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Regulatory Job Openings
  Regulatory Job Title Regulatory Job Location
Technical Manager (at Pharmilab):
Responsible for every technical issues, from regulatory affairs to the analytical Laboratory.
Main areas - pharmaceutical, cosmetics and nutraceutical Technical Manager Nottingham, Nottingham
Become part of a growing team.

Collagen Matrix, Inc. is the leader in the design and engineering of collagen and mineral-based extracellular matrices for tissue and organ repair and regeneration. The Company currently manufactures collagen and mineral-based finished medical devices in the areas of orthopedic-spine surgery, neurosurgery, oral sur Regulatory Specialist Oakland, New Jersey
We are seeking a talented director of regulatory compliance for our client, a dynamic privately held global specialty chemicals company with revenues approaching $10 Billion.

It is an exciting high profile, high impact new position that will work to establish company-wide policies and practices around compliance to product-specific regulations. Director of Regulatory Compliance Oswego, IL
KEY RESPONSIBILITY:	
Serve as a scientist for assigned preclinical research studies of basic to moderate complexity, to include study management, interpretation and reporting of study data, and assuring the regulatory compliance of these projects. 

ESSENTIAL DUTIES AND RESPONSIBILITIES:  
 With minimal guidance, serve as a as a study director Study Director General Toxicology Suzhou, Jiangsu
The position is primarily focused in preclinical vaccine development activities, including oversight/improvement of new/existing documentation systems/databases.  Candidate will help in defining programmatic milestones and assessing critical resources/timelines.  Duties include:

- Manage raw material release/qualifications for laboratories
- En Senior Program Officer, Quality Assurance and Regulatory, Vaccine Development Houston, Texas
Plan, direct and coordinate the operational activities of the microbiology and analytical labs. 
Maintain a safe and healthy work environment by establishing and enforcing organizational safety standards and adhering to legal regulations. 
Ensure quality systems are being applied in the performance and documentation of lab studies and production Laboratory Manager Sandpoint, Idaho
    *  Maintain Good Laboratory Practices (GLP)
    * Monitor and assure that all regulatory and/or applicable documentation is appropriately recorded, filed and accessible for inspections, reports, etc.
    * Ensure direct reports' compliance with departmental standard operating procedures
    * Ensure direct reports responsibilities will be co ANIMAL CARE (RESEARCH SUPPORT) SUPERVISOR Everett, WA
As a member of the leadership team, the Director, Pathology Services will be involved in activities including strategic planning, department goal setting, budgeting, and process improvement efforts with Lean Six Sigma. The Pathology Services Director will have responsibility for representing SNBL USA and interfacing successfully with clients, regul PATHOLOGY SERVICES DIRECTOR Everett, WA
Candidate will be responsible for managing and supporting projects to meet Clinical Chemistry, Histology and Immunotoxicology protocol requirements, and to meet the scientific and regulatory requirements of our clients. This individual is responsible for technical staff supervision and assuring all staff proficiencies, administrative management, en Department Head of Laboratory Services Bedford, MA
    *  The ideal candidate should have hands-on experience in development of stirred tank processes in a leading biopharmaceutical company in the late stage mammalian cell culture development facility or a pilot plant.
    * The candidate should have experience in design, development, scale-up and troubleshooting of cell culture process from labor Laboratory Scientist Electronics City, Bangalore
We are seeking a Sr. Regulatory Affairs Specialist / Manager who will define, manage and execute complex, global regulatory submission strategies to help meet growing post market compliance and change control activities.  Candidates should have some international regulatory experience and familiarity with the IVD industry.

 

DESCRIPTION OF PO Sr. Regulatory Affairs Specialist / Manager San Diego, CA
Auto req ID: 21858BR

School/Unit: Harvard School of Public Health

Department: Nutrition

Duties & Responsibilities: This position is located in Tanzania. Harvard School of Public Health (HSPH) has a long-standing collaboration with a number of medical and public health academic institutions in East Africa. Over the past 20 years, we conduct Research and Regulatory Manager Boston, Massachusetts
Regulatory Affairs Associate
Iovate is the maker of the MuscleTech family of products and a leader in the sports nutrition, diet and health supplements industry.

Opportunity:
Due to our rapid growth, Iovate has an exciting new opportunity for a Regulatory Affairs Associate within our Legal Affairs team.  As a Regulatory Affairs Associate at Io Regulatory Affairs Associate Oakville, Ontario
Auto req ID: 21391BR

School/Unit: Harvard School of Public Health

Department: Nutrition

Union: 98 - Non-Union Non-Exempt incl GF

Duties & Responsibilities: This position is located in Tanzania. Harvard School of Public Health (HSPH) has a long-standing collaboration with a number of medical and public health academic institutions in Eas Research and Regulatory Manager Boston, Massachusetts
This position is responsible for the implementation and follow through of all domestic and international regulatory requirements established by the Regulatory Affairs group of the Sherwin-Williams Company including chemical inventories, developing label precautionary language based on raw material and formula information and review of labels, data Corporate Affairs Regulatory Manager ,
The position will assist the Corporate Regulatory Affairs Group in assuring that the company and all products remain in compliance with domestic and international regulations including new acquisitions in US and international locations by properly classifying, characterizing and recording raw materials in the Sherwin Williams databases.

1 year e Corporate Regulatory Affairs Specialist ,
Juice Pharmaceutical is currently recruiting a number of temporary roles across the UK and Europe. We are interested in hearing from professional Interim Managers with 5 to 10 years experience in Pharmaceutical, Biotechnology, Healthcare and the Medical Devices industries within any area of Regulatory Affairs.
If Interim management is of interest Regulatory Manager All, All
Nutrition

Duties And Responsibilities: This position is located in Tanzania. Harvard School of Public Health (HSPH) has a long-standing collaboration with a number of medical and public health academic institutions in East Africa. Over the past 20 years, we conducted several large clinical trials on infectious diseases, maternal and child health Research and Regulatory Manager Boston, Massachusetts
Group Leader / Associate Director - Pathology (Code: ATPL/SA/PTH/BLR) 
Job Description To lead a team of staff in conducting & executing regulatory Pathology studies for domestic and international clients. 
Experience in handling of Pharmaceutical and Biotech Pathology projects is desirable. 
The incumbent is expected to have strong communicatio Associate Director ,
Pharmaceutical API, Drug Substances, Excipients and Raw Materials Testing 
Pharmaceutical Quality Control (QC) In-Process Testing 
Pharmaceutical Finished Product Release Testing 
Pharmacokinetic (PK) Studies 
Stability Studies 
Real Time Stability Studies and Testing 
Accelerated Aging Stability Studies and Testing 
Container-Content Testin Quality Assurance and Quality Control Chemist Wilmington, North Carolina,, USA, North Carolina,,
Working for this truly dynamic branded business, whose name is synonymous with healthy eating and quality, you will enjoy an active and varied position across a broad range of regulatory and nutritional accountabilities. You will play a key role in enable commercial growth in the UK via proactive Regulatory and Nutrition strategy and implementation Regulatory and Nutrition Manager (12 Month Contract) London,, Middlesex
BASF, The Chemical Company, is a Fortune 100 chemical company dedicated to making products that make our customers' products better. At BASF, we make careers better, too.      
Job Description 
The incumbent will have the unique opportunity to be based in North America supporting regional business needs as well as be part of a broader community o Product Relations Specialist Sr. Wyandotte, Michigan
McCormick Canada is a growing and prosperous leader in the spice, seasoning, flavouring and specialty food industry. Our divisions serve retail grocery and emerging channel customers, food service distributors and other food manufacturers across Canada.  McCormick Canada is part of the world leader in spice and seasonings, McCormick & Company Inc.
Regulatory Affairs Manager London, Ontario
As a Quality Assurance QA Manager at MDS Pharma Services, you will provide technical and regulatory guidance, as well as day-to-day supervision, to our Early Clinical Research and Bioanalytical Quality Assurance team.  In this position you will ensure that the records, methods and practices are in compliance with company policies, procedures and re Quality Assurance Manager Lincoln, Nebraska
Essential Responsibilities

	Provide strategic regulatory representation on assigned project teams.
	Develop, prepare and review regulatory submissions for assigned projects.
	Communicate regulatory policy to internal customers and provide clarity on regulatory expectations and timelines.
	Maintain global regulatory filings (INDs, CTAs, ND Manager, Regulatory Affairs Cambridge, MA
Qualifications: PhD in Analytical Chemistry with 3-5 Years of Experience. Or M Sc - AnalyticalChemistry / M Pharm in Pharmaceutical Analysis with 4-8 Years.

Skillsets:
 
Knowledge of Implementation of GLP and Regulatory Guidelines 
Sound knowledge in Method Development and Validation on LC-MS/MS and HPLC. 
Knowledge in preparing and reviewin Scientist/Senior Associates -BioAnalytical Hyderabad,
 Understand and comply with domestic and international cosmetic regulations including cGLPs, cGMPs, CTFA, FDA, EPA, and COLIPA guidelines 
Responsible for development and tracking of new products/promotional concepts
Work with Creative, Sales, Marketing, Brand Awareness, Packaging Engineer, and Manufacturing & Operations to ensure the products ar Regulatory /Product Development Director Renton, Washington
BC Hydro is one of the largest electric utilities in Canada, serving more than 3.6 million customers in an area containing over 94 per cent of British Columbia's population whose purpose is to provide, BC HYDRO, Manager, Regulatory Business Analysis Vancouver, BC
The primary purpose of this position is to provide support and assistance to the Regulatory Affairs Department in maintaining current regulatory knowledge of domestic and international regulations, guidelines and standards and assist in applying appropriate implementation strategies.  The individual is also required to assist with the preparation a Regulatory Affairs Specialist Winston Salem, North Carolina
Job Description
We are seeking a Director of Product Development and Regulatory Compliance to manage the development and quality control of all our products including product ideation, interacting and negotiating with vendors, project and timeline management, quality assurance, regulatory compliance, sample library maintenance, packaging stability Product Development/Regulatory Compliance Director renton, washington
COOK Endoscopy, a leading medical device manufacturer for gastrointestinal endoscopy, is seeking a qualified Regulatory Affairs Specialist.  The primary purpose of this position is to provide support and assistance to the Regulatory Affairs Department in maintaining current regulatory knowledge of domestic and international regulations, guidelines Global Regulatory Affairs Specialist Winston-Salem, NC
The Institute for Transfusion Medicine, the parent company of Central Blood Bank located in Green Tree, Pa., currently is seeking an experienced QA Manager to join our growing team of professionals. 

In this position you will be responsible for managing ITxM's (The Institute for Transfusion Medicine) Internal Audit Program that includes: schedul Quality Assurance Manager ll Pittsburgh, PA
Leading manufacturing company of functional food ingredients in Europe, located in The Netherlands

Reporting to Head of department in Switzerland

Independent Project Management role 

10-20% overnight traveling included

Internal contacts: Business Managers, Project Managers, R&D Global Regulatory Affairs Manager ,
Responsibilities include:

Timely and accurate analysis of samples to meet customer commitments. This includes, but is not limited to, sample preparation for sample analysis, data review and reduction, and providing data interpretation and opinion. 
Ensure all regulatory procedures pertaining to sample testing are followed correctly, if they are Amino Acids Chemist Des Moines. Relocation assistance is offered., IA
Responsibilities include:

·Timely and accurate analysis of samples to meet customer commitments. This includes, but is not limited to, sample preparation for sample analysis, data review and reduction, and providing data interpretation and opinion. 

·Ensure all regulatory procedures pertaining to sample testing are followed correctly, if they Senior Vitamins Chemist Des Moines. Relocation assistance is offered., IA
A growing, publicly traded organization is seeking a VP of Regulatory Affairs to oversee the Worldwide Rgulatory Affairs and Clinical and Preclinical comliance studies for the company.  Vice President of Regulatory Affairs , Maryland
TOKYO, JAPAN -- The candidate should have complete knowledge of regulatory requirements for generic prescription product and dossier registrations in Japan with supplementary knowledge of Bioequivalence study requirements, IPR, Trademark, legal and any other related issues concerning the above said registrations.  The candidate should coordinate wi Regulatory Affairs Manager (JAPAN) Minato-ku, Tokyo, TOKYO
Washington, D.C.-based consulting firm is seeking motivated individual for variable part-time position.  Job responsibilities include: contract quality assurance work not limited to testing facility audits, GLP report review, SOP review and development, and other pharmaceutical and medical device support activities.  Individual should have a minimu Quality Assurance Specialist Washington, D.C.
Accelovance is an innovative niche CRO focused on accelerating vaccine and drug advancement.  We conduct Phase II through Phase IV clinical trials.  Our clients are pharmaceutical and biotech companies.  Excellent ground floor opportunity that includes salary, bonus and stock options.   Accelovance is currently seeking qualified individuals with re Quality Assurance GCP/GLP Rockville, Maryland
Plan and consult global clinical trial IND's, NDA's and other projects for one of the worlds largest and most dynamic Contract Research Organizations - Kendle.

The Associate Director Clinical Regulatory Strategic Planning is responsible for the regulatory and business leadership and establishing its mission and goals. This responsibility include Associate Director, Clinical Regulatory Strategic Planning Cincinnati, OH
Bodycote International PLC is an UK-based public corporation. The Bodycote Materials Testing Group is the world's largest group of independent testing laboratories, with more than 60 facilities worldwide, including fifteen in Canada. 

Working in Bodycote's Health Sciences Group at the Mississauga laboratory, you will have senior responsibility f Quality Assurance Coordinator, Health Sciences Mississauga, Ontario
Conduct quality impact assessments associated with investigations on exceptions for Out-of-Specifications/Out-of-Trends reported from in-house or contract lab testing, and other exceptions during the manufacture, packaging, or holding of Raw Materials, In-Process Materials, Finished Product, and Stability Samples, Purified Water and Environmental M Quality Assurance Associate Steinbach, Manitoba
Responsible for the GLP/testing lab Quality Assurance function at the Ohio and California locations including staffing, budgeting, and training. Back up corporate management respresentative for ISO 9001 and Quality System Regulation. Secondary interface with the regulatory agencies for regulatory audits and submissions.

Manager, Quality Assurance Northwood, OH
Tyco Search has been retained by Medtronic / ERS in Seattle for a VP of Quality / Regulatory Affairs.   

Responsible for establishing and maintaining corporate systems for conformance to domestic and international quality standards and medical device laws and regulations.   Formulates long-range operating plans, budgets and programs under the di Vice President Quality / Regulatory Affairs Seattle, WA
StemCell Technologies Inc, located in Vancouver, Canada, is a leading supplier of specialized cell culture media and cell separation products for life sciences research. We are seeking an experienced and motivated technologist to be part of a dynamic ten-member QC team.

Good laboratory skills and experience in mammalian cell culture.  Experience Quality Control Technologist Vancouver, British Columbia
Summary:
Provide quality, strategic support to the US Business Development group by formulating and directing marketing plans.  The selected candidate will perform specific market research on the pharmaceutical, biotechnology industries (drug pipelines & development phases, licensing, mergers, regulatory submissions, etc) as well as on competitors Director, Strategic Marketing and Planning Newark, New Jersey
Frontage laboratories, Inc., is one of the fast growing contract research organizations based in Malvern, Pennsylvania and Shanghai, People's Republic of China. We are looking for a highly motivated toxicologist to join our newly expanded area of preclinical drug development. The successful candidate will be responsible for design, executing and re Toxicologist Malvern, PA
Frontage laboratories, Inc., is one of the fast growing contract research organizations based in Malvern, Pennsylvania and Shanghai, People's Republic of China. We are looking for a highly motivated scientist to lead the effort in the area of pharmacokinetics and drug metabolism. The successful candidate will be responsible for performing pharmacok Pharmacokinetics / Drug Metabolism Scientist Malvern, PA
We are seeking a highly motivated, team oriented individual with excellent communication skills. Skills desired include pre-formulation and formulation development of solid dosage, liquid, and IV formulations, including controlled release formulations, suspensions and emulsions. Experience in equipment selection, scale up of developed formulations, Senior Formulation Scientist Malvern, PA
Will provide veterinary support to programs in preclinical toxicology, cancer research, and biodefense. Ensures that all USDA and NIH Animal Welfare Regulations are met, and that AAALAC accreditation is maintained. This individual will ultimately assume overall responsibility for the IITRI laboratory animal medicine program. Will develop technology Clinical Veterinarian Chicago, Illinois
Will monitor non-clinical laboratory studies, raw data and reports to ensure compliance with good laboratory practice (GLP) standards. Will be expected to perform the following duties with minimal supervision:  Review all study protocols and conduct inspections to ensure that work being performed adheres to GLPs, protocols and Standard Operating P Research Quality Assurance Auditor Chicago, Illinois
CAPA system administrator, Part 11 remediation activities, Supplier Qualification, Authoring/editing/approval of investigations/deviations/SOPs, Full Time position Quality Assurance Associate Oakdale, Minnesota
Rapidly expanding contract research organization seeks scientists for Study Director positions. Studies involve compulsory pre-clinical testing of medical devices, pharmaceuticals, and biotechnology products according to numerous national and international regulatory guidelines. Opportunities exist for expanding the laboratory's testing capabilitie Study Directors, Toxicology Bedford, Massachusetts
Toxikon is seeking individuals with a minimum of a bachelor's degree in the life sciences to monitor biological and chemical studies and creating reports in conformance with GLP practices. Candidates should have at least 2 years experience in an FDA regulated environment, basic knowledge of study design and review practices, strong attention to det Quality Assurance Monitor Bedford, Massachusetts
Boston Analytical, a contract pharmaceutical laboratory located in Salem, NH, is looking for a full time QA Specialist to support the company's Quality Assurance program.  

Primary duties will include:

-Monitoring and maintaining the calibration program of the analytical and microbiological laboratory equipment.  
-Auditing results of microb Quality Assurance Specialist Salem, New Hampshire
Seeking a highly motivated Pharmaceutical Scientist to start-up a formulation development laboratory. Must be a self-starter and capable of working independently from concept to product prototype.  Familiarity with analytical techniques, regulatory requirements and GMP manufacturing is preferred. 

Quality Chemical Laboratories offers a complete Pharmaceutical Scientist (Formulation) Wilmington, North Carolina
Quality Chemical Laboratories, a contract pharmaceutical service provider in Wilmington, NC, is seeking a qualified individual for the position of Quality Assurance Director. This individual must possess strong leadership and interpersonal skills along with a thorough understanding of GMP regulations. This individual will be responsible for impleme Quality Assurance Director Wilmington, North Carolina
This position is located in our Irvine, California location. Responsibilities include fiscal and operational management of In Vitro and In Vivo Toxicology laboratory areas.

Experience:
 Practical experience in the areas of study design, data interpretation. Proven management experience required.
 
Requirements:  
 Qualifications include broa Toxicology/In Vitro Manager Irvine, California
Seeking individual with Ph.D. in environmental science with laboratory experience performing and managing aquatic
toxicology studies in compliance with OECD, OPPTS, and other international guidelines. Individual should have
demonstrated experience in writing and executing protocols, report writing, data interpretation and statistical analysis,
a Aquatic Toxicologist Bedford, Massachusetts
We are seeking a highly competent toxicologist with safety and efficacy experience with the full
range of ISO Biocompatibility and ICH testing guidelines. Strong ability to write protocols, manage studies, 
provide technical interface with clients and FDA or other agencies, and strong quality/regulatory
understanding required. Strong communicati Toxicologist Bedford, Massachusetts
Rapidly expanding contract research organization seeks scientists for Study Director positions. Studies involve compulsory pre-clinical testing of medical devices, pharmaceuticals, and biotechnology products according to numerous national and international regulatory guidelines. Opportunities exist for expanding the laboratory's testing capabilitie Toxicology Study Directors Bedford, Massachusetts
We are seeking Toxicology Technicians to work in our expanded medical device, pharmaceutical, and biotechnology testing laboratory. Responsibilities include animal handling, animal husbandry, data collection and recording, data package preparation, sample preparation, dosing, and surgical assistance. Prior animal, research, animal husbandry, and/ o Toxicology Technician Bedford, Massachusetts
Responsible for the management of the stem cell laboratory in Clinical Services, which performed 250 procedures last year. Managing the daily operations of the laboratory and supervision of the technologists in the lab. In conjunction with the Laboratory Director, the manager will ensure that the lab meets all regulatory standards including FDA, AA Stem Cell Manager , New York
Perform a thorough audit as per the requirements of the applicable SOPs, protocols, and GLP. Conduct thorough investigation. Communicate findings in a timely manner to the responsible personnel. Write audit reports. Senior Assurance Quality Auditor Laval, Quebec
The successful candidate will be responsible for coordinating the company's worldwide regulatory strategy for its lead product through to commercialization.  Beyond this immediate task this person will be responsible for worldwide regulatory activities associated with the discovery and development of new products. Director of Regulatory Affairs Melbourne, Florida
 Are you interested in working for a progressive company that is striving to improve the quality of life?  Nelson employees work with some of the best medical device, pharmaceutical, and neutraceutical companies in the world (including many fortune 500 companies).  Our staff partner with these companies to assure the quality of their unique and inn GLP Auditor Salt Lake City, Utah
Intertek Expert Services, a premier regulatory and analytical services group, is looking for an analytical scientist to initially work in our Tarrytown, New York laboratory and then transfer to Intertek's facility in Whitehouse, New Jersey.  Level and compensation commensurate with experience

Duties Include, but are not limited to:
Execute FDA Analytical Scientist Tarrytown, NY
	Coordinating, planning, and managing all Certification, Regulatory Audits by G-Med - LNE, France, UNFPA and USFDA on behalf of the Management (M.R).
	Conducting Management Reviews, Internal Audits and Trainings.
	Planning, Coordinating and supporting of External Sampling and testing of finished products.
	Monitoring and Controlling Validati General Manager - QA & RA Chennai, Pondicherry, Tamilnadu
 Monitoring the conduct of clinical study, enrollment and quality of data.
 Ensure complete and thorough study drug reconciliation and master accountability.
 Ensure compliance to Ethics Committee requirement.
 Responsible for ensuring that the study is being conducted in accordance with the protocol, standard ope Clinical research associate and as QA Auditor Ahmedabad, Gujarat
Obtain a challenging, rewarding position hospitals, pharmaceutical, 
health care .Desire a job that provide opportunity for growth and learning Regulatory Affairs Director, Quality Assurance Director, QA delhi, delhi
 Monitoring the conduct of clinical study, enrollment and quality of data.
 Ensure complete and thorough study drug reconciliation and master accountability.
 Ensure compliance to Ethics Committee requirement.
 Responsible for ensuring that the study is being conducted in accordance with the protocol, standard ope Clinical research associate and as QA Auditor Ahmedabad, Gujarat
i has participated in real time project in rheumatoid arthrities in chanre hospital,bangalore,india. pharmcovigilance,cdm,cra,regulatory affairs,bussiness analyst Bangalore, karnataka
Responsibilities:         
-	Preparation and compilation of all the relevant  technical data accurately as per guidelines
-	Co-ordination with the packaging development dept. for preparation of accurate packaging materials as per country specific requirements.  
-	Check the custom sample thoroughly for its compliance with the corresponding count Regulatory Affair Executive California, Los Angeles
regulatory affairs montreal, quebec
i has participated in real time project in rheumatoid arthrities in chanre hospital,bangalore,india. pharmcovigilance,cdm,cra,regulatory affairs,bussiness analyst Bangalore, karnataka
	Preparation & Compilation of ANDA Submission of various products for submission to USA.
	Preparation & Compilation of MRF1 of various products for submission to MCC.
	Preparation & Compilation of TGA of various products for submission to Australia.
	Preparation & Compilation of EMEA of various products for submission to Europe.
	Co-ordina Regulatory affairs hyderabad, Andhra pradesh
-Preparation and submission of dossier for international regulatory agencies as per various requirements according to regulations and 	guidelines of respective country.
-Review the following documents necessary for Dossier preparation and Submission, Batch manufacturing and packing record specification, Method of Analysis, certificate of analysis IRA EXECUTIVE AHMEDABAD, GUJRAT
In Vivo Technician
Toxikon Corporation is a preclinical contract research organization. We contract and partner with biotech, pharmaceutical and medical device industries to deliver exceptional product development services from concept to final product.
We are seeking Entry Level Technicians for our In Vivo Department to support animal studies al adg daer adgraedr, agdaer
The position is primarily focused in preclinical vaccine development activities, including oversight/improvement of new/existing documentation systems/databases.  Candidate will help in defining programmatic milestones and assessing critical resources/timelines.  Duties include:

- Manage raw material release/qualifications for laboratories
- En Senior Program Officer, Quality Assurance and Regulatory, Vaccine Development Washington, DC
My job responsibilities include:
	Involve and adhere to Quality Procedure and Analytical Methods.  Safe Handling of Lab Chemicals and Lab wastes
	Interact with Production, Sales and Logistics departments on day to day activities.
	Login all In-Process, Finished Products and Miscellaneous Samples. Analyzing and reporting o laboratory quality control supervisor easter provience, jubail
Over 14 years' of Pharmaceutical industrial experience presently associated NAARI PHARMA INDIA PVT LTD. as MANAGER- Analytical Development R&D. Expertise in 
Analytical method development, Method validation &, STP, SOP review & DMF Queries attending and Quality Innovation Projects. A dept at carrying out various tests and inspection for various pr Manager-Analytical R&D/QA/QC/RA/DQA-API Chennai,Bangalore,Hyderabad,Mumbai anywhere, TamilNadu,Karnataka,UP,AP anywhere