eBay Classifieds  » Jobs » Biotech, R&D, & science » 1-13 of 13 ads for document control in New York City

Job Title: Director of Environment, Health & Safety (EHS) Location: White Plains, NY Type: Full-time/Direct-hire Summary: The purpose of this position is twofold. It is to promote a safe and healthful workplace that protects the employees, community and environment by establishing and implementing environmentally sound business practices and complying with all state/federal and local regulations and applicable guidelines.  In addition it is to promote and coordinate (identify, establish, conduct and ...

Title: Engineering Project Manager Summary: Manages the design, specification ,and installation of new and renovated biopharmaceutical process equipment. Provides engineering support and problem solving for existing equipment and manufacturing processes. Location Country: United States State/Region: NY City: Rensselaer / Albany area Functions Manufacturing / Production Industries Pharmaceutical / Biotech Summary: Manages the design, specification ,and installation of new and renovated ...

Allied Search Partners, the only boutique laboratory staffing firm in the country is currently working to identify a qualified laboratory professional. Know someone for this position? We offer a $$ bonus if we place your referral in a position. For a complete list of current Allied Search Partners openings Nationwide please go to: http://www.alliedsearchpartners.com/careers.php Job Title: Cytopreparatory Technician (Cytoprep) Location: Port Chester, NY area Schedule: Monday-Friday 10pm-6am/Full ...

Job Description QA Documentation Associate supports functional objectives of assigned unit or team by performing a variety of activities in support of the functional processes, programs and/or services. Responsibilities: • Working on advanced department projects • Compiling and analyzing data • Creating reports • Providing information regarding function specific policies and procedures for applied use by management • Tracking and control of processes, projects and activities. • Use of new ...

QUALITY ASSURANCE MANAGER NEEDED ASAP! COMPETITIVE SALARY + BONUS & EXCELLENT BENEFITS!!~ Directs and manages all aspects and functional areas of the NY Site QA Department, ensuring compliance with all regulatory and cGMP requirements. Provides oversight of quality functions and makes quality related decisions in the following areas: compounding, packaging, inspection, product disposition. Directly responsible for the management of QA inspectors and Documentation Review Group. Reviews and approves ...

Title: Senior Packaging Engineer Location City: Tampa, FL : Functions Engineering Industries Pharmaceutical / Biotech Detailed Description The Senior Engineer - Primary Packaging is responsible for design, development, testing, manufacturing implementation and validation of sterile and non-sterile packaging systems for ophthalmic medical products. This person will drive package component specification and engineering development from concept ideation, prototyping, design evaluation, ...

QUALITY ASSURANCE MANAGER NEEDED ASAP!!! (Nyack) QUALITY ASSURANCE MANAGER NEEDED ASAP! COMPETITIVE SALARY + BONUS & EXCELLENT BENEFITS!!~ Directs and manages all aspects and functional areas of the NY Site QA Department, ensuring compliance with all regulatory and cGMP requirements. Provides oversight of quality functions and makes quality related decisions in the following areas: compounding, packaging, inspection, product disposition. Directly responsible for the management of QA ...

Below is a template job description. Every clients job description is a little different. Duties and Responsibilities: 1. If job assignment includes tissue culture: Using SOPs, accurately and efficiently performs tissue culture of assigned specimen types, including culture initiation, maintenance, and harvest. Also performs slide preparation and staining for microscopic analysis. 2. If job assignment includes microscopic analysis: Performs accurate microscopic/post-microscopic analyses of ...

Key accountabilities include: • Responsible for the day-to-day operations of the Histology laboratory and supervision of the technical and support staff. In conjunction with the Department Manager, ensures that all departmental policies and procedures meet the standards of current state and federal regulations. • Monitor and control expenses in line with department budget. Assist in the preparation of the budget and recommend capital equipment needs. • Maintain appropriate levels of supplies and ...

QA MANAGER - MUST HAVE LEAN/SIX SIGMA EXPERIENCE (ORANGEBURG AREA, NEW YORK) Directs and manages all aspects and functional areas of the NY Site QA Department, ensuring compliance with all regulatory and cGMP requirements. Provides oversight of quality functions and makes quality related decisions in the following areas: compounding, packaging, inspection, product disposition. Directly responsible for the management of QA inspectors and Documentation Review Group. Reviews and approves all ...

Plan and conduct GCP audits, issue audit reports, recommend corrective action and conduct follow up to audits and corrective actions for a company currently involved in several clinical trials Shall assist in preparing investigational sites for FDA inspection, review and recommend compliance related policies and procedures and evaluate impending regulations, guidelines and industry standards and their impact on the clinical trials and the company. Must possess at least 5 years experience in ...

SENIOR TECHNICAL PROJECT MANAGER POSITION SUMMARY: The Senior Technical Project Manager is responsible for coordinating multi-site development activities through the company's Design Control and Idea to Market process. This includes aligning and setting the project scope and objectives with all relevant stakeholders. He or she is setting and holding the team accountable for deliverable timelines, meeting performance requirements, and achieving project and development cost objectives. Development ...

Seeking a strategic leader for analytical method development team with expertise in characterization of proteins and drug products to lead a team developing, qualifying and transferring analytical methods for in-process, lot release and stability testing in early, late and commercial phase and oversee the creation and review of documents such as: method development reports, SOPs, validation protocols-reports, CMC regulatory filings (IND, IMPD, BLA, etc.), and scientific journal publications. Well ...