Mid CSV Consultant

Job Opening for Mid CSV Consultant, McPherson, KS  

We are currently working on below mentioned job opening i.,e. Job Opening for Mid CSV Consultant, McPherson, KS. Please let me know if you are interested in applying for the same.

Job Title: mid CSV Consultant
Location: McPherson, KS
Length of Assignment: 12 months
Start Date: 08/08/22

Job Description: Has a backfill position available for day to day work for about 12 months for a CSV validation work.
Looking for an automation, integration and Compliance services for the Particle Counters qualification at Pfizer McP. This person will be working on the M25 and RTU Capital projects doing the following:
CSV Staff Support
- support D2D operations
- review & approve CSV validation documents
- provide CSV guidance
- Validate Execution (IOQ,PQ)

CSV Validation Services
- Documentation Generation
- Documentation Processing
- Documentation Execution

CSV Validation Documentation Examples
• GxP Assessment
• URS (User Requirements Specification)
• VPP (Validation Project Plan)
• SIA (System Impact Assessment)
• DDS (Detailed Design Specification)
• FS (Functional Specification)
• CS (Configuration Specification)
• Alarm Assessment
• SecAP (Security Access Plan)
• ERES (Electronic Records Electronic Signatures)
• SAT (Site Acceptance Testing)
• FAT (Factory Acceptance Testing)
• IOQ (Installation/Operation Qualification)
• PQ (Performance Qualification)
• EDR (Enhanced Design Review)
• RTM (Requirements Trace Matrix)

Multiple Clinical/Scientific Across US
We are working on these current openings need help filling. If you or anyone you know might be interested in one of the following projects, please email your resume to discuss in more depth. Thanks for the help!

*SR QA/QMS Consultant – Pharma - MI
*Labview Subject Matter Expert – Pharma - CA
*SR QC Consultant – Pharma - MI
*Sr Principal Product Development Engineer – Med Device – UT or MA
*Sr Manufacturing Engineer – Med Device - CA
*SR RA Specialist – Med Device – REMOTE
*Mid-Senior CER Writer – Pharma – REMOTE
*mid or sr. Process Engineer – Pharma - MI
*Sr. EH&S Manager – Pharma - NY
*QC Lab Equipment Validation – Pharma - MD
*Senior Equipment engineer – Med Device - MA
*Utilities Engineer – Med Device - VA
*Cleaning Validation Engineer – Pharma - CA
*Equipment Validation Engineer – Pharma - CA
*Sr. Validation SME – Pharma - KS
*Design Assurance Engineer – Med Device - NC
*Senior Manufacturing engineer – Med Device – MA
*Sr. Level Serialization and Packaging Engineer – Pharma – PA
*Sr Supplier QE – Med Device – CA
*SR Medical Writer – Pharma – REMOTE
*Process Engineer – Med Device – GA
*Mid R&D Engineer – Med Device – MO
*Mid- Validation Engineer – Pharma – MO
*Mid - Automation Engineer – Pharma – MA
*SR Analytical Chemist – Pharma – AL
*Mid - Manufacturing Engineer – Pharma – NC
*Manufacturing Engineer – Pharma – CA
*Analytical Chemist – Pharma – IA
*QC Chemist – Pharma – IA
*SR Microbiology Consultant – Pharma – AL
*Mid-level CSV Consultant – Pharma - NY

Job Opening for Mid CSV Consultant, McPherson, KS  

We are currently working on below mentioned job opening i.,e. Job Opening for Mid CSV Consultant, McPherson, KS. Please let me know if you are interested in applying for the same.

Job Title: mid CSV Consultant
Location: McPherson, KS
Length of Assignment: 12 months
Start Date: 08/08/22

Job Description: Has a backfill position available for day to day work for about 12 months for a CSV validation work.
Looking for an automation, integration and Compliance services for the Particle Counters qualification at Pfizer McP. This person will be working on the M25 and RTU Capital projects doing the following:
CSV Staff Support
- support D2D operations
- review & approve CSV validation documents
- provide CSV guidance
- Validate Execution (IOQ,PQ)

CSV Validation Services
- Documentation Generation
- Documentation Processing
- Documentation Execution

CSV Validation Documentation Examples
• GxP Assessment
• URS (User Requirements Specification)
• VPP (Validation Project Plan)
• SIA (System Impact Assessment)
• DDS (Detailed Design Specification)
• FS (Functional Specification)
• CS (Configuration Specification)
• Alarm Assessment
• SecAP (Security Access Plan)
• ERES (Electronic Records Electronic Signatures)
• SAT (Site Acceptance Testing)
• FAT (Factory Acceptance Testing)
• IOQ (Installation/Operation Qualification)
• PQ (Performance Qualification)
• EDR (Enhanced Design Review)
• RTM (Requirements Trace Matrix)

Multiple Clinical/Scientific Across US
We are working on these current openings need help filling. If you or anyone you know might be interested in one of the following projects, please email your resume to discuss in more depth. Thanks for the help!

*SR QA/QMS Consultant – Pharma - MI
*Labview Subject Matter Expert – Pharma - CA
*SR QC Consultant – Pharma - MI
*Sr Principal Product Development Engineer – Med Device – UT or MA
*Sr Manufacturing Engineer – Med Device - CA
*SR RA Specialist – Med Device – REMOTE
*Mid-Senior CER Writer – Pharma – REMOTE
*mid or sr. Process Engineer – Pharma - MI
*Sr. EH&S Manager – Pharma - NY
*QC Lab Equipment Validation – Pharma - MD
*Senior Equipment engineer – Med Device - MA
*Utilities Engineer – Med Device - VA
*Cleaning Validation Engineer – Pharma - CA
*Equipment Validation Engineer – Pharma - CA
*Sr. Validation SME – Pharma - KS
*Design Assurance Engineer – Med Device - NC
*Senior Manufacturing engineer – Med Device – MA
*Sr. Level Serialization and Packaging Engineer – Pharma – PA
*Sr Supplier QE – Med Device – CA
*SR Medical Writer – Pharma – REMOTE
*Process Engineer – Med Device – GA
*Mid R&D Engineer – Med Device – MO
*Mid- Validation Engineer – Pharma – MO
*Mid - Automation Engineer – Pharma – MA
*SR Analytical Chemist – Pharma – AL
*Mid - Manufacturing Engineer – Pharma – NC
*Manufacturing Engineer – Pharma – CA
*Analytical Chemist – Pharma – IA
*QC Chemist – Pharma – IA
*SR Microbiology Consultant – Pharma – AL
*Mid-level CSV Consultant – Pharma - NY