Microbiology Quality Control Lead – Critical Systems

Simtra US LLC

Bloomington (IN)

Hybrid

USD 90,000 - 115,000

Full time

14 days+

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Benefits offered by this job

Medical & Dental Coverage
401(k) Retirement Savings Plan with 1:
Time Off Program
Education Assistance Program
Employee Assistance Program
Onsite Campus Amenities

Job summary

Simtra BioPharma Solutions (Simtra) in Bloomington, IN, seeks a Microbiology Supervisor to lead the daily operations of the Microbiology functional department within Quality Control. You will guide technicians and ensure compliance with regulatory standards.

The role requires a science degree, 5+ years in Quality, and proven leadership. You will develop SOPs, participate in audits, and analyze data trends to drive improvement while supporting a collaborative, safety‑minded lab environment.

Qualifications

  • Bachelor’s degree in a physical science required, preferably Microbiology.
  • Minimum of 5 years of experience in Quality.
  • Previous leadership experience preferred.
  • Computer proficiency in Word, Excel, and Outlook; aptitude with enterprise software.

Responsibilities

  • Lead daily operations of the Microbiology department or quality system.
  • Provide guidance and leadership to Quality Technicians and Lab Associates.
  • Prioritize workloads and assign duties/shift requirements.
  • Interviews, hires, coaches, and conducts performance reviews.
  • Develop and implement departmental policies and goals.
  • Participate in audits and cross-functional teams.
  • Serve as SME for the supervised department.
  • Write/review investigations and perform statistical analyses.

Skills

Leadership
Quality Assurance
Microbiology
MS Excel
TrackWise
JDE

Education

Bachelor's degree in Physical Science
Microbiology preferred

Tools

TrackWise
Pilgrim
JDE
BPLM

Job description

Microbiology Supervisor, Quality Control Critical Systems

Bloomington, Indiana, United States

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.

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 Microbiology Supervisor leads the daily operations of a Microbiology functional department or quality system. The supervisor serves as the leader of their respective area, and is a critical member of the Microbiology leadership team.

The responsibilities:

  • Acts as the Supervisor for their respective sub-department.
  • Provides guidance, support, direction and leadership to Quality Technicians and Quality Lab Associates through positive interactions with all personnel during daily operations.
  • Prioritizes workloads and assigns duties/shift requirements based on company needs.
  • Interviews, hires, coaches, and develops staff. Conducts annual performance reviews for all direct reports. Assist in setting performance objectives and development plans.
  • Sets local departmental policy and goals, and implement plans and systems to meet those goals.
  • Participates in the Microbiology leadership team to build systems and set goals and policy for the Microbiology department.
  • Participates in audits and as part of cross-functional teams with other Baxter departments and facilities as the
  • SME (Subject Matter Expert) of the department supervised.
  • Writes and reviews investigations for out of level results, and other microbiology related investigations as appropriate.
  • Performs statistical analysis of data and evaluates the area supervised for microbiological trends and responds appropriately.


The requirements:

  • Bachelor’s degree in a physical science required, preferably in Microbiology.
  • Minimum of 5 years of experience in Quality
  • Previous leadership experience preferred.
  • Computer proficiency in Microsoft Word, Excel, and Outlook and the ability to use enterprise software (examples include: JDE, BPLM, Pilgrim, Trackwise, etc.)

Physical / Safety Requirements:

  • Must be able to gown qualify for Grade A/B area.
  • The position sometimes requires extended periods of standing.
  • Must be able to wear applicable Personal Protective Equipment.
  • Position may require handling laboratory chemicals.
  • Duties may require overtime work, including nights and weekends
  • Use of hands and fingers to manipulate office equipment is required

In return, you’ll be eligible for[1]:

  • Medical & Dental Coverage
  • Flexible Spending Accounts
  • Life and AD&D Insurance
  • Supplemental Life Insurance
    • Spouse Life Insurance
    • Child Life 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
  • Employee Ownership Plan
  • Additional Benefits
    • Short and Long-Term Disability Insurance
    • 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 12/31/26

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.

Simtra is 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.

Interested in building your career at Simtra BioPharma Solutions? Get future opportunities sent straight to your email.

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For government reporting purposes, we ask candidates to respond to the below self-identification survey.Completion of the form is entirely voluntary. Whatever your decision, it will not be considered in the hiringprocess or thereafter. Any information that you do provide will be recorded and maintained in aconfidential file.

As set forth in Simtra BioPharma Solutions’s Equal Employment Opportunity policy,we do not discriminate on the basis of any protected group status under any applicable law.

If you believe you belong to any of the categories of protected veterans listed below, please indicate by making the appropriate selection.As a government contractor subject to the Vietnam Era Veterans Readjustment Assistance Act (VEVRAA), we request this information in order to measurethe effectiveness of the outreach and positive recruitment efforts we undertake pursuant to VEVRAA. Classification of protected categoriesis as follows:

A "disabled veteran" is one of the following: a veteran of the U.S. military, ground, naval or air service who is entitled to compensation (or who but for the receipt of military retired pay would be entitled to compensation) under laws administered by the Secretary of Veterans Affairs; or a person who was discharged or released from active duty because of a service-connected disability.

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