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Online Resumes with "CGMP"
Quality Bio-Pharmaceutical professional with ISO/GMP/TQM experience and strong data management in inventory control & distribution. Ability to design, develop and improve process systems. Bi-lingual in Spanish and English. Additional skills and knowledge include: Package & Labeling Design; Documentation Editing; Contract Facility Audits; Statistical Analysis; Return Destruction Processing; Charting Trending; Contract Vende...
Ideal Companies: Open to all Medical device and bio pharmaceutical companies
I have a hands-on experience interacting with suppliers, internal customers, and subject matter experts to ensure thorough evaluation and accuracy of discrepancies and investigations, identifying root cause, coordinating corrective and preventive action plans, writing summaries, and reviewing reference documents. I am experienced in change control process for externally initiated material changes in accordance with cGMP, U...
A science professional with greater then 4 years of extensive experience with a range of in vivo and in vitro cell culture searching for a leadership / supervisory role where my marketable skill set can be fully utilized both for the future of my career and to add value to an organization.
Experienced Product Labeling, Package Specialist; partnering with Package Engineering, Marketing, Legal, and Regulatory Groups to design, create and prepare high quality product Labeling used in Pharmaceutical Packaging. Create and Control use of labeling masters; approve implementation of all labeling and project schedules to meet deadlines for product launches, New Drug Application submissions, and Marketing presenta...
my goal is to provided the com[any with the best quality of work and more efficient to make the job easier and echo friendly. Less waste and more production. Cgmp
Salary is negotiable, my "current salary" and "Ideal salary" are not to be taken literally.
I am an accomplished process design specialist with thirteen years experience in the pharmaceutical industry involving bacterial and viral vaccine production. Achievements have included authoring and co-authoring various cGMP documents. Broad based background encompassing a strong work ethic and commitment to organizational and team goals. Experienced in recognizing, recommending and introducing new processes and equipme...
Extensive experience in developing manufacturing processes, work instructions, fixture design and Lean Manufacturing Practices.
Tags for this Online Resume: Manufacturing Processes, Work Instructions, Fixture Design, Lean Manufacturing, Cost Reduction, Six Sigma, Kaizen, Root Cause Analysis, Failure Investigations, High Performance Documentation, Training, Design for Manufacturability, New Product Introduction
Seek a position where I can contribute my technical skills and add value to a perspective employer’s goal. Look forward to contributing my strong attributes of teamwork, leadership, safety, quality and initiative towards any task set before me.
Materials Scientist – Lab Technician, looking for a strong, stable, upbeat, quality based organization to add my work experience to. I have 22 years in the medical device industry in a cGMP environment. I have been a polymer and drug analyst for 20 of those years. I am motivated, well thought of and can work alone or in a team environment. I would like the opportunity to expand or continue my skill sets with a company who ...
To get a position with a startup or well established Biopharmaceutical which has many products in their pipeline.
As an established Quality Control Manager, I have extensive experience in quality assurance, instrument qualification, procedure writing, analytical methods development, transfer and validation. I Possess expertise with FDA, ICH and EU requirements for pharmaceutical, drug substance, drug product and device testing. I Collaborate effectively with outside vendors and internal groups including assay development, manufacturing...