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IT Project Manager

Simtra US LLC
life insurance, parental leave, paid time off, paid holidays, 401(k)
United States, New Jersey, Parsippany
Aug 26, 2025

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:

Simtra BioPharma Solutions is seeking an experienced IT Project Manager to lead infrastructure and enterprise technology initiatives that support our mission of delivering high-quality sterile injectable medicines. This hybrid role based in Parsippany, NJ requires a collaborative leader with strong project management skills, pharmaceutical industry experience, and a passion for driving operational excellence.

The responsibilities:



  • Lead complex technology projects (several simultaneously) from project planning through go-live
  • Ensureprojectand resource plans are created, managed, and maintained
  • Ensureproject objectives are achieved
  • Manageprojectchangeordersas appropriate
  • EnsurePMOprocessesarefollowedinaccordancewithpolicy
  • Hire, overseeandprovideguidanceto projectstaff.
  • Manage technology project subcontractors and vendor relationships on projects
  • Lead weekly project meetings ensuring that all relevant project updates/data are shared with stakeholders and IT leadership.
  • Proactively manage risks and potential blockers andimplementcorrectivemeasures.
  • Workwithfinance and sourcing teams tomanage contracts, invoices, etc. and ensure the PMO reflects timely and relevant financial information.
  • Collaborate with the support organization to ensure that projects are properly handed over post implementation and ensure successful transition to the support teams.


Required Qualifications:



  • 5+ years of IT Project Management experience.
  • Preferable to have worked in pharmaceuticals or life sciences
  • First-hand experience running infrastructure projects (data center buildouts, infrastructure installation, migrations).
  • Experience working inside an enterprise PMO.
  • Knowledge of project management processes, such as Scrum and Agile.
  • Strong communicator and ability to manage/lead diverse teams.
  • Successful candidates will typically possess a bachelor's degree in a technical discipline.
  • Project Management designations such as PMI, SCRUM Master
  • Computer proficiency in Microsoft Project, Word, Excel and Outlook and the ability to utilize enterprise software tools.



Preferred Qualifications:



  • Experience coming from the pharmaceutical manufacturing industry.
  • Knowledge of Computer System Validation (CSV) in the pharmaceutical manufacturing industry.



In return, you'll be eligible for:



  • 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




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/


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