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- East Hanover, NJ

This is nice opportunity for a recent college graduate with a technical degree (Engineering related), who has about a years experience. This company is a manufacturer of medical instrumentation and there are excellent future growth opportunities within the company. You will primarily be involved with developing training programs for the installation, maintenance, troubleshooting, and programming of the instrumentation. Requirements:Bachelor's degree in a technical discipline.Should....


We are looking for a Production Supervisor who will be responsible for supervising all aspects of production on a daily basis and closely monitoring all manufacturing raw material and finished inventories. Responsibilities include:- Interacting on a daily basis with with Sales, Marketing, QC, QA, and Warehouse personnel, and any other internal customers to accurately plan the short-range schedule - Meeting all production commitments, working independently and making effective decisions while....


My client seeks an experienced Product Manager to support existing (and develop new) small automated devices, consumables and accessories. The Product Manager will drive product development and improvements. The ideal candidate will take on the following tasks:Develop and execute product planning and strategyDrive market research activities for both product improvement and future product planningLead product development and improvement initiatives conducted by engineering, service and....

- Seattle, WA

My client is actively seeking a technical Sales Manager to serve biotech and pharma clients. The ideal candidate will oversee a team of 4 reports and ensure the development and performance of reps.The ideal candidate will take on the following responsibilities:Establish a working relationship with the reps for the sensor product line.Develop a business plan and sales strategy for the Northwest territory.Perform a monthly and yearly business review with all Reps and Distributors to identify....

- 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,....


Job descriptionPOSITION OBJECTIVE: Conduct analytical research at an independent level using various chemistry, physical and instrumentation techniques. Independently execute experimental studies and analytical method development and summarize data. Perform pharmaceutical product development and participate in manufacturing process development, including physical and chemical compatibility, scale up, and facilitate tech transfer. Essential Job Functions/ResponsibilitiesPerform analytical and....


Job descriptionPOSITION OBJECTIVE: Provide efficient and effective programming solutions required for clinical pharmacology data analysis and reporting, including understanding clinical pharmacology components of study protocols, creation of more complex and integrated datasets, creation of graphs using more advanced programming skills, understanding and application of more advanced statistical tests, perform basic quality-checklist code reviews, develop standardized programs to automate....


Buffalo, NY, United States Full TimeAs a Nonclinical Studies Manager in Preclinical Sciences you will work closely with internal Preclinical, Toxicology, Regulatory, and Clinical staff as a subject matter expert in nonclinical study design, and you will with work with external CROs to provide oversight in the review and/or QC of study proposals, protocols, data, and reports, in support of Client development programs. You will participate in project team meetings and help to manage and drive....


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


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

- 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,....

- 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


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

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....

- Buffalo, NY

Clinical Project Manager As 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....

- 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....


Medical Affairs – Fully integrated, global biopharmaceutical company developing innovative medicines for the treatment of central nervous system (CNS) diseases. PREFER experience with Psych, Schizo, addiction, pain. The company has a diversified commercial product portfolio and a substantial clinical pipeline of product candidates for chronic diseases that include schizophrenia, depression, addiction and multiple sclerosis. In this highly visible leadership role in Medical Affairs, you will....

- Bridgewater, NJ

Job Title: Manager / Sr. Manager, Regulatory Affairs Overview:Client is a diverse pharmaceutical company that is committed to focusing on our key stakeholders while delivering consistently high performance. Our values provide the overall direction for our company, and provide us with the tools necessary to rise to any challenge by leveraging our collective hard work and effort along with our unwavering competitive spirit. These values help us set goals based on our organization’s potential and


Job Title: Senior Manager, Regulatory Affairs Overview:Client is a diverse and decentralized pharmaceutical company that is committed to focusing on our key stakeholders while delivering consistently high performance. Our values provide the overall direction for our company, and provide us with the tools necessary to rise to any challenge by leveraging our collective hard work and effort along with our unwavering competitive spirit. These values help us set goals based on our organization’s....

41-60 of 117 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.