
            <link>http://www.biotechpharmjobs.com/2012/02/alliance-oncology-physician-se.html</link>
            <guid>http://www.biotechpharmjobs.com/2012/02/alliance-oncology-physician-se.html</guid>
            
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            <pubDate>Mon, 27 Feb 2012 11:53:32 -0500</pubDate>
        </item>
        
        <item>
            <title>Doe &amp; Ingalls: Account Manager Life Sciences - MA/CT/NY, Danvers, MA</title>
            <description><![CDATA[ <center><a href="http://www.doeingalls.com/" target="_blank"><img alt="Doe &amp; Ingalls" src="http://www.biotechpharmjobs.com/images/doe_ingalls.jpg" border="0" /></a></center><br /><br />
<b>Job Description:</b><br /><br />
<b>Job Title:</b> Account Manager, Life Sciences - MA/CT/NY <br />
<b>Location:</b> Danvers, MA<br />
<b>Company:</b> Doe &amp; Ingalls<br />
<b>Job Industry:</b> Biotechnology <br />
<b>Job Industry:</b> Sales <br />
<b>Job Type:</b> Full-Time <br />
<b>Travel Required:</b> 50-75%<br />
<br /><br />
<a href="http://www.doeingalls.com" target="_blank">Doe &amp; Ingalls</a> is looking for a <b>Account Manager, Life Sciences - MA/CT/NY</b> for its <b>Danvers, MA</b> location.<br /><br />
The Account Manager is responsible for managing existing customers and developing new business for the life sciences product lines and/or chemical management services throughout central/western Massachusetts, parts of Connecticut and New York.
<br /><br />
<b>Key duties and requirements:</b><br /><br />
• Manage and grow existing accounts with manufacturers and laboratories in the pharmaceutical, medical device and environmental industry offering process materials, laboratory chemicals, and associated chemical management services
• A strong understanding of the pharmaceutical industry to be able to serve as a resource for our customers and effectively present information to engineers, managers and purchasing agents <br />
• Bachelor's Degree or equivalent experience in appropriate specialty (preference for Chemistry, Biochemistry)<br />
•  3 or more years of proven business development, sales and closing experience <br />
•  Willingness and availability to travel overnight up to 50% to visit customers, supplier facilities, and attend trade shows 
<br /><br />
Apply Here: <a href="http://www.Click2Apply.net/9826f9b" target="_blank">http://www.Click2Apply.net/9826f9b</a>
<br /><br />
<a href="http://www.doeingalls.com" target="_blank">Doe &amp; Ingalls</a> is an Equal Opportunity and Affirmative Action Employer. Any application for employment will be considered active for 30 days or until the position is filled, whichever comes first.
<br /><br />
<em>Please reference BioTechPharmJobs.com when responding.</em>
]]></description>
            <link>http://www.biotechpharmjobs.com/2011/12/doe-ingalls-account-manager-li-1.html</link>
            <guid>http://www.biotechpharmjobs.com/2011/12/doe-ingalls-account-manager-li-1.html</guid>
            
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            <pubDate>Sat, 31 Dec 2011 22:52:49 -0500</pubDate>
        </item>
        
        <item>
            <title>Doe &amp; Ingalls: Account Manager Life Sciences, Danvers, MA</title>
            <description><![CDATA[<center><a href="http://www.doeingalls.com/" target="_blank"><img alt="Doe &amp; Ingalls" src="http://www.biotechpharmjobs.com/images/doe_ingalls.jpg" border="0" /></a></center><br /><br />
<b>Job Description:</b><br /><br />
<b>Job Title:</b> Account Manager, Life Sciences<br />
<b>Location:</b> Danvers, MA<br />
<b>Company:</b> Doe &amp; Ingalls<br />
<b>Job Industry:</b> Biotechnology <br />
<b>Job Type:</b> Full-Time <br />
<b>Travel Required:</b> 50-75%<br />
<br /><br />
<a href="http://www.doeingalls.com" target="_blank">Doe &amp; Ingalls</a> is looking for a <b>Account Manager, Life Sciences</b> for its <b>Danvers, MA</b> location.<br /><br />
The Account Manager is responsible for managing existing customers and developing new business for the life sciences product lines and/or chemical management services throughout Eastern Massachusetts, parts of Connecticut and New Hampshire <br />
<br /><br />
<b>Key duties and requirements:</b><br /><br />
• Manage and grow existing accounts with manufacturers and laboratories in the pharmaceutical, medical device and environmental industry offering process materials, laboratory chemicals, and associated chemical management services 
• A strong understanding of the pharmaceutical industry to be able to serve as a resource for our customers and effectively present information to engineers, managers and purchasing agents <br />
• Bachelor's Degree or equivalent experience in appropriate specialty (preference for Chemistry, Biochemistry)<br />
• 3 or more years of proven business development, sales and closing experience <br />
•  Willingness and availability to travel overnight up to 50% to visit customers, supplier facilities, and attend trade shows 
<br /><br />
Apply Here: <a href="http://www.Click2Apply.net/97rvsyv" target="_blank">http://www.Click2Apply.net/97rvsyv</a>
<br /><br />
<a href="http://www.doeingalls.com" target="_blank">Doe &amp; Ingalls</a> is an Equal Opportunity and Affirmative Action Employer. Any application for employment will be considered active for 30 days or until the position is filled, whichever comes first.
<br /><br />
<em>Please reference BioTechPharmJobs.com when responding.</em>]]></description>
            <link>http://www.biotechpharmjobs.com/2011/11/doe-ingalls-account-manager-li.html</link>
            <guid>http://www.biotechpharmjobs.com/2011/11/doe-ingalls-account-manager-li.html</guid>
            
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            <pubDate>Wed, 23 Nov 2011 23:12:44 -0500</pubDate>
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        <item>
            <title>OMNITEC Solutions: Clinical Data Analyst, Rockville, MD</title>
            <description><![CDATA[ <center><a href="http://www.omnitecinc.com/" target="_blank"><img alt="OMNITEC Solutions, Inc." src="http://www.biotechpharmjobs.com/images/omnitec_solutions.jpg" border="0" /></a></center>
<br /><br />
<b>Job Title:</b> Clinical Data Analyst<br />
<b>Location:</b> Rockville, MD<br />
<b>Company:</b> OMNITEC Solutions, Inc.<br />
<b>Job Industry:</b> Computer Software <br />
<b>Travel Required:</b> 0-10% <br /> 
<b>Job Type:</b> Full-Time <br />
<br /><br />
<a href="http://www.omnitecinc.com/" target="_blank">OMNITEC Solutions, Inc.</a> is looking for a <b>Clinical Data Analyst</b> to join our team in <b>Rockville, MD</b> with the leading the National Database for Autism Research. We are leading the effort to make all autism research available through a single portal at the National Institutes of Health (NIH). See <a href="http://ndar.nih.gov" target="_blank">http://ndar.nih.gov</a> for more information.
<br /><br />
<b>Responsibilities:</b>
<br /><br />
• Help lead the autism bioinformatics community by making rich research data easily available to scientists seeking to gain a better understanding of autism<br />
• Focus on data harmonization, database organization &amp; effectiveness, and informatics in dealing with research data that has been gathered and then disparately stored by other Researchers<br />
• Utilize your clinical data analysis &amp; management, and database skills to ensure all data is accessible and useful to a broad audience 
<br /><br />
<b>Requirements:</b><br /> <br />
• A four-year degree is preferred, along with 5+ years experience managing clinical, imaging, and genomics research data in a complex informatics environment is needed<br />
• Excellent verbal and written communication skills, as well as a strong understanding of databases and database programming concepts are required<br />
• Oracle expertise is a plus 
<br /><br />
To apply, please send your MS Word resume and <b>reference job code 11.0066.MD</b> along with your replies to the items below to: <a href="mailto:employment@omnitecinc.com?subject=Clinical_Data_Analyst_ job_code_11.0066.MD_BioTechPharmJobs">employment@omnitecinc.com</a>
<br /><br />
1. You must be authorized to work in the United States; Please indicate if you are a US citizen or holder of an authorized green card<br />
2. Please provide brief comments regarding your past experience with data harmonization, database organization &amp; effectiveness, and informatics<br />
3. Please provide brief comments on which databases and related tools you are most skilled with <br />
4. Please provide brief comments regarding any past experience supporting Bioinformatics and/or Healthcare research efforts<br />
5. Please provide 2-3 comments on why you feel you are a good match to this opportunity<br />
6. What is your salary requirement?<br /> 
7. Please tell us how to became aware of this employment opportunity. Thank you! 
<br /><br />
<a href="http://www.omnitecinc.com/" target="_blank">OMNITEC Solutions, Inc.</a> is an Equal Opportunity Employer, m/f/d/v.
<br /><br />
<em>Please reference BioTechPharmJobs.com when responding.</em>
<br /><br />
<a href="http://www.onlineuniversities.net/" target="_blank">Online universities have information on biotech degrees</a> for those who want to further educate themselves.]]></description>
            <link>http://www.biotechpharmjobs.com/2011/10/omnitec-solutions-clinical-dat.html</link>
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            <pubDate>Thu, 27 Oct 2011 22:25:50 -0500</pubDate>
        </item>
        
        <item>
            <title>Doe &amp; Ingalls: Warehouse Specialist, Danvers, MA</title>
            <description><![CDATA[<center><a href="http://www.doeingalls.com/" target="_blank"><img alt="Doe &amp; Ingalls" src="http://www.biotechpharmjobs.com/images/doe_ingalls.jpg" border="0" /></a></center><br /><br />
<b>Job Description:</b><br /><br />
<b>Job Title:</b> Warehouse Specialist<br />
<b>Location:</b> Danvers, MA<br />
<b>Company:</b> Doe &amp; Ingalls<br />
<b>Job Industry:</b> Biotechnology <br />
<b>Job Type:</b> Full-Time <br />
<br /><br />
<a href="http://www.doeingalls.com" target="_blank">Doe &amp; Ingalls</a> is looking for a <b>Warehouse Specialist</b> for its <b>Danvers, MA</b> location.<br /><br />
<b>Responsibilities:</b>
<br /><br />
• Performs material handling required to complete receiving, storage, picking, and shipping operations<br />
• Performs receiving inspections of inbound shipments and stores products in designated warehouse locations<br /> 
• Performs order picking functions and prepares orders for shipment including required inspections of sales order and shipping manifest<br />
• Performs required warehouse and warehouse equipment maintenance and housekeeping requirements as directed by the Site Manager <br />
• Learns and executes ISO 9001 Quality System Procedures and Work Instructions related to this position's duties and responsibilities
<br /><br />
<b>Requirements:</b><br /><br />
• High School diploma or equivalent <br />
• Physical ability to perform materials handling responsibilities <br />
• 2 years Warehouse/Materials Handling experience highly desirable <br />
• HAZMAT shipping experience desirable <br />
• Forklift experience and must become forklift certified within 30 days 
<br /><br />
To apply, please send your MS Word resume along with salary requirements by applying online at:<br />
<a href="http://www.Click2Apply.net/xcnh5hr" target="_blank">http://www.Click2Apply.net/xcnh5hr</a>
<br /><br />
<a href="http://www.doeingalls.com" target="_blank">Doe &amp; Ingalls</a> is an Equal Opportunity and Affirmative Action Employer. Any application for employment will be considered active for 30 days or until the position is filled, whichever comes first.
<br /><br />
<em>Please reference BioTechPharmJobs.com when responding.</em>]]></description>
            <link>http://www.biotechpharmjobs.com/2011/08/doe-ingalls-warehouse-speciali.html</link>
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            <pubDate>Tue, 16 Aug 2011 23:02:15 -0500</pubDate>
        </item>
        
        <item>
            <title>Doe &amp; Ingalls: Sales Account Manager - Life Sciences, Tampa, FL</title>
            <description><![CDATA[<center><a href="http://www.doeingalls.com/" target="_blank"><img alt="Doe &amp; Ingalls" src="http://www.biotechpharmjobs.com/images/doe_ingalls.jpg" border="0" /></a></center><br /><br />
<b>Job Description:</b><br /><br />
<b>Job Title:</b> Account Manager, Life Sciences<br />
<b>Location:</b> Tampa, Florida<br />
<b>Company:</b> Doe &amp; Ingalls<br />
<b>Job Function:</b> Sales<br />
<b>Job Industry:</b> Biotechnology <br />
<b>Job Type:</b> Full-Time <br />
<b>Travel Required:</b> up to 50% 
<br /><br />
<a href="http://www.doeingalls.com" target="_blank">Doe &amp; Ingalls</a> is looking for an <b>Account Manager, Life Sciences</b> for its <b>Tampa, FL</b> location.<br /><br />
<b>Responsibilities:</b>
<br /><br />
• Manage existing customers and develop new business for the life sciences product lines and chemical management services throughout Florida<br />
• Manage and grow existing accounts with manufacturers and laboratories in the pharmaceutical, medical device and environmental industry offering process materials, laboratory chemicals, and associated chemical management services 
<br /><br />
<b>Requirements:</b><br /><br />
• A strong understanding of the pharmaceutical industry to be able to serve as a resource for our customers and effectively present information to engineers, managers and purchasing agents / managers<br />
• Bachelor's Degree or equivalent experience in appropriate specialty (preference for Chemistry, Biochemistry)<br />
• 3 or more years of proven business development, sales and closing experience<br />
• Willingness and availability to travel overnight up to 50% to visit customers, supplier facilities, and attend trade shows
<br /><br />
To apply, please send your MS Word resume along with salary requirements by applying online at:<br />
<a href="http://www.Click2Apply.net/jhsddvf" target="_blank">http://www.Click2Apply.net/jhsddvf</a>
<br /><br />
<a href="http://www.doeingalls.com" target="_blank">Doe &amp; Ingalls</a> is an Equal Opportunity and Affirmative Action Employer. Any application for employment will be considered active for 30 days or until the position is filled, whichever comes first.
<br /><br />
<em>Please reference BioTechPharmJobs.com when responding.</em>
<br /><br />

Some people may want to <a href="http://www.guidetoonlineschools.com/" target="_blank">learn about accredited online masters programs via Guide to Online Schools</a>.
]]></description>
            <link>http://www.biotechpharmjobs.com/2011/08/doe-ingalls-sales-account-mana.html</link>
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            <pubDate>Wed, 03 Aug 2011 21:41:12 -0500</pubDate>
        </item>
        
        <item>
            <title>Doe &amp; Ingalls: Quality Specialist cGMP, Durham, NC</title>
            <description><![CDATA[<center><a href="http://www.doeingalls.com/" target="_blank"><img alt="Doe &amp; Ingalls" src="http://www.biotechpharmjobs.com/images/doe_ingalls.jpg" border="0" /></a></center><br /><br />
<b>Job Description:</b><br /><br />
<b>Job Title:</b> Quality Specialist - cGMP<br />
<b>Location:</b> Durham, NC<br />
<b>Company:</b> Doe &amp; Ingalls<br />
<b>Job Function:</b> Quality Assurance <br />
<b>Job Industry:</b> Biotechnology <br />
<b>Job Type:</b> Full-Time <br />
<b>Experience Required:</b> 2-3 Years <br />
<b>Education Required:</b> BA/BS/Undergraduate <br />
<b>Travel Required:</b> 10-25% 
<br /><br />
<a href="http://www.doeingalls.com" target="_blank">Doe &amp; Ingalls</a> is looking for an <b>Quality Specialist - Specialty Chemicals</b> for its <b>Durham, NC</b> location.<br /><br />
<b>Responsibilities:</b>
<br /><br />
• Executing the daily sampling activities to meet and exceed our customer requirements for safe, accurate, and cGMP compliant raw material sampling<br />
• Work closely with customer quality and materials management personnel to implement and execute a raw material sampling program<br />
• Support the facility-based and corporate functions of the Quality Systems Department such as document control, records management, CAR/PAR processing, customer audit support, internal auditing, and training, etc.<br />
• Coordinate with the Site Manager and warehouse staff to execute the materials movement and other warehouse activities needed to support the raw material sampling processes<br />
• Clean, stock and maintain the raw material sampling area, equipment and instruments
• Write and follow standard operating procedures related to the raw material sampling function. 
<br /><br />
<b>Requirements:</b><br /><br />
• Bachelor's Degree in Chemistry or related science or equivalent experience in appropriate specialty <br />
• Minimum of 2 years experience in a cGMP controlled environment such as biopharmaceutical manufacturing, raw material sampling, environmental monitoring and/or quality assurance.
<br /><br />
To apply, please send your MS Word resume along with salary requirements by applying online at:<br />
<a href="http://www.Click2Apply.net/zsqq53b" target="_blank">http://www.Click2Apply.net/zsqq53b</a>
<br /><br />
<a href="http://www.doeingalls.com" target="_blank">Doe &amp; Ingalls</a> is an Equal Opportunity and Affirmative Action Employer. Any application for employment will be considered active for 30 days or until the position is filled, whichever comes first.
<br /><br />
<em>Please reference BioTechPharmJobs.com when responding.</em>]]></description>
            <link>http://www.biotechpharmjobs.com/2011/07/doe-ingalls-quality-specialist.html</link>
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            <pubDate>Mon, 11 Jul 2011 23:11:03 -0500</pubDate>
        </item>
        
        <item>
            <title>Ricerca Biosciences: Automation Engineer, Bothell, WA</title>
            <description><![CDATA[<center><a href="http://www.ricerca.com" target="_blank"><img border="0" alt="Ricerca Biosciences LLC" src="http://www.biotechpharmjobs.com/images/ricerca.jpg" /></a></center><br /><br /><b>Job Description:</b><br /><br /><b>Job Title:</b> Automation Engineer<br /><b>Location:</b> Bothell, WA<br /><b>Company:</b> Ricerca Biosciences LLC<br /><br />Customers count on <a href="http://www.ricerca.com" target="_blank">Ricerca</a> to help them bring much-needed new drugs to market - and to increase their speed, precision and productivity along the way. <a href="http://www.ricerca.com" target="_blank">Ricerca Biosciences</a> applies advanced scientific and technological expertise to the drug discovery and development process. We are looking for an <b>Automation Engineer</b> reporting to the Senior Manager of Operations.<br /><br /><b>Responsibilities:</b> <br />• Responsible for the use and performance of the automated systems in order to execute large and small-scale R&amp;D or client projects along with responsibilities for assay workflow testing, validation and implementation<br />• Works closely with laboratory personnel to accomplish project objectives<br />• Participates as a member of project teams to design new processes, or to evaluate new technologies<br /><br /><b>Essential Functions:</b><br />• Run established assays on the automation systems and/or assist end-users running established assays<br />• Integrate new equipment <br />• Develop, validate and implement new automation protocols<br />• Communicate with lab staff and scientists, in order to understand the needs and requirements of the scientific teams<br />• Maintain and troubleshoot automation equipment, including routine maintenance and periodic quality control testing<br />• Perform a variety of support functions<br />• Enter information into logs of equipment utilization, maintenance or errors, track reagent use and supply, maintain files on suppliers, writing SOPs and protocols, etc.<br />• Participate in project groups developing and/or evaluating new technologies and processes<br /><br /><b>Requirements:</b><br />• 2+ years industry experience in lab automation <br />• B.S. in biological science, engineering, or related field <br />• Hands-on experience with articulated robotic arms, liquid handling workstations, liquid dispensers, plate washers, plate readers, incubators, and automation scheduling software <br />• Experience with in vitro and cell-based assay techniques <br />• Computer programming experience a plus V11 experience a plus <br /><br />To apply, please apply online to: <br /><a href="http://www.Click2Apply.net/2dnjt9q" target="_blank">http://www.Click2Apply.net/2dnjt9q</a> <br /><br />An equal opportunity employer, m/f/d/v. <br /><br /><em>Please reference BioTechPharmJobs.com when responding.</em>]]></description>
            <link>http://www.biotechpharmjobs.com/2011/01/ricerca-biosciences-automation.html</link>
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            <pubDate>Sun, 23 Jan 2011 14:10:56 -0500</pubDate>
        </item>
        
        <item>
            <title>The NMS Group: Strategic Planning Pharma Manager, Tarrytown, NY</title>
            <description><![CDATA[ <center><a href="http://www.nms-group.com" target="_blank"><img border="0" alt="The NMS Group" src="http://www.biotechpharmjobs.com/images/nms_group.jpg" /></a></center><br /><br />

<b>Job Description:</b><br /><br />

<b>Job Title:</b> Strategic Planning Pharma Manager<br />
<b>Location:</b> Tarrytown, NY<br />
<b>Company:</b> The NMS Group
<br /><br />
<a href="http://www.nms-group.com" target="_blank">The NMS Group</a> is looking for a <b>Strategic Planning Pharma Manager</b> for its <b>Tarrytown, NY</b> office.
<br /><br /><b>Responsibilities:</b> <br /><br />
• The primary responsibility of this position is to be accountable for the strategy development, key strategic project management, and process design for the Strategic Planning and Analysis Group <br />
• Individual will conduct research, perform supply chain analysis and problem solving relative to establishing strategic supply chain direction as well as optimization of current Product Supply SAP SCM planning tools, inventory, forecasting, planning, and scheduling processes <br />
• Document current supply chain network and perform analysis on optimization opportunities <br />
• Accountability includes supply chain direction setting, management of cost savings initiatives and metrics, measurement and benchmarking for Global Product Supply <br />
• Analyze, plan, and implement on assigned DC Product Supply projects providing management with accurate and relevant information to make effective decisions in response to product supply issues or opportunities <br />
• Recommends strategies and actions based on analysis <br />
• Lead the design, implementation, and standardization of global strategic projects across multiple areas supporting DC PS requirements and organization objectives: supply chain network, sourcing, planning tools, process redesign <br />
• Lead the design, implementation, and standardization of global strategic projects across multiple areas supporting DC PS requirements and organization objectives: supply chain network, sourcing, planning tools, process redesign <br />
• Identify, redesign and implement process enhancements / improvements supporting Sales and Operations Planning, inventory management, forecasting and sourcing, new product development and other areas <br />
• Identify and recommend research projects in areas of responsibility to help optimize growth opportunities and support Product Supply strategic direction <br />
• Collaborate with PS stakeholders to extract requirements, develop plans, timelines, reporting and metrics for specific PS projects <br />
• Serve as Product Supply due diligence team member to support Business Development as required <br />
• Acquire and maintain knowledge of industry trends and professional practices and techniques within areas of responsibilities <br />
• Support Product Supply planning systems across PS organization <br />
• Identify problems/opportunities, as well as recommending solutions to problems identified by management
<br /><br />
<b>Requirements:</b><br /><br />
• Knowledge of consumer products manufacturing, Supply Chain strategies projects and problem solving <br />
• Experience in medical device or similar industry <br />
• Experience working in a global role <br />
• Experience in Supply Chain strategy and process design in both industry and consulting roles <br />
• Experience working with SAP, including implementation and network optimization analysis <br />
• Masters Degree preferred <br />
• Candidate must have a Bachelors Degree with 7 - 10 years experience <br /><br />To apply, please send your MS Word resume along with salary requirements to: <br /><a href="mailto:barnett@nms-group.com">barnett@nms-group.com</a> 
<br /><br />An equal opportunity employer, m/f/d/v. 
<br /><br /><em>Please reference BioTechPharmJobs.com when responding.</em>]]></description>
            <link>http://www.biotechpharmjobs.com/2010/11/the-nms-group-strategic-planni.html</link>
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            <pubDate>Thu, 04 Nov 2010 12:56:39 -0500</pubDate>
        </item>
        
        <item>
            <title>J R Simplot Company: Regulatory Affairs Director, Boise, ID</title>
            <description><![CDATA[<center><a href="http://www.simplot.com" target="_blank"><img border="0" alt="J.R. Simplot Company" src="http://www.biotechpharmjobs.com/images/simplot.jpg" /></a></center><br /><br /><b>Job Description:</b><br /><br /><b>Job Title:</b> Regulatory Affairs Director<br /><b>Location:</b> Boise, ID<br /><b>Company:</b> J.R. Simplot Company <br /><br /><br />The <a href="http://www.simplot.com" target="_blank">J.R. Simplot Company</a> is looking for a <b>a Regulatory Affairs Director</b> for its <b>Boise, ID</b> headquarters.<br /><br /><b>Responsibilities:</b> <br /><br />• Develop and implement a regulatory strategy, in addition to lead efforts for approval of biotech products in the U.S., Canada, Mexico, Japan and other countries as needed for export and trade protection <br />• Interface and communicate with U.S. and International Governmental Regulatory agencies to ensure the smoothest path through regulatory for Simplot and Simplot partner biotechnology products <br />• Work closely with the R&amp;D director and other Research Scientists to plan and execute all studies needed for regulatory approval <br />• Hire and manage regulatory consultants who specialize in obtaining approval in each of the countries <br />• Develop and oversee quality systems for managing successful market launches of biotech potatoes both domestically and internationally <br />• Collaborate with biotech researchers to influence regulatory agencies regarding the product safety with the goal of minimizing time and resources needed for approval <br /><br /><b>Requirements:</b><br /><br /> • 10 years related experience and/or training <br />• 5 years of practical experience in the field of plant biotechnology <br />• Requires 10 years relevant experience in the industry, with at least 5 yrs in biotechnology regulatory role <br />• Background in quality systems, project management, statistics, potato growing practices, plant biology, government regulations, and food processing desired <br />• Experience working for National level regulatory agencies desired <br />• Knowledge and experience in molecular biology is required, and knowledge of plant physiology and/or genetics is desirable <br />• Experience in the area of biotechnology is also desirable <br />• A proven track record of developing dossiers for approval of biotech plants by US and International agencies would be ideal <br />• A background in biological sciences with enough technical depth to understand and explain dossiers to regulatory agencies <br />• Strong verbal and written communication skills and a practical understanding of U.S. and International regulations for biotech products <br />• Knowledge and use of negotiation skills through executed agreements and collaborative research <br />• Candidates must excel at working collaboratively with other groups at Simplot and with external colleagues and partners <br />• This individual must be a self-starter, willing to work with minimal direction <br />• 25% travel required <br /><br /><b>Education:</b><br /><br />• B.S. (M.S. or PhD preferred) in the Sciences, which could be from Molecular Biology, Biochemistry, Genetics, Plant Physiology, Engineering, or other relevant majors<br />• The ideal candidate would have an advanced degree and at least 10 years relevant industry experience, including 5 years in biotech regulatory <br /><br />To apply, please send your MS Word resume along with salary requirements to: <br /><a href="mailto:kayce.mcewan@simplot.com">kayce.mcewan@simplot.com</a> <br /><br />An equal opportunity employer, m/f/d/v. <br /><br /><em>Please reference BioTechPharmJobs.com when responding.</em>
<br /><br /><a href="http://www.online-masters-degree-programs.org" target="_blank">Online masters
degree programs</a> are an option for people who realize that the job they
want requires advanced education.
]]></description>
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            <pubDate>Mon, 11 Oct 2010 22:18:28 -0500</pubDate>
        </item>
        
        <item>
            <title>Radiant Info Systems: Animal Technician, Cambridge, MA</title>
            <description><![CDATA[<center><a href="http://radiantinfo.com" target="_blank"><img border="0" alt="Radiant Info Systems" src="http://www.biotechpharmjobs.com/images/radiant_info_systems.jpg" /></a></center><br /><br />
<b>Job Description:</b><br /><br />
<b>Job Title:</b> Animal Technician <br />
<b>Location:</b> Cambridge, MA<br />
<b>Company:</b> Radiant Info Systems<br />
<b>Contract:</b> Duration: 12 months
<br /><br />
<a href="http://radiantinfo.com" target="_blank">Radiant Info Systems</a> is looking for an <b>Animal Technician</b> for its <b>Cambridge, MA</b> office.<br /><br />
<b>Responsibilities:</b>
<br /><br />
• Review, comprehend and comply with all SOP's and internal guidelines <br />
• Perform daily health observations and communicate issues as appropriate  <br />
• Perform husbandry duties for rats and mice <br />
• Perform cagewash and preparation activities to include usage of equipment and maintenance of adequate inventories <br />
• Perform monthly census, handle related documentation and follow reporting procedures <br />
• Utilize internal databases to assist in the receipt and processing of supplies <br />
• Perform general housekeeping and adhere to safety procedures <br />
• Performs other duties as assigned
<br /><br /> 
<b>Requirements:</b><br /><br />
• Minimum of 1-3 years directly related experience  <br />
• AALAS certification is preferred <br />
• Good working knowledge of Microsoft Word and Excel <br />
• Strong organizational skills and attention to detail  <br />
• Strong written and verbal English communication skills  <br />
• Ability to follow written and verbal instructions  <br />
• Ability to stand for extended periods of time <br />
• Ability to regularly lift/push, or pull up to 50 pounds
<br /><br />
<b>Other:</b><br /><br />
• Regular work schedule is 40 hours per week; however, the incumbent may be required to work on weekends and holidays on a rotating basis <br />
• This position is overtime eligible  
<br /><br />
To apply, please send your MS Word resume along with salary requirements to: <br />
<a href="mailto:SPalakurthi@radiants.com">SPalakurthi@radiants.com</a>
<br /><br />
An equal opportunity employer, m/f/d/v.
<br /><br />
<em>Please reference BioTechPharmJobs.com when responding.</em>]]></description>
            <link>http://www.biotechpharmjobs.com/2010/10/radiant-info-systems-animal-te.html</link>
            <guid>http://www.biotechpharmjobs.com/2010/10/radiant-info-systems-animal-te.html</guid>
            
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            <pubDate>Mon, 11 Oct 2010 21:53:49 -0500</pubDate>
        </item>
        
        <item>
            <title>Radiant Info Systems: Staff Analyst Statistical Programming, Cambridge, MA</title>
            <description><![CDATA[<center><a href="http://radiantinfo.com" target="_blank"><img border="0" alt="Radiant Info Systems" src="http://www.biotechpharmjobs.com/images/radiant_info_systems.jpg" /></a></center><br /><br />
<b>Job Description:</b><br /><br />
<b>Job Title:</b> Staff Analyst - Statistical Programming<br />
<b>Location:</b> Cambridge, MA<br />
<b>Company:</b> Radiant Info Systems<br />
<b>Contract:</b> Duration: 6 months
<br /><br />
<a href="http://radiantinfo.com" target="_blank">Radiant Info Systems</a> is looking for a <b>Staff Analyst - Statistical Programming</b> for its <b>Cambridge, MA</b> office.<br /><br />
<b>Responsibilities:</b>
<br /><br />
• Supports statistical programming activities in the production of the analysis datasets, tables, listings, figures, electronic submission components, and complex ad hoc analyses<br />
• Monitors and meets assigned study and program milestones and requests resources as needed<br />
• Leads a small team of support statistical programmers to accomplish tasks and communicate issues to senior management as necessary<br />
• Provides input to policy, operations, and capability building in Statistical Programming and Operations<br />
• Leads cross-functional teams to implement policy, operations, and capability initiatives<br />
• Develops and implements standard programming practices while also ensuring that they are employed across studies and programs<br />
• Mentors less experienced programmers
<br /><br /> 
<b>Requirements:</b><br /><br />
• 5-10 years SAS Base programming, with 5-7 years using SAS STAT, GRAPH and MACRO<br />
• 5-10 years relevant industry experience<br />
• 5-10 years clinical trial experience<br />
• At least 2 years clinical database experience<br />
• Excellent knowledge of drug development process<br />
• Knowledge of drug submission requirements 
<br /><br /> 
<b>Education:</b><br /><br />
• Must have a Bachelor's degree or equivalent, preferably in a scientific discipline (i.e. Statistics, Mathematics, Economics, Computer Science, IT, Biology, Life Science) 
<br /><br />
To apply, please send your MS Word resume along with salary requirements to: <br />
<a href="mailto:SPalakurthi@radiants.com">SPalakurthi@radiants.com</a>
<br /><br />
An equal opportunity employer, m/f/d/v.
<br /><br />
<em>Please reference BioTechPharmJobs.com when responding.</em>]]></description>
            <link>http://www.biotechpharmjobs.com/2010/10/radiant-info-systems-staff-ana.html</link>
            <guid>http://www.biotechpharmjobs.com/2010/10/radiant-info-systems-staff-ana.html</guid>
            
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            <pubDate>Mon, 11 Oct 2010 21:38:59 -0500</pubDate>
        </item>
        
        <item>
            <title>Radiant Info Systems: Clinical Business Planning Manager, Cambridge, MA</title>
            <description><![CDATA[<center><a href="http://radiantinfo.com" target="_blank"><img border="0" alt="Radiant Info Systems" src="http://www.biotechpharmjobs.com/images/radiant_info_systems.jpg" /></a></center><br /><br />
<b>Job Description:</b><br /><br />
<b>Job Title:</b> Clinical Business Planning Manager<br />
<b>Location:</b> Cambridge, MA<br />
<b>Company:</b> Radiant Info Systems<br />
<b>Contract:</b> Duration: 4 months
<br /><br />
<a href="http://radiantinfo.com" target="_blank">Radiant Info Systems</a> is looking for a <b>Clinical Business Planning Manager</b> for its <b>Cambridge, MA</b> office.<br /><br />
<b>Responsibilities:</b>
<br /><br />
• Responsible for financially managing overall programs and highly complex, large volume trial budgets, determining the methodology for forecasting each account<br />
• Supervises or performs monthly financial planning, accrual calculations, accrual reconciliations, and justification of liability held on accounting books<br />
• Responsible for the leadership of the monthly budget review meetings<br />
• Analyzes, finalizes, and is accountable for all variance commentary<br />
• Creates, as needed, ad hoc financial and operational reports<br />
• Builds financial scenarios to support program decisions<br />
• Develops annual Long Range Planning projections reflecting approved Clinical Development Plans<br />
• Involved with, or manages, initiatives that are rooted in the details of clinical trial financial management<br />
• Responsible for maintaining compliance for financial transactions within the clinical trial area by careful management of Purchase Orders (PO), PO requests, work approvals, and vendor contract amendments related to clinical trials<br />
• Will participate in or may lead complex, multifunction initiatives<br />
• Will contribute to the development of SOPs and Work Instructions that support clinical trial financial resource management<br />
• May take on roll of supervisor or manager<br />
• Operates and responsible for driving activities/influencing beyond individual department<br />
• Establishes and implements standard practices, processes and procedures for group/department/program<br />
• Will supervise professional subordinates to handle direct workload<br />
• Helps to develop departmental budget and prioritizes resources and timelines to complete multiple projects within budget<br />
• Ready to mentor and train new CBP personnel<br />
• Interacts with Clinical Program Leads, Contract Managers, Contracts Associates, Clinical Trial Managers, Clinical Trial Coordinators of studies to which CBP is assigned by supporting the operational strategy/planning with relevant industry and BIIB-specific benchmarks<br />
• Interacts with accountant to assist with monthly accrual process and subsequent reconciliation<br />
• Interacts with R&D Finance counterpart to communicate significant budget/scope changes on studies/programs assigned<br />
• Will directly interact with external vendors on business terms
<br /><br />
To apply, please send your MS Word resume along with salary requirements to: <br />
<a href="mailto:SPalakurthi@radiants.com">SPalakurthi@radiants.com</a>
<br /><br />
An equal opportunity employer, m/f/d/v.
<br /><br />
<em>Please reference BioTechPharmJobs.com when responding.</em>]]></description>
            <link>http://www.biotechpharmjobs.com/2010/10/radiant-info-systems-clinical.html</link>
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            <pubDate>Mon, 11 Oct 2010 21:24:52 -0500</pubDate>
        </item>
        
        <item>
            <title>Radiant Info Systems: Statistical Submissions Management Senior Analyst III, Cambridge, MA</title>
            <description><![CDATA[<center><a href="http://radiantinfo.com" target="_blank"><img border="0" alt="Radiant Info Systems" src="http://www.biotechpharmjobs.com/images/radiant_info_systems.jpg" /></a></center><br /><br />
<b>Job Description:</b><br /><br />
<b>Job Title:</b> Statistical Submissions Management Senior Analyst III<br />
<b>Location:</b> Cambridge, MA<br />
<b>Company:</b> Radiant Info Systems<br />
<b>Contract:</b> Duration: 12 months
<br /><br />
<a href="http://radiantinfo.com" target="_blank">Radiant Info Systems</a> is looking for a <b>Statistical Submissions Management Senior Analyst III</b> for its <b>Cambridge, MA</b> office.<br /><br />
<b>Responsibilities:</b>
<br /><br />
• Coordinating, preparing, reviewing and managing Biostatistics electronic submission ready components for complex regulatory submissions  <br />
• Monitoring and meeting assigned project milestones and requesting resources while providing adequate submission status tracking reports, as well as metrics reports, to communicate progress and trends of electronic submission activities (i.e. submissions plans)  <br />
• Developing or implementing standard electronic submission practices and standards, while also ensuring that they are employed across studies and drug programs  <br />
• Providing submission support to complex ad-hoc and response requests from regulatory agencies 
<br /><br />
<b>Requirements:</b><br /> <br />
• Able to handle a large volume of highly complex tasks and work effectively under pressure and tight deadlines <br />
• Able to use SAS programming software intensively and to review SAS programs and prepare the submission components <br />
• Must have experience with clinical trial data and software used for electronic submissions purposes <br />
• Must have great general computer proficiency, including Microsoft Suite applications <br />
• Must have 5-10 years Adobe Acrobat and electronic submission applications experience utilized for electronic submission purposes <br />
• Must have 5-10 years SAS experience with some demonstrated programming language experience <br />
• Must have 5-10 years relevant experience in the pharmaceutical, biotechnology industry or CRO <br />
• Must have a demonstrated ability in supporting project teams and management <br />
• Must have extensive knowledge and application of applicable industry principles, concepts, techniques, and standards <br />
• Must have full knowledge of applicable regulations and industry practices and ability to utilize the knowledge in the practice <br />
• Must have excellent application of concepts and principles of electronic submission and drug development process 
<br /><br />
<b>Education:</b><br /><br />
• Must have a Bachelor's degree or equivalent, preferably in a scientific discipline (i.e. Statistics, Mathematics, Economics, Computer Science, IT, Biology, Social Science, etc.)
<br /><br />
To apply, please send your MS Word resume along with salary requirements to:<br />
<a href="mailto:SPalakurthi@radiants.com">SPalakurthi@radiants.com</a>
<br /><br />
An equal opportunity employer, m/f/d/v.
<br /><br />
<em>Please reference BioTechPharmJobs.com when responding.</em>]]></description>
            <link>http://www.biotechpharmjobs.com/2010/10/radiant-info-systems-statistic.html</link>
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            <pubDate>Mon, 11 Oct 2010 20:58:43 -0500</pubDate>
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