Automation Engineer
Bloomington, IN · On-site
... sterile crystallization. Our product types include biologics and small molecules, cytotoxics ... These positions are 100% onsite at the Bloomington, Indiana facility and reports directly to the ...
Automation Engineer
Bloomington, IN · On-site
... sterile crystallization. Our product types include biologics and small molecules, cytotoxics ... These positions are 100% onsite at the Bloomington, Indiana facility and reports directly to the ...
Sr. Process Engineer
Bloomington, IN · On-site
$96K - $124K/yr
... sterile crystallization. Our product types include biologics and small molecules, cytotoxics ... This position is 100% onsite at the Bloomington facility and reports directly to the Sr. Manager ...
Sr. Process Engineer
Bloomington, IN · On-site
$96K - $124K/yr
... sterile crystallization. Our product types include biologics and small molecules, cytotoxics ... This position is 100% onsite at the Bloomington facility and reports directly to the Sr. Manager ...
Sr. Process Engineer
Bloomington, IN · On-site
$96K - $124K/yr
... sterile crystallization. Our product types include biologics and small molecules, cytotoxics ... This position is 100% onsite at the Bloomington facility and reports directly to the Sr. Manager ...
Sr. Process Engineer
Bloomington, IN · On-site
$96K - $124K/yr
... sterile crystallization. Our product types include biologics and small molecules, cytotoxics ... This position is 100% onsite at the Bloomington facility and reports directly to the Sr. Manager ...
... sterile crystallization. Our product types include biologics and small molecules, cytotoxics ... Demonstrated experience authoring and executing process validation protocols and reports Preferred ...
... sterile crystallization. Our product types include biologics and small molecules, cytotoxics ... Demonstrated experience authoring and executing process validation protocols and reports Preferred ...
... sterile crystallization. Our product types include biologics and small molecules, cytotoxics ... Demonstrated experience authoring and executing process validation protocols and reports Preferred ...
... sterile crystallization. Our product types include biologics and small molecules, cytotoxics ... Demonstrated experience authoring and executing process validation protocols and reports Preferred ...
... reports, regulatory submissions, and lab notebooks to a high standard. * Drive cross-functional ... Working knowledge of key organic chemistry unit operations (crystallization, distillation ...
... reports, regulatory submissions, and lab notebooks to a high standard. * Drive cross-functional ... Working knowledge of key organic chemistry unit operations (crystallization, distillation ...
... sterile crystallization. Our product types include biologics and small molecules, cytotoxics ... The position reports to the Associate Director Engineering & Maintenance Operations. The ...
... sterile crystallization. Our product types include biologics and small molecules, cytotoxics ... The position reports to the Associate Director Engineering & Maintenance Operations. The ...
... sterile crystallization. Our product types include biologics and small molecules, cytotoxics ... The position reports to the Associate Director Engineering & Maintenance Operations. The ...
... sterile crystallization. Our product types include biologics and small molecules, cytotoxics ... The position reports to the Associate Director Engineering & Maintenance Operations. The ...
... reports, regulatory submissions, and lab notebooks to a high standard. * Drive cross-functional ... Working knowledge of key organic chemistry unit operations (crystallization, distillation ...
... reports, regulatory submissions, and lab notebooks to a high standard. * Drive cross-functional ... Working knowledge of key organic chemistry unit operations (crystallization, distillation ...
Process Engineer, Kilo and High Potency Lab, Lilly Medicine Foundry
Lebanon, IN · On-site
$103 - $172/hr
... reports, regulatory submissions, and lab notebooks to a high standard. * Drive cross-functional ... Working knowledge of key organic chemistry unit operations (crystallization, distillation ...
Process Engineer, Kilo and High Potency Lab, Lilly Medicine Foundry
Lebanon, IN · On-site
$103 - $172/hr
... reports, regulatory submissions, and lab notebooks to a high standard. * Drive cross-functional ... Working knowledge of key organic chemistry unit operations (crystallization, distillation ...
Tableau Developer
Indianapolis, IN · On-site
$60K/yr
And we do it every single day - for both temporary and permanent assignments and across virtually ... reporting tools such as Cognos, SAS & QlikView. Understand business requirements very clearly then ...
Tableau Developer
Indianapolis, IN · On-site
$60K/yr
And we do it every single day - for both temporary and permanent assignments and across virtually ... reporting tools such as Cognos, SAS & QlikView. Understand business requirements very clearly then ...
Senior Critical Utilities Engineer
Bloomington, IN · On-site
$96K - $132K/yr
... sterile crystallization. Our product types include biologics and small molecules, cytotoxics ... This position is 100% onsite at the Bloomington facility and reports to the Manager of Process ...
Senior Critical Utilities Engineer
Bloomington, IN · On-site
$96K - $132K/yr
... sterile crystallization. Our product types include biologics and small molecules, cytotoxics ... This position is 100% onsite at the Bloomington facility and reports to the Manager of Process ...
Senior Critical Utilities Engineer
Bloomington, IN · On-site
$96K - $132K/yr
... sterile crystallization. Our product types include biologics and small molecules, cytotoxics ... This position is 100% onsite at the Bloomington facility and reports to the Manager of Process ...
Senior Critical Utilities Engineer
Bloomington, IN · On-site
$96K - $132K/yr
... sterile crystallization. Our product types include biologics and small molecules, cytotoxics ... This position is 100% onsite at the Bloomington facility and reports to the Manager of Process ...
... crystallization method and morphology engineering, cGMP analytical method development and testing ... Day-to-day activities include reviewing and approving test records and reports, performing internal ...
New
... crystallization method and morphology engineering, cGMP analytical method development and testing ... Day-to-day activities include reviewing and approving test records and reports, performing internal ...
New
This role designs and executes developmentally appropriate programming, supports positive youth ... Reporting * Track attendance, participation, and required program data accurately. * Support ...
This role designs and executes developmentally appropriate programming, supports positive youth ... Reporting * Track attendance, participation, and required program data accurately. * Support ...
senior .net developer
Indianapolis, IN · On-site
$52.50 - $67/hr
And we do it every single day - for both temporary and permanent assignments and across virtually ... Should be able to write reports using various reports generation tools and languages Custom ...
senior .net developer
Indianapolis, IN · On-site
$52.50 - $67/hr
And we do it every single day - for both temporary and permanent assignments and across virtually ... Should be able to write reports using various reports generation tools and languages Custom ...
Quality Engineer
Indianapolis, IN · On-site
$70K - $85K/yr
Review and approve supplier First Article Inspection Reports * Facilitate root cause, corrective ... We offer excellent opportunities for contract, temporary, temp-to-hire, and direct assignments. We ...
Quick apply
Quality Engineer
Indianapolis, IN · On-site
$70K - $85K/yr
Review and approve supplier First Article Inspection Reports * Facilitate root cause, corrective ... We offer excellent opportunities for contract, temporary, temp-to-hire, and direct assignments. We ...
Quality Engineer
Indianapolis, IN · On-site
$70K - $85K/yr
Review and approve supplier First Article Inspection Reports * Facilitate root cause, corrective ... We offer excellent opportunities for contract, temporary, temp-to-hire, and direct assignments. We ...
Quality Engineer
Indianapolis, IN · On-site
$70K - $85K/yr
Review and approve supplier First Article Inspection Reports * Facilitate root cause, corrective ... We offer excellent opportunities for contract, temporary, temp-to-hire, and direct assignments. We ...
SQL developer
Indianapolis, IN · On-site
$80K/yr
And we do it every single day - for both temporary and permanent assignments and across virtually ... Reports directly to Automated Data Sourcing Manager * Interacts with other colleagues at all levels ...
SQL developer
Indianapolis, IN · On-site
$80K/yr
And we do it every single day - for both temporary and permanent assignments and across virtually ... Reports directly to Automated Data Sourcing Manager * Interacts with other colleagues at all levels ...
... sterile crystallization. Our product types include biologics and small molecules, cytotoxics ... Required Qualifications: • Bachelor's degree in Engineering, Industrial Technology, Maintenance ...
... sterile crystallization. Our product types include biologics and small molecules, cytotoxics ... Required Qualifications: • Bachelor's degree in Engineering, Industrial Technology, Maintenance ...
Temporary Crystal Report Developer information
What is the difference between Temporary Crystal Report Developer vs Temporary SQL Report Developer?
| Aspect | Temporary Crystal Report Developer | Temporary SQL Report Developer |
|---|---|---|
| Required Skills | Experience with Crystal Reports, report design, data visualization | Proficiency in SQL, report writing, database management |
| Work Environment | Business intelligence teams, reporting departments | Data analysis teams, database administration |
| Certifications | Crystal Reports certifications often preferred | SQL certifications beneficial |
Both roles involve report development but focus on different tools: Crystal Reports vs SQL-based reporting. The Crystal Report Developer specializes in designing reports with Crystal Reports software, while the SQL Report Developer emphasizes writing SQL queries for data extraction and report generation. Your choice depends on the specific reporting tools used by the employer and your skill set.
What are the most commonly searched types of Crystal Report Developer jobs in Indiana?
The most popular types of Crystal Report Developer jobs in Indiana are:
What are popular job titles related to Temporary Crystal Report Developer jobs in Indiana?
For Temporary Crystal Report Developer jobs in Indiana, the most frequently searched job titles are:
What job categories do people searching Temporary Crystal Report Developer jobs in Indiana look for?
The top searched job categories for Temporary Crystal Report Developer jobs in Indiana are:
What cities in Indiana are hiring for Temporary Crystal Report Developer jobs?
Cities in Indiana with the most Temporary Crystal Report Developer job openings:
Full-time
Medical, Dental, Vision, Life, Retirement, PTO
Re-posted yesterday
Job description
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 Automation Engineers (level depends on experience) that are responsible for leading the identification, implementation, optimization, and maintenance of process automation and controls systems in pharmaceutical processing, packaging, and facilities. These engineers ensure efficient, quality, functional, and compliant process automation systems and supports engineering systems, capital projects, technical services, and plant support, as applicable. These positions are 100% onsite at the Bloomington, Indiana facility and reports directly to the Sr. Manager, Automation Engineering.
The responsibilities:
Required qualifications:
Physical/safety requirements:
In return, you'll be eligible for[1]:
[1] Current benefit offerings are in effect through 12/31/26
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.
Data Privacy
To learn more about Simtra's approach to data privacy, please review the Simtra Recruitment Platform Global Privacy Policy: https://simtra.com/privacy-policy/
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 Automation Engineers (level depends on experience) that are responsible for leading the identification, implementation, optimization, and maintenance of process automation and controls systems in pharmaceutical processing, packaging, and facilities. These engineers ensure efficient, quality, functional, and compliant process automation systems and supports engineering systems, capital projects, technical services, and plant support, as applicable. These positions are 100% onsite at the Bloomington, Indiana facility and reports directly to the Sr. Manager, Automation Engineering.
The responsibilities:
- Lead various aspects of support needed in the design, development, and implementation of the site process automation and controls systems
- Develop, modify, and troubleshoot PLC & HMI programs
- Specify and configure ins
- Identify and drive improvement opportunities for equipment, instrument, and process optimization, efficiency, and cost reduction through automation technologies and lead initiatives to implement projects
- Lead the deployment of the full system lifecycle for process automation and control systems including the design, assessment, selection, commissioning, validation, and implementation of systems
- Troubleshoot automation and controls systems issues, conduct root causes analysis, and implement corrective actions to minimize downtime and ensure continuous operations
- Conduct risk assessments of automation and controls systems
- Ensure automation and controls systems meet regulatory requirements by conducting and assisting with validation activities
Required qualifications:
- BS in Engineering (Computer, Electrical, Computer Science, Systems Engineering and Design, or related field), plus 6+ years of relevant experience
- Work experience in process automation and controls systems (including programming PLCs, SCADA, and HMI systems) in pharmaceutical and/or manufacturing environments
- Experience in reading and interpreting electrical schematics and Process & Instrumentation Diagrams (P&IDs)
- Experience in Ignition SCADA/HMI
- Knowledge of coding in Rockwell and Siemens (PLCs and HMIs)
- Knowledge of automation and controls hardware and software systems
- Ability to prioritize projects and workload
- Excellent verbal communication and technical writing skills
Physical/safety requirements:
- Duties may require overtime work, including nights and weekends
- Position requires sitting for long hours, but may also involve walking or standing for long periods of time
- Variable travel of 0-10% could be expected
- Must be able to lift, push, pull, and carry up to 50 lbs
- Must be able to lift 20 lbs overhead
- Must be able to wear personal protective equipment (PPE), as required
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
- 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
- Employee Ownership Plan
- Additional Benefits
- Short and Long-Term Disability Insurance
- 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 12/31/26
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.
Data Privacy
To learn more about Simtra's approach to data privacy, please review the Simtra Recruitment Platform Global Privacy Policy: https://simtra.com/privacy-policy/