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Pharmaceutical general production in Health & Medical Jobs

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Contact Us   4 days ago
Senior Quality Assurance Engineer, cGMP - Tustin

At TSS-Tustin/SSF, we provide innovative quality medical device assembly and packaging, as well as engineering services and combination products to our customers. We are a USA ISO 13485 certified company, with all services performed in California. Currently, there is an opportunity in our Quality Assurance Department, for a Senior Quality Assurance Engineer, specializing in cGMP. TSS-Tustin/SSF is

Contact Us   6 days ago
Manager Validation - Norwich

SUMMARY OF POSITION The Manager Validation manages day to dayactivities of the validation group Thisposition conducts validation assessments of equipment facilities and processsystems makes recommendations for changes and or improvements and approvesappropriate change control documentation ORGANIZATION STRUCTURE The Manager Validation reports directly to theDirector Operations Pharmaceutical Techn

Contact Us   1 week ago
Director, Manufacturing Operations - Winchester

Job DescriptionJob Title Director, OperationsPosition Summary The Operations Director will be directing and providing scientific and technical leadership for the overall manufacturing of the Oral Solids technologies at the site, and to support customer-driven product development and commercial work for the Winchester facility. The role is responsible for:Organizing, managing and improving Operatio

Contact Us   1 week ago
Aseptic Filling Operator Lg3Union1st Shift, Mon-Fri, 600am-230pm - St. Joseph

Description:Description\\\\: To perform duties in the manufacturer of high quality biological products. As an employee of Boehringer Ingelheim, you will actively contribute to the discovery, development and delivery of our products to our patients and customers. Our global presence provides opportunity for all employees to collaborate internationally, offering visibility and opportunity to directl

$10.00   1 week ago
Clinical Research Associate - CRA Experienced Late Phase - Up to $10K - Lincoln

Seeking Clinical Research Associates (CRAs) in phases II-IV in all therapeutic areas! Seeking all levels of CRAs Up to $10,000 Sign On Bonus! The Clinical Research Associate conducts site monitoring responsibilities for Clinical trials, according to Covance Standard Operating Procedures, ICH guidelines and GCP, including Pre-study, Site Initiation, Routine Monitoring and Close-out Visits. Job Duti

$10.00   2 weeks ago
Clinical Research Associate - CRA Experienced Late Phase - Up to $10K - Lincoln

Seeking Clinical Research Associates (CRAs) in phases II-IV in all therapeutic areas! Seeking all levels of CRAs Up to $10,000 Sign On Bonus! The Clinical Research Associate conducts site monitoring responsibilities for Clinical trials, according to Covance Standard Operating Procedures, ICH guidelines and GCP, including Pre-study, Site Initiation, Routine Monitoring and Close-out Visits. Job Duti

Contact Us   2 weeks ago
Senior Quality Assurance Engineer, cGMP - Tustin

At TSS-Tustin/SSF, we provide innovative quality medical device assembly and packaging, as well as engineering services and combination products to our customers. We are a USA ISO 13485 certified company, with all services performed in California. Currently, there is an opportunity in our Quality Assurance Department, for a Senior Quality Assurance Engineer, specializing in cGMP. TSS-Tustin/SSF is

Contact Us   2 weeks ago
Production Associate II, 2nd Shift Medical Device Manufacturer - Kimball Electronics

Job Description:/h3:Shift/Hours: 2nd Shift, 3:00pm: 11:00pm, M:FOvertime: When requiredPosition OverviewThe mission of the Production Associate II is to operate high speed and semi:automated assembly equipment, pack parts per production procedures, and document production processes while meeting goals of quality, cost and delivery for our customers. This position reports to a Production Supervisor

$10.00   3 weeks ago
Clinical Research Associate - CRA Experienced Late Phase - Up to $10K - Lincoln

Seeking Clinical Research Associates (CRAs) in phases II-IV in all therapeutic areas! Seeking all levels of CRAs Up to $10,000 Sign On Bonus! The Clinical Research Associate conducts site monitoring responsibilities for Clinical trials, according to Covance Standard Operating Procedures, ICH guidelines and GCP, including Pre-study, Site Initiation, Routine Monitoring and Close-out Visits. Job Duti

Contact Us   3 weeks ago
Quality Engineer - Cincinnati

Position SummaryThe Quality Engineer is responsible for providing quality oversight to all manufacturing and packaging areas to ensure product quality and SOP/GMP compliance at the Cleveland Manufacturing Facility. Works closely with Production personnel to complete on-the-floor, in process batch record review, resolve all batch related issues or escalate to the Quality Assurance Manager as approp

Contact Us   1 month ago
Quality Assurance Associate III - North Augusta

Quality Assurance Associate III:The Quality Assurance Associate III is an advanced level position with hands-on QA experience in a pharmaceutical environment. Working independently and under minimum supervision, the individual will be working primarily in quality operations providing quality assurance support to in-house production, testing and systems and Regulatory team. The individual will be i

Contact Us   1 month ago
Director, Biostatistics - Swiftwater

Provide leadership and guidance as the statistical expert on a project team or within a therapeutic area. For one or more projects, be accountable for all statistical aspects of clinical studies and submissions, including quality, relevance to regulatory perspective, and scientific validity. Act as key statistical consultant within company. Responsible for project staffing, resource planning and a

Contact Us   1 month ago
Sr Process Validation Engineer - Moscow

Job Description The Principal Process Engineer supports manufacturing processes and techniques utilized for the production of vaccines and biologics manufactured at industrial sites for a Life Sciences leader. Experience in pharmaceutical/biopharmaceutical industry or related industry/cGMP environment with experience in plant utilities, clean utilities, HVAC, Filling lines, CTUs, component prep eq

Contact Us   1 month ago
Quality Assurance Associate III - North

Quality Assurance Associate III: The Quality Assurance Associate III is an advanced level position with hands-on QA experience in a pharmaceutical environment. Working independently and under minimum supervision, the individual will be working primarily in quality operations providing quality assurance support to in-house production, testing and systems and Regulatory team. The individual will be

Contact Us   1 month ago
Director, Biostatistics - Swiftwater

Provide leadership and guidance as the statistical expert on a project team or within a therapeutic area. For one or more projects, be accountable for all statistical aspects of clinical studies and submissions, including quality, relevance to regulatory perspective, and scientific validity. Act as key statistical consultant within company. Responsible for project staffing, resource planning and a

$10.00   1 month ago
Clinical Research Associate - CRA Experienced Late Phase - Up to $10K - Lincoln

Seeking Clinical Research Associates (CRAs) in phases II-IV in all therapeutic areas! Seeking all levels of CRAs Up to $10,000 Sign On Bonus! The Clinical Research Associate conducts site monitoring responsibilities for Clinical trials, according to Covance Standard Operating Procedures, ICH guidelines and GCP, including Pre-study, Site Initiation, Routine Monitoring and Close-out Visits. Job Duti

Contact Us   1 month ago
Pain Management Nurse Practitioner - Redding

Job Description Pain Management NP or PA needed! Looking for at least 1 year of experience. ESSENTIAL DUTIES AND RESPONSIBILITIES Provides primary or specialty medical care with the supervision of a physician Provides services by collecting data required for diagnosis and performing authorized and approved procedures and services Obtains and evaluates medical histories, performs physical examinati

Contact Us   1 month ago
Director, Biostatistics - Swiftwater

Provide leadership and guidance as the statistical expert on a project team or within a therapeutic area. For one or more projects, be accountable for all statistical aspects of clinical studies and submissions, including quality, relevance to regulatory perspective, and scientific validity. Act as key statistical consultant within company. Responsible for project staffing, resource planning and a

Contact Us   1 month ago
Physician Urgent Care Pennsylvania Permanent Physician Urgent Care Pennsylvania

General Position Summary: To support and direct the highest quality urgent care services available to the public while always assuring the MedExpress mission, vision and values are met. All duties and responsibilities are to be performed in compliance with state and federal laws and regulations governing the legal scope of medical practice. MedExpress Core Responsibilities: Has a contagious and po

Contact Us   1 month ago
Director, Biostatistics - Swiftwater

Provide leadership and guidance as the statistical expert on a project team or within a therapeutic area. For one or more projects, be accountable for all statistical aspects of clinical studies and submissions, including quality, relevance to regulatory perspective, and scientific validity. Act as key statistical consultant within company. Responsible for project staffing, resource planning and a


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Last Updated on: June 26, 2017
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