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The Regional Sales Manager is responsible for managing the sales representatives and the sales activities of the Particle Characterization, Rheology, and Nanomaterials Testing product lines within the Western Region (eleven western states). This position reports to the Regional Vice President. Responsibilities & QualificationsAssists the Vice President of the region to build sales territories within assigned region.Interviews, makes hiring and firing recommendations, develops new hires,....


Designs, develops, implements and supports all aspects of electrical control systems, equipment, and machinery related to site utilities, production equipment, and facilities. Is a technical resource to the Engineering, Maintenance and Validation departments to meet all regulatory and company specific policy requirements and to improve plant efficiency, capacity, and capability via continuous improvement and modernization objectives. Responsible for the research, development, design, layout,....


This position is responsible for providing the managerial and technical expertise necessary to direct the efforts of a project team. The project team consists of contractors from various crafts as well as members of department as assigned. Responsibilities include analysis, recommendation, implementation, cost justification and follow-up on projects designed to increase or improve productivity, capacity, or safety.Product transfer process design and development.Organizes and analyzes product....

- Cincinnati, OH

This function is responsible for supporting the daily manufacturing and facility operations along with project support. This is a Quality role in support of sterile manufacturing operations. Functions include proactive support of change control assessments, documentation reviews and validation review/support. Functions also include reactive support of discrepancy identification and resolution on the floor, Investigation Team Support, TrackWise (assessing product impact), and reporting....

- Buffalo, NY

Independently responsible for the efficient and thorough investigation of process deviations and customer complaints, determination of root cause, and initiation of corrective/preventative actions designed to adequately address and correct the Quality related deficiencies identified during the investigation process. Responsible to provide proactive corrections based on noted trends to minimize the potential for repeat incidents that may lead to, or result in, the issuance of Product Discards,....

- Cranford, NJ

Clinical Project ManagerAs a Clinical Project Manager (CPM), you will work in a matrix management environment and serve as the primary contact for interdepartmental and external study contacts. This experienced CPM role is responsible for managing all stages of a clinical study within GCP and ICH guidelines when direct management by the sponsor is required. The CPM may also function as the liaison and provide support for sponsor managed studies in an international setting, and, may oversee CRO

- Cranford, NJ

Cranford, NJ, United States Full TimePOSITION OBJECTIVE: Work within a clinical team setting to ensure compliance with protocol and overall clinical objectives. This position is based in Client's Cranford, New Jersey office. Essential Job Functions/ResponsibilitiesParticipates in the preparation and/or review of draft protocol and informed consent documentsPossesses detailed knowledge of the study protocol and its associated activities and timelinesParticipates in conference calls,....


POSITION OBJECTIVE: Provide accurate, efficient and effective programming solutions required for clinical trial analysis and reporting. Perform a wide range of activities that include: understanding study protocols, study designs and SAP; creation of complex datasets, tables, listings and figures using SAS; follow and validate CDISC standards; perform basic quality-checklist code reviews; develop standardized programs to automate routine tasks; design, write and debug macro routines.....


Buffalo, NY, United States Full TimePOSITION OBJECTIVE: Provide accurate, efficient and effective programming solutions required for clinical trial analysis and reporting. Perform a wide range of activities that include: understanding study protocols, study designs and SAP; creation of complex datasets, tables, listings and figures using SAS; follow and validate CDISC standards; perform basic quality-checklist code reviews; develop standardized programs to automate routine tasks; design, write

- Pittsburgh, PA

My client is expanding and seeks a Scientist with aseptic fill experience. The ideal candidate will take on the following tasks:Support tech transfer and scale-up of products and processes to ensure smooth transition from process development into cGMP manufacturing.Assist with process-related issues and investigations.Participate in start-up efforts of new equipment and processes in manufacturing.Assist in documenting updates to manufacturing processes and working with manufacturing,....


POSITION OBJECTIVE: The Clinical Research Physician will be dedicated to providing a leadership role on a matrix team dedicated to stage appropriate clinical development of multiple innovative compounds. He or she will lead the development of clinical strategies for compounds and drive their successful implementation. This position is based in Client's New Jersey office. It is an office based position. Remote candidates will not be considered for this role. Essential Job....

- Cranford, NJ

Senior Clinical Research Associate POSITION OBJECTIVE: Work within a clinical team setting to ensure compliance with protocol and overall clinical objectives. . Essential Job Functions/ResponsibilitiesParticipates in the preparation and/or review of draft protocol and informed consent documentsPossesses detailed knowledge of the study protocol and its associated activities and timelinesParticipates in conference calls, prepares agenda and summariesCoordinates with project team and other study....

- Cranford, NJ

As a Clinical Study Monitor, you will work within a clinical team setting to ensure study compliance with protocol, FDA and ICH guidelines. Essential Job Functions/Responsibilities · Ensure the Sponsor, Investigator, and study team adhere to current FDA regulations, applicable ICH/GCP guidelines, local policies and standard operating procedures. · Adhere to monitoring plan protocols; e.g. monitoring visit type, frequency, and required critical monitoring activities by utilizing monitoring....


The Manager, Medical Information will assist in the operational oversight of medical information within the Medical Affairs function under the guidance of the Lead of Medical Information. The manager will be responsible for providing and supporting the provision of accurate, scientifically balanced and timely responses to inquiries received from health care professionals, consumers and other customers. The manager will monitor the scientific literature and communicate new data to relevant....


Safety Physician POSITION OBJECTIVE: Supports the Pharmacovigilance team in reviewing, querying, documenting and reporting on all serious adverse events (SAE) & Suspected Unexpected Serious Adverse Reactions (SUSAR) cases related to clinical studies. Essential Job Functions/ResponsibilitiesProvide timely and sound medical review of individual case safety reports (ICSR) from clinical trials.Actively participates in the case initiation process (case triage) and case data inputting/data entry

- Irvine or Madison NJ, CA

PLEASE NOTE THIS POSITION CAN BE BASED IRVINE, CA OR MADISON, NJ.Tope Tier Global Pharmaceutical company is expanding and adding a Director of Medical Science Library- competitive compensation package - including base, bonus, stock, and other incredible Long Term Incentives The Director of the Global Medical Science Library provides a vision for, leads, and is accountable for the administration, oversight, and propagation of this department, including the acquisition, planning, staffing, and....


This key leadership role in the Regulatory Affairs organization and will report directly to the Senior Vice President, Regulatory Affairs & Medical Writing. The incumbent in this role will lead the regulatory strategy group for the defined therapeutic area(CNS) to this position will provide expert leadership and managerial oversight for pre-approval and post-approval projects to ensure delivery of high quality regulatory strategy and submissions. Further, this position will guide....

- Adams, NE

HOT JOB ********* HOT JOB *********** HOT JOB ********** HOT JOB Working with chemical plant in need of technically strong production manager to help build culture. Our client is a state of the art facility. They opened the plant for business in 2006. Looking to grow output and need someone to help drive this challenge. Reports to a plant manager. The Production Manager is responsible for the operation of the plant to ensure production optimization and maximizing product quality along with....

- Lancaster, SC

We are looking for a Brand Manager who will be accountable for developing the brand innovation and communication strategies for a product (within a brand) to build consumer demand and market share. Brand Manager will be involved in development of brand strategy, pricing strategy, innovation, product portfolio management, new launches and integrated brand activation plans. The Brand Manager will plan and coordinate the retail marketing and promotional campaigns for assigned product lines. The....

- Boston, MA

My client is a rapidly growing firm, and they seek a Data Scientist to collaborate with the global data science group and provide innovative solutions. The ideal candidate will take on the following tasks:Provide data analysis support and lead in the design, analysis, and interpretation of translational research experiments.Offer statistical consultation to collaborators.Promote innovative study design and analysis methodology.Supply statistical input in planning translational experiments to....

41-60 of 162 results
Unless noted above, applicants MUST be authorized to work in the US without Visa Sponsorship. US citizens and Green Card holders ONLY. We do not provide relocation assistance for those living outside the continental US. Please only click apply if you meet the specific requirements of the job listing, you are able to work in the location listed, and are comfortable with the salary range indicated above. Thanks for your interest. We look forward to working with you.