Verista

6044 - Manufacturing Project Manager (Pharma) / Project Manager

Manufacturing Project Manager

Bachelor’s degree in engineering; 3+ years solid dosage form manufacturing; granulation, spray drying, tablets, coating expertise; cGMP/FDA/EMA knowledge; onsite in Indianapolis, IN.

6022 - Manufacturing Process Engineer (Pharma) / Senior Process Engineer

Manufacturing Process Engineer

Bachelor's degree in Chemical Engineering, Pharmaceutical Sciences, Mechanical Engineering (or related); minimum 3 years solid dosage form manufacturing; experience in granulation, spray drying, tablet compression, coating; onsite in Indianapolis, IN.

6018 - Annual Product Review Coordinator - Pharma / Validation Engineer

Annual Product Review Coordinator

Entry-level APR coordinator in Pharma; 1-3 years experience; engineering/STEM degree preferred; onsite in Indianapolis; strong communication; proficiency with MS Office.

6001 - Project Engineer / Risk Management (Pharma/Med Device)

Project Engineer / Risk Management

3-5 years in medical device development or risk management; ISO 14971 knowledge; FMEA experience; strong cross-functional communication; proficient in MS Office.

Bloomington CQV/CSV Validation Engineers

Validation Engineer

3+ years in validation engineering within pharmaceuticals or biotech, expertise in equipment qualification, Delta V, GMP compliance, and more.

RTP Quality Assurance Specialists

Quality Assurance Specialist

3+ years in quality assurance within pharmaceuticals or biotech, overseeing compliance with cGMP, GDP, and other regulatory standards.

RTP Project Managers

Project Manager

3+ years in project management within pharmaceuticals or biotech, with skills in leading complex projects and ensuring regulatory compliance.

RTP CQV/CSV Validation Engineers

RTP Automation Engineers

Automation Engineer

3+ years in automation engineering within pharmaceuticals or biotech, skilled in DeltaV, Rockwell/Allen-Bradley PLCs, and Siemens PLCs.

CQV Engineer / Deviation Investigator (New Grad)

CQV Engineer

Entry level CQV Engineer position in the Pharma industry. Client will train the resource on Deviation Investigation.

CQV/Process Engineer (New Grad)

Process Engineer

Bachelor’s degree in chemical, biomedical/biochemical engineering, biological/chemical sciences or equivalent required. Strong communication and teamwork skills are essential.

CQV Engineer (New Grad)

Bachelor’s Degree or equivalent required (STEM degree highly preferred) with demonstrated experience in leading CQV activities specific to Process Equipment.

Bachelor’s or equivalent STEM degree required, demonstrated experience in leading CQV activities, proficiency in Microsoft Office, strong problem-solving skills.

Title	Location	Date
6044 - Manufacturing Project Manager (Pharma) / Project Manager Full Time · $85K-$136K · 3+ YOE Columbus or Fishers or Indianapolis · Onsite	Columbus or Fishers or Indianapolis Onsite	Nov 20, 2025
6022 - Manufacturing Process Engineer (Pharma) / Senior Process Engineer Full Time · $85K-$134K · 3+ YOE Indianapolis, Indiana, United States · Onsite	Indianapolis, Indiana, United States Onsite	Nov 11, 2025
6018 - Annual Product Review Coordinator - Pharma / Validation Engineer Full Time · $60K-$94K · 1+ YOE Indianapolis, Indiana, United States · Onsite	Indianapolis, Indiana, United States Onsite	Nov 5, 2025
6001 - Project Engineer / Risk Management (Pharma/Med Device) Full Time · $80K-$114K · 3+ YOE Indianapolis, Indiana, United States · Onsite	Indianapolis, Indiana, United States Onsite	Oct 24, 2025
Bloomington CQV/CSV Validation Engineers Full Time · 3+ YOE Bloomington, Indiana, United States · Onsite	Bloomington, Indiana, United States Onsite	Jul 29, 2025
RTP Quality Assurance Specialists Full Time · 3+ YOE Raleigh or Durham · Onsite	Raleigh or Durham Onsite	Jul 24, 2025
RTP Project Managers Full Time · 3+ YOE Raleigh or Durham · Onsite	Raleigh or Durham Onsite	Jul 24, 2025
RTP CQV/CSV Validation Engineers Full Time · 3+ YOE Raleigh or Durham · Onsite	Raleigh or Durham Onsite	Jul 24, 2025
RTP Automation Engineers Full Time · 3+ YOE Raleigh or Durham · Onsite	Raleigh or Durham Onsite	Jul 24, 2025
CQV Engineer / Deviation Investigator (New Grad) Full Time · 0+ YOE Indianapolis, Indiana, United States · Onsite	Indianapolis, Indiana, United States Onsite	Jan 22, 2025
CQV/Process Engineer (New Grad) Full Time Kalamazoo, Michigan, United States · Onsite	Kalamazoo, Michigan, United States Onsite	Jan 22, 2025
CQV Engineer (New Grad) Full Time Columbus, Ohio, United States · Onsite	Columbus, Ohio, United States Onsite	Jan 22, 2025
CQV Engineer (New Grad) Full Time · 0+ YOE Portland, Maine, United States · Onsite	Portland, Maine, United States Onsite	Jan 8, 2025

Activities	compliance consultingvalidation engineeringindustrial automationquality managementmanufacturing solutions
Headquarters	US
Industries	Life SciencesProfessional Services
Name	Verista
Employees	500
Type	Private
Subsidiaries	Delta Project ManagementILB EnterprisesClarke SolutionsCovexAcquire Automation
Tagline	Provides compliance, automation, and validation services to life sciences.
Founded	2,020
Website	verista.com
Latest Funding Round	Private Equity
Latest Funding Year	2,022
Latest Investors	Lightview Capital

Verista

About Verista