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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 –....

- San Jose, CA

Excellent oppt'y for a Medical Technologist to work for a medical lab manufacturer and utilize their lab knowledge as a Technical Support Specialist. Will be instrumental during the installation process as a trainer, and documenting the lab procedures. Area to be covered is approx 150 mile radius of San Jose (Sacramento - Stockton - San Jose), and maybe a bit south of San Jose. Can reside almost anywhere is this area. Will also be involved with direct problem solving covering reagents, kits,....

- 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).....


Traditional SHE leader's role dealing with a Chemical manufacturing facility. MUST HAVE PSM BACKGROUND AND EXPERIENCE. Will not even look at anyone without it. Lead the plant’s safety, health, environmental and security programs, as well as the operation of the Utilities function. Take the lead on all compliance with all safety and environmental regulations and policies. Lead effort in compliance with environmental regulations, permits and reporting requirements. Responsible for the operation....

- Waltham, MA

Incredibly successful publicly traded Biotech in Waltham , Massachusetts is expanding due to their clinical trial success. Looking for a Strong Clinical Trials Manager or Senior Clinical Trials Manager to help lead their Phase 2 and 3 trials in anti-cancer partner drugs. This company has three wholly owned therapies- in late stages, with a fourth starting in phase I. This CTM is focused on the anti- cancer phase III trials. If you are an experienced Clinical Trials Manager with oncology....

- 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....


The Head of Device SRM (Supplier Relationship Management) manages device supplier relationships. This is a strategic role that will develop and implement internal policies and be influential in decision making across major functional areas: - Develop and manage Suppliers for clinical and commercial devices - Development and implementation for legal and financial aspects of the alliance - Contribute to negotiation of contract terms and conditions, including the management of amendment....


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....

- Lancaster, SC

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....


The Manager Regulatory Affairs will be responsible for the following: Leading the preparation and filing of regulatory applications (IND, NDA, BLA).Coordinating/meeting with various functional areas in order to identify and obtain information required for regulatory submissions.Developing and/or reviewing regulatory documents (IND, NDA, BLA) in order to ensure that all submissions are of high quality.Leading the preparation of responses to questions from Regulatory Authorities.Developing and....


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....

81-98 of 98 results