... sterile crystallization. Our product types include biologics and small molecules, cytotoxics ... risk management, cleaning validation, inspection/packaging validation, and computer systems ...
... sterile crystallization. Our product types include biologics and small molecules, cytotoxics ... risk management, cleaning validation, inspection/packaging validation, and computer systems ...
Warehouse Coordinator/Driver - Weekend PM shift
Bloomington, IN · On-site
$16.75 - $21.25/hr
... sterile crystallization. Our product types include biologics and small molecules, cytotoxics ... Complete daily vehicle inspections, cleaning, fueling, and temperature control checks. * Prepare ...
Warehouse Coordinator/Driver - Weekend PM shift
Bloomington, IN · On-site
$16.75 - $21.25/hr
... sterile crystallization. Our product types include biologics and small molecules, cytotoxics ... Complete daily vehicle inspections, cleaning, fueling, and temperature control checks. * Prepare ...
Crystal Clean information
What is the difference between Crystal Clean vs Janitorial Technician?
| Aspect | Crystal Clean | Janitorial Technician |
|---|---|---|
| Required Credentials | High school diploma, cleaning certifications | High school diploma, cleaning certifications |
| Work Environment | Commercial and industrial cleaning sites | Office buildings, schools, healthcare facilities |
| Employer & Industry Usage | Cleaning service companies, facilities management | Cleaning service providers, facilities management |
| Common Search & Comparison | Yes | Yes |
Crystal Clean and Janitorial Technician roles often require similar credentials and work in comparable environments within the cleaning industry. While Crystal Clean may refer to a specific company or brand, Janitorial Technician is a general job title used across many organizations. Both positions focus on maintaining cleanliness in commercial settings, making them closely related in terms of duties and industry usage.
What are the key skills and qualifications needed to thrive as an industrial cleaner at Crystal Clean, and why are they important?
To thrive as an Industrial Cleaner at Crystal Clean, you need attention to detail, physical stamina, and knowledge of cleaning protocols, often supported by a high school diploma or equivalent. Familiarity with industrial cleaning equipment, hazardous waste handling procedures, and safety certifications such as OSHA training is typically required. Reliability, teamwork, and strong communication skills help employees excel in maintaining safety and efficiency. These skills ensure compliance with regulations, minimize risks, and deliver high-quality cleaning services in industrial environments.
What are Crystal Clean jobs?
Crystal Clean jobs typically refer to positions at Heritage-Crystal Clean, a company specializing in environmental services such as parts cleaning, hazardous and non-hazardous waste disposal, and used oil recycling. Employees may work in roles ranging from drivers and service technicians to sales and corporate support staff. These jobs involve helping businesses manage their environmental impact by safely handling, transporting, and processing industrial waste and cleaning products. Working at Crystal Clean often requires compliance with strict safety and environmental regulations and may involve customer-facing responsibilities. The company offers training and career development opportunities for those interested in the environmental services industry.
What are some common challenges faced by Crystal Clean technicians in the field, and how can they be addressed?
Crystal Clean technicians often encounter challenges such as managing a busy service schedule, adhering to strict environmental regulations, and ensuring proper handling of hazardous materials. Staying organized and making use of route optimization tools can help manage time effectively. Ongoing training and clear communication with supervisors and customers are essential for meeting compliance standards and resolving any on-site issues. Building strong teamwork with other technicians and support staff also contributes to a safer and more efficient work environment.
What are popular job titles related to Crystal Clean jobs in Indiana? For Crystal Clean jobs in Indiana, the most frequently searched job titles are:
What job categories do people searching Crystal Clean jobs in Indiana look for? The top searched job categories for Crystal Clean jobs in Indiana are:
What cities in Indiana are hiring for Crystal Clean jobs? Cities in Indiana with the most Crystal Clean job openings:
Full-time
Medical, Dental, Vision, Life, Retirement, PTO
Re-posted 29 days ago
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.
The role:
The Bloomington facility is a full-service contract manufacturing plant providing formulation, aseptic filling and finishing services. The Technical Services Director is a member of the plant senior leadership team and is responsible for the development, coordination and execution of clinical and commercial technical transfer and validation operations for syringe and vial filling/packaging activities. This includes providing guidance and technical expertise to multiple disciplines and serving as the technical liaison between the customer and manufacturing. The Director is also responsible for the strategic planning of the department. This position reports to the Site Director.
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.
The role:
The Bloomington facility is a full-service contract manufacturing plant providing formulation, aseptic filling and finishing services. The Technical Services Director is a member of the plant senior leadership team and is responsible for the development, coordination and execution of clinical and commercial technical transfer and validation operations for syringe and vial filling/packaging activities. This includes providing guidance and technical expertise to multiple disciplines and serving as the technical liaison between the customer and manufacturing. The Director is also responsible for the strategic planning of the department. This position reports to the Site Director.
The responsibilities:
- Site Director delegate
- Lead cross-functional teams in technical transfer, commercial product support, sterility assurance validation, process validation, risk management, cleaning validation, inspection/packaging validation, and computer systems validation for filling and packaging operations
- Establish and deploy validation strategies in compliance with global regulatory requirements
- Direct the development and implementation of new processes requiring new technologies
- Understand and integrate information from more than one discipline and apply to complex problems requiring innovative techniques
- Budget development (>$10MM) and maintenance to meet business needs
- Responsible for final approval on product/process documentation, including CAPAs, deviation investigations and change controls
- Responsible for strategic planning, deployment, execution and after-action reviews
- Represent the site during regulatory inspections, client visits, and internal audits
- Collaborate with site Quality to drive improvements and risk reduction
Required qualifications:
- Bachelor's Degree in technical discipline required, preferably in science or engineering
- Minimum 10 years of experience in aseptic manufacturing operations required
- Minimum 8 years of technical management experience including cross-functional teams, resource and budget management and strategic development experience
- Strong knowledge of aseptic processing and validation in a globally regulated industry (FDA, EMEA, PIC/S, Japan PMDA, etc.)
- Computer proficiency in Microsoft Word, Excel, and Outlook and the ability to use quality enterprise software systems
Physical / Safety Requirements:
- Duties may require overtime work, including nights and weekends
- Use of hands and fingers to manipulate office equipment is required
- Position requires sitting for long hours but may involve walking or standing for periods of time.
- Ability to meet Grade C gowning requirements.
- Global travel may be required (10%)
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/