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- New Ulm, MN
new job!

Minimum Requirements:B.S. Degree (Engineering or Chemistry preferred)10+ years of total experience and 3+ years of plant/production management experienceExperience supervising 30+ personnel out of the Food, Chemical or Pharmaceutical industriesStrong background with quality and FDA/GMP experiencePlus would be experience with drying and the management $5 million budgets Job Description:Our client is a leading, publicly traded, food additives producer with 15 production facilities....


Job Type: W-2 contract Duration: 9 months Location: New Haven, CT Position Summary Our client is seeing an experienced Research Associate who will support research and development programs through method development and validation of novel cell-based assays and ligand binding assay to support pharmacokinetic, pharmacodynamics, and exploratory biomarker studies. Principal Responsibilities: · Work with common mammalian cell culture practices, including passaging, cryopreservation, DNA/RNA/siRNA....

- Sleepy Hollow, NY
new job!

We are currently seeking a Senior Manager of Alignments for a direct-hire employee role with our client in Sleepy Hollow NY (10591). Compensation depends upon experience level. The ideal candidate has multiple years of experience with software platforms related to Field Alignment and Sizing. This position will be responsible for executing projects on Field Force Alignment and Sizing. The ideal candidate should have hands on technical expertise with various software tools/ methodologies used in

- Lancaster, SC
new job!

The QA Supervisor reports to the Assistant QA Manager. This person supervises Quality Assurance Generalists and label Issuance but may include other personnel in Quality Assurance Department. The QA Supervisor is responsible for all of the day to day operations, techniques, documentation, and activities associated with those departments that are used to fulfill the Quality Assurance requirements of the product and/or service. Floor presence is required to be successful in this roleRoles and....


IT CYBERSECURITY ANALYST - TOP SECRET CLEARANCERESTON, VA QUALIFICATIONS:Current & Active Top Secret ClearanceComputer security expertise with a strong track record of identifying solutions to problems and guiding teams to develop those solutionsCyber Security Incident response experienceStrong Identity and Access Management experience (IAM)Experience responding to and handling / resolving incidents and eventsTechnical experience using network security, incident response, digital forensics

- New Ulm, MN
new job!

Minimum Requirements:S. Science Degree (Engineering or Chemistry)5+ years of total experience and 3+ years of production management experienceExperience supervising the production out of the Pharmaceutical or Food industriesStrong background with quality and FDA/GMP experiencePluses would be drying and experience serving as interim plant manager Job Description:Our client is a leading, publicly traded, food additives producer with 15 production facilities across the US. These plants....

- Los Angeles, CA
new job!

Description: The Service Manager is responsible for the day-to-day management of in-house and field service and support activities in the Western Region (west coast and inter-mountain west). The Service Manager manages a team of highly skilled degreed technicians who troubleshoot, repair and calibrate bench top analytical instrumentation used in R&D Labs. This is not a Service Manager position for a copier company. Responsibilities:Bachelor’s degree required in electrical, mechanical or....

- Los Angeles, CA
new job!

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,....

- 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....

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