Process Supervisor

RXinsider LTD.; Cherry Hill Township (NJ); On-site; USD 85,000 - 110,000; Full time

Job summary

Hikma Pharmaceuticals USA Inc. in Cherry Hill, NJ seeks a Process Supervisor to manage shift operations in pharmaceutical manufacturing. The role focuses on meeting budget, quality, and production goals while interpreting policies and procedures.

Responsibilities include supervising daily operations, driving process improvements, and ensuring safety and regulatory compliance. The position is full-time and onsite at the facility.

Qualifications

• BS or equivalent, preferred technical discipline, or 10 years site pharma injectables experience.
• 5-7 years experience in all aspects of the manufacturing process.

Responsibilities

• Meet production requirements while delivering quality products on time and cost-efficiently.
• Identify resources to help meet operating plans and budgets.
• Supervise daily manufacturing operations across departments.
• Lead shift training and implement controls to reduce discrepancies.
• Maintain a positive, equitable work environment emphasizing respect and results.
• Support safety and quality commitments of the department.
• Make staffing decisions and resolve disciplinary issues up to suspensions/terminations.
• Drive operational excellence and Lean manufacturing initiatives.
• Must become gown-qualified.
• Ensure regular onsite attendance and punctuality.

Skills

People management

Data analysis

Lean manufacturing

Regulatory knowledge

Education

BS or equivalent in technical discipline

10 yrs site pharma injectables experience

Tools

Statistical tools

Quality systems

Job description

Job Title: Process Supervisor

Location: Cherry Hill, NJ

Job Type: Full-time

DESCRIPTION: We continue to be committed to building a diverse and inclusive team and encourage applications from candidates of all backgrounds. We are seeking a talented and motivated Process Supervisor.

JOB PURPOSE

This Process Supervisor role manages shift or multiple shift operations within manufacturing departments. Responsible for meeting budget, quality, and production goals, setting standards, and making employment and staffing decisions. Interprets manufacturing policies, procedures, and programs.

KEY ACCOUNTABILTIES

• Responsible for meeting production requirements, delivering quality products to customers in a timely fashion and cost-efficient manner.
• Identify/prioritize/provide resources to assist the department manager to meet the annual operating plan and budgetary commitments.
• Supervise the daily manufacturing operations across a department or multiple departments.
• Emphasize training and implement control systems on the shift or multiple shifts to eliminate product discrepancies.
• Commit to employee feedback and developmental processes.
• Provide a positive and equitable working environment emphasizing Respect/Responsiveness/Results.
• Support and emphasize the Safety and Quality commitments of the department.
• Make staffing decisions.
• Investigate and resolve disciplinary issues up to and including suspensions and terminations.
• Responsible for driving operational excellence and flawless execution in the areas of cost reduction, discard reduction, annual productivity improvements, inventory turnover, regulatory excellence including exception reduction and internal/external regulatory commitment management, on time delivery and lead time reduction, improving the overall safety of the work environment, leadership development and the ability to create a Lean Manufacturing, total employee involvement workplace
• Must be become gown-qualified.
• Regular and predictable onsite attendance and punctuality.

QUALIFICATIONS / EXPERIENCE

• B.S. or equivalent, preferably in a technical discipline, required or 10 yrs. site experience in pharmaceutical injectables manufacturing as an alternative to a 4 year degree.
• 5-7 years experience in all aspects of the manufacturing process required.

SKILLS

• Ability to manage activities of departments through subordinates who exercise full supervision in terms of cost, methods, and employees.
• Ability to interpret and analyze statistical data and information and financial reports, understand and resolve technical difficulties, interface with internal engineering/technical experts and external technical representatives, manage multiple priorities in a manufacturing plant setting, be resourceful to a large manufacturing department.
• Knowledge of World Class manufacturing methods ( Lean ), Good Manufacturing Practices, Food Drug and Administration guidelines and process validation.

Equal Opportunity Employer:

Hikma Pharmaceuticals USA Inc. is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status, or other characteristics protected by law