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Job info
 
Company
Location
Hillsboro, OR
Posted Date
Jan 23, 17
Info Source
Employer  - Full-Time   

Job ID: 00450265 The Position Main Purpose of the Position: The key objective of this intern project is to improve communication between Direct Material end users, Supplier Quality Management, and Direct Material Suppliers regarding quality issues and continual improvement. The candidate will ...

 
Company
Location
South San Francisco, CA
Posted Date
Jan 23, 17
Info Source
Employer  - Full-Time   

Job ID: 00450224 The Position The key objective of this intern project is to improve and obtain alignment across Supplier Quality Management (SQM) on a number of processes relating to supplier management. The candidate will work with the Global SQM team, including colleagues in Europe, Asia, Rio, ...

 
Location
San Rafael, CA
Posted Date
Jan 21, 17
Info Source
Employer  - Full-Time   

... . Qualifications: Have at least 8 years of working in QA & Testing Experience with Life Sciences and Pharma is must Experience with testing in Validated environment Experience in HPQC is required Experience in ...

 
Location
Lexington, MA
Posted Date
Jan 20, 17
Info Source
Recruiter  - Full-Time   

This is a contract job opportunity Position: Quality Assurance Compliance Specialist Pharma 152 Location: Lexington MA Projected duration: 6 months Job Code: 6008152 Support CAPA development and serve ...

 
Company
Location
Boston, MA
Posted Date
Jan 18, 17
Info Source
Employer  - Full-Time   

Lead Validation Quality Analyst in Boston, MA. Pharmaceutical / Biopharm is required for onsit... Lead Validation Quality Analyst in Boston, MA. Pharmaceutical / Biopharm is required for onsite person. * strong written and verbal communication skills. * Validation knowledge of ...

 
Location
Fort Collins, CO
Posted Date
Jan 17, 17
Info Source
Employer  - Full-Time   

Purpose and Scope Responsible for the development and execution of validation activities including, design, installation, and operational qualification of equipment/utilities/facilities, cleaning, and process validation for all manufacturing processes in an aseptic environment.  Writes, executes, or ...

 
Location
Raritan, NJ
Posted Date
Jan 13, 17
Info Source
Employer  - Full-Time   

... QA compliance experience within a software and hardware environment Software test experience in a regulated environment, ideally Pharma R&D Experience in Life Sciences industry preferred Ability to work at a strategic level with key client ...

 
Company
Location
Boston, MA
Posted Date
Jan 12, 17
Info Source
Employer  - Full-Time   

Associate GMP Quality Assurance Manager The Manager of Quality Assurance will report to the Associate Director or Director of Quality Assurance. This position will ensure... Requirements: Associate GMP Quality Assurance Manager The Manager of Quality Assurance will report to the Associate Director ...

 
Location
Boston, MA
Posted Date
Jan 11, 17
Info Source
Recruiter  - Contract     

Associate GMP Quality Assurance Manager The Manager of Quality Assurance will report to the Associate Director or Director of Quality Assurance. This position will ensure that procedures are implemented to maintain compliance to the quality systems requirements as defined by the quality system ...

 
Location
Morris Plains, NJ
Posted Date
Jan 11, 17
Info Source
Recruiter  - Contract     

Quality Assurance Associate needed for a contract opportunity with Yoh's client located in Morris Plains NJ The Big Picture - Top Skills You Should Possess: BS/BA in Biological Sciences or equivalent relevant career experience Minimum of 1 year GMP manufacturing and/or QA related experience PLEASE ...

 
Company
Location
Madison, WI
Posted Date
Jan 10, 17
Info Source
Employer  - Full-Time   

... regulatory requirements.   This position reports directly to the QA Manufacturing Lead – Pharma Project Lead and is directly responsible for the support, maintenance and verification of ... /GED (±11 years)','','Full-time','Regular','Experienced','QA Pharma Compliance Lead - Nutrition and Health

 
Company
Location
Madison, WI
Posted Date
Jan 10, 17
Info Source
Employer  - Full-Time   

... requirements. This position reports directly to the QA Manufacturing Lead - Pharma Project Manager for the Madison site and is directly responsible for the ... Pharmaceutical API compliance.Act as the primary backup to the QA Pharma Compliance Lead.Contribute to the review and assessment of Deviations, ...

 
Location
Swiftwater, PA
Posted Date
Jan 06, 17
Info Source
Employer  - Full-Time  90  

Manager Analytical Chemistry [cGMP/Quality Control - Pharma-Biotech]','POS_00404706-1','!*!Sanofi Pasteur, the vaccines division of Sanofi, provides more than 1 billion ... -Swiftwater','','Sep 30, 2016','Regular','Regular','Manager Analytical Chemistry [cGMP/Quality Control - Pharma-Biotech]']); api.

 
Location
Swiftwater, PA
Posted Date
Jan 06, 17
Info Source
Employer  - Full-Time   

Manager Compliance [Quality Assurance/cGMP pharma-biotech]','POS_00406604-1','!*!Who We AreSanofi Pasteur, the ... the Change Control System  Technical Competencies:Quality Assurance experience in a Pharma/Vaccine production facilityWorking knowledge of cGMPs and regulatory requirements Knowledge of ...

 
Location
Knoxville, TN
Posted Date
Jan 03, 17
Info Source
Employer  - Full-Time   

Director, Quality Systems (Pharma)','16000XIZ','!*!PURPOSE AND SCOPE: Directs and monitors the Quality System programs across the assigned manufacturing ... Orientation/Gender Identity','Quality','United States-Tennessee-Knoxville','','Full-time','Day Job','Director, Quality Systems (Pharma)

 
Location
Swiftwater, PA
Posted Date
Oct 27, 16
Info Source
Employer  - Full-Time   

Deputy Director of External Quality [cGMP pharma-biotech]','POS_70058368-1','!*!Sanofi Pasteur, the vaccines division of Sanofi, provides more than 1 billion doses ... -Pennsylvania-Swiftwater','','Oct 27, 2016','Regular','Regular','Deputy Director of External Quality [cGMP pharma-biotech]']); api.

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