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Company Jobs - Novartis Pharmaceuticals



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Shannon @ Novartis Pharmaceuticals

   


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Manufacturing Assembler (Material Handling for LenSx products)

Irvine CA

• High School diploma or GED • 3 - 5 years of manufacturing experience in a manufacturing environment preferred (preferably in the medical field) • Must be able to read, speak and write English fluently. • Basic knowledge of assembly and measurement tools.

Posted On - 5/26/2015 7:33:14 AM

SOP System Specialist

East Hanover NJ

BS degree in science or related field • 2+ years experience in drug development, preferrably 1+ year within Novartis • Good technical/IT knowledge • Understanding impact of work on compliance with GxP regulations and quality requirements • Good negotiation skills (ability to facilitate compromise, and to manage and implement change) • Demonstrate fast learning in new software management • Excellent interpersonal, communication and coordination skills • Excellent administration and organizational skills • Understanding the Pharma Development organization

Posted On - 5/26/2015 7:33:14 AM

Dir. E&C Investigations & Analytics

East Hanover NJ

Ability to think strategically and further develop and execute compliance data analytics schemes Experience in data mining techniques and procedures and knowing when their use is appropriate Ability to present complex information in an understandable and compelling manner Proficient in visualization software such as Tableau or Spotfire Ability to build interactive management dashboards for real time and what if analysis Strong analytical and problem solving skills with emphasis on utilizing business processes and technology to solve business problems. Demonstrated ability to work at both conceptual and detailed levels. Creative thinker with ability to translate strategies into actions Ability to develop investigation strategies and work closely with NPC's employment law attorneys to seek guidance, as necessary. Proficient in data querying / statistical analysis tools (e.g., SQL, Toad, SAS, COGNOS, MS Access, MS Excel, etc.). Strong written and oral communication skills Ability to maintain professional demeanor even when confronted with stressful and/or potentially adversarial situations Demonstrated ability to effectively interact and work collaboratively with multiple cross functional teams (IT, HR, Compliance, Security, Legal, Field force etc) Must be capable of simultaneously handling multiple investigations and various related tasks; meet investigative and project deadlines Demonstrated project management experience and problem-solving as a member of a cross-functional team Ability to work in a matrixed organization and influence others Adept at report writing Excellent interpersonal, consulting, and relationship management skills. Must be able to clearly document and communicate complex information; communicate business requirements and methodologies Successfully manage tight deadlines

Posted On - 5/26/2015 7:33:14 AM

Professional Sales Assoc-Charleston/Huntington

Charleston WV

• BS/BA in related field. • Fluent in English. • Generally, 2-4 years' experience in related field with emphasis in business to business sales. • Preferred, 4-6 years of sales experience with: Industry and/or technical knowledge and experience. • Experience in business consultative selling. • Significant business to business selling.

Posted On - 5/26/2015 7:33:14 AM

Sr. Global PLR Administrator

Fort Worth TX

Education: Bachelor's degree Exerience: 3 years' experience in Pharmaceutical manufacturing/ materials management environment.

Posted On - 5/26/2015 7:33:14 AM

Principal Eng I - Software

Fort Worth TX

•Computer Science, or related discipline - PhD + 9 yrs.; 5 yrs. Med. Industry preferred. - MS + 12 yrs. 5 yrs. Med. Industry preferred. - BS + 15 yrs.; 5 yrs. Med. Industry preferred. •Fluent verbal and written English is required. • 10 + years hands-on Windows development experience. •Experience with .NET, C# and C++. •Familiarity with hardware design constraints as applied to software interfaces. Preferred Experience •Experience developing medical device software in an FDA-regulated environment. •Experience developing Graphic User Interfaces using Windows Forms or Windows Presentation Foundation (WPF) for embedded applications. •Experience with multi-threading, and interprocess communication. • Familiarity with Windows 7 Embedded. •Strong working knowledge of advanced design principles that facilitate maintainability, reuse, and clarity of design.

Posted On - 5/26/2015 7:33:14 AM

Mgr, Information Technology

Fort Worth TX

Minimum Education: • Preferred Education: Bachelor's Degree in Computer Science or an Information Technology field of study • Alternate Education: Master's Degree in Math, Computer Science, or equivalent technical field with 8 to 9 years' experience Minimum Experience: • 10 years of experience supporting Information Technology applications Preferred Experience: 10+ years of experience supporting Information Technology applications with management experience (Alternate Experience - requires Leadership Team approval )

Posted On - 5/26/2015 7:33:14 AM

MS&T_ Technical Transfer Steward

Broomfield CO

Education: BS required. MS or equivalent experience for Expert level. Languages: Fluent in written and spoken English Experience: 4+ years pharmaceutical experience. Experience with technical transfers preferred

Posted On - 5/26/2015 7:33:14 AM

Engineering_ Engineer III, Validation (Equipment Validation)

Broomfield CO

Education: BS or MS in a technical discipline such as chemistry, engineering, biology. Languages: Fluent in written and spoken English Experience: 6-9 years of related experience, preferably in a GMP environment. • Strong knowledge and technical understanding of pharmaceutical unit operations • Strong knowledge in two or more of the following validation / qualification fields: pharmaceu-tical equipment, facilities, utilities and automation • Strong knowledge of cGMPs and Good Document Practices (GDPs) • Detail orientated, organizational, technical writing and presentation skills • Must demonstrate good negotiation skills • Must be a team player prepared to lead, work in and embrace a team-based culture • Ability to communicate and collaborate with technical and management staff within Manufac-turing, Engineering, Technical Services and Quality • Project management skills, including creating / managing project budgets, resources (internal and external) and schedules • Ability to lead and direct complex assignments with no guidance • Ability to provide solutions to a variety Validation issues • Ability to manage multiple projects at one time • Execute small capital projects and preventative action plans.

Posted On - 5/26/2015 7:33:14 AM

Assoc. Product Mgr. Endocrinology

Princeton NJ

BA degree (with 6 - 9 years of experience); MBA degree (with 4 - 7 years of experience) English 6 - 9 Years (with BA); 4 - 7 Years (with MBA)

Posted On - 5/26/2015 7:33:14 AM

Production Tech - Compression or Granulation (3rd shift)

Wilson NC

Education: High school degree required Languages: Fluent in written and spoken English Experience: Minimum 3 months of solid, oral dosage pharmaceutical experience in Manufacturing/Packaging. Prefer Sandoz contractor experience.

Posted On - 5/26/2015 7:33:14 AM

QC Analyst Associate

Melville NY

AAS or higher in Biology, Microbiology or related field. English Minimum one (1) year pharmaceutical or biological or related industrial experience. Pharmaceutical experience preferred.

Posted On - 5/26/2015 7:33:14 AM

QC Scientist

Melville NY

BS, MS, PhD, JD, MD, DVM English Minimum 7yrs. Pharmaceutical method development/validation experience with PhD preferred. BS or MS with significant method development/validation experience in a pharmaceutical environment will be considered.

Posted On - 5/26/2015 7:33:14 AM

Senior HR Manager

East Hanover NJ

BA / BS university degree in social science or business degree required and professional HR qualification desired. English speaking with 5 - 7 years experience in HR in a generalist role or as a specialist ( i.e. Training & Development, Coaching, Organizational Development, Comp&Ben), Complete understanding and use of human resource planning concepts/principles. Knowledge of pharmaceutical industry practices. Solves a variety of complex problems. Talent acquisition and development a plus International/Global experiences in a highly complex matrix environment Organizational development and learning experience highly preferred. Position will be filled at level commensurate with experience. Experience in a manufacturing environment preferred.

Posted On - 5/22/2015 9:15:33 AM

Medical Science Liaison (Tennessee and Kentucky)

Nashville TN

BA/BS required. Advanced scientific degree (MD, PhD, or PharmD highly preferred) or oncology nurse with advanced degree required. Minimum of 5 years Oncology experience with a strong current working knowledge of Oncology preferred. Teaching experience preferred. Previous pharmaceutical industry experience preferred. Thought leader development experience is a plus. Knowledge of treatment guidelines, clinical research processes, FDA regulations and OIG guidelines is preferred. Excellent interpersonal communication and presentation skills are required. Ability to network and partner with important external customers, including medical thought leaders, academic institutions, large group practices, medical directors and pharmacy directors is required. Must be able to prioritize and work effectively in a constantly changing environment. Must have the ability to gain customer feedback, uncover business opportunities for Novartis and pair customer's unmet needs with available internal resources. Active membership in professional society (ies) is a plus. Must be a strong team player who can effectively interface cross-functionally with Novartis clinical and commercial personnel. Working knowledge of Microsoft Office Suite (Word, PowerPoint, Excel) and associated hardware is required. The position is associated with approximately 65% travel. Position will be filled at level commensurate with experience.

Posted On - 5/22/2015 9:15:33 AM

Software Engineer- Interfacing

Carlsbad CA

Education Requires a bachelors degree in computer science, related field, or equivalent experience 3 years of experience in software development with a focus on c#, windows and web services and web applications in the healthcare industry Knowledge of HL7 interfacing and interfacing engines desired Qualifications Excellent communication skills; Strong desire to seek out problems and resolutions; Capability to multitask efficiently and desire to be a strong team player in a small to medium sized team; Flexibility in adjusting schedule based on workload; Capability to establish standards and procedures and advocate best practices; Ability to understand high level and low level system details simultaneously. The applicant should also have experience with HL7, interfaces written to send/receive files, and various ways of formatting data. Required Skills C#, JavaScript, SQL HL7 and XML Web services Windows services Web applications Interfacing engines Why you should work here: Genoptix offers competitive compensation and benefits programs that include vacation and sick pay, extensive medical insurance coverage, flexible spending accounts, 401 (k) with company match, childcare savings account, commuter benefits and much more! Career development opportunities and educational tuition reimbursement programs. We offer various fitness programs, discounted gym memberships and encourage eco-friendly initiatives like the "Bike to Work Day". Fluid and consistent communications on a quarterly basis from the executive team. Fun and exciting events including "Lab Week" and the annual employee appreciation events. If you or someone you know is looking for a career opportunity with a great company, apply online at www.genoptix.com/careers Genoptix is more than a laboratory - we deliver actionable results to improve quality of life.

Posted On - 5/22/2015 9:15:33 AM

Sr. Clinical Trial Leader

Holly Springs NC

Job Purpose: Novartis is seeking a Sr. Clinical Trial Leader to provide overall accountability for clinical trial management and execution of clinical trial objectives. This will include the management of clinical trial timelines, authorship of clinical trial documents, budget management and overall trial oversight, in adherence with GCP-ICH guidelines, corporate SOPs & policies. Major Accountabilities: • Contributes to the project strategy and to the Clinical Development Plans. • Primary responsibility ( together with Cluster Physician, Clinical Scientific Lead or Senior Clinical Research Scientist) for preparing trial protocol, amendments and informed consent form, and taking active part in study design internal discussion/meetings • Coordinating the preparation of other clinical trial documents including: CRF, diary cards, study manuals, IND updates, and clinical summaries • Maintaining accurate and up-to-date information in project management systems and trial specific tracking systems (Clin Track) • Management of overall timelines for internal study document approval and trial allocation • Ensuring that appropriate documents are available to regional teams for timely submission to Ethics Committees and/or Regulatory Authorities according to local requirements • Supports cluster MD/Clinical scientific lead in preparation of investigators' brochure • Contributes to preparation of Clinical Trial Reports/Clinical Study Reports • Contributes to clinical parts of regulatory dossiers and assists in the preparation of regulatory filings • Typically responsible for 1-4 trials of average design and protocol complexity (on lower end of capacity if responsible for trials of greater size and complexity, or across regions)

Posted On - 5/22/2015 9:15:33 AM

Global Clinical Operations Lead

Holly Springs NC

• Bachelor degree required (or comparable), preferably in a science or health related discipline. Post graduate degree in a life science field desirable • At least 5 years but preferably 7+ years hands-on experience in clinical research scope (i.e. responsible for trial document preparation, site management, study and team coordination) • At least 2 years of experience in regional clinical trial leadership desirable • Project Management skills and general understanding of project management tools (e.g. MS Project) • Previous experience in the field of vaccinology desirable • In depth knowledge of GCPs and ICH Guidelines • Solid understanding of clinical trial design, trial execution and operations • Understand business implication of clinical trial design and execution • Excellent communication and presentation skills (both written and verbal), attention to detail, good organizational skills and proactive approach to problem solving • Demonstrated solid experience working on teams with a broad range of cultures including team leadership is desirable • Fluent in English language NOTE: This position can be based in Holly Springs, NC or Cambridge, MA sites. .

Posted On - 5/22/2015 9:15:33 AM

Chemist II, QC

Wilson NC

BS/BA in Chemistry, or life sciences preferred. Fluent in written and spoken English 2-4 years related experience

Posted On - 5/22/2015 9:15:33 AM

Specialist I, Development QA

Holly Springs NC

• Bachelor's degree in Science/ Engineering discipline preferred and 0+ years' experience or equivalent experience in biotech or pharmaceutical industry (high school diploma and 4+ years or equivalent). • Experience in Quality Assurance and/or in a GMP regulated environment within the pharmaceutical industry preferred • Experience with early stage development of Vaccines or Biopharmaceuticals preferred.

Posted On - 5/22/2015 9:15:32 AM

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