Operations Lead, Inspection

Jubilant HollisterStier LLC

$102K — $136K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's Degree in Engineering, Operations, or Life Sciences
  • 5+ years of experience or a high school diploma with significant experience
  • Project management experience
  • Strong analytical skills with proficiency in data analysis tools
  • Effective communication skills across various audience levels
  • Ability to influence and network within the organization
  • Proficient in Microsoft Office and production planning

Responsibilities

  • Provide subject matter expertise on standards and best practices for product integration
  • Develop inspection test sets and author best practices for qualification
  • Integrate cross-functional teams for seamless cGMP operations
  • Lead continuous improvement projects for capacity optimization
  • Develop Operational Excellence programs with stakeholders
  • Review and revise standard operating procedures and documentation
  • Assist with regulatory inspections and provide training for new personnel

Benefits

  • Medical, Dental & Vision coverage
  • Flexible Spending Accounts (FSA) & Health Savings Accounts (HSA)
  • Life & AD&D Insurance
  • Short-Term & Long-Term Disability Insurance
  • Employee Assistance Program
Full Job Description
Job Description:

The Operations Lead, Inspection, will ensure operational excellence and continuous improvement within the shift manufacturing teams. Reporting directly to the Manager, Secondary Manufacturing, you will provide technical and operational support, maintain a strong working knowledge of the manufacturing equipment set, control systems, and site operating systems.
  • Provide Subject Matter expertise on industry standards, best practices, and site capabilities to enable successful integration of new products and processed into the existing and future facility inspection equipment.
  • Support and own development of inspection test sets, authoring means and methods for performing inspection, and best practices for inspection qualification & requalification.
  • Serve as a key integrator for cross-functional teams supporting seamless operation of cGMP production, ensuring readiness of manufacturing areas for start-up, process qualification, and validation activities.
  • Support the manufacturing operations team as a key contributor for projects that implement new technologies and operational process improvements in the GMP manufacturing environment, maintaining processing suites in a compliant and validated state.
  • Lead or participate in continuous improvement projects, including capacity optimization and cost reduction programs.
  • Support the development of the Operational Excellence programs and lead Manufacturing Projects with cross-functional stakeholders.
  • Work with cross functional teams to review, author and revise standard operating procedures and batch records, review technical reports, assist with conducting deviation investigations, and write deviation reports.
  • Document and communicate all aspects of work and learnings, providing training and mentorship for new personnel.
  • Assist with metrics tracking and reporting to leadership teams.
  • Support and participate in internal and external regulatory inspections as necessary.

Qualifications:

Required
  • Bachelors Degree in Engineering, Operations, or Life Sciences
  • 5+ Years experience in lieu of a degree (must have H.S. degree)
  • Experience in project management and coordination.
  • Strong analytical skills and proficiency in data analysis tools and techniques.
  • Ability to communicate effectively to various audiences.
  • Ability to influence network with multiple levels and functions of the organization.
  • Tasks require entering manufacturing areas which require wearing appropriate PPE.
  • Microsoft Office
  • Production Planning
  • Managing conflict and influencing outcomes
  • Strong leadership skills
  • Prolonged sitting or standing
  • Exposure to allergens
  • Working in aseptic areas

Preferred
  • Pharmaceutical experience

Location: Spokane, WA - On Site, Full-Time

Shift: Monday-Friday 8am-5pm

Compensation & Benefits That Start on Day One - Because Your Well Being Matters

Hiring Wage: $102,100 - $136,100 annually, with opportunities for growth, promotion, and annual raises.

At Jubilant HollisterStier, we don't believe in waiting periods. From the moment you join us, you and your family have access to a full suite of benefits designed to support your health, stability, and long-term success.

Starting on your first day, you receive:
  • Medical, Dental & Vision coverage
  • Flexible Spending Accounts (FSA) & Health Savings Accounts (HSA)
  • Life & AD&D Insurance
  • Short-Term & Long-Term Disability Insurance
  • Employee Assistance Program

Similar Jobs

More Jobs at Jubilant HollisterStier LLC

More Pharmaceuticals & Biotech Jobs

  • BridgeBio Pharma, Inc.
    Sr. MSL/MSL - New England
    $225K — $250K *
    BridgeBio Pharma, Inc.
    Remote
  • Senior Validation Specialist
    $95K — $115K *
    Katalyst HealthCares and Life Sciences
    Raleigh, NC 27610 (Wake County)
  • CSV Lead
    $110K — $130K *
    Katalyst HealthCares and Life Sciences
    Salt Lake City, UT 84118 (Salt Lake County)
  • Supplier Quality Specialist
    $80K — $95K *
    Katalyst HealthCares and Life Sciences
    Indianapolis, IN 46227 (Marion County)
  • Quality Control Engineer
    $95K — $115K *
    Katalyst HealthCares and Life Sciences
    Annapolis, MD 21401 (Anne Arundel County)

Find similar Operations Lead, Inspection jobs: