Sr. Scientist | Lakewood, OH

improving billions of lives around the world. We value diversity in professional backgrounds and life experiences. By enabling a consistent, unbiased, and transparent recruitment process, Lubrizol seeks to create a positive experience for candidates so we can get to know them at their best.

We recognize unique work and life situations and offer flexibility, ensuring our employees feel engaged and fulfilled in every aspect of life. The Lubrizol Corporation, a Berkshire Hathaway company, is committed to enabling a sustainable future. Our unmatched science unlocks immense possibilities at the molecular level, driving sustainable and measurable results to help the world Move Cleaner, Create

Smarter and Live Better. Our solutions are used by people every day, improving billions of lives around the world The Lubrizol Corporation currently has an opening for a safety-minded and results-oriented Research Chemist at our facility in Brecksville, Ohio.

This role will support the Temp Rite business in the following key areas: Ensure excellent personal and process safety, regulatory, and housekeeping performance in laboratory operations. Perform independent research in CPVC chemistry, processing, and characterization of CPVC resin to improve processing and product performance. Identify and utilize new analytical techniques to advance understanding of CPVC resin structure and physical

properties. Lead cross-functional project teams to achieve business goals.

Become a recognized subject matter expert in Temp Rite CPVC resin technology. Maintain accurate and clear records and written reports on experimental data and interpretation of results. Evaluate experimental and production data and identify trends. Oversee resin characterization and chlorination lab operations including operation and troubleshooting of instruments. Develop a good understanding of the intellectual property landscape and track pertinent literature. Support plant resin evaluations to ensure new material implementations meet necessary quality, processing, material handling and approval body certification requirements.

Design and review outcomes of plant trials for quality and process improvements. Communicate effectively to a global audience between key stakeholders across all levels of the organization. Provide technical support and training to internal and external customers. Experience and Qualifications Ph. D. in chemistry from an accredited college/university 5+ years of experience in a research & development or plant production role Required Competencies: Ability to take initiative, lead decisively, and work independently with minimal supervision. Excellent organizational and written and verbal communications skills.

Demonstrated ability to utilize chemistry expertise to solve problems and develop product technology. Experience in writing technical reports to communicate information to internal and external stakeholders. Willingness to adhere to all lab safety and personal protective equipment requirements, including use of a respirator as needed. Strong PC skills including MS Office Suite Ability to travel as required (less than 10%) Preferred Skills and Qualifications: Knowledge of polymer processing and associated testing and analysis techniques Knowledge of Design of Experiments (DOE) and statistical analysis principles Experience in chlorination chemistry, reactions and associated processes Industrial/manufacturing experience What Lubrizol offers: Competitive salary with performance-based bonus plans 401K Match plus Age Weighted Defined Contribution Competitive medical, dental & vision offerings Health Savings Account Paid Holidays, Vacation, Parental Leave Flexible work environment Learn more at benefits.

If you’re interested in the position, we encourage you to apply. Lubrizol is always looking for candidates who embody our cultural beliefs in everything they do.

If you’re All In, Lead Decisively, Take Action, Think External, and can Be Courageous, Lubrizol could be the place for you.

of lives around the world. We value diversity in professional backgrounds and life experiences. By enabling a consistent, unbiased, and transparent recruitment process, Lubrizol seeks to create a positive experience for candidates so we can get to know them at their best.

We recognize unique work and life situations and offer flexibility, ensuring our employees feel engaged and fulfilled in every aspect of life. Lubrizol has an immediate need for a Jr. Scientist in our global Beauty Applications Team. This person will work collaboratively as a member of cross-functional project teams to evaluate, identify and deliver new ingredients and concepts for the skin cleansing and hair care markets.

DUTIES/RESPONSIBILITIES: Work collaboratively as a member of cross-functional project teams to introduce new value-added solutions to the skin cleansing and hair care markets.

Plan, organize and conduct experiments to develop new formulations, concepts, and testing methodologies to support global product launches. Explore new applications and enhanced formulation benefits with leveraged ingredients for the skin cleansing and hair care markets. Ensure experimental products and new formulation concepts are evaluated against appropriate benchmarks using accepted protocols clearly demonstrating value proposition. Conduct and manage scientific experiments: Accurately record, interpret, analyze,

and draw conclusions from data. Use focused development tools such as Design of Experiments (DOE) as needed.

Follow safe laboratory practices. Communicate results and recommendations to project and leadership teams as needed. Support marketing to develop technical literature for new products and applications concepts. Maintain detailed records of experiments, results, and conclusions. Train internal colleagues, distributors, and customers on new concepts and product launches Up to 10% travel SKILLS, QUALIFICATIONS, EXPERIENCE, SPECIAL PHYSICAL REQUIREMENTS: Bachelor’s degree in Chemistry, Biochemistry, Chemical Engineering, Materials Science, or related field from an accredited college/university.

3-5 years’ experience formulating and testing hair care and skin cleansing ingredients/products. Knowledge of global hair care and skin cleansing trends, product formats, and customer base. Ability to work well individually and in team settings. Ability to plan and organize multiple assignments with minimal supervision. Strong verbal and written communication skills. Self-starter, highly motivated toward achievements, results oriented. Solid record keeping skills. Proficient computer skills including MS Office. Ability to travel up to 10% as needed to support commercialization of new products.

Ability to work safely within Lubrizol laboratories. What Lubrizol offers: Competitive salary with performance-based bonus plans 401k Match plus Age Weighted Defined Contribution Competitive medical, dental and vision offerings Health Savings Account Paid Holidays, Vacation, Parental Leave If you’re interested in the position, we encourage you to apply. Lubrizol is always looking for candidates who embody our cultural beliefs in everything they do. If you’re All In, Lead Decisively, Take Action, Think External, and can Be Courageous, Lubrizol could be the place for you. #LI-JM1

Science Jobs refer to employment opportunities within the various fields of science, such as biology, chemistry, physics, and environmental science. These positions often require a strong educational background in their respective disciplines and can range from academic research and teaching roles to industry-based positions in pharmaceuticals, technology, and more. Unique features of Science Jobs include a focus on innovation, evidence-based analysis, and the exploration of the natural world. They contribute significantly to technological advancements and the betterment of society through scientific discovery and application.

inspection of safe and effective sterile (injectable) medical products.

Operation of secondary packaging line equipment, labelling, and equipment cleaning. Interacts with Quality, Technical Services, Maintenance, Warehouse Departments, and other departments as required.

Ensures that daily production is carried out according to current SOP's ensuring absolute compliance to quality standards. The Operator is responsible for documenting daily production outputs and efficiencies and keeps other stakeholders involved and informed. Challenges during production are documented and resolved by means of various LEAN tools. Collaborates in the training of colleagues. Key Responsibilities:

Set-up, operation, and troubleshooting of manufacturing equipment: including (but not limited to) Manual Inspection Booths, Semi-Automated Inspection Machine, Secondary Packaging Machines and ancillary equipment (conveyors, pallet jacks, etc.

) within validated parameters and in compliance with c GMP's. Operation of automated equipment through a Human Machine Interface (HMI). Clear and concise written documentation to support GMP activities. Performs line change overs and simple-to-moderate equipment adjustments. Supports the creation and updating of procedures enabling the improvement of quality, compliance, and overall process performance. React to issues on the production line

and start up systematic problem-solving enabling colleagues to support root cause analysis.

Adhere to c GMP's, SOP's, Batch Record processing steps, and site environmental and safety policies. Support a continuous improvement culture and mind set within the department. Possess strong commitment to quality and compliance. Guide colleagues in the importance of proactive behavior regarding improving the work environment towards zero accidents. Work closely together with quality to solve quality issues as they occur and ensure timely release of products. Responsible for execution and completion of individual Training per required curriculum. Ensure processes and products are in compliance with all local, state, and federal rules and regulations.

Oversee that processes are in CGMP compliance, and establish systems that identifies opportunities for improvement and makes constructive suggestions for change to improve process effectiveness to heighten quality. Develop knowledge of and understand regulatory requirements such as 21CFR Parts 210 and 211, c GMP's, FDA, OSHA and other regulatory agencies. Requirements: High School Diploma or GED; Associates Degree in a natural science or technical curriculum preferred Prior experience in a regulated environment; medical or medical device manufacturing experience preferred Must be able to learn and develop a working knowledge of c GMP's; previous knowledge of c GMP requirements preferred Prior experience with complex high speed packaging equipment Experience with quality control technology including vision, robots or automation preferred Ability to clearly read and write English Demonstrates a strong desire to continuously learn and improve Personnel engaged in the manufacture, processing, packing, or holding of a drug product shall wear clean clothing appropriate for the duties they perform.

Protective apparel, such as head, face, hand, and arm coverings, shall be worn as necessary to protect drug products from contamination. Candidate will not be permitted to wear (in the classified manufacturing areas) jewelry, makeup, hair extension, or any exterior adornment (religious articles will be evaluated on a case-by-case basis as to backss impact on controlled environment and drug product). Physical Requirements of the Role: Adequate vision required, must be able to successfully pass visual acuity requirements (20/20 corrected vision, distinguish colors as required. Visual Acuity requirements are tested annually).

Ability to stand, sit, and/or walk for long period of time. Ability to operate material handling equipment. Ability to lift, push, and/or pull up to 50 lbs frequently. Position requires continuous standing and walking. Must be able to be gown qualified. Any person shown at any time (either by medical examination or supervisory observation) to have an apparent illness or open lesions that may affect the safety or quality of a drug product shall be excluded from direct contact with components, drug product containers, closures, in-process materials, and drug products until the condition is corrected or determined by competent medical personnel not to jeopardize the safety or quality of drug products.

All personnel shall be instructed to report to supervisory personnel any health conditions that may have an adverse effect on drug products. #LI-AH1#LI-Onsite Xellia medicals is owned by Novo Holding A/S and is a specialty medical company leading in the development, manufacture and supply of anti-infective treatments. Headquartered in Copenhagen, Denmark, Xellia has global facilities in Europe, North America, and Asia, currently employing over 1700 people.

With over 100 years of industry experience in developing last resort treatments for infectious diseases, Xellia is focused on the supply of products which not only save lives, but also improve and enhance patients' quality of life. Together with us, you can help lead the fight against bacterial infections. Read more about Xellia medicals here