Pharma Manufacturing Project Lead — Flexible Hours

Kindeva Drug Delivery; Clitheroe; On-site; GBP 65,000 - 90,000; Full time

Benefits offered by this job

Private Medical Insurance

Company pension scheme

25 days holiday per year

Free on-site parking

Cycle to work scheme

Life assurance

Job summary

Kindeva Drug Delivery is seeking a project/operations leader to oversee technical development of manufacturing processes at commercial sites and with Outsource Partners. You will manage schedules, budgets, and COGs while coordinating cross-functional teams to ensure GMP compliance and successful phase-gate reviews.

You will lead project charters, develop detailed plans, and mentor staff to drive process transfers, product optimization, and new technology introductions.

Qualifications

• Bachelor’s degree in Engineering, Science or related technical field.
• 3+ years’ experience in a technical role within pharmaceutical operations/product development/process development.
• 4+ years’ experience with project management.
• Experience working within ISO9001.
• Requires track record of detailed program management exhibiting comprehensive planning and thorough communication.
• Must be proficient acting in and leading integrated process teams, coordinating and communicating project requirements.

Responsibilities

• Lead development of Project Charter and initial requirements.
• Scope project requirements for NPI, line extension, tech transfers and optimization.
• Ensure design, system performance, quality, and COGs alignment with specs.
• Adhere to Health, Safety, Environmental and GMP requirements.
• Mentor teams and manage high-level strategic projects affecting the organization.
• Establish risk management and contingency plans for each project.

Skills

Engineering degree

PM experience

ISO 9001 experience

Cross-functional coordination

Technical pharma ops

Education

Bachelor’s degree in Engineering/Science

Job description

Kindeva Drug Delivery is seeking a project/operations leader to oversee technical development of manufacturing processes at commercial sites and with Outsource Partners. You will manage schedules, budgets, and COGs while coordinating cross-functional teams to ensure GMP compliance and successful phase-gate reviews.

You will lead project charters, develop detailed plans, and mentor staff to drive process transfers, product optimization, and new technology introductions.