Principal Chemist Jobs

Job Title: LABORATORY MANAGER Company: Matheson Tri-Gas, Inc. Location: New Johnsonville, TN Description: LABORATORY MANAGER Matheson Inc. is seeking a Laboratory Manager for our New Johnsonville, Tennessee facility. The Laboratory Manager is responsible for the day-to-day operations of the facility including all aspects of Data Generation and Reporting, Staffing, Financial Performance, Quality, Customer Service, and Environmental Health and Safety.This is a full-time, exempt position with a starting salary commensurate with experience. Relocation allowance is available to the right candidate.The New Johnsonville laboratories analyze a wide variety of specialty and electronic gas products. Analytical equipment utilized includes gas chromatographs, atomic absorption, FTIR, CRDS, and various process analyzers.The ideal candidate will possess: A relevant science degree with a minimum of 7 years experience working in a specialty, electronics or environmental laboratory operation with progressive responsibilities, including personnel management. Familiarity with a wide variety of bench level techniques, processes, equipment and data systems for routine environmental testing procedures. Demonstrated experience leading or managing a team at the department and/or laboratory level. The ability to relate professionally with people through both verbal and written communications. Excellent time management and organizational skills with the ability to handle multiple priorities simultaneously, and operate in a fluid environment while managing and coordinating projects and staff. Familiarity with ISO Accreditation and Quality Programs A high degree of motivation to lead a laboratory team to meet stated Goals and Objectives. Excellent compensation & benefits package, including medical, dental, vision, 401(k) Retirement Savings Plan with employer match. Send resume & salary requirements. to: Matheson Tri-Gas, Inc., Attn: H.R. Manager, Fax: Register to View or e-mail: HR- Register to View -Trigas.com No phone calls or agencies please. EOE M/F/D/V MATHESON TRI-GAS www.matheson-trigas.com

Job Title: SR CHEMIST Company: Professional Services of America Inc. Location: Beltsville, MD Description: The government has a need for chemist services to develop analytical methods and protocols on tobacco products in support of the Bureau's enforcement programs. GOVERNMENT-FURNISHED PROPERTY, EQUIPMENT and SUPPLIES Existing workspace, utilities, furniture, laboratory equipment, laboratory supplies and personal safety equipment except for prescription eyewear. Task specific training such as training on theory and operation of analytical equipments, such as a smoking machine, as well as general training on the following SSD Technical Procedure Document (TPD) and Quality Procedure Document (QPD)

Job Title: Pharmaceutical Chemist Company: Lachman Consultants Location: US and International , ZZ Description: PHARMACEUTICAL CHEMISTS: Lachman Consultants, a worldwide, renowned pharmaceutical consulting firm is looking for: FORMER FDA INVESTIGATOR CHEMISTS OR PHARMACEUTICAL INDUSTRY CHEMISTS / SUPERVISORS FOR INDEPENDENT CONSULTING OPPORTUNITIES: Chemists must have experience in performing GMP / GLP audits covering laboratory procedures and practices for Quality Control, Bioanalytical and Analytical Research and Development Laboratories; documentation practices; analytical methods development, validation and transfer; instrument qualification; training programs; stability studies, investigations; CAPAs, etc. and assist in project management. Experience must also include electronic data reviews, remediation of laboratory control systems, laboratory investigations including OOS and mitigation, deviations, and change control records. Quality Assurance or Regulatory Agency experience a plus. Qualifications: B.S. / M.S. / Ph.D. in Chemistry Minimum of 10 years' laboratory experience, preferably in a Quality Control setting Detailed knowledge of current FDA, ICH, and USP regulations / guidances and expectations Strong communication / presentation skills, verbal and written, are required for interaction with clients and coworkers Ability to recognize and differentiate importance of issues and prioritize accordingly All candidates must have verifiable and recent "hands on" experience, including demonstrated remediation skills in the pharmaceutical industry. Only competent, well qualified, and highly motivated chemists with a proven track record of success need submit resume for consideration to be engaged as an independent consultant. Must be willing to travel both domestically and internationally. Send resume which includes dates of employment history to Register to View

Job Title: PRINCIPAL SCIENTIST, PRODUCT DEVELOPMENT Company: Johnson & Johnson Location: Los Angeles, CA Description: Neutrogena a division of Johnson Johnson Consumer Companies, Inc. is currently recruiting for a Principal Scientist.Neutrogena Corporation develops, manufactures and markets premium skin and hair care products sold worldwide and recommended by medical professionals. The regulatory classification of the products is principally OTC. The product line includes acne treatment products, sun protection, facial care as well as other hair and skin care products.Under minimal supervision of management, the Principal Scientist will exhibit extensive expertise in personal care and sun care formulations and effect of ingredient chemistries and process on product properties and stability. Work in conjunction with the formulation team to ensure that the formulations and processes developed are robust and scalable into full scale manufacturing. To do such, the Principal Scientist will challenge the formulation for ingredients selected (correct and business continuity planning for alternates), levels defined (to ensure properties result in consumer acceptable attributes), attributes and ranges (to ensure that all meet consumer needs at and beyond specification limits) as well as the formulation and process to ensure that the combination is robust. Takes initiative and champion leadership of scientists on techniques to build robustness into the formula and process during the product development process, GMP lab batching and initial process identification. Demonstrate critical thinking skills on the evaluation of the data generated from development work to assess the robustness and predict success of new formulations. Supervise and provide technical guidance to fellow scientific staff. Consumer focused to deeply understand the consumer needs for product attributes and how variations in such will affect product performance. Leader with influence and possess effective communication skills.

Job Title: Principal Scientist Company: Briston Myers Squibb Location: Hopewell, NJ Description: The Clinical Biomarker - Oncology Group uses state of the art technologies to discover and implement biomarker strategies for furthering development of the BMS oncology pipeline. Members of this team work on various projects in concert with multiple groups within Discovery and Exploratory Clinical Research Global Development and Medical Affairs and have impact at many different levels of the organization. This team is responsible for the synergistic application of genetic, genomic and proteomic technologies for identification and development of novel biomarkers to enable the clinical development of the right drugs at the right dose for the right patients The successful candidate will be responsible for managing oncology projects for biomarker discovery, validation and clinical application. This will include development of biomarker strategic plans, identification, implementation and evaluation of clinical biomarkers for multiple programs; leading efforts for data generation, interpretation and communication to the team. The candidate will also be responsible for coordinating collaborations and alliances both internally and with external partners.

Job Title: PRINCIPAL SCIENTIST Company: HealthMedia, Inc Location: Somerville, NJ Description: PRINCIPAL SCIENTIST Register to View ) Job Description PRINCIPAL SCIENTIST Register to View Description . The Advanced Technologies and Regenerative Medicine (ATRM) group performs early stage research of innovative ideas in all areas of health care. The recently formed, 120 person groups is a results-driven R&D organization developing technologically convergent products for our customers by Being a powerful growth engine for J&J; Driving innovation and scientific excellence; Focusing on our business partners needs; Generating new business opportunities; Fostering an environment of creativity, exploration, and risk-taking; Maintaining our unique capacity to create products not being addressed elsewhere in J&J; and Building diverse talent that can be leveraged across J&J. Principal Scientist Seeking highly motivated and innovative person to lead and conduct investigation, applying skills and learnings from cell biology, developmental biology, and regenerative medicine. This individual will be well versed in emerging technologies in regenerative medicine such as pluripotent cell technologies, cell reprogramming, lineage specific differentiation and have made significant contributions in the field of regenerative medicine. The applicant will ensure effective communication and teamwork with co-workers as well as proper interactions with internal and external collaborators. The candidate will be expected to maintain state-of-the-art knowledge in the fields of interest. The candidate will prepare reports, patent memos and publications and present results in internal and external forums. Qualified candidate must have the ability to work independently and as part of a team. Responsibilities will include: Lead individual contributors who design and execute critical projects Identify and bring internally, emerging technologies in regenerative medicine Develop strategic plans for regenerative medicine opportunities with novel emerging technologies Execute on plans and deliver on milestones Collaborate with key internal stakeholders across JNJ Develop strong academic collaborations and partnerships Establish clear criteria and Go/No-go path for moving program forward Develop strong IP portfolio in collaboration with in-house counsel Qualifications . A PhD in biology/biochemistry/developmental biology with 10 years of experience in industry or academic setting leading groups. Candidate should also be well versed in emerging technologies in regenerative medicine, including pluripotent cell technologies, and lineage reprogramming technologies and should have made significant contributions in the area of regenerative medicine. Brings a track record of successful multi-disciplinary team leadership with demonstrable results and/or successes Intelligent thinker with demonstrated ability to see beyond an initial strategy and with ability to develop long term plans Ability to think creatively and make connections across disciplines Has a strong sense of urgency and focus Track record of delivering results independently and in teams Demonstrates critical judgment skills and proven capability to achieve goals Strong written and oral communication skills. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! Primary Location North America-United States-New Jersey-Somerville Organization Advanced Technologies and Regenerative Medicine, LLC (6164) Send this job to a friend Send this job description to a friend by email. All the relevant details will be included in the message.Send this job to a friendPlease refer to job code Register to View when responding to this ad.

Job Title: Senior Principal Scientist Company: Boehringer Ingelheim GmbH Location: Ridgefield, CT Description: The Department of CardioMetabolic Diseases Research at Boehringer Ingelheim Pharmaceuticals, Inc. in Ridgefield, CT has an opening in the Chronic Kidney Disease Therapeutic Indication for a Laboratory Head position. The successful candidate will be expected to lead an in vivo pharmacology/physiology laboratory as well as manage and expand a significant research program directed at the understanding of the mechanisms/pathways involved in the progression of renal disease. The candidate is expected to provide strong scientific and technical leadership in the chronic kidney disease (CKD) area and must be able to lead and manage a laboratory ensuring productivity, compliance and career development of direct reports. The laboratory is responsible for: 1) developing and establishing animal models of CKD including diabetic nephropathy models, 2) studying the mechanisms/pathways contributing to pathophysiological processes of CKD progression; 3) identifying druggable targets that drive these processes and 4) effectively evaluating therapies that may delay or prevent the progression of CKDAs an employee of Boehringer Ingelheim, you will actively contribute to the discovery, development and delivery of our products to our patients and customers. Our global presence provides opportunity for all employees to collaborate internationally, offering visibility and opportunity to directly contribute to the companies' success.We realize that our strength and competitive advantage lie with our people. We support our employees in a number of ways to foster a healthy working environment, meaningful work, diversity and inclusion, mobility, networking and work-life balance. Our competitive compensation and benefit programs reflect Boehringer Ingelheim's high regard for our employees.Responsibilities:Contributes to defining project team goals and collaborates with scientists within and outside functional area in achieving them. Assumes departmental responsibility for projects and/or acts as representative on multiple project teams. The candidate is expected to both lead teams and projects supporting multi-disciplinary research and contributing to overall program goals. Provides guidance and expertise to advance specific projects. Manages and prioritizes projects within the laboratory. Directs and oversees experimental design and results of technicians and junior level scientists The candidate will provide high quality scientific guidance, and promote internally and externally scientific research. Develop and manage external collaborations and outsourcing projects. The candidate is expected to communicate effectively with all levels of the organization including technical reports and oral presentations. The candidate will assume responsibility for direct reports including recruiting, managing, mentoring, developing and retaining high quality scientific staff The candidate is expected to comply with all applicable regulations, ensure that work performed in area of responsibility is conducted in a safe and compliant manner and maintain proper records in accordance with SOPs and policies

Job Title: Principal Scientist, Toxicology Company: Biogen Idec Inc Location: Cambridge, MA Description: The ideal candidate will be required to design preclinical toxicology studies, and have some experience in managing/conducting GLP-compliant toxicology studies at contract facilities. The candidate needs to possess conceptual and technical expertise in toxicology and drug development and have strategic initiative with regard to biologic and small molecule development. The candidate will represent the department at inter and intra departmental meetings and be responsible for cross functional dialogue and communication of a nonclinical development strategy. The candidate will be responsible for the preparation of regulatory submissions. The candidate must have excellent organizational and communication skills.Background in both biologics and small molecules preferred; experience in oncology, autoimmune disease, or CNS disease preferred.Qualifications10 or more years experience in preclinical drug development (Industry)Experience with regulatory submissionsEducationPhD in a toxicology/pharmacology relevant disciplineBoard certification in toxicology is preferred

Job Title: Senior Scientist Principal Scientist DMPK Company: GlaxoSmithKline Location: Research Triangle Park, NC Description: Basic qualifications:BS/MS in chemistry, biochemistry or related field with a minimum of 5 years relevant pharmaceutical industry experiencePreferred qualifications:? Demonstrated ability to think outside the box and achieve results when conventional analytical approaches were unsuccessful? Demonstrated experience analyzing drug compound and metabolites in a variety of biological matrices? Demonstrated experience programming and using automation platforms (Tecan, Hamilton, Biomek, etc) to improve bioanalytical process efficiency? Knowledge of drug metabolism/pharmacokinetics and in-vitro ADME science is desired? Hands on experience performing in-vitro ADME studies and preparing pre-clinical animal study formulations is a plus? Strong communication, written, interpersonal and teamwork skillsArea(s) of Expertise: Bio-analysis; Mass Spectrometry, HPLC; LC-tandem MS; and QuantitationDetails:The Department of Drug Metabolism and Pharmacokinetics at GlaxoSmithKline is seeking an experienced and motivated Scientist to be part of a team providing bioanalytical support to the Infectious Diseases Center of Emphasis for Drug Discovery (CEDD) small molecule portfolio.Primary Responsibilities include:? Provide hands-on quantitative and qualitative analysis of small molecules from in vitro and in vivo DMPK studies.? Manage/troubleshoot mass spectrometry, liquid chromatography and automation systems? Explore/implement new techniques, technologies or processes to improve data quality and increase bioanalysis throughput? Act as a mentor and provide necessary LC/MS/MS training to junior scientists.? Provide scientific input and guidance to project teams and DMPK colleagues.? Work with fellow DMPK colleagues and line management setting strategy and ensuring goals and timelines are metContact information:You may apply for this position online by selecting the Apply now button.

Job Title: Sr Principal Scientist Company: General Dynamics Information Technology Location: Silver Spring, MD Description: General Dynamics Information Technology is a top-tier IT integrator that provides information technology, systems engineering and professional services to customers in the defense, intelligence, homeland security, federal civil and commercial sectors. With approximately 17,000 professionals worldwide, the company has the customer knowledge, domain expertise and proven performance to manage large-scale, mission-critical IT programs.Scientist to support and manage a Genomics/Proteomics Core Facility. 1. Work with committees of scientists and managers to establish requirements for the Core Facility capabilities as instrumentation and technological requirements change.2. Acquire, install, and train investigators and technicians on proteomic/genomics instrumentation such as the SOLiD 3 System, next-generation sequencers, Real-time PCR, Luminex, multiparameter flow cytometry, cell sorting.3. Establish a Bioinformatics/Statistical Competency to support genomics/proteomics research as well as structural biology modeling.4. Work with supervisors, scientists and training specialists to develop a core curriculum for education in the application of genomics/proteomics technologies to problems of biomedical importance to the research institute.5. Work with SMEs and training specialists to establish a series of workshops to: (a) analyze the impact of core technologies on human clinical research and animal models, including the volumes and types of samples required, their appropriate preservation, and the strategy for extracting far larger volumes of information from a fewer, well-selected, clinical samples obtained earlier in the product development pathway, and (b) apply Core technologies to pharmacogenomics. 5. Collaborate with scientists to plan for and implement the leveraging of the genomics/proteomics competency to attract outside funding and collaborative projects that can extend and enhance the scientific mission of the institute.Requires PhD. Requires 10-15 years experience.