Verista · 2 weeks ago
6022 - Manufacturing Process Engineer (Pharma) / Senior Process Engineer
Indianapolis, IN
Full-time
Onsite
Mid, Senior Level
$85K/yr - $134K/yr
3+ years expVerista is a company that collaborates with leading brands in the life sciences sector to address critical healthcare challenges. They are looking for a skilled Process/Project Engineer with hands-on experience in solid dosage form pharmaceutical manufacturing to provide technical support and lead process improvement initiatives.
ComplianceHealth CareLife ScienceManufacturingPharmaceutical
Responsibilities
Provide technical support for the manufacturing of solid dosage forms, ensuring processes operate safely, efficiently, and in compliance with cGMP regulations
Lead or support process improvement and scale-up projects for granulation, spray drying, compression, and coating operations
Conduct process investigations, identify root causes, and implement corrective/preventive actions to resolve manufacturing issues
Develop and optimize process parameters to achieve consistent product quality and yield
Prepare and review process documentation including batch records, SOPs, validation protocols/reports, and change control documents
Collaborate with cross-functional teams (R&D, Quality, Validation, Maintenance, and Production) to ensure successful technology transfer and process validation
Support equipment qualification and process validation activities for new or modified equipment/processes
Analyze production data, generate reports, and recommend process or equipment improvements to enhance performance and efficiency
Ensure compliance with all safety and regulatory requirements within the manufacturing environment
Qualification
Required
Bachelor's degree (or higher) in Chemical Engineering, Pharmaceutical Sciences, Mechanical Engineering, or related field
Minimum 3 years of hands-on experience in solid dosage form manufacturing (pharmaceutical industry required)
Strong knowledge of granulation, spray drying, tablet compression, and tablet coating processes
Familiarity with cGMP, FDA, and EMA regulatory requirements
Excellent problem-solving, analytical, and communication skills
Proven ability to work independently and in cross-functional teams within a fast-paced manufacturing environment
Proficiency with process data analysis tools and process control systems preferred
Onsite requirement in Indianapolis, IN
Preferred
Experience with fluid bed granulation and/or spray drying systems
Direct involvement in tablet compression and film coating process development or troubleshooting
Exposure to process validation, technology transfer, and scale-up activities
Benefits
High growth potential and fast-paced organization with a people-focused culture
Competitive pay plus performance-based incentive programs
Company-paid Life, Short-Term, and Long-Term Disability Insurance.
Medical, Dental & Vision insurances
FSA, DCARE, Commuter Benefits
Supplemental Life, Hospital, Critical Illness and Legal Insurance
Health Savings Account
401(k) Retirement Plan (Employer Matching benefit)
Paid Time Off (Rollover Option) and Holidays
As Needed Sick Time
Tuition Reimbursement
Team Social Activities (We have fun!)
Employee Recognition
Employee Referral Program
Paid Parental Leave and Bereavement
Company
Verista
Verista offers transformative compliance, automation, packaging solutions for the life sciences, pharmaceutical and manufacturing.
501-1000 employees
H1B Sponsorship
Verista has a track record of offering H1B sponsorships. Please note that this does not
guarantee sponsorship for this specific role. Below presents additional info for your
reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (7)
2024 (4)
2023 (13)
2022 (6)
2021 (1)
Funding
Current Stage
Late StageLeadership Team
Bill Murray
Chief Financial Officer
Dan White
Chief Operating Officer
Recent News
2023-12-22
2023-12-22
Company data provided by crunchbase