Search Jobs: Results: Process Validation Engineer - Aseptic Pharmaceutical, Sterile Media Filling and Lyophilization
Multiple Process Validation Engineers 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:
These Process Validation Engineers will be faced with the challenges of:
1) Supporting quality investigations resulting from process deviations and provides CAPA support.
2) Working around the Production Department to gain access to production equipment which needs to be validated.
3) Emergency response to breakdowns of Production equipment.
4) Performance of critical validations during shutdown or other holiday periods.
Salary: Base salary should be in the low 60’s to 80’s -depending on experience and growth potential. Excellent relocation package and bonus available too
Location: Ohio
Contact: Apply below and/or contact Ira Mann at iram@fpccareers.com
Requirements:
1. While a BS degree and relevant Aseptic Pharmaceutical process validation experience in required, IT IS MORE IMPORTANT THAT YOU SHOW YOUR EXPERIENCE WITH:
- Development of Process Validation and Technical Transfer protocols
2. Experience with any of the following: Media Filling, Cleaning Validation, Critical Systems or Sterilization Validation.
3. Providing technical assistance via rationales or validation studies to support manufacturability.
4. PQ experience in addition to IQ and OQ
5. Ability to work non standard shift or periodically working 2nd or 3rd shifts to meet aggressive timetables.
Keyword (s): process validation, CIP, media fill, technology transfer, cleaning validation, investigations, deviations, DOE, critical process parameters, contract manufacturing, Lyophilization, critical systems, HVAC, WFI, water systems, autoclaves, lyophilizers, utilities, computerized systems validation, dry heat, sterilization, protocols, SOP’s
Job Details
| Name: | Ira Mann | Date Posted: | 8/30/2010 |
| Office: | Atlanta | Telephone: | (770) 246-9757 |
| Email: | iram@fpccareers.com | Fax: | |
| Category: | Biotechnology, Contract Manufacturing, Pharmaceutical, Quality Assurance, Validation | ||
| Keywords: | process validation, CIP, media fill, technology transfer, cleaning validation, investigations, deviations, DOE, critical process parameters, contract manufacturing, Lyophilization, critical systems, HVAC, WFI, water systems, autoclaves, lyophilizers, utilities, computerized systems validation, dry heat, sterilization, protocols, SOP?s | Region: | |
| State: | OH | City: | |
| Education: | BS | Job Number: | J84316-ATLA-15155-IM |
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