Issaquah
WA
Qualifications/Requirements: 1. Associates degree, or a High School diploma and 5 years technical experience
2. Proficiency to logically troubleshoot at subsystem and system level, using identifiable problem solving techniques
3. Ability to draw accurate conclusions from test data, malfunctions, or deviations, and assist with corrections to the existing design or process
4. Proficiency to understand and interpret basic written technical information
5. Demonstrated ability to work well with limited direction and information
6. Ability to communicate using English
7. Must be legally authorized to work in the United States
8. Must be willing to work in our Issaquah, WA facility
9. Must be willing to submit to a drug test and background check
10. Must submit application for employment through gecareers.com to be considered
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: Bachelor?s degree in Manufacturing, Engineering or Technology related fields
Posted On -
5/16/2013 6:30:27 AM
Piscataway
NJ
Qualifications/Requirements:
- BS in Engineering, Science , Business, Finance or Economics
- Min 3 years? experience working in projects in area of operations, supply chain, IT within complex organizations
- Experience with project management in a highly structured environment
- Analytical, troubleshooting and planning skills
- High Computer Skills: MS Excel, MS Access, MS Office, MS Visio, Oracle and GE Support Central
- High Level of Flexibility and passion/engagement
- Demonstrated Team working skills
- Demonstrated ability to create, design, implement, and compete a project
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:
- Change Agent experience
- Green Belt Certified
- Field Sales Experience
- MBA Degree
Posted On -
5/14/2013 6:13:55 AM
Princeton
NJ
Qualifications/Requirements:
* Bachelor's degree in Nursing or PharmD
* Minimum 5 years of pharmaceutical and/or biotechnology industry experience in Pharmacovigilance.
* Basic understanding of data mining in the evaluation of safety signals
* Strong post-marketing and investigational event and aggregate assessment/review/documentation skills.
* Strong working knowledge of US/EU/AP/LA regulations and ICH guidelines.
* Experience in developing case series retrieval strategies.
* Strong knowledge of MedDRA coding.
* Available for domestic and international travel
* Must be legally authorized to work in the United States
* Must be willing to work in Princeton, NJ facility
* 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:
* Knowledge of other languages desirable.
* Ability to work collaboratively with PV Physicians in all pharmacovigilance-related activities.
* 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 li>Experience in working with epidemiologists to develop and implement strategies that lead to an understanding of a product-event relationship desirable.
* Prior experience in pharmacovigilance and risk management strategies regarding products under increased regulatory scrutiny and in assisting PV Physicians in providing the medical safety content of all documents required to implement and monitor the progress of risk management plans and responses to ad hoc safety issues to regulatory authorities.
* Advanced knowledge and understanding of safety database search strategies to support the Pharmacovigilance Physician in the identification and evaluation of safety signals.
- Accepting constructive criticism and dealing calmly and effectively with high-stress situations. This includes continuing to persevere and remaining calm in challenging or frustrating circumstances
- External Focus: Understanding customer needs, marketplace dynamics, industry trends, and the competitive landscape in the industry/function and considering the external impact of business activities and decisions on the external environment
- Inclusiveness: Energizing others by building a connection with the team through personal involvement and trust and providing feedback and coaching to help develop others
- Clear thinker: 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
* Basic understanding of pharmacovigilance -related information systems other than safety databases, such as health claims databases for the identification of safety signals using data mining techniques.
Posted On -
5/14/2013 6:13:55 AM
Princeton
NJ
Qualifications/Requirements: - Bachelor?s Degree
- Minimum 5 years regulatory affairs experience in the pharmaceutical industry
- Minimum 1 year post-marketing regulatory affairs experience
- Minimum 2 years experience reporting/negotiating to FDA and EU health authorities
- Prior experience using spreadsheet and presentation software
-Legal authorization to work in the U.S. is required. We will not sponsor individuals for employment visas, now or in the future, for this job opening.
-Must be willing to work in our Princeton, NJ facility
-Must be willing to submit to a drug test and background check
-Must submit application for employment through gecareers.com to be considered
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: - Regulatory Affairs Certification (RAPS). - Knowledge of Quality Management Systems (QMS) - Ability to work across cultures/countries/sites - Demonstrated experience prioritizing conflicting demands from multiple business entities in an extremely fast paced environment. - Strong problem solving, negotiation and influencing skills - Ability to work well independently & in a team setting to provide timely, constructive and authoritative regulatory opinion and advice on all regulatory aspects. - Demonstrated understanding of healthcare environment and knowledge of current competitive, commercial or political situations and their impact on GEHC regulatory strategies. - Ability to prioritize, plan & evaluate deliverables to established strategic goals. - Demonstrated experience operating in a highly regulated environment; Proven application of analytical skills in a regulatory environment - Demonstrated knowledge & experience conducting scientific, regulatory, legal, or business research. - Excellent verbal and written communication and presentation skills with the ability to communicate business issues in English in an easy to understand manner
Posted On -
5/8/2013 6:30:05 AM
Princeton
NJ
Qualifications/Requirements:
* MD degree
* Minimum 3 years of pharmaceutical and/or biotechnology industry experience in Pharmacovigilance functioning as a Pharmacovigilance Physician
* Successful completion of medical residency and possess clinical/patient care work experience before moving into PV/pharma industry
* Minimum 6 years of experience in both clinical trials and postmarketing pharmacovigilance
* Minimum 6 years of experience in signal detection and evaluation.
* Strong post-marketing and investigational event and aggregate assessment/review/documentation skills.
* Strong working knowledge of US/EU/AP/LA regulations and ICH guidelines.
* Strong experience in risk management plan preparation and review, including European Union Risk Management Plans (EU ? RMPs) and US Risk Evaluation and Mitigation Strategies (REMS).
* Experience in communicating with the FDA, EMA , and other global health authorities.
* Experience in developing case series retrieval strategies.
* Working knowledge of MedDRA coding
* Available for domestic and international travel
* Must be legally authorized to work in the United States
* Must be willing to work in our Princeton, NJ facility
* Must be willing to submit to a drug test and background check
* Must submit application for employment through gecareers.com to be considered
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:
* Knowledge of other languages desirable.
* Collaborative internal relations with Regulatory Affairs, Medical Affairs, Quality and Legal Counsel, with a mindset to share information regarding potential or confirmed safety issues as soon as safety information allows
* High integrity, sense of urgency, ability to recognize time sensitivity, willingness to be a ?player/coach? as necessary, and an appetite to lead all activities within the medical affairs and clinical development functions
* Excellent written and verbal communication skills, exceptional listening skills, strong presentation skills, and good negotiating and influencing skills
* Accepting constructive criticism and dealing calmly and effectively with high-stress situations. This includes continuing to persevere and remaining calm in challenging or frustrating circumstances
* External Focus: Understanding customer needs, marketplace dynamics, industry trends, and the competitive landscape in the industry/function and considering the external impact of business activities and decisions on the external environment
* Inclusiveness: Energizing others by building a connection with the team through personal involvement and trust and providing feedback and coaching to help develop others
* Clear thinker: 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
* Demonstrated success in building effective teams, systems, and processes; proven ability to identify, select and manage a variety of external resources.
* Ability to lead a team of functional experts and negotiate the multi-disciplinary environment in which they operate
* Understanding of pharmacovigilance -related information systems.
* Experience in working with epidemiologists to develop and implement strategies that lead to an understanding of a product-event relationship.
* For PV Physicians serving as the EU-QPPV and Deputy QPPV, an excellent working understanding of the roles and responsibilities of the QPPV as outlined in Volume 9A of the European Union.
* Oversight of the pharmacovigilance and risk management strategy regarding products under increased regulatory scrutiny, with responsibility for the medical safety content of all documents required to implement and monitor the progress of risk management plans and for responses to ad hoc safety issues to regulatory authorities.
* Expert in Aggregate Report preparation and review.
Posted On -
5/7/2013 6:09:02 AM
NA
PA
Qualifications/Requirements:
- Bachelor Degree in Science or Engineering.
- 3 to 5 years working in bioprocessing e.g., bioprocess engineering, bioprocess project management, bioprocess line management, downstream purification lead.
- 1 to 2 years in sales.
- Good overview knowledge of upstream and downstream processes.
- Sales expertise in downstream is a highly desired.
- Ability to interface with both internal and external team members as part of solutions based sales approach.
- Ability to develop and build rapport at all levels within an organization.
- Strong team player.
- Excellent verbal and written communication skills in English.
- Strong presentation skills with ability to synthesize and explain complex issues.
- Valid motor vehicle license
- Location: Philadelphia area, easy access to King of Prussia.
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:
Posted On -
4/29/2013 6:21:15 AM
Princeton
NJ
Qualifications/Requirements: - MD degree
- Minimum 3 years of pharmaceutical and/or biotechnology industry experience in Pharmacovigilance or Drug Safety
- Completed a medical residency and possess clinical/patient care work experience before moving into PV/pharma industry
- Strong post-marketing and investigational event and aggregate assessment/review/documentation skills.
- Strong working knowledge of US/EU/AP/LA regulations and ICH guidelines.
- Experience in communicating with the FDA, EMA , and other global health authorities.
- Experience in developing case series retrieval strategies.
- Working knowledge of MedDRA coding
- Available for domestic and international travel
- Must be legally authorized to work in the United States
- Must be willing to work in our Princeton, NJ facility
- Must be willing to submit to a drug test and background check
- Must submit application for employment through gecareers.com to be considered
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: - Knowledge of other languages desirable. - Collaborative internal relations with Regulatory Affairs, Medical Affairs, Quality and Legal Counsel, with a mindset to share information regarding potential or confirmed safety issues as soon as safety information allows - High integrity, sense of urgency, ability to recognize time sensitivity, willingness to be a ?player/coach? as necessary, and an appetite to lead all activities within the medical affairs and clinical development functions - Excellent written and verbal communication skills, exceptional listening skills, strong presentation skills, and good negotiating and influencing skills - Accepting constructive criticism and dealing calmly and effectively with high-stress situations. This includes continuing to persevere and remaining calm in challenging or frustrating circumstances - External Focus: Understanding customer needs, marketplace dynamics, industry trends, and the competitive landscape in the industry/function and considering the external impact of business activities and decisions on the external environment - Inclusiveness: Energizing others by building a connection with the team through personal involvement and trust and providing feedback and coaching to help develop others - Clear thinker: 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 - Demonstrated success in building effective teams, systems, and processes; proven ability to identify, select and manage a variety of external resources. - Ability to lead a team of functional experts and negotiate the multi-disciplinary environment in which they operate - Understanding of pharmacovigilance -related information systems. - Experience in working with epidemiologists to develop and implement strategies that lead to an understanding of a product-event relationship. - For PV Physicians serving as the EU-QPPV and Deputy QPPV, an excellent working understanding of the roles and responsibilities of the QPPV as outlined in Volume 9A of the European Union. - Oversight of the pharmacovigilance and risk management strategy regarding products under increased regulatory scrutiny, with responsibility for the medical safety content of all documents required to implement and monitor the progress of risk management plans and for responses to ad hoc safety issues to regulatory authorities.
Posted On -
4/25/2013 5:51:55 AM
NA
CA
Qualifications/Requirements:
- Bachelor's Degree
- Minimum of 7 years of consultative sales experience.
- Experience managing sales professionals.
- Excellent communication skills. Strong computer skills, with demonstrated capabilities utilizing the Microsoft OfficeTM suite of products
- Willingness and ability to frequently travel within the specified geographic zone, as well as occasional travel outside the Zone
- Basic forecasting skills and an understanding of fundamental financial principals
- Ability to safely operate a GE owned/leased or rental vehicle for company business (you must be willing to submit to a check of your driving record).
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:
- Experience in a commercial organization serving the BioProcess segments
- Masters degree in Business or Life Sciences
- Prior experience working for a large company in a matrix organization
- Experience selling capital equipment and long-sales cycle products and services
- Range of technical knowledge across all BioProcess applications (e.g. Cell Culture, Filtration, Chromatography, etc.)
Posted On -
4/23/2013 5:47:16 AM
NA
CA
Qualifications/Requirements:
- PhD in Biologics, Molecular Biology, Chemistry, Molecular Pathology or related field
- Minimum 7 years of clinical technology & business leadership experience in the areas of diagnostics or life sciences industry
- Proven successful pipeline development experience, and implementation success of content management, especially in the areas of Oncology, Cardiology and/or Neurology. Minimum of seven years experience.
- Significant global experience and understanding of technology development in the life sciences and diagnostic industries.
- Legal authorization to work in the U.S. is required. We will not sponsor individuals for employment visas, now or in the future, for this job opening.
- Must be willing to work in our Menlo Park, CA or Aliso Viejo, CA facility
- 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:
- PhD and/or MD, experience in oncology translational science.
- Ability to work in a matrix organization and to interact with senior executives
- Product, Technology & Scientific Knowledge: Excellent knowledge of scientific methods/theory with an affinity for clinical solutions and workflow in a diagnostic space
- Clear thinking: Simplifying strategy into actions with clear accountability, making fast, accurate decisions based on available information, and communicating priorities clearly.
- Organizational leadership, influencing, and problem solving, with strong interpersonal skills and excellent written and verbal communication.
Posted On -
4/16/2013 5:34:24 AM
Westborough
MA
Qualifications/Requirements:
* Bachelors degree in Life Sciences, Healthcare or other related degree; knowledge of BioProcess
* Leadership experience in a biotechnology business
* Regulatory background, within Life Sciences or other highly regulated industry
* Must demonstrate large network in the Biopharma industry
* Excellent networking, communication and presentation 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:
* Five to ten years of senior leadership with a large Biopharmaceuticals Company
* Active in trade organizations
* FDA contacts and knowledge
* Advanced degree, PhD preferred in BioProcess related Chemistry, Chemical Engineering, etc.
* Enjoys speaking in front of large, highly educated groups
* Organized, driver with positive and inspiring attitude
Posted On -
4/10/2013 5:38:29 AM
Piscataway
NJ
Qualifications/Requirements: 1. Minimum of a Bachelor's Degree in Science, Finance, Economics, Business Administration, or and at least 5 minimum of 7 years of experience, in positions of increasing responsibility, in patent licensing or the in a life sciences, diagnostic or bioprocess markets technology.
2. A minimum of two years of experience negotiating contracts in the life sciences, biopharmaceutical, or healthcare diagnostic industry.
3. Strong demonstrated skills in writing proposals/strategic documentsskills, articulating complex ideas in an easy to understand manner and delivering presentations at a senior or executive level.
4. Demonstrated experience analyzing, and negotiating and closing business transactions within the life sciences market including acquisition evaluation, modeling and financial analysis
5. Proven track record supporting and managing transactions
6. Ability to understand the various business unit goals and proactively identify inorganic opportunities to meet them
6. Ability to make revenue commitments and engage resources across business units and sites to deliver on them.
7. Experience and demonstrated aptitude both managing and prioritizing multiple projects and initiatives
8. Strong working knowledge of English language (oral and written)
9. Integrity: Accepting and adhering to high ethical, moral, and personal values in decisions, communications, actions, and when dealing with others
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. Masters in Science, Finance or a related function
2. Working knowledge of intellectual property analysis and landscape.
3. Ability to work lead and work within a matrix organizational environment and to interact with executives at the most senior levels
4. Strong interpersonal skills and demonstrated teamwork skills
5. Adaptable/Flexible: Being open to change in response to new information, different or unexpected circumstances.
6. External focus: Understanding customer needs, marketplace dynamics, industry trends, and the competitive landscape in the Life Science industry
Posted On -
2/21/2013 5:26:26 AM
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