Location: Aibonito, PR
Pay Rate: $15.50 p/h
Shift E: Thursday–Friday (8-hour shifts from 10:00 PM to 6:30 AM) and Saturday–Sunday (12-hour shifts from 6:00 PM to 6:30 AM).

Summary:
Assists in implementing and coordinating daily activities in the manufacturing area to ensure manufacturinggoals 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.

Essential Duties and? Responsibilities:

• Focus on creating a positive and equitable working environment emphasizing the company Shared 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 andprocedures.
• Supports and assures compliance with all the Operational Excellence projects implemented inhis/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 with a Minimum of 5+ years of experience in a manufacturing processes, preferably in pharmaceutical/solutions filling manufacturing environment or Bachelor Degree with a Minimum of 3+ years of experience in a manufacturing processes, preferably in pharmaceutical/solutions filling manufacturing environment.
• Bilingual (English & Spanish) 
• Drivers license category 3 or higher (applicable for Catao Logistics Center).
• Computer literate.
• Hands-on experience on computer programs, such as MS Word, Excel, PowerPoint.
• Excellent interpersonal and leadership skills with ability to interface well with other departments, andlead operators effectively and efficiently in a team environment.
• Ability to manage multiple priorities in a manufacturing plant setting.
• Strong writing skills and ability to prepare reports, write business correspondence and proceduremanuals in English.
• Able to effectively prepare and present information and respond to questions.
• 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.
• Ability to follow written procedures and/or verbal instructions communications by phone, fax or shortwave radios.

Physical Demand:

• Medium Work: Exerting 20 to 50 pounds of force occasionally, and/or 10 to 25 pounds of force frequently, and/orgreater than negligible up to 10 pounds of force constantly to move objects. Physical demands requirements are in excess of those for Light Work.

 
 
At SPECTRAFORCE, we are committed to maintaining a workplace that ensures fair compensation and wage transparency in adherence with all applicable state and local laws. This position’s starting pay is: $ 15.50/hr.