Under supervision, provide strategic and operational global CMC regulatory direction and documentation for projects/products covering development, registration and approval/post approval activities. The following activities may be performed within this capacity:
Provide and/or implement global CMC regulatory strategy for development projects or marketed products
Lead or contribute to global CMC submission activities (planning, authoring, reviewing, coordination, submission) for ...
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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 ...
This is a permanent position. Must have strong experience in Solid Tumor and/or Oncology.
Canidates to be located in: NJ, NY, or CT
Region to cover: NJ, NY, CT, and PA
Job Key Duties and Responsibilities:
This position is responsible for performing any/all of the following tasks and responsibilities, as well as any other tasks deemed appropriate by the Supervisor:
Monitor activities at assigned clinical study sites to assure adherence to ICH GCPs, local regulatory requirements, Standard ...
For details and to apply, please visit
Job Title: Pharmacy Tech / Technician
Company Name: CSI Health
Location: Fairfield, New Jersey
Job Type: Full-Time
Profession: Pharmacy Technician
Career Level: Experienced
Experience: 1-2 years
Education Level: Certification
Pharmacy Tech / Technician
The CSI Companies is a national recruitment firm that specializes in placing professionals in contract, right to hire, and direct ...
Currently seeking 2 Lead Clinical Data Managers for a permanent opportunity with a leader in the pharmaceutical industry. Ideally looking for individuals to start as soon as possible.
Will lead & manage project activities at the study level for clinical data management and ensure coordination between teams. Will act as single point of contact for all data management deliverables during study set-up, conduct, and close out phases.
Responsible for the creation/review ...
Heartland Payment Systems
Are You A Relationship Manager?
Integrity. Honesty. Advocacy. Tenacity. These are the core values of Heartland. If you possess these attributes and are determined to be a high-income earner, personal and financial fulfillment can be earned selling the truth for a company known for its integrity and merchant advocacy. Heartland employs nearly 3,000 dedicated employees throughout the country and ...
Our client, a fast paced, growing pharmaceutical company in Central NJ is seeking a Safety Data Specialist for about 6 months. This position pays up to $47/hour, depending upon experience.
• Responsible for collection and processing of spontaneous and clinical trial adverse event and pregnancy reports, which includes data entry and verification of information into the safety database.
• Responsible for medical evaluation of relevant reports, which includes narrative generation, ...
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