GMP Quality Validation Engineer
- Contract
Company Description
MEDVACON Life Sciences works with leading pharmaceutical companies to hire consulting, contract and full-time employees to join client organizations.
Our focus is providing consulting and talent acquisition services for cGMP Quality and Compliance, Validation and Regulatory for pharmaceutical and biotechnology companies.
We have a 6+ month contract role located ON-SITE in Bloomington INDIANA:
PPQ - PROCESS PERFORMANCE QUALIFICATION - ASEPTIC PROCESSING contractor
SCOPE:
- Process Control Strategies
- Validation Master Plans
- Developing a Process Performance Qualification (PPQ) protocol
- Executing a PPQ protocol
- Sampling
- Mixing Studies
- Hold Studies
Job Description
We have a 6+ month contract role located ON-SITE in Bloomington INDIANA:
PPQ - PROCESS PERFORMANCE QUALIFICATION - ASEPTIC PROCESSING contractor
- Process Control Strategies
- Validation Master Plans
- Developing a Process Performance Qualification (PPQ) protocol
- Executing a PPQ protocol
- Sampling
- Mixing Studies
- Hold Studies
Qualifications
Successful candidates require solid Process Validation background.
This role is not for Equipment, Cleaning or Computer Systems.
Key areas of interest – if several apply to you.
• Technical Transfer
• Process Control Strategies
• Validation Master Plans
• Developing a Process Performance Qualification (PPQ) protocol
• Executing a PPQ protocol • Sampling
• Mixing Studies
• Hold Studies
• cGMP
• Aseptic processing
Additional Information
Please attach a WORD resume to your submission
All of your information will be kept confidential according to EEO guidelines.
ON-SITE only on W2
This is a contract role and does not offer benfits
40-hour week