Project Manager - PMO

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 Bloomington facility is a full-service contract manufacturing plant providing formulation, aseptic filling, and finish services. This individual should be a strong team player with highly developed communication and problem-solving skills. This position reports to the Associate Director of Operational Execution (OPEX) and is 100% onsite.

The responsibilities:
Evaluate potential projects from a variety of sources to determine site priority and resourcing requirements
Develop and monitor project plans and adjust to ensure successful delivery
Communicate progress regularly to key stakeholders and escalate potential roadblocks when identified
Facilitate After Action Reviews (AAR) for projects to identify opportunities for improvement
Collaborate with cross-functional team members from Operations, Quality, Technical Services to effectively and efficiently drive projects to completion

Required qualifications:
BS degree, preferably in science or project management related field
MS degree and/or PMP certification is a plus, but not mandatory
3+ years of project management experience, preferably within the pharmaceutical or other regulated industry
Ability to manage multiple projects at the same time
Experience leading and/or working with cross-functional teams with the ability to negotiate, influence, and drive change
Strong oral and written communication skills
Experience with project management tools: MS Project, Minitab, Excel (or similar programs)
Advanced proficiency in Microsoft Office Suite (Word, PowerPoint, Outlook, Teams)

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 12/31/24
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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