CMMS Administrator

Posted 18 Days Ago
Be an Early Applicant
Bloomington, IN
Senior level
Pharmaceutical • Manufacturing
The Role
The CMMS Administrator oversees the CMMS system, collaborates with departments to manage work orders, maintains SOPs, provides training, and presents reports. They ensure adherence to quality standards in a hybrid work setting.
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:

The Computerized Maintenance Management System (CMMS) Administrator is responsible for maintaining and overseeing the CMMS system, including training and system access. The CMMS Administrator will collaborate with applicable departments to create and track work orders (WO) and associated tasks in order to support batch release and CAPA closure. This role will report to the Director of Maintenance and Reliability, and it is a hybrid position at our Bloomington, Indiana facility.

 

The responsibilities:

  • Subject Matter Expert of the CMMS system and will provide training to internal stakeholders/users and manage the access to the system
  • Collaborate with Action Owners/Approvers and facilitate the resolution of work order backlog
  • Provides oversight to work order completion for batch release/CAPA closure
  • Amends and maintains standard operating procedures (SOPs) and supports system updates/upgrades
  • Supports facility Fit and Finish program and ensures adherence to schedule
  • Generate work order report and present site metrics to leadership and at the quarterly Quality Review meeting
  • Responsible for speaking to client auditors and regulatory personnel to explain work order process and the CMMS system

 

Required qualifications:

  • Associates (AS) Degree
  • 5+ years experience (in lieu of education) with work order, preventive maintenance, and/or inventory systems
  • Advanced proficiency in Microsoft Office Suite (Word, Excel, Outlook)
  • Preferred experience in Maximo, Dynamics 365, and/or TrackWise
  • Excellent attention to detail and organization skills
  • Strong oral and written communication skills
  • Strong leadership skills with the ability to persuade, influence, and negotiate
  • Experience in a regulated industry, preferably knowledge of FDA regulations current Good Manufacturing Practices (cGMP)
  • Must be able to work overtime, including nights, weekends, and during facility shutdowns


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 12/31/25


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/

Am I A Good Fit?
beta
Get Personalized Job Insights.
Our AI-powered fit analysis compares your resume with a job listing so you know if your skills & experience align.

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)

Similar Jobs

Novo Nordisk Logo Novo Nordisk

Senior Representative, Regulatory Affairs

Healthtech • Software • Pharmaceutical
Bloomington, IN, USA
69000 Employees

Thrive Market Logo Thrive Market

Operations Manager, Fulfillment

Consumer Web • eCommerce • Food • Healthtech • Natural Language Processing • Social Impact
Batesville, IN, USA
1000 Employees
85K-100K Annually

Magna International Logo Magna International

Assoc, Production-Complex Mach

Automotive • Hardware • Robotics • Software • Transportation • Manufacturing
Hybrid
Muncie, IN, USA
171000 Employees

Magna International Logo Magna International

Lead Operator

Automotive • Hardware • Robotics • Software • Transportation • Manufacturing
Hybrid
Muncie, IN, USA
171000 Employees

Similar Companies Hiring

Accuris Thumbnail
Software • Manufacturing • Machine Learning • Information Technology • Generative AI • Conversational AI
Denver, CO
1200 Employees
Zealthy Thumbnail
Telehealth • Social Impact • Pharmaceutical • Healthtech
New York City, NY
13 Employees
Cencora Thumbnail
Pharmaceutical • Logistics • Healthtech
Conshohocken, PA
46000 Employees

Sign up now Access later

Create Free Account

Please log in or sign up to report this job.

Create Free Account