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

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Job DescriptionJob Description

Description

Verista's 500 experts team up with the world's most recognizable brands in the life science industry to solve their business needs. The nature of our business is to empower growth and innovation within the scientific community and to help researchers, organizations, and companies solve some of the world's most pressing healthcare challenges. Verista provides innovative solutions and services that empower informed decision-making and are the result of our significant investment in our people and our capabilities.

Our ability to grow is driven by world-class people who thrive in a team environment and share our mission to enable life sciences clients to improve lives. Our talented and dedicated professionals are committed to making an impact every day.

Company Culture Guidelines & Values:

• We empower and support our colleagues
• We commit to client success at every turn
• We have the courage to do the right thing
• We encourage an inclusive environment where our colleagues feel respected, engaged, and challenged.
• We constantly acquire new skills and learn from our experiences to enhance our collective expertise

Manufacturing Process Engineer position summary:

We are seeking a skilled Process/Project Engineer with hands-on experience in solid dosage form pharmaceutical manufacturing to join our team. The ideal candidate will have a strong technical background in process design, optimization, and troubleshooting for solid oral dosage forms, including granulation, spray drying, tablet compression, and coating operations. This role will support both day-to-day manufacturing activities and capital or process improvement projects to enhance product quality, process robustness, and operational efficiency.

Key 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

Qualifications:

• 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
• Onsite requirement in Indianapolis, IN

Qualifications:

• 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

For US geography, the salary range for this position is shown below. The actual salary is dependent upon a variety of job-related factors such as professional background, training, work experience, location, business needs, market demand, and competitive market practice. Therefore, in some circumstances, the actual salary could fall outside of this expected range. This salary range is subject to change and may be modified in the future.

*Verista is an equal opportunity employer.

(US) Range$85,000—$134,409 USD

Benefits

Why Choose Verista?

• 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 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

Verista collects and processes personal data in accordance with applicable data protection laws. If you are a California Job Applicant, see the privacy notice for further details.

For more information about our company, please visit us at Verista.com

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