Search Jobs: Results: Cleaning Validation and Process Validation Supervisor - Media Filling and Lyophilization
Cleaning Validation / Process Validation Supervisor sought for an expanding state of the art pharmaceutical manufacturing facility at one of the fastest growing sterile pharmaceutical companies in the world. Actually, multiple new opportunities have been created for process validation experts; media fill experts, cleaning experts, sterilization experts and even quality leaders.
Challenges:
This Cleaning and Process Validation Supervisor will be faced with the challenges of:
1) Supervising a growing team and being a subject matter expert on validation processes related to cleaning, CIP and SIP. :
2) Define, develop and execute cleaning processes for certain automated equipment processes, lyophilizers and cold room equipment.
3) Leading the cleaning validation of multiple products migration through tech transfer and into production. This will involve troubleshooting, making recommendations and suggesting corrective actions.
Salary: Base salary should be in the low 80's to 90's -depending on experience – and also will include a string bonus and relocation package
Location: Ohio
Contact: Apply below and/or contact Ira Mann at iram@fpccareers.com
You also will be challenged with:
- Determining how new technologies may be applied to increase process efficiency and implement.
- Evaluate the existing validation processes, compile relevant data packs, address deviations and recommend and implement corrective actions
- Reviewing or approving technical reports, validation test protocols and final reports; ensuring compliance with protocol test procedures and specifications; evaluating deviations which occur during the validation test process.
Requirements:
1. While a BS degree and 3+ years of relevant Aseptic Pharmaceutical cleaning validation experience in required, IT IS MORE IMPORTANT THAT YOU SHOW YOUR EXPERIENCE WITH:
-Supervising cleaning processes for certain automated equipment processes, lyophilizers and cold room equipment as well as developing process validation protocols.
2. Experience with TOC, Media Filling, Critical Systems, and lyophilizers.
3. Providing technical assistance via rationales or validation studies to support manufacturability.
4. PQ expertise
Keyword (s): cleaning validation, TOC, process validation, CIP, media fill, technology transfer, investigations, deviations, contract manufacturing, Lyophilization, critical systems, utilities, water systems, autoclaves, lyophilizers, protocols, SOP’s
Job Details
| Name: | Ira Mann | Date Posted: | 7/27/2010 |
| Office: | Atlanta | Telephone: | (770) 246-9757 |
| Email: | iram@fpccareers.com | Fax: | |
| Category: | Contract Manufacturing, Pharmaceutical, Validation | ||
| Keywords: | cleaning validation, TOC, process validation, CIP, media fill, technology transfer, investigations, deviations, contract manufacturing, Lyophilization, critical systems, utilities, water systems, autoclaves, lyophilizers, protocols, SOP?s | Region: | |
| State: | OH | City: | |
| Education: | BS | Job Number: | J12851-ATLA-15152-IM |
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