Lead Pharma Clean Room CQV Engineer
Verista, Inc.
Verista, Inc. in Miami, FL is seeking a qualified candidate to lead the Clean Room qualification process within a pharmaceutical facility. Responsibilities include authoring and executing technical documentation, running test scripts, and maintaining detailed records. The ideal candidate will have a Bachelor’s degree and experience in Clean Room validation. Verista offers competitive pay, performance-based incentives, and a supportive team environment that thrives on innovation. The role requires strong communication skills, attention to detail, and the ability to work onsite in a fast-paced setting. #J-18808-Ljbffr Verista, Inc.
$70.49k - $118.94k
...an impact every day. Senior Validation Engineer Responsibilities Authoring, editing, and... ...Specific demonstrable experience leading validation efforts in pharma Clean Room environments Demonstrated experience in leading CQV activities specific to Process Equipment...SuggestedTemporary workWork experience placementWork at office$70.49k - $118.94k
...expertise Senior Validation Engineer Responsibilities: This role leads the process of Clean Room qualification and the associated... ...leading validation efforts in pharma Clean Room environments Demonstrated experience in leading CQV activities specific to Process...SuggestedTemporary workWork experience placementWork at office- Verista is seeking a Senior Validation Engineer to join their team in Miami. This role involves authoring... ...for equipment and processes in pharma environments. Candidates must have a Bachelor's Degree and experience leading validation efforts. The position offers competitive...Suggested
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