Group Leader, IP - 2nd Shift

Job Title: Group Leader, IP - 2nd Shift

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 Group Leader, IP. In this role, you will be responsible for providing support to Manufacturing. Provides the necessary leadership to achieve product quality, cost control, cGMP compliance, safety and the execution of the production schedule to support the customer service requirements. Through leadership, commits to employee feedback and developmental processes. Coordinates all functions and lead efforts related to Filling, Inspection and/or Packaging. Oversees the work of other employees, gives direction and prioritizes work assignments. 

 

Key Responsibilities:

• Adheres to all environmental, health and safety SOPs, policies and procedures, including any department specific requirements.
• Coordinates and oversees daily activities of hourly production staff providing leadership assistance and necessary coaching.
• Initiates and completes investigative reports for production related process deviations.
• Provides phase-in training for new and existing employees.
• Provides conflict resolution and handles general problems/requests when necessary.
• Evaluates/enforces current practices within areas of responsibility.
• Coordinates orders for production related materials.
• Provides problem investigation and resolution. Supports management and engineering projects as assigned.
• Maintains training records for individual departments and production areas.
• May create and run reports on Access, Excel, ISO Train and Line Management Systems including tracking line performance
• Performs inspection processes as necessary based on line/room running (startup samples, House samples, in-process inspection).

 

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:

• High School diploma or equivalent required with a minimum of five [5] years experience in a non GMP environment or a minimum of two [2] years experience within a GMP manufacturing environment. Has demonstrated leadership skills or has shown potential leadership abilities in his/her work. Ability and working knowledge how to use a computer. Knowledgeable in site training management systems preferred. Knowledgeable in site label verification vision systems preferred. Knowledgeable in line management data capture systems preferred.

or

• Associates Degree with a minimum of two [2] years work experience in a GMP or non GMP environment Minimum of two [2] years work experience in a GMP or non GMP environment. Has demonstrated leadership skills or has shown potential leadership abilities in his/her work. Ability and working knowledge how to use a computer.
• Language Skills: Candidate should have strong interpersonal skills and be an excellent communicator who can successfully interact and coordinate activities across departmental boundaries and at varying levels within the organization. Excellent English language comprehension, both written and verbal.
• Mathematical Skills: Able to perform mathematical calculations associated with production documentation analysis and problem solving.
• Reasoning Ability: Technically oriented with ability to analyze problems and suggest solutions.
• Physi