Oral Solid Dose Manufacturing Lead - Ops & Growth

KVK Tech, Inc.

Newtown (PA)

On-site

USD 90,000 - 120,000

Full time

14 days+

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Benefits offered by this job

401(k) with company match
Health, vision, and dental insurance
Tuition reimbursement
Annual bonus eligibility
Annual merit increases
Paid Time Off and Flexible Holidays

Job summary

KVK Tech, Inc. in Newtown, PA is seeking an experienced Manufacturing Group Lead to oversee daily oral solid dosage operations. You will lead group leads and operators, ensure safety, quality, and compliance with cGMP and approved procedures, and drive efficient production scheduling.

The role focuses on staffing, floor oversight, documentation quality, training compliance, and continuous improvement within a regulated manufacturing environment.

Qualifications

  • Minimum 5 years of pharmaceutical manufacturing experience in a cGMP environment.
  • Experience leading groups and coordinating production activities.
  • Strong knowledge of batch records, SOPs, and compliance expectations.

Responsibilities

  • Supervise daily oral solid dosage manufacturing activities and ensure safe, compliant execution.
  • Direct staffing assignments, room coverage, and labor utilization based on priorities.
  • Oversee floor execution and ensure adherence to batch records and cGMP requirements.
  • Review and approve production documentation for accuracy and compliance.
  • Lead issue escalation and cross-functional support for timely resolution.
  • Coach employees and support training, onboarding, and succession planning.
  • Support deviations, investigations, CAPAs, and continuous improvement.

Skills

Leadership
Coaching
Communication
Problem-solving
cGMP knowledge
Documentation review

Education

High school diploma
Bachelor's degree preferred

Job description

KVK Tech, Inc. in Newtown, PA is seeking an experienced Manufacturing Group Lead to oversee daily oral solid dosage operations. You will lead group leads and operators, ensure safety, quality, and compliance with cGMP and approved procedures, and drive efficient production scheduling.

The role focuses on staffing, floor oversight, documentation quality, training compliance, and continuous improvement within a regulated manufacturing environment.

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