Project Engineer, Multiple Openings
- Simtra BioPharma Solutions
- Bloomington, Indiana
- Full Time
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 Project Engineers (level depends on experience) that are responsible for the engineering execution and technical oversight of capital projects (expansion and sustainability) within the pharmaceutical manufacturing facility. This role ensures that all projects are delivered safely, on time, within budget, and in compliance with Good Manufacturing Practices (GMP) regulatory requirements and company standards. The positions work closely with cross-functional teams including manufacturing, quality, EHSS, maintenance, validation, and procurement to ensure successful project delivery. This position is 100% onsite at the Bloomington, Indiana facility.
The responsibilities:
- Leads team in defining project strategies, developing goals and ensures project scope, budgets, and schedules are defined to meet project requirements
- Continuously interacts with all functions and levels of management ensuring effective, ongoing communications across teams and stakeholders
- Assists project manager to ensures identification and communication of projects risks, development of risk plan and leads team in the proactive
management of risk response strategies
- Anticipates potential conflict situations and manages to a successful outcome
- Assists Project Manager to track team deliverables for project completion, to create and maintain project schedules, to control project scope, and to review contractor/engineering firm submittals
- Establish, track and communicate project risks in collaboration with project team
- Participates in all collaborations with external engineering firms in feasibility assessments, concept design, basic design and detail design
- Participates in technical review of all external engineering design reviews
- Develop project URS, RFQs, CCMs, Work Orders, preventative maintenance plans, P&ID redlines, spare parts management among other activities directly
related to project documentation.
- Collaborates with multifunction teams to develop project Capital Expenditure Requests (CERs) and Front-End Loading (FEL) documents among other documents
required to obtain project approvals.
- Assists with project CQV (commissioning, qualification, and validation) activities
- Participates in training site stakeholders as project is turned over to the site
- Presents project technical scope to site stakeholders and project sponsors/endorsers
- Participates/leads project technical reviews for assigned projects
Required qualifications:
BS degree in Engineering (Chemical, Mechanical, Electrical, Packaging, Pharmaceutical, Biomedical), or a related technical field
0-2 years of experience (Level I)
2-5 years of experience (Level II)
5-8 years of experience (Level III/Sr.)
8-15 years of experience (Level IV/Principal)
15+ years of experience (Level V/Sr. Principal)
Experience with capital project execution, from concept to commissioning
Knowledge of the basic principles in aseptic processing and/or inspection & packaging engineering best practices
Must be able to lead and execute engineering projects and lead multiple projects simultaneously
Strong understanding of inspection and packaging materials, processing, and testing methods
Experience and/or knowledge of PLC, HMI, Vision Systems and Building Management Systems
Strong oral and written communication skills
Lean Six Sigma or continuous improvement experience
Must be able to read mechanical, electrical, and P&ID drawings
Advanced proficiency in Microsoft Office Suite (Word, Excel, and Outlook)
Proficient in project management tools (MS Project, Primavera, JIRA, etc.)
Experience and the ability to use enterprise software (examples include: JDE, Microsoft Dynamics, BPLM, Veeva, Trackwise, etc.)
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
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.
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