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Mount Laurel, New Jersey, United States · Hybrid
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Winslow Township, New Jersey, United States · On-site
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Warren Township, New Jersey, United States · Hybrid
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Hamilton Township, New Jersey, United States · On-site
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Asbury Park, New Jersey, United States · Hybrid
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Iselin, New Jersey, United States · Hybrid
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Newark, New Jersey, United States · On-site
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Newark, New Jersey, United States · On-site
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Cherry Hill Township, New Jersey, United States • On-site
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Manage shift operations within manufacturing departments to meet budget, quality, and production goals. Drive operational excellence through cost reduction, regulatory compliance, and the implementation of Lean Manufacturing principles.
Requires a B.S. in a technical discipline or 10 years of experience in pharmaceutical injectables manufacturing. Candidates must have 5-7 years of experience in all aspects of the manufacturing process and knowledge of GMP and FDA guidelines.
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:
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:
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*:
*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.
Offices: 1809 WILSON RD, Columbus, Ohio 43228, us
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