Our Large Global Pharmaceutical Client is looking for a Director of Quality to do the following:
Ensures corporate compliance to Regulatory Agency requirements (i.e., FDA, EU, DEA, etc.) from a Quality perspective throughout the clients manufacturing plants within his oversight (and to some degree regarding contract manufacturing companies where this position acts as Quality liaison interact for limited third party cGMP oversight).
Head QA/QC Designee for US Operations within the Corporate CQMS ...
Support the operational execution of the clinical study strategies related to biomarker and pharmacokinetic assessments in oncology protocols, in compliance with client’s processes and regulatory requirements and in collaboration with Oncology Clinical Teams.
• Sample tracking for biomarker and pharmacokinetic samples from clinical site to analytical laboratory.
• Setting up the laboratory procedures, being the primary point of contact and providing ongoing ...
Assigns, oversees, and reviews the work of employees. Directs all phases of work, quality, service, and costs; and performs tests or assays as required.
Candidate must possess strong leadership skills and will direct activities in the laboratory within a managed hospital environment. Required competencies will include but not limited to the following: High level of efficiency in dealing with various levels in the organization, possesses high stress tolerance ...
We are seeking sales representatives to sell our solid Phase extraction line of chromatography products. As a leader in this field we are looking for a successful sales candidate to will work with our sales and support teams, for the purpose of attracting new customers and growing our customer base while giving customer satisfaction. We are looking for candidates with previous sales experience within the chemical sales environment only. You must be a proven revenue generator. Someone comfortable ...
Our client is seeking a long term Regulatory Associate for about 2 years with full benefits. This is an excellent opportunity paying up to $40 an hour.
The Regulatory Associate's responsibilities:
• Provide labeling assistance to Regulatory Affairs (RA) Department and assists RA with the preparation and approval of product labeling
• Prepare labels using Structured Product Labeling (SPL) authoring tool, Text Verification Tool (TVT), LOLA Workflow
• Perform manual proofing of labels in a ...
If Interested, please send your resume to Shangda at ajuliaexecutivesearch.com , 732-993-6810 ex14
Job Title: Product Manager Biocides
Reports to: Managing Director
Job Purpose Statement:
CM responsibility for biocides business.
Establish business strategy and marketing concepts; Develop / Initiate / Execute business plans.
Manage / Coordinate all Market Unit’s related activities (Sales, Technical, Development, Production, Sourcing, Advertising).
Develop market information of competitive ...
Apr 3 -
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