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Director, Medical Information for this leading pharmaceutical company in New England S Headquarters in Waltham, MA Looking for Senior Engineer for drug product unit operations- leadership scale-up and optimization in development from R&D to cGMP Phase 3 manufacture to process validation. Experience with continuous manufacturing, scale-up and PAT implementation is strongly desired. The individual is expected to integrate QbD principles, guide experimental design with a focus on process....


Our client is a world leader in the manufacturing and distribution of analytical instrumentation used in R&D Laboratories. Due to continuing growth they have opening for a Field Service Engineer to be based in the Kansas City, St. Louis or Springfield. This position may also conduct supplemental travel into other territories on a regular basis.Requirements:Duties include the preventative maintenance, troubleshooting, repair, and calibration of instruments in R&D Labs in the assigned....


Two MD contractors needed for Global Pharmaceutical company in Cambridge, MA two roles-Contract Role Only One year contract (renewal up to 4 years), w-2 with benefits offered Has to be office based in Cambridge- we will only consider local candidates at this time. We need PV experience within submissions specifically We have a submission approaching for a product. Need someone with good clinical trial experience. Worked in clinical trial as opposed to post trial setting SPA or European....


Our client is a world leader in the manufacturing and distribution of analytical instrumentation used in R&D Laboratories. Due to continuing growth they are adding a new Field Service Engineer to be based in the Sacramento, CA area. The Field Service Engineer provides on-site service including preventative maintenance, calibration, installation, and training across all product lines.Responsibilities & QualificationsThis position will be based in or near the Sacramento, CA area but will

- Lancaster, SC

We are looking for a Manufacturing Engineer, the ideal candidate will possess 5 years' experience in a cGMP facility, including experience with Continuous Improvement and Project Management. This individual will be responsible for identifying, development, and execution of projects necessary for process improvements geared towards company goals and objectives. Responsibilities of the Manufacturing Engineer Learn and understand all company products, systems and Manufacturing operations in all....

- Lancaster, SC

We are looking for a qualified individual who has the understanding and knowledge of development of chromatographic, spectroscopic, titrimetric and wet chemistry methods. Implements strategies to ensure effective achievement of scientific objectives. Monitors and evaluates completion of tasks and projects.Roles and Responsibilities:Has hands on knowledge and can begin the development and validation of scientifically sound analytical methods for Product release and stability testing.Familiarity


Our client is a world leader in the manufacturing and distribution of analytical instrumentation used in R&D Laboratories. Due to continuing growth they are adding a new Field Service Engineer to be based in Boston or Albany, NY or Hartford, CT. Requirements:Duties include the preventative maintenance, troubleshooting, repair, and calibration of instruments in the assigned region.Managing inventory and reporting for accuracy.This position requires up to 75% overnight travel within the....


Our client is a world leader in the manufacturing and distribution of analytical instrumentation used in R&D Laboratories. They have an opening for a Field Service Engineer to be based in the Chicago area or Milwaukee. The Field Service Engineer provides on-site service including preventative maintenance, calibration, installation, and training across all product lines.Responsibilities & QualificationsThis position will be based in or near the Chicago area but will also conduct....

- Cleveland area, OH

Our client is a world leader in the manufacturing and distribution of analytical instrumentation. They have an opening for a Field Service Engineer covering a Midwestern territoryRequirements:Duties include the preventative maintenance, troubleshooting, repair, and calibration of instruments in the assigned region.Managing inventory and reporting for accuracy.This position requires up to 75% overnight travel within the United States.The preferred candidate will possess a BS degree in Electric....

- Madison, WI

Director - QC Stability & Release Testing (GMP), your basic purpose will be to ensure efficient and effective management. You will supervise and assist group leaders and scientists in laboratory operations with tasks such as scheduling, resource management, technical and compliance related issues. In addition, you will plan, direct and implement improvements in systems, processes and procedures to increase efficiency, productivity and quality in the laboratory. You will assist the division


Validation Engineer Process Engineer Global Chemical /Biotech company looking to hire: Greenville, Soth Carolina location competitive salary and full relocation and full benefits Would love someone who has: affiliation with: IVT (International Validation Technology), KEN X (Knowledge Exchange Network), PDA, ISPE ResponsibilitiesRemain current on cGMP practices for Process Validation and ensure local Process Validation SOPs and validation documents reflect current industry practices.Provide....


Leading Pharmaceutical Company with marketed products and strong Neurology Pipeline is looking for a Director, Medical Information for their growing US Headquarters in Waltham, MA Competitive Base, Bonus, Long Term Incentives and Relocation The Director, Medical Information (MI) will be responsible for leading the MI function within the Medical Affairs. The Director, Medical Information will be responsible for managing the member of the MI function who are providing and supporting the....

- Somerset, NJ

Specialty Pharmaceutical Company is hiring a Safety Coordinator for Somerset, NJ Competitive Salary, bonus and incentives Provide support for environmental, health and safety matters for the Somerset site including maintaining compliance with federal, state, and local regulations. ESSENTIAL FUNCTIONS: Include the following. Other duties may be assigned. Responsible for coordinating regulatory programs, audits, permits and ensure compliance. Support the development and coordination of all EHS....


Here is an excellent growth opportunity with a prominent food products manufacturer! Plant Sanitation Manager -- Cleveland, OH -- 6 day week (6 days, 10 hours per day) -- $78-85,000 -- Excellent benefits -- Relocation Assistance Responsibilities of the Sanitation Manager: - Manages the company's sanitation department. to requirements for food processing machinery, equipment, and facility - Includes assisting in planning, scheduling, assigning and directing of sanitation personnel (approx:....

- Larwill, IN

SUMMARY OF POSITION: Responsible for the overall management of customer complaints and CAPA’s for the corporation. Develop, analyze and publish divisional and corporate quality metrics. Function as both the corporate and divisional resource in conducting field complaint investigations. Provide quality engineering expertise (including investigations, CAPAs and training) to support both corporate and divisional activities. Evaluate and recommend process/procedure improvements as necessary and....


We are looking for an experienced Environmental Water Quality Program Specialist (Project Manager). Duties and Responsibilities : Project set-up, Sample Receipt, Reporting, Account Maintenance- Provide courteous and efficient telephone and e-mail support to clients; Schedule/coordinate access and/or on-site escort for field staff; Interface/liaison between the lab and internal and external customers; Works with Lab Operations to ensure adequate capacity and capability and communicates that to....


We are looking for a Quality Assurance Auditor who has worked in a cGMP environment to be responsible for developing, maintaining and ensuring compliance. Roles and Responsibilities:Manage audit planning, scheduling, and execute internal audits in Facilities to assess compliance to the regulations.Function as a backup as well as support the efforts of Supplier Quality Engineer.Determine the level of risk of findings identified and follow up on corrective actions ensuring they address the....

- Manhattan, NY

As a Study Leader Team Lead/Assistant Director, you will manage and mentor a group of approximately 10 study leaders and associates in order to maximize their capabilities to deliver high quality clinical studies. People Management · Coach and develop global staff to maximize their contribution to the delivery of studies across various therapeutic areas · Manage performance of direct reports through regular dialog and throughout the year in accordance with the Roche performance management....


Strong Player in the Pharmaceutical Industry is looking to hire a Medical Director for their new Phase one Unit (24 bed) Looking for a true Medical Director (not just a PI) who can interact and engage other Key Opinion Leaders in the Medical Community This role include VERY competitive base salary, long term incentive and full relocation (will make it stress free- pack up, moving and temp housing, real estate assistance and more) The primary responsibilities of this position include medical....

- Decatur, IL

Global Specialty Pharmaceutical company is expanding in their Decatur, IL location Need Process Engineer III will relocate competitive and comprehensive salary and benefits hile a member of the Technical Services organization, the Process Engineer will be located on the manufacturing site located in Decatur, IL. The Process Engineer will be responsible to provide the plant operations unit technical process expertise for a variety of pharmaceutical configurations produced on-site. The scope of....

41-60 of 76 results