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