• Performing orienting and preparatory tasks after deliberation with the supervisor in such a way that the project at hand is prepared almost autonomously.
• Implementing in consultation with the supervisor of tasks related to product development, product maintenance, sales and production support. 
• Impact on the improvements in the fields of working methods and efficiency.
• Formulating and introducing approved formulas and test cards for new or changed products and distribution via the usual channels.
• Follow experimental procedures, generate reliable data, and consistently demonstrates the ability to chip in to the design of experiments. 
• Manage independent projects or portions of larger project.
• Follows independently the industrial pilot batches with the process department.
• Checking the progress of activities and adjusting these, adjusting the method to get the result.
• Establishing an action plan and naming the management aspects
• Implementing the plan in collaboration.
• Solve problems through the application of knowledge of appropriate scientific, experimental, and statistical methods (i.e. DOE).
• Working in compliance with QMS system and 5S and EHS requirements.

Skills: Project Preparation, Product Development, Process Improvement, Formula Management, Experimental Design, Independent Project Management, Pilot Batch Monitoring, Problem Solving

• Act as a point of expertise for chemical analysis, training and calibration and manage the Microbiology function in providing an effective and efficient testing support for the factory
• Identify/lead/implement quality improvement initiatives
• Identify, lead and implement projects which deliver improved efficiency and cost saving benefits
• Maintain the ISO9001, SGS & BRC quality management systems to ensure continued accreditation
• Manage HACCP improvement exercises
• Ensure that all actions from laboratory visits, audits and internal non-conformances are captured and regularly reviewed
• Promote Health & safety awareness and improvement in by being actively involved in safety management systems
• Point of expertise for product/component analysis, raw material issues, and technical support in blending / filling
• Lead process improvement projects value engineering, NPD and EPD
• Monitor supplier conformance and quality via KPI tracking systems
• Identify, lead and implement projects which deliver improved efficiency and cost saving benefits
• Maintain the ISO9001, SGS & BRC quality management systems for the laboratory to ensure continued accreditation
• Strives to reduce costs within its own area wherever possible without compromising quality or service.

Skills: Chemical Analysis, Quality Improvement, Project Leadership, Quality Management, HACCP Management, Safety Promotion, Technical Support, Supplier Monitoring

• Conduct laboratory scale organic chemistry experiments in accordance with the work plan and under the close direction of the project leader or designate. 
• Seeks input from other more experienced chemists
• Document comprehensive, accurate and timely experimental observations in lab books
• Report observations to project leader or designate
• Register spectra and chromatograms
• Acquire skills and knowledge necessary to perform analytical methods on various samples
• Prepare a summary of laboratory experiments for project updates to be discussed with project team leader
• Perform the accurate input of hours and comments in TIMS for post project reviews
• Read and follow R+D Manuals and SOP’s
• Participate in opportunities to develop a current knowledge of chemistry and technology
• Ensure safe and clean lab operations
• Interact with cross-functional staff on projects. 
• Develop knowledge of other departments and functions
• Perform departmental tasks such as inventory control, supply ordering, etc

Skills: Organic Chemistry, Experimental Documentation, Data Reporting, Analytical Techniques, Project Summarization, SOP Compliance, Lab Safety, Cross-functional Collaboration

• Routinely evaluates current product formulas for performance improvements, process efficiencies, and cost containment/reduction.
• Re-formulates current products to meet changing regulatory requirements.
• Leads investigations into and implements solutions to manufacturing challenges with scale-up, raw material substitutions, packaging, stability, or other quality issues that may arise.
• Ensure sampling, examining, and testing all merchandise, ingredients and finished products for compliance with quality standards and ensure that retention samples are stored properly after release.
• Establish the testing capability and develop the testing methods for all new ingredients and finished products to ensure new product launches in a defined timeframe.
• Perform analysis using advanced analytical techniques, eg. GC, HPLC/UHPLC, UV, FT-NIR, Particle Sizer, AAS, IC, ICP-MS etc, including basic preparation of samples for analysis
• Development of analytical methods and conducting calibration and validation for all existing and new lab equipment at a defined frequency to ensure it generates accurate and precise testing results consistently.
• Arrange the analysis of ingredients, finished products, in-process samples and samples for new supplier approval in a timely, accurate manner.
• Conduct review of scientific, governmental, or other literature in order to maintain and improve laboratory knowledge/skills and identify appropriate analytical techniques for projects/studies
• Work as an internal expert on his/her working group by supporting other chemists/technicians on complicated technical processing review
• Organize workflow and task schedules to maximize laboratory efficiency
• Perform data audits in order to ensure accuracy of data and analytical processes, which may include testing records and calibration records, statistical process control, correlation studies, notebook review, and/or traceability exercises

Skills: Formula Evaluation, Regulatory Reformulation, Manufacturing Investigation, Quality Testing, Analytical Techniques, Method Development, Workflow Organization, Data Auditing

• Perform a broad range of chemical analyses, test methods, and procedures required for determining the quality of petroleum and lubricating fuel samples, adhering to laboratory protocols, work instructions and regulations.
• Analyze test results, perform routine calculations, maintain records of fuel tests, interpret test results, and notify the Responsible Officer and Regional Chemist of any questionable findings.
• Manage the laboratory resources to include equipment, adequate inventories of consumables, reagents, and chemicals necessary to carry out testing
• Coordinate contractor support of equipment calibration efforts as well as perform limited in house maintenance /repair on laboratory test equipment.
• Ensure that solvents and reagents used in the performance testing are disposed of in accordance with applicable permit requirements and environmental regulations.
• Scales up of successful experimental formulations and writes manufacturing and quality instructions and specifications
• Provide subject-matter expertise to support and occasionally lead New Product Development projects
• Develops, validates, and maintains analytical test methods and instrument calibration processes for use by R&D and QC.
• Qualify, direct and support contract manufacturers of items within the supported product lines.
• Perform HPLC and testing of raw materials.
• Perform instrument qualification and maintenance
• Perform test method validation/verification

Skills: Chemical Analysis, Test Interpretation, Laboratory Management, Equipment Maintenance, Environmental Compliance, Product Scale-up, Method Validation, Supplier Qualification

• Actively promotes safe behavior in the workgroup and takes responsibility for personal safe lab operations. 
• Maintains a clean, orderly, and safe working environment. 
• Maintains documentation and equipment including testing equipment, process equipment, lab notebooks, electronic databases, and organized files. 
• Plans and executes experimental work programs, analyzes data and documents results in reports, tables, and databases. 
• Communicates project progress at the Team level both in writing and verbally. 
• Learns and develops Lithium-Ion Battery expertise to support R&D overall objectives.
• Review analytical data for completeness, accuracy, and compliance
• Perform training on procedures, equipment, or quality systems
• Responsible for critical metrics statistics.
• Manage & Responsible for the investigation and disposal of nonconforming products.
• Responsible for daily maintenance of QC lab
• Responsible for IQC, IPQC, FQC and other daily inspection work

Skills: Lab Safety, Documentation Management, Experimental Planning, Data Analysis, Communication Skills, Battery Expertise, Quality Training, Inspection Management

• Analyze the application feasibility from the literature and competition benchmark.
• Identify technology gaps and potential solutions, develop the application concept and all the relevant tests.
• Understand the technology capabilities and limitations in the application's scope.
• Develop the right inkjet ink formulation specification /parameters in correlation with the technology and application constraints (rheology, adhesion, resistance…).
• Contribute to the external communication on applications and on the technologies, participate to supplier/partner meetings, conferences and external events.
• Communicate project progress with appropriate media
• Write technical notes and reports
• Present findings to engineers, scientists, and other colleagues
• Formulate hair-related products with low level of supervision and direction. 
• Engage in research activities to develop innovative hair product technologies, identify new opportunities and application methodologies.
• Understand, utilize and document within a laboratory notebook and Ingenuity every batch made with details of the reason for the batch, batching notes, batch specification results and other test results.

Skills: Application Analysis, Technology Assessment, Ink Formulation, External Communication, Technical Reporting, Presentation Skills, Product Formulation, Research Development

• Lead the development of new and existing chemical formulas for the product range
• Lead the testing of new and existing chemical formulas for the product range
• Plan, develop and conduct experimental programmes and guidelines
• Develop and maintain accurate reporting processes and protocols
• Compile and present test findings, interpretations, and recommendations to different stakeholders across the business
• \Responsible for the laboratory equipment and ensure this is used to the highest standard
• Maintain Health, Safety and Environmental standards and procedures throughout the laboratory
• Support in the development of continuous improvement projects, work processes and problem-solving
• Manage, oversee, and liaise with external service providers, suppliers, and licensing authorities
• Lead in the formulation of regulatory reviews and product safety assessments
• Responsible for regular risk assessments
• Seek cross-functional solutions to address scientific and operational issues

Skills: Formula Development, Experimental Testing, Program Planning, Reporting Accuracy, Stakeholder Communication, Equipment Management, Safety Compliance, Continuous Improvement

• Independently performing the manufacture and characterization of oligonucleotides for research and pre-clinical use
• Maintaining, calibrating, and troubleshooting synthesis and purification processes on varying synthesis and purification platforms
• Identifying, developing processes, and resolving technical challenges and difficulties
• Delivering new and custom products and involvement in tech transfer and scale-up of oligonucleotides.
• Evaluating and extending new chemistries as well as providing innovations that can be developed into new product advantages
• Develop/optimize the conjugation of oligos to biological compounds such as proteins or antibodies
• Adherence to Quality Assurance and Management policies and processes
• Understand, follow and adhere to project cost objectives and timelines for each project and develop cost estimates with a supervisor.
• Follow the requirements of the new product development process and follow through with action plans to meet the goals and timeline of the project.
• Conduct stability by department policy, i.e., track stability, update results charts and summarize data for review at each test period
• Design and develop, as well as conduct efficacy testing for projects and requested by the supervisor

Skills: Oligonucleotide Manufacture, Process Troubleshooting, Technical Development, Product Scale-up, Chemistry Innovation, Conjugation Optimization, Quality Compliance, Project Management

• Researching and synthesizing new polymer formulations from the lab scale through production scale-up, with a focus on polyurethane technology
• Identifying regulatory status of new polymer formulations and working with the team to ensure compliance with TSCA, FDA, REACH and customer restricted substance requirements
• Evaluating and developing/compounding new formulations in the areas of urethanes, thermoplastic extrusions and solvent and waterborne adhesives (latex, natural/synthetic rubbers, PSAs) and testing from the lab bench to manufacturing
• Utilize internal analytical resources including GC-Headspace, FTIR, DSC, and instrumentation techniques, to characterize properties and performance of materials
• Outline, organize and perform technical service experiments and projects for its assigned end-use(s), as approved by the Polymer Lab manager, in co-operation with the various business units servicing both external and internal customers.
• Maintaining a lab notebook and documentation of experimental results. 
• Draft project status reports for sharing with the Polymer Lab team
• Share and communicate technical information in informal conversation, phone calls, written report, or presentation format to customers, raw material suppliers, Worthen employees and visitors.
• Provide technical & project leadership to the Polymer Lab team for the successful completion of R&D projects and related activities performed by various business units and/or staff for a business or product line.
• Direct & coordinate the effective and on-time implementation of multiple projects through successful project management, i.e. following timelines and fully utilizing resources available from the polymer group to manufacturing and quality
• Protect the company's technology through adherence to all Intellectual Property standards throughout the area of responsibility and the effective use of IP tools. 

Skills: Polymer Synthesis, Regulatory Compliance, Formulation Development, Analytical Techniques, Technical Experimentation, Documentation Management, Technical Communication, Project Leadership

• Experience managing research projects
• Experience presenting at conferences and writing technical papers.
• Experience reading and interpreting documents such as safety rules, laboratory operating procedures, operating and maintenance instructions, and procedure manuals.
• Ability to write routine reports and correspondence.
• Advanced-level Microsoft Office including, among others, Word, Excel, and PowerPoint.
• Ability to speak effectively before groups of customers or employees of the organization
• Experience working with oilfield chemical-related projects.
• Knowledge of surfactant chemistry and experience in product development
• Demonstrated technical knowledge and creativity to solve technical problems.
• Strong work ethic and ability to work independently on multiple projects.

Qualifications: BS in Chemistry with 4 years of Experience

• Skills necessary for the analysis, production, isolation and purification of biomaterials, which include basic skills in wet chemistry (extraction, filtration and precipitation) and analytical skills to characterize and qualify the biomaterials (LC, GC, GPC) and mechanical testing.
• Ability to conduct assigned tasks under the supervision of senior scientific staff
• Ability to perform assigned tasks by applying general procedures, methods, and scientific techniques
• Good communication and data management skills are needed to communicate and document research findings and for record keeping.
• Ability to guide/coach laboratory technicians and/or temporary employees with clear direction and prioritization.
• Excellent business sense, oral and written communication skills and presentation skills
• Familiarity with analytical testing and instrumentation
• Demonstrated strong analytical skills and the ability to work independently against multiple deadlines.
• Experience in general laboratory techniques (reagent preparation and measurement)
• Experience working with automated filling equipment
• Ability to follow procedure and conduct documents following GMP/GLP

Qualifications: BA in Biochemistry with 5 years of Experience

• Knowledge of GSK Quality standards, GLP and GMP requirements.
• Knowledge of validations, calibration systems, and instrumentation.
• Knowledge of applicable GSK policies and procedures.
• Problem-solving/continuous improvement skills.
• Developed skills in coaching, interpersonal communications, team building and training facilitation.
• High level of computer literacy with working knowledge of Microsoft Word, Microsoft Excel and Laboratory Information System (LIMS).
• Ability to interact with all levels of the organization.
• Experience in implementing Quality Systems in regulated environments.
• Experience in writing, reviewing and revising SOPs.
• Excellent written and oral communication
• Ability to set priorities and work on multiple projects simultaneously.
• Familiar with statistical software (ex, Statistica)

Qualifications: BS in Chemical Engineering with 4 years of Experience

• Strong computer, scientific, and organizational skills
• Excellent communication (oral and written) and attention to detail
• Ability to work independently and as part of a team with internal and external clients, self‑motivation, adaptability, and a positive attitude
• Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies
• Proficiency in IT-related skills such as Microsoft Excel, Word, PowerPoint etc
• Knowledge of instrumentation used for environmental analysis (i.e. GC/MS, ICP, GC-ECD, IC, etc.)
• Proficient in standard office computer applications and software, including Microsoft Word, Excel, and Access
• Experience in laboratory or environmental chemistry
• Familiarity with out-of-specification (OOS) and out – of –trend (OOT) investigations
• Experience in an FDA-related environment, inclusive of 21 CFR Part 11 compliance criteria.
• Experience or understanding of inorganic analytical techniques e.g. IC, ICP GC-MS XRF etc

Qualifications: BA in Environmental Science with 5 years of Experience

• Proficient knowledge in synthetic organic chemistry, particularly in route development and optimization.
• Ability to think critically and innovatively, combined witha  willingness to challenge
• Strong analytical capability and ability to carry out large-scale reactions in the laboratory.
• Demonstrated ability in troubleshooting and solving complex issues.
• Embrace and participate in PPI (Practical Process Improvement) initiatives to identify improvements and cost savings to the business.
• Experience in supporting plant processes.
• Excellent technical writing skills and oral communication to interact with all levels of the organization and clients.
• Ability to work with cross-functional teams and engage with employees and customers at all levels
• Experience with High Pressure Liquid Chromatography, Infra-Red (IR), Gas Chromatograph (GC), Ultra Violet/Visible, Particle Size Analysis, KF Titration and wet chemistry skills
• Familiarity with HPLC/GC analytical software.
• Familiarity with GLP/GMP guidelines..

Qualifications: BS in Pharmaceutical Science with 6 years of Experience

• Experience with a variety of computational tools and methodologies including docking, virtual screening, molecular dynamics, free energy perturbation, homology modeling, quantum mechanics, pharmacophore elucidation, and machine learning.
• Experience in data mining and data analysis.
• Familiarity with organic and synthetic chemistry concepts.
• Ability to provide project teams with computational strategies to inform, influence, and prioritize designs for potency/selectivity and improve ADME/Tox endpoints.
• Ability to contribute to the development and deployment of design and/or AI platforms to impact drug discovery.
• Ability to identify and implement novel computational chemistry algorithms, technologies, and workflows.
• Familiarity with standard computational chemistry software including Schrodinger Suites, KNIME, and more.
• Proficiency in scientific scripting and programming languages.
• Ability to write OOS and OOT reports.
• Experience with USP/EP monographs.
• Good Communication and writing skills.

Qualifications: BA in Molecular Biology with 4 years of Experience

• Strong communication skills & proven ability to interact across a range of functions & leadership groups and deal with people from multicultural backgrounds.
• Good Verbal/written Communication skills, ability to influence peers, key stakeholders and various partners.
• Well understand product development principles, R&D processes and protocols, good ability to identify the risk and mitigation plan.
• Good digital acumen, always design products with E-commerce & Social commerce 'genes'
• Ability to work under high pressure and good problem-solving skills
• Experience testing Inhalation products, especially MDI
• Knowledge of Good Documentation practices. 
• Knowledge of USP/ICH/FDA
• Ability to learn quickly and decision-making skills
• Experience following detailed instructions, maintaining accurate records and notes, and carrying out assignments in a thorough, conscientious fashion while adhering to safe laboratory practices.
• Experience with problem-solving and troubleshooting in a laboratory environment.

Qualifications: BS in Materials Science with 5 years of Experience

• Knowledge of a variety analytical techniques, and proficiency in some, including the following USP dissolution equipment, Gas chromatography (GC), high pressure liquid chromatography (HPLC), atomic absorption (AA), infrared spectrophotometer (IR), ultraviolet/visible spectrophotometer (UV/VIS), pH meter, flurometer, melting point apparatus, viscometers, muffle furnace, polarimeter, vacuum oven, distillations, titrations, centrifuge, sonicator, conductivity meter.
• Familiar with compendial guidelines such as USP and EP.
• Familiar with the following written procedures such as Standard Operating Procedures (SOPs) and methods
• Familiar with data acquisition systems such as TotalChrom.
• Familiar with a LIMS system.
• Knowledge of regulatory guidelines such as cGMP.
• Good interpersonal, written and verbal communication skills.
• Ability to work with minimal direction/supervision.
• Ability to follow detailed instructions, maintain accurate records and notes, and carry out assignments in a thorough, conscientious fashion while adhering to safe laboratory practices.
• Knowledge of a variety of lab equipment and its operation 

Qualifications: BA in Forensic Science with 6 years of Experience

• Knowledge of cGMP, USP/NF, and FDA guidelines and regulations
• Experience in analytical methods and lab instrumentation (e.g. HPLC, GC, dissolution, wet chemistry)
• Excellent oral and written communication skills
• Strong organization and time management skills
• Ability to work as part of a cross-functional team
• Knowledge of Microsoft Word and Excel
• Experience with software associated with a Laboratory Information Management System (LIMS) and a Chromatography Data System (CDS)
• Proficient with computer software applications and data analysis (Word, Excel, etc.).
• Excellent organizational skills, strong interpersonal skills, independent problem solver.
• Experience with aqueous formulations
• Strong analytical/laboratory and mechanical skills, precision, attention to detail, and record keeping.

Qualifications: BS in Biophysics with 5 years of Experience

• Strong interpersonal skills with the ability to interact with personnel at all levels in a team environment.
• Understanding of analytical methodologies and protein biochemistry (e.g. IC, HPLC, GC, etc.).
• Strong organizational, analytical, and problem-solving skills with the ability to make structured decisions on a routine basis.
• Ability to effectively prioritize and manage multiple tasks to meet targeted deadlines.
• Experience with various chemistries (latex, moisture curing, reactive, etc.) in sealants, adhesives, coatings, repair or related field
• Experience and familiarity with various analytical techniques wet chemistry, titrations, microscopy, rheology, thermal analysis, tensile testing, etc.
• Skills evident as risk taking, result seeking, and idea integration
• Experience operating lab-scale mixing equipment as well as lab-scale analytical and test apparatus
• Excellent interpersonal, written, and verbal communication and presentation skills
• Knowledge of lab equipment (HPLC, GC, UV, IR)
• Knowledge of GMP regulations

Qualifications: BA in Food Science with 4 years of Experience