Pharmaceutical Materials Specialist Jobs in Texas

Currently, there are no Pharmaceutical Materials Specialist jobs available in Texas which match this search. You may wish to explore similar job titles on the Biotech jobs in Texas page or view related jobs below.
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Job Title: RA I, CV & Metabolic Diseases Position Description Will perform in vivo and ex vivo experiments to assess pharmacodynamics and efficacy of novel therapeutics in the relevant disease models. He/she will be responsible for execution of standard CV and renal rodent methodology (surgical and non-surgical). Position Responsibilities Under supervisor's direction, he/she will design and ex...
CorePharma LLC is a fast growing mid-size generic pharmaceutical company with approximately 250 employees, located in Middlesex, New Jersey. We are a fourteen year old firm principally in the business of developing, manufacturing, and distributing pharmaceutical products for the United States market. JOB SUMMARY: Under the direct supervision of the Supervisor, Quality Control Laboratory, the inc...
Chemist Glori Energy Inc is seeking a Chemist to join our Technology team. Glori Energy’s mission is to sustainably and efficiently recover billions of barrels oil trapped in existing oil reservoirs. Glori’s AERO™ technology utilizes existing infrastructure and enhances oil production by stimulating a reservoir’s naturally-occurring microbes to release previously unrecoverable oil. The Chemist w...
Our client, a global medical device company, is seeking an experienced, high caliber Clinical Data Manager (Analyst II) to join the team. Working under general direction, this experienced employee is responsible for all data management aspects of clinical studies. Within the first three months on the job, the new hire will be trained on our devices, regulations, data management and platforms and w...
We currently have an excellent opportunity for a Sr. Packaging Engineer located at our Princeton, NJ Location. The Sr. Packaging Engineer will lead packaging development projects from initiation through manufacture (launch). Projects will consist of modifications of packaging for existing products as well as the packaging for new products. Additional scope includes consideration of new, explorat...
Job Summary: Provide statistical analysis and expertise to multi-disciplinary teams supporting a variety of programs in the engineering and physical sciences; conduct statistical consulting including the design of experiments, the development and implementation of data analysis approaches to address customer needs and the statistical analysis of data; utilize statistical software packages to perf...
Pall is a Fortune 1000 materials science and engineering company with the broadest filtration, separation and purification capabilities in the world. Our process and product enabling technologies help our customers make good products better, safer and even possible. We provide innovative products to customers in health care, biotechnology, pharmaceutical, semiconductor, municipal drinking water, a...
The Senior Environmental Engineer will ensure compliance with environmental regulations and permits. Other responsibilities include, but are not limited to: Development, modification, and implementation of environmental permits, plans, and company procedures to ensure compliance with environmental regulations and corporate programs, procedures, policies, and manuals. Leading internal departments...
Oversees all aspects of management of laboratory operations within the different functional groups of the GMP, GCL, Vaccines & Biologics or Bio-Analytical laboratories. Ensures productivity, efficiency and quality of the work are maintained and financial objectives of the business are achieved. Oversees the development and implementation of laboratory systems and processes. Ensures client delivera...
GENERAL: Participate in and manage both stability and sterility activities in the stability program for PharMEDium?s services. RESPONSIBILITIES: Assist in the design and acceptance of method validation protocols preparation and execution of stability testing protocols. Manage new product evaluations based on current stability data. Identify potential areas where current stability data and lite...
Novum is looking for an individual that possess strong management skills, good clinical practices, experience with FDA regulations, research studies and other regulatory standards. Position Summary Day to day staff management and clinic conduct of Phase I investigations. Responsibilities Coordinate all clinic activities and support service, to ensure coverage; for example, clinic set-up, scree...
Hays is currently recruiting for a Project Manager for our global pharmaceutical client located in Northern NJ. This hands-on, process driven Project Manager position is a 6 month contract job. This position is an excellent opportunity to leverage your Drug Development and Regulatory Filing experience in a tangible project-based setting. This position will be responsible for hands-on daily projec...
Global Stability Operations works closely with each Hospira plant to ensure all stability commitments are met, including the annual placement of each Hospira product required on stability, reconciliation of special stability commitments, compilation of reports used by Regulatory Affairs for use in submissions and annual updates. The gropu controls the Stability database where all stability data is...
As part of the iCAD/Xoft Clinical Affairs team, the Clinical Affairs Project Manager will be responsible for the coordination of all activities associated with the conduct of multiple clinical trials (develops study protocols, CRFs; supervises study tasks and mentors other CRAs; assists in the generation and oversight of trial budgets and contracts; and communicates trial status to management). In...
Assist in monitoring and collecting data from sponsor initiated clinical study. RESPONSIBILITIES: Travel to clinical research sites to collect clinical data for publication Check the data for compliance with study/site protocol, consistency and quality assurance Post-process, analyze the collected data using various software tools Document and report the analysis results Work with Investigat...
If you are a confident and highly motivated individual looking for a great sales opportunity with uncapped earnings and growth potential, join our team at MedSupply Partners! MedSupply Partners is a nationwide distribution company that specializes in providing high quality laboratory equipment, reagents and consumables to academic research laboratories and biotechnology/pharmaceutical companies. ...
To maintain and coordinate Quality Systems related documents namely deviation reports, change controls and product complaints for compliance with cGMP and company procedures with minimal supervision. To review and write cGMP procedures under supervision. To process changes in analytical methods, test specifications and batch records. To issue effective documents including procedures, forms, report...
RMC is seeking an environmental protection specialist with a bachelor’s degree and 7 years experience or a master’s degree and 3 years experience with environmental impact assessment and NEPA (AICP certification is a plus). The candidate should have background in transportation planning for transit project development and/or city/urban planning. Must have a working knowledge of NEPA, NHPA/Section ...
At St. Jude Medical every one of us plays a role in our collective ability to save and improve lives. As an organization, we want to continue to grow and lead our industry in changing the way the world views the treatment of expensive, epidemic diseases. By seeing things from a different perspective, using our imagination, leading with character, and working with passion, we all have a role to pla...
The scientist will be part of a team effort to provide cell banking services to the Client, other R&D customers, Client Supply Chain and other clinical and commercial manufacturing sites. The scientist will perform cell culture according to Standard Operating Procedures using Good Manufacturing Practices. Primary responsibilities will be: Culture and cryopreservation of a variety of cell lines ...

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Biotech Career Tools

Pharmaceutical Materials Specialist

Salaries

$22,000.00 - $78,174.00
Typical Salary for Pharmaceutical Materials Specialist in Texas
(2873 Respondents)
Source: Monster.com Careerbenchmarking Tool

Education / Training

Bachelor's
51.6%
Master's
23.7%
Doctorate
7.1%
Some College Coursework Completed
7%
Associates
5.5%
High School
2.4%
(2114 Respondents)
Source: Monster.com Careerbenchmarking Tool
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