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Manufacturing Science and Technology (MSAT

Job in Bloomington, Monroe County, Indiana, 47401, USA
Listing for: Simtrabps
Full Time position
Listed on 2026-08-02
Job specializations:
  • Quality Assurance - QA/QC
    Regulatory Compliance Specialist, Quality Engineering
Salary/Wage Range or Industry Benchmark: 85000 - 110000 USD Yearly USD 85000.00 110000.00 YEAR
Job Description & How to Apply Below
Position: Manufacturing Science and Technology (MSAT)

Job Overview

The Manufacturing Science and Technology (MSAT) role is part of a team of experienced pharmaceutical professionals responsible for the technical onboarding and process development of new drug product projects s includes designing the process(es) required for the new project. The Tech Transfer Senior Associate will work closely with a cross‑functional group consisting of Program Management, Sales, Supply Chain, Process Validation, Research and Development (R&D) and others, during development and transfer of new projects to Simtra.

This position is 100% onsite at the Bloomington facility and reports to the Sr. Technical Transfer Manager.

Responsibilities
  • Lead the onboarding and process development activities for the manufacture of new drug products, including the supporting development studies
    • Lead the cross‑functional team through technical activities, development studies and PPQ batches
    • Create technical transfer documents supporting this goal (Technical Transfer Plan, Process Development studies, Demonstration batch records, PPQ master batch record)
    • Heavy participation/co‑lead with Process Validation representative on PPQ strategy and protocol development
    • Lead during hand‑off to the commercial team following PPQ batches
  • Provide technical support to daily manufacturing operations while being visible on the manufacturing floor and resolving issues during manufacturing
  • Lead process improvement activities
  • Independently conduct Non‑Conformance Report (NCR) investigations and create, provide ownership, and implementation of Corrective Actions/Preventive Actions (CAPA)
  • Change Control Management (CCM) owner and impact assessment
  • Ownership of Fill Volume Dosing Qualification (FVOQ) documentation
  • Critical evaluation of product impact and responsible for advising if product meets release criteria and regulatory requirements
  • Participate in new project reviews to determine acceptable fit
  • Reviews Master Batch Records of junior colleagues and provides guidance
  • Independently represents Simtra in regulatory, client and internal audits as product/process Subject Matter Expert (SME). Ownership of audit responses and related CAPAs
  • Participate independently in client calls and on‑site visits to discuss and set strategy for projects and issue resolutions
  • Standard Operating Procedures (SOP) owner & process subject matter expert (SME)
  • Perform filter troubleshooting
  • Develop and present in‑depth SME courses on pharmaceutical industry topics
  • Mentor new hires in Technical Services Department and helps with training and on‑boarding
Required Qualifications
  • BS degree, preferably in a science or engineering related field
  • 7+ years pharmaceutical manufacturing experience
  • 3+ years of applicable Technical Transfer/Process Development experience
  • In‑depth knowledge of systems and equipment – including scales, mixing systems, mixing monitoring methods, aseptic formulations, fill volume limit setting, disposable formulation technology, homogeneity testing, control charting, identification and response to trends
  • Expertise in aseptic processing, sterile filtration, and Process Validation
  • Microsoft Office Suite advanced proficiency – Word, Excel, Outlook
  • Knowledge and ability to use enterprise software (JDE, BPLM, Minitab, Trackwise, etc.)
Physical / Safety Requirements
  • Duties will require overtime work on occasion, including nights and weekends
  • Position requires sitting for long hours but may involve walking or standing for periods of time
  • Must be able to qualify for Grade A/B area gowning
  • Must be able to wear applicable personal protective equipment (PPE)
Benefits

In return, you’ll be eligible for the following benefits:

  • 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…
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