Jobs in Manat, PR

At Bristol Myers Squibb, we are inspired by a single vision - transforming patients' lives through science. In oncology, hematology, immunology and cardiovascular disease - and one of the most diverse and promising pipelines in the industry - each of our passionate colleagues contribute to innovations that drive meaningful change. We bring a human touch to every treatment we pioneer. Join us and make a difference. Position: Calibration Technician Location: Manati, Puerto Rico At Bristol Myers Squibb, we are inspired by a single vision - transforming patients' lives through science. In oncology, hematology, immunology and cardiovascular disease - and one of the most diverse and promising pipelines in the industry - each of our passionate colleagues contribute to innovations that drive meaningful change. We bring a human touch to every treatment we pioneer. Join us and make a difference. Key Responsibilities 1 .Verifies and/or calibrates instrumentation as required per current CMMS System 2.Documents Calibration process using current CMMS. 3.Revises calibration sheets to ensure proper documentation, calculation, and process completion. 4.Modifies or update CMMS documentation as required 5.Repairs instruments and equipment as required. 6.Uses several test equipment and tools (e.g. pressure, temperature indicators, etc.) 7.Contacts supplier for quote external calibration of the instrument and standards 8.Performs inventory of the standards in the calibration shop 9.Initiates, participates, and assists in resolution of quality investigations 10.Attends to all mandatory training for GMP's EHS and company Policies 11.Attends to all mandatory meetings as staff, PAT, or MAT as required. 12.Revises, improves, or creates calibration procedures based on observation or current experience. 13.Participates actively in special projects as required 14.Troubleshoots manufacturing and utility equipment 15.Participates and assist validation and qualification process 16.Writes and reviews SOP's for instruments and controls. 17.Prepares reports and keeps records on calibration inspection, testing, and repair. 18.Ensures low cost of the calibration department (Reducing overtime, implementing new ideas) 19.Plans, justify and implement cost reduction small projects. Qualifications & Experience 1. Associate degreein Electronics or Instrumentation Engineering 2.Four(4) relevant experience in calibrations of processing, utilities, and facilities equipment for a pharmaceutical manufacturing plant. Experience in parenteral areas desirable. 3.Computer literate (CALMAN/Maximo program highly desirable). 4.Knowledge of the principle of calibrations and basic principles of mechanical and electrical engineering. 5.Excellent organizational skills and sense of urgency. 6.Customer service-oriented and self-starter 7.Ability to review SOP's and operating instructions 8.Knowledge of cGMPs and regulatory agencies guidelines 9.Bilingual Spanish/English. Read, write and speak are required 10.Knowledge of computer systems 11.Solid technical writing skills related to investigation reports 12.Ability to create and organize cGMP systems procedures based on regulatory and compliance requirements 13.Should read technical English and equipment manuals 14.Ability to perform the complex mathematical calculation for sample analysis Working Conditions This is a *Third-Shift* Position. 8 Hrs. Shift BMSCO-OP Around the world, we are passionate about making an impact on the lives of patients with serious diseases. Empowered to apply our individual talents and diverse perspectives in an inclusive culture, our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues. Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Physical presence at the BMS worksite or physical presence in the field is an essential job function of this role which the Company deems critical to collaboration, innovation, productivity, employee well-being and engagement, and enhances the Company culture. To protect the safety of our workforce, customers, patients and communities, the policy of the Company requires all employees and workers in the U.S. and Puerto Rico to be fully vaccinated against COVID-19, unless they have received an exception based on an approved request for a medical or religious reasonable accommodation.Therefore, all BMS applicants seeking a role located in the U.S. and Puerto Rico must confirm that they have already received or are willing to receive the full COVID-19 vaccination by their start date as a qualification of the role and condition of employment.This requirement is subject to state and local law restrictions and may not be applicable to employees working in certain jurisdictions such as Montana. This requirement is also subject to discussions with collective bargaining representatives in the U.S. Our company is committed to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace adjustments and ongoing support in their roles. Applicants can request an approval of accommodation prior to accepting a job offer. If you require reasonable accommodation in completing this application or if you are applying to a role based in the U.S. or Puerto Rico and you believe that you are unable to receive a COVID-19 vaccine due to a medical condition or sincerely held religious belief, during or any part of the recruitment process, please direct your inquiries to adastaffingsupport@bms.com. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement. Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

At Bristol Myers Squibb, we are inspired by a single vision - transforming patients' lives through science.

Satellite Industries Application for Employment Ethical Please indicate what location you are looking to apply for and thank you for applying at Satellite Industries. Satellite Companies are smoke-free workplaces.

Experience Level: Entry Level About Actalent: Actalent connects passion with purpose.

At Bristol Myers Squibb, we are inspired by a single vision - transforming patients' lives through science.

Validation & Engineering Group, Inc.

Through our dedicated associates, Conduent delivers mission-critical services and solutions on behalf of Fortune 100 companies and over 500 governments creating exceptional outcomes for our clients and the millions of people who count on them. Have prior clerical/ customer service work experience You will help customers with their account issues while providing them with exceptional customer service.

& RESPONSIIBILITITES Accountable for the design and execution of IQ/OQ/PQ studies of process for parenteral and oral solid drug dosages products manufactured at Client's facility. Accountable for designing and executing qualification studies for sterilization/Dehydrogenation/bio-decontamination equipment (autoclaves & SIP, tunnel, isolator), utilities and facilities to support their effectiveness in the manufacture of parenteral/oral solid drug dosages products. This position must comply with all Security guidelines, Environmental Health and Safety regulations and the current Good Manufacturing Practices required for the job function. 1. Conducts process/packaging equipment installation/operational/performance qualification studies to test their functionality for the manufacture of parenteral and OSD products. 2. Conducts critical sterilization/Dehydrogenation/bio-decontamination equipment (tanks, autoclaves & SIP, tunnel, isolator), utilities and facilities qualification studies (Critical utilities/systems includes Purified Water, HVAC, compressed gases) to ensure that a system functions as to routinely produce results that meet predetermined specifications. 3. Conducts temperature/relative humidity mapping qualification studies (cold boxes, freezers, and incubators) to ensure that a system functions as to routinely produce results that meet predetermined specifications. 4. Prepares operational qualification assessments to support that validated critical operating parameters are within qualified parameters for specific parenteral and OSD products. Identify and evaluate equipment enhancements to support intended qualified operational ranges. 5. Hands on experience in the use/troubleshooting of validation equipment such as KAYE Validator, thermocouples and temperature/relative humidity data loggers. 6. Supports the evaluation of Change Controls to establish qualification assessments and performance qualification requirements during process and/or equipment modifications. 7. Supports process capability and statistical analysis related to equipment performance within parenteral and OSD manufacturing process 8. Serves as Subject Matter Expert for qualifications during regulatory audits (internal and external). 9. Supports the periodic review of equipment/system qualifications studies. 10. Assists and performs as the liaison person with the Information Technology Department in the implementation and qualification of upgraded equipment control systems and automation initiatives. 11. Prepares well-documented protocols for all equipment/utilities qualification exercises in compliance with corporate guidelines, procedures, FDA Regulations and industry current practices. 12. Executes and ensures successful and timely equipment/utilities qualification activities as per established protocol in support of the manufacturing operation at the site. 13. Executes activities according to the Time and Event schedule developed by the site team. 14. Performs in process test as required, analyze qualification data and generate conclusions based on test results and reports the results in an accurate and timely manner. 15. Performs successful and on time resolution of incidents and deviations related to equipment/utilities qualification exercises. 16. Proposes and formalizes alternatives for enhancement of site qualification program. 17. Investigates and conducts troubleshooting and root-cause analysis of unexpected trends or results during equipment/utilities qualification activities, implements accurate and timely solutions and; develop and manage plans as needed. 18. Evaluates deviations with respect to their causes and corrective actions to prevent recurrence. 19. Identifies, plans, and implements quality and productivity initiatives associated to equipment/utilities qualification activities based on business needs and priorities. 20. Assures the accuracy and correctness of documentation used during equipment/utilities qualification activities. 21. Trains manufacturing and QC/QA personnel on the qualification documentation. 22. Assures compliance to corporate guidelines and site procedures governing overall operation. 23. Maintains documentation in accordance with cGMP and FDA regulations. 24. Maintains equipment/utilities qualification program in conformance with department standards and government/corporate regulations. MINIMUM REQUIREMENTS • Bachelor Degree in Pharmacy, Chemistry or Engineering. • Five (5) years of experience in a pharmaceutical industry with at least three (3) years in solid oral dosage forms. • Proficient technical knowledge/expertise in pharmaceutical manufacturing processes/technologies and processing equipment for oral dosage forms, including packaging technologies. • Proficient knowledge of equipment/utilities qualification, continuous process improvement and troubleshooting processes. • Ability to effectively manage multiple projects at the same time with minimum supervision and to incorporate a wide array of technical principles, concepts and theories in innovative ways to equipment/utilities qualification. • Strong project management skills. • Proficient time management skills, planning and organization capabilities. • Proven ability to influence and work with people at different levels and departments. • Proven leadership & teamwork skills, self starter, results oriented and build and maintain strong relationships with multiple groups.

Since we opened our first door in 1976 with a single kiosk in Williamsville, New York, Vitamin World has been passionate about good nutrition. Maintain a professional attitude with sincerity and enthusiasm reflecting Vitamin World s commitment to our customer. Vitamin World is looking for Part-Time Store Associates for our retail store located at Plaza Rio Hondo in Bayamon, PR. All Vitamin World Employees will be vaccinated by September 20. Collaborate with the store team to support and achieve the goals of Vitamin World.

Why deliver with DoorDash Choose your own hours: When and where you work is totally up to you. Sign Up Details Requirements 18 or older Any car, scooter, or bicycle (in select cities) Driver's license number Social security number (only in the US) Final Step: consent to a background check How to sign up Click Apply Now and complete the sign up Get the app and go Earn extra money for your goals: Achieve your short-term goals or long-term dreams by driving or biking with DoorDash. What is DoorDash Available in over 4,000 cities in the U.S, DoorDash connects local businesses and local drivers (called Dashers) with opportunities to earn, work, and live.

** Our site in Manati Puerto Rico is hiring for a Quality Control Technician. **Please note that DuPont has announced the intended divestiture of a majority of its M&M business to Celanese Corporation. This includes the Engineering Polymers business; Vamac & Hytrel product lines; Microcircuit & Component Materials; and DuPont Teijin Films.

As part of the Thermo Fisher Scientific team, you'll discover meaningful work that makes a positive impact on a global scale.

Conduct virtual and on-site presentations to position the value of Aflac s products and services. Raised and donated more than $140+ million to the Aflac Cancer and Blood Disorders Center of Children s Healthcare of Atlanta. Aflac s family of insurers includes Aflac and/or Aflac New York, and/or Continental American Insurance Company and/or Continental American Life Insurance Company. World s Most Admired Companies list FORTUNE magazine named Aflac to the list for the 20th consecutive year in 2021.

• Conocimiento básico en la industria de materiales de construcción • Conocimiento en instalaciones, terminaciones, tareas generales de mantenimiento. • Conocimiento en electricidad, instalación de objetos en pared y pintura. • Gran sentido de urgencia, responsabilidad y compromiso. • Habilidad para trabajar bajo poca supervisión. • Entre otras tareas de mantenimiento. - Lunes a Viernes 8am a 5pm Powered by JazzHR YvazYBwOfC

Associates who remain unvaccinated must either undergo weekly negative COVID testing OR wear a mask at all times while in a Humana facility or while working in the field. Also visits doctors offices and elderly homes to help increase Humana presence and beneficiaries. + **COVID VACCINATION:** Humana and its subsidiaries require vaccinated associates who work outside of their home to submit proof of vaccination, including COVID-19 boosters.

* Drive employee engagement and satisfaction through promotion of a positive One Thermo Fisher company culture while balancing employee concerns with all levels of company goals.

Hilton is dedicated to continuing its tradition of providing exceptional guest experiences across its global brands . Today, Hilton remains a beacon of innovation, quality, and success. We support the mental and physical wellbeing of all Team Members, so they can Thrive, thanks to innovative programs and benefits such as workplace flexibility, career growth and development, and our Go Hilton travel discount program. Check out the Hilton Careers blog and Instagr For nearly a century, Hilton has offered business and leisure travelers the finest in accommodations, service, amenities and value. Hilton is proud to have an award-winning workplace culture, and we are consistently named among one of the World's Best Workplaces. The future of hospitality is bright at Hilton : a leading global hospitality company with a diverse portfolio of world-class brands . Hilton has been a leader in the hospitality industry. Hilton prioritizes understanding and integrating our Team Members' unique perspectives and voices-along with those of our Guests, Owners, Suppliers, and Partners-to cultivate a diverse and inclusive environment for all. Hilton is the leading global hospitality company, spanning the lodging sector from luxurious full-service hotels and resorts to extended-stay suites and mid-priced hotels. A Security Director is also responsible for the safety and security of the hotel premises. Specifically, the Security Director will perform the following tasks at the highest level of service

About RCM:RCM IT & Life Sciences is a leading provider of IT Business Solutions and Engineering Services to over 1,000 clients in the commercial and government sectors. RCM partners with clients to define implement and manage a broad range of technologies across multiple platforms, systems, and networks. Scope of JobRCM is seeking several experienced CSV and CQV consultants to support a Packaging Project for our pharmaceutical client in Manati, Puerto Rico. Job Title: CSV and CQV Consultants (Packaging and Facility)

At Bristol Myers Squibb, we are inspired by a single vision - transforming patients' lives through science.

At Bristol Myers Squibb, we are inspired by a single vision transforming patients lives through science.

Qualification Engineer / Scientist: Change Control, VP Development, & IOQ Development and Execution Validation & Engineering Group, Inc.

At Bristol Myers Squibb, we are inspired by a single vision - transforming patients' lives through science.

Validation & Engineering Group, Inc. (V&EG) is a leading services supplier 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.

Please indicate what location you are looking to apply for and thank you for applying at Satellite Shelters. Satellite Shelters Application for Employment

We're looking for a Travel MRI Technologist , working in the Healthcare Systems & Services industry in San Juan, Puerto Rico, Puerto Rico . Performing MRI diagnostic imaging procedures on appropriate anatomical regions according to department procedures and protocols. Locating and recording internal elements of the body, and identifying any anomalies indicative of disease, injury, or other medically significant conditions. Adjusting equipment and calming patient to eliminate test artifacts. Monitoring the patient for potentially dangerous physical and emotional changes. Evaluating test results for clarity and accuracy. Reviewing tests with peers and physician. Informing physicians of preliminary findings as requested according to department procedures. Distributing completed test results to physicians and service providers. Preparing diagnostic information for physician interpretation. Maintaining patient charts, entering diagnosis and billing codes, logging data into patient information systems, and updating file systems for tests performed. Cleaning and sterilizing equipment and work space. Recognizing equipment malfunctions and readjusting equipment or writing referrals for repair. Instructing patients in pretest preparation, answering questions, and explaining procedures. Performing additional duties as required. Experience Required for Your Success Clinical Radiographer background with a minimum of 2 years MRI clinical experience required Siemens equipment experience required Valid ARRT license, registered in MRI Strong communication skills both written and verbal needed Ability to interact with client personnel and team members in an autonomous responsible, professional and ethical manner Must be flexible, reliable and demonstrate sound judgment and initiative

At Bristol Myers Squibb, we are inspired by a single vision - transforming patients' lives through science.

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.

Through our dedicated associates, Conduent delivers mission-critical services and solutions on behalf of Fortune 100 companies and over 500 governments - creating exceptional outcomes for our clients and the millions of people who count on them.

Conduct virtual and on-site presentations to position the value of Aflac s products and services. Raised and donated more than $140+ million to the Aflac Cancer and Blood Disorders Center of Children s Healthcare of Atlanta. Aflac s family of insurers includes Aflac and/or Aflac New York, and/or Continental American Insurance Company and/or Continental American Life Insurance Company. World s Most Admired Companies list FORTUNE magazine named Aflac to the list for the 20th consecutive year in 2021.

Why deliver with DoorDash Choose your own hours: When and where you work is totally up to you. Earn extra money for your goals: Achieve your short-term goals or long-term dreams by driving or biking with DoorDash. What is DoorDash Available in over 4,000 cities in the U.S, DoorDash connects local businesses and local drivers (called Dashers) with opportunities to earn, work, and live.

Company: C&S Wholesale Grocers, Inc. Use your prior warehouse order selector experience to join a team that travels the country completing assignments at one of our 30+ distribution centers. C&S Wholesale Grocers, Inc. , based in Keene, NH, is the largest wholesale grocery supply company in the U.S. and the industry leader in supply chain innovation.

When you're part of the team at Thermo Fisher Scientific, you'll do important work, like helping customers in finding cures for cancer, protecting the environment or making sure our food is safe. At Thermo Fisher Scientific, each one of our 90,000 extraordinary minds has a unique story to tell.

This position is located at the Community Club-Conference Center, Fort Buchanan, Puerto Rico. To better expedite the hiring process, we recommend including full contact information (name, address, phone number, email, etc.) for professional and personal references on your resume. Responsibilities Manages a business activity as an assistant manager. Recommends and enforces operating procedures. Represents the activity to the public. Conducts surveys, reviews activity reports and makes recommendations concerning services, promotional activities and revenue improvements. Supervises assigned staff. Requirements Conditions of Employment Qualifications Minimum Qualifications: 1. Work experience or education directly related to the duties to be performed. PLEASE NOTE: Your resume & application package must reflect the qualifications stated in the announcement and questionnaire to be rated eligible. Education YOU MUST UPLOAD TRANSCRIPTS AT THE TIME OF APPLICATION See Minimum Qualifications above to ensure you meet the minimum educational qualifications if applicable, and ensure all appropriate transcripts are provided. Additional Information Area of Consideration: The Area of Consideration for this vacancy announcement is worldwide. (Military Spouse Preference (MSP) and Involuntarily Separated Military Preference (ISMP) eligible candidates are included in the area of consideration.) Manual Applications: If you are unable to apply online, you may submit your application package using a manual application method. Please contact the NAF Human Resources Office or representative listed on this job announcement to request a copy of the manual application form. All completed manual application forms (along with resume and other supporting documentation) must be received no later than 2:00pm by 08/24/2022 in order to process your application in a timely manner. Please note that neglecting to respond to the job related questions may result in an ineligible rating. Allowances, Incentives, and PCS Costs: Allowances, differentials, or incentives will not be paid. Payment Permanent Change of Station (PCS) costs are not authorized, based on a determination that a PCS move is not in the Government's interest. Please check out our Applicant Information Kit: It contains additional information applicants may find useful when applying for our jobs. (To view the kit, click or copy and paste this URL: https://publicfileshare.chra.army.mil/Applicants/NAF%20Applicant%20Information%20Kit.pdf ). Other: Information may be requested regarding the vaccination status of selectees for the purposes of implementing workplace safety protocols. For more information, visit https://www.saferfederalworkforce.gov/faq/vaccinations/ Additional referrals may be made from this vacancy announcement for up to 90 days after the closing date. Applications are valid for 90 days after submission date. Applicants will be referred to selecting officials as additional vacancies occur. This is a Standing Register Job Announcement meaning it will stay announced for up to 90 days and as new applicants apply & management needs to fill the position, applications will be reviewed and sent to management if they meet the minimum qualifications set forth in this job announcement.

Also visits doctors offices and elderly homes to help increase Humana presence and beneficiaries. **Responsibilities** The MarketPoint Sales Representative - PR makes sales presentations to qualified Medicare participants at Points of Sales, their homes, doctors' offices, etc. using approved presentation material and guidelines. The MarketPoint Sales Representative - PR work assignments involve moderately complex to complex issues where the analysis of situations or data requires an in-depth evaluation of variable factors. + **COVID VACCINATION:** Humana and its subsidiaries require vaccinated associates who work outside of their home to submit proof of vaccination, including COVID-19 boosters. Associates who remain unvaccinated must either undergo weekly negative COVID testing OR wear a mask at all times while in a Humana facility or while working in the field. The MarketPoint Sales Representative - PR sells individual health plan products and services in a field setting.

1. Supports manufacturing operations areas (OSD and Parenteral product) such as Compounding, Filling, preparation, capping, Inspection, compression and packaging to assure that appropriate cGMPs are in place through frequent operations audit. 2. Manages audit observations, investigations and CAPAs records in Trackwise on timely manner and participates in the investigations management process to identify root cause, evaluate and approves Corrective and Preventive actions (CAPAs).and provides appropriate recommendations for the lot disposition. 3. Reviews and approves the investigations occurred in the manufacturing process (OSD and Parenteral products), facility and utilities, microbiology and warehouse areas. 4. Reviews and approves the master documentation related to manufacturing and support areas such as CRs, SOPs, WPPs, BOMs, qualification and validation Protocols with government regulations and Policies. 5. Provides technical guidance and compliance support in the transfer of new products and process to maintain quality standards. 6. Manages audit observations, investigations and CAPAs records in Trackwise on timely manner. 7. Maintains management informed (via frequent written reports) of any problem that might affect the quality and/or timely release of materials. 8. Assures that electronic systems (PMS, Syncade, Maximo, Quasar etc) are aligned and in compliance with cGMPs, Regulatory Standards and requirements for domestic and international markets. 9. Provides support and training to other departments as required. 10. Participates in the risk analysis process when a quality event has happened that cannot be solved immediately and assesses the needs to be completed to continue or prior to resumption of manufacturing process. 11. Keeps track of the Department performance and attainment to deadlines and goals by means of the QC/QA Metric System. 12. Performs product Acceptance Quality Level (AQL) during inspection (parenteral products) stage and distribute reserve and/or stability samples to the appropriate area. 13. Supports Media Fill activities in order to assure that typical and atypical interventions are performed as established. 14. Reviews and approves the instrumentation and equipment Calibration records and engineering drawings ensuring there are effective systems for the maintenance and calibration of critical equipment and, approves calibration requests.. 15. Participates in PAT, department staff and planning meetings as required. 16. Reviews and approves equipment, utilities and facilities qualification and system life cycle documentation. 17. Reviews and approves all executed batch production records and laboratory testing records before release of the product for distribution to assure that no deviations have occurred, or if deviations have occurred, that they have been fully investigated. 18. Reviews and approves all process, product and computer systems validation protocols and reports, change control documentation, redressing / reprocessing / rework operations, investigation reports related to manufacturing process and microbiology laboratory, and Annual Product Quality Review (APQRs) elements. 19. Supports the resolution of product and process issues associated to Quality Events. 20. Reviews supporting data for compliance with cGMP documentation practices. 21. Approves or reject procedures and specifications impacting drug products, raw material or packaging components. 22. Verifies compliance with Policies and Guidelines. 23. Participates as quality representative or liaison in site projects 24. Assures that the manufacturing and packaging procedures are properly followed and adequate for their use. 25. Verifies consistency with other site procedures and/or specifications. . 26. Ensures the designation and monitoring of storage conditions for quarantine materials and products. Skills: capa, audit, batch record review, document control Top Skills Details: capa,audit,batch record review,document control Additional Skills & Qualifications: * Bachelor Degree in Science, Chemical Engineering, Biology, Pharmacy or Microbiology. * 3 years of experience in the pharmaceutical industry. * Minimum 1 year of experience in Quality Assurance responsibilities in a pharmaceutical industry. * Knowledge of manufacturing operations of Solid Dosage and Parenteral Products Manufacturing. * Strong knowledge of relevant GMP, FDA, EU regulations and the ability to interpret and apply them for intended use. * Fully bilingual (Spanish/English) communication skills, both written and verbal are required. * Self-motivated, creative and team work oriented. * Excellent interpersonal skills and the ability to interact with people at all levels. * Proficient knowledge of computer systems (Microsoft Office, etc.) and applications like Trackwise and SAP. * Solid ability for analyzing data detecting deviations, inconsistencies and interpret sampling test results. * Knowledge of problem solving and root cause analysis methodologies (i.e. Kepner Tregoe) Experience Level: Entry Level About Actalent: Actalent connects passion with purpose. Our scalable talent solutions and services capabilities drive value and results and provide the expertise to help our customers achieve more. Every day, our experts around the globe are making an impact. We're supporting critical initiatives in engineering and sciences that advance how companies serve the world. Actalent promotes consultant care and engagement through experiences that enable continuous development. Our people are the difference. Actalent is an operating company of Allegis Group, the global leader in talent solutions. The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

We are looking for a one resource to provide the services for the development, configuration, verification and qualification of electronic records in MES ( Manufacturing Execution System) at our client's site in Vega Baja, Puerto Rico. This is a temporary position for 12 months with the possibility of extension. JOB /SERVICE SUMMARY: Develop and maintain Master Electronic Batch Records (EBR) recipes within the Manufacturing Execution System (MES). Support the implementation of the continuous improvements culture. ESSENTIAL FUNCTIONS: Subject Matter Expert (SME) of the site recipes/process. Create and maintain MES master data. Audit process and equipment operations to assure compliance with Electronic Batch Records (EBR) Provide support MES System authoring related incidents. Ensure EBRs comply with GMP, PQS, safety and process standards. Developing and/or revising MES related procedures to ensure production quality. Support BT compliance team and System Audits/Periodic Reviews of the application as per company's policies. Assure training compliance with all applicable regulations (EHS, HR, GMP, etc.). Support/executes training plans at the site. Train end user in the MES System. Develop and maintain recipe testing life cycle documentation. Responsible for Recipe Change requests, if applicable. PRINCIPAL RELATIONSHIPS: Inside the Company: Planning Team Mfg. and Pkg. operations Quality Operations Site Leadership Team Material Planners Hourly Colleagues Outside the Company: MES Core Team QUALIFICATION REQUIREMENTS: EDUCATION: BS Degree in Science. Preferable in Computer Engineering, Electrical Engineering (Electronic) and/or Computer Programming. EXPERIENCE: Three to five years of experience in pharmaceutical industries (Manufacturing and/or Packaging). Experience with the electronic batch record authoring process. Preferable knowledge in Rockwell Factory Talk (MES) Application . Excellent communication skills (verbal and written). Excellent conflict management skills. Computer literate. OTHER REQUIREMENTS: Technical Skills Technical writing Teaching skills Computer Literacy Pharmaceutical Process Bilingual (English/Spanish) Competencies Presentation skills Creativity Communication skills Leadership Develop People Analysis Listening Drive Changes ENVIRONMENTAL, HEALTH AND SAFETY REQUIREMENTS: WORK ENVIRONMENT: While performing the duties of this job, the employee very frequently works in a normal office temperature environment. The noise of the work environment is usually normal. ENVIRONMENTAL, HEALTH AND SAFETY (EHS): Audits area to assure compliance with safety, environmental regulation and safety equipment Advises and keeps inform the operators in all E.H.S. related issues. Ensures that product / process / equipment comply with Company's E.H.S. standards during