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Company Jobs - GE Healthcare


 

Lead - Quality Assurance Engineer

Sunnyvale CA

1. Bachelor's Degree in an engineering or technical discipline (or non-technical degree with 5 years of experience in engineering, manufacturing, or quality assurance experience in addition to any other experience requirements). 2. Demonstrated understanding or aptitude to understand Medical Device QMS requirements and regulatory requirements including but not limited to FDA CFR 21 820 and ISO 13485. 3. Demonstrated understanding of product development lifecycles, design change and document change control, process verification and validation methodologies, manufacturing / production process control methodologies, and servicing in a medical device environment. 4. Demonstrated expertise to effectively communicate within all levels of the organization around concepts of design controls, design verification and validation activities; production &process controls; Corrective & Preventive Action (CAPA), complaints & risk management; & product quality improvement using tools such as six sigma, DFR, etc. 5. Demonstrated collaboration, negotiation & conflict resolution skills Additional Eligibility Qualifications GE will only employ those who are legally authorized to work in the United States for this opening. Any offer of employment is conditioned upon the successful completion of a background investigation and drug screen. Desired Characteristics 1. Demonstrated knowledge of Quality Management System tools, continuous improvement methodologies & in-depth understanding of site level products & related processes 2. Proven skills in driving operational rigor & ability to multi-task, handle tasks with competing priorities effectively 3. Excellent oral communication & report, business correspondence & procedure-writing skills 4. Demonstrated ability to lead, acknowledge, develop, communicate & implement a strategy under crisis situations to ensure compliance 5. Change agent with energy, passion & enthusiasm to drive change 6. Exceptional analytical, problem solving & root-cause analysis skills 7. Clear thinker: Simplifying strategy into specific actions with clear accountability, making decisions with speed & accuracy based on best available information & communicating priorities clearly & concisely 8. Prior GE Healthcare experience 9. 4 or more years of Quality Assurance or Quality Engineering experience within a medical device or pharmaceutical environment

Posted On - 6/30/2015 7:18:03 AM

Flex Factory Trainer

Marlborough MA

• Technical competence in either upstream bioprocessing (especially mammalian cell culture) or purification, with exposure to the other • Experience as a hands-on operator in a GMP biomanufacturing operation • A strong interpersonal skillset, including good technical communications and an ability to uphold GE company values during customer interactions • Working knowledge of Excel, Word and PowerPoint, Outlook • Bachelor's Degree in Biology, Chemistry, Chemical Engineering or related discipline or Bachelor's Degree and 1 year experience within technical discipline or equivalent (defined as High School Diploma/GED/Biotech training program and 3 years progressive experience within bioprocess-related positions) • Must be able to travel internationally without restrictions • Must be able to sustain up to 50% travel, including multi-week assignments Must be able to reside in the U.S. or the Netherlands Additional Eligibility Qualifications GE will only employ those who are legally authorized to work in the United States for this opening. Any offer of employment is conditioned upon the successful completion of a background investigation and drug screen. Desired Characteristics • At least one year of hands-on GMP manufacturing experience • Expertise in bioreactor operation and cell culture or chromatography and tangential flow filtration • Experience in any of the following areas is beneficial: field service, bioprocess development, customer service, training, facility start-up • Experience with one of the following platforms: Wonderware ArchestrA, Emerson Delta V, Allen-Bradley SLC/PLC, Panel View, RSView32, Intellution/iFix, Siemens PLC Step 7, WinCC control system, Rockwell RSLogix 5000 software or equivalent.

Posted On - 6/30/2015 7:18:03 AM

Scientist I-HC

Marlborough MA

•Bachelor's degree in Chemistry, Physics, Biomedical Engineering, Chemical Engineering or related Life Sciences field •1+ years industrial experience in bioprocess development, scale-up, tech transfer or manufacturing U.S. (Country) Specific Qualifications: •Must be legally authorized to work in the United States full-time •Must be willing to work in our [city, state] facility full-time •Must submit application for employment through gecareers.com (or COS if internal) to be considered •Must be 18 years of age or older •Must be willing to take a drug test as part of the selection process •Must be willing to submit to a background investigation, including for example, verification of your past employment, criminal history, and educational background Additional Eligibility Qualifications GE will only employ those who are legally authorized to work in the United States for this opening. Any offer of employment is conditioned upon the successful completion of a background investigation and drug screen. Desired Characteristics •MS Degree in Life Sciences, Chemistry, Physics, Biomedical Engineering, Chemical Engineering or related Life Sciences field •4+ years of Vaccine, MAb plasma, recombinant protein manufacturing, R&D and/or process development experience •Willing to gain scientific understanding of principles and theory behind unit operations for processing biologicals with knowledge in principles of scale up, validation, disposable, hybrid and traditional set ups and GMP manufacturing •Cell culture, filtration and/or chromatography experience •Prior teaching and/or presenting scientific material experience would be highly desirable •Excellent oral and written communication skills •Experience with research collaborations •Self-starter, energizing, results oriented, and able to multi-task •Demonstrated problem solving ability and results orientation

Posted On - 6/30/2015 7:18:03 AM

Global Coordinator, Pharmacovigilance

Marlborough MA

• Bachelor of Science degree • Minimum of 2 years of pharmaceutical/biotechnology industry with experience in pharmacovigilance including clinical trials and postmarketing. Global experience highly preferred. • In-depth knowledge of Individual Case Safety Report (ICSR) processing with hands-on experience coordinating and monitoring ICSR workflows and reporting ICSRs to global regulatory agencies • Proficient in performing data entry, retrieval and electronic reporting in global drug safety databases (ARISg highly preferred) • Familiar with US/EU/AP/LA regulations and ICH guidelines pertaining to adverse event reporting • Proficient in use of Microsoft Office (Word, Excel, PowerPoint, Outlook) • Must be permitted to work in USA • Must be willing to submit to a background investigation, including for example, verification of your past employment, criminal history, and educational background Additional Eligibility Qualifications GE will only employ those who are legally authorized to work in the United States for this opening. Any offer of employment is conditioned upon the successful completion of a background investigation and drug screen. Desired Characteristics • High integrity, sense of urgency and ability to recognize time sensitivity • Excellent organizational, interpersonal skills, problem solving and negotiation skills • Excellent written and verbal communication skills • Being open to change (positive or negative) in response to new information, different or unexpected circumstances, and/or to work in ambiguous situations

Posted On - 6/30/2015 7:18:03 AM

QA Lead Engineer

Westborough MA

1. Bachelor's Degree or a minimum of 4 years work experience. 2. Minimum of 1 year experience working in a regulated industry or a Masters degree 3. Ability to communicate effectively in English (both written and oral). 4. Demonstrated experience and proficiency with MS Office word processing, spreadsheet, presentation, and database applications. Additional Eligibility Qualifications GE will only employ those who are legally authorized to work in the United States for this opening. Any offer of employment is conditioned upon the successful completion of a background investigation and drug screen. Desired Characteristics 1. Minimum of 3 years experience in a regulated industry is preferred 2. Demonstrated understanding or aptitude to understand Medical Device QMS requirements and regulatory requirements including but not limited to FDA CFR 21 820 and ISO 13485. 3. Demonstrated knowledge of Quality Management System tools, continuous improvement methodologies & in-depth understanding of site level products & related processes 4. Demonstrated expertise to effectively communicate within all levels of the organization around concepts of design controls, design verification and validation activities; production &process controls; Corrective & Preventive Action (CAPA), complaints & risk management; & product quality improvement using tools such as six sigma, DFR, etc. 5. Demonstrated collaboration, negotiation & conflict resolution skills 6. Excellent communication skills (written and oral) 7. Demonstrated ability to lead, acknowledge, develop, communicate & implement a strategy under crisis situations to ensure compliance 8. Demonstrated understanding of product development lifecycles, design change and document change control, process verification and validation methodologies, manufacturing / production process control methodologies, and servicing in a medical device environment. 9. Demonstrated understanding of continuous quality / process improvement tools: (As defined by the local site, e.g. DMIAC, SPC, Lean SS, 5S) 10. Experience leading and implementing change 11. Experience performing internal audits and participating in external audits 12. Exceptional analytical, problem solving & root-cause analysis skills 13. Ability to multi-task & handle tasks with competing priorities effectively 14. Strong technical aptitude (i.e. able to read & comprehend technical documentation & execute procedures), global regulatory experience & demonstrated experience interfacing with regulators. 15. Prior GE Healthcare experience

Posted On - 6/30/2015 7:18:03 AM

Product Manager-Cell Culture

Logan MA

1. Bachelor's Degree in technical (Science or Engineering) or business (Marketing, Business Administration) field. 2. Minimum 3 years combined experience in product management, marketing or a related technical field 3. Excellent oral and written communications skills 4. Strong analytical and process skills 5. Strong project management skills 6. Ability to work effectively within a matrix environment 7. Strong leadership qualities Additional Eligibility Qualifications GE will only employ those who are legally authorized to work in the United States for this opening. Any offer of employment is conditioned upon the successful completion of a background investigation and drug screen. Desired Characteristics 1. MSc or Master's degree in Marketing, Engineering, Science, Business Administration or other related field 2. 5+ years combined experience in product management, marketing or a related technical field 3. Product Management/Marketing expertise, including: market trends/analysis, NPI process, product roadmap development, product life-cycle management, 4. Life science product/industry/technical acumen 5. Team oriented - ability to motivate and work well with diverse, cross-functional teams 6. Proven ability to work globally

Posted On - 6/30/2015 7:18:03 AM

QA Manager - GCP/GLP

Marlborough MA

• Bachelor's degree in science or higher degree, with 5+ years of GCP /GLP related experience (QA experience in the drug or device industry highly preferred). • A strong understanding of GxPs and an ability to apply them to clinical research and/or related processes is required. • Inspection experience in clinical trial conduct, support laboratory evaluation • Experience in auditing or certified auditor for compliance in computer validation, pharmacovigilence systems and knowledge of compliance issues related to commercial drug product promotion is highly desirable • Excellent knowledge of GCP/GLP regulations • Excellent technical report writing skills • Strong Communications, interpersonal and problem solving skills and detail oriented • Domestic, international overnight travel is required • Multi-lingual fluency highly desirable Additional Eligibility Qualifications GE will only employ those who are legally authorized to work in the United States for this opening. Any offer of employment is conditioned upon the successful completion of a background investigation and drug screen. Desired Characteristics 1. Master's Degree or PhD in Engineering or Technical Discipline. 2. CRA experience. 3. Demonstrated expertise to effectively communicate within all levels of the organization around concepts of design controls, design verification and validation activities; production &process controls; Corrective & Preventive Action (CAPA), complaints & risk management; & product quality improvement using tools such as six sigma, DFR, etc. 4. Demonstrated collaboration & conflict resolution skills 5. Excellent communication skills (written and oral) 6. Demonstrated ability to lead, acknowledge, develop, communicate & implement a strategy under crisis situations to ensure compliance 7. Demonstrated understanding of product development lifecycles, design change and document change control, process verification and validation methodologies, manufacturing / production process control methodologies, and servicing in a medical device environment. 8. Demonstrated understanding of continuous quality / process improvement tools: (As defined by the local site, e.g. DMIAC, SPC, Lean SS, 5S) 10. Experience leading and implementing change 9. Experience performing internal and external audits 10. Exceptional analytical, problem solving & root-cause analysis skills 11. Ability to multi-task & handle tasks with competing priorities effectively 12. Strong technical aptitude (i.e. able to read & comprehend technical documentation & execute procedures), global regulatory experience & demonstrated experience interfacing with regulators.

Posted On - 6/30/2015 7:18:03 AM

Strategic Marketing Analysis

Marlborough MA

Quality Specific Goals: 1. Aware of and comply with the GEHC Quality Manual, Quality Management System, Quality Management Policy, Quality Goals, and applicable laws and regulations as they apply to this job type/position 2. Complete all planned Quality & Compliance training within the defined deadlines 3. Identify and report any quality or compliance concerns and take immediate corrective action as required Required Qualifications and Skills: • Bachelor's Degree or higher in Finance, Economics, Business Administration, or in a relevant scientific field • Experience analyzing business transactions including evaluation, modeling and financial analysis. Excellent skills in Excel. • Ability to analyze and synthesize multiple, complex sources of information into actionable recommendations. • Ability to network and build rapport with external customers as well as payer and policy decision makers • Strong working knowledge of English language (oral and written) • Integrity: Accepting and adhering to high ethical, moral, and personal values in decisions, communications, and actions Additional Eligibility Qualifications GE will only employ those who are legally authorized to work in the United States for this opening. Any offer of employment is conditioned upon the successful completion of a background investigation and drug screen. Desired Characteristics • Having both a business and a science background or education, ideally with an understanding of the pharmaceutical industry • Excellent written and verbal communication skills with the ability to effectively communicate complex business issues • Ability to work within a matrix organization plus strong interpersonal and teamwork skills • Adaptable/Flexible: Being open to change in response to new information, different or unexpected circumstances, and/or to work in ambiguous situations • Clear thinking: Simplifying strategy into specific actions with clear accountability, making decisions with speed and accuracy based on best available information, and communicating priorities clearly and concisely • External focus: Understanding customer needs, marketplace dynamics, industry trends, and the competitive landscape, and considering the external impact of business activities and decisions on the external environment

Posted On - 6/29/2015 7:34:06 AM

Customer & Market Insights Leader

Marlborough MA

1. Bachelor's Degree in Marketing, Business Administration or Statistics/Economics or a related science field 1. 5+ years' experience in market research or related field 2. Ability to influence and make recommendations at all levels of the company 2. Excellent oral and written communications skills 3. Strong analytical and process skills Additional Eligibility Qualifications GE will only employ those who are legally authorized to work in the United States for this opening. Any offer of employment is conditioned upon the successful completion of a background investigation and drug screen. Desired Characteristics 1. Master's or Ph.D. in Marketing, Statistics or Economics 2. 8+ years' experience in market research or related field 3. Ability to interpret large amounts of information, e.g. from clinical studies, scientific papers, financial reports and in-depth market research studies 4. Excellent project management skills - able to lead and manage complex matrix teams 5. High energy works proactively and demonstrates flexibility in approach to changing work priorities. 6. Life Sciences/Bioscience product/industry acumen 7. Team oriented - ability to motivate and work well with diverse, global and cross-functional teams 8. Influencing skills - ability to motivate individuals and demonstrate organizational influence 9. Broader commercial or consulting experience

Posted On - 6/29/2015 7:34:06 AM

Anatomic Pathology Technician III - Immunohistochemistry

Houston TX

1. AA, AS or minimum 2 year equivalent combination of education and experience 2. Minimum 3 years of experience in a Histology/IHC lab as a technician 3. Ability to troubleshoot intermediate to advanced issues on IHC platforms, histology, and/or general workflow. 4. Able to demonstrate initiative, balanced assertiveness, team orientation and take a leadership role with staff and/or new hires when the leadership team is indisposed. 5. Advanced skills in microtomy and tissue embedding, must be able to complete these skills in an efficient manner and/or experience working in the IHC lab environment. 6. Ability to handle biological samples and potentially hazardous chemicals. 7. Ability to operate equipment with sufficient proficiency to successfully execute test procedures. 8. Computer skills and extensive automation knowledge for AP instruments. 9. Ability to communicate effectively and follow written and verbal instructions. 10. High School Diploma or equivalent 11. Successful candidate must have an extensive understanding of general laboratory techniques. 12. Able to demonstrate excellent time management skills. 13. All candidates must pass a color vision test. Additional Eligibility Qualifications GE will only employ those who are legally authorized to work in the United States for this opening. Any offer of employment is conditioned upon the successful completion of a background investigation and drug screen. Desired Characteristics 1. HT (ASCP) Certification preferred 2. HTL (ASCP) Certification preferred 3. QIHC (ASCP) Certification preferred

Posted On - 6/23/2015 7:32:47 AM

Solutions Marketing Manager

Marlborough MA

1. Aware of and comply with the GEHC Quality Manual, Quality Management System, Quality Management Policy, Quality Goals, and applicable laws and regulations as they apply to this job type/position 2. Complete all planned Quality & Compliance training within the defined deadlines 3. Identify and report any quality or compliance concerns and take immediate corrective action as required Qualifications: 1. 8+ years experience in marketing, product marketing, sales, business development or related field 2. Experience of marketing and/or selling products through distribution partners 3. Excellent oral and written communications skills 4. Strong analytical and process skills 5. Capable of quickly understanding and interacting with customers at senior levels within organizations 6. Capable of quickly grasping technical and clinical concepts to drive solutions 7. Ability to deal with abstract concepts and handle ambiguity well. 8. Ability to proactively look 1-3 years out and anticipate how global, regulatory and business operating changes might impact segment value and need 9. Able to drive change 10. Clear Thinker - Strong decision making skills: takes proactive steps to generate results, uses data and other inputs to make decisions, owns decision, and takes accountability for work using strong organizational and analytical skills. Additional Eligibility Qualifications GE will only employ those who are legally authorized to work in the United States for this opening. Any offer of employment is conditioned upon the successful completion of a background investigation and drug screen. Desired Characteristics 1. Life Sciences product/industry acumen 2. Leadership skills to lead teams and shape/lead growth vision and marketing strategy 3. Able to drive change 4. Collaborative leadership skills - exhibits willingness to engage other business partners within the organization, is innovative, creative and a team player with a solution-based approach capture opportunities and remove barriers. 5. Team oriented - ability to motivate and work well with cross-functional teams 6. Assertiveness - strong influencing skills across business functions; confidence to share difficult messages and defend decisions and make judgment calls

Posted On - 6/23/2015 7:32:47 AM

Viral Production Lab Associate 2

Lafayette CO

Minimum Requirements/ Qualifications: • Bachelor's Degree in Biology or a closely related field; • Typically 1-3 years current laboratory experience; • Proficient in mammalian tissue culture and DNA cloning; • Familiarity with standard concepts, practices, and procedures of a BSL 2 laboratory; • Professional and clear communication skills, both written and verbal; • Must be able to use a computer with previous work experience in MS Outlook and Excel; and • Proficient typing skills. Physical Requirements/ Working Conditions: • Duties of this job are regularly performed indoors. • Work is primarily in a laboratory environment and may include some work in office environment to include cubicles and/or in and around shipping/receiving docks, stock rooms, and storage locations. • This position is regularly required to talk, hear, stand, sit, walk, reach and pull with hands and arms. • Work includes standing on your feet for the majority of each shift. • Associate is regularly required to climb or balance, stoop, kneel, crouch or crawl. • Personal protective equipment must be worn to include lab coats, safety gloves, and safety glasses. • Must be able to work overtime as required. • Must be able to work in a BSL2 laboratory with exposure to non-replicating viral particles. Quality Specific Goals: 1. Aware of and comply with the GEHC Quality Manual, Quality Management System, Quality Management Policy, Quality Goals, and applicable laws and regulations as they apply to this job type/position 2. Complete all planned Quality & Compliance training within the defined deadlines 3. Identify and report any quality or compliance concerns and take immediate corrective action as required 4. Ensures the QC processes are established and followed as required. 5. Ensures QI metrics are established and followed as required. 6. Ensure laboratory operates with no major systematic deficiencies as determined by external audits (CAP, NYS). Additional Eligibility Qualifications GE will only employ those who are legally authorized to work in the United States for this opening. Any offer of employment is conditioned upon the successful completion of a background investigation and drug screen. Desired Characteristics The ideal candidate will possess all of the following: • Good analytical skills and laboratory practices; • Inherently focused and self-motivated; • Excellent interpersonal skills with the talent for teamwork; • Experience with sequence analysis; • A high level of emotional intelligence; and • Exceptional attention to detail and accuracy. • Master's degree plus 1-3 yrs. relevant work experience is preferred.

Posted On - 6/23/2015 7:32:47 AM

Marketing Operations Analyst

Marlborough MA

Quality Specific Goals: • Aware of and comply with all Quality, Regulatory, and Legal policies and guidelines, as well as applicable laws and regulations as they apply to this job type/position • Complete all required Quality & Compliance training within the defined deadlines • Identify and report any compliance concerns and take immediate corrective action as required • Establish a commitment to quality within ongoing simplification of Marketing processes and mechanisms Required Qualifications: • Bachelor's degree in Marketing, Operations, Business Administration, or related field • 2 years experience in marketing operations, marketing, product management, and/or commercial operations • Strong analytical skills with passion for data, financial modeling and reporting • Demonstrated process-driven orientation and execution focus • Determined drive for results leading to high quality outputs • Strong project management skills and attention to details • Ability to work effectively within a matrix environment • Highly effective interpersonal and communication skills • Highly collaborative team player with ability to develop effective relationships across an organization • Extensive knowledge and use of Microsoft Office • Ability to travel up to 10% of time Additional Eligibility Qualifications GE will only employ those who are legally authorized to work in the United States for this opening. Any offer of employment is conditioned upon the successful completion of a background investigation and drug screen. Desired Characteristics • Master's degree in Business Administration, Marketing, Operations, or related field • Professional experience from a top strategy consulting firm • Deep knowledge of both life sciences and diagnostics industries • Familiarity with CRM databases and marketing automation platforms • Proven ability to work globally • Proven ability to influence internal stakeholders

Posted On - 6/23/2015 7:32:47 AM

Project Leader II - Clinical Development

Marlborough MA

1. BS/MS Degree in Life Sciences, Chemistry, Physics 2. Minimum of 5 years project leadership experience pharmaceutical and/or clinical development 3. Demonstrated leadership of cross-functional project teams and an ability to drive project plans to completion 4. Familiarity with FDA/EMEA/PMDA/CFDA and other regulatory standards and guidelines 5. Demonstrated understanding/experience with the New Product Introduction (NPI) cycle Additional Eligibility Qualifications GE will only employ those who are legally authorized to work in the United States for this opening. Any offer of employment is conditioned upon the successful completion of a background investigation and drug screen. Desired Characteristics 1. PhD Degree in Life Sciences, Chemistry, Physics, 2. Strong written and verbal communication skills 3. Experience with conflict resolution 4. Self-starter, energizing, results oriented, and able to multi-task 5. Demonstrated problem solving ability and results orientation. Creative problem solver and solution developer when presented with conflicting requirements, business demands and technical risks/issues 6. Demonstrated ability to work in a collaborative, matrixed, and customer focused environment 7. Excellent communication, influencing skills and ability to gain buy-in for initiatives 8. Project management certification 9. Demonstrated skills in proactively identifying, facilitating and driving closure of a product 10. Knowledge of GE Healthcare engineering tools and processes 11. Attention to detail and ability work independently toward timely completion of a variety of assignments 12. Ability to develop unique concepts/solutions for complex products

Posted On - 6/22/2015 7:25:20 AM

Courier

Houston TX

1. Willingness to submit to a drug test and background check 2. High School Diploma or GED 3. Valid drivers license to operate in necessary delivery area 4. Ability to accommodate shift changes based on business needs Quality Specific Goals: 1. Aware of and comply with the GEHC Quality Manual, Quality Management System, Quality Management Policy, Quality Goals, and applicable laws and regulations as they apply to this job type/position. 2. Complete all planned Quality & Compliance training within the defined deadlines. 3. Identify and report any quality or compliance concerns and take immediate corrective action as required Additional Eligibility Qualifications GE will only employ those who are legally authorized to work in the United States for this opening. Any offer of employment is conditioned upon the successful completion of a background investigation and drug screen. Desired Characteristics 1. Previous delivery driving experience 2. Previous experience handling/transporting pharmaceuticals or radioactive materials 3. Ability to prioritize job duties, handle multiple tasks quickly without compromising quality

Posted On - 6/22/2015 7:25:20 AM

Client Billing Specialist

Aliso Viejo CA

•High school diploma or equivalent •Minimum of one year related job experience and/or training in the medical billing field •Extensive medical billing knowledge •Advanced computer skills •Working knowledge of Microsoft Office •Excellent typing and data entry skills •High level of accuracy and attention to detail •Ability to multitask, adapt to change, and work in a fast paced team environment •Ability to communicate effectively and follow written and verbal instructions Additional Eligibility Qualifications GE will only employ those who are legally authorized to work in the United States for this opening. Any offer of employment is conditioned upon the successful completion of a background investigation and drug screen. Desired Characteristics •Job experience and/or training in the Clinical Laboratory/Anatomic Pathology setting

Posted On - 6/22/2015 7:25:20 AM

Hourly Shipping Coordinator

Lafayette CO

Required Qualifications: • High school Diploma/GED or local equivalent • Typically 2 years or more professional working experience; • Must be able to use a computer with previous work experience in MS Outlook and Excel; • Proficient typing skills; • Excellent interpersonal skills with the talent for teamwork; • Exceptional attention to detail and accuracy; • Ability to communicate well and work with others; and • Ability to interface with Customers and Suppliers in a business professional manner on the phone and through e-mail Physical Requirements/ Working Conditions: • Duties of this job are regularly performed indoors, with occasional work done out of doors. • Work is in office environment to include cubicles and/or in and around shipping/receiving docks, stock rooms, storage locations and laboratory environments. • This position is regularly required to talk, hear, stand, sit, walk, reach and pull with hands and arms. • Work includes standing on your feet for the majority of each shift. • Associate is regularly required to climb or balance, stoop, kneel, crouch or crawl. • Must regularly lift and/or move up to 70 pounds. • Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception and the ability to adjust focus. • Depending on area of building, personal protective equipment may be worn to include lab coats, safety gloves, and safety glasses. • Must be able to work overtime as required. Quality Specific Goals: 1. Aware of and comply with Stop Order, Concession, Defect Awareness, ESD, Non-conforming Material, Material Identification/Segregation and Good Documentation Practices procedures as associated with this job type/position. 2. Aware of and comply with the GEHC Quality Manual, Quality Management System, Quality Management Policy, Quality Goals, and applicable laws and regulations as they apply to this job type/position 3. Complete all planned Quality & Compliance training within the defined deadlines 4. Identify and report any quality or compliance concerns and take immediate corrective action as required Additional Eligibility Qualifications GE will only employ those who are legally authorized to work in the United States for this opening. Any offer of employment is conditioned upon the successful completion of a background investigation and drug screen. Desired Characteristics Preferred Qualifications: Familiarity or previous experience with the following items is highly desired: • Inventory management and/ or inventory cycle count; • Familiarity with dangerous goods shipping as well as dry ice packaging requirements; • Previous experience or familiarity with Oracle system

Posted On - 6/22/2015 7:25:20 AM

Regulatory Affairs Leader

Milwaukee WI

1. Bachelor's Degree or a minimum of 4 years work experience. 2. Minimum of 1 year experience working in a regulated industry or a Masters degree 3. Ability to communicate effectively in English (both written and oral). 4. Demonstrated experience and proficiency with MS Office word processing, spreadsheet, presentation, and database applications. Quality Specific Goals: 1. Aware of and comply with the GEHC Quality Manual, Quality Management System, Quality Management Policy, Quality Goals, and applicable laws and regulations as they apply to this job type/position. 2. Complete all planned Quality & Compliance training within the defined deadlines. 3. Identify and report any quality or compliance concerns and take immediate corrective action as required Additional Eligibility Qualifications GE will only employ those who are legally authorized to work in the United States for this opening. Any offer of employment is conditioned upon the successful completion of a background investigation and drug screen. Desired Characteristics 1. Minimum of 3 years experience in a regulated industry is preferred 2. Advanced degree in scientific, technology or legal disciplines 3. Regulatory Affairs Certification (RAPS) 4. Statistics education and or training 5. Ability to work independently in fast-paced environment with little supervision. 6. Ability to adapt to constant change and influence positive change effectively. 7. Team-oriented and responsive to customer needs. 8. Attention to Detail and Results-Oriented. 9. Ability to understand technical documentation and execute associated procedures

Posted On - 6/19/2015 7:30:02 AM

Pharmacovigilance Compliance Coordinator

Marlborough MA

• Bachelor's of Science degree with RN or Pharmacy Degree preferred • Minimum of 2 years in pharmaceutical/biotechnology industry experience in PV, including clinical trials and postmarketing experience. Global experience and experience in Pharmacovigilance compliance monitoring is preferred. • Proficient in US/EU/AP/LA regulations and ICH guidelines • Proficiency working in Windows-based word processing and medical/scientific/regulatory databases/resources • Must be permitted to work in USA • Must be willing to submit to a background investigation, including for example, verification of your past employment, criminal history, and educational background Additional Eligibility Qualifications GE will only employ those who are legally authorized to work in the United States for this opening. Any offer of employment is conditioned upon the successful completion of a background investigation and drug screen. Desired Characteristics • High integrity, sense of urgency, ability to recognize time sensitivity, willingness to work in a matrix environment and assume the role of "player/coach" as necessary • Excellent written and verbal communication skills, exceptional listening skills, strong presentation skills, and good negotiating and influencing skills

Posted On - 6/18/2015 7:30:08 AM

Field Marketing Manager, Nuclear Medicine

Marlborough MA

1. Bachelor's Degree in Marketing, Business Administration or related field 2. 5+ years' experience in marketing or related field 3. Healthcare product/industry acumen 4. Excellent oral and written communications skills 5. Planning and project management skills 6. Experience working with Sales teams and supporting commercial teams with programs to drive awareness and sales. Additional Eligibility Qualifications GE will only employ those who are legally authorized to work in the United States for this opening. Any offer of employment is conditioned upon the successful completion of a background investigation and drug screen. Desired Characteristics 1. MBA or Master's degree in Marketing, Business Administration or related field 2. 7+ years' experience in marketing 3. Marketing experience in market & customer insights, product commercialization and branding 4. Healthcare product/industry acumen, preferably in diagnostic imaging, nuclear medicine and pharmaceutical imaging agents 5. Experience developing/adapting and implementing marketing campaigns and programs across multiple customer targets 6. Innovation - ability to develop/execute on new ideas through collaboration 7. Team oriented - ability to work well with diverse, cross-functional teams 8. Leadership and initiative to drive business objectives 9. Digital Marketing and Social media experience 10. Can learn quickly and communicate effectively across multiple stakeholders in a fast paced environment

Posted On - 6/18/2015 7:30:08 AM

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