Capital Projects Manager

Simtra BioPharma Solutions · Minneapolis–Saint Paul, MN

Company

Simtra BioPharma Solutions

Location

Minneapolis–Saint Paul, MN

Type

Full Time

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.


This role:

The Capital Projects Manager ensures projects and related activities meet committed timelines and budgets to ensure these projects' compliance and requirements for on-time delivery. This position oversees a group of Project Managers, Project Engineers and other professional.  This position reports to the Director, Engineering and Technology. 


The responsibilities:

  • Provides guidance, support, direction and leadership through positive interactions with all personnel during daily operations (24/7)
  • Interviews, hires, coaches, and develops staff. Conducts annual performance reviews for all direct reports. Assist in setting performance objectives and development plans
  • Manages a team of senior level and other engineering professionals to support a variety of projects at the Bloomington, Indiana plant - projects support, but is not limited to, the following areas: facilities, utilities (critical and non-critical), aseptic processing, and filling & packaging equipment processes
  • Oversees and develops departmental capital equipment budgets, Value Improvement Projects, and equipment/process optimization
  • Ensures department compliance for master change control management and validation protocols
  • Utilizes lean principles to manage the successful completion of departmental tasks within the boundaries of quality, time, safety and budget
  • Manages project timelines associated with generating design specifications, procurement, design of experiments, factory acceptance testing, installation, coordination of validation activities, standard operating procedure (SOP) generation, and transfer to functional area for in-service status
  • Provides guidance on design and technical direction to engineering staff
  • Provides review and approval of Engineering Work Orders, Master Change Controls, Exception Reports, Technical Summaries, Validation protocols, expense approvals and CAPA's
  • Leads the processes governing site master and long-range planning 

  
Desirable qualifications:

  • Bachelor’s degree in an Engineering discipline, or equivalent experience, required (Advanced degree preferred)
  • 8+years of experience in a pharmaceutical manufacturing environment
  • Demonstrated effective leadership skills. 
  • Must be self-motivated, have good interpersonal skills, and be capable of analyzing and solving complex problems through innovative thought and experience
  • Knowledge of GMPs and regulatory guidelines
  • MS Office Suite proficiency (Word, Excel, PowerPoint, Outlook)
  • Experience using enterprise software (Autocad, JDE, BPLM, Pilgrim, Trackwise, Maximo etc.) 

 
Physical / Safety Requirements:

  • Must be able to lift up to 50lbs.
  • Duties may require overtime work, including nights and weekends
  • Use of hands and fingers to manipulate office equipment is required
  • Position requires sitting or standing for long hours



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



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:

[ENTER DESCRIPTION SUMMARY]

 

The responsibilities:

  • [ENTER EACH TASK/RESPONSIBILITY]


The work environment:

[ENTER DESCRIPTION SUMMARY]

 

Desirable qualifications:

  • [ENTER EACH QUALIFICATION]

 

Physical / safety requirements:

  • [ENTER EACH REQUIREMENT, IF APPLICABLE TO ROLE. OTHERWISE, OMIT THIS SECTION.]


Additional requirement(s):

  • [ENTER EACH REQUIREMENT, IF APPLICABLE TO ROLE. OTHERWISE, OMIT THIS SECTION.]


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.
                                                                                                                                                            
EEO is the Law 
EEO is the law - Poster Supplement 
Pay Transparency Policy


Data Privacy

To learn more about Simtra's approach to data privacy, please review the Simtra Recruitment Platform Global Privacy Policy:

https://biopharmasolutions.baxter.com/simtra-recruitment-platform-privacy-policy



Apply Now

Date Posted

08/22/2024

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