Jobs in Maunabo, PR

Job Description Se habla español. Para aplicar en español, haga clic trabajos.compassgroupcareers.com(opens in a new tab). We have an opening for full time JANITOR positions. Note: online applications accepted only. Schedule: Full time schedule. Days and hours may vary. More details upon interview. Requirement: Maintenance experience required. Fixed Pay Rate: $10.50 per hour. ESFM is the corporate Integrated Facilities Management (IFM) division of Compass Group USA and a Keystone member of the International WELL Building Institute (IWBI). We Make Applying Easy! Want to apply to this job via text messaging? Text JOB to 75000 and search requisition ID number 1459592. The advertised program is a conversational recruiting assistant that helps you apply to jobs with Compass Group. Message frequency varies. Message and data rates may apply. Text STOP to opt out or HELP for help. Terms and conditions: *************************** Skg Rooted in hospitality, ESFM elevates the workplace experience as the single source of innovative FM solutions that ensure a safe, healthy, and sustainable environment. ESFM's clients include many household names from Life Science, Technology, Oil & Gas and Manufacturing markets. ESFM self-performs 80% of all IFM solutions provided to clients. Their portfolio of service categories includes Environment, Health & Safety, Facilities Maintenance & Engineering, Sustainability, Janitorial & Industrial Cleaning, Laboratory Support and Workplace solutions. This self-performance model creates a consistent hospitality experience for clients, resulting in higher engagement and productivity from their employees. In 2020, ESFM (formerly Eurest Services) won the George Graves Award for Facility Management Achievement from the International Facilities Management Association (IFMA). Job Summary Summary: Keeps buildings clean and orderly. Performs heavy cleaning duties, including cleaning floors, shampooing rugs, washing walls and glass, and removing rubbish. Essential Duties and Responsibilities: Collects and disposes of trash following approved procedures and infection control plans. Dusts and damp mops floors following approved procedures. Moves equipment and furniture for proper cleaning and place furniture back in correct placement. Cleans assigned areas with the use of assigned materials and equipment. Sanitize all surfaces. Follows the eight-step cleaning procedure. Washes walls, windows, furniture, baseboards and other items to maintain a clean, safe environment for patients, visitors and staff. Seeks out areas requiring cleaning; takes initiative to complete the task. Completes all tasks assigned by supervisor. Performs tasks in accordance with all federal, state and county guidelines. Strips, scrubs, buffs and refinishes floors; shampoos carpet. Contributes to the team; exhibits professionalism with customers, fellow employees and others. Performs other duties as assigned. Associates at ESFM are offered many fantastic benefits. Full-time and part-time positions offer the following benefits to associates: Retirement Plan, Associate Shopping Program, Health and Wellness Programs, Discount Marketplace, Identity Theft Protection, Pet Insurance, Voluntary Benefits, including Critical Illness Insurance, Accident Insurance, Hospital Indemnity Insurance, Legal Services, and Choice Auto and Home Program Full-time positions also offer the following benefits to associates: Medical, Dental, Vision, Life Insurance/AD, Disability Insurance, Commuter Benefits, Employee Assistance Program, Flexible Spending Accounts (FSAs) Associates may also be eligible for paid and/or unpaid time off benefits in accordance with applicable federal, state, and local laws. For positions in Washington State, Maryland, or to be performed Remotely, click here for paid time off benefits information. About Compass Group: Achieving leadership in the foodservice and facility management industry Compass Group is an equal opportunity employer. At Compass, we are committed to treating all Applicants and Associates fairly based on their abilities, achievements, and experience without regard to race, national origin, sex, age, disability, veteran status, sexual orientation, gender identity, or any other classification protected by law. Qualified candidates must be able to perform the essential functions of this position satisfactorily with or without a reasonable accommodation. Disclaimer: this job post is not necessarily an exhaustive list of all essential responsibilities, skills, tasks, or requirements associated with this position. While this is intended to be an accurate reflection of the position posted, the Company reserves the right to modify or change the essential functions of the job based on business necessity. Applications are accepted on an ongoing basis. ESFM maintains a drug-free workplace. ESFM

Eaton's Electrical Sector is hiring a Plant Manager for their Assemblies & Residential Solutions (ARS) business. This position will be based in Las Piedras, Puerto Rico. Reporting to the Operations Director for the Residential and Wiring Devices Division (RWDD), the Plant Manager is responsible for driving strategic and operational leadership. This person will drive profit and loss, growth strategy and organizational direction to meet and exceed short and long-term business goals. This is a non-union site with over 400 employees. This operation is a feeder site to Eaton's assembly site in the Dominican Republic. This person will maintain a close and collaborative relation with the Plant Manager and will encourage and guarantee good communication and engagement of the team with their peers in the Dominican. The Plant Manager will drive plant performance as defined by regional and local objectives. This person has overall responsibility for all strategic and day-to-day activities impacting the Plant including Safety, Quality, Delivery, Cost and Inventory. (High 5 Metrics). This person will also maintain a workforce of highly motivated employees with a morale that is conductive to high performance with performance being measured at or above minimum acceptable levels, drive performance to achieve or exceed financial plans and strategic goals. Essential Functions: * Develop and implement local policies and procedures to meet the needs of the Eaton Business System, Values and Philosophy for both plant operations. * Drive Plant profitability through participation with Sales, Product Line Strategy Teams and Cost Out councils. * Maintain and improve employee relationships with both hourly and salaried employees. * Develop and maintain ongoing manufacturing strategy. * Develop and manage Plant Profit Plan departmental budgets * Develop and implement capital plans to support manufacturing strategy. * Monitor product quality levels and introduce and implement new programs to assure continued improvement that meets customer requirements. * Direct and coordinate the implementation of new product lines. * Direct cost estimating and cost savings programs. * Direct an R&D effort to ensure that manufacturing keeps abreast and takes advantage of the latest technology and manufacturing systems. * Active member to facilitate risk assessment at the location to identify critical EHS hazards and aspects. Works with leadership team to create targets and objectives based on key EHS risks. Required Qualifications: * Minimum ten (10) years of experience with progressive levels of accountability and responsibility in roles focused on Manufacturing, Supply Chain, Finance, OPEX and/or related support functions in a manufacturing/production environment. * Lean Six Sigma and/or continuous improvement experience. * Minimum three (3) years of manager of people experience. * Fluent in English and Spanish Eaton Leadership Attributes: * Effectively drives and manages change, challenges the status quo and champions new and innovative ideas. * Demonstrates professional presence, communicates articulately and confidently. * Effectively leverages functional and cross-functional resources to solve problems, improve processes and meet objectives. * Demonstrated written, verbal, and interpersonal communications skills. * Demonstrated success in effectively and confidently providing "leadership" to employees in a constantly changing environment. Education: * An undergraduate degree is required. A Master's degree is preferred. Compensation: * Eaton recognizes this role as a critical position within the corporation and will create a compelling package consisting of a base salary, employee incentive compensation and complete benefits. Location: * This position will be based in Las Piedras, Puerto Rico About Eaton: Sustainability Report: **************************************************************************************************** At Eaton, we strive to provide compensation and benefits that attract, engage, and retain the best talent. This includes competitive pay and a variety of benefit programs for eligible employees. The expected annual salary range for this role is $169000 - $248000 a year. This role is also eligible for a variable incentive program. Please note the salary information shown above is a general guideline only. Salaries are based upon candidate skills, experience, and qualifications, as well as market and business considerations. We are committed to ensuring equal employment opportunities for all job applicants and employees. Employment decisions are based upon job-related reasons regardless of an applicant's race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, marital status, genetic information, protected veteran status, or any other status protected by law. You do not need to disclose your conviction history or participate in a background check until a conditional job offer is made to you. After making a conditional offer and running a background check, if Eaton is concerned about conviction that is directly related to the job, you will be given the chance to explain the circumstances surrounding the conviction, provide mitigating evidence, or challenge the accuracy of the background report. To request a disability-related reasonable accommodation to assist you in your job search, application, or interview process, please call us at ************** to discuss your specific need. Only accommodation requests will be accepted by this phone number. We know that good benefit programs are important to employees and their families. Eaton provides various Health and Welfare benefits as well as Retirement benefits, and several programs that provide for paid and unpaid time away from work. Click here for more detail: Eaton Benefits Overview. Please note that specific programs and options available to an employee may depend on eligibility factors such as geographic location, date of hire, and the applicability of collective bargaining agreements.

For utility services in the manufacturing area. WHAT MAKES YOU A FIT: The Technical Part: Associate Degree with two (2) years of experience in industrial mechanics within the pharmaceutical or regulated industry. Bilingual (English & Spanish). Project Management skills. Shift: 12-hour rotational shift, and according to business needs. 5:00 PM - 5:00 AM 5:00 AM - 5:00 PM Experience in: Preventive maintenance HVAC, pumps, Utilities, and HEPA certification The Personality Part: If you have excellent communication skills and aren't afraid to ask for help when you need it (in addition to your excellent Maintenance skills), this might be the job for you! Sprinkle on a love of the scientific method, teamwork, and, above all else, being ethical, and you just might have what it takes to take on this new challenge. Bring it on! AS A PIECE OF FITS, YOU WILL: (The day-to-day on the job) Execute intermediate maintenance activities or operate and monitor plant support equipment, referring to complex issues or problems. Assist the team with maintaining an up-to-date working spare parts inventory system for the equipment/systems the team is responsible for. Perform various "Housekeeping " activities (e.g., keeping work areas clean, cleaning equipment, etc.). Ensure that operational log paperwork, daily log files, and work order documentation are completed with accurate information. Provide a detailed training program to develop one's knowledge in the maintenance and operations field and other plant areas. Maintain an up-to-date cGMP training book. Develop, revise, and review related SOPs or job plans/work plans for work-related areas. Assist in the evaluation of the current maintenance procedures and recommend changes to optimize the maintenance program. Perform intermediate troubleshooting of utility, process, and HVAC-related equipment/ systems. Plan and schedule own work activities with operations staff to minimize impact on production activities. WHO WE ARE: We are a Service Provider company different from the rest. We pride ourselves in how we treat the most important piece of our company's puzzle: you! We integrate Engineering, Construction, Maintenance, Utilities and Specialized Technical services across the Island (and in the US as well!). Our company is flexible, family-oriented and focused on our resources' well-being, while providing our Pharmaceutical, Medical Device and Manufacturing industry clients with top-notch quality talent. We're FITS! Are you the next piece?

Responsible for the efficient operation of the plant calibration program, including the performance of the calibrations, maintaining and repair of Manufacturing and Laboratory Instruments, filling/organize calibration documents, and distributing the calibration documents to the affected parties. Will also be responsible for maintaining the utility equipment, will include the preventive maintenance and repair of these systems to maintain them in good operation. Will also keep a minimum stock of spare parts required for the Laboratory Manufacturing & instrument equipment. Other duties related to technical support may be assigned. Job Description We are the makers of possible BD is one of the largest global medical technology companies in the world. Advancing the world of health is our Purpose, and it's no small feat. It takes the imagination and passion of all of us-from design and engineering to the manufacturing and marketing of our billions of MedTech products per year-to look at the impossible and find transformative solutions that turn dreams into possibilities. We believe that the human element, across our global teams, is what allows us to continually evolve. Join us and discover an environment in which you'll be supported to learn, grow and become your best self. Become a maker of possible with us. DUTIES AND RESPONSIBILITIES * Will maintain the documentation related to the calibration program, including certificates, reports, and Out of Tolerance conditions on automatic, mechanical, and electrical instruments or equipment. Will also follow calibration related procedures. * Will be responsible for the information loaded and retrieved from the calibration software in order to maintain the system fully operational. * Will support the utilities maintenance systems, will perform repairs and preventive maintenance to the systems * Perform Preventive Maintenance (PM) to the assigned equipment following the procedure. * Coordinate all PM's Programs with each Supervisor as to the time when the work can be performed. * Diagnose the sources of malfunction in both mechanical and electrical components of equipment or instrument; disassemble to repair or replace defective parts. * Check inventories to assure those required repair parts are available prior to shutting down equipment to perform repair or preventive maintenance. * Maintain equipment logbooks on all instrument equipment or tasks. * Maintain proper procedure of clean-up tools while performing duties in the production or facilities areas. * Interpret and work with blueprints, drawings, schematics, layouts, diagrams, written specifications and/or oral instructions in diagnosing and fixing equipment malfunction using various measuring and test instruments. * Observes and enforces QSR, Safety Laws, ISO requirements and Company Policies. * Inform supervisor of any improper equipment usage, hazardous situation, or potential safety risk. * Identify and inform operational problems, equipment malfunctioning and recommend on the improvement or replacement of the concerned equipment, part or section. * Stays up to date on the fundamental requirements for alignment in own area of work and aligns with those requirements. Participates as required in training on regulatory issues affecting own area of work. Brings regulatory compliance questions/issues to the attention of management. * Promotes a safe work environment. May provide recommendations on maintaining the safety of the work environment. Participates in Environmental Health and Safety programs. Addresses corrective actions whenever a hazard is identified. Notifies supervisor of all observed hazardous conditions or unsafe work practices. * Provide recommendations to support systems that continuously improve product/process quality and product availability, reduce cost, and increase production capability. * To assist the Calibration Area in handling and completing BMRAM or SAP data entry promptly. * To support in maintain a minimum inventory of spare parts of Lab Instruments and production machinery, keep backup of critical instruments to support the manufacturing and Laboratory operations as required. * To offer technical assistance as needed in fixing Manufacturing and lab equipment as needed. * Performs other related duties and assignments as required. KNOWLEDGE AND SKILLS * Instrument calibration knowledge including pneumatics, electronics. * Demonstrated ability to perform diligent work with a high degree of accuracy. * Demonstrated ability to follow established policies and procedures. * Effective oral and written communication skills. * Effective organization and planning skills. * Effective analytical, quantitative, and problem-solving skills. * Effective interpersonal skills. * Bilingual, fluent in English and Spanish, oral and written. * Hands-on experience in computer systems including Word, Excel, e-mail, and similar software. * Must be capable of prioritizing and working with minimum supervision in a results-oriented environment. * Good interpersonal skills. * Knowledge of GMP, QSR or ISO requirements. * Ability with reading and interpreting drawings, operational/maintenance manuals and parts breakdown diagrams. * Attendance and punctuality are an essential function of the job position. EDUCATION & EXPERIENCE * Requires an Associate/Technical Degree in Industrial Mechanics, Engineering Technology, Instrumentation or similar academic background, or combination of academic background stated above and a minimum of five (5) years of previous experience as Technician or a similar position, within a manufacturing organization, preferably in a Medical Device, Pharmaceutical Biotechnology company related industry or similar academic background, or combination of academic background stated above and proven experience. * Experience with laboratory instrument calibration (i.e.: HPLC). * Basic experience in management of spare parts supply, and programmable controllers (PLC's). At BD, we prioritize on-site collaboration because we believe it fosters creativity, innovation, and effective problem-solving, which are essential in the fast-paced healthcare industry. For most roles, we require a minimum of 4 days of in-office presence per week to maintain our culture of excellence and ensure smooth operations, while also recognizing the importance of flexibility and work-life balance. Remote or field-based positions will have different workplace arrangements which will be indicated in the job posting. For certain roles at BD, employment is contingent upon the Company's receipt of sufficient proof that you are fully vaccinated against COVID-19. In some locations, testing for COVID-19 may be available and/or required. Consistent with BD's Workplace Accommodations Policy, requests for accommodation will be considered pursuant to applicable law. Why Join Us? A career at BD means being part of a team that values your opinions and contributions and that encourages you to bring your authentic self to work. It's also a place where we help each other be great, we do what's right, we hold each other accountable, and learn and improve every day. To find purpose in the possibilities, we need people who can see the bigger picture, who understand the human story that underpins everything we do. We welcome people with the imagination and drive to help us reinvent the future of health. At BD, you'll discover a culture in which you can learn, grow, and thrive. And find satisfaction in doing your part to make the world a better place. To learn more about BD visit ********************** Becton, Dickinson, and Company is an Equal Opportunity Employer. We evaluate applicants without regard to race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, and other legally-protected characteristics. #earlycareer Required Skills Optional Skills . Primary Work Location USA PR Cayey - Vicks Drive (BDB) Additional Locations Work Shift PR 200pm-1030pm M-F (United States of America)

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. Responsibilities: Create Environmental reports. Conduct inspections and enforce adherence to laws and regulations governing the health and safety of individuals. Implement and evaluate programs designed to limit chemical, physical, biological, and ergonomic risks to workers. Participate in SEPC reviews, routine environmental inspections, audits, assessments, and incident investigations, making appropriate recommendations. Conduct audits at hazardous waste sites or industrial sites and participate in hazardous waste site investigations. Conduct environmental training and education programs and demonstrate the use of safety equipment. Coordinate "right-to-know" programs regarding hazardous chemicals and other substances. Inspect and evaluate workplace environments, equipment, and practices, to ensure compliance with safety standards and government regulations. Examines credentials, licenses, or permits to ensure compliance with licensing requirements. Prepare Construction Permits, Air Permits and Título V applications. Verify Air Emissions data and calculations Prepare necessary emissions assumptions and calculations to support permitting and regulatory compliance Implement strategies for air condensers monitoring Validation of tanks throughput tanks data Projects Inspections Other responsibilities as assigned by supervisor/management, and/or client. Requirements/Education: Technical College Science Degree as a minimum BS / BA in Sciences/Environmental or related fields preferred. 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.

Develop, implement, and manage environmental and safety programs in compliance with federal, state, and local regulations. Monitor and report on pollution prevention, waste management, and compliance auditing activities. Conduct EHS impact assessments for new construction projects, process changes, and permit modifications. Review and interpret environmental documentation issued by regulatory agencies (EPA, OSHA, PR Environmental Quality Board). Evaluate proposed regulations and determine their financial, operational, and environmental implications. Serve as the company liaison with regulatory agencies, resolving compliance issues and supporting audits. Develop and deliver employee training programs on environmental, health, and safety topics. Lead incident investigations and ensure appropriate corrective and preventive actions are implemented. Promote continuous improvement and employee engagement through proactive EHS initiatives and safety leadership. *Other duties may be assigned.* Requirements Education and Experience Requires a Bachelor Degree and a minimum of 4 years of relevant experience, or an Advanced degree with a minimum of 2 years of relevant experience. Key Experience Areas 1. EHS Programs and Regulatory Expertise Proven experience managing EHS programs within a manufacturing environment. Hands\-on experience in Lockout\/Tagout (LOTO), Electrical Safety, and Waste Management programs. 2. Regulatory Compliance and Risk Management Strong knowledge of OSHA, EPA, DOT, and local Puerto Rico environmental regulations. Skilled in conducting risk assessments, ergonomics reviews, and safety audits in regulated environments. Demonstrated experience in developing and executing CAPA to resolve EHS findings. 3. Leadership in Safety Culture and Continuous Improvement Ability to influence and coach leadership at all levels to foster a proactive safety culture. Proven track record in leading EHS training programs and driving employee engagement. Experience using data analytics and metrics to enhance environmental performance and safety outcomes. "}}],"is Mobile":false,"iframe":"true","job Type":"Full time","apply Name":"Aplicar ahora","zsoid":"6314569","FontFamily":"Arial, Helvetica, sans\-serif","job OtherDetails":[{"field Label":"Industry","uitype":2,"value":"Manufacturing"},{"field Label":"City","uitype":1,"value":"Juncos"},{"field Label":"State\/Province","uitype":1,"value":"Juncos"},{"field Label":"Zip\/Postal Code","uitype":1,"value":"00777"}],"header Name":"Sr. EHS Specialist","widget Id":"118922000006310086","is JobBoard":"false","user Id":"118922000000026001","attach Arr":[],"custom Template":"1","is CandidateLoginEnabled":true,"job Id":"118922000017183001","FontSize":"15","location":"Juncos","embedsource":"CareerSite","indeed CallBackUrl":"https:\/\/recruit.zoho.com\/recruit\/JBApplyAuth.do","logo Id":"nrt0md43109f3de4c490e9975771d2b120574"}

Job Description PharmEng Technology has been providing quality services to leading manufacturers of healthcare and pharmaceutical products since 1997. Our specialists hold expertise in Commissioning & Qualification, Validation, Quality Systems, Regulatory Affairs, Engineering, and Training to ensure that our clients can keep on providing the world with their cost-effective and high-standard healthcare products. At PharmEng Technology, we strive to cultivate the best working environment where empowerment, passion and perseverance are nurtured while serving our clients to achieve their unique business goals. Data integrity specialists are responsible for ensuring that data is accurate and consistent across an organization. They commonly work with databases or other large pools of information, looking for errors or inconsistencies that may have been introduced during the collection, storage, or transmission process. Responsibilities Ensure the accuracy and completeness of data across multiple platforms through analysis, auditing, and reporting. Develop and maintain data integrity policies and procedures in alignment with organizational goals. Conduct regular audits of data to identify errors, discrepancies, or missing information. Investigate root causes of data issues and work with relevant teams to resolve them. Generate reports on data integrity findings for internal and external stakeholders. Keep abreast of new developments in data management and data integrity best practices. Train staff on data integrity procedures and policies Assist with the development and implementation of data governance framework. Monitor compliance with data integrity policies and procedures. Escalate non-compliance issues to senior management as needed. Maintain up-to-date knowledge of relevant laws, regulations, and industry best practices. Perform other duties as assigned. Required Skills and Qualifications Bachelor's degree in computer science, information technology, or related field 3-5 years professional experience working with Data Integrity Experience developing and implementing data quality control processes. Exceptional attention to detail and strong analytical skills Ability to work independently and as part of a team. Proficient in Microsoft Excel and Access

Job Description Type: Full Time Overtime Exempt: Yes Reports To: ARMADA HQ Travel Requirement: YES, nationwide to support onsite credentialing operations as mission needs require. Security Clearance Required: N/A *************CONTINGENT UPON AWARDING OF GOVERNMENT CONTRACT******** Credentialing Specialists will provide credentialing service and support to operate IRS credentialing sites utilizing the GSA scheduling tool to manage credentialing appointments, run reports through the USAccess system, and use credentialing equipment to conduct post issuance and enrollment activities. These duties and responsibilities include, but are not limited to the following: Duties & Responsibilities: The Credentialing Specialists shall: View, manage, and check daily appointments in time trade scheduling tool Credentialing Specialists shall perform enrollment and Issuance of Identification Cards to include PIV/Smart IDs, Access Cards, PAC Cards, issue and activate SmartID Cards, Perform Certificate Rekey, Pin Reset, and Card Update Credentialing Specialists shall perform card inventory and log cards on the Credential Inventory Tool (CIT) Store cards in a lockable container (file cabinet) Credentialing Specialists shall contact employees and contractors to schedule pick-up and activate SmartID Credentialing Specialists shall issue PAC Cards and Access Cards Issue Pocket Commission Credentials Collect SmartID Cards and PAC Cards; return terminated credentials to the Security Officer for destruction Credentialing Specialists shall keep a log of Cards issued and collected Perform Registrar and Activator duties as required Credentialing Specialists shall perform Card Custodian duties Credentialing Specialists shall mail SmartID Cards to Light Activation Kit Operators Applicant Communications regarding credential status Credentialing Specialists shall take photo, capture digital signatures, and assemble Pocket Commission inserts, and other ID Media duties as directed by ICAM Credentialing Specialists shall perform IRS credentialing functions and may be required to travel up to 40% of their annual work hours to support IRS credentialing and activation efforts. Short-term shiftwork to support the standard workday, night shift and weekend hours, shall be required Other duties as assigned. Knowledge, Skills, and Abilities (KSAs): Ability to complete required online credentialing training and maintain compliance with PIV-II SmartID credential requirements. Knowledge of ICAM and USAccess credentialing processes, including enrollment, activation, and verification procedures. Ability and willingness to travel nationwide to support onsite credentialing operations as mission needs require. Knowledge of credentialing hardware such as FCUs, MCUs, and LAKs. Knowledge of PII handling and federal credentialing policies. Skill in managing daily credential operations, workstations and equipment. Strong customer service and communication skills. Skill in preparing and submitting daily site reports. Strong attention to detail and documentation accuracy. Ability to follow federal credentialing standards and procedures. Minimum/General Experience: Experience with or ability to complete USAccess Registrar and Activator training or a comparable credentialing program. Experience preparing, reviewing, and submitting required reports and documentation in accordance with established procedures. Ability and willingness to travel nationwide to support onsite credentialing operations as mission needs require. Minimum Education: High School Diploma, or equivalent Disclaimer: The above information has been designed to indicate the general nature and level of work to be performed. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities, and qualifications required of the contractor assigned to this position. Applying: If you feel you have the knowledge, skills and abilities for this position visit our careers page at ****************** Special Notes: Relocation is not available for these jobs. ARMADA provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, gender, sexual orientation, gender identity or expression, national origin, age, disability, genetic information, marital status, amnesty, or status as a covered veteran in accordance with applicable federal, state and local laws. ARMADA complies with applicable state and local laws governing non-discrimination in employment in every location in which the company has facilities. This policy applies to all terms and conditions of employment, including, but not limited to, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training. Must be able to successfully pass a background check, and pre-employment drug testing. Job offers are contingent upon results of background check and drug testing.

The smartphones industry is looking for a promoter to support sales and implement and maintain their promotional material and equipment in-stores. If you are passionate person, focused in customer service and sales, this opportunity is for you! Job Responsabilites: Go to the right stores following the established itinerary Manage in-store displays (maintain “perfect store” standard): keep display clean and in recommended alignment, display pop material, enhance display of iconic products, seek new in-store display opportunities, and negotiate better display areas Build strong interpersonal relationships with the store manager and salespeople Generate and submit quantitative and qualitative reports on time and accurately Transfer product knowledge and service skills to store staff Execute promotions to customers and store vendors according to the indications given by the brand Job Requirements: Proven experience in visual marketing Ability to use promotional material following the guidelines Proven experience in customer service Basic knowledge of MS Office Strong teamwork spirit Excellent communication skills Ability to work autonomously, managing your own time and schedule Accustomed to working based on objectives (KPIs) Availability to travel, own car and valid license Required Availability: Monday to Saturday 8:00am - 6:00pm Route: Municipalities you may visit: From Humacao - San Lorenzo - Juncos - Carolina - Canóvanas - Fajardo Compensation: Base pay: $13.00 per hour, full time Monthly incentives based on KPIs metrics Car allowance Cellular Service TPIS is an Equal Opportunity Employer (EEO Employer/Affirmative Action for Women/Disabled/Veterans). We comply with all federal, local and state laws regarding non-discrimination) Required Availability: Monday - Saturday 8:00am - 6:00pm

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, PR, Boston, MA & San Francisco, CA and we serve life sciences clients in six global markets: United States, Puerto Rico, Dominican Republic, Mexico, Germany, Canada, and South America. Essential Functions: The GMP Cleaning and Sanitization Technician is responsible for providing facility/equipment cleaning, and sanitization, in support of GMP manufacturing and technical areas. All work to be completed to assure minimal impact to production while aligning with Standard Operating Procedure's (SOP's), Current Good Manufacturing Practices (cGMP's) and client/site facilities regulations. You will be asked also to perform housekeeping activities such as keep clearing work areas, equipment, facility, utility, mezzanine and office areas in addition to keep process and results documents up-to-date. You will also assist the team with maintaining an up-to-date working inventory for the equipment/supplies that the team is responsible for to ensure everything runs smoothly. Responsibilities: Complete all cleaning/sanitization of the manufacturing and technical areas and equipment (outside), as required. Coordinate with clients to ensure environmental support activities are performed with no delay to production. Communicate with partners, as required, to complete tasks. Maintain an up-to-date working inventory for the equipment/supplies. Document and review appropriate paperwork, daily logs, files, and work order documentation per Good Documentation Practices. Will also be responsible for documenting and entering data into applicable GMP forms, including electronic records. Provide on-the-job training for new staff. Plan and schedule collaboration activities with production staff to minimize impact to production activities. All work must be completed in accordance with Code of Federal Regulations(CFR's), cGMPs, SOPs, and Amgen policies. Ability to work in an environment where cleaning products are used (i.e., bleach, isopropyl, sporicidal, and other disinfectants) Perform moderately physical activities for up 2-3 hours and the ability to lift 25 lbs. Ability to work all shifts in support of 7/24 operations Perform various "Housekeeping" activities. (i.e. keeping work areas clean, cleaning of equipment exterior, facility, utility, mezzanine and office areas). Participate in a detailed training program in order to develop one's knowledge in the cleaning and other areas of the plant. Prepare, handle and dispense chemicals for cleaning and sanitization with required PPE. Responsible for labeling, storage, movement and disposition of cleaning materials. Assist the Group Leader or Supervisor in performing regular building areas inspections regarding cleaning and sanitization activities. Follow the process to remove trash, recyclables, garments, biowaste, garbage from facilities, and move them into proper containers. Qualifications Requirements/Knowledge/Education/Skills: Associate's degree and 4 years of hands-on leadership experience within manufacturing facilities environment or other related field OR High school diploma / GED and 6 years of hands-on leadership experience within manufacturing facilities environment or other related field. Experience working in a cleanroom environment is highly preferred. Experience in Current Good Manufacturing Practices (cGMP) and Good Documentation Practices (GDP) is required. Computer Software Skills: Microsoft office (Word, Excel, Outlook) in a beginner to intermediate level. Work in a team environment with the flexibility to work shifts as scheduled (weekends, holidays as required) Excellent interpersonal and communication skills. - Intermediate Intermediate math skills with an ability to calculate with percentages and decimals is required. Ability to understand and interpret both written and oral communication in English is a plus. The COVID-19 vaccine is / may be a condition of employment. Physical Requirements and Working Environment: No make-up, nail polish, and/or jewelry may be worn in the GMP process areas. Ability to fully gown including head covering, facemask, gloves, plant shoes, safety glasses/goggles and/or face shield. Ability to wear PPE face covers for pandemics compliance when required. Ability to wear full face respiratory protection including PAPR as applicable. 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. 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. 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.

The Licensed Pharmacist is responsible for ensuring compliance with all applicable pharmaceutical regulations, Good Manufacturing Practices (GMP), and company policies. This role oversees the proper handling, storage, and distribution of pharmaceutical products, guarantees adherence to regulatory requirements, and serves as the primary liaison with health authorities. The Pharmacist -in -Charge ensures that all operations maintain product integrity, patient safety, and legal compliance. Key Responsibilities: Act as the Pharmacist -in -Charge for the site, maintaining an active professional license in accordance with local regulations. Ensure compliance with FDA, EMA, ICH, and local health authority requirements. Oversee the receipt, storage, and dispensing of raw materials and finished products. Review and approve batch records, labeling, and documentation for accuracy and compliance. Monitor and enforce adherence to GMP, SOPs, and quality standards throughout the facility. Participate in audits and inspections, providing documentation and regulatory expertise. Train and mentor staff on pharmaceutical regulations and best practices. Manage controlled substances in compliance with legal and regulatory requirements. Support validation, quality control, and regulatory submissions as needed. Requirements Bachelor's or Doctor of pharmacy degree (PharmaD) from an accredited institution. Active Pharmacist license in good standing. Minimum 5 years of experience in a pharmaceutical manufacturing or regulatory environment. Strong knowledge of GMP, regulatory compliance, and quality systems. Excellent organizational, communication, and leadership skills.

mirus Consulting Group is a local company based in Humacao, Puerto Rico that provides computer system validation and information technology consulting services to pharmaceutical companies and other organizations across the Island and parts of the United States. Its services include the assessment and validation of automation equipment, network infrastructures and business processes, as well as the involved project management. Job Description Independently provides and/or directs the characterization of process optimization strategies and/or troubleshooting of operational issues in the operations, manufacturing, pilot plant or capital projects environment. Applies advanced and diverse engineering principles to the design and implementation of major system modifications, experiments, process and/or capital projects. Develops, organizes, analyzes and presents interpretation of results for operational issues or engineering projects of significant scope and complexity Complete complex or novel assignments requiring development of new and/or improved engineering techniques and procedures. Develop engineering policies and procedures that affect multiple organizational units. Supervise, coordinate and review work of a small staff of engineers, associates and/or technicians on an ongoing basis as well as on a project basis. Employ advanced engineering techniques and/or modifications of advanced techniques within area of engineering expertise. Apply knowledge of engineering principles and practices outside of area of discipline expertise to broad variety of assignments in related fields. Serves as a peer-recognized engineering technology specialist in at least one area, with overall responsibility for determining methodologies in that area. Application of mature engineering knowledge in planning and conducting projects. Other functions may be assigned Design Engineering: Develop technical solutions to complex problems requiring the regular use of ingenuity and creativity. Work with research, manufacturing, process development, utilities, facilities, quality assurance and validation departments in developing requirements and recommendations for large and/or highly complex system/facility modifications Work with project managers to complete design and engineering projects within schedule, budget and quality constraints. Coordinate the work of consultants, architects and engineering firms on development of standard design documents. Develop departmental budgets or project budgets encompassing multiple disciplines for area within project or entirety of smaller project Preferred Qualifications Validation Life Cycle (IQ, OQ PQ) Documentation Change control Commissioning & Decommissioning Previous experience in Characterization Bachelors Degree in Mechanical Engineer or Electrical Engineer. This Company is an equal employment opportunity employer. We adhere to a policy of making employment decisions without regard to race, color, religion, sex, sexual orientation, national origin, citizenship, age or disability. We assure you that your opportunity for employment with this Company depends solely on your qualifications.

Clorox is the place that's committed to growth - for our people and our brands. Guided by our purpose and values, and with people at the center of everything we do, we believe every one of us can make a positive impact on consumers, communities, and teammates. Join our team. #CloroxIsThePlace Your role at Clorox: The Plant Maintenance Leader coordinates and supervises Clorox Puerto Rico's plant maintenance, facilities, utilities, and manufacturing engineering programs to ensure high equipment reliability and extend asset life across all facilities, grounds, and structures. The role also leads specialized and complex plant-wide engineering initiatives supporting critical systems, operations, and maintenance activities, applying both standard and advanced engineering principles to identify root causes and develop permanent solutions. In this role, you will: Maintenance & Reliability Leadership * Develop and implement an effective preventive, predictive, and reliability-based maintenance program, including work orders and spare parts management, using World Class Organization (WCO) methodologies. * Lead the plant's Maintenance function, ensuring the reliability and efficiency of equipment and facilities. * Drive improvement of maintenance skills across team members; promote a strong reliability and safety culture. * Lead the preventive maintenance system, ensuring operational predictability and sustainable performance. Engineering, Projects & Capital Management * Supervise the Engineering function, providing technical guidance and ensuring alignment with standards and business needs. * Lead, implement, and support plant engineering projects, improvements, and the Capital Plan using internal and external resources. * Lead the Master Site Plan, making sure it follows the capital projects, space utilization, and future expansion needs. * Define scope, schedule, budget, and resources for each project, actively identifying and mitigating project risks. * Prepare and be responsible for the annual and 3-year capital program; review all AFEs (Authorization for Expenditure) for transparency and validated business justification. * Ensure project execution meets deadlines, budget, and quality standards, coordinating with Technical Project Managers as needed. * Maintain ongoing communication with OEMs regarding major equipment and technology decisions. * Lead construction/contractor safety programs to ensure full regulatory compliance. Operations, Vendor Management & Site Support * Supervise plant facility management, including security, utilities, safety systems, and required permits. * Collaborate with suppliers and contractors to ensure compliance with service agreements and secure favorable cost, delivery, and performance terms for NGSS-related purchases. * Coordinate engineering support for productivity, cost reduction, environmental compliance, safety, and new product initiatives. * Prepare periodic reports on project status, maintenance activities, and resource utilization following Clorox standards. * Provide quarterly SAP updates on planned spending, cash flow forecasts, and one-time expense estimates. Leadership & People Development * Serve as part of the Plant Leadership Team, under the direction of the Plant Manager, and contribute to strategic planning using the Engineer's Guide to Career Development. * Lead and develop maintenance personnel through coaching, performance management, and capability building (PMP, Objectives, IDP, career discussions). * Mentor and coach engineering personnel, including those not reporting directly to the role. * Assign work, evaluate performance, and ensure alignment with individual and team objectives. * Communicate technical priorities optimally across the plant. Documentation, Standards & Asset Management * Own and govern plant user documentation, ensuring it is current, accurate, and aligned with company standards. * Develop a regular revision schedule for technical documents and maintain the Facility Improvement Plan (FIP) with a 3-5 year horizon. * Ensure availability, operation, and life-cycle management of critical equipment and facilities; provide asset retirement recommendations. * Drive plant equipment standardization and secure approvals for modifications from the Platform Team. Safety, Compliance & Standards * Ensure full compliance with Clorox and regulatory requirements related to safety, security, health, and the environment-including maintenance practices, inspections, training, and record-keeping. * Actively partner with Operations to support safety programs, metrics, and continuous improvement. * Review and provide feedback on engineering work to ensure alignment to Clorox Engineering Standards and safety/regulatory requirements. What we look for: * Bachelor's degree in Mechanical, Electrical, or Industrial Engineering (PE license preferred). * At least 5 years of experience in a Maintenance Coordinator role within a manufacturing environment, with a strong focus on preventive and corrective Maintenance. * Experience in Engineering Projects Management and Facilities Management. * Strong leadership, coaching, and team-building skill. * Excellent planning, organizing, analytical, and problem solving abilities * Effective interpersonal and communication skills (written and verbal). * Ability to work in a dynamic environment and handle multiple priorities * Bilingual proficiency in Spanish and English. * Ability to resolve technical and project-related issues reliably and proactively. * Collaboration skills and the ability to navigate interdepartmental challenges constructively. Our values-based culture connects to our purpose and empowers people to be their best, professionally and personally. We serve a diverse consumer base which is why we believe teams that reflect our consumers bring fresh perspectives, drive innovation, and help us stay attuned to the world around us. That's why we foster an inclusive culture where every person can feel respected, valued, and fully able to participate, and ultimately able to thrive. Learn more. Benefits we offer to help you be well and thrive: * Competitive compensation * Generous 401(k) program in the US and similar programs in international * Health benefits and programs that support both your physical and mental well-being * Flexible work environment, depending on your role * Meaningful opportunities to keep learning and growing * Half-day Fridays, depending on your location Please apply directly to our job postings and do not submit your resume to any person via text message. Clorox does not conduct text-based interviews and encourages you to be cautious of anyone posing as a Clorox recruiter via unsolicited texts during these uncertain times. To all recruitment agencies: Clorox (and its brand families) does not accept agency resumes. Please do not forward resumes to Clorox employees, including any members of our leadership team. Clorox is not responsible for any fees related to unsolicited resumes.

**Join Amgen's Mission of Serving Patients** At Amgen, if you feel like you're part of something bigger, it's because you are. Our shared mission-to serve patients living with serious illnesses-drives all that we do. Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest diseases. With our focus on four therapeutic areas -Oncology, Inflammation, General Medicine, and Rare Disease- we reach millions of patients each year. As a member of the Amgen team, you'll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives. Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you'll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career. **Executive Director, Drug Substance Process Development** **What you will do** Let's do this. Let's change the world. In this vital role, you are responsible for scientific and technical leadership of Drug Substance (DS) manufacturing processes and Attribute Sciences functions at Amgen's Puerto Rico site. Oversight responsibilities span commercialization through full scale process validation and life-cycle management of processes and methods for Amgen's mammalian and microbial DS manufacturing facilities in Puerto Rico. This executive leader will work in close collaboration with Manufacturing, Engineering, Finance, Supply Chain and Quality functions to enable progressive improvements in commercial processes and analytical methods. You will have direct strategic responsibility for leading a team of 80+ scientists/engineers to support a growing portfolio with increased volumes. This position reports to the Vice President of Drug Substance Manufacturing, Amgen Manufacturing Limited (AML) and has a dotted line reporting to Vice President of Drug Substance Technologies, Process Development. **Responsibilities:** + Drug substance technology and analytical method transfer to and from the site + Process validation at scale across the two DS manufacturing plants + Drug substance and Attribute science CMC authoring activities for products, the latter in partnership with Attribute Sciences + Process monitoring activities, including real time multi-variate statistical process monitoring + Life cycle improvements in commercial process, including improvements to increase yields and reduce cost of goods manufactured + Ensure manufacturing operations are aligned with the registered process + Provide oversight and support for technical investigations + Safety and compliance of process development activities + Developing strategy, setting goals and priorities, allocating resources, monitoring project progress, and managing the organization's budget **What we expect of you** We are all different, yet we all use our unique contributions to serve patients. The executive we seek is a leader with these qualifications. **Basic Qualifications:** + Doctorate degree and 6 years of Scientific, Process Development and/or Technical Service experience OR + Master's degree and 10 years of Scientific, Process Development and/or Technical Service experience OR + Bachelor's degree and 12 years of Scientific, Process Development and/or Technical Service experience And + 6 years of managerial experience directly managing people and/or leadership experience leading teams, projects, programs or directing the allocation of resources **Preferred Qualifications:** + PhD with 15+ years technical experience or a MS with 20+ years of technical experience in the field of biochemical engineering, chemical engineering, biochemistry, or appropriate technical discipline and 10+ years of managerial experience in a cGMP environment. + Practical knowledge of the technologies related to analytical technologies, mammalian and microbial cell culture, protein purification, automation, validation and process engineering + Strong technical communication skills, both written and verbal, to interact effectively with all stakeholders + Experience in authoring marketing authorization applications + Well-recognized in the scientific community through a record of peer-reviewed publications and/or patents + Demonstrated success developing staff, including effective feedback and coaching + Demonstrated collaborative experience and ability to effectively work through others + Business acumen with track record of innovation and continuous improvement that provided strong financial benefits **What you can expect of us** As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we'll support your journey every step of the way. The annual base salary range for this opportunity in the U.S. is $268,622 - $321,865. In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include: + Comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts. + A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan + Stock-based long-term incentives + Award-winning time-off plans and bi-annual company-wide shutdowns + Flexible work models, including remote work arrangements, where possible As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease. Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation. Amgen does not have an application deadline for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position.

Job Description We are seeking an experienced Operations Director to oversee the daily operations of our Bayamn Campus. As the Operations Director, you will be responsible for ensuring the smooth and efficient functioning of all departments, while maintaining a high level of customer satisfaction. You will be expected to develop and implement strategies to improve productivity, reduce costs, and increase revenue. Your ultimate goal will be to ensure that the Bayamn Campus operates at peak performance, while maintaining the highest standards of quality and safety. Minimum Qualifications: Bachelor's degree in Operations Management, Business Administration, or a related field 5+ years of experience in operations management, with a proven track record of success Strong budgeting and financial management skills Excellent leadership and communication skills Ability to work well under pressure and meet tight deadlines Preferred Qualifications: Master's degree in Operations Management, Business Administration, or a related field Experience in restructuring and turnaround management Experience in a higher education setting Responsibilities: Develop and implement operational policies and procedures to ensure the efficient functioning of all departments Manage and oversee the budgeting and forecasting processes, ensuring that financial targets are met Identify areas for cost reduction and implement strategies to achieve savings Oversee facilities management, ensuring that all buildings and equipment are well-maintained and meet safety standards Ensure a high level of customer satisfaction by monitoring and improving service delivery Skills: As the Operations Director, you will be using your skills in operations management, production management, budgeting, budget management, forecasting, cost reduction, facilities management, and customer satisfaction on a daily basis. You will be responsible for ensuring that all departments are functioning efficiently and effectively, while maintaining a high level of customer satisfaction. Your ability to lead and communicate effectively will be critical to your success in this role. “Patrono con Igualdad de Oportunidades en el Empleo y Acción Afirmativa para Mujeres, Veteranos y trabajadores/as con Discapacidad”.

Job Description Validation & Engineering Group, Inc. (V&EG) is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services. We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position: CQV Lead - Upstream & Downstream Biotech Process Equipment The CQV Lead will be responsible for overseeing all commissioning, qualification, and validation activities related to upstream and downstream process equipment in a biotech GMP manufacturing facility. This includes strategic planning, resource coordination, protocol development, execution oversight, and stakeholder engagement across the CQV lifecycle. The role requires a strong technical background in cell culture and purification systems, as well as leadership experience in cross-functional environments supporting project delivery, regulatory compliance, and schedule milestones. Key Responsibilities: Leadership & Project Management Lead CQV efforts for upstream and downstream equipment, ensuring alignment with overall project schedule and quality standards. Manage CQV engineers and contractors; assign responsibilities and oversee protocol development and execution activities. Represent CQV function in cross-functional meetings with QA, Manufacturing, Automation, Process Engineering, and Project Controls. Develop CQV strategy, work plans, and schedules in alignment with URS, risk assessments, and cGMP expectations. Support the resolution of deviations, non-conformances, and issues identified during commissioning and qualification. Documentation & Execution Oversight Oversee the preparation and approval of commissioning plans, IQ/OQ/PQ protocols, risk assessments, and summary reports. Ensure traceability from URS to qualification deliverables (RTM). Approve system walkdowns, punchlist resolutions, and impact assessments. Lead or support FAT/SAT coordination and vendor engagements. Compliance & Quality Assurance Ensure CQV activities are conducted in accordance with FDA, EMA, ICH Q8-Q10, ISPE Baseline Guide Vol. 5, and ASTM E2500. Collaborate with QA to ensure timely approvals of protocols and reports. Ensure all validation deliverables support readiness for regulatory inspections and PPQ readiness. Equipment in Scope: Upstream Systems: Bioreactors (single-use and stainless steel) Media preparation systems and skids Cell culture support equipment (incubators, mixing tanks) Control systems for pH, DO, temperature, agitation Seed train and expansion systems Downstream Systems: Chromatography systems (Protein A, IEX, etc.) Tangential flow filtration (TFF) skids Virus filtration/inactivation systems Centrifuges and depth filtration units Bulk hold tanks and transfer skids CIP/SIP systems interfacing with both upstream and downstream trains Qualifications: Bachelor's or Master's degree in Engineering, Biotechnology, or related Life Sciences field. Minimum 7-10 years of CQV experience in GMP biopharmaceutical manufacturing. Demonstrated experience leading CQV teams in facility startups, tech transfers, or capital projects. Strong technical knowledge of both upstream (cell culture) and downstream (purification) processes. In-depth understanding of validation lifecycle and GMP documentation. Excellent communication, coordination, and problem-solving skills. Preferred Experience: Use of electronic validation platforms (e.g., Kneat, Valgenesis). Familiarity with DeltaV, Rockwell, or Siemens PCS automation. Previous experience on large-scale biotech capital projects (greenfield/brownfield). Experience interfacing with Quality Assurance and regulatory auditors.

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: Responsible for production support engineering with respect to testing methods, procedures, and problems; device specification and yield problems; minor redesign of devices and masks; analysis of customer returns; supplier related engineering changes and optimizing device production relative to cost constraints. Assumes responsibility for device and/or internally produced or externally purchased components after transfer into high-volume production and usually responsible for entire device manufacturing operations other than wafer fabrication. May assist customer in device usage problems or customer testing of complex devices Formulates, delivers and/or manages projects assigned and works with other stakeholders to achieve desired results. The majority of time is spent delivering R&D, systems or initiatives related to new technologies or therapies - from design to implementation - while adhering to policies, using specialized knowledge and skills. Qualifications: Bachelor's degree in Engineering Entry level with experience in support or equivalent capstone experience. Can do attitude able to work with orientation and bring ideas to the table. Able to work weekend shifts and/or night shift. Shift: 3rd and 2nd Shift Quality Consulting Group, LLC 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.

Responsibilities may include the following and other duties may be assigned. TECHNICIAN SUPPORT CAREER STREAM: Works from schematics, engineering drawings and written or verbal instructions. Gathers, maintains, formats, compiles, and manipulates technical data using established formulae and procedures, and performs detailed mathematical calculations. Provides engineering support to the manufacturing line. Conducts experiments \/ tests for engineers. Collects and analyzes numeric data. Assists in the adequate disposition to non\-conforming product\/material (P.R.B.). Requirements Associate Degree in Electronics, Mechanical, Engineering Technology, or related field). 0\-2 years of experience Knowledge in Non\-Conformance Process Intermediate knowledge in English Computer knowledge Willing to work 100% on\-Site. "}}],"is Mobile":false,"iframe":"true","job Type":"Full time","apply Name":"Aplicar ahora","zsoid":"6314569","FontFamily":"Arial, Helvetica, sans\-serif","job OtherDetails":[{"field Label":"Industry","uitype":2,"value":"Manufacturing"},{"field Label":"City","uitype":1,"value":"Juncos"},{"field Label":"State\/Province","uitype":1,"value":"Juncos"},{"field Label":"Zip\/Postal Code","uitype":1,"value":"00777"}],"header Name":"Technician I \- 1st & 2nd Shift","widget Id":"118922000006310086","is JobBoard":"false","user Id":"118922000000026001","attach Arr":[],"custom Template":"1","is CandidateLoginEnabled":true,"job Id":"118922000016123001","FontSize":"15","location":"Juncos","embedsource":"CareerSite","indeed CallBackUrl":"https:\/\/recruit.zoho.com\/recruit\/JBApplyAuth.do","logo Id":"nrt0md43109f3de4c490e9975771d2b120574"}

For Project Management services in the Manufacturing and Engineering area. WHAT MAKES YOU A FIT: The Technical Part: Bachelor's Degree in Engineering or related field and at least eight (8) years of previous exposure to Project Management activities within the regulated industry. Bilingual: (Spanish and English) Shift: Administrative & according to business needs Experience in: Capital project management Regulatory compliance (cGMP/cGLP/cGCP) Engineering coordination Contractor supervision Cost estimation & scheduling The Personality Part: Our Next Piece is someone who treats everyone they meet like family, especially our resources, clients and team members. In other words, being a customer service pro is one your (many) talents. Being the Piece means you're full of bright ideas and eager to innovate, always bringing top-quality results to the table. Are you ready to take on this new challenge? AS A PIECE OF FITS, YOU WILL: (The day-to-day on the job) Lead execution of assigned capital projects, ensuring timely documentation and alignment with site processes and systems. Ensure all activities comply with company policies, SOPs, values, and global regulatory standards. Manage multi-disciplinary projects from concept to completion, supporting site operations and business needs. Apply engineering principles to identify and resolve technical issues during project execution. Promote and enforce safety and cGMP compliance across all project phases and work environments. Oversee design development, including selection and coordination with A&E firms and internal stakeholders. Facilitate design reviews, meetings, and documentation of team decisions. Prepare and track project estimates, forecasts, schedules, and cost reports. Manage contractor activities, including bid reviews, inspections, and compliance with safety and quality standards. Provide technical support to site operations through investigations, assessments, and design input. WHO WE ARE: We are a Service Provider company different from the rest. We pride ourselves in how we treat the most important piece of our company's puzzle: you! We integrate Engineering, Construction, Maintenance, Utilities and Specialized Technical services across the Island (and in the US as well!). Our company is flexible, family-oriented and focused on our resources' well-being, while providing our Pharmaceutical, Medical Device and Manufacturing industry clients with top-notch quality talent. We're FITS! Are you the Next Piece?