Chemist Jobs in Sunrise, FL

About Us: Come join a rapidly growing biotechnology company dedicated to advancing scientific research and developing innovative solutions. We are committed to excellence and are seeking a highly skilled Analytical Scientist to join our dynamic team. Job Summary: The Analytical Scientist will play a crucial role in our research and development efforts, focusing on method development, analytical techniques, and documentation within a GMP (Good Manufacturing Practice) environment. The ideal candidate will have extensive experience in developing methods from scratch, drafting Standard Operating Procedures (SOPs), and utilizing various analytical techniques such as HPLC, UPLC, GC, and Empower. Key Responsibilities: Develop and validate analytical methods from scratch to support product development and quality control. Draft and revise SOP documentation to ensure compliance with GMP regulations. Perform routine and non-routine analysis using HPLC, UPLC, GC, and Empower software. Troubleshoot and optimize analytical methods to improve accuracy and efficiency. Maintain accurate and detailed records of all analytical activities and results. Collaborate with cross-functional teams to support research and development projects. Ensure all laboratory activities comply with GMP, GLP (Good Laboratory Practice), and other regulatory requirements. Participate in internal and external audits and inspections. Stay current with industry trends and advancements in analytical techniques and technologies. Qualifications: Ph.D. or Master's degree in Chemistry, Biochemistry, Analytical Chemistry, or a related field. Minimum of 2 years of experience in analytical method development and validation in a GMP environment. Proficiency in HPLC, UPLC, GC, and Empower software. Strong knowledge of GMP regulations and SOP documentation. Excellent problem-solving skills and attention to detail. Ability to work independently and as part of a team. Strong written and verbal communication skills. Experience with statistical analysis and data interpretation is a plus. Benefits: Competitive salary and benefits package. Opportunities for professional growth and development. Collaborative and innovative work environment.

Mackenzie Stuart are currently partnered with a Personal Care Contract Manufacturer seeking a Senior R&D Chemist. The role of Senior R&D Chemist involves developing robust formulations across all personal care categories. This position will collaborate with Regulatory, Quality Control (QC), and Compliance teams to ensure FDA compliance for product formulation. Additionally, the Senior R&D Chemist will manages multiple projects concurrently within tight deadlines whilst adhering to Good Manufacturing Practice (GMP) guidelines, Standard Operating Procedures (SOPs), and safety requirements. Responsibilities for this role include (but are not limited to): Independently formulates skin, hair and body care products, focusing on product stability and exploring reformulation alternatives. Develops innovative and robust skincare formulations and processes, understanding the interplay between formulation and production. Collaborates effectively across R&D and related departments to advance projects. Possesses expertise in considering processing, operating, and design factors impacting skincare formulations. Works closely with Regulatory, QC & Compliance to ensure FDA compliance for product formulation. Manages multiple projects concurrently, meeting tight deadlines. Gains proficiency in relevant software systems or other required platforms. Adheres to GMP guidelines, SOPs, and safety protocols. To be considered for the role, the following education, experience and qualifications are required: Bachelor's degree in chemistry or a related field. Over 5 years of formulation experience. Proven track record in developing innovative skincare/hair/OTC products. Comprehensive understanding of cosmetic raw materials and cutting-edge technologies. Proficiency in laboratory and scale-up production equipment. Familiarity with cosmetic manufacturing practices and operations. Demonstrated ability to work independently and collaboratively. Confidence to mentor junior chemists. Excellent team-building skills. Creative and out-of-the-box thinker. This role offers a competitive salary, with a great compensation package, and a strong progression pathway. Please submit your CV/resume if you have the requisite skills as outlined above and are a highly competitive individual with excellent communication skills. Unfortunately, due to the high volume of expected responses we are only able to acknowledge successful applications. If you have not been contacted within 2 weeks, on this occasion your application has been unsuccessful. About Mackenzie Stuart Global Executive Search & Selection Mackenzie Stuart is a leading executive search and selection business. From our offices in Leeds/London we provide retained and contingency recruitment solutions across industry and have specialist recruitment consultants that work within the Oil & Gas, Mining, Construction, Medical, Life Sciences, Renewable Energy, Cyber Security, FMCG, Ingredients, and Manufacturing sectors.

The R&D Lab Chemist is responsible for working on various Technical Service and R&D Projects to support our Customers, Principals, Various product lines in our portfolio, and Sales Team in laboratory/office setting, resulting in making Barentz Always a better solution ESSENTIAL DUTIES AND RESPONSIBILITIES Position/Department Data management - acquiring, validating, and maintaining data for the lab projects. Perform, interpret, and record lab project data. Data processing and documentation using common software tools such as Excel, PowerPoint as well as Datacor/Chempax, eChempax, and BRM. Generation of various Lab Reports to summarize testing, results & conclusions. Ensure safety procedures and housekeeping are maintained to protect yourself, co-workers, and the environment. General lab duties including clean-up, maintenance of equipment, track and order chemicals and disposables used in the lab as needed. Leadership/ Teamwork Conduct necessary lab work to provide Technical Support to our Customers, Principals, Sales Team and Product Line Portfolio. Communicate with other Lab Technicians throughout the organization to stay up to date on processes, protocols and trends Provide additional documentation and supporting information cross-departmentally upon request Continuous Improvement/Problem Solving Ensure adherence to all applicable facility requirements, certifications and designations Contribute to and support continuous improvement of our processes and systems Seek opportunities to share best practices with the team, support staff and other divisions Barentz Culture/Fundamentals Support and lead by example, following Barentz' purpose, strategies, and values Act legally and ethically in all professional relationships in adherence with Barentz' culture, values and fundamentals Contribute to an environment of trust and mutual respect Maintain a strong commitment to teamwork and concern for others Maintain a high level of personal responsibility and ownership Use effective communication and listening skills Foster an inclusive and diverse workplace where every team member feels valued and respect Learning and Development Seek out and participate in ongoing growth and personal development opportunities Embrace and promote Barentz' learning and development culture Other Duties and Responsibilities: Duties and responsibilities may be amended at any time per business need Education Bachelor's degree in Chemistry, Biology, Engineering or other Sciences or equivalent of education and experience (required) Experience Minimum 3-5 years of previous experience in a laboratory setting (required) Certifications Any industry related certification (i.e., Laboratory Technician, Sales Techniques, Project Management, Regulatory, Quality Management, etc.) (preferred/encouraged) Position/Product/Industry Requirements Experience using industry related technologies and equipment Champion a safety-first mindset for yourself and others in the facility SKILLS AND KNOWLEDGE Self-motivated, high energy, and engaging level of enthusiasm and positive outlook Demonstrated organizational, complex problem-solving, and analytical skills. Effective written and verbal communication skills and the ability to adapt communication style to the audience as needed Software knowledge of Microsoft Office including Outlook, Word, Excel and Power Point Must be able to effectively prioritize work assignments for self and others Ability and desire to develop meaningful/productive business relationships

Essential Duties and Responsibilities NOTE: This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US without visa sponsorship or visa transfer. Conduct laboratory activities with limited supervision including for example analyzing raw materials, in-process materials and finished pharmaceutical products for quality, safety, purity, strength and identity using applicable methods or manufacturing drug product, following the cGMP, EH&S and other relevant guidelines of Corporate, FDA and other governing bodies. Independently set up and operate lab equipment, prepare reagents, solvents and solutions for analytical and formulation activities. Prepare and maintain accurate records in lab notebooks of all testing performed. Process analytical data on lab equipment such as HPLC/UPLC, enter data in spreadsheets and conduct routine calculations. Support the manufacture of inhalation drug product. Prepare samples for blend uniformity. Perform equipment qualification and calibrations as directed. Execute approved method transfer protocols. Assist in the training of other scientists. Perform other tasks as assigned. Participate in project activities and support project timelines and proactively contribute to meeting the team objectives. Communicates effectively with team members. Establish and maintain effective relationships with team members. Conduct lab work in accordance with SOPs & STPs; follow Corporate safety rules and procedures Comply with all Corporate guidelines and policies Qualification Requirements Must be eligible to work in the United States without any visa sponsorship or visa transfer requirements. Not open to H1B holders. Must be willing to work 2nd shift. Must be able to work On-site in Weston, FL. (West of Ft. Lauderdale) Must have at least 2-3 years of experience of pharmaceutical industry R&D experience Must have strong HPLC and Empower experience. BSc in Chemistry, Pharmacy or related fields with 3-6 years of experience MSc in Chemistry, Pharmacy or related fields with 2+ years of experience in Pharmaceutical R&D Proven ability and/or experience with compendial test methods or pharmaceutical manufacturing equipment. Understanding of pharmaceutical equipment and computerized systems for operation and troubleshooting. Specific experience with analytical and/or process equipment used in laboratories such as HPLC, IR/FTIR, UV-Vis AA, powder blender etc. Knowledge and understanding of the FDA cGMP requirements as it applies to the Pharmaceutical industry. Effective English written and oral communication skills. Ability to write short technical documents such as memos, laboratory investigations, protocols and reports.

Now Hiring: Quality Control Analyst I Duration: 5-month contract Industry: Pharmaceutical / Biotech / environmental lab We are looking for a Quality Control Analyst with: Bachelor's degree in Chemistry or Microbiology 2+ years of experience in a CGMP pharmaceutical, biotech, or environmental lab Microbiology testing experience (environmental samples, purified water, RM/FP - USP) Experience with Labware LIMS v7 Experience using Learning Management Systems (LMS) Strong understanding of data integrity (ALCOA+) and lab documentation practices Key Responsibilities: Perform testing on raw materials and finished products Wet chemistry methods (LOD, pH, titration, etc.) Equipment calibration checks Peer review of lab results Support production, validation, and stability timelines

This position performs testing of raw materials and drug products, maintenance, and calibration of analytical equipment instruments, prepares standard and sample solutions, and maintains appropriate records. Core essential skill sets candidates must have to be considered for the role: Bachelor's degree, preferably in Chemistry or Microbiology, or equivalent education/experience Minimum of two years of experience in Quality Control in CGMP pharmaceutical, biotechnology, or environmental laboratory Experience Labware LIMS V7 and laboratory auditing processes Microbiology testing experience on Environmental Samples for surface and air, Purified Water Samples, and RM/FP Microbial Limit Test following USP Computer proficiency with a comprehensive working knowledge of MS Office products, Learning Management Systems (LMS) Ability to communicate effectively with excellent written and oral communication skills for scientific and/or technical ideas Acts independently and proactively recommends methods and procedures for problem resolution Self-directed with the ability to organize and prioritize work Understand Data Integrity (ALCOA+) and laboratory documentation practices Essential Areas Of Responsibility All areas of responsibility listed below are essential for the satisfactory performance of this position by any incumbents with reasonable accommodation if necessary. Any non-essential functions are assumed to be included in other related duties or assignments. Carries out responsibilities under the organization's policies, procedures, and state, Federal, and local laws. Complies with all safety rules and regulations. Perform analysis on raw materials, finished goods, API, and control substances Ensures that balances are reviewed and calibrated. Perform peer review of laboratory testing as required. Responsible for Wet Chemistry testing (such as LOD, PH, titration, etc.) Work within a team to meet production, validation, stability, and request deadlines. Participates in troubleshooting of analytical test methods and laboratory instruments. Responsible for completing all training requirements and maintaining 100% compliance with all assignments. Responsible for maintaining work areas and performing job functions in a safe and efficient manner in accordance with company policies and procedures, Good Manufacturing Practices (cGMP's), and Standard Operating Procedures (SOP's) instructions. Responsible for performing additional related duties as assigned.

Introduction “Quality and safety above everything”. That is the unassailable theme that guides everything that we do, every day. We have an unwavering commitment to quality and the production of safe and effective products. Our science and risk-based compliant quality culture is innovative, and healthcare oriented. Whether you are involved in development, operations, maintenance, compliance or analysis, through research and manufacturing programs, your contribution will directly impact our success. Your Diligence Means Our Success At Pherros, we combine development and safety to improve the lives of those around us. Our employees bring life-changing medicines to people in need and improve the understanding and management of disease. We give our best to putting people first and we are looking for people who are determined to improve life for everyone. You will be a member of Pherros' dedicated and highly effective quality control operations team. Our aseptic manufacturing facility for parenteral pharmaceuticals presents an exciting opportunity to be an important part of a state-of-the-art facility and quality system. The Quality Control Laboratory assures patients worldwide that our drug products are safe and effective and of the highest quality and integrity. We exceed these standards through effective execution of process, environmental, supply and product testing. General Requirements As a Quality Control Chemist, you will perform accurate and timely testing of routine and non-routine samples in accordance with appropriate Good Manufacturing Practices (“GMP”), Good Laboratory Practices (“GLP”), and safety guidelines, to support site production and stability requirements. The Chemist and Chemistry Supervisor roles are focused on the quality control testing of the various pharmaceutical products manufactured at Pherros Biosciences. All testing performed is in accordance with the established drug product specifications. The candidate will participate in and perform development and validation of analytical test methods associated with finished dosage form (FDF) drug products as well as investigate, resolve, and mitigate deviations, non-conformances, and OOS (Out of Specification) events associated with products tested at the facility. The Quality Control Scientist utilizes technical skills to perform in-depth problem solving, proactively identify opportunities for continuous improvement, and assist in resolving laboratory investigations of atypical data and results. Additional key objectives and deliverables include the capability to: Be an inspirational part of a vibrant and growing group of professionals. Accurately and safely perform timely testing of routine and non-routine lab samples in accordance with appropriate GMP, GLP, and safety guidelines. Accurately record data in reports or Laboratory Information Management System (“LIMS”) in accordance with laboratory procedures, Good Laboratory Practices (“GLP”), standards, and GMP requirements. Recognize deviations from procedures, methods, etc., and initiate an investigation as required. Verify analytical data generated by other analysts within the lab as required. Adhere to all Environmental, Health, and Safety (“EH&S”) standards. Identify and communicate opportunities for improvement initiatives in daily work activities. Troubleshoot equipment and methods as required. Provide technical support for non-routine (e.g., deviation) investigations. Maintain inventory of all supplies and consumables for the laboratory. Gown for activities within aseptic manufacturing suites typical of a GMP environment. Engage in training exercises to fulfill compliance requirements associated with the position. Conduct chemical and physical testing of raw materials, API, in-process, finished products, and stability samples, and other in process samples, using established test methods to provide accurate and reliable data to assure their strength, identity and purity. Work with materials using safe protocols and participate in and contribute to the maintenance and calibration of analytical instruments within the quality control laboratories. Collaborate with other facility team members and regulatory colleagues to establish release and stability specifications for starting materials, intermediates, drug substances, and drug products. Work well in a fast-paced team environment. Collaborate with management to identify training needs and ensure appropriateness of training plans, creating and assigning curricula as required. Contribute to the training, education, guidance, and influence of operational and support areas on quality control policy and practices. Foster a culture of collaboration, partnership, teamwork, and a drive for change and continuous improvement. Take initiative and have the ability to work independently as well as collaboratively with exemplary enthusiasm amongst other team members. Perform other duties as assigned. Educational, Experience and Training Requirements Bachelors, Masters or Ph.D. degree in Chemistry with three (3) to seven (7) years of relevant experience in a GMP Chemistry Lab environment, including knowledge of analytical chemistry testing, excellent understanding and knowledge of analytical instrumentation technologies, chromatography methods, USP compendial test methods, ICH guidelines, and cGMP, experience with HPLC and LCMS analytical testing, method development, and method validation is required, experience with GCMS, FTIR and ICPMS is required for supervisors, strong communication and organizational skills, proficiency in Microsoft Office suite applications (Excel, Word, PowerPoint), ability to handle multiple tasks simultaneously while meeting deadlines, ability to investigate, collect data, and analyze trends investigations, ability to work as needed for off-hours stability timepoints and potential early start times, excellent communication (written and verbal), interpersonal, organizational and negotiation skills, project management skills, experience in process improvement, and the ability to be solution focused on the design and implementation of quality and process improvements. Additional Preferences: Experience with a LIMS system. Ability to lead and to inspire others. Experience with a Quality Management System (“QMS”) such as Master Control. Demonstrated problem solving and analytical thinking skills. Understanding of statistical tools and analysis. Excellent interpersonal skills and networking skills. Experience in a GMP QC Lab environment. Demonstrated written and verbal communications skills. Strong attention to detail. Ability to organize and prioritize multiple tasks. Experience with Root Cause Analysis. Demonstrated ability to work both independently and as a part of a team. Additional Information The position is full-time non-remote, Monday through Friday, with flexibility to support weekends. Applicants will work in various areas within the site. Some allergens may be present in the facility. Exposure to allergens should be considered when applying for this position. Tasks may require repetitive motion (e.g., keyboarding). Minimal travel required. Sunshine Act Pherros reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations. These laws and regulations require Pherros to provide government agencies with information such as a health care provider's name, address and the type of payments or other value received, generally for public disclosure. Subject to further legal review and statutory or regulatory clarification, which Pherros intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act. Therefore, if you are a licensed physician who incurs recruiting expenses as a result of interviewing with Pherros that we pay or reimburse, your name, address and the amount of payments made currently will be reported to the government. If you have questions regarding this matter, please do not hesitate to contact your Talent Acquisition representative. EEO & Employment Eligibility Pherros is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status. Pherros also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA. Quality Control About Us Careers at Pherros Biosciences are like no other. We believe in our ability to improve future healthcare, and potential to transform millions of lives. We're looking for new talent to join our global community in order to bring innovative therapies to market and to make the world a healthier place.

The Amazon Web Services Professional Services (ProServe) team is seeking a skilled Delivery Consultant to join our team at Amazon Web Services (AWS). In this role, you'll work closely with customers to design, implement, and manage AWS solutions that meet their technical requirements and business objectives. You'll be a key player in driving customer success through their cloud journey, providing technical expertise and best practices throughout the project lifecycle. Possessing a deep understanding of AWS products and services, as a Delivery Consultant you will be proficient in architecting complex, scalable, and secure solutions tailored to meet the specific needs of each customer. You'll work closely with stakeholders to gather requirements, assess current infrastructure, and propose effective migration strategies to AWS. As trusted advisors to our customers, providing guidance on industry trends, emerging technologies, and innovative solutions, you will be responsible for leading the implementation process, ensuring adherence to best practices, optimizing performance, and managing risks throughout the project. The AWS Professional Services organization is a global team of experts that help customers realize their desired business outcomes when using the AWS Cloud. We work together with customer teams and the AWS Partner Network (APN) to execute enterprise cloud computing initiatives. Our team provides assistance through a collection of offerings which help customers achieve specific outcomes related to enterprise cloud adoption. We also deliver focused guidance through our global specialty practices, which cover a variety of solutions, technologies, and industries. Key job responsibilities As an experienced technology professional, you will be responsible for: - Designing, implementing, and building complex, scalable, and secure GenAI and ML applications and models built on AWS tailored to customer needs - Providing technical guidance and implementation support throughout project delivery, with a focus on using AWS AI/ML services - Collaborating with customer stakeholders to gather requirements and propose effective model training, building, and deployment strategies - Acting as a trusted advisor to customers on industry trends and emerging technologies - Sharing knowledge within the organization through mentoring, training, and creating reusable artifacts About the team About AWS: Diverse Experiences: AWS values diverse experiences. Even if you do not meet all of the preferred qualifications and skills listed in the job below, we encourage candidates to apply. If your career is just starting, hasn't followed a traditional path, or includes alternative experiences, don't let it stop you from applying. Why AWS? Amazon Web Services (AWS) is the world's most comprehensive and broadly adopted cloud platform. We pioneered cloud computing and never stopped innovating - that's why customers from the most successful startups to Global 500 companies trust our robust suite of products and services to power their businesses. Inclusive Team Culture - Here at AWS, it's in our nature to learn and be curious. Our employee-led affinity groups foster a culture of inclusion that empower us to be proud of our differences. Ongoing events and learning experiences, including our Conversations on Race and Ethnicity (CORE) and AmazeCon (diversity) conferences, inspire us to never stop embracing our uniqueness. Mentorship & Career Growth - We're continuously raising our performance bar as we strive to become Earth's Best Employer. That's why you'll find endless knowledge-sharing, mentorship and other career-advancing resources here to help you develop into a better-rounded professional. Work/Life Balance - We value work-life harmony. Achieving success at work should never come at the expense of sacrifices at home, which is why we strive for flexibility as part of our working culture. When we feel supported in the workplace and at home, there's nothing we can't achieve in the cloud. Basic Qualifications - Experience developing software code in one or more programming languages (java, python, etc.) - Bachelor of Science degree in Computer Science, or related technical, math, or scientific field (or equivalent experience) - 3+ years of cloud based solution (AWS or equivalent), system, network and operating system experience - 2+ years of experience hosting and deploying GenAI/ML solutions (e.g., for training, fine tuning, and inferences) Preferred Qualifications - AWS Experience preferred, with a proficiency in a wide range of AWS services (e.g. SageMaker, Bedrock, EMR, S3, OpenSearch Service, Step Functions, Lambda, and EC2) - AWS Professional level certifications (e.g., Solutions Architect Professional, DevOps Engineer Professional) preferred - Experience with automation and scripting (e.g., Terraform, Python) - Knowledge of security and compliance standards (e.g., HIPAA, GDPR) - Strong communication skills with the ability to explain technical concepts to both technical and non-technical audiences - Masters or PhD degree in computer science, or related technical, math, or scientific field - Hands on experience with deep learning (e.g., CNN, RNN, LSTM, Transformer), machine learning, CV, GNN, or distributed training Amazon is an equal opportunity employer and does not discriminate on the basis of protected veteran status, disability, or other legally protected status. Los Angeles County applicants: Job duties for this position include: work safely and cooperatively with other employees, supervisors, and staff; adhere to standards of excellence despite stressful conditions; communicate effectively and respectfully with employees, supervisors, and staff to ensure exceptional customer service; and follow all federal, state, and local laws and Company policies. Criminal history may have a direct, adverse, and negative relationship with some of the material job duties of this position. These include the duties and responsibilities listed above, as well as the abilities to adhere to company policies, exercise sound judgment, effectively manage stress and work safely and respectfully with others, exhibit trustworthiness and professionalism, and safeguard business operations and the Company's reputation. Pursuant to the Los Angeles County Fair Chance Ordinance, we will consider for employment qualified applicants with arrest and conviction records. Our inclusive culture empowers Amazonians to deliver the best results for our customers. If you have a disability and need a workplace accommodation or adjustment during the application and hiring process, including support for the interview or onboarding process, please visit ********************************************************* for more information. If the country/region you're applying in isn't listed, please contact your Recruiting Partner. Our compensation reflects the cost of labor across several US geographic markets. The base pay for this position ranges from $118,200/year in our lowest geographic market up to $204,300/year in our highest geographic market. Pay is based on a number of factors including market location and may vary depending on job-related knowledge, skills, and experience. Amazon is a total compensation company. Dependent on the position offered, equity, sign-on payments, and other forms of compensation may be provided as part of a total compensation package, in addition to a full range of medical, financial, and/or other benefits. For more information, please visit ******************************************************* . This position will remain posted until filled. Applicants should apply via our internal or external career site.

Florida Power & Light Company is the largest electric utility in the U.S., delivering clean, affordable, and dependable electricity to over 12 million Floridians. With one of the nation's cleanest power generation fleets and top-tier reliability, we are setting new standards in the energy industry. Ready to make an impact? Join our exceptional team today and help shape the future of energy! Position Specific Description The candidate in this position will be expected to perform the following Additional Job Duties and Responsibilities: * Performs and documents laboratory analyses in a safe and timely manner in accordance with standard operating procedures based on EPA, ASTM, and Standard Methods. * Generate reports of analyses through use of the laboratory information management system. * Maintain instruments for reliable operation. * Properly manage waste generation. * Availability to take after-hours work as needed. * Job may include other miscellaneous duties as assigned. Job Overview

Perform routine tests of finished product and stability samples, raw materials, and CV samples, including assays, chromatographic purity, content uniformity using UV and HPLC, particle size distribution using different techniques including water determination by KF, and tests according to in-house monographs and USP in a regulated laboratory environment. Evaluate test results and decide the acceptability of the samples based on the test results. Maintain accurate lab notebooks and complete all related analytical reports, write summaries, and keep proper documentation in compliance with SOPs. Maintain the laboratories with good housekeeping practices and in compliance with cGMP. Ensure notebooks are reviewed promptly, in accordance with SOPs. Analyze and interpret results in written and oral format. Assist in the training of new analysts. Conduct laboratory investigations and initiate Quality Events, CAPA, and Change Controls as needed. Follow all SOPs and Safety Guidelines to ensure compliance with a cGMP environment. Responsibilities * Perform routine tests of finished product and stability samples, raw materials, and CV samples, including assays, chromatographic purity, content uniformity using UV and HPLC, particle size distribution using different techniques including water determination by KF, and tests according to in-house monographs and USP in a regulated laboratory environment. * Evaluate test results and decide the acceptability of the samples based on the test results. * Maintain accurate lab notebooks and complete all related analytical reports, write summaries, and keep proper documentation in compliance with SOPs. * Maintain the laboratories with good housekeeping practices and in compliance with cGMP. * Ensure notebooks are reviewed promptly, in accordance with SOPs. * Analyze and interpret results in written and oral format. * Assist in the training of new analysts. * Conduct laboratory investigations and initiate Quality Events, CAPA, and Change Controls as needed. * Follow all SOPs and Safety Guidelines to ensure compliance with a cGMP environment. Essential Skills * Proficiency in HPLC, UPLC, UV-Vis, and other analytical techniques. * Strong background in chemistry and pharmaceutical analysis. * Experience in working in FDA and GMP regulated environments. * Ability to maintain accurate lab notebooks and documentation in compliance with SOPs. * Competence in analyzing and interpreting results in both written and oral formats. * Experience in training new analysts and conducting laboratory investigations. Additional Skills & Qualifications * Bachelor's degree in Chemistry or related scientific field with 1-2 years of related experience in pharmaceutical analysis. * Master's degree in Chemistry or related scientific field with 1 year of related experience in pharmaceutical analysis. * Ability to deal with problems involving several concrete variables in standardized situations. * Ability to carry out necessary computations and to draw and interpret graphs. * Working knowledge of instrumentation software used in the laboratories. Work Environment Lab environment; FDA and GMP regulated. Hours are Monday-Friday: 8am-5pm OR 2pm-11pm Pay and Benefits The pay range for this position is $28.00 - $32.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: * Medical, dental & vision * Critical Illness, Accident, and Hospital * 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available * Life Insurance (Voluntary Life & AD&D for the employee and dependents) * Short and long-term disability * Health Spending Account (HSA) * Transportation benefits * Employee Assistance Program * Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Hollywood,FL. Application Deadline This position is anticipated to close on Apr 25, 2025. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. Diversity, Equity & Inclusion At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through: * Hiring diverse talent * Maintaining an inclusive environment through persistent self-reflection * Building a culture of care, engagement, and recognition with clear outcomes * Ensuring growth opportunities for our people The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Job Details Level: Experienced Position Type: Full Time Education Level: 4 Year Degree Salary Range: Undisclosed Travel Percentage: None Job Category: Pharmaceutical Description ADMA Biologics is a biopharmaceutical company relentlessly committed to creating superior products for immunodeficient patients at risk for infection. It is our devotion to this underserved population that fuels us and our hands-on approach to production and development that sets us apart. If you are looking for a dynamic, innovative, growing company in the biopharmaceutical industry that is committed to excellence and integrity, then consider ADMA Biologics. We currently have an exciting opportunity available for a Chemist II, Bioanalytics in Boca Raton, FL! The Chemist II, Bioanalytics will perform quality control testing of raw materials, in-process, and final products with minimal supervision, with a concentration in immunoassays. Uses knowledge of corporate policies to resolve routine problems and ensure compliance with procedures. Qualifications ESSENTIALS OF THE JOB: * Perform quality control testing for raw materials, in-process, and final product samples, according to approved Standard Operating Procedures (SOPs) and cGMP guidelines * Complete testing documentation and data entry as required for procedures and tests performed * Apply knowledge of analyzing issues and uses judgment to make decisions * Knowledge of immunoassays, specifically plate-based assays and ELISAs * Utilize cGMP practices in documentation and execution of job functions * Perform instrument calibration or qualification according to written procedures * Write and revise SOPs and/or participate in validation protocol execution, as needed * Perform testing, as needed, to generate data for qualification/validation and special projects * Fulfill requests from management for assistance in other matters, as needed * Accountable for following SOPs and adhering to cGMP guidelines * Review documentation on trained tasks as assigned by QC management * Use technical and scientific knowledge to recommend solutions to problems as directed by QC management * Mentor junior analysts and provide training as requested on QC assays Education Requirements: Bachelor's degree in Chemistry, Biochemistry, Molecular Biology, or related science discipline. Experience Requirements: At least three years of experience performing chemical/biochemical testing or developing immunoassays. Work in a regulated environment (FDA, EPA, etc.) is highly preferred. In addition to competitive compensation, we offer a comprehensive benefits package including: * 401K plan with employer match and immediate vesting * Medical, Vision, Life and Dental Insurance * Pet Insurance * Company paid STD and LTD * Company Paid Holidays * 3 Weeks' Paid Time Off (within the first year) * Tuition Assistance (after the first year) * Easily accessible to Tri-Rail * Company paid shuttle to the Boca Tri-Rail station ADMA Biologics uses E-Verify to confirm the employment eligibility of all newly hired employees. To learn more about E-Verify, including your rights and responsibilities, please visit ********************* ADMA Biologics is an Equal Opportunity Employer.

div name="main"div class="cl HeadSecondary"h2Job Details/h2/divdiv aria-label="Job Details" class="row" name="local_row"div class="col-md-6 local-tax-col local-ee" id="job DetailsLeftColumn" name="local_left"div class="row form RowStandard" id="Level-row" div class="form Line"div aria-label="Level" name="Level"span aria-label="Level" class="" name="level"Experienced/span/div/div/divdiv class="row form RowStandard" id="Job Location-row" div class="form Line"div aria-label="Job Location" name="Job Location"span aria-label="Job Location" class="" name="level"ADMA Biologics FL - Boca Raton, FL/span/div/div/divdiv class="row form RowStandard" id="Position Type-row" div class="form Line"div aria-label="Position Type" name="Position Type"span aria-label="Position Type" class="" name="level"Full Time/span/div/div/divdiv class="row form RowStandard" id="Education Level-row" div class="form Line"div aria-label="Education Level" name="Education Level"span aria-label="Education Level" class="" name="level"4 Year Degree/span/div/div/div/divdiv class="col-md-6 local-tax-col local-client" name="local_right"div class="row form RowStandard" id="Travel Percentage-row" div class="form Line"div aria-label="Travel Percentage" name="Travel Percentage"span aria-label="Travel Percentage" class="" name="level"None/span/div/div/divdiv class="row form RowStandard" id="Job Shift-row" div class="form Line"div aria-label="Job Shift" name="Job Shift"span aria-label="Job Shift" class="" name="level"Day/span/div/div/divdiv class="row form RowStandard" id="Job Category-row" div class="form Line"div aria-label="Job Category" name="Job Category"span aria-label="Job Category" class="" name="level"Pharmaceutical/span/div/div/div/div/divdiv class="cl HeadSecondary"h2Description/h2/divdiv aria-label="Description" class="row" name="description" style="word-wrap: break-word;"div class="row form RowStandard" id="job Desc-row" div class="form Line"span class="fb Text ignore-global-css" name="job Desc"p style="margin-left:0in;margin-right:0in;"span style="font-size:16px;"span style="font-family:Arial, Helvetica, sans-serif;"strong ADMA Biologics/strong is a biopharmaceutical company relentlessly committed to creating superior products for immunodeficient patients at risk for infection. It is our devotion to this underserved population that fuels us and our hands-on approach to production and development that sets us apart. If you are looking for a dynamic, innovative, growing company in the biopharmaceutical industry that is committed to excellence and integrity, then consider ADMA Biologics. We currently have an exciting opportunity available for a strong Chemist II in Boca Raton, FL!/strong/span/span/p p style="margin-left:0in;margin-right:0in;" /p p style="margin-left:0in;margin-right:0in;"span style="font-size:16px;"span style="font-family:Arial, Helvetica, sans-serif;"The strong Chemist II/strong will perform quality control testing of raw materials, in-process goods, and final products with minimal supervision. Uses knowledge of corporate policies to resolve routine problems. /span/span/p/span/div/div/divdiv class="cl HeadSecondary"h2Qualifications/h2/divdiv aria-label="Qualifications" class="row" name="qualifications" style="word-wrap: break-word;"div class="row form RowStandard" id="job Qualifications-row" div class="form Line"span class="fb Text ignore-global-css" name="job Qualifications"ul lispan style="font-size:16px;"span style="font-family:Arial, Helvetica, sans-serif;"Perform quality control testing for raw materials, in-process and final product sample testing according to approved Standard Operating Procedures. /span/span/li /ul ul lispan style="font-size:16px;"span style="font-family:Arial, Helvetica, sans-serif;"Complete testing documentation and data entry as required for procedures and tests performed./span/span/li /ul ul lispan style="font-size:16px;"span style="font-family:Arial, Helvetica, sans-serif;"Apply knowledge of analyzes issues and uses judgment to make decisions./span/span/li /ul ul lispan style="font-size:16px;"span style="font-family:Arial, Helvetica, sans-serif;"Utilize cGMP practices in documentation and execution of job functions./span/span/li /ul ul lispan style="font-size:16px;"span style="font-family:Arial, Helvetica, sans-serif;"Perform instrument calibration or qualification according to written procedures./span/span/li /ul ul lispan style="font-size:16px;"span style="font-family:Arial, Helvetica, sans-serif;"Write and revise SOPs and/or Validation Protocols./span/span/li /ul ul lispan style="font-size:16px;"span style="font-family:Arial, Helvetica, sans-serif;"Perform testing as needed to generate data for Validation and Special Projects./span/span/li /ul ul lispan style="font-size:16px;"span style="font-family:Arial, Helvetica, sans-serif;"Fulfill requests from management for assistance in other matters as needed./span/span/li /ul ul lispan style="font-size:16px;"span style="font-family:Arial, Helvetica, sans-serif;"Accountable for following Standard Operating Procedures (SOPs) and adhering to cGMP guidelines./span/span/li /ul ul lispan style="font-size:16px;"span style="font-family:Arial, Helvetica, sans-serif;"Review documentation on trained tasks as assigned by /span/spanspan style="font-family:Arial, Helvetica, sans-serif;"span style="font-size:16px;"manager./span/span/li /ul p style="margin-left:0in;margin-right:0in;" /p p style="margin-left:0in;margin-right:0in;"span style="font-family:Arial, Helvetica, sans-serif;font-size:16px;"strong Education Requirements: /strong /span/p p style="margin-left:0in;margin-right:0in;text-align:left;"span style="font-size:16px;"span style="font-family:Arial, Helvetica, sans-serif;"B.S. in Chemistry, Biochemistry, Molecular Biology, or related science discipline./span/span/p p style="margin-left:0in;margin-right:0in;text-align:left;"span style="font-size:16px;"span style="font-family:Arial, Helvetica, sans-serif;" /span/span/p p style="margin-left:0in;margin-right:0in;text-align:left;"span style="font-size:16px;"span style="font-family:Arial, Helvetica, sans-serif;"strong Experience Requirements: /strong /span/span/p p style="margin-left:0in;margin-right:0in;text-align:left;"span style="font-size:16px;"span style="font-family:Arial, Helvetica, sans-serif;"At least three years of experience in a laboratory setting. Work in a regulated environment (FDA, EPA, etc). is /span/span/p p style="margin-left:0in;margin-right:0in;text-align:left;"span style="font-size:16px;"span style="font-family:Arial, Helvetica, sans-serif;"preferred, but not required./span/span/p p style="margin-left:0in;margin-right:0in;" /p p style="margin-left:0in;margin-right:0in;"span style="font-size:16px;"span style="font-family:Arial, Helvetica, sans-serif;"strongemspan style="color:#000000;"In addition to competitive compensation, we offer a comprehensive benefits package including:/span/em/strong/span/span/p ul lispan style="font-size:16px;"span style="font-family:Arial, Helvetica, sans-serif;"401K plan with employer match and immediate vesting/span/span/li lispan style="font-size:16px;"span style="font-family:Arial, Helvetica, sans-serif;"Medical, Vision, Life and Dental Insurance /span/span/li lispan style="font-size:16px;"span style="font-family:Arial, Helvetica, sans-serif;"Pet Insurance /span/span/li lispan style="font-size:16px;"span style="font-family:Arial, Helvetica, sans-serif;"span style="color:#000000;"Company paid STD and LTD/span/span/span/li lispan style="font-size:16px;"span style="font-family:Arial, Helvetica, sans-serif;"span style="color:#000000;"Company Paid Holidays /span/span/span/li lispan style="font-size:16px;"span style="font-family:Arial, Helvetica, sans-serif;"span style="color:#000000;"3 Weeks' Paid Time Off (within the first year)/span/span/span/li lispan style="font-size:16px;"span style="font-family:Arial, Helvetica, sans-serif;"span style="color:#000000;"Tuition Assistance (after the first year)/span/span/span/li lispan style="font-size:16px;"span style="font-family:Arial, Helvetica, sans-serif;"span style="color:#000000;"Easily accessible to Tri-Rail/span/span/span/li lispan style="font-size:16px;"span style="font-family:Arial, Helvetica, sans-serif;"span style="color:#000000;"Company paid shuttle to the Boca Tri-Rail station/span/span/span/li /ul p style="margin-left:0in;margin-right:0in;" /p p style="margin-left:0in;margin-right:0in;"span style="font-size:16px;"span style="font-family:Arial, Helvetica, sans-serif;"span style="color:#000000;"strong ADMA Biologics/strong uses E-Verify to confirm the employment eligibility of all newly hired employees. To learn more about E-Verify, including your rights and responsibilities, please visit ********************* /span/span/span/p p style="margin-left:0in;margin-right:0in;" /p p style="margin-left:0in;margin-right:0in;"span style="color:#000000;font-family:Arial, Helvetica, sans-serif;font-size:16px;"strong ADMA Biologics/strong is an Equal Opportunity Employer./span/p/span/div/div/div/div

The R&D Lab Chemist is responsible for working on various Technical Service and R&D Projects to support our Customers, Principals, Various product lines in our portfolio, and Sales Team in laboratory/office setting, resulting in making Barentz Always a better solution

PLEASE NOTE: Must be authorized to work lawfully in the United States for any employer without sponsorship. For immediate consideration, please apply. Kelly Science & Clinical is seeking an Associate Scientist II for a direct hire position at a leading client in Weston, FL. If you're passionate about bringing the latest scientific discoveries to life and are ready to take the next step in your career, trust The Experts at Hiring Experts. **Pay Rate:** $65-85,000/Year (commensurate with experience) **Overview:** Our client has immediate needs for multiple Associate Scientist IIs to join a growing client located in the Fort Lauderdale/Miami area. This is a great direct hire opportunity that can offer room to grow within the organization, full relocation package, and 10% bonus potential. **Schedule:** Monday - Friday, 2nd/Swing: 4:00 PM - 12:00 AM **Responsibilities:** - Conduct laboratory activities with limited supervision, including analyzing raw materials, in-process materials, and finished pharmaceutical products for quality, safety, purity, strength, and identity, following applicable methods and relevant guidelines (cGMP, EH&S, FDA, and other governing bodies). - Independently set up and operate lab equipment, prepare reagents, solvents, and solutions for analytical and formulation activities. - Maintain accurate records in lab notebooks for all testing performed. - Process analytical data using lab equipment such as HPLC/UPLC and enter data into spreadsheets; conduct routine calculations. - Support the manufacture of inhalation drug products and prepare samples for blend uniformity. - Perform equipment qualification and calibrations as directed. - Execute approved method transfer protocols. - Assist in training other scientists and team members. - Perform additional tasks as assigned. - Participate in project activities, support project timelines, and proactively contribute to meeting team objectives. - Communicate effectively with team members and maintain effective relationships. - Conduct lab work in accordance with SOPs and STPs and follow corporate safety rules and procedures. - Comply with all corporate guidelines and policies. **Qualifications:** - BSc in Chemistry, Pharmacy, or related fields with at least 3 years of experience in Pharmaceutical R&D, or MSc in Chemistry, Pharmacy, or related fields with 0-2 years of experience in Pharmaceutical R&D. - 2 years minimum industry experience with HPLC method development and Empower software - Proven ability and/or experience with compendial test methods or pharmaceutical manufacturing equipment. - Understanding of pharmaceutical equipment and computerized systems for operation and troubleshooting, including experience with analytical and/or process equipment such as HPLC, IR/FTIR, UV-Vis, AA, powder blenders, etc. - Knowledge and understanding of FDA cGMP requirements as it applies to the pharmaceutical industry. - Strong written and oral communication skills in English, with the ability to write short technical documents such as memos, laboratory investigations, protocols, and reports. **What Happens Next:** Once you apply, you'll proceed to next steps if your skills and experience look like a good fit. But don't worry - even if this position doesn't work out, you're still in our network. That means our team of expert Science & Clinical recruiters will have access to your profile, making your opportunities limitless. 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.

Job Title: Innovation Senior Chemist Summary: Designs, implements, & reports experiments with the goal of addressing technical challenges facing Perfume R&D process. Collaborates with Technology Division as the liaison at the Fort Lauderdale Site. Essential Duties and Responsibilities: Include the following, but not limited to: Design, implement, & report experiments addressing technical challenges in the R&D process Collaborate with Technology division in the testing and validation of new products for market introduction Meets with Sales team & Clients to discuss Projects/ Technology/ Technical difficulties. Maintain organized records of raw material regulatory documents, cosmetic formulas, and stability reports used in application lab. Revise formluations to identify chemicals triggering instabilitites/ challenges. Perform other incidental and related duties as required and assigned. Competencies: To perform the job successfully, an individual should demonstrate the following competencies: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. About The Organization Cosmo International Fragrances is a privately owned company that has been in operation for over 40 years. We work with well-established and indie brands globally and manufacture fragrance oils for fine fragrance, personal care, home, hair care, and household products. With production plants, creative centers, and R&D sites in the US, Europe, Asia, and the Middle East, we bridge the gap between fragrance creation, consumer needs, and emerging innovations. Cosmo is proud to be an international company. We are a diverse entity with employees from diverse backgrounds and over thirty (30) countries worldwide. We value our diversity and foster a culture of community with respect towards each other, inclusion, and equity. People Parfum, Purpose We offer competitive pay, career growth opportunities, and outstanding benefits programs. Our benefits package includes health insurance coverage, wellness and family support programs, life and disability insurance, retirement savings plans, paid leave programs, education-related programs, paid holidays and vacation time, year-round summer Fridays, and many others...

JOB QUALIFICATIONS: BS or MS in Chemistry or equivalent combination of education and experience 1-3 years of industry experience Demonstrated use of the analytical techniques in support of product development activities Understanding of the fundamentals of analytical chemistry and instrumentation Knowledge of current Good Manufacturing Practices (cGMP) Demonstrated ability to work well in a fast-paced setting with excellent organizational skills Excellent written and verbal communication skills, problem solving skills and basic computer skills POSITION RESPONSIBILITIES: Performs testing on raw material, in-process & finished product samples Executes method transfer, verification and validation protocols Documents all data in corresponding laboratory notebook and files documentation according to approved SOP and data integrity guidelines Evaluate and interpret the test results and other related technical documentation Writes methods and reports Performs routine lab maintenance including equipment calibration, glassware cleaning, chemical and supplies inventory management (includes ordering, cleaning and organization) Other duties may be assigned as deemed appropriate by management PHYSICAL REQUIREMENTS: Employees are required to wear eye protection and lab coats while in the lab Work safely and follow all OSHA regulations and company safety policies and procedures Ability to frequently lift and/or move up to 25 lb. Ability to occasionally lift and/or move up to 35 lb. Ability to regularly stand, sit and walk to perform tasks

Empower, Innovate, Impact! At Team A-TEK, we EMPOWER people to drive INNOVATION that IMPACTS mission! A-TEK operates at the intersection of mission and innovation by applying our deep domain expertise across the federal markets. Embracing our digital-first strategy, A-TEK provides enhanced capabilities in application development, digital transformation, enterprise IT, and scientific services. Our solutions are designed to modernize, automate, secure, protect, and enhance the operations of our federal clients, ensuring they stay ahead in a rapidly evolving digital landscape. Our work is fueled by a passion to serve our clients' needs and to protect the safety and welfare of Americans. That passion shapes how we nurture our most valuable asset - Our Employees. A-TEK actively cultivates the talent that drives our success and fosters a creative, challenging, and mission-driven work environment for current and future employees. This position will be responsible for performing non-research molecular testing to rapidly identify and characterize potential pathogenic bacterial and viral threat agents. Ensures incoming biological samples are processed and triaged maintaining chain of custody. Performs and interprets a variety of specialized tests and strains, detection, and identification of pathogenic microorganisms. Prepares written and oral reports, answers questions, troubleshoot and makes recommendations to the supervisor for inclusion in comprehensive reports on test findings. Maintains and operates equipment including performing calibrations, adjustments, and to operate equipment and instruments properly and in a safe manner. Participates in cross training related to bioterrorism and other public health emergencies. Additionally, will be responsible for maintaining knowledge and skills related to position and program and to carry out all procedures in accordance with proper handling and storage of various biological materials. Must be available 24/7/365 to respond in case of emergency. Rotating weekends and some holidays are required. Kindly be aware that drug screening is a mandatory condition of employment for this position. REQUIRED QUALIFICATIONS: Bachelor's degree from an accredited university in microbiology, molecular biology, or related course work in biological sciences. REQUIRES at least one year of laboratory bench experience, utilizing PCR, aseptic techniques and experience with biological assays. Laboratory training that is assigned or accompanies an associated course is not considered applicable training. Biological Safety Level (BSL)-3 experience is highly desirable. This position supports a federal contract which requires that all employees and job applicants hold a valid Green Card or US Citizenship at the time of application. #LI-OnSite A-TEK, Inc. is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or status as a qualified individual with a disability, or Vietnam era or other protected Veteran status.

Job Details Miramar, FL $75000.00 - $85000.00 Salary/year AnyDescription About Us: Aveva Drug Delivery Systems is a pharmaceutical manufacturer at the forefront of innovative drug delivery technologies. We are dedicated to advancing solutions that optimize the efficacy, safety, and precision of pharmaceutical treatments. Join our team and help shape the future of healthcare by contributing to the development of groundbreaking drug delivery systems that improve patient outcomes worldwide. Job Summary: Laboratory position which involves development and validation of analytical methodology in support to the research projects involving testing of pharmaceutical components and/or drug products. This position also involves designing and completion experiments and providing scientifically sound recommendations based on the data obtained. Key Responsibilities: Developing new analytical methods using innovative solutions for actives, excipients, drug release, residual solvents and to support product development. Validating analytical methodologies following ICH guidance Executing complex experiments in support to R&D for development and validation of process under minimum supervision. Ability to identify creative and innovative solutions of non routine analytical tasks Improves analytical applications by implementing new analytical techniques Clearly interpret problems, make scientific judgment based on outcome of the obtained data and take appropriate actions to resolve the issues. Writing/reviewing protocols, reports, SOP's, specifications & test procedures. Compiling necessary documentation to support regulatory submissions such as Abbreviated New Drug Applications (ANDAs) or New Drug Applications (NDA), as required. Adhering to laboratory SOP guidelines, GMP requirements and safety rules. Maintaining analytical instrumentation through the proper performance and/or maintenance as required. Train junior scientists and QC chemists as necessary. Demonstration ability of problem solving and offer necessary recommendations. Works as a member of a team to achieve all outcomes Operates in accordance with our Code of Conduct and Business Ethics, and all established regulatory, compliance and safety requirements. Performs all work in support of our Values: Collaboration, Courage, Perseverance, and Passion All other relevant duties as assigned Qualifications Education Bachelor's degree (B.S.) in chemistry or related field Master's degree (M.S.) or Ph.D. Experience At least five (5) years experience in pharmaceutical laboratory (B.S) At least two (2) years laboratory experience (M.S.) Knowledge, Skills and Abilities Proficiency in using analytical equipments such as UV/Visible and Infrared spectrophotometers, automatic titrators, pH potentiometers, dissolution apparatus, HPLC, GC, GC/MS, LC/MS/MS and other techniques as needed. Strong verbal and written communication skills, interpretation of experimental results, technical protocols and reports writing. Broad knowledge of methods development in support Active Pharmaceutical Ingredients, Intermediates, excipients and drug products. Ability to clearly indentify problems and take appropriate actions based on available information Organization skills and ability to plan and prioritize work to meet deadlines. Proficiency in the use of computer hardware, software and databases such as Word processing software, MS office, TrackWise, Empower, or other applicable to analytical instrumentation software. Demonstrate accuracy and thoroughness of work and adhere to high quality standards related to cGMPs. Benefits: Aveva Drug Delivery Systems and DifGen Pharmaceuticals provides a comprehensive benefits plan Medical/Dental/Vision Insurance Paid Time Off 401k with employer match Paid Holidays and Floating Holiday Equal Opportunity Employer

Current Employees: If you are a current Staff, Faculty or Temporary employee at the University of Miami, please click here to log in to Workday to use the internal application process. To learn how to apply for a faculty or staff position using the Career worklet, please review this tip sheet. The University of Miami/UHealth Department of SCCC - Human Genetics has an exciting opportunity for a Full Time Associate Scientist to work at the UHealth Medical Campus in Miami, FL CORE JOB SUMMARY The Associate Scientist supports the University's research goals and objectives by performing laboratory experiments in his/her areas of interest, expertise, or assignment. Moreover, the incumbent performs various analytical procedures involving method development and application development and synthesis. This position will report to Dr. Reinberg's lab. CORE JOB FUNCTIONS 1. Contributes to basic and applied research activities including authorship of scientific publications, technical and agency reports, and patent preparations. 2. Publishes in refereed journals in collaboration with department leadership or independently. 3. Supervises research employees and non-exempt staff. 4. Writes extramural proposals with approval of senior managing staff. 5. Creates and conducts experiments and analyzes results. 6. Works with other researchers to use and develop end products. 7. Provides ready access to all experimental data for the faculty researchers, supervisors, and other relevant staff. 8. Requests or acquires equipment and supplies for assigned project(s). 9. Applies for grants to continue research and prepares materials for submission to granting agencies and foundations. 10. Adheres to University and unit-level policies and procedures and safeguards University assets. This list of duties and responsibilities is not intended to be all-inclusive and may be expanded to include other duties or responsibilities as necessary. CORE QUALIFICATIONS Education: Doctorate degree - Philosophy (PhD) required Experience: Minimum 5 years of relevant experience required Certification and Licensing: Refer to department description for applicable certification requirements Knowledge, Skills and Abilities: * Learning Agility: Ability to learn new procedures, technologies, and protocols, and adapt to changing priorities and work demands. * Teamwork: Ability to work collaboratively with others and contribute to a team environment. * Technical Proficiency: Skilled in using office software, technology, and relevant computer applications. * Communication: Strong and clear written and verbal communication skills for interacting with colleagues and stakeholders. #LI-YC1 The University of Miami offers competitive salaries and a comprehensive benefits package including medical, dental, tuition remission and more. UHealth-University of Miami Health System, South Florida's only university-based health system, provides leading-edge patient care powered by the ground breaking research and medical education at the Miller School of Medicine. As an academic medical center, we are proud to serve South Florida, Latin America and the Caribbean. Our physicians represent more than 100 specialties and sub-specialties, and have more than one million patient encounters each year. Our tradition of excellence has earned worldwide recognition for outstanding teaching, research and patient care. We're the challenge you've been looking for. The University of Miami is an Equal Opportunity Employer - Females/Minorities/Protected Veterans/Individuals with Disabilities are encouraged to apply. Applicants and employees are protected from discrimination based on certain categories protected by Federal law. Click here for additional information. Job Status: Full time Employee Type: Staff Pay Grade: A11