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Global Pharmaceutical Leader is looking for consultant (all levels) Clinical Managers for their growing Clinical Development team Accountable for leading the operational study team, which is responsible for the execution and delivery of quality studies, including in-process quality control activities (e.g. quality checks and balances to ensure inspection readiness, enrollment, metrics, milestones, timelines and budget). This position requires advanced knowledge of the functional disciplines....


Our client is a world leader in laboratory equipment and services, and has an opportunity for a Technical Sales Representative (TSR) for its industry leading analytical instrumentation used in R&D laboratories. The Technical Sales Representative will be responsible for direct sales of mechanical surface characterization instrumentation and services to customers covering OR, WA, ID, MT, CO, WY, & UT with an ideal base close to Portland or Seattle. The product lines include Atomic Force....


Top Tier Pharmaceutical company (with focus in RESPIRATORY, CNS, Diabetes, Cardio, GI and more) in Madison, NJ is looking for three Clinical Trials Manager Consultants for Clinical Trials Group This is a one year contract and can continue for up to 4 years (1099 or w-2)SummaryParticipate in all aspects of clinical development and study management under the direction of the Director, or designee, which includes providing scientific, and/or logistical support to planned and ongoing trials CTM –....

- Swifwater, PA

Global Pharmaceutical and Vaccine company is expanding the Marketing division: Objective: To maximize company dose and dollar sales volume in a manner consistent with profit goals. Expectations: ·Achieve forecast as planned. ·Develop realistic and achievable forecast in concert with Marketing and Sales Management. ·Use information systems and reports to monitor and direct the progress of sales and profits toward monthly, trimester and annual sales objectives. PRODUCT LINE MANAGEMENT Objective:


Global Pharmaceutical company (headquarted in West Palm BEach, Florida) is growing and needs a Strong Clinical Lead (someone who mas managed the CRAs and the clinical study trials but can also monitor when needed as Snr CRA). Snr Clinical Research Associate for oncology trials. Must have five to eight years of experience with at least two years of oncology experience. Must come from a Sponsor company (Pharma or Biotech) and be bi-lingual (spanish speaking - many sites are in Latin America).....

- Charlotte, NC

Summary of the Position:. Develops and deploys the quality system for entire manufacturing facilities to assure systems and procedures are compliant pursuant to government regulations, industry standards and Company specifications and policies. Periodically reviews the suitability and effectiveness of the quality systems with Executive Management. He/She has ultimate responsibility for making the quality decisions on the identity, purity, strength or composition of nutritional products in the....

- Lancaster, SC

Summary of the Position:. Develops and deploys the quality system for entire manufacturing facilities to assure systems and procedures are compliant pursuant to government regulations, industry standards and Company specifications and policies. Periodically reviews the suitability and effectiveness of the quality systems with Executive Management. He/She has ultimate responsibility for making the quality decisions on the identity, purity, strength or composition of nutritional products in the....

- Cranford, NJ

Global Pharmaceutical company is hiring a \ for their growing company. Our Clinical Trainer is responsible for identifying and implementing Clinical Development staff training needs. They may benchmark Clinical SOPs and insure SOP training is completed and up to date. The Clinical Operations Trainer may also periodically co-monitor and evaluate staff performance and provide guidance for performance, improvement and adherence to FDA and SOP requirements. They may liaise with US and Taiwan....

- Rock Hill, SC

We are looking for a Metrology Technician to perform accurate measurements of complex molded components using advanced programmable optical measuring systems. Job Responsibilities: 1. Interpret and apply metrology programs 2. Perform day to day metrology functions by following established standard operating procedures 3. Produce dimensional report, collect & analyze data, and understanding of statistical process control rules 4. Interpret charts, graphs, and data 5. Determine the most....

- Trona, CA

Lab Manager - QA/QC - Trona, CA Excellent high desert/mountainous location for the outdoors type without the expense of the crowded coastal areas of California located in the Bakersfield / Ridgecrest / Mojave area. In this very large 500+ person inorganics production facility you will be responsible for providing management and technical expertise on large and complex engineering and construction projects through all phases of project development and execution. Responsible for leading,....


Manufacturing Engineer – Injection Molding Experience a must!! Camden SC COMPANY PROFILE:50 plus years as a provider to the automotive and engine industry State of the art products individually tailored to customer needs (Tier one / Tier two Automotive OEM and aftermarket)Global Company - International presence at 9 locations in Europe, North America, South America and Asia / This location is the corporate and main manufacturing location in the USWHAT THIS COMPANY OFFERS YOU:Growing Company....


Our client is a world leader in laboratory equipment and services, and has an opportunity for a Technical Sales Representative (TSR) for its industry leading analytical instrumentation used in R&D laboratories. The TSR will be selling products for Atomic Force Microscope and Nanomaterials Testing include indentation testers, scratch testers, tribometers (high temperature and linear reciprocating), and calotest instruments (coating thickness characterization).This position will be covering....

- Monroe, NC

We are looking for a Project Manager with cGMP/Pharma experience who will be responsible for delivering projects on time within budget and scope. The Project Manager should have a background in business skills, management, budgeting and analysis.Roles and Responsibilities:Coordinate internal resources or third parties/vendors for the flawless execution of projectsEnsure that all projects are delivered on-time, within scope and within budgetDeveloping project scopes and objectives, involving....

- Charlotte, NC

We are looking for a Project Manager with cGMP/Pharma experience who will be responsible for delivering projects on time within budget and scope. The Project Manager should have a background in business skills, management, budgeting and analysis.Roles and Responsibilities:Coordinate internal resources or third parties/vendors for the flawless execution of projectsEnsure that all projects are delivered on-time, within scope and within budgetDeveloping project scopes and objectives, involving....


Specialty Pharmaceutical company is expanding the Somerset, NJ location- Looking for a Supervisor, QA Documentation This position serves as a dedicated resource for the administration of controlled documentation and documentation systems at the companys Somerset site. Associated documentation, systems and activities provide support for all facets of material, process and product development, validation, manufacture, testing, storage, service and distribution. It also applies to controlled....

- Palo Alto, CA

The Director is primarily accountable for nonclinical toxicology, working in collaboration with nonclinical pharmacology and pharmacokinetic scientists to drive the overall global nonclinical regulatory submission strategy and coordination for multiple company portfolio products, from research to registration and beyond. The individual has experience in evaluating and responding to inquiries from regulatory authorities addressing global nonclinical development issues in support of IND and....

61-76 of 76 results