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Sr. Group Leader, Operations

3 months ago

Cherry Hill, United States Hikma Pharmaceuticals Full time

This is a 3rd Shift Position

Under the general direction of Operations Management provides 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.

Regular and predictable onsite attendance and punctuality. 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 online/room running (start-up samples, House samples, in-process inspection).

QUALIFICATIONS

Minimum: High School diploma or equivalent required with a minimum of eight [8] years’ experience in a non GMP environment or a minimum of five [5] years’ experience within a GMP manufacturing environment Preferred: Associates Degree with a minimum of five [5] years’ work experience in a GMP or non GMP environment Minimum of three [3] years’ work experience in a GMP or non GMP environment

SKILLS

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. Able to perform mathematical calculations associated with production documentation analysis and problem solving. Technically oriented with ability to analyze problems and suggest solutions. Lifting and bending requirements are possible and candidate should be able to lift 5 – 40 lbs in order to support line activities. Good visual acuity with or without eyeglasses/contacts (eye exam required). Noise levels are moderate to high. Ear protection may be required in some areas.  The work environment for this position involves walking, lifting (up to 40 lbs.), bending and sitting. Majority of the time is spent in the performance of manual inspection, paperwork and coordination of line activities. 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. Has demonstrated leadership skills or has shown potential leadership abilities in his/her work. Ability and working knowledge how to use a computer.

What We Offer

Clean climate-controlled working environment (Operator roles at the top) Annual performance bonus potential 401k employer match up to 6% of your contributions 23 vacation/personal days 11 paid Company holidays Generous healthcare benefits Employee discount program Wellbeing rewards programs Safety and Quality is a top organizational priority Career advancement/growth opportunities Tuition Reimbursement Maternity and Parental Leave