JT976 - GROUP LEADER

QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and enthusiastic to join our team. In this role, you’ll work with a highly enthusiastic team, contributing in a world-class manufacturing industry in Puerto Rico & USA.

Responsibilities:

• Focus on creating a positive and equitable working environment emphasizing the Values and Leadership Expectations and Culture Levers.
• Assists in implementing and coordinating daily activities in the manufacturing area to ensure manufacturing goals and project deadlines are met while maintaining compliance with current good manufacturing practices (cGMPs), environmental health and safety (EHS) guidelines and any other regulations that apply.
• Monitors and control labor efficiency, downtime, scrap, conversion loss and other key performance indicators.
• Identifies and supports VIP projects.
• Aids and assists in equipment troubleshooting problems.
• Audits manufacturing areas assuring compliance with specifications, batch record documentation and procedures.
• Supports and assures compliance with all the Operational Excellence projects implemented in his/her area.
• Conducts periodic meetings with employees as required.
• Collaborates in the investigation and solution of quality issues and complaints.
• Assigns employees to specific jobs/job rotations and monitors personnel performance. Provides feedback to supervisor/manager and director concerning employee job performance.
• Track completion of monthly/quarterly ACE's Check-Ins with all line/ area employees.

Qualifications:

• Associate Degree in Science, Engineering, Business Administration or Technology
• Minimum of 5+ years of experience in a manufacturing processes, preferably in pharmaceutical/solutions filling manufacturing environment
• Hands-on experience on computer programs, such as MS Word, Excel, Power Point.
• Excellent interpersonal and leadership skills with ability to interface well with other departments, and lead operators effectively and efficiently in a team environment.
• Strong writing skills and ability to prepare reports, write business correspondence and procedure manuals in English. 
• Ability to understand GMPs and other regulatory guidelines applicable to the medical/pharmaceutical industry.
• Strong analytical, problem solving and troubleshooting skills.
• Must be able to work rotating shift & weekends.
• Ability to understand technical drawings.
• Availability for 3rd shift