Catalent
Pharmaceutical
Manager,ManufacturingScience&Technology
“Manager, Manufacturing Science & Technology at Catalent. Skills: Manufacturing Science & Technology, process performance, troubleshooting, technology transfer, continuous improvement, formulation, non‑sterile fill/finish operations. Plan and execute defined experimental studies, process evaluations, and equipment qualification activities. Maintain process, analytical, and raw material knowledge needed to support ongoing production and investigations”
What You'll Achieve.
maintain product quality; ensure compliance; drive operational efficiency; ensure production schedules maintained; processes are run reliably and compliantly; detect trends and recommend corrective actions
Industry & Context.
troubleshooting; investigations; root cause analysis; CAPA development; structured problem‑solving tools
100% on-site
What They're Looking For.
Must Have
Master’s Degree in Biochemistry, Chemical Engineering, Bioengineering, or related technical field with 5 + years of GMP pharmaceutical manufacturing experience OR Bachelor’s Degree in Biochemistry, Chemical Engineering, Bioengineering, or related technical field 7 + years of GMP pharmaceutical manufacturing experience, Experience supporting formulation or non‑sterile fill/finish operations in a GMP environment is required, Familiarity with cGMP regulations for non‑sterile liquid products and basic validation/qualification principles is required
Nice to Have
Working knowledge of 21 CFR Part 4 and 21 CFR Part 820 expectations for nasal spray combination products is preferred, Experience with DOE/statistical tools and analytical method development is preferred
What You'll Do.
Plan and execute defined experimental studies
and equipment qualification activities
and raw material knowledge needed to support ongoing production and investigations
Provide technical support for formulation
and labeling operations
Assist with technology transfer activities for clinical and commercial manufacturing
Monitor critical quality attributes (CQAs) and critical process parameters (CPPs) to detect trends and recommend corrective actions
Lead investigations to determine root cause and support CAPA development
How You'll Work.
Team & Collaboration
collaborates closely with Manufacturing, Quality, and Development; coordination with internal and external partners
Process & Methodology
Plan and execute defined experimental studies, assist with technology transfer activities
Applying for this Manager, Manufacturing Science & Technology role?
Most applicants get filtered before a human reads their resume. See if yours makes the cut.
How to Apply on Workday
- Workday has a multi-step form — save your progress after every section.
- "Apply With LinkedIn" can fail or lose data; manual entry is more reliable.
- Watch for the "Submit for Review" final step — hitting "Save" alone does not submit.
- Job requisition numbers are useful when following up with HR by email.
ANONYMOUS · UNFILTERED
What do employees actually say about Catalent?
Real rants from real employees. Read before you apply.