Environmental Maintenance Services Supervisor- Tercer Turno, Juncos

MENTOR Technical Group Corporation; Juncos (PR); On-site; USD 70,000 - 90,000; Full time

Job summary

MENTOR Technical Group Corporation in Juncos, Puerto Rico, is looking for candidates with at least five years of experience in manufacturing or quality roles in the Pharmaceutical industry. The position requires strong leadership skills, bilingual communication in Spanish and English, and proven technical knowledge. Candidates must be willing to work irregular hours and be adept in GMP cleaning activities and environmental monitoring.

This role promises a dynamic work environment with opportunities for personal and professional growth.

Qualifications

• 5+ years experience in manufacturing or quality role in Parenteral or Pharmaceutical industry.
• 2 years experience in GMP Cleaning or Environmental Monitoring.
• Proven technical knowledge in environmental monitoring programs.
• Knowledge of cGMP, GLP, and FDA regulations.
• Fully bilingual in Spanish and English with excellent writing skills.
• Strong leadership, planning, and organizational skills.

Responsibilities

• Ensure compliance with aseptic operations and sterilization processes.
• Execute GMP cleaning activities in a Clean Room environment.
• Provide supervision and leadership in a manufacturing setting.
• Interact with stakeholders at all levels to communicate technical information.
• Analyze data related to environmental monitoring and detect deviations.

Skills

Bilingual Communication (Spanish/English)

Leadership Skills

Time Management

Technical Writing

Judgment and Decision-Making

Interpersonal Skills

Education

Experience in Manufacturing or Quality Role in Parenteral or Pharmaceutical Industry (5+ years)

Experience in GMP Cleaning Activities

Supervisory/Managerial Experience (5+ years)

Tools

Microsoft Office Suite (Word, Excel, Power Point)

Laboratory Management System (LIMS)

Particle Analyzers

Job description

Mentor Technical Group (MTG) provides a comprehensive portfolio of technical support and solutions for the FDA-regulated industry. As a world leader in life science engineering and technical solutions, MTG has the knowledge and experience to ensure compliance with pharmaceutical, biotechnology, and medical device safety and efficacy guidelines. With offices in Caguas, Puerto Rico, and Boston, United States, we serve life sciences clients in six global markets: United States, Puerto Rico, Dominican Republic, Mexico, Germany, Canada, and South America.

Job Description

• At least five (5) years of directly experience in a manufacturing operation or quality role in Parenteral or Pharmaceutical Industry
• Two (2) years of experience in GMP Cleaning activities, Clean Room (preferred), and/or Environmental Monitoring
• Previous experience with five (5) years of experience in a supervisory/managerial position
• Proven technical knowledge in Parenteral or Pharmaceutical environmental monitoring program, aseptic operations, isolators, sanitization and sterilization process
• Must have knowledge in compendium requirements, cGMP, GLP, and FDA regulations and the ability to interpret and apply them
• Fully bilingual (Spanish/English) communication skills, both written and verbal. Excellent technical writing skills (English/Spanish)
• Strong leadership skills, time management, planning and organization capabilities
• Computer Literate in Microsoft Office Suite (Word, Excel, Power Point) and Laboratory Management System (e.g. LIMS) and in instrumentation such as viable and nonviable particle analyzers, among others
• Strong sense of urgency
• Judgment and decision-making skills
• Knowledge in environmental, health and safety matters as it relates to the site operation
• Knowledge and experience on manufacturing and sterility isolators is highly preferred
• Excellent interpersonal skills and the ability to interact with people at all levels
• Knowledge of industry trends & best practices related to pharmaceutical cleanrooms & environmental monitoring. Ability to analyze data, detect deviations, inconsistencies and interpret sampling test results
• Proven experience in planning/organizing, managing execution & using resources & time effectively
• Able to communicate technical information & ideas to a wide variety of audiences
• Willing to work irregular hours, rotating shifts, weekends and holidays when needed

Position Qualifications

• At least five (5) years of directly experience in a manufacturing operation or quality role in Parenteral or Pharmaceutical Industry
• Two (2) years of experience in GMP Cleaning activities, Clean Room (preferred), and/or Environmental Monitoring
• Previous experience with five (5) years of experience in a supervisory/managerial position
• Proven technical knowledge in Parenteral or Pharmaceutical environmental monitoring program, aseptic operations, isolators, sanitization and sterilization process
• Must have knowledge in compendium requirements, cGMP, GLP, and FDA regulations and the ability to interpret and apply them
• Fully bilingual (Spanish/English) communication skills, both written and verbal. Excellent technical writing skills (English/Spanish)
• Strong leadership skills, time management, planning and organization capabilities
• Computer Literate in Microsoft Office Suite (Word, Excel, Power Point) and Laboratory Management System (e.g. LIMS) and in instrumentation such as viable and nonviable particle analyzers, among others
• Strong sense of urgency
• Judgment and decision-making skills
• Knowledge in environmental, health and safety matters as it relates to the site operation
• Knowledge and experience on manufacturing and sterility isolators is highly preferred
• Excellent interpersonal skills and the ability to interact with people at all levels
• Knowledge of industry trends & best practices related to pharmaceutical cleanrooms & environmental monitoring. Ability to analyze data, detect deviations, inconsistencies and interpret sampling test results
• Proven experience in planning/organizing, managing execution & using resources & time effectively
• Able to communicate technical information & ideas to a wide variety of audiences
• Willing to work irregular hours, rotating shifts, weekends and holidays when needed

Mentor Technical Group es un empleador que ofrece igualdad de oportunidades y todos los solicitantes calificados recibirán consideración para el empleo sin importar raza, color, religión, sexo, orientación sexual, identidad de género, información genética, origen nacional, estado de veterano protegido, estado de discapacidad o cualquier otro grupo protegido por ley.

Mentor Technical Group is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, protected veteran status, disability status, or any other characteristic protected by law.