ARIAD Pharmaceuticals, Inc.
Cambridge, Massachusetts
This position is responsible for the planning, delivery and execution of the Good Clinical Practice QA program on assigned projects/products and global GCP audit activities. The role is responsible for GCP oversight, and for assuring the compli...
Source: CareersInPharmaceutical.com
Updated
7 days
16 hours
ago
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Amphastar Pharmacuticals Inc.
Rancho Cucamonga, California
Amphastar Pharmaceuticals, Inc. is a progressive company that will recognize your talents, challenge you, and reward your efforts competitively. We invite you to explore employment opportunities with Amphastar and its subsidiaries.
Amphastar is commit...
Source: CareersInPharmaceutical.com
Updated
11 days
17 hours
ago
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Amphastar Pharmacuticals Inc.
Rancho Cucamonga, California
Amphastar Pharmaceuticals, Inc. is a progressive company that will recognize your talents, challenge you, and reward your efforts competitively. We invite you to explore employment opportunities with Amphastar and its subsidiaries.
Amphastar is commit...
Source: CareersInPharmaceutical.com
Updated
11 days
17 hours
ago
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Jim Crumpley & Associates
Southeastern US, North Carolina
Job Title: SENIOR VALIDATION ENGINEER
Location: Southeastern US
Salary: $105,000 + 20% Bonus
Last Updated: 08/26/2008
Will be responsible for validation of sterile processing equipment within a new plant start-up and once it is completed, prov...
Source: CareersInPharmaceutical.com
Updated
19 days
18 hours
ago
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Jim Crumpley & Associates
Rocky Mountains, Colorado
Job Reference Code: AFF-450
Job Title: DIRECTOR OF QUALITY ASSURANCE
Location: Rocky Mountains
Salary: $170K + 25% Bonus Target
Last Updated: 09/09/2008
Must have solid dose experience.
This person will direct resources to assure GMP complianc...
Source: CareersInPharmaceutical.com
Updated
19 days
18 hours
ago
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Jim Crumpley & Associates
Midwest, Missouri
DIRECTOR, OPERATIONS EXCELLENCE
POSITION OVERVIEW
--Seeks a Director, Operations Excellence who will direct and manage all aspects of master batch records for bulk manufacturing from “R&D Draft” stage to final approval. The successful candidate wil...
Source: CareersInPharmaceutical.com
Updated
19 days
18 hours
ago
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Jim Crumpley & Associates
Florida, Florida
Requirements:
Bachelor's degree in Engineering or other scientific discipline. 1-3 years in Quality Assurance, Supervisory experience preferred. Candidate must have proven project management skills and demonstrated experience using statistical process co...
Source: CareersInPharmaceutical.com
Updated
19 days
18 hours
ago
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Jim Crumpley & Associates
Texas
Will be responsible for total oversite of plant-wide quality operations to include FDA escort, PAI's, documentation, compliance, audit and lab operations. Must have a demonstrated track record of management of a quality organization of at least 30 people ...
Source: CareersInPharmaceutical.com
Updated
19 days
18 hours
ago
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Jim Crumpley & Associates
Texas
Extremely visible position at a leading drug manufacturer involved in oversite of GMP and continuing education training. This includes manufacturing and quality assurance training to foster an effective teamwork environment and increases employee involvem...
Source: CareersInPharmaceutical.com
Updated
19 days
18 hours
ago
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Jim Crumpley & Associates
Southeast US, North Carolina
Job Reference Code: AFF-105
Job Title: SR. PROCESS DEVELOPMENT ENGINEER
Location: Southeastern US
Salary: $90,000 + Bonus
Last Updated: 08/12/2008
Will have responsibility of working with R&D teams to assure smooth transition of product from R&D...
Source: CareersInPharmaceutical.com
Updated
19 days
18 hours
ago
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Jim Crumpley & Associates
Southeastern US, North Carolina
Job Reference Code: AFF-100
Job Title: QUALITY ASSURANCE MANAGER
Location: Southeastern US
Salary: $100,000 + Bonus
Last Updated: 08/12/2008
Will have primary responsibility for oversite of a QA group devoted to preparation and approval of all S...
Source: CareersInPharmaceutical.com
Updated
19 days
18 hours
ago
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Valeant Pharmaceuticals
Aliso Viejo, California
The incumbent provides leadership for the Corporate Quality Operations, Corporate Quality CTM, and Corporate Quality Compliance programs. The incumbent is charged with establishing corporate policies for quality and compliance that are commensu...
Source: CareersInPharmaceutical.com
Updated
20 days
17 hours
ago
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TalentWRx, LLC
Doral, Florida
Job Summary
This position is responsible for the inspection and microbial testing of all raw materials for production. This includes physical examination, reviews of C of A’s and microbiological examination. Conducts the microbiological examination o...
Source: CareersInPharmaceutical.com
Updated
48 days
21 hours
ago
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TalentWRx, LLC
Miami, Florida
Job Responsibilities:
• Devises and directs monitoring programs to protect facilities and laboratory personnel from radiation hazards.
• Conducts research to develop inspection standards, radiation exposure limits for personnel, safe work methods, and d...
Source: CareersInPharmaceutical.com
Updated
48 days
21 hours
ago
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TalentWRx, LLC
Ormond Beach, Florida
GENERAL DESCRIPTION: Directs the assessment, upgrade and execution of all facets of a company-wide quality system. Provides direction to company's Quality organization and establishes policies, procedures and accountability measures that ensure regulatory...
Source: CareersInPharmaceutical.com
Updated
48 days
21 hours
ago
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