Process Supervisor - 2nd Shift

Hikma Pharmaceuticals; Cherry Hill Township (NJ); On-site; USD 56,950 - 95,000; Full time

Benefits offered by this job

Annual performance bonus

401(k) with company match

20 days PTO + holidays

Job summary

Hikma Pharmaceuticals USA Inc. is hiring a Process Supervisor for the 2nd shift in Cherry Hill, NJ. The role leads shift operations to meet production targets, quality standards, and budget goals, with emphasis on Lean practices and safety.

You will oversee staffing decisions, drive continuous improvement, and ensure regulatory compliance across manufacturing activities. Employment is full-time with competitive benefits and growth opportunities.

Qualifications

• BS or equivalent in a technical discipline, or 10 years in pharmaceutical injectables manufacturing as an alternative.
• 5–7 years experience in all aspects of the manufacturing process.
• Ability to manage department activities through subordinates with cost, methods and staffing control.
• Knowledge of World Class manufacturing, Lean, GMP, FDA guidelines and process validation.

Responsibilities

• Meet production requirements and deliver quality products on time and cost‑efficiently.
• Identify resources to help department head meet annual operating plan and budget.
• Supervise daily manufacturing operations across one or more departments.
• Provide training and implement control systems to reduce discrepancies on shifts.

Skills

Lean manufacturing

GMP

Statistical data analysis

Process control

Education

BS in a technical discipline or 10 years pharma experience

Job description

Process Supervisor - 2nd Shift

Job Title: Process Supervisor - 2nd Shift (Monday to Friday, 3:00PM to 11:30PM)

Location: Cherry Hill, New Jersey

Job Type: Full-time

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. Through our global footprint of 30+ manufacturing plants, 8+ R&D centers, and 9,000+ empowered employees, we are committed to making high‑quality medicines accessible to the people who need them.

Description: We are 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. In this role, you will be responsible for managing 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

• 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

• B.S. or equivalent, preferably in a technical discipline, required or 10 years in pharmaceutical injectables manufacturing as an alternative to a 4‑year degree.
• 5‑7 years experience in all aspects of the manufacturing process required.
• 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: $56,950 to $95,000 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. The Talent Acquisition team can provide more details about the specific salary range for the job location during the hiring process.

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

Eligibility requirements apply to some benefits and depend on the job classification, role, and length of employment. Benefits are subject to change as well as specific plan or program terms.

Recruiters

Please note that Hikma has a set roster of approved recruiters for specific roles agreed to in advance and does not accept unsolicited resumes or calls from third‑party recruiters or employment agencies regarding open positions. In the absence of a signed agreement and approval from Hikma’s Human Resources department to submit resumes for a specific position, Hikma will not approve, nor will be under an obligation to make, any payment to such non‑approved third‑parties in the event a candidate they refer is hired by Hikma.

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.