Quality control analyst jobs in Guaynabo, PR

**At Kelly** ** ** **Science, we're passionate about helping you find a job that works for you. How about this one?** We're seeking **Specialist QC** to work for one of our top **Biotechnology Industry client at Juncos, PR** . **Salary: $38.00 p/h** **Requirements:** + PHD or MS degree and 2 years of directly related experience OR BS degree and 4 years of directly related experience OR AD degree and 8 years of directly related experience. Preferable scientific background in Science or Engineering Preferable experience as Microbiologist, Chemist, Biochemistry, Molecular Sciences, or Chemical Engineering + Scientific Data Analysis + Strong Technical Writing (English and Spanish) mainly focuses + Strong knowledge in Microsoft Excel as a Tool for Data Analysis + Knowledge in Computer System and Method Validation (Experience preferable) + Strong knowledge and experience with quality process management + Ability to develop inspection or qualification protocols in a short timeframe period. The **Specialist QC** will be responsible for: + Providing technical guidance, provide reports, data analysis and ensure flow of communication between technical groups including following up on and resolving issues that arise. + Resolve technical issues and troubleshoot for assays as necessary + Ensure lab compliance which includes: Implementing procedures that enhance GMP, GLP and safety. + Manage existing and/or develop and implement new programs, processes and methodologies. + Develop, revise and audit various complex controlled documents that may have multi-organizational and/or multi-site impact. + Approve lab investigations, Lead audit teams **Kelly** ** ** **Science PR Offers!** + Exposure to a variety of career opportunities as a result of our expansive network of client companies + Career guides, information and tools to help you successfully position yourself throughout every stage of your career + Access to more than 3,000 online training courses through our **Kelly** ** ** **Learning Center** + **Biweekly pay ( W2)** + **Sick, Vacations & Holidays paid*** + **Christmas bonus*** + * Must comply with minimum established requirements to qualify. **APPLY TODAY!** As part of our promise to talent, Kelly supports those who work with us through a variety of benefits, perks, and work-related resources. Kelly offers eligible employees voluntary benefit plans including medical, dental, vision, telemedicine, term life, whole life, accident insurance, critical illness, a legal plan, and short-term disability. As a Kelly employee, you will have access to a retirement savings plan, service bonus and holiday pay plans (earn up to eight paid holidays per benefit year), and a transit spending account. In addition, employees are entitled to earn paid sick leave under the applicable state or local plan. Click here (********************************************************************* for more information on benefits and perks that may be available to you as a member of the Kelly Talent Community. Why Kelly ? As a worker today, it's up to you to take charge of your career and look for opportunities to learn, grow, and achieve your potential. Helping you find what's next is what we're all about. We know what's going on in the evolving world of work-just ask the 440,000 people we employ each year. Connecting with us means getting the support, guidance, and opportunities needed to take your career where you may have never imagined. About Kelly Work changes everything. And at Kelly, we're obsessed with where it can take you. To us, it's about more than simply accepting your next job opportunity. It's the fuel that powers every next step of your life. It's the ripple effect that changes and improves everything for your family, your community, and the world. Which is why, here at Kelly, we are dedicated to providing you with limitless opportunities to enrich your life-just ask the 300,000 people we employ each year. Kelly is committed to providing equal employment opportunities to all qualified employees and applicants regardless of race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or any other legally protected status, and we take affirmative action to recruit, employ, and advance qualified individuals with disabilities and protected veterans in the workforce. Requests for accommodation related to our application process can be directed to the Kelly Human Resource Knowledge Center. Kelly complies with the requirements of California's state and local Fair Chance laws. A conviction does not automatically bar individuals from employment. Kelly participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S. Kelly Services is proud to be an Equal Employment Opportunity and Affirmative Action employer. We welcome, value, and embrace diversity at all levels and are committed to building a team that is inclusive of a variety of backgrounds, communities, perspectives, and abilities. At Kelly, we believe that the more inclusive we are, the better services we can provide. Requests for accommodation related to our application process can be directed to Kelly's Human Resource Knowledge Center. Kelly complies with the requirements of California's state and local Fair Chance laws. A conviction does not automatically bar individuals from employment.

At TE, you will unleash your potential working with people from diverse backgrounds and industries to create a safer, sustainable and more connected world. Establishes appropriate product design or testing processes; oversees the design or testing processes and associated test equipment. Job Requirements At TE Connectivity, you'll be part of an innovative, fast-paced environment where your contributions directly impact cutting-edge technologies that shape the future. Specifically, the Digital Data Networks Business Unit is seeking a highly skilled and detail-oriented Engineering Designer to join our Advanced Technology team. This role plays a pivotal part in bridging the gap between conceptual design and manufacturable components. Core Responsibilities: Collaborate with Product Development Engineers to refine and finalize part and tool designs. Create detailed, toleranced 3D CAD models using Creo (MBD - Model Based Definition). Generate accurate 2D drawings using AutoCAD. Apply GD&T principles to ensure manufacturability and functional performance. Develop dimensioned drawings for both components and tooling. Ensure designs meet manufacturing capabilities and constraints (stamping, molding, assembly). Support design reviews and receive input on design for manufacturability (DFM). Maintain drawing standards and documentation practices. Assist in troubleshooting design-related issues during prototyping and production phases. What your background should look like Associate or bachelor's degree in mechanical engineering, Design Engineering, or related field. Proven experience in engineering, drafting and design. Proficiency in Creo 3D CAD software; SpaceClaim experience is a plus. Proficiency in AutoCAD 2D CAD software. Strong understanding of GD&T principles and application. Experience designing high-speed, high-density connectors is highly desirable. Knowledge of manufacturing processes including stamping, molding, and assembly. Ability to create dimensioned drawings for both parts and tooling. Excellent attention to detail and organizational skills - can manage multiple tasks simultaneously. Strong communication and collaboration skills - fluent in English. Ability to work in a global environment -capable of collaborating with individuals across geographies. Ability to offer creative solutions to complex problems is a desirable differentiating skill. Competencies Values: Integrity, Accountability, Inclusion, Innovation, Teamwork ABOUT TE CONNECTIVITY TE Connectivity is a global industrial technology leader creating a safer, sustainable, productive, and connected future. Our broad range of connectivity and sensor solutions enable the distribution of power, signal and data to advance next-generation transportation, renewable energy, automated factories, data centers, medical technology and more. With more than 85,000 employees, including 8,000 engineers, working alongside customers in approximately 140 countries. TE ensures that EVERY CONNECTION COUNTS. Learn more at ********** and on LinkedIn, Facebook, WeChat, Instagram and X (formerly Twitter). COMPENSATION • Competitive base salary commensurate with experience: $76,300 - $114,400(subject to change dependent on physical location) • Posted salary ranges are made in good faith. TE Connectivity reserves the right to adjust ranges depending on the experience/qualification of the selected candidate as well as internal and external equity. • Total Compensation = Base Salary + Incentive(s) + Benefits BENEFITS • A comprehensive benefits package including health insurance, 401(k), disability, life insurance, employee stock purchase plan, paid time off and voluntary benefits. EOE, Including Disability/Vets IMPORTANT NOTICE REGARDING RECRUITMENT FRAUD TE Connectivity has become aware of fraudulent recruitment activities being conducted by individuals or organizations falsely claiming to represent TE Connectivity. Please be advised that TE Connectivity never requests payment or fees from job applicants at any stage of the recruitment process. All legitimate job openings are posted exclusively on our official careers website at te.com/careers, and all email communications from our recruitment team will come only from actual email addresses ending **********. If you receive any suspicious communications, we strongly advise you not to engage or provide any personal information, and to report the incident to your local authorities.

Under general direction, functions as the technical specialist for testing and development in areas of molecular biology and microbiology. Focus is on the complex technical issues and scope is typically multi-organizational and/or multi-site and /or involving outside resources. FUNCTIONS: Responsible for providing technical guidance, Provide reports, data analysis and ensure flow of communication between technical groups including following up on and resolving issues that arise. Resolve technical issues and troubleshoot for assays as necessary Ensure lab compliance which includes: Implementing procedures that enhance GMP, GLP and safety. Manage existing and/or develop and implement new programs, processes and methodologies. Develop, revise and audit various complex controlled documents that may have multi-organizational and/or multi-site impact. Approve lab investigations, Lead audit teams May serve as subject matter expert to develop technical training. May perform routine work in a specific area of responsibility as necessary. Represents the department/organization on various teams, Independently responsible for following through on multi-site action items. May interact with regulatory agencies regarding area(s) of responsibility including written responses. May resolve issues with outside resources. Performs special projects as requested by supervisor, May supervise employees as necessary to meet technical requirements. REQUIREMENTS: EDUCATION High school/GED + 10 years of directly related experience. Associates + 8 years of directly related experience Bachelors + 4 years of directly related experience Masters + 2 years of directly related experience Preferable Scientific Background (Science or Engineering) with experience in Pharmaceutical Industry, Quality Control, Laboratory Testing, Project Management and Quality processes. Preferable experience as Microbiologist, Chemist, Biochemistry, Molecular Sciences, or Chemical Engineering PREFERRED QUALIFICATIONS Scientific Data Analysis Strong Technical Writing (English and Spanish) mainly focuses. Strong knowledge in Microsoft Excel as a Tool for Data Analysis. Good Communication skills Project Management Knowledge in Computer System and Method Validation (Experience preferable). Strong knowledge and experience with quality process management. Basic Knowledge on equipment preventive maintenance and troubleshooting. Agile on prioritization of critical tasks. Ability to develop inspection or qualification protocols in a short timeframe period. Strong negotiation skills COMPETENCIES/ SKILLS: Understand, support and demonstrate the AMGEN values. Excellent communication skills, facilitation and presentation skills. Excellent technical writing skills. Strong computer operation skills including work processing, presentation, database and spreadsheet application skills. Excellent project management and organizational skills including the ability to independently understand, follow, implement complex instructions and follow assignments through to completion. Advanced skill in handling multiple responsibilities, tasks and projects simultaneously including ability to shift priorities. Excellent knowledge of and experience with processes involved in quality analytical labs, validation, manufacturing, quality assurance, process development and distribution. Extensive knowledge of all testing including the development and validation of assays and the ability to perform all testing in specific area of responsibility. Knowledge of pharmaceutical processes. Strong knowledge of U.S. regulations and practices pertaining to the testing of pharmaceutical/biological products. Knowledge of basic international regulations and practices pertaining to the testing of pharmaceutical/biological products. Extensive knowledge and application of GMPs/CFRs. Ability to evaluate compliance issues. Skill in evaluating and documenting according to Company and various guidelines. Proficient at maintenance, troubleshooting and operation of equipment in area of expertise. Advanced scientific data analysis and interpretation skills. Advanced skills in solving complex problems. Advanced data trending and evaluation. Strong skill in working independently and to effectively interact with various levels. Ability to interact with regulatory agencies both orally and in writing. Initiate, coordinate and lead cross functional teams. Excellent skill in leading, motivating, influencing, and negotiating. WORK METHODOLOGY: Full on site job in Juncos, PR Full time job Expected project duration: 7 months for the first contract Administrative shift from Monday to Friday Professional services contract with potential extension based on performance and budget Expected hiring date: January 2026

This position is responsible for all QA activities that directly support execution of the process, both within the PET and in assigned areas outside the PET, ensuring compliance. These activities may include, but are not limited to, Quality on-line review, batch release, change control and documentation, equipment and process validation, investigations, SOPs, supplier management and regulatory interactions. In addition, in the QC area, must perform testing of raw materials, finished products, stability, and other samples received according to business needs and following approved procedures, cGMP's, cGLP's, corporate policies, and any other applicable regulatory requirements. At the Senior Level will be trained and demonstrate some level of proficiency in all of the major responsibilities of the role. The incumbent must demonstrate a strong understanding of the area to which the individual is aligned. The incumbent will act as execution lead/process owner for one or more processes. This position will be able to provide assistance to either QA or QC areas. The support will be given on one specific area only and is not allowed to be executed in both areas at the same time. General Accountabilities Escalate to QA management (i.e., QA Manager/QC Manager or Head of Quality) any discrepancies (potential or real) during daily operations. Provide expert advice on Good Manufacturing Practice / Good Development Practice / Good Laboratory Practice to Operations and ensure compliance with the associated quality standards. Support major and critical site investigations. Conduct QA / QC area investigations. Support local complaint investigations, identify and rectify any trends. Collate the required documentation for product quality reviews within the required timescales. Apply the first level of risk management by using analytical skills and experience to make decisions, develop solutions, or more complicated judgments, within general operating guidelines. Look for opportunities to identify change and make efficiency savings, influence decisions and deliver the results whilst ensuring an appropriate level of compliance. Produce and deliver Good Manufacturing Practice training within the Manufacturing Teams. Identify QA / QC enhancement opportunities, and actively participate and coordinate with QA / QC Management the required activities to implement these opportunities. Ensure plant readiness for any regulatory inspections including periodic walkthroughs. Execute and/or support local audits (both internal and external) to aid in developing follow-up improvement plans to ensure ongoing compliance. Review and approve documentation generated as a result of experimentation, validation, new product technology introduction (i.e., Experimental Programs and Reports, Process and Cleaning Validation, Release Requirements Determination, Computer Validation Lifecycle documents, Risk Assessment for Qualification purposes, Installation Qualification, Operation Qualification, Technical Projects, Applications Change Controls). Support development and implementation of systems or CAPAs identified during audits, regulatory inspection, and pre or post-approval negotiation. Participate in the development and implementation of Quality Risk Assessments (QRA). Participate in project teams created towards problem solving or specific issues, to ensure GMP and regulatory compliance. Train and mentor junior members of the Quality organization and providing QA / QC coaching to other non-QA / QC employees within the area supported. Generates or revises associated documentation including procedures, analytical methods, and other documents with additional technical complexity such as but not limited to special study reports, technical reports or analytical method validation protocols. Builds productive and effective relationship with internal and external customers, such as Manufacturing, Quality Assurance, Planning, and other Laboratory areas to ensure customer satisfaction and business success. Proactively participates in company initiatives toward continuous improvement (New Products Introduction, GMP Improvement Programs, Kaizen events, GENBA walks) while providing guidance in the area knowledge and deliver timely results while contributing to business success. Actively identifies, develops, establishes, monitors and maintains area Key Performance Indicators as required. Take any action needed to prevent situations that may jeopardize the patient safety, quality of the product or supply to market. QA Area Accountabilities Perform product release activities and recommend batch disposition. Ensure compliance with change management processes within the Process Execution Team (PET) and approval of associated documentation at a local level. Available to work 2nd shift. QC Area Accountabilities Conducts testing following applicable procedures, cGMP's, corporate and any other applicable regulation. Ensure is trained and qualified on the corresponding procedures before starting any test or doing any laboratory operation related task. Certifies analytical reports generated in the laboratory ensuring compliance with cGMP's and applicable specifications, procedures, among others, if applicable. Evaluates data trends and actively participates in the investigation of OOS and atypical events and/or quality issues placing particular attention to root cause analysis, technical completion and scope while ensuring accuracy of documentation contents. Actively support the implementation of compendial changes for raw materials, analytical methods or finished products tests in accordance with applicable Pharmacopoeias such as USP/NF, European Pharmacopoeia, British, and Japanese Pharmacopoeia. Performs instrumentation troubleshooting and preventative maintenance as deemed required to maintain the operational status of instrumentation. Assists in ensuring the laboratory operations are fully an integral part of the LEAN culture and that visual boards are continuously updated representing the current operation. Provide guidance to laboratory activities including the review of quality documentation, such as, product specifications, chemical methods, chemical (analytical) report forms, SOPs, and quality and compliance guidelines. Education, Qualifications, Skills and Experience • Bachelor's degree in a Sciences / Technical field such as Pharmacy, Biology, Chemistry or Engineering and at least three (3) years related experience in the pharmaceutical industry with emphasis in Quality or Compliance position; or equivalent combination of education and experience. Language • Fully Bilingual (English & Spanish) Digital Literacy • Advance knowledge of Microsoft Office applications (i.e., Word, Excel, Project, Power Point, Outlook) or similar computer applications. • Advance knowledge of databases/application systems (i.e., SAP, Global LIMS, Documentum, Saba, EQV, Change Controls, Complaints). Knowledge, Skills and Abilities • Adaptable to changing environment. • Up to date knowledge of cGMP regulations and end-to-end supply chain management principles. Knowledge of pharmaceutical operations processes: warehouse, manufacturing, packaging, laboratory, in process, etc. • Strong ability and motivation to learn. • Capable of making timely decisions with facts on hand, even when under pressure. • Good communication across all levels or the organization and capable of building and maintaining open lines of communication. • Strategic and tactical customer stakeholder management. • Understanding of statistical data and capable of drawing or reaching conclusions from supporting data concepts (i.e. normal distribution, percentages, ratios and proportions to practical situations). • Ability to read, analyze and interpret common scientific and technical journals, financial reports and technical documents. • Ability to interpret a variety of instructions furnished in written, oral, diagram, or schedule form. • Monitors own work to ensure quality. Meets productivity standards. Completes work in timely manner. • Demonstrates accuracy and thoroughness. • Looks for ways to improve and promote quality. Applies feedback to improve performance. • Willing to make decisions. Exhibits sound and accurate judgment. • Knowledge in ANSI/ASQ Z1.4 Standard and auditing of documents for GMP compliance. • Business Knowledge focused on ensuring continuity of supply, cost-savings and reducing non-value adding activities. • Balances team and individual responsibilities. Exhibits objectivity and openness to others' views. Gives and welcomes feedback. Supports everyone's efforts to succeed. • Ability to solve practical problems and deal with variables in situations where only limited standardization exists. 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. Would you like to be part of an excellent team of professionals? Apply Today! IPR provides a comprehensive benefits package for its employees. It includes: Health, Pharmacy, Dental and Vision Insurances, STD and LTD Insurances, Retirement Plan with company match and Profit Sharing among others. To be considered for this exciting opportunity, please complete the full application on our website at your earliest convenience - it is the only way that our Recruiter and Hiring Manager can know that you feel well qualified for this opportunity. If you know someone who would be a great fit, please share this posting with them. 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. iPR Pharmaceuticals & AstraZeneca embraces diversity and equality of opportunity! We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We follow all applicable laws and regulations on nondiscrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements. Date Posted 12-Dec-2025 Closing Date 18-Dec-2025 Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.

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. Responsibilities: Scientific Data Analysis Strong Technical Writing (English and Spanish) mainly focuses Strong knowledge in Microsoft Excel as a Tool for Data Analysis Good Communication skills Project Management Knowledge in Computer System and Method Validation (Experience preferable) Strong knowledge and experience with quality process management Basic Knowledge on equipment preventive maintenance and troubleshooting Agile on prioritization of critical tasks Ability to develop inspection or qualification protocols in a short timeframe period. Strong negotiation skills Qualifications Requirements/Knowledge/Education/Skills: Bachelor's Degree in Engineering, Science or Business field and 5 years of experience. Preferable Scientific Background (Science or Engineering) with experience in Pharmaceutical Industry, Quality Control, Laboratory Testing, Project Management and Quality processes. Preferable experience as Microbiologist, Chemist, Biochemistry, Molecular Sciences, or Chemical Engineering. Knowledge in Pharmaceutical and Medical Devices. PMP Certification Preferred Fully Bilingual 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.

For Quality Control in the Technical Resources area. WHAT MAKES YOU A FIT: The Technical Part: Bachelor's Degree with four (4) years of experience in a Scientist within the pharmaceutical or regulated industry. Bilingual (English & Spanish). Project Management skills. Shift: Administrative, and according to business needs. Experience in: Scientific Data Analysis and Technical Writing. Computer System and Method Validation. Quality process management and equipment preventive maintenance and troubleshooting. Develop inspection or qualification protocols in a short timeframe period. The Personality Part: Picture yourself in a lab… with all the equipment you need to put your multitasking, scientific, creative (to come up with all those experiments!) skills to work. Picture as well an environment of healthy competition, teamwork, being ethical and of using the scientific method in all ways possible. If you like how this sounds, then this might be the job for you. Bring it on! AS A PIECE OF FITS, YOU WILL: (The day-to-day on the job) Responsible for providing technical guidance. Provide reports, data analysis and ensure flow of communication between technical groups. Resolve technical issues and troubleshoot for assays as necessary. Ensure lab compliance which includes: Implementing procedures that enhance GMP, GLP and safety. Manage existing and/or develop and implement new programs, processes and methodologies. Develop, revise and audit various complex controlled documents that may have multi-organizational and/or multi-site impact. Approve lab investigations, Lead audit teams May serve as subject matter expert to develop technical training. May perform routine work in a specific area of responsibility as necessary. Represents the department/organization on various teams, Independently responsible for following through on multi-site action items. May interact with regulatory agencies regarding area(s) of responsibility including written responses. May resolve issues with outside resources. Performs special projects as requested by supervisor, May supervise employees as necessary to meet technical requirements. 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?

Our team members are at the heart of everything we do. At Cencora, we are united in our responsibility to create healthier futures, and every person here is essential to us being able to deliver on that purpose. If you want to make a difference at the center of health, come join our innovative company and help us improve the lives of people and animals everywhere. Apply today! Job Details Summary of Role: Under general direction, functions as the technical specialist for testing and development in areas of molecular biology and microbiology. Focus is on the complex technical issues and scope is typically multi-organizational and/or multi-site and /or involving outside resources. Responsibilities: * Responsible for providing technical guidance, Provide reports, data analysis and ensure flow of communication between technical groups including following up on and resolving issues that arise. * Resolve technical issues and troubleshoot for assays as necessary * Ensure lab compliance which includes: Implementing procedures that enhance GMP, GLP and safety. * Manage existing and/or develop and implement new programs, processes and methodologies. * Develop, revise and audit various complex controlled documents that may have multi-organizational and/or multi-site impact. * Approve lab investigations, Lead audit teams * May serve as subject matter expert to develop technical training. * May perform routine work in a specific area of responsibility as necessary. * Represents the department/organization on various teams, Independently responsible for following through on multi-site action items. * May interact with regulatory agencies regarding area(s) of responsibility including written responses. * May resolve issues with outside resources. * Performs special projects as requested by supervisor, May supervise employees as necessary to meet technical requirements. Shift: Administrative Location: Juncos, PR Education: Doctorate OR Masters + 2 years of directly related experience OR Bachelors + 4 years of directly related experience OR Associates + 8 years of directly related experience OR High school/GED + 10 years of directly related experience. Preferred Qualifications: * Scientific Data Analysis * Strong Technical Writing (English and Spanish) mainly focuses * Strong knowledge in Microsoft Excel as a Tool for Data Analysis * Good Communication skills * Project Management * Knowledge in Computer System and Method Validation (Experience preferable) * Strong knowledge and experience with quality process management * Basic Knowledge on equipment preventive maintenance and troubleshooting * Agile on prioritization of critical tasks * Ability to develop inspection or qualification protocols in a short timeframe period. * Strong negotiation skills Skill: * Understand, support and demonstrate the values. * Excellent communication skills, facilitation and presentation skills. * Excellent technical writing skills. * Strong computer operation skills including work processing, presentation, database and spreadsheet application skills. * Excellent project management and organizational skills including the ability to independently understand, follow, implement complex instructions and follow assignments through to completion. * Advanced skill in handling multiple responsibilities, tasks and projects simultaneously including ability to shift priorities. * Excellent knowledge of and experience with processes involved in quality analytical labs, validation, manufacturing, quality assurance, process development and distribution. * Extensive knowledge of all testing including the development and validation of assays and the ability to perform all testing in specific area of responsibility. * Knowledge of pharmaceutical processes. * Strong knowledge of U.S. regulations and practices pertaining to the testing of pharmaceutical/biological products. * Knowledge of basic international regulations and practices pertaining to the testing of pharmaceutical/biological products. * Extensive knowledge and application of GMPs/CFRs. * Ability to evaluate compliance issues. * Skill in evaluating and documenting according to Company and various guidelines. * Proficient at maintenance, troubleshooting and operation of equipment in area of expertise. * Advanced scientific data analysis and interpretation skills. * Advanced skills in solving complex problems. * Advanced data trending and evaluation. * Strong skill in working independently and to effectively interact with various levels. * Ability to interact with regulatory agencies both orally and in writing. * Initiate, coordinate and lead cross functional teams. * Excellent skill in leading, motivating, influencing, and negotiating. This position is for a fixed term contract supporting one of ECHO Consulting Group (a Cencora company) partners on site at their facility. What Cencora offers We provide compensation, benefits, and resources that enable a highly inclusive culture and support our team members' ability to live with purpose every day. In addition to traditional offerings like medical, dental, and vision care, we also provide a comprehensive suite of benefits that focus on the physical, emotional, financial, and social aspects of wellness. This encompasses support for working families, which may include backup dependent care, adoption assistance, infertility coverage, family building support, behavioral health solutions, paid parental leave, and paid caregiver leave. To encourage your personal growth, we also offer a variety of training programs, professional development resources, and opportunities to participate in mentorship programs, employee resource groups, volunteer activities, and much more. For details, visit ************************************** Full time Equal Employment Opportunity Cencora is committed to providing equal employment opportunity without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, age, disability, veteran status or membership in any other class protected by federal, state or local law. The company's continued success depends on the full and effective utilization of qualified individuals. Therefore, harassment is prohibited and all matters related to recruiting, training, compensation, benefits, promotions and transfers comply with equal opportunity principles and are non-discriminatory. Cencora is committed to providing reasonable accommodations to individuals with disabilities during the employment process which are consistent with legal requirements. If you wish to request an accommodation while seeking employment, please call ************ or email ****************. We will make accommodation determinations on a request-by-request basis. Messages and emails regarding anything other than accommodations requests will not be returned Affiliated Companies Affiliated Companies: Echo Consulting Group Inc

Job Description The position focuses on complex technical issues, multi-department and/or multi-site initiatives, and coordination with external resources when needed. Responsibilities include advanced troubleshooting, method support, documentation oversight, compliance, and cross-functional leadership. Key Responsibilities Provide technical guidance and ensure effective communication between scientific and technical groups. Analyze data, generate reports, and follow up on technical issues to ensure timely resolution. Troubleshoot assay and testing challenges as necessary. Ensure laboratory compliance by implementing and maintaining GMP, GLP, and safety procedures. Manage, develop, and implement programs, processes, and methodologies that support laboratory operations. Develop, revise, and audit complex controlled documents with multi-department or multi-site impact. Approve laboratory investigations and lead internal audit teams. Serve as a subject matter expert (SME) and support the development of technical training. Perform routine work within area of responsibility as required. Represent the department on cross-functional teams and independently manage multi-site action items. Interact with regulatory agencies as needed, including preparing written responses. Support issue resolution with external partners and resources. Lead or assist with special projects assigned by leadership. May supervise or mentor employees to meet technical and operational requirements. Core Competencies & Skills Excellent communication, facilitation, and presentation skills. Strong technical writing abilities. Advanced computer proficiency (word processing, presentations, databases, spreadsheets). Strong project management and organizational abilities; able to manage complex tasks independently. Ability to manage multiple priorities and shift focus as needed. Extensive experience in quality analytical labs, validation, manufacturing, QA, process development, or distribution. Deep understanding of assay development, validation, and laboratory testing. Knowledge of pharmaceutical and biological product testing processes. Strong understanding of U.S. regulations, GMPs, CFRs, and basic international regulatory practices. Ability to evaluate and document compliance-related issues. Skilled in interpreting scientific data and solving complex technical problems. Proficient in trending, analyzing, and evaluating data. Strong ability to work independently and collaborate across organizational levels. Capable of interacting with regulatory agencies both orally and in writing. Ability to lead, motivate, influence, negotiate, and drive cross-functional teams. Requirements Required Education & Experience Doctorate, OR Master's degree + 2 years of directly related experience, OR Bachelor's degree + 4 years of directly related experience, OR Associate degree + 8 years of directly related experience, OR High school diploma/GED + 10 years of directly related experience. Preferred Qualifications Strong scientific data analysis expertise. Advanced technical writing skills in English and Spanish. High proficiency with Microsoft Excel for data analysis. Excellent communication and project management skills. Knowledge of Computer System Validation (CSV) and Method Validation. Experience with quality process management. Basic understanding of equipment preventive maintenance and troubleshooting. Ability to prioritize critical tasks with agility. Experience developing inspection or qualification protocols on short timelines. Strong negotiation and influencing skills. Benefits Administrative Shift 6-months contract

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 providing technical guidance, provide reports, data analysis and ensure flow of communication between technical groups including following up on and resolving issues that arise. Resolve technical issues and troubleshoot for assays as necessary. Ensure lab compliance which includes: Implementing procedures that enhance GMP, GLP and safety. Manage existing and/or develop and implement new programs, processes and methodologies. Develop, revise and audit various complex controlled documents that may have multi-organizational and/or multi-site impact. Approve lab investigations, lead audit teams. May serve as subject matter expert to develop technical training. May perform routine work in a specific area of responsibility as necessary. Represents the department/organization on various teams, independently responsible for following through on multi-site action items. May interact with regulatory agencies regarding area(s) of responsibility including written responses. May resolve issues with outside resources. Performs special projects as requested by supervisor, may supervise employees as necessary to meet technical requirements. Qualifications: Bachelor's degree in preferably with Scientific Background (Science or Engineering) with experience in Pharmaceutical Industry, Quality Control, Laboratory Testing, Project Management and Quality processes. +4 years of directly related experience. (Preferable experience as Microbiologist, Chemist, Biochemistry, Molecular Sciences, or Chemical Engineering). Knowledge of pharmaceutical processes. Extensive knowledge and application of GMPs/CFRs. Knowledge in Scientific Data Analysis. Strong Technical Writing (English and Spanish) mainly focuses. Strong knowledge in Microsoft Excel as a Tool for Data Analysis. Good Communication skills Project Management skills Knowledge in Computer System and Method Validation (Experience preferable) Strong knowledge and experience with quality process management. Basic Knowledge on equipment preventive maintenance and troubleshooting. Proficient at maintenance, troubleshooting and operation of equipment in area of expertise. Agile on prioritization of critical tasks. Ability to develop inspection or qualification protocols in a short timeframe period. Strong negotiation skills Administrative 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.

In a world of possibilities, pursue one with endless opportunities. Imagine Next! At Parsons, you can imagine a career where you thrive, work with exceptional people, and be yourself. Guided by our leadership vision of valuing people, embracing agility, and fostering growth, we cultivate an innovative culture that empowers you to achieve your full potential. Unleash your talent and redefine what's possible. **Job Description:** Parsons is looking for an amazingly talented **QC Inspector** to join our team! **This job is not remote but located in Puerto Rico!** **What You'll Be Doing:** + Performing inspections and surveillances based on training and project requirements. + Interacting with project team members and management to support quality initiatives. + Implementing and documenting inspection, examination, and testing procedures. + Planning and setting up evaluations and tests, including equipment preparation. + Assessing and reporting the validity of inspection and testing results. + Reviewing training programs for inspection personnel and evaluating their effectiveness. + Conducting and documenting inspections of subcontractor work. + Overseeing subcontractor inspections and auditing quality records. + Performing First-Article and In-Process Inspections, including source inspections as needed. + Ensuring compliance with Health, Safety, and Environmental (HSE) requirements. + Supporting the development and implementation of a Quality Control Inspectors certification program. + Communicating inspection results clearly and concisely. + Understanding and applying contract and subcontractor requirements. **What Required Skills You'll Bring:** + Experience in quality control inspection within a project or functional environment. + Knowledge of inspection, examination, and testing procedures. + Ability to document and communicate inspection results effectively. + Familiarity with subcontractor oversight and quality record auditing. + Understanding of HSE compliance related to inspection activities. **What Desired Skills You'll Bring:** + Experience with First-Article and In-Process Inspections. + Prior involvement in inspector certification programs. + Ability to evaluate training programs for inspection personnel. + Strong cross-functional collaboration and communication skills. **Security Clearance Requirement:** None This position is part of our Corporate team. For over 80 years, Parsons Corporation, has shaped the future of the defense, intelligence, and critical infrastructure markets. Our employees work in a close-knit team environment to find new, innovative ways to deliver smart solutions that are used and valued by customers around the world. By combining unique technologies with deep domain expertise across cybersecurity, missile defense, space, connected infrastructure, transportation, smart cities, and more, we're providing tomorrow's solutions today. Salary Range: $29.95 - $52.40 We value our employees and want our employees to take care of their overall wellbeing, which is why we offer best-in-class benefits such as medical, dental, vision, paid time off, Employee Stock Ownership Plan (ESOP), 401(k), life insurance, flexible work schedules, and holidays to fit your busy lifestyle! This position will be posted for a minimum of 3 days and will continue to be posted for an average of 30 days until a qualified applicant is selected or the position has been cancelled. Parsons is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, veteran status or any other protected status. We truly invest and care about our employee's wellbeing and provide endless growth opportunities as the sky is the limit, so aim for the stars! Imagine next and join the Parsons quest-APPLY TODAY! Parsons is aware of fraudulent recruitment practices. To learn more about recruitment fraud and how to report it, please refer to *********************************************** . About Us Parsons is a digitally enabled solutions provider focused on the defense, security, and infrastructure markets. With nearly 75 years of experience, Parsons is uniquely qualified to deliver cyber/converged security, technology-based intellectual property, and other innovative services to federal, regional, and local government agencies, as well as to private industrial customers worldwide. Parsons is an equal opportunity, drug-free employer committed to diversity in the workplace. Minority/Female/Disabled/Protected Veteran/LGBTQ+. For more about Parsons, visit parsons.com and follow us on Facebook, Twitter, LinkedIn, and YouTube.

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas - immunology, oncology, neuroscience, and eye care - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at *************** Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok (******************************* . Job Description Purpose Describe the primary goals, objectives or functions or outputs of this position. Performs laboratory testing within a GMP environment in support of one or more of the following areas; raw materials, in-process product, finished product, stability, and/or validation. Uses scientific education and/or experiences to generate results in accordance with GMP/procedural requirements and scientific principles. Interprets data output to determine conformance with product specifications. Reviews and verifies data generated by others to determine conformance with product specifications. Understands internal business process, to make appropriate prioritization of their assigned work duties. Has experience and command of multiple laboratory techniques to perform them with minimal error. Can train other laboratory personnel on any technique they currently have in their training matrix. Responsibilities List up to 10 main responsibilities for the job. Include information about the accountability and scope. + Understands,implements,and maintains GMP with respect to laboratory records, procedures, and systems in accordance with procedural requirements. + Proposes and implements changes to maintain procedural requirements. + Performs analytical test methods as written to support product/material release with minimal error. + Proposes and implements changes to improve laboratory techniques and methodology. + Can independently troubleshoot and resolve analytical techniques and instrument issues. + Interprets experimental data for conformance with product/material specifications. + Understands and identifies laboratory technique or instrumental performance in accordance with scientific principles. + Initiates appropriate exception documents in accordance with procedural requirements. + Implements and ensures improvement ideas are completed to facilitate team objectives. + Proposes and implements scientific protocols to determine exception event cause. Qualifications Qualifications List required and preferred qualifications (up to 10). Include education, skills and experience. + Bachelor's degree in Science, preferably Microbiology, Biology, Chemistry or Bio-Chemistry with 6 years of experience in related field. Master's Degree in Science, preferably Microbiology, Biology, Chemistry or Bio-Chemistry with 4 years of experience in related field. PhD in Science, preferably Microbiology, Biology, Chemistry or Bio-Chemistry with 2 years of experience in related field. + Manages multiple priorities and comply with deadlines. + Maintains their certifications as needed for assigned job tasks. + Demonstrates strong analytical skills and logical thought process. + Method Transfer, Method Validation, Equipment Qualification Additional Information Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law: + The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future. + We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees. + This job is eligible to participate in our short-term incentive programs. Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company's sole and absolute discretion, consistent with applicable law. AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled. US & Puerto Rico only - to learn more, visit ************************************************************************* US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: *************************************************************

Performs complex tests and analyses to assure that products comply with established specifications. Carries out difficult calculations and prepares documentation that shows the results of tests performed. Completes record of inspection results, acceptance, rejection and disposition. Enters data into log books or computer databases. Compiles data and prepares reports on findings. Conducts scheduled calibration and maintenance on test equipment. Establishes maintenance and calibration schedule for test equipment based on manufacturers' recommendations and maintains equipment records. Coordinates specialized product\/customer quality testing. Prepares custom reports on results. Recommends and implements revisions, corrections and changes to test equipment, procedures and methods. Troubleshoots defective products returned by customers to determine root causes of failure. Compiles data to identify trends and proposes corrective action. Initiates and coordinates discussions with quality, engineering and other relevant departments to develop corrective actions for reoccurring problems. Requirements Minimum 4 to 6 years of relevant experience in the regulated industry. Bilingual. High school, technical or associate degree completed. "}}],"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":"Anasco"},{"field Label":"State\/Province","uitype":1,"value":"Anasco"},{"field Label":"Zip\/Postal Code","uitype":1,"value":"00610"}],"header Name":"QC\/QA Technician","widget Id":"118922000006310086","is JobBoard":"false","user Id":"118922000000026001","attach Arr":[],"custom Template":"1","is CandidateLoginEnabled":true,"job Id":"118922000017022001","FontSize":"15","location":"Anasco","embedsource":"CareerSite","indeed CallBackUrl":"https:\/\/recruit.zoho.com\/recruit\/JBApplyAuth.do","logo Id":"nrt0md43109f3de4c490e9975771d2b120574"}

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: Quality Control Scientist III Qualifications: Bachelor's Degree in Science. Minimum of 8 years of experience in direct pharmaceutical quality control areas and regulatory operations. Must be fully bilingual (English / Spanish) with excellent oral skills. Must be proficient using MS Windows and Microsoft Office applications. Strong knowledge in cGxP and regulatory guidance as well as understanding of how they are applied to regulatory compliance. Strong knowledge (according to related area). Technical Writing skills and investigations processes. Available to work extended hours, possibility of weekends and holidays. Responsibilities: Evaluate compendial changes from the different pharmacopeias. Generate trend reports of investigations based on the company's procedures. Evaluate global documents against site-specific procedures and update the site procedure accordingly. Draft technical documents such as methods, specifications, method validation protocols and reports, method transfer protocols and reports, based on corporate policies, SOPs, compendial guidelines, ICH, DEA, and FDA regulatory guidance. Generate required change requests for analytical documents and route documents for review and approval. Conduct laboratory event/out-of-specification/out-of-trend investigations and close them on time.

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. Responsibilities: • Laboratory experience in a GMP environment within the Pharmaceutical and/or Biotech industry • Fully bilingual communications skills (English and Spanish) • Good communications and presentation skills in English and Spanish • Project management skills • Strong organizational skills, including ability to follow assignments through to completion • Enhanced skills in leading, influencing and negotiating • Knowledge of and experience with processes involved in manufacturing and distribution, QA, QC, validation and process development • Basic Knowledge and skills of word processing, presentations, and spreadsheet applications Qualifications Requirements/Knowledge/Education/Skills: • Educational background in Chemistry, Microbiology, Biology or Life Sciences 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.

In a world of possibilities, pursue one with endless opportunities. Imagine Next!At Parsons, you can imagine a career where you thrive, work with exceptional people, and be yourself. Guided by our leadership vision of valuing people, embracing agility, and fostering growth, we cultivate an innovative culture that empowers you to achieve your full potential. Unleash your talent and redefine what's possible. Job Description: Parsons is looking for an amazingly talented QC Inspector to join our team! This job is not remote but located in Puerto Rico! What You'll Be Doing: Performing inspections and surveillances based on training and project requirements. Interacting with project team members and management to support quality initiatives. Implementing and documenting inspection, examination, and testing procedures. Planning and setting up evaluations and tests, including equipment preparation. Assessing and reporting the validity of inspection and testing results. Reviewing training programs for inspection personnel and evaluating their effectiveness. Conducting and documenting inspections of subcontractor work. Overseeing subcontractor inspections and auditing quality records. Performing First-Article and In-Process Inspections, including source inspections as needed. Ensuring compliance with Health, Safety, and Environmental (HSE) requirements. Supporting the development and implementation of a Quality Control Inspectors certification program. Communicating inspection results clearly and concisely. Understanding and applying contract and subcontractor requirements. What Required Skills You'll Bring: Experience in quality control inspection within a project or functional environment. Knowledge of inspection, examination, and testing procedures. Ability to document and communicate inspection results effectively. Familiarity with subcontractor oversight and quality record auditing. Understanding of HSE compliance related to inspection activities. What Desired Skills You'll Bring: Experience with First-Article and In-Process Inspections. Prior involvement in inspector certification programs. Ability to evaluate training programs for inspection personnel. Strong cross-functional collaboration and communication skills. Security Clearance Requirement: NoneThis position is part of our Corporate team.For over 80 years, Parsons Corporation, has shaped the future of the defense, intelligence, and critical infrastructure markets. Our employees work in a close-knit team environment to find new, innovative ways to deliver smart solutions that are used and valued by customers around the world. By combining unique technologies with deep domain expertise across cybersecurity, missile defense, space, connected infrastructure, transportation, smart cities, and more, we're providing tomorrow's solutions today.Salary Range: $29.95 - $52.40We value our employees and want our employees to take care of their overall wellbeing, which is why we offer best-in-class benefits such as medical, dental, vision, paid time off, Employee Stock Ownership Plan (ESOP), 401(k), life insurance, flexible work schedules, and holidays to fit your busy lifestyle!This position will be posted for a minimum of 3 days and will continue to be posted for an average of 30 days until a qualified applicant is selected or the position has been cancelled.Parsons is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, veteran status or any other protected status.We truly invest and care about our employee's wellbeing and provide endless growth opportunities as the sky is the limit, so aim for the stars! Imagine next and join the Parsons quest-APPLY TODAY! Parsons is aware of fraudulent recruitment practices. To learn more about recruitment fraud and how to report it, please refer to ************************************************

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas - immunology, oncology, neuroscience, and eye care - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at *************** Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok (******************************* . Job Description Purpose The QC Lab Supervisor II is responsible for the organization, administration, and supervision of Lab Analysts and other Lab employees; properly overseeing the day-to-day operations by prioritizing shop floor presence. Oversees the processes of the chemical analysis and release of raw materials, in-process, and final products in compliance with current quality criteria while respecting deadlines and managing costs. Ensures effective and efficient utilization of laboratory resources through management of laboratory support activities. The QC Supervisor II is expected to work independently and serve as a mentor to other supervisors. Responsibilities + Responsible for leading and developing a high performing team while prioritizing shop floor presence. This includes hiring, setting performance expectations, providing continuous and on-time performance feedback, coaching staff, assisting in problem-solving, and handling employee matters. Ensures that the department has the appropriate talent and level of performance to meet business objectives. Monitors administration of training, identifies training needs, and ensures development of team. + Oversees the operation and functions of the laboratory group which may include Raw Materials, Finished Products, Projects/validation samples, MEC, and stability samples. Organizes laboratory activity by coordinating the activity of personnel depending on the demands of planning. Controls the products (raw materials, intermediates, and finished products) by following procedures (general, specific, of analysis and use, and qualification of equipment) to meet the lab testing schedule. + Identifies aspects of the tests or results warranting further attention and implements corrective actions. + Reviews and approves Analytical data (may relate to analytical product release depending on regional regulatory requirements). + Supports laboratory investigations, including out-of-specification test results, and ensures effective corrective actions are implemented. + Effectively understands, communicates, and presents QC Metrics. Attends and leads Tier meetings. + Ensures appropriate procedures are in place and that QC activities are executed in line with internal procedures, requirements of cGMP, and relevant safety standards. Identifies improvement opportunities to lab processes and participates in continuous improvement projects. Assesses impact of changes to Laboratory Operations and communicates changes to team. + Assists analysts with analytical/microbial instrumentation. Assures instrumentation availability to achieve schedule and improves capacity by ensuring that preventive and repair maintenance as well as material qualifications are carried out in a timely matter. Plans the needs of instruments by maintaining permanent technical and technological intelligence. Applies systematic corrections and/or corrective actions that mitigate the risk of recurrent instrumentation failures. + Participates in periodic inspection of laboratory facilities to ensure that they are operated and administered according to Good Manufacturing Practices (GMP) and Good Laboratory Practices, maintaining laboratory audit readiness. When required, support supplier, internal, and regulatory audits. + May serve as a backup when the Lab Manager is unavailable. Provides mentorship and guidance to other supervisors who are developing leadership capability. Qualifications Qualifications + Bachelor's Degree required, preferably in a Scientific field (Chemistry, Microbiology, or Biology) + 2+ years of experience supervising a team and at least 2 years of experience working in a QC Lab. + Demonstrated advanced scientific knowledge and technical expertise in chemistry, technical writing, investigations, analytical laboratory equipment, and laboratory operations required. + General knowledge in cGMPs, compendia, and regulations required. + Effective problem-solving, decision-making, teamwork, influence, negotiation, and conflict resolution skills required. + Demonstrated leadership skills and ability to foster an inclusive environment. Ability to effectively train and mentor other supervisors. + Ability to work cross-functionally and coordinate work both within the department and with other departments. + Ability to interpret the impact of laboratory data for appropriate and effective actions. + Ability to identify, develop, communicate, and follow through to completion necessary corrective action plans to resolve problems. *The selected candidate must be available to work on a 1st Shift, Monday to Friday. Additional Information Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law: + The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future. + We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees. + This job is eligible to participate in our short-term incentive programs. Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company's sole and absolute discretion, consistent with applicable law. AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled. US & Puerto Rico only - to learn more, visit ************************************************************************* US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: *************************************************************

**Kelly Science & Clinical** is seeking **_Stability Chemist_** for a **contract** position at client in **Naguabo, Puerto Rico.** **Salary: $16.00 per/hour** **Schedule:** 1st shift & 2 nd shift, overtime hours and weekends may be required as necessary _In this role you'll be responsible for Performs chemical and physical analysis to stability products and is involved in the development and validation of analytical procedures following R&D guidelines_ **Responsibilities:** + Perform analytical testing on stability products and samples from other plants. + Assure that test activities are performed in accordance with written procedures + Prepares reports of analytical results. + Maintain informed the progress of test schedules. + Inform the Lab. Manager of supplies needs, standards, and instrument change parts. + Discuss with Lab. Manager of any failure in the analysis results + Manage and handling of hazardous waste in the generation area and coordinate the proper manage to the hazardous waste shed. + Records all analytical result in the analysis forms and laboratory notebooks following specifications, SOP'S and CGMP Guidelines. + Prepares all test solutions to be used in the laboratory, following appropriate specification or analitical procedures. + Maintains Laboratory area in an orderly and clean manner, always following the Current Good Manufacturing Practices (cGMP) and Good Laboratory Practices (cGLP + Performs other specific stability work as assigned by the Lab Manager or designee. + Notifies Lab Manager when errors, incongruities or out specification conditions are observed on documentation and in the analytical data. **Qualifications:** + Bachelor's Degree in Chemistry and at least two years of experience in an analytical laboratory, or equivalent combination of education and experience. + Laboratory equipment: HPLC, GC, UV/VIS, pH meters, IR, RI,Karl Fisher Titrators, analytical balances, scientific calculators and others. + Spanish/English communication skills, both written and verbal. **For this position Kelly** ** ** **Science PR Offers!** + Exposure to a variety of career opportunities as a result of our expansive network of client companies + Career guides, information and tools to help you successfully position yourself throughout every stage of your career + Access to more than 3,000 online training courses through our Kelly Learning Center + Weekly pay + **Sick, Vacations &** **H** **olidays paid *** + **Christmas bonus*** + **_*_** **_Must comply with minimum established requirements to qualify._** **Apply to be a Stability** **_Chemist_** **today! ** **Recruiter: Lilly Abouomar** **\#SETTPuertoRico** As part of our promise to talent, Kelly supports those who work with us through a variety of benefits, perks, and work-related resources. Kelly offers eligible employees voluntary benefit plans including medical, dental, vision, telemedicine, term life, whole life, accident insurance, critical illness, a legal plan, and short-term disability. As a Kelly employee, you will have access to a retirement savings plan, service bonus and holiday pay plans (earn up to eight paid holidays per benefit year), and a transit spending account. In addition, employees are entitled to earn paid sick leave under the applicable state or local plan. Click here (********************************************************************* for more information on benefits and perks that may be available to you as a member of the Kelly Talent Community. Why Kelly Science & Clinical? Kelly Science & Clinical is your connection to premier scientific and clinical companies looking to hire industry experts just like you. Our team creates expert talent solutions to solve the world's most critical challenges. Every day, we match science professionals with dream jobs that fit their skills, interests, and career goals-it's the way we think job searching should be. Nearly 100 percent of our science recruiters have a professional background and education in science, so we know a thing or two about the science market and how to get your expertise noticed. About Kelly Work changes everything. And at Kelly, we're obsessed with where it can take you. To us, it's about more than simply accepting your next job opportunity. It's the fuel that powers every next step of your life. It's the ripple effect that changes and improves everything for your family, your community, and the world. Which is why, here at Kelly, we are dedicated to providing you with limitless opportunities to enrich your life-just ask the 300,000 people we employ each year. Kelly is committed to providing equal employment opportunities to all qualified employees and applicants regardless of race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or any other legally protected status, and we take affirmative action to recruit, employ, and advance qualified individuals with disabilities and protected veterans in the workforce. Requests for accommodation related to our application process can be directed to the Kelly Human Resource Knowledge Center. Kelly complies with the requirements of California's state and local Fair Chance laws. A conviction does not automatically bar individuals from employment. Kelly participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S. Kelly Services is proud to be an Equal Employment Opportunity and Affirmative Action employer. We welcome, value, and embrace diversity at all levels and are committed to building a team that is inclusive of a variety of backgrounds, communities, perspectives, and abilities. At Kelly, we believe that the more inclusive we are, the better services we can provide. Requests for accommodation related to our application process can be directed to Kelly's Human Resource Knowledge Center. Kelly complies with the requirements of California's state and local Fair Chance laws. A conviction does not automatically bar individuals from employment.

Validation & Engineering Group (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. Job Description Under general direction, functions as the technical specialist for testing & development in areas of molecular biology and microbiology. Focus is on the complex technical issues and scope is typically multi-organizational and/or multi-site and /or involving outside resources. Functions: Responsible for providing technical guidance, Provide reports, data analysis and ensure flow of communication between technical groups including following up on and resolving issues that arise. Resolve technical issues and troubleshoot for assays as necessary, Ensure lab compliance - which includes implementing procedures that enhance GMP, GLP and safety. Manage existing and/or develop and implement new programs, processes and methodologies, Develop, revise and audit various complex controlled documents that may have multi-organizational and/or multi-site impact. Approve lab investigations, Lead audit teams May serve as subject matter expert to develop technical training. May perform routine work in a specific area of responsibility as necessary. Represents the department/organization on various teams, Independently responsible for following through on multi-site action items.. May interact with regulatory agencies regarding area(s) of responsibility including written responses. May resolve issues with outside resources. Performs special projects as requested by supervisor, May supervise employees as necessary to meet technical requirements. Competencies/Skills: Understand, support and demonstrate values. Excellent communication skills, facilitation and presentation skills. Excellent technical writing skills. Strong computer operation skills including work processing, presentation, database and spreadsheet application skills, Excellent project management and organizational skills including the ability to independently understand, follow, implement complex instructions and follow assignments through to completion. Advanced skill in handling multiple responsibilities, tasks and projects simultaneously including ability to shift priorities. Excellent knowledge of and experience with processes involved in quality analytical labs, validation, manufacturing, quality assurance, process development and distribution. Extensive knowledge of all testing including the development and validation of assays and the ability to perform all testing in specific area of responsibility. Knowledge of pharmaceutical processes, Strong knowledge of U.S. regulations and practices pertaining to the testing of pharmaceutical/biological products. Knowledge of basic international regulations and practices pertaining to the testing of pharmaceutical/biological products Extensive knowledge and application of GMPs/CFRs. Ability to evaluate compliance issues. Skill in evaluating and documenting according to Company and various guidelines. Proficient at maintenance, troubleshooting and operation of equipment in area of expertise. Advanced scientific data analysis and interpretation skills. Advanced skills in solving complex problems. Advanced data trending and evaluation. Strong skill in working independently and to effectively interact with various levels. Ability to interact with regulatory agencies both orally and in writing. Initiate, coordinate and lead cross functional teams. Excellent skill in leading, motivating, influencing, and negotiating Qualifications Expertise in Technical Writing, must have written reports for investigations, method transfers/validations, • Root Cause Analysis experience and CAPA identification and implementation • Fully bilingual English/Spanish • Meeting and conference calls facilitator, with multilevel audience (Upper level Management to analysts) • Presentation skills • Oriented to solve problems and troubleshoot, technical proficiency • Simple statistical assessments Doctorate degree in Sciences or Master's degree in Sciences & 3 years of directly related experience or Bachelor's degree in Sciences & 5 years of directly related experience • BS in Chemistry or Biochemistry preferred • Knowledge in TrackWise, CDOCS, Maximo • Knowledge in PowerPoint, Excel, Word, One Note Additional Information Positions available for Puerto Rico. Validation and Engineering Group, Inc. is an Equal Employment Opportunity employer.

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: Laboratory experience in a GMP environment within the Pharmaceutical and/or Biotech industry Fully bilingual communications skills (English and Spanish) Good communications and presentation skills in English and Spanish Project management skills Strong organizational skills, including ability to follow assignments through to completion Enhanced skills in leading, influencing and negotiating Knowledge of and experience with processes involved in manufacturing and distribution, QA, QC, validation and process development Basic Knowledge and skills of word processing, presentations, and spreadsheet applications Qualifications Requirements/Knowledge/Education/Skills: Ph.D OR MD + 2 years of directly related experience OR BS + 4 years of directly related experience OR Associates + 8 years of directly related experience OR High school/GED + 10 years of directly related experience. Educational background in Chemistry, Microbiology, Biology or Life Sciences 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.