Process Engineer II

Posted 9 Hours Ago
Be an Early Applicant
Bloomington, IN
Entry level
Pharmaceutical • Manufacturing
The Role
The Process Engineer II develops, implements, and optimizes pharmaceutical manufacturing processes, enhancing efficiency and quality. Responsibilities include developing specifications for equipment, executing protocols, conducting validation reviews, and proposing energy-saving improvements. The role collaborates with cross-functional teams to solve issues and ensure compliance with safety and regulatory standards.
Summary Generated by Built In

Simtra BioPharma Solutions (Simtra) is a world-class Contract Development Manufacturing Organization, partnering with pharmaceutical and biotech companies to bring their sterile injectable products to market. With facilities in Bloomington, Indiana, US and Halle/Westfalen, Germany, we offer a wide range of delivery systems including pre-filled syringes, liquid/lyophilized vials, diluents for reconstitution, powder-filled vials and sterile crystallization.  

Our product types include biologics and small molecules, cytotoxics, highly potent compounds, diluents for reconstitution and vaccines – which are all directly injected into patients worldwide.  As such, there is a strong emphasis on quality and continuous improvement at Simtra.  We hold ourselves to the highest quality and regulatory standards.

While our primary focus is cGMP manufacturing, we offer many support services including formulation and development, lyophilization optimization, global regulatory support and secondary packaging.  Our teams are driven to help clients scale, innovate and bring life-changing medicines to patients worldwide.

 

Why join Team Simtra? Because we:

Make it HAPPEN – We bring a growth mindset to every opportunity, developing new skillsets and exceeding our expectations and those of our customers.

Make it TOGETHER – We work as one, respecting each voice and tapping into our unique strengths across teams—so we can solve problems in new ways.

Make it RIGHT – We hold ourselves to a high standard of excellence, fulfilling our commitments to the customer, their patients, and our team members.

Make it COUNT – We take pride in our day-to-day work, knowing the impact we make – taking on challenges big and small to improve patient health.




This role:

We are looking for a Process Engineer II that is responsible for developing, implementing, and optimizing manufacturing packaging processes to improve efficiency, quality, and productivity. This engineer will work closely with cross-functional teams to identify areas for process improvement, troubleshoot issues, and ensure compliance with safety and regulatory standards in the packaging area. This position is 100% onsite at the Bloomington facility and reports directly to the Process Engineering Manager.

 

The responsibilities:

  • Develop user requirements, technical specification and design specifications for new automated packaging equipment or upgrades to existing equipment
  • Author and execute protocols to include commissioning, qualification, and validation activities (FAT, SAT, IQ and OQ) for packaging systems
  • Implement improvement projects for packaging processes and systems that enhance efficiency and reduce costs
  • Develop and maintain project schedules using MS Project
  • Collaborate with suppliers to source packaging equipment parts to ensure quality standards are met
  • Provide technical support and training to operations on packaging equipment and processes

 

Desirable qualifications:

  • BS degree in Packaging Engineering, Mechanical Engineering, or a related field
  • 3+ years of experience in process/packaging engineering in the pharmaceutical industry
  • Knowledge of the basic principles in various packaging engineering best practices
  • Knowledge of aseptic manufacturing
  • Must be able to lead and execute engineering projects
  • Strong understanding of packaging materials, processing, and testing methods
  • Experience with PLC, HMI, Vision Systems and Building Management systems
  • Must be able to read mechanical and electrical drawings
  • AutoCAD or equivalent component design knowledge
  • Advanced proficiency in Microsoft Office Suite (Word, Excel, and Outlook)
  • Experience and the ability to use enterprise software (examples include: JDE, BPLM, Pilgrim, Trackwise, etc.)


In return, you’ll be eligible for [1]:

  • Day One Benefits
    • Medical & Dental Coverage
    • Flexible Spending Accounts
    • Life and AD&D Insurance
    • Supplemental Life Insurance
      • Spouse Life Insurance
      • Child Life Insurance
    • Short and Long-Term Disability Insurance
    • 401(k) Retirement Savings Plan with Company Match
    • Time Off Program
      • Paid Holidays
      • Paid Time Off
      • Paid Parental Leave and more
    • Adoption Reimbursement Program
    • Education Assistance Program
    • Employee Assistance Program
    • Community and Volunteer Service Program
  • Additional Benefits
    • Voluntary Insurance Benefits
      • Vision Coverage
      • Accident
      • Critical Illness
      • Hospital Indemnity Insurance
      • Identity Theft Protection
      • Legal and more
    • Onsite Campus Amenities
      • Workout Facility
      • Cafeteria
      • Credit Union

[1] Current benefit offerings are in effect through 12/31/24



Disclaimer

This job description is intended to provide the minimum knowledge, skills and abilities necessary to perform the job.  It may not be inclusive of all the duties and responsibilities of the job.  Simtra reserves the right to make modifications based on business requirements.

 

Equal Employment Opportunity

Simtra is proud to be an equal opportunity employer. Simtra evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status or any other legally protected characteristic.
                                                                                                                                                            
EEO is the Law 
EEO is the law - Poster Supplement 
Pay Transparency Policy


Data Privacy

To learn more about Simtra's approach to data privacy, please review the Simtra Recruitment Platform Global Privacy Policy:

https://biopharmasolutions.baxter.com/simtra-recruitment-platform-privacy-policy


The Company
HQ: Bloomington, Indiana
375 Employees
On-site Workplace

What We Do

As a premier, independently owned CDMO with over 65 years of sterile injectable manufacturing experience, Simtra BioPharma Solutions offers world-class cGMP sterile fill/finish, technical expertise, quality service, and a uniquely collaborative approach. Pharmaceutical and biotech companies partner with us when they face formulation challenges, clinical supply hurdles, surges in demand due to market fluctuations, or risk mitigation concerns. Our teams are driven to offer our clients tailored and versatile solutions to help them bring their products to market so they can get to the patients who need them.
(Simtra is a tradename of Baxter Oncology GmbH and Baxter Pharmaceutical LLC)

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