This is a benefit for CBSA Members. If you would like to post your available positions or internships, please submit it along with a brief statement to Mae Desaire. If your company is not a member, we will still post a field related position for $100.00 each.

Internship Resources and Programs

Posted 8/30/2010

Novus Biologicals

Senior Lab Technician:  Novus is seeking an experienced scientist to join our Antibody Quality Control department.    The position requires extensive experience in antibody characterization techniques including Western blot, Immunocytochemistry, cell culture and FACs.  Experience in chromatin IP a plus.  Candidate must be able to work independently, be extremely detail oriented, have experience troubleshooting antibody techniques and be able to prioritize and meet deadlines.  Advanced degree preferred but not required.  Minimum three to five years lab experience required.  Salary commensurate with experience. Please send CV or resume and cover letter to jobs@novusbio.com

Novus offers competitive benefits for all full-time employees, including:

• 100% employer paid medical and dental insurance premiums for employee, with reduced premiums for families
• Profit sharing/401K,  long term disability, life insurance

Novus Biologicals, LLC
PO Box 802
Littleton, CO 80120
jobs@novusbio.com

Posted 8/30/2010

An Aerotek client is looking for a Research Scientist (Biochemistry), based in Englewood, Colorado.  The protein biochemist will independently provide analysis and characterization of enzymes relevant for the production of C4-C5 alcohols in engineered yeast. He/she will provide enzymology data for the biocatalyst development as well as for the fermentation team.

Requirements include:
• PhD Biochemistry
• 5 - 10 years of work experience in a lab, working with Biochemical Research.
• At least 3 years of work experience, working with Protein characterization, as well as Assay and screen development.
• Would prefer candidate with at least 50% of experience acquired in private industry, as well as having experience in project and people management.
• Strong background in biochemistry.
• Extensive knowledge of protein chemistry.
• Demonstrated ability to purify proteins.
• Demonstrated ability to work under strict timelines.
• Working in a team oriented environment.
• Demonstrated ability to quickly learn and apply new concepts and techniques.
• Ability to interpret experimental results to assess success of experiments.

Responsibilities include:
• Development of in vitro enzyme activity assays
• Author and review SOPs for enzyme analysis
• Review and troubleshoot results of enzyme assay analysis of fermentation samples
• Measurement of enzyme kinetics
• Detailed enzymological studies
• Preparation of samples for HPLC and GC analysis
• Interpretation of biochemical and analytical data
• Protein purification (AKTA, IEC, SEC, HIC, AFC)
• High throughput assay development
• Use of automated liquid handling equipment

This is an immediate, full time opportunity - if interested please immediately contact Nesli Orhon at 303.224.4558 or email in a resume to norhon@aerotek.com

Posted 8/26/2010

Analytical Chemist, 1-2 years experience

Aerotek Scientific is actively seeking Analytical Chemists in Boulder, Colorado.

Qualified candidates will offer the following:
-Strong knowledge of HPLC
-Experience in a GMP environment
-Large Protein experience
-Previous experience with Electronic Lab Notebooks

Interested candidates, who meet the above qualifications, please email a copy of your Microsoft Word formatted resume to jhertzbe@aerotek.com.

Posted 8/26/2010

Bionovo, Inc. is a drug discovery and development company focused on developing safe and effective drugs for the treatment of unmet medical needs in women’s health and cancer. Our mission is to improve the quality of women’s health and defeat life-threatening cancers.  www.bionovo.com
Current Openings in Colorado (due to an expansion)
Analytical QC Chemist
Research Scientist
Job Title:  Analytical QC Chemist
Responsibilities:

• Perform routine sample preparation and analysis with experience in at least 1 of the following instrumentation; (ICP-MS, AAS, GC-MS, LC-MS/MS), for in-process, finished, stability, raw materials and various biological samples created during R&D and process development activities.
• Assay (ICP-MS, AAS, GC-MS, LC-MS/MS) development and validation.
• Troubleshooting skills for routine instruments, equipments and data interpretation.
• Follow SOPs and maintain good documentation during work: data management and maintenance to ensure compliance for audit preparation.
• Write analysis reports and data QC or review.

Requirements:

• BS degree in analytical chemistry or a related science with a minimum of 2 years experience in a research/pharmaceutical environment on small molecular analysis.
• Familiar with GMP/GLP and FDA requirements and possess good documentation skills.
• Strong organizational and professional communication skills with team members internally, externally, and cross-functionally.
• Person needs to be highly motivated and flexible, with excellent problem solving and interpersonal skills. The ability to work as part of a small team with other scientists and analysts are essential.

• Select individual must be: detail orientated, high attention to accuracy, team player, and ability to multi-task.

• Administrative: Must be proficient in the use of a computer as well as Microsoft Office applications.
• Fluent in English and able to write SOPs, reports, etc.
• Salary commensurate with skills and experience.

Standard work week is Monday through Friday.
Email resume to: kim.plath@bionovo.com

Job Title:  Research Scientist
Responsibilities:

• Perform routine various biological sample preparation and analysis by multiple instrumentations: ICP/MS, AAS, GC/MS and/or LC-MS/MS for heavy metals, aflatoxins, pesticides and/or profiling of small molecules.
• Develop, validate and implement methods for heavy metals, aflatoxins, pesticides and/or profiling of botanical raw materials with ICP-MS, AAS, GC-MS and/ or LC-MS/MS.
• Trouble shooting for instrumentation and data interpretation.
• Review and update SOPs
• Write method development and validation reports
• Review and QC data

Requirements:

• M.S. or Post Doc in Analytical Chemistry with at least 2 yrs. of industry experience
• Preferred instrumentation experience with ICP-MS, AAS, GC-MS and/or LC-MS/MS.
• Development and execution of methods and quality control of botanical raw materials.
• Strong GMP/GLP experiences at pharmaceutical or related areas.
• Select individual must be: detail orientated, high attention to accuracy, team player, and ability to multi-task.

• Person needs to be highly motivated and flexible, with excellent problem solving and interpersonal skills. The ability to work as part of a small team with other scientists and analysts are essential.

• Administrative: Must be proficient in the use of a computer as well as Microsoft Office applications.

• Fluent in English and able to write SOPs, reports, etc.
• Salary commensurate with skills and experience.

Standard work week is Monday through Friday.
Email resume to: kim.plath@bionovo.com

Posted 8/20/2010

SomaLogic is a recognized industry leader in producing high quality, revolutionary health care products based upon biomarker discovery. Our innovative clinical diagnostics using our proprietary SOMAmer technology platform will revolutionize diagnosis and treatment in clinical medicine.

Building a team of bright, energetic, and committed individuals, SomaLogic is dedicated to shaping the future of clinical diagnostics.

 Senior Accountant Position Summary:

This position will be responsible for general accounting functions in a medical diagnostic device company. Reporting to the Corporate Controller this individual will work in the areas listed under key responsibilities.

Key Job Responsibilities:

• Accounts Payable
• General Ledger
• Account Reconciliations
• Monthly Closing
• Systems Implementation
• Government Grant Management/Accounting
• General Revenue and Project Management

Contributes to positive work environment, this includes but is not limited to:

• Able to work in a team environment in a scientific environment
• Communicating with others in a courteous and professional manner
• Accepting and completing specific projects as assigned by the Controller

Education and Experience:

• Degreed Accountant (CPA preferred)
• 5 plus years of accounting experience
• Strong Excel skills
• Quick Books preferred but not required
• Public accounting a plus

Physical Requirements:
The physical demands of the position are those required in a typical office environment. 

We offer competitive salaries, comprehensive benefits including a 401(k) plan, relocation assistance, and stock options commensurate with level of responsibility.

Apply to careers@somalogic .com

LABS

Posted 8/5/2010

LABS’ has a temporary position open for Senior Microbiologist with a minimum of 7 years of experience. This position will work in our Research & Development department. Job functions include process and develop validations, microbial log and reduction study. Flexibility in shift is helpful – days and/or mid shift Monday - Friday. If you are interested in this position please send resume to resumes@labs-inc.org.

Fitzsimons Redevelopment Authority (FRA)

Posted 8/3/2010

Request for Proposals

Industry Analysis/Technology Evaluation Services

The FRA is seeking proposals from qualified consultants to complete a database and website development project as needed for the development of the Colorado Institute for Drug Device and Diagnostic Development (www.cid4.com) under a grant from the Small Business Administration. 

Scope of Work:
Consultant will be responsible for developing a database of industry data to assist CID4 in making decisions about investment opportunities. In addition, the consultant will be responsible for transitioning the CID4 website to a new server and redesigning the site to be more easily usable by visitors.  He/she will also assist in developing new content for the site.  The consultant will be responsible for working with and evaluating an industry database that will be purchased by CID4, with the objective of making it a useful tool in the technology evaluation and selection process.

Proposals must be received by FRA by close of business on or before August 13, 2010.   Proposals and questions should be addressed to jfarnham@colobio.com and kevin.smith@cid4.com

Technology Evaluation/Therapeutic Drug Development Consulting Services

The FRA is seeking proposals from qualified consultants to undertake technology evaluation and therapeutic drug development projects as needed for the development of the Colorado Institute for Drug Device and Diagnostic Development (www.cid4.com) under a grant from the Small Business Administration. 

Consultant will be responsible for developing due diligence materials and processes to evaluate therapeutic drug development proposals to assist CID4 in making decisions about investment opportunities. In addition, the consultant will be responsible for developing detailed pre-clinical and clinical development plans for two to three projects that will include CMO and CRO selection, animal and clinical trial protocol development, pre-IND and IND package preparation, and budget and timeline projections.

Proposals must be received by FRA by close of business on or before August 13, 2010.   Proposals and questions should be addressed to jfarnham@colobio.com and richard.duke@cid4.com

Clovis Oncology, Inc.

Posted 8/3/2010

Manager, Pharmaceutical Development
Boulder, CO or San Francisco, CA

Clovis Oncology is a biopharmaceutical company focused on acquisition, development, and worldwide registration and marketing of new cancer therapies.  The company leverages expert contract research and manufacturing services for activities related to development and manufacturing.

The Manager, Pharmaceutical Development position will be responsible for definition and management of contractor activities related to development and manufacturing of drug substances and/or drug products, and development and validation of analytical methods.  The scope of work will support products all stages of development up to and including commercialization.  Some travel, possibly international, will be required.
Responsibilities will include:

• Identification and resolution of technical challenges in the areas of drug substance process development and manufacturing, drug product formulation development, drug product process development and manufacturing, analytical method development, and technology transfer
• Creation and execution of CMC development plans for new products
• Creation and execution of process (drug substance and drug product) and analytical method validation plans
• Identification and management of contract research and contract manufacturing organizations to support product development
• Coordination with supply chain and clinical operations groups for production of clinical trial materials
• Assistance in batch record review
• Assistance in deviation investigations
• Assistance in the preparation and review of regulatory documentation
• Assistance in due diligence technical assessments of potential new products

If you would like to submit a resume for our files, please send a resume and a cover letter to: careers@clovisoncology.com

Sharklet Technologies, Inc.

Posted 8/3/2010

MICROBIAL RESEARCH ASSOCIATE

BASIC REQUIREMENTS:
1) M.S. degree in microbiology, environmental science or related field or BS with 2 years experience in relevant laboratory or field research;
2) Knowledge of and experience with research methods in microbiology, experimental design, and statistical data analysis.
HOURS: 25 hours a week, Monday - Friday, Weekends, Holidays, Evenings, Overtime as required

Conduct research related to the microbiology of alternative antimicrobial technologies.

Qualified applicants should submit a CV/resume and a cover letter to:
Shravanthi Reddy
Director of Research
Sharklet Technologies, Inc.
sreddy@sharklet.com

SomaLogic

Posted 8/2/2010

SomaLogic is building a team of bright, energetic, and committed individuals dedicated to shaping the future of clinical diagnostics. We offer competitive salaries, comprehensive benefits including a 401(k) plan, relocation assistance, and stock options commensurate with level of responsibility. SomaLogic is an equal opportunity employer.

Current Openings:
Analytical Chemistry Lab Tech 1 - Temp - As a scientist you will to join the Analytical Chemistry Group.  Primary responsibilities for this position include following SOPs to analyze raw materials and prepare media/reagents, and monitoring/maintaining laboratory inventories. Attention to detail is critical.  Experience with basic biochemical techniques (spectrophotometry, gel electrophoresis, and dialysis) plus data base and GLP experience is helpful.  A BS in biochemistry or a related field and a minimum one year relevant experience is required. Duties include:

• QC analysis of raw materials and reagents
• preparation of media and reagents
• monitoring/maintaining laboratory inventories
• data base entry

Education and Experience:

• BS with a minimum of 1 year experience
• Degree in biochemistry or related field
• The candidate must possess excellent analytical skills
• Detail oriented
• Excellent interpersonal, communication, planning and organizational skills
• Able to working in a cross-functional team environment
• Strong initiative and a can-do attitude
• Experience with basic biochemical techniques (spectrophotometry, gel electrophoresis, and dialysis)
• experience with data bases and GLP

Chemistry Research Associate - 4 month assignment - We are looking for an experienced scientist to join the Nucleic Acid (Aptamer) Chemistry Group. Primary responsibilities for this position are synthesis, purification, and characterization of synthetic oligonucleotides. Secondary responsibilities include supporting research chemistry projects and developing novel methods for modified nucleic acids. Duties include:

• Synthesis of oligonucleotides using automated synthesizers
• Purification of oligonucleotides.
• Running automated analytical systems to characterize new batches of oligonucleotides
• Documenting, filing, and tracking oligonucleotide process steps and experimental results
• Support of related chemistry research projects

Education and Experience:

• Degree in chemistry, biochemistry, or related field
• BS or MS with a minimum of 4 years research experience
• The candidate must possess a knowledge of nucleic acid synthesis and purification methods
• The position requires a working knowledge of organic chemistry
• Applicants should be skilled in basic computer programs for analyzing and presenting data. 
• Excellent written and verbal communication skills are required. 
• Applicants should have desire to work collaboratively and effectively in a team oriented, fast-paced environment

Applications may be submitted using the following methods:
By fax: 303-449-1057, Attn: Human Resources
By e-mail : careers@somalogic.com

Novus Biologicals

Posted 7/28/2010

Customer/Technical Service Representative - Littleton, CO

Novus Biologicals is seeking a full-time Customer Service/Technical Service Representative to join our rapidly growing, Littleton, CO based company.  The ideal cadidate will have a scientific degree as well as an outgoing and upbeat phone personality.  The job will entail answering calls and taking customer orders as well as answering pre-sale and post-sale technical questions.  Training will be provided, but actual lab experience working with antibody assays is a definite plus.

Novus offers fully paid employee healthcare and dental coverage as well as long term disability and 401K match.  We have a very fast paced, yet casual work environment where customer service is a key to our success.  Interested candidates should email their resumes to jobs@novusbio.com.

Merck

Posted 7/7/2010

Laboratory Manager

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.

The Lab Manager will cover the following site-specific issues: Lab Equipment and Instruments: The lab manager will be responsible for laboratory equipment support for the site, which includes equipment and instruments in R&D and Analytical Services. This includes selection, service, calibration, repairs, spares parts inventory, maintenance of the Merck required instrument qualification status. Lab Safety: The lab manager will over see the implementation and maintenance of the various EHS initiatives surrounding lab safety at Merck. They will be accountable to the EHS department and site management in these areas. Lab Operations Support: The lab manager will provide laboratory operations support to R&D and AS. This includes procurement, storage, use, and disposal of materials used in these labs. They will also provide an interface to the Technical Services department for Work Orders, projects, etc.

Responsible for securing and managing resources for multidisciplinary projects, with the objective to effectively manage the change process by ensuring the achievement of projects to time, cost and specification. At the higher levels the incumbents manage large multifaceted projects; at the lower levels incumbents may be concerned with clearly identifiable elements or functions within a larger project. Typically incumbents matched to this function are working towards or have achieved certification in project management.

Leads or coordinates cross-functional research science project/program teams conducting basic theoretical and experimental scientific and technological investigation directed toward the acquisition of new knowledge. Ensures successful project/program completion and implementation as defined by the research science leadership. Monitors performance and recommends schedule changes, cost adjustments or resource additions. Investigates facts and develops solutions to problems during the design and planning phases. Provides timely and accurate information and status updates to research leadership. Participates in budget development and evaluating how project plan changes impact cost and schedule

Provides technical support to engineers and scientists on a variety of technical tasks. Working with EHS, prepares and maintains written standard operating procedures (SOPs) and job safety analyses (JSAs). Modifies, refines, adapts, or develops lab techniques and analytical procedures to meet specific experimental goals. Installs, operates, maintains and repairs laboratory test equipment, apparatus and systems, and maintains laboratory supplies.
Selects and procures instrument spare parts to minimize instrument downtimes. Coordinates calibration with outside contractors for equipment that can not be done internally. Provides business technical support for Laboratory Information Management System (LIMS) including development of templates, providing system generated reports, and daily resolution of customer system issues.
Conducts laboratory support functions such as stocking and distributing supplies and equipment; arranging and dismantling apparatus; and collecting, washing, and storing glassware. Performs technical and record keeping duties in conformance with company and regulatory policies and standards to meet quality and accuracy requirements. May analyze compounds and manage corporate compound collection. Performs technical procedures in one or more of the following areas: Production, Research and Development, Quality Control/Assurance, and/or Compliance/Environmental.

EDUCATION: B.S., B.A., or M.S. degree in Science, Engineering or Business or equivalent experience. EXPERIENCE: At least five years of manufacturing, quality control, or staff support experience or equivalent. The successful candidate must demonstrate a strong working knowledge of pharmaceutical laboratory GMP's/GLP's and be familiar with pharmaceutical/biopharmaceutical manufacturing and bulk chemical operations. Strong written and verbal communication skills, as well as interpersonal skills and proven project management skills are also essential. In addition, the successful candidate must have the ability to demonstrate leadership and problem solving skills in a team based environment.

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.ecentralmetrics.com/url/?u=7534366324-187 to create a profile and submit your resume for requisition # RES000870 Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.

Search Firm Representatives Please Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

AmideBio

Posted 6/28/2010

Research Scientist (Biotechnology)
Company:    AmideBio,  LLC,  an early stage biotechnology company, specializing in novel manufacturing of peptides and proteins. (www.amidebio.com)
Location:    Boulder, CO

Job Description:
A full-time contract position with the possibility of permanent employment.  Job responsibilities include all phases of gene cloning, protein expression and purification to produce company products and various custom proteins including quality control.  Job will also include all aspects of lab and equipment maintenance, ordering and organization of lab supplies, record keeping, interaction with customers and filling of orders.

Requirements:
Bachelors Degree in Biology or related science and minimum of 5 years industry experience in cloning, protein expression and purification from E. coli.  Candidate should be familiar with a variety of chromatography methods/resins and with other protein purification equipment and techniques.

Expertise in basic molecular biology techniques, such as PCR, RT-PCR, plasmid minipreps, subcloning, protein quantitation, bacterial cell culture, SDS-PAGE, and western blots. Experience in FPLC and HPLC desired.

Proficient with standard MS Office tools (Word, Excel and PowerPoint).
Excellent communication skills, both written and oral.
Self-starter - ability to work independently.

Compensation:
Salary commensurate with skills and experience.

Application:    Email résumé and cover letter to hramidebio@gmail.com.

OPX Biotechnologies, Inc.

http://opxbiotechnologies.com/careers/

Posted 6/23/2010

Scientist, Strain Development:  Requires a PhD in biochemical engineering, molecular biology or related field; a Masters plus 3+ years experience; or equivalent combination. 

Scientist, Genomics:  Requires a PhD in biochemical engineering, molecular biology or related field; a Masters plus 3+ years experience; or equivalent combination. 

Research Associate, Genomics:  Requires a Bachelors degree in molecular or microbiology with 3+ years related work experience or equivalent combination. 

Research Associate, Biochemistry:  Requires a Bachelors degree in biochemistry or molecular biology with 3+ years related work experience or an equivalent combination.

Research Associate, Quantitative Physilogy:  Requires a Bachelors degree in chemical engineering, molecular biology or related field with 3+ years related work experience or an equivalent combination. 

Fermentation Microbiologist: This position provides industrial microbiology expertise in the areas of fermentation, process development, process scale-up and contamination control/mitigation.

Take your next career step with OPXBIO, where a collaborative and creative environment is producing economically viable and environmentally friendly bio-products.  We offer a competitive total compensation package including health/dental insurance, life & disability coverage, a 401(k) plan with company match, incentive and stock option programs.  OPXBIO is an Equal Opportunity Employer.  Please apply by email to resumes@opxbio.com.

AlloSource

Process Equipment Specialist I

Posted 6/15/2010

To apply, please visit: https://home.eease.adp.com/recruit/?id=508160

POSITION PURPOSE:
Perform scheduled calibration and maintenance of all measurement and test equipment enrolled in the Equipment Management System. Ensure the timely completion of scheduled work in accordance with established work instruction, standard operating procedure, and company policy. Provide technical support to all departments owning and utilizing measurement and test equipment.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Calibrate, maintain, and repair all measurement and test equipment in accordance with established work instructions, standard operating procedures, and company policy.

• Monitor equipment schedules and reports and ensure all work activity is completed within the scheduled timeframe.
• Complete associated documentation of all calibration, maintenance, and repair activity and ensure information is accurately recorded.
• Clean, organize, and maintain work areas as required.
• Investigate and close measurement and test equipment related incident reports, product evaluation reports, and corrective/preventative action reports.
• Adhere to all safety guidelines and company policies.
• Carry on call pager during scheduled rotation.
• Other duties as assigned.