Managing 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: 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: 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: Biopharm R D - Principal Scientist Company: GlaxoSmithKline Location: King of Prussia, PA Description: Basic qualifications:PhD in Immunology, Cell Biology or relevant area with 2-8 years of industry experience is required.Preferred qualifications:PhD candidate in Immunology or Biology with relevant laboratory experience in immunoassay development and validation is preferred. The capability to work independently in a team environment is a must. Knowledge and experience of GLP/GMP is a plus.Details:As part of the expansion of the Clinical Immunology group within the Biopharm R&D, we have an exciting opportunity available for an immunologist to join us at our Upper Merion, PA site. We are looking for a talented, highly motivated scientist to join our successful team working on Clinical Biomarker and Immunogenicity assessment. The qualified candidate will be able to:Design, develop, analytically validate and troubleshoot clinical immunoassays for Biomarker and Immunogenicity evaluation.Be able to apply advanced immunological and analytical techniques to improve immunoassay design and throughput.Generate high quality and timely clinical study immunoassay data. Ensure smooth transfer of data to data management and other business partners and participate in evaluation and interpretation of data.Perform laboratory work to GLP/GcLP quality standard to support the clinical development of biopharmaceutical products.Provide laboratory and assay training to other members of the section and department when required.Work with external partners to bring externally established assays and technologies in-house and/or transfer in-house assays externally as required. Provide guidance, trouble-shooting and quality oversight as required.Author or approval SOP's, reports and other technical documentation to a high scientific standard.Contact information:You may apply for this position online by selecting the Apply now button.

Job Title: Development Microbiologist (Principal Scientist I) Company: Company Confidential Location: Waltham, MA Description: Operational development microbiology in support of antibacterial global product teams: works with Development Microbiology Directors; and Clinical, Regulatory, Commercial and Discovery Medicine colleagues to create and deliver clinical and non-clinical microbiology plans and reports of experimental and review work in an outsourcing model. Depending on experience: might support Clinical Project Teams as Development Microbiology representative. Major Responsibilities [it is recognized that the successful candidate might not have experience of all of these activities: see minimum requirements] Create plans for delivery of the agreed microbiology strategies of global product teams using an outsourcing model, and forecast the resources needed (FTEs, $$). Work with the microbiology standards agencies, CLSI and EUCAST, and susceptibility-testing device manufacturers, to implement the project's susceptibility-testing and breakpoint strategy. Deliver the clinical and non-clinical microbiology plans using an outsourcing model. Contribute to microbiology sections of regulatory submissions (NDA, MAA, etc), core data sheets, and product labels. Write microbiology sections of investigator brochures, in collaboration with colleagues from other functions. Work with purchasing and legal colleagues to set up contracts for external work with appropriate external providers and medical and scientific experts; performing due-diligence investigations as appropriate. Make presentations of completed work and proposed plans to clinical project teams, the research management team, global product teams, and discovery colleagues as required. Analyze the competitive environment for specific antibacterial compounds in clinical development under the guidance of Development Microbiology directors. In collaboration with colleagues in medical affairs and other commercial functions, provide scientific summaries to support the launch of new antibacterial compounds. Be proficient in the use of relevant software tools at AstraZeneca. Requirements: Qualifications: PhD in microbiology, infection pharmacology, or a related discipline and experience of publishing relevant research in the academic literature. -5 or more years experience in the microbiology of the clinical development of antibacterial agents. Familiarity with the work of CLSI and EUCAST. Working knowledge of internet search tools such as Pubmed, Highwire, Google scholar, Science direct, Scifinder etc. Experience of creating good scientific proposals and presenting them authoritatively at project meetings. Skills and Competencies Can address the needs of multiple customers: development microbiology directors and colleagues, project team and discovery medicine colleagues, doctors, regulators and patients. Holds self and others accountable. Self-development orientation: can listen to and respond to feedback and provide constructive feedback to others. Ability to work under pressure and to deadlines. Good collaborator: respects and integrates different views. Ability to analyze data and make consequent recommendations for action. Results orientation. Preferred Background PhD in microbiology and a publication track record. Seven or more years' experience in the microbiology of the clinical development of antibacterial agents. Experience of preparing microbiology plans to support antibacterial drug development projects, including planning non-clinical microbiology in accordance with the project strategy and regulatory guidance. Experience of conducting the microbiology associated with clinical trials. Experience at presenting microbiology work to project teams to monitor progress against agreed strategies. Knowledge of key members of CLSI and EUCAST, and microbiology outsource provider companies. Knowledge of antibacterial PK-PD.

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 - Toxicologist Company: Medtronic Location: Fridley, MN Description: Medtronic Job Details Principal Scientist - Toxicologist Requisition 73606 Category Scientist Business Corporate-US Headquarters Division MDT Ventures a New Therapies Location USA-MN-Fridley Relocation Relocation eligibility to be determined Job Type Full Time - Regular Exempt/Non-Exempt Exempt Shift First Travel Percentage less than 10% Experience Required 6 years Education Required Master of Science Medtronic is an Equal Opportunity/Affirmative Action Employer Position Description MAIN PURPOSE OF JOB: 1.Plan, coordinate and perform activities to research and develop new products and therapies using local or systemic drug and biologic delivery to treat chronic disease. 2.Provide technical expertise and tactical project leadership to one or more projects or programs. Execute for impact. Foster innovation. 3.Establish and maintain relationships with other Medtronic R&D groups and with organizations external to Medtronic. Position Responsibilities MAIN JOB DUTIES/RESPONSIBILITIES (most important duties first) Provide technical expertise to one or more project teams. Use in-depth knowledge of drug toxicology to design and execute IND-enabling safety studies. oSupport regulatory filings (i.e. IND) for drug delivery development programs Participate as an individual contributor in your area of expertise. oAs a technical leader: R&D projects or Business Unit problem solving. oHelping to identify new therapy and technology opportunities. oScouting for technologies that support Ventures and New Therapies (VNT) programs. oTechnical due diligence of investment opportunities that support Medtronic Corporate or Business Unit strategic goals. Effectively communicate to internal and external audiences oBuild communication skills to manage up two levels (Director). oMake technical presentations of data in team and departmental meetings, as well as internal and external meetings and conferences. oDocument experimental plans and results in laboratory notebooks and in written reports. Cultivate relationships. oActively partner with and connect VNT teams; foster collaborations. oMaintain and expand network with Medtronic Business Units. oActively partner to establish cross-business projects. Generate intellectual property to support novel therapy and technology development. Mentor and educate other scientists in your area(s) of expertise. Adhere to all applicable Medtronic policies and procedures. Basic Qualifications KNOWLEDGE/EDUCATION Masters Degree in Toxicology or Related Science JOB EXPERIENCE 6+ Years experience with Masters or 4+ years experience with Doctorate Experience in designing and executing IND-enabling toxicology studies Experience with medical device and/or pharmaceutical product development SKILLS/COMPETENCIES R&D project leadership Desired/Preferred Qualifications PhD in Toxicology DABT certification Strong understanding of protein and peptide pharmacology Formal training and/or experience in pharmacology 5+ years experience in research and development of medical devices or pharmaceutical products Track record of innovation Track record of transferring technologies and/or products from R&D to business units Advanced critical thinking skills Innovation skills Proven ability to mentor and coach Consulting skills Technology assessment skills SKILLS/COMPETENCIES Communication, influence and interpersonal skills Ability to effectively work across organizational boundaries Physical Job Requirements Sit/Stand/Walk up to 8 hrs./day

Job Title: Principal Scientist Company: Biogen Idec Inc Location: Cambridge, MA Description: The person in this position will be responsible for development and the implementation of Bioanalytical strategies in support of early and late stage Development Program in the BiogenIdec pipeline. Responsibilities will include the development, qualification/validation of appropriate assays to measure protein therapeutics, immune response to such therapeutics, and pharmacodynamic/disease biomarker changes in support of Preclinical and clinical studies in accordance with current guidelines and industry standards for PK immunogenicity and biomarker assays. The successful candidate should be able to balance hands-on laboratory work with managerial responsibilities. The candidate should have strong managerial capabilities and will lead a group of BS/MS/PhD scientists, as well as have a strong interest in evaluating and implementing novel assay technologies, and the ability to work and lead effectively in a collaborative environment. The incumbent will present data in a variety of team settings, prepare technical & regulatory documents, and work within cross-functional project teams. May interact with contract research organizations to transfer the assays developed and oversee study support. This individual will work closely with colleagues in other departments on projects ranging from early to late stage development. Close interactions and collaborations with peers in the group to ensure optimum progression of projects and impact of collective assay data on projects will be essential for this position. Working with senior management, this individual will use his/her scientific expertise and insights to weigh in on strategic decision-making. This individual will be responsible for incorporating the latest assay and automation technologies to optimize the bio-therapeutics development process; this position involves working concurrently on multiple projects in a fast paced environment. Successful candidate will have demonstrated experience in the Bioanalytical area, an interest and aptitude in learning new technologies, attention to detail, flexibility and strong work ethics to meet demanding timelines and excellent written and verbal communications skills.QualificationsA strong interest and demonstrated accomplishments in developing novel cell based and biochemical assay technologies are essential. Extensive knowledge of Biomarkers, Molecular Biology and Cell Biology is highly desirable. The successful candidate should have an extensive scientific track record (publications, presentations, etc.), possessEducationPh.D. in immunology, cell biology or related field 10+ years of relevant experience in the biotechnology and/or pharmaceutical industries along with 4-5 years recent protein therapeutic experience is required.

Job Title: Principal Scientist ? New Technologies R Company: HealthMedia, Inc Location: Skillman, NJ Description: Principal Scientist ? New Technologies R&D (409100421) Job Description Principal Scientist ? New Technologies R&D-409100421 Description Johnson & Johnson Consumer & Personal Products Worldwide, a member of Johnson & Johnsons Family of Companies is recruiting for a Principal Scientist - New Technologies R&D, located in Skillman, NJ. Johnson & Johnson Consumer Products Company, a division of Johnson & Johnson Consumer Companies, Inc. develops and markets baby care, wound care and skin care products that address the needs of consumers and health care professionals and incorporate the latest innovations. The portfolio includes heritage brands JOHNSONS® Baby and BAND-AID® Brand, as well as leading skin care brands such as AVEENO® and CLEAN & CLEAR®. The Principal Scientist - New Technologies R&D will report to an Associate Director in the Research, Technology & Professional Products group. This individual will have responsibilities spanning multiple technology platforms. For each platform, the Principal Scientist - New Technologies R&D will work on developing new device technologies, focusing on products for committed franchise partners under Design Controls. This individual will become expert in the scientific literature in specific fields and be responsible for leveraging that expertise to create opportunities for additional franchises. Qualifications A minimum of a Masters Degree and 5 years of professional experience OR a PhD Degree and 3 years of professional experience is required. A focused degree in biomedical science and/or engineering is preferred. Previous experience in working within a Consumer business is preferred. Previous experience designing clinical trials is preferred, either independently or with clinical partners. Experience with Design Controls is preferred. Strong communication skills are required. This candidate will be able to work independently on multiple projects/platforms. The ability to successfully partner and influence cross-functional team members is required. This position may require up to 10% overall travel and is based out of Skillman, NJ. 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-Skillman Organization Johnson & Johnson Consumer Inc. (6071) 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 409100421 when responding to this ad.

Job Title: Principal Scientist Investigator Company: GlaxoSmithKline Location: Research Triangle Park, NC Description: Basic qualifications:MS or PhD degree in Chemistry, Biological Sciences or related scientific field.Preferred qualifications:Excellent written and verbal communication skills required. Three or more years of experience in molecular/cell biology of skeletal muscle, mitochondrial biology, or muscle molecular physiology is required.Details:The Muscle Metabolism Discovery Performance Unit at GlaxoSmithKline, Inc. in Research Triangle Park, North Carolina, seeks a highly motivated scientist to join a research group whose goal is to develop novel therapies for age related muscle dysfunction and muscle wasting diseases. The successful candidate will perform research in areas such as mitochondrial function and biogenesis, protein anabolism/catabolism, and the relationship between metabolic stress responses and the maintenance of muscle cell function in aging.Contact information:You may apply for this position online by selecting the Apply now button.