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Food Chemist Jobs

20 matches | 1 - 20 displayed
  1  
date  location  job detail
Jan 13,2019 USA-MD-Frederick Clinical Research Associate
Frederick, MD
What you'll be doing
Works primarily in an in house position, assists with the implementation of clinical trials, tracking studies and subject informations and coordinating project activities associated with the monitoring functions of clinical studies. Assists with the review of proto
Jan 11,2019 USA-NJ-East Hanover Quality Control Manager at Pharmaceutical Company in East Hanover, New Jersey, United States
Job Description
Primary Purpose/Objectives of the Job:
The primary responsibilities of the Quality Control Sales Order Associate are to create Certificates of Analysis and allocate, release and transfer material for sales orders and manufacturing purposes. This role with also review internal and ext
Jan 15,2019 USA-CA-Orange Inpatient Speciality Pharmacy Manager
A reputable 400 bed medical center in southern California is looking for a meticulous Senior Pharmacy Manager PharmD to joining their prestigious medical center. This facility has been ranked as one of the best hospitals in the nationwide for over 15 consultative years.??This prestigious academic
Jan 20,2019 USA-TX-Carrollton QC Supervisor-Pharmaceutical Manufacturing
QC Supervisor-Pharmaceutical Manufacturing
in
Carrollton
Texas
Kelly Scientific Resources is currently seeking a FSQA Supervisor for a major pharmaceutical manufacturer in the Dallas/Ft Worth geographical area of Texas. This company is a consistent leader in its field and is highly respected for its
Jun 07,2018 USA-NJ-Princeton Regulatory Affairs Project Leader
Responsible for tracking and timely completion of regulatory strategies and issues, scientific substantiation for product claims, and label/promotional material activities.
Responsible for effective communication of regulatory requirements to project teams and internal customers.
Assists in definiti
Dec 31,1969 USA-CA-Redwood City Senior Manager/Associate Director, Regulatory Affairs
Job description:
Develop and implement competitive and effective global regulatory strategies for various oncology products including clinical, nonclinical and CMC aspects and identify potential risks associated with proposed strategies.
Manage and participate in the creation, review, assembly and s
Jan 26,2019 USA-NJ-Madison Medical Information Analyst
Research and respond to requests for scientific/medical information using various search and retrieval techniques and medical literature database (product label, published and unpublished studies).
Develop a medical/scientific response that is accurate, fair balanced, complete and delivered in a
Jan 24,2019 USA-FL-Kendall 3rd Shift Washroom Technician (Pharmaceutical)
\n\nJob Description\nWashroom Technician-3rd shiftA growing pharmaceutical company in Miami are looking for a 3rd shift Washroom Technician.  M-F,  10pm-6:30am.  This is a permanent position up to $15.50/hr. depending on skill set. ESSENTIAL DUTIES\n\nEnsures work area is kept in a clean and tid
Jan 22,2019 USA-NC-Charlotte Manager Regulatory Affairs
\n\nJob Description\nAn exciting and growing medical device team out of the Charlotte, NC area is looking to bring on a Regulatory Manager in a strategic and hands-on role that is a high priority role for this regulatory group. This company is a global pioneer and leader within textiles, compression
Jan 24,2019 USA-TX-Carrollton QC Supervisor-Pharmaceutical Manufacturing
QC Supervisor-Pharmaceutical Manufacturing
Kelly Services
?
Carrollton
TX
75007
Job #821230404
Kelly Scientific Resources is currently seeking a FSQA Supervisor for a major pharmaceutical manufacturer in the Dallas/Ft Worth geographical area of Texas. This company is a consistent leader in its field
Jan 29,2019 USA-NJ-Saddle Brook Regulatory Review Manager
\n\nJob Description\nRef ID: 02710-9501743235Classification: Copywriter - Sr.Compensation: $40.00 to $50.00 per hourThe REGULATORY REVIEW MANAGER (RRM) must follow the protocol established by our pharmaceutical company clients when submitting marketing materials for regulatory review. This includes
Jan 30,2019 USA-TX-Richardson Quality Control Instrument Technician
Renowned Systems Integrator seeks:
QC inspections, testing Instruments & Control Panels
Wiring, fabrication testing
Instrument and control systems including transmitters, PLC's and instrument loops.
Flow meters, pressure probes, temperature probes, and level probes.
PLC logic and software platforms
Feb 04,2019 USA-UT-Salt Lake City Regulatory Affairs Associate
Position: Regulatory Affairs Associate
Location: Salt Lake City , UT
Duration:4 months (possibilities of extension)
Essential Duties & Responsibilities
Prepare, review and approves regulatory submissions (i.e. ANDAs, amendments, supplements, etc.) to the Food and Drug Administration (FDA) to ensure
Feb 04,2019 USA-KS-Overland Park Quality Assurance - Clinical Trials
Job Description
QA Professionals
- Are you ready to give your career a boost by bringing your talents and expertise to one of the cities fastest growing and expanding
clinical trials companies???
Come be part of the exciting
LIFE SAVING
cancer research conducted by our client, help advance the worl
Feb 04,2019 USA-CA-Foster City Regulatory Affairs Associate - II //Foster City, CA
Job Title: Regulatory Affairs Associate - II
Work Location: Foster City, CA
Length of Assignment: 6 Months
Position Type: Contract Full Time
Client:  A Big Pharmaceutical Company

Job Description:
Under supervision of a Regulatory Affairs Manager, the associate will work with cross-functio
Feb 09,2019 USA-NC-Lenoir Scientist I
\u003Cp\u003E\u003Cb\u003ECurrently seeking an experienced Chemist. Please contact Stephen Frazer at sfrazer@apexsystems.com or 704.521.6100\u003C/b\u003E\u003C/p\u003E\u003Cp\u003EThe \u003Cb\u003EScientist I, API Synthesis \u003C/b\u003Ewill be responsible in process development to support ongoin
Feb 08,2019 USA-NJ-Mahwah Regulatory Affairs Associate
Title:
Regulatory Affairs Associate
Location:
Mahwah, NJ
Duration:
6 months
Responsibilities:
Work with minimum supervision, conferring with more senior staff when indicated. Keep supervisor regularly apprised of project status. 
Collaborate with New Product Development Teams to ensure US, EU and o
Feb 07,2019 USA-NJ-Allendale Lead Coordinator, Regulatory Affairs
Title:
Lead Coordinator, Regulatory Affairs
Location:
Allendale, NJ
Schedule:
8am to 5pm Mon ? Fri ? Up top 20% travel may be required.
Type:
Temporary (12 months) 
Start date:
2/11/19
Responsibilities:
Support Regulatory Affairs product life cycle management and sustaining activities.
Responsible
Feb 08,2019 USA-NJ-Summit Project Coordinator
Title:
Project Coordinator
Location:
Summit, NJ
Schedule:
8am to 5pm Mon ? Fri.
Type:
Temporary
Start date:
Responsibilities:
Responsible for creating and maintaining all records in accordance with record retention policies and legal requirements
Update and maintain departmental electronic records u
Feb 08,2019 USA-NJ-Summit Sr. Clinical Trial Associate (CTA)
Title:
Sr. Clinical Trial Associate (CTA)
Location:
Summit, NJ
Schedule:
8am to 5pm Mon - Fri.
Type:
Temporary
Start date:
3/2/19
Responsibilities:
Creating and or reviewing study plans, specification documents, materials and tools.
Ability to communicate clearly both verbally and written to sites,
20 matches | 1 - 20 displayed
  1  

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