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Online Resumes with "SOP writing"

Quality Control Analytical Chemist II. 4yrs of GMP experience,IQ/OQ/PQ and validation experience as well as HPLC, GC/MS, FTIR, Flame AA and more

To help out an established Quality Control department to further and continue their track record of excellence by bringing my expertise in various types of spectrophotometry as well as HPLC,Particle Sizers, etc. I am aiming for the role of QC Analyst II or III or QC Analytical Chemist.

Tags for this Online Resume: QC Analytical Chemist, GMP, IQ, OQ, PQ, Chemist, Validation, Quality Analyst II, Analyst, Pharmacovigilance , QA, GDP, Metrology, Flame AA, Method , HPLC, Spectrophotometry, SOP writing, Particle Size, Data logger

Sr. Clinical research Associate/ Director of clinical research

Can undertake most of the tasks and works independently. Very much focussed on the timelines and quite goal tending. Willing to help others in their prioritized tasks. Excellent planning, design and implementation. Highly experienced in writing reports and data analyses.

Ideal Companies: Pharmaceutical industries, Biotech companies, Research institutes, hospitals and for profit mid to large companies.

Tags for this Online Resume: Director of clinical research, Manager of drug safety, Senior clinical research associate, Regional clinical research associate

Analytical Chemist, Lab Manager, Lab Supervisor, Quality Control Officer

Methods Development • Procedure/SOP Writing • Method Validation Quality Control (NELAP, cGMP, GLP, ISO, FDA) • Organics Lab Start-up and Initialization • Process Improvement • Effective Communications Relationship Building • Strategic Planning • Resource Management • Problem Solving • Budgeting • Lab Safety • Laboratory Certification

Compliance Manager/Auditor

To obtain a position working as a Microbiology Business Analyst and Project Manager in a pharmaceutical/biotech validation environment, oriented toward management advancement. Over 20 years of experience in the Pharmaceutical Industry, 16+ years of those years are with GxP (GMP, GLP, GCP) systems compliance/QA and 21 CFR Part 11. Experience includes GxP system implementation projects, documentation/SOP writing/review.

Quality Assurance Management

Tags for this Online Resume: Lab Auditing, SOP writing, NELAC, DoD ELAP, traceability



M.S Biomedical Engineering (USC, Los Angeles)

Quality engineer has the thorough knowledge about the product and all the processes involved in making that product and minimizes the errors and improves the use of resources using the tools of Six Sigma. They also maintain the standard procedures and regulations set by the company as well as the ISO and FDA. My Green Belt in Six Sigma and ASQ CQIA has given me the confidence to tackle statistical data and help conform the...

Tags for this Online Resume: ASQ certified Quality Improvement Associate, Green Belt in Six Sigma, Quality Engineer, CAPA, Interned at Natiopnal Chemical Lab, India, Medical devices

Food Safety,Food Quality-20 years of experience

Motivated Quality Professional who applies exceptional analytical skills and acute attention to detail to craft and implement rigorous quality processes that protect product integrity and ultimately the company brand. Work effectively both independently and within team environments.

Tags for this Online Resume: HACCP, GMP Auditor, Food Microbiology, ISO 22000, SOP writing, pathogen testing

Featured Profile

Director of Manufacturing

I am looking for a company that can utilize my extensive talents. Probably my best attribute is my personnel skills. I have interviewed hundreds of people, hired dozens and terminated a few as necessary. I would like a position that is a Production Director or Manager in the Biotech area. I have interfaced with ISO dozens of times and have done so with the FDA when they arrived for inspections as well. I am well versed ...

Tags for this Online Resume: Corrective Actions, Validations, Process Control, Product Transfer, Personnel Management, Biotech Manufacturing

Stability Program Coordinator - 20 Years Experience - New Jersey

Highly energized and versatile stability coordinator with extensive experience in Fortune 500 Pharmaceutical companies. Experience include sample and chamber management, technical/SOP writing, and LIMS.

Chemical Engineer - 17 Years of Experience - Indianapolis Near 46231

Extensive experience in Chemical Management, operation of wastewater treatment plant, staff management, JES and SOP writing, team and committee projects from conception to implementation, waste reduction and cost savings identification and attainment, and environmental permit application preparation and proofing.

Tags for this Online Resume: Indianapolis, Maximo, Microsoft Office, Project Management, Lab Technician