Process Supervisor

Hikma Pharmaceuticals; South Brunswick (NJ); On-site; USD 66,000 - 134,000; Full time

Job summary

A pharmaceutical company in South Brunswick is seeking a Process Supervisor to manage shift operations in manufacturing. This role involves meeting production goals, supervising teams, and ensuring compliance with regulatory standards. Candidates should have a degree in a technical discipline or extensive experience in pharmaceutical manufacturing. Competitive salary and comprehensive benefits are offered.

Benefits

Annual performance bonus

401(k) matching

Generous paid time off

Comprehensive health benefits

Tuition reimbursement

Qualifications

• Minimum of 10 years experience in pharmaceutical injectables manufacturing as an alternative to a 4-year degree.
• 5-7 years experience in aspects of the manufacturing process.

Responsibilities

• Supervise daily manufacturing operations across a department.
• Meet production requirements and deliver quality products.
• Drive operational excellence and regulatory compliance.

Skills

Ability to manage activities

Knowledge of Lean manufacturing

Ability to analyze statistical data

Education

B.S. in a technical discipline or equivalent experience

Job description

Title: Process Supervisor

About Us: As a developer, manufacturer, and supplier of essential medicines, Hikma Pharmaceuticals USA Inc. and its affiliates’ purpose is to put better health within reach, every day for millions of patients around the world.

We are a trusted, reliable partner and dependable source of over 760 high-quality generic, specialty and branded pharmaceutical products that hospitals, physicians and pharmacists need to treat their patients across North America, the Middle East, North Africa and Europe.

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 highly skilled and motivated Process Supervisor through subordinate supervisors, 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 Responsibilities:

• Regular and predictable onsite attendance and punctuality.
• 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.

Qualifications:

We value the skills and experiences candidates bring to the table. While we have listed some qualifications below, we encourage candidates to apply even if they do not meet all of them:

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

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.

Compensation:

Base Salary: $66,600 - $133,750 annually. The compensation for this position will be determined during the interview process and will vary based on multiple factors, including, but not limited to, work location, prior experience and job-related knowledge, relevant skills and expertise, current business needs, and market factors.

What We Offer:

• Annual performance bonus, commission, and share potential
• Auto enrollment in a Hikma-sponsored 401(k) program at a pre-tax contribution rate of 3% of eligible pay. Hikma will match 100% of the first 6% of eligible pay that you contribute
• A generous paid time off (PTO) bank starting with 20 days (prorated based on hire date). Additional days granted upon reaching work milestone anniversaries
• 3 personal days (prorated based on hire date)
• 11 company paid holidays
• Comprehensive benefits including health, dental, vision, mental health, disability, life insurance, prescription drug coverage, and a variety of voluntary benefits
• Employee discount program
• Wellbeing rewards program
• Safety and Quality is a top organizational priority
• Career advancement and growth opportunities
• Tuition reimbursement
• Paid maternity and parental leave

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.