We are seeking a highly motivated scientist to join our research group focusing on pre-clinical development of novel targeted therapeutics in cancer metabolism.

Responsibilities:

The candidate will lead and participate in the evaluation of antibody drug candidates in vivo models; including proof of concept, target validation and efficacy studies. The candidate must have a proven record of scientific achievement in metabolic and/or inflammatory diseases, the ability to work as part of a dynamic multidisciplinary team and excellent oral and written communication, organizational and interpersonal skills.

Qualifications:

• PhD in the life sciences with a minimum of two years postdoctoral experience.
• Extensive hands-on experience in animal models of inflammatory and/or metabolic diseases.
• Working knowledge of molecular biology, broad biochemical techniques with an emphasis on oncology pathways or metabolic diseases, and general histology and immunohistochemstry.
• Strong scientific record and proficiency in experiemntal design, troubleshooting and data interpretation.

We welcome your expertise, your insight and your enthusiasm to help us develop and commercialize novel drugs that bring new hope to cancer patients.

• CLICK HERE TO SUBMIT YOUR RESUME TODAY!

AVEO is an Equal Employment Opportunity employer that values the strength diversity brings to the workplace.

About AVEO

AVEO Oncology (NASDAQ: AVEO) is Passionate in Our Pursuit of Improving the Lives of Patients with Cancer. We are united in our efforts to provide patients with reasons to believe that they can receive effective treatments while carrying on with their daily living. AVEO Oncology is founded on a unique drug discovery and development approach called the Human Response Platform™. With it, we aim to translate cancer biology insights into next generation therapeutics targeted to specific patients living with cancer who will benefit most. The Human Response is more than a novel biology platform – it is our way of responding to the needs of the cancer community with integrity, fierce determination and compassion combined with the confidence that we will transform the lives of those impacted by cancer. This is the AVEO Way – The Human Response.

Agency Notice

AVEO Oncology does not accept unsolicited resumes from any third-party recruiters, agencies or individuals. Any such third party recruiters, agencies or individuals seeking to work with AVEO Oncology must first contact the staffing group at careers@aveooncology.com. Only approved staffing vendors will be allowed to provide services to AVEO Oncology. Unsolicited resumes will be deemed the property of AVEO Oncology to follow up with as it sees applicable and no fee will be paid in the event the candidate is hired as a result of the referral or by other means. Submission of unsolicited resumes does not create any implied obligation on the part of AVEO.

Responsible for planning and executing integration projects. The incumbent will utilize skills in mechanics, software, electronics, robotics, systems engineering and applications to design, develop, test, and install turnkey automation solutions using automation, liquid handling, detection and sample preparation devices for life science customers.

Responsibilities:

• Evaluate customer needs and adapt existing products with a minimum amount of alteration.
• Provide project quotes and planning
• Light CAD design for system architecture and hardware components
• Software scripting and test/debug, cabling/connectivity and applications testing

Qualifications:

• B.S degree in life science (e.g. molecular biology, cell biology, or biochemistry) or engineering (e.g. biomedical, systems) curriculum
• 5+ years total experience in a commercial life science company with demonstrated experience in designing and developing customized laboratory automation systems by integrating commercial components and devices such as hotels, incubators, plate sealers, washers and readers to the liquid handling robot
• Demonstrated ability to plan and execute in a fast-paced, dynamic team environment
• Excellent planning, customer relationship, and communication skills are a must
• Up to 30% travel is required

  PERKINELMER IS AN EEO/AA EMPLOYER 

PerkinElmer provides competitive compensation plans / Top notch training and development / Comprehensive benefits package / Paid time off and holidays / Generous tuition reimbursement plan / 401(k) with match and immediate vesting / An environment that fosters career growth.

Toxikon Corporation, originally founded in 1977, is a Contract Research and testing company with laboratories in Bedford, MA and Belgium.  Our mission continues to focus on providing quality services, competitively priced, with on-time delivery for the Pharmaceutical, Medical Device and Biotech industries. 

In this Quality Assurance role, the appropriate candidate will be responsible for the implementation, functioning, and monitoring of quality assurance activities in the Analytical and Bioanalytical Chemistry Depts. This includes monitoring biological and chemical studies, and creating reports in conformance with GLP practices.  Candidates will review both GLP and non-GLP reports for accuracy with reference to protocols, Quality Assurance Standards, Standard Operational Procedures, laboratory precision and accuracy limits, as well as reviewing all protocols for compliance and accuracy.  

Other quality assurance responsibilities include maintaining equipment performance, calibration records and preventative maintenance logs.  Included duties are performing system and phase audits according to GLP and ISO guidelines, as well as all other activities required from quality assurance.  

A bachelor’s degree in life sciences is required, preferably in Chemistry. Candidates should also have at least 2 years experience in an FDA regulated environment, with basic knowledge of study design and review practices.  Must have strong knowledge of a life science as well as documentation and coordination practices. Must be detail oriented and enjoy high work volume via computer.  

For additional information about Toxikon, please visit our website at www.toxikon.com.   

Submit resumes to:

Human Resources

Toxikon Corporation

15 Wiggins Avenue

Bedford, MA  01730

Email:              hr@toxikon.com

Toxikon employs 160 people and offers a generous benefit program including health, dental, fsa, std, ltd, life insurance and matching 401K plan. Toxikon is an EOE.

TESARO is a growing oncology-focused biopharmaceutical company whose passionate associates are dedicated to improving the lives of cancer patients by developing and providing safer and more effective therapeutics and supportive care products.

 Position Summary

The Senior Medical Writer will prepare clinical/regulatory documentation (protocols, study reports, sections of NDA/MAA in CTD format, etc.) to support successful submissions in the US, EU, and rest of world.  Reporting to the Head of Regulatory Writing, the Senior Medical Writer also may be responsible for oversight and review of clinical documentation prepared by vendors/contractors.  This position will be on-site at TESARO's office in Waltham.

 Responsibilities

• Produce clinical protocols, clinical study reports, summaries of safety/efficacy, other regulatory documents (annual reports, briefing documents), safety reports, Investigator brochures/updates
• Oversee clinical documentation as necessary for IND and/or NDA/MAA filing
• Ensure consistency of style, format, content for all IND and NDA documents
• Oversee quality and timely output of deliverables delegated to contracted personnel
• Ensure that all clinical study reports (Mod 5) at TESARO:

-   Comply with ICH, 21 CFR, GCP, pertinent local regulations

-   Adhere to SOP and guidance documents

-   Are completed in accordance to internal timelines

• Ensure accuracy of study-specific and department information disseminated both internally and externally.

Education/Experience

• Undergraduate degree in a scientific or health-related field required; graduate degree preferred
• Minimum 5 years of clinical research/drug development experience in biotech, pharmaceutical, or contract research organization (oncology experience a plus)
• Excellent organizational, managerial, and communication skills
• Self-motivated, assertive, self-confident, working under general supervision
• Resourceful, creative, energetic, results-oriented
• Ability to accept and integrate input from diverse sources and work effectively across multi-disciplinary work teams
• Must enjoy working in a fast-paced, small-company environment
• Working knowledge of GCP, 21 CFR, CTD, and ICH guidelines/regulations is required

Diagnostics For All (DFA) is an exciting non-profit organization focused on improving global health by creating and commercializing very low cost, easy-to-use, point-of-care medical diagnostic devices for underserved populations in the developing world.  Conveniently located in Cambridge, Massachusetts, we are creating a new generation of diagnostic devices using elegantly simple paper-microfluidics technology originally developed in the lab of Professor George Whitesides at Harvard University. DFA has received several grants to develop this technology from varied sources including the Bill & Melinda Gates Foundation, USAID, and DARPA.  Please learn more at www.dfa.org.

The Situation:

DFA is a group of committed scientists working collaboratively on number of projects from infectious diseases to vaccine surveillance to novel nucleic acid technologies.  DFA has a series of diagnostics tests in various stages of development; some tests are in concept stage, others are working prototypes and others are near completion with field tested clinical data behind them.  The atmosphere is informal but intense, with a real sense of urgency.

 DFA now needs to convert these late-stage tests into deliverable products, with the first product – a liver function test – due out this year

 Some Questions:

• Can you rapidly come up to speed on the liver function test first – understand the biochemical reaction, the paper based platform, the mechanics of the platform? 

• Are you interested in solving problems of minute detail, prepared to “go to the bench” if necessary, seek solutions from colleagues, consultants and the wider community, and take personal ownership? 

• Be able to design the minimum necessary experiments to optimize and validate the design for production?  And then deal with inevitable set-backs? 

• Have you built a product before? 

• Are you comfortable collaborating with a manufacturing sub-contractor to get a manufacturing line up and running, or modify an existing manufacturing line? 

• Will you recognize equipment gaps if present specify equipment and negotiate with suppliers for laboratory and test equipment necessary to complete this project?

• Can you work within an embryonic quality system and help build that quality system in to an appropriate one for DFA?  Be able to document a Design Control process and follow it?

•  In the future, take on wholly new tests with wholly new challenges and take them too into production?

 If you can answer yes to some of these questions and you are not put-off by them, then we would love to hear from you.  The right answers to these questions are more important than an MS or a PhD, but one of these could help you.  Ideally in the past you might also have shepherded a product through the 510k FDA process, or had experience of the clinical studies necessary.  None of this would you have to do on your own, you would be supported by a close knit team.  

If you are interested in an exciting opportunity to change the way health care is delivered in much of the world, contact us at careers@dfa.org.  Please reference PDE-001 in the subject line.

We are scientists, researchers, biotechnologists, physicians, and businesspeople working to bring new medicines to market. Faster. Because we know this isn't about us. It's about the millions of patients waiting to benefit from our discoveries Co-founded in 1994 by Garo Armen and Pramod Srivastava as Antigenics, our company has outgrown its name but never its raison d'être: to develop and commercialize breakthrough immunotherapies for cancer and infectious diseases.

Job Description:

This is a newly developed Executive Administrative position in which you would provide high level support and assistance to 2 of the organization’s Executives. We are seeking a highly competent Executive Assistant with a strong background in biotechnology/pharmaceuticals support and scientific acumen. 

• Manages calendars; schedules meetings, makes travel arrangements and manages expense reporting  for executives and others.
• Accountable for meeting planning and organization (schedule attendees, books conference rooms, arrange catering, prepares presentations, compiles notebooks, meeting materials, handouts, etc.).
• Provides phone support; assumes responsibility for copying, faxing etc. 
• Creates and distributes general correspondence, letters, memos, charts, graphs, contracts, agreements, minutes, spreadsheets reports, and assists in presentation building.
• Proactively responds to questions, concerns, and requests for information and resolves routine questions and information requests.
• Manages the administrative priorities of senior executives, solves conflicting priorities.
• Ad hoc projects, as assigned, including involvement in Board meetings.
• Works on complex problems in which analysis of situations or data requires an in-depth evaluation of various factors.
• Exercises judgment within broadly defined practices and policies in selecting methods, techniques and evaluation criteria for obtaining results.

Desired skills and Experience:

• Must have bachelor’s degree.
• Must have experience supporting senior level management in a complex environment;  5+ years preferred.
• Extensive and advanced working knowledge of MS Outlook, Word, Excel & PowerPoint.
• Strong interpersonal skills; position continually requires demonstrated poise, tact, and diplomacy.
• Must be able to interact and communicate effectively with individuals at all levels of the organization up to and including Board level.
• Confident, self-starter who can work well with minimum supervision
• Requires strong attention to detail in composing and proofing materials, establishing priorities, scheduling and meeting deadlines
• Must be able to work in a fast paced environment with demonstrated ability to simultaneously manage multiple competing tasks and demands.
• Must be flexible in handling multiple tasks of a different nature and have the ability to prioritize efficiently.
• Problem solver who is quick to figure solutions and make things happen.
• Must be able to handle confidential information and issues effectively and without breach of confidentiality.
• Makes decisions concerning business priorities on Executive’s calendar, as well as decisions on operational arrangements for meetings.

The Vertex Medical Writing group is located in Cambridge, MA. The Manager of Medical Writing Operations has the opportunity to lead a dynamic team of quality-minded professionals to improve the quality of clinical and regulatory documents.  The Manager is responsible for the day-to-day operations of the QC team, planning and resourcing QC reviews, and applying technical expertise to develop solutions to complex problems. In addition, the Manager is expected to oversee the development, implementation, and maintenance of business processes for Medical Writing.

The Medical Writing Operations Group is responsible for quality control review of documents authored by Medical Writing; creating and compiling clinical study report (CSR) appendices; editing and formatting documents; developing and maintaining Medical Writing processes, including document templates and SOPs; supporting Medical Writers with computer applications and dependent work flows; providing expertise in formatting documents for submission to regulatory authorities; and innovating and training on Medical Writing processes.

Key Responsibilities
- Provides guidance and leadership for the Medical Writing Operations group
- Manages activities of direct reports and contractors
- Maintains a high level of knowledge related to current developments in the field, including pharmaceutical regulations pertaining to documentation for regulatory submissions

Prepares and delivers effective presentations for internal and external audiences, as needed
- Participates in discussions regarding Medical Writing process strategy
- Represents Medical Writing on cross-functional teams, including those related to document quality control, formatting, and electronic submissions
- Has solid technical and analytical skills and is able to recommend changes to or troubleshoot systems
- Continually evaluates and improves processes
- Contributes to the design of functional area goals
- Provides Medical Writing management with updates on resourcing and metrics for Medical Writing Associates’ work
- May be required to supervise other Medical Writing staff

Minimum Qualifications:
- A bachelor’s degree and 5+ years of work experience in the pharmaceutical industry;
- Or a master’s degree and 4+ years of experience in the pharmaceutical industry
- Direct supervisory experience

Preferred Qualifications:
- 5+ years of work experience in a quality control, quality auditing, medical editing, regulatory writing, or medical writing function in the pharmaceutical industry
- Proven ability to manage teams working on complex tasks
- Proven ability to design and/or execute procedures and communicate those procedures to others
- Demonstrates an in-depth understanding of applicable regulations
- Displays ability to influence within technical area of expertise
- Proven ability to manage projects of moderate scope and complexity
- Exhibits understanding of technical disciplines beyond own specialty area
- Proactively identifies and resolves problems
- Demonstrates strong oral and written communication skills

Vertex creates new possibilities in medicine. Our team discovers, develops and commercializes innovative therapies so people with serious diseases can lead better lives. Vertex scientists and our collaborators are working on new medicines to cure or significantly advance the treatment of hepatitis C, cystic fibrosis, rheumatoid arthritis and other life-threatening diseases. Founded more than 20 years ago in Cambridge, Mass., we now have ongoing worldwide research programs and sites in the United States, United Kingdom and Canada. Vertex has consistently been recognized as one of the industry's top workplaces by leading publications such as Science magazine, The Boston Globe, Boston Business Journal, San Diego Business Journal and The Scientist.

For more information and to view Vertex's press releases, please visit www.vrtx.com.

Vertex is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person’s race, color, gender, age, religion, national origin, ancestry, disability, veteran status, genetic information, sexual orientation or any characteristic protected under applicable law. Vertex will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law.

To Apply for this position, please CLICK HERE

https://home.eease.adp.com/recruit/?id=3708961

Research Associate

Toxikon Corporation, originally founded in 1977, is a Contract Research and testing company with laboratories in Bedford, MA and Belgium. Our mission continues to focus on providing quality services, competitively priced, with on-time delivery for the Pharmaceutical, Medical Device and Biotech industries.

Seeking Research Associates to work in our expanded medical device, pharmaceutical, and biotechnology testing facility. Responsibilities include data collection and recording, data package preparation, sample preparation, dosing, bleeding, necropsy and surgical assistance. Prior animal, research, and/ or animal laboratory experience is preferred. Must be willing or have experience in working with large animal models. Excellent communication skills needed as this position works closely with other research associates, scientists, veterinarians, and regulatory affairs. Studies are conducted under numerous guidelines, protocols, and Standard Operating Procedures. Requirements include ALAT certification and/or bachelors degree in a life science and 2-5 years experience, however willing to train the right candidate.

For additional information about Toxikon, please view our website at www.toxikon.com

Submit resumes to: 

Human Resources

Toxikon Corporation

15 Wiggins Avenue

Bedford, MA 01730

Fax: (781) 271-1137

Email: hr@toxikon.com

Toxikon employs 160 people and offers a generous benefit program including health, dental, fsa, std, ltd, life insurance and matching 401K plan. Toxikon is an EOE.

Harvard Medical School invites applications for the position of Analytical Chemist. Under supervision by senior faculty, this position will be responsible for establishing and operating an analytical chemistry core facility serving investigators from Harvard Medical School and other Longwood-based institutions. The facility will focus on analysis of diverse small molecules (molecular mass

The Analytical Chemist will have a high degree of independence, opportunities to work on collaborative projects with senior investigators, and opportunities to present results in meetings and publications.  Key responsibilities will include performing routine analytical analysis of samples submitted by multiple users, HPLC purification of samples submitted by multiple users, developing more complex analytical methods in the context of a research collaboration, and direct oversight of the workflow and instrumentation needed to accomplish these purposes.

Candidates should hold a Ph.D. in Analytical Chemistry, have a thorough knowledge of chromatographic and mass spectrometry techniques (HPLC, MS, and NMR), and be able to perform routine maintenance and repair of HPLC and MS instrumentation. The position requires attention to detail; excellent communication, interpersonal, and administrative skills; and demonstrated ability to work productively with a diverse set of investigators, including many non-specialists.

Interested parties should submit a letter of application, curriculum vitae, and references to:

Dr. Su Chiang, Ph.D.

Seeley Mudd 604, Harvard Medical School

250 Longwood Avenue

Boston, MA 02115

Our client is seeking a Research Associate to perform laboratory experiments in a product development, molecular biology and assay development setting.  In this position you will have an opportunity to analyze, review and evaluate data to form conclusions and present findings in oral and written form.  You will also assist in the development of new analysis methods.  This position requires an individual who can maintain accurate and precise records and laboratory notebooks.  This position requires a BS or MS in molecular biology or microbiology with previous experience with molecular diagnostics.  Previous experience with real-time PCR & instrument usage, such as TaqMan is required.  Experience in purifying nucleic acids, cloning & gel electrophoresis is also required. 

Whether you are seeking a career change or simply interested to become part of our network, you will appreciate the ethics guiding each StratAcuity team member. We build lasting relationships with exceptional scientists and take great care to protect your personal information. Upon receiving your inquiry, you may be directly contacted by a StratAcuity team member to discuss your career goals. We will not share your information with anyone without your direct prior consent.

StratAcuity, CHEMISTRY IS EVERYTHING.

We are searching for an experienced Chemist with laboratory experience in QC to lead analytical experiments using HPLC. 

• Bachelor's or Master's Degree in Chemistry or scientific background.
• 3-5 years experience in QC/R&D background using HPLC and other analytical instruments.
• Attention to detail, proactive attitude, sense of urgency and ownership over the project
• Industry experience in a GMP environment, preferably pharmaceuticals. Familiarity with change control, investigation, deviation and CAPA processes.

Local Biotech company is searching for a Batch Record Specialist for a contract position immediately available. The successful candidate will be performing batch record, Quality Control data and raw material review and disposition. Review, assessment and approval of Quality System documents such as deviations, OOS and environmental excursions is also required. Additional responsibilities may include release of packaged product to Distribution, document change review and approvals and conducting audits.

KEY RESPONSIBILITIES

• Perform the review of production and cell bank batch records, Quality Control data, data forms, raw materials and other associated documentation. Identify discrepancies and works to obtain correction of the discrepancies with the responsible individual(s) or teams.
• Enter raw material and product lot information and data into the MBR database(s).
• Review and approve deviations, OOS and EM Excursions.
• Assist in the transfer of finished products, from the Manufacturing group to the Distribution/Shipping group.

PREFERRED EDUCATION AND EXPERIENCE

Bachelor of Science Degree in a scientific discipline preferable, with a minimum of 3-6 years of related experience in a GMP/GLP regulated environment. Previous batch record review experience is required.

Functions:

Identify and evaluate potential new business opportunities to sell the Company’s products to other companies to be used by them on an OEM basis and/or license Company’s intellectual property to third parties. Initiate and develop productive client relationships in multiple functions (e.g R&D, in-licensing, production, procurement, marketing, quality, regulatory affairs) with client companies and at multiple levels within them (scientist, project manager, manager and occasionally executive levels), as may be necessary.  Develop pricing proposals for large, complex, often multi-year deals and contracts. Make highly informed judgments of value to the customer upon which to develop pricing proposals for highly customized products, for which easy benchmarks are often unavailable. Negotiate other terms and conditions. Coordinates technical support to determine client needs, respond to inquiries, and resolve problems in a timely fashion. Investigates product issues and ensures satisfactory resolution of customer complaints.

Background:

Requires a bachelor’s degree in any life science, or the equivalent combination of education and experience. Advanced degree and/or MBA preferred.Requires a minimum of 5 years of international sales experience as well as experience with diagnostics. Knowledge of intellectual property
landscape. Demonstrated ability to lead teams without being the manager both internally and externally. Experience integrating complex products with third party solutions. Advanced regulatory and compliance knowledge and experience. Demonstrated proficiency with computer applications,
including word processing, spreadsheet, and slide presentations required.

Candidates must live local and be a US Citizen or Green Card Holder
 
Email resume to: jobs@cwsciences.com
 
Commonwealth Sciences is a professional recruiting firm specializing in Science, Engineering and Green Technologies. We unite industry professionals with exciting career opportunities by leveraging our technical expertise, advanced recruiting tools and years of staffing experience. CWS works with a
variety of disciplines and levels from Research Associates to Scientists, Engineers, Managers and Directors. Our clients value the basic integrity, customer service and industry expertise that defines our organization.
 
Commonwealth Sciences, Inc.
www.cwsciences.com

Description:
 
Candidate will join a group focused on the development of a diagnostic. Responsibilities will include developing and troubleshooting assays and protein purification and characterization.

Candidates must live local and be a US Citizen or Green Card Holder
 
Email resume to: jobs@cwsciences.com 
 
Commonwealth Sciences is a professional recruiting firm specializing in Science, Engineering and Green Technologies. We unite industry professionals with exciting career opportunities by leveraging our technical expertise, advanced recruiting tools and years of staffing experience. CWS works with a variety of disciplines and levels from Research Associates to Scientists, Engineers, Managers and Directors.
Our clients value the basic integrity, customer service and industry expertise that defines our organization. 
 
Commonwealth Sciences, Inc.

www.cwsciences.com

Candidate will perform chromatography immunoassay and other analytical method development in support of vaccine process and product development programs. 

Requirements:Experience with protein characterization techniques and associated instrumentation such as HPLC/UPLC (RPC, SEC, IEX), Mass Spectrometry, Capillary Electrophoresis, etc.
Hands-on experience with bioanalytical assay development and qualification of large molecule, such as ELISA, Western Blot
MS/PhD – 2+ years relevant experience 

Candidates must live local and be a US Citizen or Green Card Holder

Email resume to: jobs@cwsciences.com 

Commonwealth Sciences is a professional recruiting firm specializing in Science, Engineering and Green Technologies. We unite industry professionals with exciting career opportunities by leveraging our technical expertise, advanced recruiting tools and years of staffing experience. CWS works with a variety of disciplines and levels from Research Associates to Scientists, Engineers, Managers and Directors. Our clients value the basic integrity, customer service and industry expertise that defines our organization. 

Commonwealth Sciences, Inc.
www.cwsciences.com

Candidate will join a team dedicated to the discovery of drug products.

Requirements:

BS/MS with 3+ years experience using techniques including qPCR, ELISA and westerns
 

Candidates must live local and be a US Citizen or Green Card Holder

Email resume to: jobs@cwsciences.com

Commonwealth Sciences is a professional recruiting firm specializing in Science, Engineering and Green Technologies. We unite industry professionals with exciting career opportunities by leveraging our technical expertise, advanced recruiting tools and years of staffing experience. CWS works with a variety of disciplines and levels from Research Associates to Scientists, Engineers, Managers and Directors. Our clients value the basic integrity, customer service and industry expertise that defines our organization.

Commonwealth Sciences, Inc.
www.cwsciences.com

• Expression and purification of recombinant HIV-1 proteins, IgGs and Fabs, and characterize protein-antibody interactions.
• Design of novel HIV antigens using protein structure knowledge
• BS/MS with 1-2 years of experience in protein expression in eukaryotic expression systems,
• protein purification and characterization.
• Knowledge of analytical techniques such as AUC, SPR, RP-HPLC, SE-HPLC and MALS is highly desirable.

Candidates must live local and be a US Citizen or Green Card Holder

Email resume to: jobs@cwsciences.com

Commonwealth Sciences is a professional recruiting firm specializing in Science, Engineering and Green Technologies. We unite industry professionals with exciting career opportunities by leveraging our technical expertise, advanced recruiting tools and years of staffing experience. CWS works with a variety of disciplines and levels from Research Associates to Scientists, Engineers, Managers and Directors. Our clients value the basic integrity, customer service and industry expertise that defines our organization.

Commonwealth Sciences, Inc.
www.cwsciences.com

Duties:
Troubleshoot problems with antibody-related applications (western blot, ELISA, IHC, etc) and provide optimal solutions to customers. Candidate will answer technical inquiries and product complaints by phone, working toward department goal of eliminating missed calls.

Requirements:
B.S. in a life sciences field with 2+ years experience with Western Blots.
Must have strong communication skills and willingness to work in a customer liason capacity.

Candidates must live local and be a US Citizen or Green Card Holder
 
Commonwealth Sciences is a professional recruiting firm specializing in Science, Engineering and Green Technologies. We unite industry professionals with exciting career opportunities by leveraging our technical expertise, advanced recruiting tools and years of staffing experience. CWS works with a variety of disciplines and levels from Research Associates to Scientists, Engineers, Managers and Directors.
Our clients value the basic integrity, customer service and industry expertise that defines our organization.
 
Commonwealth Sciences, Inc.
 
www.cwsciences.com

Description:  Candidate will be responsible for developing, performing and evaluating viral antigen purification to support vaccine development  

Requirements:  BS/MS with 1-3 years experience with protein biochemistry Experience with viral particle and protein purification Experience with HPLC and FPLC

Candidates must live local and be a US Citizen or Green Card Holder

Email resume to: jobs@cwsciences.com

Commonwealth Sciences is a professional recruiting firm specializing in Science, Engineering and Green Technologies. We unite industry professionals with exciting career opportunities by leveraging our technical expertise, advanced recruiting tools and years of staffing experience. CWS works with a variety of disciplines and levels from Research Associates to Scientists, Engineers, Managers and Directors. Our clients value the basic integrity, customer service and industry expertise that defines our organization.

Commonwealth Sciences, Inc.
www.cwsciences.com