Job Title: GC/MS & LC/MS Field Serv Tech
Company: GenTech Scientific, Inc.
Location: Los Angeles, CA
Description:
Complete initial set-up, perform preventive maintenance, troubleshooting, repair, equipment modifications, and installation of GC, LC and MS equipment. Factory-trained candidate required. Candidate must be able to provide excellent customer service.
Minimum of 3+ years in the repair and maintenance of GC, LC and MS equipment preferred. Factory-trained candidate required. Excellent interpersonal and communication skills required. Strong technical and troubleshooting skills. Proficiency in computer and Windows software required. Strong organization and problem-solving skills. Ability to work independently and without close supervision. Flexibility to handle multiple and changing priorities. Ability to work flexible hours and travel as required. Clean driver’s license required.
General knowledge of principals and methods of analytical equipment. Basic knowledge and experience with electrical and mechanical systems.
A major Personal Care Private Label Mfg. located in Los Angeles, CA area has an opening for a Product Development Chemist. Minimum qualifications B.S. in Chemistry, 2 to 5 yrs of exp.in developing Emulsions,
and OTC Prods. and command of Microsoft Office.
Job Title: Senior Chemist
Company: Kuo Testing Labs, Inc.
Location: Othello, WA
Description:
We have immediate opening for an experienced chemist. Preference will be given to those with previous practical experience in soil or environmental laboratories. Higher graduate degree in soil chemistry or soil environmental chemistry will be a plus.The candidate should possess excellent oral and written communication skills. The candidate should have demonstrated work ethics from previous jobs. Our company offers excellent salary, bonus, health insurance, vacation, and simplied retirement package.
Job Title: Laboratory manager
Company: Northern Lake Service, Inc
Location: Crandon, WI
Description:
Northern Lake Service, Inc (NLS), an environmental compliance laboratory in Northern Wisconsin is searching for an energetic, highly motivated individual to manage laboratory operations (approximately 15 chemists and technicians). NLS is recognized by clients and regulators for its extremely high level of data quality and client service. Laboratory manager works closely with IT, QC and client services managers and acts as a liaison with technical staff in meeting client needs and sample load requirements. Candidates must have a strong technical background and very good communication/people skills. NLS has a great staff (average ~10 years), cutting edge instrumentation, a powerful LIMS, and an unmatched reputation for quality and service. If you are looking for a challenging opportunity to be an integral part of our operation, apply today.
Position is full-time salaried with health benefits, 401(k) match, long-term disability, bonuses, two weeks of personal leave (annually) and two weeks of annual leave.
From: Gary Smith
Phone: Register to View SciTech Services, Inc.
Baton Rouge, LA 70879
website: http//:www.scitechservices.com
REFERENCE: JO-128 ( Register to View )
POSITION TITLE: Laboratory/Technical Manager, reporting to the Global Technology Manager
KNOWLEDGE, SKILLS, AND ABILITIES NECESSARY FOR THE JOB:
Experience in a laboratory associated with lightweight liquids derived from petroleum is highly desired. Due consideration will be given to experience in related low molecular weight organic liquids
Hands-on experience in formulating, blending, and testing of these and / or similar materials
Solid understanding of basic laboratory practices and equipment
Experience in safely conducting synthesis, development, and / or blending experiments
Ability to pay close attention to detail and coordinate various activities simultaneously
Ability to communicate with customers, suppliers, blending / production facilities, carriers, co-workers and other business contacts in a courteous and professional manner ¡V own excellent communication skills
Ability to work with minimal supervision for a remotely located manager
Ability to maintain confidentiality
Ability to be flexible with a strong desire to learn continuously
Solid problem solving skills
Computer skills including MS Word, Excel, PowerPoint, E-mail, etc.
EDUCATION AND EXPERIENCE:
Four year college degree is required preferably in chemistry
At least several years of laboratory experience matching the above noted criteria
ADDITIONAL REQUIREMENT:
Potential candidates for this position must be currently located in the Houston, Texas area or be able to relocate to that area without expense to the employer
GENERAL RESPONSIBILITIES:
Organize all laboratory activities required to support the Specialty and Industrial Products group while also undertaking varied aspects of the laboratory workload, including duties such as synthesis, blending, and testing / analysis using a variety of classical and instrumental techniques involving the highest standards of accuracy possible by modern instrumentation and methods.
Independently direct the lab activities based on general guidelines regarding priorities and expectations.
Support product quality control and innovative product development.
Daily organize analytical activity, accurately reflecting the priorities of the business team.
Direct the daily activities of a laboratory technician and lead by example in demonstrating high standards of laboratory efficiency and accuracy.
Interface daily with team members in the USA, UK, and Asia-Pacific, effectively communicating and accurately reporting laboratory information with a variety of team members from diverse cultures.
Implement an internal quality control program to address customer complaints.
Assist with the development of new products.
Responsible for sample preparation, sending samples to customers, requesting samples from vendors, logging of samples, and follow up after sample has been sent.
Provide technical and laboratory assistance to other teams, departments, and marketing as required.
Responsible for dealing with hazardous materials and associated regulations.
Job Title: GC/MS & LC/MS Field Serv Tech
Company: GenTech Scientific, Inc.
Location: San Francisco, CA
Description:
Complete initial set-up, perform preventive maintenance, troubleshooting, repair, equipment modifications, and installation of GC, LC and MS equipment. Factory-trained candidate required. Candidate must be able to provide excellent customer service.
Minimum of 3+ years in the repair and maintenance of GC, LC and MS equipment preferred. Factory-trained candidate required. Excellent interpersonal and communication skills required. Strong technical and troubleshooting skills. Proficiency in computer and Windows software required. Strong organization and problem-solving skills. Ability to work independently and without close supervision. Flexibility to handle multiple and changing priorities. Ability to work flexible hours and travel as required. Clean driver’s license required.
General knowledge of principals and methods of analytical equipment. Basic knowledge and experience with electrical and mechanical systems.
Job Title: Principal Scientist
Company: Delta
Location: Mundelein, IL
Description:
We are looking for a Principal Specialist - preferably with an expertise in polymers. The Principal Scientist conducts exploration of subject areas for novel concepts and approaches; demonstrates depth of understanding of industry developments and related technology trends; applies intensive and diversified knowledge of scientific principles and practices in broad areas of assignments; modifies and extends theories, concepts, and practices of his/her own field and related disciplines; demonstrates advanced analytical problem-solving abilities with some synthetic abilities; as well as develops detailed reports documenting research results & advancing recommendations.________________________________________________________________________ Position ResponsibilitiesA. Technology Development - Lead internal technology development, as well as partner through external relationships to drive application of new technology opportunities which benefit the company's products and processes. Reduce to practice new inventions and ideas.B. New Product Development - Establish new product vision and/or demonstrate proof of concept through exploratory development of new product prototypes. Direct technical assessments & evaluate technology performance in new products. Determine success criteria for product development and advance new ideas through commercialization.C. Research fundamental relationships - Guide innovation by identifying, adapting, -and- advancing novel technology initiatives which may realize new benefits for clinicians & consumers, and provide a competitive advantage for our company. Conduct sophisticated analyses of test data in the course of developing new scientific theories & hypotheses. Our company’s expert for Polymer & Material technologies.D. Project Leadership & Technical Mentorship - Provide technical leadership for project team activities. Mentor & consult team members, peers and cross-functional counterparts. Contribute to project planning, controlling & organizing to establish priorities and related activities. Qualifications· Technical PhD, preferably with post-Doctoral research experience, strong fundamental expertise in Polymers/Materials, and at least 4 years relevant industry experience.· Established success in innovation and research effectiveness as demonstrated by patents and/or publication in peer-reviewed journals, presentations at industry / academic forums, etc.· Strong statistical analysis skills are welcome· Excellent communication, interpersonal, and writing skills. Must be computer literate with MS Office & Windows applications· Significant experience in intellectual property and/or patent law, as well as the patent process, is desired Preferred Qualifications - Significant Chemical, Medical Device, Hygiene, and/or Packaging Industry experience.
Job Title: Principal Scientist Drug Delivery (SC)
Company: Atrium Medical Corporation
Location: Hudson, NH
Description:
Founded in 1981, Atriumis a privately held healthcare products company located in Hudson, NH. Atrium is a market leading manufacturer of breakthrough medical device technologies used in open heart surgery, emergency chest trauma, thoracic drainage and surgical repair of diseased blood vessels. More recently, Atrium is known for its high technology presence in coronary stents, minimally invasive intervention of peripheral blood vessels, state-of-the-art hernia repair, drug delivery research, hemodialysis access, and market leadership in facial plastic surgery. Atrium manufactures over 1,000,000 sterile medical products each year which are distributed to over 60 countries. Maintaining a commitment to innovation in research, market development and manufacturing has enabled the company to excel in many global medical device markets. With more than two decades of experience, Atrium has been an innovator of new technologies designed to meet the clinical needs of the patient. Whether it is chest drainage, drug delivery, drug coated stents, or new ways to deal with vascular disease and general surgery, Atrium is working on a new and innovative ways to solve unmet clinical needs. Atrium offers a unique opportunity with exciting challenges for the qualified candidate. OverviewLeads drug delivery projects.Position Specific RequirementsProvide technical and project leadership over complex design, development and research projects.Management of formulation development, pre-clinical studies, development of test methods.Management of regulatory requirements, design control and support of technology transfer to manufacturing for drug coated/eluting stents.Responsible for the direct supervision and management of personnel.Responsible for achieving project and objectives as specified by management team by promoting investigaation and creativity.Maintain compliance to all Regulatory Standards for project and personnel safety.Recommend the addition, expansion or termination of projects.Assure technical soundness of programs.Provide technical presentation support and consultation to Marketing.Prepare project requests detailing proposed work costs and timetables.Analyze and translate experimental results into development criteria.Evaluate and select optimum alternatives.Provide application/formulation support to customers.Develop potential applications to exploit new business opportunities.Collect and analyze information on competitive products.Assist in the development of budgets.Evaluate competitive patents and recommend alternative options.Vendor contract and specification development.Prepare reports and document progress with Senior Management.Assists with other projects as needed. Contributes to team effort by accomplishing related duties as required.Qualifications:Bachelors or Masters Degree in Chemistry, Chemical Engineering or related core area. Demonstrated experience managing proejct teams, and transfer of projects to manufacturing. Experience with medical product development and FDA requirements. Good knowledge of project management techniques. Excellent organizational, interpersonal and communication skills. Strong project management skills. Comprehensive understanding of design control and product development systems. Strong communication skills (both oral and written).Atrium Medical Corporation offers competitive salaries, exceptional benefits, and a business casual dress code. We do not accept unsolicited Agency Resumes. Atrium Medical Corporation is an equal opportunity employer dedicated to workforce diversity and a drug and smoke-free environment. Drug screening is required.
Job Title: CPR&D Principal Scientist
Company: Johnson Matthey
Location: Paulsboro, NJ
Description:
A Pharmaceutical Material company in West Deptford, NJ is seeking a Principal Scientist. SUMMARY OF POSITION This position has the following responsibilities: · Manages the design and execution of effective research programs directed toward developing and implementing safe and robust API manufacturing processes. Oversees the resolution of production problems and contributes to problem solving on a high level. Plays a key role in regulatory filing and filing strategy. Assesses new product opportunities and identifies resource, technology, and capital needs. · Manages project leaders and guides the design of effective research programs, including negotiating deliverables and timelines with Commercial and ensures the creation of interdepartmental project plans. Has primary responsibility for high level projects as well as for the success of projects managed by direct reports. Provides assessments of process costs for local R&D program and for prospective processes and projects. Is fully responsible for evaluating processes to be transferred in from other sites and provides sound assessments for feasibility and cost. Reviews assessment performed by others. Manages or participates in intersite transfer. · Undertakes laboratory R&D, and prepares GMP and non GMP lab batches to support internal and external customers. · Maintains ownership and expertise with respect to assigned processes across their life cycle. Reviews process performance against KPI’s, is the internal expert for problem solving, and represents the process to customers or regulatory bodies. · Principal author on papers or meets inventorship criteria if co-author within proprietary constraints. EDUCATION/BACKGROUND Ph.D. plus 15-20 years, MS plus 25 years, BS plus 30 years of additional relevant experience or equivalent required. Proven project management and group management skills required. Excellent communication skills as well as computer skills. Please send your resume and salary requirements to Register to View if you meet the qualifications and have an interest in this position.
Job Title: Principal Scientist
Company: Aerotek Professional Services
Location: Rockville, MD
Description:
Aerotek's client in Montgomery County, MD seeks qualified candidates who will be responsible for the following duties:- Support non-clinical development of countermeasures for biodefense- Mainly working with vaccines and immunotherapeutics against anthrax- Design and implementation of non-clinical studies to meet regulatory requirements- Interaction with scientists, CRO's, and PMs- Evaluate and respond to government RFPs, BAAs, RFIs, and RFAsMinimum qualifications:- 3+ years Post-Doc experience- Design and execution of animal studies- Strong familiarity with GLP environment\- Knowledge of FDA "Animal Rule"- PhD in Microbiology, Immunology, Biochemistry, or related fieldQualified candidates please contact Travis Hurley at Register to View or [Click Here to Email Your Resumé]
Join Aerotek Professional Services. Our customized employment solutions and personalized approach give job seekers access to great opportunities with competitive salaries. Aerotek offers comprehensive benefits that can include medical, dental, optical, and optional 401k. Don't put your career in the hands of just anyone; put it in the hands of a specialist. Launch or rejuvenate your career today with Aerotek Professional Services! Allegis Group and its subsidiaries are equal opportunity employers.
CompetenciesDesired:Biodefense, Non-Clinical Development, Animal Studies, GLP, FDA "Animal Rule", Experience with In Vivo Studies
Contact Information
Contact:
Hurley,Travis G
-->
Email
this job
Email:
Send Email Now
Address:
US-MD-Rockville
Phone:
Register to View
Fax:
Register to View
Reference Code:
1818184
Click
here to see all