Chemist Jobs in Tampa, FL

As a Lab Technician you will perform a variety of routine analytical and physical testing on mining, coatings, and road materials, research and development samples and finished products. You will also make detailed observations and provide basic interpretation of data and accurate reporting of results. Primary Duties and Responsibilities: Analytical services that the Lab Technician will perform include samples from all departments mining, coatings and road products. Analytical Equipment that the Lab Technician will be operating include Auto Titrator, Digital diluter, UV/Vis Spectrophotometer, Spectrophotometer, X-Ray fluorescence and ICP-OES, GC-FID, HPLC with UV, ELSD and RI detectors. FTIR, DSC and Particle Size Analyzer. Physical prep equipment includes BICO Grinder, Ball Mill Grinder, and Pellet Press. Also, any new technique added due business growth. Maintains lab equipment and supplies. Works safely and maintains a clean and sanitary work area in accordance with standard laboratory practice and procedures. Work in accordance with laboratory chemical hygiene plan. Other job duties, as assigned. Education/Experience Requirements: Associate degree in a Physical Science, minimum or Minimum of two years working in a laboratory environment. Internship experience will be considered. Skills and Competencies: Must be self-motivated with a can-do attitude. Must be able to work independently. Must be proficient in math and possess knowledge of basic chemistry, lab equipment, instrumentation and related manufacturing processes. Attention to detail and accuracy are critical. Proficiency with MS Office products - Word, Excel, PowerPoint and Outlook, required. Excellent verbal and written communication skills. Ability to work effectively in a team-based environment. Basic knowledge of standard lab safety procedures including personal protection equipment (PPE).

Job Title: Chemist Schedule: Monday-Friday 8am-4:30pm Hourly Pay Rate: $25-$33 Temp to hire role for 3-6 months before converting Responsible for conducting chemical, physical, and instrumental laboratory tests on materials to support research and development, quality control, and environmental standards. This role involves the experimental, theoretical, or practical application of chemistry and related sciences to ensure product and process quality. Essential Functions and Responsibilities: \t \t Monitor raw material and finished product quality to ensure they meet specified standards. \t \t \t Analyze organic and inorganic compounds to determine their chemical or physical properties, using techniques such as chromatography, spectroscopy, or spectrophotometry. \t \t \t Prepare technical reports, graphs, and charts to document experimental findings. \t \t \t Review, compile, and interpret test results, ensuring accurate and timely reporting. \t \t \t Coordinate with contract laboratories to send samples and track testing progress. \t \t \t Prepare chemical solutions for analysis and, when necessary, develop and verify testing methods. \t \t \t Perform routine maintenance and troubleshooting of laboratory instruments. \t \t \t Clean, sterilize, and maintain laboratory instruments and equipment. \t \t \t Manage inventory and order necessary materials to maintain supply levels. \t \t \t Adhere to and comply with standard operating procedures (SOPs), safety policies, and cGMP guidelines. \t \t \t Assess and evaluate the quality, identity, and safety of raw materials and finished products. \t \t \t Collaborate with Quality Assurance, Formulations, and Purchasing teams to review new raw materials. \t \t \t Establish specifications for raw materials and finished products alongside Quality Assurance. \t \t \t Ensure proper laboratory procedure flow and assist in general lab operations. \t \t \t Follow safety protocols, report unsafe conditions, and correct hazardous situations. \t \t \t Perform other tasks as needed or directed by management. \t Knowledge: \t \t Proficient in the use of arithmetic, algebra, geometry, calculus, and statistics in QC laboratory functions. \t \t \t Strong understanding of the chemical composition, structure, properties, and chemical processes of substances, including their interactions and disposal methods. \t \t \t Familiar with the theoretical and practical aspects of Analytical Chemistry, including chromatographic and spectroscopic techniques for isolating, identifying, and quantifying chemicals. \t \t \t Knowledgeable in the operation, design, repair, and maintenance of laboratory instruments and equipment. \t \t\t\t\t \t\t\t\t\t \t\t\t\t \t\t\t\t \t\t\t\tAs 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. \t\t\t \t\t\t \t\t\t\t \t\t\t\t\t \t\t\t\t \t\t\t\t \t\t\t\t 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. \t\t\t \t\t\t

PRIMARY PURPOSE: Develop, transfer and validation of HPLC, Gas Chromatography, ICP and AA methodology. Must have extensive cGMP experience and be able to provide leadership and mentoring to Chemist I and Chemist II in QC Laboratory. Must have thorough understanding of Good Laboratory Practices and Good Documentation Practices, as well as compendial methodology. Must have experience in writing Standard Operating Procedures, Protocols and Reports. MAJOR DUTIES AND RESPONSIBILITIES: Perform all the activities for development, transfer and validation of analytical methods. Revise and write Validation Protocols, Test Methods, Validation Reports and SOP's. Testing of incoming materials, using compendial test methods (USP, PhEUR, JP) Testing of stability samples, in process samples and finished product testing, using a variety of techniques, such as HPLC, GC, AA, ICP, UV/Vis, etc. Accurately records raw data and analyzes, as well as calculates and interprets the results. Occasional customer interaction in a professional environment. Responsible for out of specification test results, investigation, and implementation of corrective actions. Ensure testing is performed accurately and in compliance with GLP, cGMP, cUSP, SOP and other approved test methods and protocols. Maintain analytical reagents in laboratory including but not limited to: inventory, current MSDS, PPE required for handling, waste generation and disposal. Assist Validation teams in cleaning validation activities. Support laboratory troubleshooting needs by interacting with vendors, customers and other relevant SMEs. Promote GMP and safety throughout the facility. Promote continuous improvement and customer satisfaction. Follow-up on OOS's and CAPAs to verify compliance. Potential exists for exposure to potentially harmful chemicals. Participate in other activities as assigned by the Lab Manager or VP Quality. QUALIFICATIONS: Required Knowledge of Compendia testing. Knowledge of the chemical composition, structure, and properties of substances and of the chemical processes and transformations that they undergo. This includes uses of chemicals and their interactions, danger signs, production techniques, and disposal methods. Knowledge of raw materials, production processes, quality control, and other techniques for maximizing the effective manufacture of goods. Working knowledge of FDA regulations for laboratory testing and disposition. Ability to use a personal computer and peripheral equipment to accurately enter an analyze data and produce reports. Knowledge of chemical safety and protective equipment. Expertise in various analytical equipment and techniques utilized in an analytical laboratory including but not limited to pH, viscosity, specific gravity, infrared spectroscopy, HPLC, GC, ICP, UV/VIS, atomic absorption. Ability to establish priorities, work independently, productively, and proceed with objectives without supervision. Ability to handle and resolve recurring problems. Understanding the implications of new information for both current and future problem-solving and decision-making. Ability to troubleshoot HPLC, GC, ICP and AA analyses Ability to communicate effectively, concisely in a professional manner with clients and others. Ability to work in a dynamic fast paced environment-sometimes rapidly shifting priorities. Ability to concentrate in such an environment and perform quality work. Must be able to lift up to 15 pounds. EDUCATION AND TRAINING: Bachelor's degree in Chemistry or related discipline. Must have three or more years' experience working in an analytical laboratory in an FDA regulated industry.

Senior Chemist Analytical Laboratory Employment Type: Contract to hire About the Company Join a leading contract development and manufacturing organization (CDMO) known for transforming great ideas into remarkable health and wellness products. Our team supports a wide range of pharmaceutical and personal care innovations, emphasizing scientific excellence, quality compliance, and continuous improvement. We foster a collaborative environment where your expertise directly impacts the success of both customers and consumers worldwide. This position ensures continuity in laboratory operations with expertise in HPLC, Gas Chromatography (GC), and Atomic Absorption (AA) techniques. The Senior Chemist will play a leadership role by mentoring Chemist I and II personnel while maintaining strict compliance with cGMP, GLP, and GDP standards. Experience in Method Validation, including development, protocol generation, and reporting, is essential. Key Responsibilities Qualify, validate, and maintain laboratory equipment Execute method transfer and validation activities Revise and author Test Methods and Standard Operating Procedures (SOPs) Perform testing on raw materials, in-process, and finished product samples Record raw data, analyze results, and interpret findings accurately Investigate and document Out-of-Specification (OOS) results; implement corrective actions Ensure compliance with GLP, GMP, USP, and other regulatory standards Maintain analytical reagent inventory, MSDS documentation, and proper disposal procedures Support cleaning validation efforts alongside the Validation Team Promote safety, GMP compliance, and continuous improvement within the lab Follow up on OOS findings and CAPAs for compliance verification Participate in other duties as assigned by Lab Manager or VP of Quality Required Skills & Knowledge Strong knowledge of compendial (USP, EP) testing Familiarity with FDA regulations specific to lab testing in drug/device industries Proficient in MS Office and laboratory software systems Skilled in chemical safety protocols and PPE requirements Hands-on experience with pH meters, viscometers, IR, HPLC, GC, and atomic absorption Strong problem-solving, multitasking, and organizational skills Effective verbal and written communication skills Ability to work independently in a fast-paced, changing environment Education & Experience Bachelor s Degree in Chemistry or related scientific discipline 4 5 years of experience in an analytical laboratory within an FDA-regulated environment EOE/ADA IND123 #LI-KC1

Automation Personnel Services is looking for a Laboratory Chemist for a company based in Oldsmar, FL. In this role, you will have the opportunity to advance your career while being a key part of a leading dietary supplement manufacturer. Pay Rate $20.00 - $25.00 per hour Schedule and Hours Monday through Friday, 8:00 am to 5:00 pm. Laboratory Chemist Duties and Responsibilities• Function as the technical specialist for testing & development in molecular biology and microbiology.• Provide technical guidance and ensure effective communication between technical groups.• Conduct chemical analyses and quality control testing on raw materials, in-process samples, and finished dietary supplements.• Develop and validate analytical testing methods in compliance with industry standards.• Maintain, calibrate, and operate laboratory equipment such as HPLC, GC, UV-Vis Spectroscopy, and FTIR.• Prepare chemical reagents and solutions in accordance with laboratory protocols.• Record, analyze, and interpret experimental data, preparing technical reports for internal and regulatory use.• Ensure compliance with Good Manufacturing Practices (GMP), FDA regulations, and other industry standards.• Manage existing and/or develop and implement new programs, processes, and methodologies.• Develop, revise, and audit complex controlled documents with multi-organizational and/or multi-site impact.• Approve lab investigations and lead audit teams.• Interact with regulatory agencies, providing written responses when necessary.• Perform troubleshooting and root cause analysis for assays and technical issues.• May supervise employees to meet technical requirements. Laboratory Chemist Qualifications and Requirements • Doctorate or Master’s degree in Sciences, Chemistry or Biochemistry.• 3+ years proven work experience in a laboratory setting.• Experience in quality analytical labs, validation, manufacturing, quality assurance, process development, and distribution.• Strong knowledge of U.S. regulations and practices pertaining to the testing of pharmaceutical/biological products, including GMPs/CFRs.• Expertise in technical writing, including experience with investigations, method transfers/validations, and CAPA identification/implementation.• Strong problem-solving skills, with experience in root cause analysis and CAPA implementation. Job Type Full-time, Temporary to Hire Benefits • Weekly Pay• 401(k) retirement plan• Medical, dental, vision, short-term disability and life insurance• 5 paid Vacation Days after 1 year of continuous service (paid as a service bonus)• 6 paid Holidays after 1500 continuous hours of service within a calendar year Interested in this job? Click Apply Now, email your resume to aps Tampa@apstemps.com, or call us at 813.888.7508 to learn more. You can also apply in person at our office located at Automation Personnel Services Tampa Branch 3918 West Hillsborough Ave. Tampa, FL 33614 Bonus Opportunity! We are also offering a $50.00 referral bonus. Both employee and referral must stay on assignment for 30 days to receive the payout. About Automation Personnel ServicesAutomation Personnel Services is an award-winning staffing agency with more than 30 years of experience in manufacturing and light-industrial staffing. Automation Personnel Services is the winner of the ClearlyRated® Best of Staffing Talent Award from 2019-2024, and the ClearlyRated® Best of Staffing Client Award from 2016-2024. Automation Personnel Services is also the recipient of the Safety Standard of Excellence Award by the American Staffing Association and was named one of the Best Staffing Companies to Work For 2022 by CIO Views Magazine. Our goal is finding you the right job! Equal Opportunity Employer APSTampa

The Product Development Scientist role: Responsible for developing and leading scaleup of new products to commercialization. Creative and self-motivated, the Product Development Scientist plays a key role in introducing novel ideas and techniques to the product development and commercialization process - leading directly to improved commercial results for the company. Duties & Responsibilities: Research and develop creative and novel products with a focus on extracts and distillates - bringing them to commercial fruition. Utilize and maintain a range of laboratory and pilot-plant equipment (introducing new equipment and techniques where necessary) during product development. Identify unique raw materials for the development of new products. Work with the Innovation, QC teams, VP of Innovation, and Category Managers in the planning of R&D project priorities. Provide Senior Innovation Manager-Coffee and Tea with ongoing and consistent communication of status of R&D efforts and commercial implications of R&D work. Lead in planning, monitoring and documentation of plant trials leading to successful commercialization of new products. Execute shelf life and stability studies of new product development. Support the Production Supervisor to determine, define and improve product tolerance limits of new and existing products. Lead projects relating to quality or cost improvement. Lead Continuous improvement projects as pertinent. Lead projects and evaluation of alternate raw material sources with detailed reports of findings Participate in sensory evaluation of R&D projects, new products, reformulations, ingredient substitutions, and competitive products. Maintain and share accurate records of lab work, and documentation of used ingredients, formulation modifications and provide statistical evaluations and reports. Develop product and raw material specifications suitable for QA, QC, Regulatory, and Customer Display understanding of HACCP, GMP, and Acidified Foods Filing Demonstrate proficient use of internal Systems (JDE, STARS, SharePoint, GICP etc.) Coordinate with Quality Control in scheduling the use of laboratory facilities and equipment to ensure the appropriate levels of R&D, application and QA testing are performed. Stay abreast of current, worldwide R&D efforts and transfer new knowledge to Treatt product lines. Continually explore and identify ways to tailor Treatt product lines to appeal to untapped markets. Provide/Support Capex planning by identifying and costing out potential solutions that may grow business. Provide both technical and non-technical articles and reports for internal publication. Cultivate sales opportunities with current customers and other industry contacts by building strong partnering relationships with key technical personnel in these organizations. Participate in customer call and/or product demonstrations as needed. Work with customers as needed on new product developments and reformulations. Partner with sales team members to identify and analyze consumer market trends that might provide increased sales and product development opportunities. Act in the best interest of Treatt at all times. All other duties as customary or as delegated. Work primarily independently or with minimal supervision to complete required tasks. Education & Traininig: A bachelor's degree in chemistry, Food Science or a related Scientific field, plus a minimum of 1 years lab and product development experience in a closely affiliated field. Knowledge & Experience: A proven independent worker with strong creativity and problem-solving skills. An in-depth understanding of fundamental chemistry principles. Demonstrate knowledge of regulations, policies, procedures and processes in food science and product development. Superior ability to research and analyze information and data to arrive at valid conclusions and plans of actions. Effective communication skills at all levels - both orally and in writing. Basic knowledge in the use of various laboratory equipment and methodologies. Including: Gas chromatography, mass spectrometry and other analytical measurement methods a plus Ability to use various spreadsheets, word-processing and database computer software. Environment: Normal laboratory and manufacturing working conditions.

We are currently accepting applications for future Quality Control Chemists. WHY CORERX CoreRx, a dynamic pharmaceutical technology company that empowers its employees with responsibility and offers a supportive and highly progressive work environment. At CoreRx you will find a challenging career path directed towards growth and opportunity. We employ talented, motivated people - team players who are innovative thinkers. We offer our employees a comprehensive, competitive program of benefits and a corporate culture based on core values that include innovation, a results-oriented focus and ethical behavior. If we do not have any positions that fit your needs at this time; We invite you to join our talent network and stay informed about future opportunities by submitting your resume. Thank you for choosing CoreRx as your employer of choice. DESCRIPTION The Analytical Chemist II is an integral part of the team, contributing to our success by performing raw materials and clinical and commercial pharmaceutical products testing according to compendial method and/or methods provided by analytical development team or clients. ESSENTIAL DUTIES AND RESPONSIBILITIES Performs relevant QC testing, such as HPLC, GC, Dissolution, Malvern and wet chemistry testing as required in compliance with cGMP requirements, compendia standards, and internal procedures Ensures testing is properly conducted and documented for all performed activities with emphasis on data integrity Prepare test solutions, volumetric solutions, and samples used in analysis Performs assigned physical tests, chemical tests and assay on raw materials, active pharmaceutical ingredients, in-process, finished, and stability products in an FDA regulated lab environment Perform analysis with a practical understanding of the test procedure and instrument operation Perform laboratory analysis right first time, contemporaneous documentation, analyze and document the results Conducts laboratory investigation under the supervision of laboratory manager. Complies with all regulatory/ in-house requirements may include but not be limited to safety, housekeeping, laboratory chemical waste, cGMP, documentation Maintain required level of training needed to perform a GMP task Notify manager immediately of nonconforming data or unexpected occurrences Organize work schedule to complete assigned tasks efficiently and on schedule Work under direction provided by manager Conscientious with safety procedures and knowledgeable of hazardous waste procedures Performs other related duties as assigned by management EXPERIENCE AND EDUCATION REQUIREMENTS Experience in UPLC/HPLC GMP operations Knowledge with analytical equipment and Part 11 compliant software, such as Chemstation™, Chromeleon™, EMPOWER™, and Laboratory Information Management System. Demonstrated ability to work as an independent, self-motivated, detail-oriented, result-driven and highly flexible team-player in a fast-paced working environment Proficient in Microsoft Office Suite or similar software Minimum of 2 years experience preferred in an FDA-regulated pharmaceutical environment Experience in other highly regulated laboratory settings will be considered BS/BA in life science or chemistry required Equivalent experience may substitute for stated requirements PHYSICAL DEMANDS Regularly required to stand. Frequently required to sit, walk, talk, hear, handle or feel tools or controls Occasionally required to reach with hands and arms, stoop, crouch, climb or balance, kneel Vision suitable for performing detailed inspections May be required to move items weighing up to 25 lb Ability to communicate clearly in both written and verbal form We are an equal opportunity/equal access/affirmative action employer fully committed to achieving a diverse workforce and complies with all applicable Federal and State laws, regulations, and executive orders regarding nondiscrimination and affirmative action with our hiring activities. We do not discriminate based on race, color, religion, ethnic or national origin, gender, genetic information, age, disability, sexual orientation, gender identity, gender expression, and veteran's status. Notification to Agencies: Please note that CoreRx Inc. does not accept unsolicited resumes from recruiters or employment agencies. In the absence of a signed Master Service Agreement, and specific approval to submit resumes to an approved requisition, CoreRx Inc. will not consider or approve payment regarding recruiter fees or referral compensation.

Short Description: FL-DEA-Long Term Care Ombudsman Program-QC Analyst (PT 20hr/s per week) -4 hrs a day, Monday thru Friday. Hours worked are flexible as long as they are the same each day. Complete Description: FL-DEA-Long Term Care Ombudsman Program-Quality Control Analyst Dress Code: Business Work Environment: Professional Business Office Candidate Responsibilities: * Answering phones * Typing * Strong data entry * Imputing data into RTC Data Base * Working with Microsoft Office Suite (Excel, Word, Outlook, Adobe) * Handling customer complaints Experience Required: * 1 year of professional office experience * Strong data entry skills * Attention to detail * Proofreading/Grammar * Strong typing skills

Hybrid role in St. Petersburg, FL At Vault we specialize in providing personal insurance for highly successful individuals and their families. As a fast-growing disrupter Vault is fueled by a team inspired to protect our customers' most prized possessions. When others say it can't be done Vault's unrivaled business model equips our underwriters with the ability to offer more coverage and customized solutions for the most exquisite homes, automobiles and collectibles. Our in-house risk managers are experts when it comes to understanding the unique intricacies of insuring successful customers, ensuring proper coverage, loss prevention and emergency preparations. Why Choose Vault Voted Best Places to work in Tampa Bay An innovative, open-minded environment, built on trust and empowerment A diverse and inclusive organization where we value each individuals' strengths and expertise A team committed to charity and community involvement Mentorship from the top minds in the industry A forward-thinking team backed by cutting edge technology A-Financial Strength rating by AM Best Comprehensive benefits tailored to your lifestyle Job Responsibilities include but are not limited to: · Conduct market research to identify opportunities for new products and enhancements to existing offerings. · Analyze data related to customer preferences, market trends, and competitive products. · Collaborate with product managers, marketing teams, and engineers to develop product specifications and requirements. · Support the product development process, including prototyping, testing, and validation. · Monitor and report on product performance post-launch, providing insights and recommendations for improvements. · Assist in the preparation of product documentation, including business cases, feasibility studies, and project plans. · Maintain strong relationships with internal stakeholders and external partners. · Ensure Personal Lines policy forms are accurate, in compliance, producing effectively and supporting our company's goal to offer a competitive coverage product to our members · Work closely with Actuarial, Underwriting, Marketing, and Claims to develop forms, product manuals, product comparisons and product communications · Create and enhance the company's product including, but not limited to, forms, manuals, member policy package, implementation of forms, etc., to ensure competitiveness in the marketplace · Draft and prepare filings and responses to negotiate approval for form and rule filings with the Department of Insurance (DOI) and Office of Insurance Regulation (OIR) through to completion · Research primary competitors for opportunities for improvement · Interpret insurance forms, statutes, rules, regulations, develops conclusions, and makes recommendations · Perform analysis of existing forms and manuals on a regularly schedule basis for effectiveness · Research and analyze external information sources to provide updated, accurate competitive analysis including rates, guidelines, and forms coverage information · Compile, analyze and report on product market trends to assist in determining product strategy · Consistently perform User Acceptance Testing for accuracy of enhancements and modifications of forms installations, identify, document and report discrepancies found · Perform all responsibilities using established department processes, quality control procedures and checklists Job Requirements include but are not limited to: - Bachelor's degree in Business, Marketing, or a related field -5-7 years of P&C insurance experience, preferably high net worth experience - 2+ years of experience in product development or a related field - Strong analytical and problem-solving skills - Excellent communication and collaboration skills - Ability to work independently and manage multiple projects simultaneously - Proficiency in Microsoft Office and project management tools Benefits include but are not limited to: Flexible Spending Accounts & Health Savings Accounts, with company contributions Company paid comprehensive life & disability insurance plans. 24/7 Telehealth Doctor Access, Virtual wellness screenings, Employee Assistance Programs Company 401k retirement plan with Day 1 eligibility (5% company match, 100% immediate vesting) 23 PTO days/yr + 10 paid holidays... and so much more! We believe diversity makes us better, and we seek to create a workplace where all feel a sense of belonging.

If you are a strategic thinker passionate about driving solutions and mitigating risk; you have found the right team. The Testing CoE (Center of Excellence) team is responsible for ensuring a strong and consistent control environment across the firm. This role is a great opportunity to be working with a large Controls Testing team and help establish a newly formed organization which provides the potential hire a good starting point within the firm. As a Controls Testing Associate in the Testing Center of Excellence, you will be responsible for the execution of independent risk-based, point-in-time evaluations of the control design adequacy and execution effectiveness, to mitigate compliance, conduct and operational risks. The role requires overseeing the performance of complex evaluations of business processes through a comparison of actual processes against expected practices (policies, standards, procedures, laws, rules and regulations). Testing activities often include sophisticated data analytics on large datasets and regular engagement with senior stakeholders across the firm. This is an exciting opportunity to work on key risk initiatives as they become the focus of the firm and across the financial services industry. You will excel at creative thinking and problem solving; be self-motivated, confident and ready to work in a fast-paced, energetic environment. Through collaboration and analytical skills, you will contribute to the Testing CoE's overall success and strengthen the firm's compliance with regulatory obligations and industry standards. Job Responsibilities: Lead comprehensive control evaluations and substantive testing to independently assess the design and effectiveness of controls within the Consumer and Community Banking (CCB) sector. Ensure compliance with internal policies, procedures, and external laws, rules, and regulations, while identifying necessary remediation actions. This includes developing and executing testing procedures, meticulously documenting results, drawing informed conclusions, making actionable recommendations, and distributing detailed compliance testing review reports. Foster collaboration with Compliance and Operational Risk Officers on various engagements. This includes developing detailed test scripts, facilitating issue discussions, participating in business meetings, and drafting comprehensive final reports to ensure alignment and clarity. Utilize advanced critical thinking skills to apply substantive testing techniques, thoroughly evaluating the effectiveness of high-risk business processes and identifying potential areas for improvement. Proactively assess and monitor risks, ensuring adherence to firm standards, regulatory requirements, and industry best practices. Implement strategies to mitigate identified risks effectively. Collaborate with cross-functional teams and stakeholders to support the design and effectiveness of controls. Drive initiatives that enhance the business control environment through recommended updates to the Compliance and Operational Risk Evaluation (CORE) application. Develop and execute robust control test scripts aimed at identifying control weaknesses, determining root causes, and recommending practical solutions to enhance operational efficiency and control effectiveness. Document test steps and results in a comprehensive and organized manner, ensuring sufficient support and justification for testing conclusions. Maintain a high standard of documentation to facilitate transparency and accountability. Lead meetings with business owners at various management levels, delivering testing results and supporting sustainable control enhancements. Identify and capitalize on opportunities to strengthen controls and improve operational efficiency. Required qualifications, capabilities, and skills A minimum of 3+ years of experience or equivalent expertise in risk management, assessment, control evaluations, or a related field, within the financial services industry. Possess a strong understanding of industry standards and regulatory requirements. Demonstrated ability to analyze complex issues, develop and implement effective risk mitigation strategies, and communicate insights and recommendations clearly to senior stakeholders. Proficient knowledge of risk management frameworks, regulations, and industry best practices. Ability to stay updated with evolving regulatory landscapes and adapt strategies accordingly. Exceptional ability to develop and communicate well-founded recommendations based on regulatory guidance and standards, ensuring alignment with organizational goals and compliance requirements. Highly organized and detail-oriented, with a proven track record of managing multiple priorities and delivering results in a fast-paced environment. Strong analytical and communication skills, with the ability to convey complex information in a clear and concise manner to diverse audiences. Preferred qualifications, capabilities, and skills CISM, CRISC, CISSP, CISA, CCEP, CRCM, CRCMP, GRCP, or other industry-recognized risk and risk certifications preferred. A background in auditing and the ability to understand of internal controls is beneficial. Proficiency in MS (Microsoft Suite) Office - Microsoft Word, Excel, Access, and PowerPoint. Knowledge of data analytical tools such as Tableau, Altryx or Pythyon is a plus.

The CRIU Senior Analyst is responsible for performing complex and high-risk AML Reviews/Investigations of account activity from automated and/or manual sources, recommending the filing of Suspicious Activity Reports ("SARs"), relationship termination, and/or escalating matters to Senior Management, as appropriate. Cases are worked from beginning to completion in accordance with relevant Citi AML policies and procedures. The overall objective is to perform complex reviews/ investigations and provide analysis/ recommendations on AML cases. **Responsibilities:** + Business relationships, potential network activity, prominent/high-profile clients, entities designated as SDN/money laundering concern, and other sensitive matters. + Conduct independent research and analyze data on potentially suspicious and/or high-risk client cases using financial statements and documents + Document and report the review/investigation findings and prepare case files with required supporting documentation (e.g. media search results, copies of statements/checks, results from internal system searches etc.) + Follow-up with additional Point(s) of Contact (POC) as needed to identify additional information in support of the case. + Utilize pertinent information to write clear and concise summaries on the findings of investigations for management to determine next steps + Draft and file Suspicious Activity Reports (SARs) consistent with FinCEN requirements, and recommend relationship retention or termination + Communicate with senior management on compliance, legal and business AML issues + Appropriately assess risk when business decisions are made, demonstrating particular consideration for the firm's reputation and safeguarding Citigroup, its clients and assets, by driving compliance with applicable laws, rules and regulations, adhering to Policy, applying sound ethical judgment regarding personal behavior, conduct and business practices, and escalating, managing and reporting control issues with transparency. **Qualifications:** + 4-7 years relevant experience + Experience in writing and preparing Suspicious Activity Reports (SARs) in accordance with applicable regulatory requirements preferred + Proficient in MS Office + Proven analytical skills + Effective verbal and written communication skills + Comprehensive knowledge of AML regulations preferred **Education:** + Bachelor's/University degree or equivalent experience ------------------------------------------------------ **Job Family Group:** Compliance ------------------------------------------------------ **Job Family:** AML Execution ------------------------------------------------------ **Time Type:** Full time ------------------------------------------------------ **Primary Location:** Tampa Florida United States ------------------------------------------------------ **Primary Location Full Time Salary Range:** $79,120.00 - $118,680.00 In addition to salary, Citi's offerings may also include, for eligible employees, discretionary and formulaic incentive and retention awards. Citi offers competitive employee benefits, including: medical, dental & vision coverage; 401(k); life, accident, and disability insurance; and wellness programs. Citi also offers paid time off packages, including planned time off (vacation), unplanned time off (sick leave), and paid holidays. For additional information regarding Citi employee benefits, please visit citibenefits.com. Available offerings may vary by jurisdiction, job level, and date of hire. ------------------------------------------------------ **Anticipated Posting Close Date:** Apr 28, 2025 ------------------------------------------------------ _Citi is an equal opportunity employer, and qualified candidates will receive consideration without regard to their race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other characteristic protected by law._ _If you are a person with a disability and need a reasonable accommodation to use our search tools and/or apply for a career opportunity review Accessibility at Citi (*************************************************************************** ._ _View Citi's EEO Policy Statement (*********************************************** and the Know Your Rights (*********************************************************************************************** poster._ Citi is an equal opportunity and affirmative action employer. Minority/Female/Veteran/Individuals with Disabilities/Sexual Orientation/Gender Identity.

We are seeking a Food Science Analyst to join our New Product Development (NPD) team. This role will support the formulation, testing, and commercialization of innovative food and fresh-cut fruit products. The ideal candidate has a strong background in food science, product development, and quality assurance. They will work cross-functionally with QA, production, procurement, marketing, and food safety teams to ensure new products meet consumer expectations, quality standards, and regulatory requirements. Accountabilities: * NPD product formulation, including iterative testing in a food-safe environment to optimize ingredients for sensorial and shelf-life objectives. * Conduct sensory and shelf-life testing to assess product quality, flavor retention, and microbial stability. * Research and analyze in-market products, performing reverse-engineering of competitor formulations to identify innovation opportunities. * Ensure NPD processing and operational efficiencies, collaborating with production teams to streamline scale-up processes. * Prepare prototypes and mock-up samples for internal evaluations, consumer testing, and sales presentations. * Conduct analytical testing (e.g., pH, Brix, organoleptic) to assess product performance and ensure food quality and safety. * Research and test new ingredients, processing techniques, and preservation methods to enhance product quality and extend shelf life. * Work with suppliers and vendors to source high-quality raw materials for product development. * Maintain a food and ingredient inventory for NPD purposes, ensuring materials are available for ongoing trials. * Collaborate with cross-functional teams to ensure new products align with food safety regulations, labeling requirements, and industry standards. * Support sensory evaluation panels and consumer testing to optimize product flavor, texture, and appearance. * Document testing results, prepare reports, and present findings to internal stakeholders * Proactively brings thoughtful product recommendations to cross-functional teams that drive brand and business results. * Ability to substantiate recommendations with research, reasoning, and data. * Ability to work closely with suppliers in developing and improving their processes to achieve commercial viability of products. * Fosters an innovative, curiosity-inspired, food-forward mindset in the organization. Minimum Skills Required: * 1-3 years of work experience in food/beverage product/process development, quality assurance, or R&D. (fresh produce experience a plus) * Bachelor's degree in Food Science, Food Technology, Microbiology, or a related field. * Strong Knowledge of food processing, ingredient functionality, and packaging technologies. * Strong analytical skills with experience in food testing methodologies (e.g., microbiological, chemical, and physical testing). * Familiarity with food science equipment required * Experience with consumer insights, culinary innovation, and nutrition. * Familiarity with HACCP, GMPs, FDA, USDA, and other food safety regulations. * Ability to work in a fast-paced environment, manage multiple projects, and meet deadlines. * Excellent problem-solving skills, attention to detail, and teamwork capabilities. * Please note: This position does not qualify for relocation expenses. * * -------------------------------------------------------------------------------- DEL MONTE FRESH PRODUCE IS AN EEO/AA/V/H

Job title: Quality Control Analyst (US) Reporting to: Quality Control Supervisor Hours: 40 hours per week The objective of this role is to perform full analysis of flavor and fragrance raw materials that pass through the Quality Control laboratory. This encompasses the classical wet analysis, instrumental analysis to assess the acceptability of the profile, and organoleptic evaluation, to ensure that any material that enters or leaves the site is fit for purpose. What it's like to work here We've been making the world taste better since 1886 and sell over 3000 products in more than 90 countries, but we're only just getting started. We're on an exciting journey and have ambitious plans to become the indispensable partner of choice for the world's leading flavor and fragrance houses, beverage and consumer brands. On joining Treatt, you'll become one of over 300 international experts, working together to collectively surprise and delight our customers. Nothing is more important to us than the happiness of our people as without them, we'd never succeed. We think Treatt's a great place to work, but don't just take our word for it: "Everyone wants your feedback and opinion; it feels like a place of study where nurturing and encouragement are the standard. It is very clear the hard work that goes into providing excellence for customers, but it is also very apparent that managers have the same goals for helping us all to progress." - Anita, Innovation Scientist "Joining my close and supportive team was the most enjoyable way to gain more skills and increase my knowledge" - Ashley, Distillation Control Team Leader "Treatt creates an environment to help you be the best you can, with no two days the same and opportunities always available to help you learn and develop. The people and the culture create a fantastic company to be part of" - Rebecca, Commercial Coordinator What you'll be doing The duties and tasks of a Quality Control Analyst (QCA) involves the following: * Measure physical parameters of flavor and fragrance raw materials originating from various departments and external sources, which includes but is not exclusive to density, pH, refractive index, optical rotation, %Aldehyde, and Peroxide values. * Perform instrumental analysis on the above products which includes but is not exclusive to, UV spectroscopy, gas and liquid chromatography, and gas chromatography/mass spectroscopy. * Collect and analyze chromatographic data, being able to make conclusions on sample suitability and identify potential contamination, adulteration, or chromatography issues. * Perform general essential oil analysis but with further tests specific to the substance under analysis. * Participate in organoleptic evaluation of the products. * Prepare tasting solutions, arrange for a representative number of individuals to carry out analysis, and report data. * Prepare reagents for routine and non-routine analysis as well as analytical standards, to include accurately weighing and diluting stock standard materials for calibration purposes. * Identify problems, whether it be with a sample, process, or instrument, and propose solutions to address issues in a timely manner. * Carry out regular calibration and maintenance of the measuring instruments as prescribed by the working practices in the laboratory. * Perform internal microbiological testing. * Communicate with relevant departments for analytical samples to be sent for external analysis and collate the results. * Revise and review SOPs to ensure methods are up to date. * Assist in sample receipt to the Quality Control laboratory to maintain workflow of sample analysis to the required areas of the department. * Carry out day-to-day laboratory checks and housekeeping tasks, these includes washing up glassware and emptying the waste at the end of each day. * Capable of working independently and as a team player. * Contribute to the continuous improvement in the Quality Department (e.g. suggestions on improvements in efficiency, cost cutting, improvements in effectiveness of operations). * Follow any task and request as requested by Quality Control Supervisor or Quality Control manager. General tasks within the department: * Assist Quality Control Supervisor in maintaining chemical inventory for the Quality Control laboratory and in the purchase of any items necessary for routine analysis. * Ensure that the working area in the laboratory is maintained in a clean and orderly condition and that any hazard or potential hazard is reported to the Quality Control Supervisor or Quality Control Manager. * Report any faults or deficiencies in equipment or analytical practices to the Quality Control Supervisor or the Quality Control Manager. * Always maintain your own and other staff's healthy and safety ensuring a safe working environment. * Undergo training in areas specific to Treatt PLC business as required. * Undergo training in additional practices to those to aid the efficiency of the Quality Department as a whole. * Perform such other tasks that may be required from time to time. * Undertake a shift pattern where necessary to continue a high level of service to internal customers. * Act in the best interest of Treatt PLC always. What we're looking for A Quality Control Analyst will either have a degree in a science-based discipline, preferably with chemistry-based modules, or industry experience relevant to the role. Specific training on procedures whilst being desirable is not required as full training is provided by Treatt. * Analyst will have extensive chromatography experience (at least 2 yrs) and is comfortable operating, maintaining, troubleshooting, and calibrating GC and LC instrumentation, as well as confident analyzing the data for trends and anomalies. * Analyst will have the following skills: attention to detail, multitasker, effective communicator, and be able to lead when necessary. * Analyst must have a track record of taking the initiative to better themselves, the team, the business, systems/processes, etc. We want you to love your work and bring that energy to the job every day, no matter what the task. You'll be someone who keeps up to date with the latest technologies and is always willing to share their knowledge with colleagues. Our department is busy. We need someone who can run with the pack but also bring their own personality to their work. You should be personable, friendly and supportive, acknowledging that you'll get to work with colleagues from all seniority levels across all departments on a daily basis. What we'll do for you We offer an excellent package which includes a competitive salary; vacation time as well as the opportunity to purchase additional vacation, we also offer a discretionary annual bonus, medical (including family cover), dental and vision coverage, AFLAC, 401k employer matching up to 6%, company-paid short term and long-term disability insurance, company-paid life insurance and stock purchase options. With the encouragement and development you need, we help you to become your ultimate you. Beyond building a successful career, we also support the wishes and ambitions of our staff outside of the office in achieving a health work/life balance - the wellbeing of our staff is paramount to us, which we actively promote and support by regularly delivering a variety of wellbeing initiatives. There will also be opportunities to be actively involved in community and charity projects and to take part in numerous subsidized social events. M/F/D/V EOE DFWP SO Polite Notice We politely request that we are not contacted by any recruitment agencies. We have a preferred supplier list and high volumes of speculative calls from agencies negatively impact upon the efficiency of our business. Please help us to maintain the highest levels of customer service by respecting our wishes.

IEH Laboratories, a Leader in Food Safety, is now accepting applications for a Laboratory Analyst - 12hr Rotational Day Shift position at its facility in Lakeland, FL. Ideal candidates will possess the following: * A BS or BA in the biological sciences or related field (required) * Proficiency with data entry and computer applications * Ability to multitask and work in a fast-paced environment * Strong written and verbal communication skills * Strong attention to detail * Strong understanding of aseptic technique in the laboratory Laboratory Analyst duties include: analysis of food samples for pathogens via PCR and immunoassay, various microbe enumerations, data entry, laboratory reporting, quality control, media preparation, and other duties as assigned. This is a full-time position and is eligible for standard benefits after a brief waiting period. The schedule for this position is on a rotating shift basis: the first week is Wednesday-Thursday, from 1:00pm to 1:00am; the second week is Monday, Tuesday, Friday, Saturday, and Sunday, from 1:00pm to 1:00am. Due to exposure to various food allergens in the laboratory environment, applicants with moderate-to-severe food allergies are discouraged from

Job Details Sarasota, FL $20.00 - $22.00 HourlyDescription Manage the development, implementation and maintenance of the company policies and contract regulations. Duties & Responsibilities: Responsible for maintaining contract schedules and detailed agreements Responsible for preparing, maintaining, updating and organizing all relevant records pertaining to contract jobs Proactively communicate with project management and superintendents, keeping all abreast of any upcoming issues, opportunities and change orders Oversight of site and sub-contractor performance Other duties may be assigned. Essential Qualifications Bachelor's Degree in Engineering, Architecture or Construction Management A minimum of 3 years construction experience Ability to read and interpret documents such as safety rules, operating and maintenance instructions, and procedure manuals Organizational skills and attention to detail Comfortable in office start-up situations Travel flexibility Excellent verbal and written communication skills Working knowledge of MS Office including, Excel, Word, and Access Clean driving record Desired Qualifications Prior experience with Quality Control in construction or disaster recovery work Identifies and resolves problems in a timely manner; develops alternative solutions Contributes to building a positive team spirit Commits to long hours of work when necessary to reach goals Exhibits sound and accurate judgment First Aid/CPR certification Prioritizes and plans work activities; uses time efficiently; plans for additional resources Looks for ways to improve and promote quality Meets productivity standards; strives to increase productivity Observes safety and security procedures. Reports potentially unsafe conditions and uses equipment and materials properly Physical Demands While performing the duties of this Job, the employee is regularly required to stand and walk. The employee is frequently required to use hands to finger, handle, or feel; reach with hands and arms; climb or balance and talk or hear. The employee is occasionally required to sit and stoop, kneel, crouch, or crawl. The employee must occasionally lift and/or move up to 50 pounds. Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception and ability to adjust focus. May vary from site to site and in some cases be greater or lesser than indicated here. Work Environment While performing the duties of this Job, the employee is regularly exposed to moving mechanical parts and outside weather conditions. The employee is occasionally exposed to wet and/or humid conditions; high, precarious places; fumes or airborne particles; risk of electrical shock and vibration. The noise level in the work environment is usually loud. Ceres Environmental is an Equal Opportunity and Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to age, race, color, sex, sexual orientation, gender identity, national origin, religion, disability status, or protected veteran status.

The Production Floor Quality Control Inspector will maintain quality standards by inspecting production orders for quality imprints and customer specified attributes and recording quality results and coach fellow employees on quality requirements. Essential Job Functions: Maintaining quality standards on the production floor Signs off each order along with Supervisor and/or Manager signoffs when order is acceptable to produce. Uploads pictures and information into app for each order signoff. Monitors orders for quality as Operators produce them. Perform audits of printed material and provide feedback to the operators and management regarding any quality issues. Stops and advises orders need fixes during production. Removes unacceptable product from floor and places in appropriate location. Notifies Supervisor/Manager of major quality issues. Checks quality picture in app for running shortages and verify to compare placement. Quality training and coaching Mentor and coach production floor operators and packers on quality requirements. Create and document ways to improve the quality of the parts being produced. Accomplish quality and organization mission by completing related results as needed. Read and follow printed instructions within the Traveler. Determine color match to PMS color book. Determine correct location and centering for printing applications. Keep work area clean and follow all safety rules.

PRIMARY PURPOSE: Develop, transfer and validation of HPLC, Gas Chromatography, ICP and AA methodology. Must have extensive cGMP experience and be able to provide leadership and mentoring to Chemist I and Chemist II in QC Laboratory. Must have thorough understanding of Good Laboratory Practices and Good Documentation Practices, as well as compendial methodology. Must have experience in writing Standard Operating Procedures, Protocols and Reports. MAJOR DUTIES AND RESPONSIBILITIES: Perform all the activities for development, transfer and validation of analytical methods. Revise and write Validation Protocols, Test Methods, Validation Reports and SOP's. Testing of incoming materials, using compendial test methods (USP, PhEUR, JP) Testing of stability samples, in process samples and finished product testing, using a variety of techniques, such as HPLC, GC, AA, ICP, UV/Vis, etc. Accurately records raw data and analyzes, as well as calculates and interprets the results. Occasional customer interaction in a professional environment. Responsible for out of specification test results, investigation, and implementation of corrective actions. Ensure testing is performed accurately and in compliance with GLP, cGMP, cUSP, SOP and other approved test methods and protocols. Maintain analytical reagents in laboratory including but not limited to: inventory, current MSDS, PPE required for handling, waste generation and disposal. Assist Validation teams in cleaning validation activities. Support laboratory troubleshooting needs by interacting with vendors, customers and other relevant SMEs. Promote GMP and safety throughout the facility. Promote continuous improvement and customer satisfaction. Follow-up on OOS's and CAPAs to verify compliance. Potential exists for exposure to potentially harmful chemicals. Participate in other activities as assigned by the Lab Manager or VP Quality. QUALIFICATIONS: Required Knowledge of Compendia testing. Knowledge of the chemical composition, structure, and properties of substances and of the chemical processes and transformations that they undergo. This includes uses of chemicals and their interactions, danger signs, production techniques, and disposal methods. Knowledge of raw materials, production processes, quality control, and other techniques for maximizing the effective manufacture of goods. Working knowledge of FDA regulations for laboratory testing and disposition. Ability to use a personal computer and peripheral equipment to accurately enter an analyze data and produce reports. Knowledge of chemical safety and protective equipment. Expertise in various analytical equipment and techniques utilized in an analytical laboratory including but not limited to pH, viscosity, specific gravity, infrared spectroscopy, HPLC, GC, ICP, UV/VIS, atomic absorption. Ability to establish priorities, work independently, productively, and proceed with objectives without supervision. Ability to handle and resolve recurring problems. Understanding the implications of new information for both current and future problem-solving and decision-making. Ability to troubleshoot HPLC, GC, ICP and AA analyses Ability to communicate effectively, concisely in a professional manner with clients and others. Ability to work in a dynamic fast paced environment-sometimes rapidly shifting priorities. Ability to concentrate in such an environment and perform quality work. Must be able to lift up to 15 pounds. EDUCATION AND TRAINING: Bachelor's degree in Chemistry or related discipline. Must have three or more years' experience working in an analytical laboratory in an FDA regulated industry.

It is the primary responsibility of the Analytical Chemist to maintain the instrumentation and analytical methods in the Analytical Sciences laboratory in a state of readiness for the analysis of essential oils and isolates for agricultural residues and other trace contaminants. DUTIES & RESPONSIBILITIES: Preparation, dilution and extraction, where appropriate, of samples for trace analysis Calibration of analytical balances and pipettes Instrument preparation including creation of sequences (GLC, GC-MS, GC-MSMS, GC-XSD and UHPLC) Data analysis, interpretation and reporting of trace analytical results (GLC, GC-MS, GC-MSMS, GC-XSD and UHPLC) Maintenance of the analytical calibration and verification spreadsheets (GC; GC-MS; GC-MSMS, GC-XSD and UHPLC) Advanced instrument maintenance & troubleshooting (GC; GC-MS; GC-MSMS, GC-XSD and UHPLC) Maintenance of the equipment down time log Method development and maintenance of advanced quantitative methods Preparation and appropriate storage of calibration standards for trace analysis Assist and contribute to Global Technical projects Maintain the supply of gas to the instrumentation by changing gas cylinders when required Monitor and log the ordering, receipt and return of gas cylinders on site including maintenance of the gas usage log Perform classical and/or instrumental analysis on any QC samples as and when requested by the Global Analytical Innovation Manager or the Quality Control Manager. Raise purchase orders where appropriate to replenish consumables and reagents. Report and address any deficiencies in equipment or analytical practices to Global Analytical Innovation Manager Undergo training in areas specific to Treatt PLC business Statistical data evaluation of new and existing analytical methods Write Quality Policies, Procedures and Operating Instructions. Ensure that the working area in the laboratory is maintained in a clean and orderly condition and that any hazard or potential hazard is reported to the Line Manager or H&S Officer Act in the best interest of Treatt PLC at all times Employees have a legal duty to take reasonable care of their own health and safety and that of others who may be affected by what they do at work. EDUCAION & TRAINING: Bachelor of Science Degree with Science Major or Master of Science Degree KNOWLEDGE & EXPERIENCE: Strong analytical skills with a minimum of 3 years' laboratory experience. Significant experience in working with GC-FID, HPLC, GC/MS Some experience in working with GC/MSMS and LC/MSMS preferred Knowledge of analytical disciplines, methods, developments and troubleshooting. Significant experience in data collection, extraction and analysis with strong analytical, problem-solving and research skills. Passionate about keeping up to date with relevant scientific and technological developments. The capability to organize and prioritize with a strong eye for detail. Excellent interpersonal and relationship skills with the ability to support teams and colleagues. Intermediate classical analytical skills. Exposure to hazardous Chemical WORKING CONDITIONS: Exposure to hazardous Chemical Open Office - typical spacious room, desks close together Shop floor, including some time inside and outside production

WHY CORERX? CoreRx is a dynamic pharmaceutical technology company that empowers its employees with responsibility and offers a supportive and highly progressive work environment. At CoreRx, our biggest asset is our people, and the service and solutions they provide to our partners; you will find a challenging career path directed towards growth and opportunity. We employ talented, motivated people - team players who are innovative thinkers. We offer our employees a comprehensive, competitive program of benefits and a corporate culture based on core values that include innovation, a results-oriented focus, and ethical behavior. Our employees enjoy a competitive benefits package, including: Competitive compensation with an annual discretionary incentive bonus! Affordable healthcare insurance (Medical, Dental, Vision) Health Care Flexible Spending Account Employer paid LTD, STD, and Life Insurance coverage Paid Time Off (PTO), 15 days pro-rated your first year + 10 Paid Holidays 401k with 100% employer match up to 3% Tuition Reimbursement, Perks at Work Employee Discounts, Employee Assistance Program, and Adoption Assistance Program The Senior Microbiologist is an integral part of the team, contributing to our success by leading all activities related to the microbiology laboratory. ESSENTIAL JOB DUTIES Primary Responsibilities/functions: Oversee microbiology laboratory compliance to ensure all microbiological testing procedures/methods are properly performed and manage efficiency of operations and continuous improvement activities Provide training, mentoring, and career development to team members Prepare SOP's, work instructions, reports and all other documents related to microbiological testing Ensure testing is properly conducted and documented for all performed activities with emphasis on data integrity Ensure all materials (media, reagents, standard organisms, etc.) and equipment used for testing are valid, qualified or calibrated as required Oversee and perform as necessary microbiological testing of raw materials, finished and stability pharmaceutical drug products, environments monitoring samples from utilities and facilities, and equipment cleaning validation samples Responsible for media, reagents, standards, tools, and instrument/equipment procurement Notify management immediately of nonconforming data or unexpected occurrences and conducts deviation and laboratory investigations as required Complies with all regulatory/in-house requirements may include but not be limited to safety, housekeeping, laboratory waste, cGMP, documentation Performs other related duties as assigned by management REQUIRED SKILLS/ABILITIES Experience in environmental monitoring and microbial testing of pharmaceutical products Knowledge with microbiological equipment Working knowledge of Health Authority expectations for microbiology laborator facilities and procedures Demonstrated ability to work as an independent, self-motivated, detail-oriented, result -driven and highly flexible team-player in a fast-paced working environment Proficient in Microsoft Office Suite or similar software WORK EXPERIENCE AND REQUIREMENTS Minimum of 2 year's experience preferred in an FDA-regulated pharmaceutical environment Experience in other highly regulated laboratory settings will be considered EDUCATION REQUIREMENTS MS in Microbiology preferred BS/BA in microbiology or life sciences required Equivalent experience may substitute for stated requirement PHYSICAL DEMANDS Regularly required to stand for long periods. Frequently required to sit, walk, talk, hear, handle or feel tools or controls Occasionally required to reach with hands arms, stoop, crouch climb or balance, kneel Vision suitable for performing detailed inspections May be required to move items weighing up to 25lb Ability to community clearly in both written and verbal form WORK ENVIRONMENT Pharmaceutical microbiology laboratory environment General office setting Notification to Agencies: Please note that CoreRx Inc. does not accept unsolicited resumes from recruiters or employment agencies. In the absence of a signed Master Service Agreement, and specific approval to submit resumes to an approved requisition, CoreRx Inc. will not consider or approve payment regarding recruiter fees or referral compensation. Job Type: Full-time