Fort Worth
TX
Min Requirements
? BS in a scientific discipline such as biology, chemistry, or pharmacology from a respected institution, an advanced degree preferred, MS in Information Science
? At least three years of relevant industry or research experience, working in information sciences, knowledge management or competitive intelligence
? Solid understanding of the pharmaceutical industry with inisghts into the entire R&D process with focus on development / clinical information
? Fundamental understanding of information engineering technology applications such as semantic web technology and text mining techniques and tools
? Solid knowledge of MS Office Word, Power point, Excel and other office business tools
Posted On -
6/18/2013 6:10:44 AM
East Hanover
NJ
Minimum requirements
1. Over 4 years of practical experience in chemical / pharmaceutical industry or over 4 years of experience in field of expertise
2. Recognized expertise in related field. Good (IT) application know how.
3. Good knowledge about the Drug Development process
4. Comprehensive knowledge about project management
5. Knowledge of relevant regulations (e.g. GMP, HSE etc.) and Novartis specific standards.
6. Demonstrates cross-functional problem-solving and idea generation skills
7. Advanced presentation skills
8. Good leadership skills
9. Excellent organization and planning skills. Ability to work in interdisciplinary and cross-cultural teams
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6/18/2013 6:10:44 AM
Emeryville
CA
? B.S. Degree in Engineering and/or Science: advanced degree preferred.
? 9+ years of systems engineering experience developing diagnostic products.
? 3+ years? experience developing automated track or robotic solutions.
? Experience with leading development efforts in a cross functional environment.
? Ability with solving complex systems engineering issues and problems, for systems including instrumentation, consumables, assays and reagents.
? Experience with design of experiments and statistical analysis to solve complex problems.
? Demonstrated product development experience using lifecycle methodologies and under FDA design control.
? Ability to convey complex information in both written and oral form.
? Experience with managing external vendor relationships.
? Ability to influence others, gain acceptance and build consensus.
? Excellent communication and interpersonal skills.
? Working knowledge in worldwide IVD regulatory processes and clinical evaluations highly desired
? Knowledge of molecular biology is a plus.
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6/18/2013 6:10:44 AM
Irvine
CA
4-year college Degree in non-Liberal Arts course of study.
4-years of Manufacturing, experience with a minimum of one year in the capacity of a production planner or materials planner and one year as a buyer.
Posted On -
6/18/2013 6:10:41 AM
East Hanover
NJ
BA/BS degree preferred (Business administration, legal services, finance, science discipline preferred) OR equivalent on the job experience considered. Minimum three years of experience in pharmaceutical services with three/four years contract management and/or study start-up activities including contract negotiations and management highly desirable. High degree of organizational, analytical, and team management skills. Computer literacy with document and spreadsheet applications. Ability to work on complex, multi-faceted projects. Excellent negotiation skills and vast knowledge of clinica trial agreements. Novartis is an EEO/AA employer M/F/D/V.
Posted On -
6/18/2013 6:10:40 AM
Holly Springs
NC
Bachelor of Science in a discipline relevant to pharmaceutical or biological drug manufacture (e.g. microbiology, biochemistry, pharmacy) or appropriate education and experience in pharmaceutical industry.
Minimum of 7 years? experience in the Pharmaceutical industry which must include experience in Quality Assurance, Quality Control, orQuality Systems & Compliance and Technical Development (product and/or process) in a GMP regulated environment.
Multinational experience highly desirable.
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6/18/2013 6:10:40 AM
Fort Worth
TX
Bachelors required in Finance, IT or other applicable field Fluent in English 9 Years with Bachelors 7 Years with Masters. English 12+ years of information systems maintenance/support within finance or procurement, including experience with end-to-end involvement implementing projects for large ERP systems. 10+ years of SAP implementation projects with responsibilities within procurement and accounts payable processing required.
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6/18/2013 6:10:37 AM
Wilson
NC
High school diploma or GED equivalent
?3+ years experience in a production environment and at least one year of solid dosage pharmaceutical experience
Posted On -
6/18/2013 6:10:34 AM
Fort Worth
TX
Bachelor's degree in Computer Science, Math, or Information Systems or Equivalent Technical degree and/or internal experience
Minimum: 5 years + IT Business Analyst
Fluent in English
Posted On -
6/18/2013 6:10:34 AM
Holly Springs
NC
? BS with 15+ years, MS 12+ years, or Ph.D. 7+ years
Education should be in mathematics/statistics or related field
? Applies deep specialized and/or broad expertise and is viewed as a subject matter expert (?SME?) in a particular discipline
? Leads projects that focus on complex and challenging technical issues and provides critical contributions to drug development
? Uses sophisticated analytical thinking to solve complex problems by analyzing a range of alternatives
? Experience working in biotech or pharmaceutical industry.
? Provides on-going support on projects, including guidance to others as needed; applies knowledge of broader project objectives to provide input that furthers project success
? Analyzes information and standard practices to solve problems of moderate complexity in straightforward situations
? Accountable for developing own self to enhance contribution
? Excellent working knowledge on statistical software (e.g. SAS, R, JMP etc.)
? Experience in modeling and simulations techniques (desirable)
Posted On -
6/18/2013 6:10:33 AM
San Carlos
CA
Bachelors degree in an Engineering discipline is required. Equivalent experience may be accepted. ?A minimum of 8 years industry work experience is required. ?A minimum of 5 years experience in a GMP operational or manufacturing pharmaceutical or other regulated environment. ?Knowledge of a process oriented organization and self-directed culture a plus. ?Sound knowledge of maintenance and operational processes.?Proven project management and leadership skills of cross-functional teams.?Interdisciplinary knowledge advantageous. - -
Posted On -
6/18/2013 6:10:33 AM
Holly Springs
NC
Requirements:
? Bachelor?s degree in related scientific field or equivalent; master?s degree or PhD preferred.
? 7+ years in Quality Assurance and/or in a GMP regulated en-vironment within the pharmaceutical industry.
? 5+ years of demonstrated leadership of staff or projects
? Advanced knowledge and experience using Quality Systems required
? Advanced knowledge and experience in sterile product man-ufacturing, biological processes, and laboratory operations required.
? Excellent leadership skills required with a proven ability to manage and mentor multi-functional teams in a fast paced environment.
? Demonstrated ability to think strategically and to work collaboratively using a proactive approach to operations problem-solving.
? Multinational experience preferred
? Early stage development experience preferred
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6/18/2013 6:10:24 AM
Fort Worth
TX
Minimum: Bachelor degree and/or relevant business experience in the area of computer science in Life Science in dustry English At least 8 years experience in Project Quality Management as project manager or team lead or in SAP support respectively. Knowledge about CSV (FDA and EMEA regulations) and financial compliance requirements (SOX) Experience in leading small teams (project teams) Experience in dealing with difficult/complex client relationships / engagements Experience in working in multidisciplinary/multicultural teams Proven track record of delivering work/projects within tight deadlines Excellent communication skills Be able to "jump in" and align communication activities with ERP IGM topics Be experienced in the common MS office tool like excel etc. & SharePoint Pro-active and independent on bringing the assigned tasks to a successful completion The position requires travelling up to 50 Percent.
Posted On -
6/18/2013 6:10:24 AM
East Hanover
NJ
Bachelors Degree required. Experience negotiating ICF language with research centers and IRBs highly preferred. Experience working with the HIPAA Privacy Rules preferred. Strong Computer Skills, specifically Microsoft Word, Excel and PowerPoint.
Novartis is an EEO/AA employer. M/F/D/V
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6/18/2013 6:10:24 AM
Cambridge
MA
Education:
? Facility operations management and construction background required
? Advanced management sciences degree preferred
Experience:
? Previous experience in a senior operational role preferably within a pharmaceutical environment.
? Previous construction oversight experience
? Management of large international projects and exposure to general management disciplines (HR, Finance etc).
? Experience of working within a matrix organisation across countries and cultures.
? Strong strategic vision, superior leadership, excellent communication, consensus building, well developed influencing and negotiation skills.
? Demonstrated ability to work globally and effectuate change within the company.
? A clear sense of accountability, an ability to empower people and a high degree of mutual respect and integrity are essential factors to succeed.
? The candidate will be required to travel internationally.
? Next to English, which is mandatory, additional language skills are considered to be a plus.
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6/18/2013 6:10:23 AM
East Hanover
NJ
Education: Ph.D. in pharmacokinetics, drug metabolism or a related discipline, or a Pharm. D. with appropriate post-doctoral training.
Experience / Skills:
? 3 - 7 years of relevant post doctoral, academic, industry or government experience
? Strong knowledge of related disciplines (e.g. DMPK, toxicology, regulatory) and the drug development process
? Demonstrated proficiency using in silico analysis tools (e.g. WinNonlin, SAS, NonMEM, Trial Simulator, GastroPlus, SymCyp)
? Demonstrated ability to work as part of cross functional team in a highly dynamic, matrixed, project team environment
? Strong oral and written communication skills
? Strong organizational and project skills
? Strong critical thinking and problem solving skills including publications / presentations
Posted On -
6/18/2013 6:10:22 AM
East Hanover
NJ
Education (minimum/desirable):
? MD or equivalent medical degree required. Advanced knowledge in medical/scientific area (e.g., internal medicine or sub-specialty training) required
Languages: Fluent oral and written English
Experience/Professional requirement:
>3 years clinical trial experience with demonstrated ability to manage several trials in parallel with multidisciplinary trial teams
Demonstrated ability to establish strong scientific partnership with key investigators
Thorough knowledge of GCP, clinical trial design, statistics, and regulatory/clinical development process
Advanced knowledge of assigned therapy area is desired, with the capability to interpret, discuss and present trial or section level data
Strong interpersonal skills
Ability to work under pressure
Excellent negotiation and conflict resolution skills
Ability to resolve issues with minimal supervision and understand when to escalate
Excellent scientific writing skills
Demonstrated knowledge and application of statistical analysis methodology; can identify trends and interpret/report results effectively
Posted On -
6/18/2013 6:10:20 AM
Fort Worth
TX
? Master?s in life science is preferred
? 5+ years of experience in Drug/Device Development, especially in managing global multiple site clinical studies
? Solid understanding of the clinical study process of devices or pharmaceuticals
Fluent in English 4 years of clinical experience in a major international pharmaceutical company. The experience must be in the pharmaceutical field with a demonstrated record of success.
Must have assisted as scientific support of at least two major product.
Expertise/Experience/Skills:
Ability to formulate a hypothesis
? Understanding of the disease (project specific), natural course, standard of care and expected (reported) treatment outcome
? Knowledge of disease specific clinical efficacy and safety endpoints
? Logical & critical thinking
? Experience in writing clinical protocols
Ability to interpret data:
? Sufficient disease (project specific) and treatment knowledge to identify critical data
? Scientific thinking allowing to identify bias and validity issues
Conduct of clinical studies:
? Several years of experience in running clinical studies independently without significant supervision
? Ability to proactively identify issues and respond appropriately
? Solid understanding of the regulations (FDA, EMA, ICH, ISO etc.)
Leadership:
? Organizational awareness to operate in a cross-functional team
? Communicates effectively to provide clear directions of what has to be done
? Builds support from others in situations with no direct authority
? Ability to embrace and communicate change
? Well organized / solid project management skills
Posted On -
6/18/2013 6:10:20 AM
Dallas
TX
BA/BS Nursing, Pharmacy and or equivalent experience. English Position will be filled at level commensurate with experience. Technical Business Knowledge in drug development process; regulatory requirements 3-5 years experience in monitoring clinical data/clinical trials as CRA/Clinical Trial monitor in Phase I-IV required. Oncology clinical trial monitoring experience required. Ability to travel 50%: Ability to interact/communicate in matrix organization.
Posted On -
6/18/2013 6:10:20 AM
Cambridge
MA
BS or MS degree in immunology, biology, physiology, pharmacology, cellular biology, or related discipline; minimum of 3 years of academic or industry experience in inflammatory disease research in the eye
Direct experience establishing models of ocular inflammation in the cornea and/or ocular adnexa and performing pharmacology experiments to investigate potential new therapies
Excellent oral and written communication skills
Posted On -
6/18/2013 6:10:19 AM
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