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Life Sciences Account Executive

http://www.eglifesciences.com/internal-careers/account-executive

Quality Assurance and Systems. FDA Consent Decree Remediation. FDA Corporate Warning Letter Remediation Post Market Surveillance. FDA Pre-Approval Inspection PAI Preparation. Technical File Updates Medical Device Company. Purpose of the Position:. Must have proven successful track record of selling Staffing Solutions in the greater Boston area with a strong focus on hunting and developing new business OR have proven sales experience in a highly competitive and transactional environment. The above stateme...

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Life Sciences Staffing & Consulting – Quality Management

http://www.eglifesciences.com/services/quality-management-systems

Quality Assurance and Systems. FDA Consent Decree Remediation. FDA Corporate Warning Letter Remediation Post Market Surveillance. FDA Pre-Approval Inspection PAI Preparation. Technical File Updates Medical Device Company. Assessments, GAP Analyses, and Optimization. Reviews of process and procedures to identify opportunities for improvement. Implementation and Turn-key Project Management. Complete management of projects from task execution, resource planning, schedule management, team meetings, etc.

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Life Sciences Staffing & Consulting - Regulatory

http://www.eglifesciences.com/services/regulatory-affairs

Quality Assurance and Systems. FDA Consent Decree Remediation. FDA Corporate Warning Letter Remediation Post Market Surveillance. FDA Pre-Approval Inspection PAI Preparation. Technical File Updates Medical Device Company. Regulatory Submissions (ex.- Premarket Approval PMA, 510(k), CE Mark, INDs, ANDAs, etc.) and Compliance. Lead and assist client companies with product approvals and submissions for both U.S. and International markets. Labeling, Advertising, and Promotional Materials Review. Lead and ass...

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Life Sciences Staffing & Consulting – Quality Assurance

http://www.eglifesciences.com/services/quality-assurance-and-control

Quality Assurance and Systems. FDA Consent Decree Remediation. FDA Corporate Warning Letter Remediation Post Market Surveillance. FDA Pre-Approval Inspection PAI Preparation. Technical File Updates Medical Device Company. Quality Assurance and Control. Specification Development and Review. Establish and document product requirements and specifications. Process Establishment, Implementation, and Improvement initiatives. Document and formal release of process parameters and procedures. FDA Guidance Doc on ...

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EG Life Sciences Resources

http://www.eglifesciences.com/resources

Quality Assurance and Systems. FDA Consent Decree Remediation. FDA Corporate Warning Letter Remediation Post Market Surveillance. FDA Pre-Approval Inspection PAI Preparation. Technical File Updates Medical Device Company. FDA Guidance Doc on UDI Labeling. Center For Diseases and Radiological Health (CDRH) News and Updates. 2015 FDA Enforcement Activities - Drugs. FDA Guidance Doc on UDI Labeling. Center For Diseases and Radiological Health (CDRH) News and Updates. 2015 FDA Enforcement Activities - Drugs.

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Life Sciences Principal Consultant

http://www.eglifesciences.com/internal-careers/sme-principal-consultant

Quality Assurance and Systems. FDA Consent Decree Remediation. FDA Corporate Warning Letter Remediation Post Market Surveillance. FDA Pre-Approval Inspection PAI Preparation. Technical File Updates Medical Device Company. Purpose of the Position:. Key Tasks and Responsibilities. Develop new client engagements through your personal network as well as targeted client companies. Help with the growth of existing client relationships. Ensure that all scope of work projects developed with client are attainable.

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About EG Life Sciences

http://www.eglifesciences.com/about

Quality Assurance and Systems. FDA Consent Decree Remediation. FDA Corporate Warning Letter Remediation Post Market Surveillance. FDA Pre-Approval Inspection PAI Preparation. Technical File Updates Medical Device Company. EG Life Sciences is committed to providing our clients with the best talent available in the market. Similarly, our Professional Service and Consultant practices are committed to driving business value and results for our clients. Warning Letter/Consent Decree Remediation.

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consultant-advocate

http://www.eglifesciences.com/consultant-advocate

Quality Assurance and Systems. FDA Consent Decree Remediation. FDA Corporate Warning Letter Remediation Post Market Surveillance. FDA Pre-Approval Inspection PAI Preparation. Technical File Updates Medical Device Company. Reward yourself by referring your network! Chances are you’ve worked with some great performers in the past you may still even work with them now! Why not be rewarded for surrounding yourself with extraordinarily talented people? How does the referral bonus work? What will you receive?

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Life Sciences Staffing & Consulting – Validation

http://www.eglifesciences.com/services/validation

Quality Assurance and Systems. FDA Consent Decree Remediation. FDA Corporate Warning Letter Remediation Post Market Surveillance. FDA Pre-Approval Inspection PAI Preparation. Technical File Updates Medical Device Company. Master Validation Plan (MVP) Development. Establish and document plans for how, who and when validation activities shall be executed. Process Validation (IQ, OQ, PQ). Protocol development to show processes have been appropriately validated. Packaging/Storage Stability and Labeling.

eglifesciences.com

Life Sciences Team Lead Recruiter

http://www.eglifesciences.com/internal-careers/team-lead-recruiter

Quality Assurance and Systems. FDA Consent Decree Remediation. FDA Corporate Warning Letter Remediation Post Market Surveillance. FDA Pre-Approval Inspection PAI Preparation. Technical File Updates Medical Device Company. Jayne Gill (Managing Director). Purpose of the Position:. Key Tasks and Responsibilities. Lead and develop the recruiting team through daily goal setting and individual accountability. Ensure that all recruiters are following procedure regarding data collection and communication. Respon...