analytical chemist

Novelis

<div>
 
 
 
 Position Overview
 
 
 
 
 The Novelis Kennesaw team is seeking an
 
 Analytical Chemist
 
 in ECA lab. The person in this role will report to the Laboratory Leader. The ideal candidate will be responsible for operating XRD, XRF, ICP, FTIR and XPS. This position will bring its experience in handling different analytical experiments and handle them according to the Novelis safety guidelines.
 
 
 
 
 
 
 Responsibilities
 
 
 <ul>
 <li>
 Demonstrates personal commitment to safety and good EHS awareness by following established safety rules and practices during all activities. Ensure all users and visitors are compliant with all Safety Absolutes and other EHS initiatives.
 </li>
 <li>
 Accountability for maintaining the analytical equipment situated in the area of responsibility to ISO 17025 standards
 </li>
 <li>
 Operate and maintain
 
 ICP-OES
 
 instruments for elemental analysis of alloys and beverage matrices.
 </li>
 <li>
 Perform
 
 XRD
 
 analysis for phase identification and crystallographic characterization of metallic samples
 </li>
 <li>
 Conduct
 
 XRF
 
 testing for rapid compositional screening of solid samples.
 </li>
 <li>
 Utilize
 
 FTIR
 
 spectroscopy for organic compound identification and beverage quality assessment.
 </li>
 <li>
 Prepare samples using appropriate digestion, grinding, or dilution techniques.
 </li>
 <li>
 Interpret and report analytical data with accuracy and clarity.
 </li>
 <li>
 Develop and validate analytical methods in compliance with industry standards and regulatory guidelines.
 </li>
 <li>
 Collaborate with cross-functional teams including R&amp;D, Quality Assurance, and Manufacturing.
 </li>
 <li>
 Maintain laboratory documentation, calibration records, and safety protocols.
 </li>
 <li>
 Run qualitative and quantitative analysis of elements, coatings and lubricants using different spectroscopic techniques such as FTIR, NIR and GDOES.
 </li>
 <li>
 Communicate the research findings to the project managers and stakeholders on routine basis
 </li>
 </ul>
 
 
 
 
 
 Minimum qualifications
 
 
 <ul>
 <li>
 Entry to this level typically requires 3-5 years of progressive experience in analytical chemistry and a BS in chemistry, metallurgy, metallurgical engineering, material science, physics or equivalent.
 </li>
 <li>
 Minimum 3 years of experience in an analytical laboratory setting.
 </li>
 <li>
 Proficiency in operating and troubleshooting
 
 ICP-OES
 
 ,
 
 XRD
 
 ,
 
 XRF
 
 , and
 
 FTIR
 
 instruments.
 </li>
 <li>
 Experience with sample preparation techniques for metals and beverages.
 </li>
 <li>
 Strong understanding of analytical chemistry principles and data interpretation.
 </li>
 <li>
 Familiarity with laboratory information management systems (LIMS) is a plus.
 </li>
 <li>
 Excellent communication and organizational skills.
 </li>
 <li>
 Willing to collaborate with other Novelis R&amp;D labs by undergoing training in other areas where resources are necessary for high priority testing
 </li>
 <li>
 Hands on experience working with wet chemistry techniques with an emphasis on material science.
 </li>
 <li>
 Desire and ability to collaborate and communicate across functions are essential to this position.
 </li>
 <li>
 Knowledgeable about overall chemical safety.
 </li>
 </ul>
 
 
 
 
 
 Preferred qualifications
 
 
 <ul>
 <li>
 Master&rsquo;s in chemistry with 3 years of experience in handling different analytical equipment
 </li>
 <li>
 Experience in
 
 metallurgical analysis
 
 and
 
 food/beverage testing
 
 .
 </li>
 <li>
 Knowledge of
 
 ISO
 
 ,
 
 ASTM
 
 , or
 
 FDA
 
 standards relevant to analytical testing.
 </li>
 <li>
 Ability to work independently and manage multiple projects simultaneously.
 </li>
 </ul>
 
 
 
 
 
 What We Offer:
 
 
 
 Novelis' benefits say a lot about how we care for each other. Our employees and their families have many different needs. As a result, our benefits offer choices on many levels and are high in quality, driven by the marketplace, and affordable. In addition to core benefits, we provide these unique to the industry benefits:
 
 <ul>
 <li>
 Family Growth Programs: Paid parental Leave, Adoption Assistance, Fertility Treatment, Childcare Discount and Nursing Mom Support
 </li>
 <li>
 Employee Assistance Programs: free resources available 24/7 to you and your family in the areas of mental health, family life, and career and financial guidance
 </li>
 <li>
 Wellness Programs: incentives for wellness activities, wellness spending account, programs for building healthy habits, virtual physical therapy for joint, back, and pelvic health, health management programs and more.
 </li>
 <li>
 Diabetes Management Program
 </li>
 <li>
 Pet insurance
 </li>
 <li>
 Identity Theft Protection
 </li>
 <li>
 PerkSpot Discount Program
 </li>
 <li>
 Tuition assistance and career development programs
 </li>
 </ul>
 
 
</div>

Analytical Chemist

Catalent Pharma Solutions

<div>Senior Analytical Chemist
The Senior Analytical Chemist will perform routine and non-routine analytical testing in support of pharmaceutical products following all applicable safety, quality, and regulation requirements.
Position Summary
This position is 100% on-site at the Greenville site.
Catalent&rsquo;s Greenville, N.C. facility specializes in end-to-end turn-key solutions for oral solid dosage forms, including integrated formulation development, analytical services, commercial manufacturing, and packaging. This state-of-the-art facility has had over $100M of investments in recent years and features fit-for-scale capacity with potent handling capabilities, ideal for orphan or targeted drug development.
This role provides laboratory troubleshooting for a team to assist in the successful and timely execution of laboratory analyses.
The Role<ul><li>
Independently perform routine and complex testing for chromatographic and spectrophotometric methods (HPLC, GC, UV) of analysis for excipients, new chemical entities and/or drug products.</li><li>
Interpret data and make recommendations to management for improvement or potential concerns.</li><li>
Compare laboratory data against specifications, prepare reports, and trend data where applicable to determine if results meet requirements.</li><li>
Ensure proper usage, care, and return of calibration standards including, but not limited to, reference standards, timers, thermometers, and instrumentation.</li><li>
Ensure accuracy of testing by following method/standard instructions and adhering to internal SOPs to eliminate the potential for repeat testing, deviations, and investigations.</li><li>
Independently author standard operating procedures, analytical testing procedures, final submission ready documents, and create document templates for use by junior team members.</li><li>
All other duties as assigned.
</li></ul>The Candidate<ul><li>
Associate degree in Biotechnology, Chemistry or equivalent science degree with seven years of professional experience in pharmaceutical analytical chemistry required or;</li><li>
Bachelor&rsquo;s degree in a science-related field (e.g. Biology, Chemistry, Pharmaceutical Sciences) with six years of professional experience in pharmaceutical analytical chemistry required or;</li><li>
Master&rsquo;s degree in a science-related field with five years of professional experience in pharmaceutical analytical chemistry required or;</li><li>
PhD in a science-related field with two years of relevant experience in pharmaceutical analytical chemistry required.</li><li>
Experience in a Catalent analytical laboratory in a role that is independent and proficient in Chromatography and data review as well as troubleshooting and technical understanding may be substituted for 2 years of professional experience.</li><li>
Position requires the ability to lift 10-50lbs, unassisted.</li><li>
Majority of the work day is performed while standing, walking, lifting, pulling, and pushing.</li><li>
Requires bending, squatting, crawling, climbing, and reaching.</li><li>
Some exposure to hazardous chemicals and other active chemical ingredients.</li></ul>
Why You Should Join Catalent<ul><li>
Competitive medical benefits and 401K</li><li>
152 hours of PTO + 8 Paid Holidays</li><li>
Dynamic, fast-paced work environment</li><li>
Opportunity to work on Continuous Improvement Processes</li></ul>
Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.
personal initiative. dynamic pace. meaningful work.
Visit Catalent Careers to explore career opportunities.
Catalent is an Equal Opportunity Employer, including disability and veterans.
If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to DisabilityAccommodations@catalent.com. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process. 
Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written &amp; signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.
Important Security Notice to U.S. Job Seekers:
Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond&mdash; it is a fraudulent request. Please forward such requests to spam@catalent.com for us to investigate with local authorities.
California Job Seekers can find our California Job Applicant Notice HERE.</div>

Senior Analytical Chemist

Corden Pharma - A Full-Service CDMO

<div>
 
 CordenPharma
 
 is a leading full-service Contract Development and Manufacturing Organization (CDMO) specializing in active pharmaceutical ingredients (APIs), excipients, drug products (DPs), and packaging. With around 3,000 employees worldwide, we help pharmaceutical, and biotech companies manufacture medicines with the ultimate goal of improving people&rsquo;s lives.
 
 
 Our network, spanning Europe and the U.S., provides flexible and specialized solutions across six technology platforms: Peptides, Lipids &amp; Carbohydrates, Injectables, Highly Potent &amp; Oncology, Small Molecules, and Oligonucleotides. We strive for excellence in supporting this network and are committed to delivering the highest quality products for patient well-being.
 
 
 
 Our People Vision
 
 
 
 We strive for excellence. We share our passion. Together, we make a difference in patients' lives.
 
 
 
 Summary
 
 
 
 Performs analytical research and development activities for the purpose of designing/improving a manufacturing process or technology by performing the following duties.
 
 
 
 Essential Duties And Responsibilities
 
 
 
 Include the following. Other duties may be assigned.
 
 
 <ul>
 <li>
 Participates in development of new processes by applying analytical skills and training
 </li>
 <li>
 Participates in the development of new and innovative analytical chemistry and methodology, supporting manufacturing, and regulatory needs. Facilitates and supports analytical technology transfers
 </li>
 <li>
 Participates in the development of key technologies and transfer strategies that function well in a manufacturing environment
 </li>
 <li>
 Plans and formulates aspects of analytical research and development proposals such as objectives or purpose of project, applications that can be utilized from findings, cost of project, equipment, and human resource requirements
 </li>
 <li>
 Develops, implements, and validates analytical methods and procedures
 </li>
 <li>
 Keeps accurate records and documents experimentation
 </li>
 <li>
 Develops a comprehensive understanding of internal, corporate, and ICH stability guidelines to provide support to the Corden Pharma Stability Program
 </li>
 <li>
 Participates in manufacturing site activities, such as troubleshooting and analytical problem resolving
 </li>
 <li>
 Develops an understanding of QEH&amp;S principles and regulatory affairs
 </li>
 <li>
 Analyzes batches of drug substance, intermediates and raw materials to be used in clinical or registration programs
 </li>
 <li>
 Responsible for properly managing the generation and accumulation of hazardous and non-hazardous waste
 </li>
 <li>
 Works flexible hours including weekends and nights to accommodate the production/validation schedule
 
 
 </li>
 </ul>
 
 LEADERSHIP &amp; BUDGET RESPONSIBILITIES
 
 
 
 Demonstrates positive attitude. Supports a positive, healthy, and flexible work environment that encourages employees and coworkers to develop their full potential and expand their horizons.
 
 
 
 Safety &amp; Environmental Responsibilities
 
 
 
 Every individual is personally responsible for the safety and environmental aspects of his or her activities in the workplace. Each employee is expected to perform their job duties in a safe manner utilizing all their knowledge, training, ability and experience.
 
 
 
 Qualifications
 
 
 
 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.
 
 
 
 EDUCATION And/or EXPERIENCE
 
 
 
 Bachelor&rsquo;s degree in Chemistry or related sciences with 3 years of relevant experience.
 
 
 
 Language Skills
 
 
 
 Ability to read, analyze, and interpret common scientific and analytical journals, financial reports, and legal documents. Ability to respond to common inquiries or complaints from customers, regulatory agencies, or members of the business community. Ability to write speeches and articles for publications that conform to prescribed style and format. Ability to effectively present information to top management, public groups, and/or boards of directors.
 
 
 
 Mathematical Skills
 
 
 
 Ability to apply advanced mathematical concepts such as exponents, logarithms, quadratic equations, and permutations. Ability to apply statistical concepts such as significant figures and analysis of variance.
 
 
 
 REASONING ABILITY
 
 
 
 Ability to define problems, collect data, establish facts, and draw valid conclusions. Ability to interpret an extensive variety of technical instructions in mathematical or diagram form and deal with several abstract and concrete variables.
 
 
 
 CERTIFICATES, LICENSES, REGISTRATIONS
 
 
 
 Domestic and international travel required.
 
 
 
 PHYSICAL DEMANDS
 
 
 
 The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
 
 
 While performing the duties of this job, the employee is regularly required to work with hands; and talk or hear. The employee frequently is required to stand, walk, and sit. The employee is occasionally required to reach above shoulder height; climb or balance; stoop, kneel, crouch, or crawl; and taste or smell. The employee must occasionally lift and/or move up to 50 pounds. Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception, and ability to adjust focus.
 
 
 
 WORK ENVIRONMENT
 
 
 
 The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
 
 
 While performing the duties of this job, the employee frequently uses toxic and/or caustic chemicals as well as high potent compounds and there is a risk of exposure. The employee is occasionally exposed to moving mechanical parts, outside weather conditions, and risk of electrical shock. The noise level in the work environment is usually moderate.
 
 
 
 CORE COMPETENCIES
 
 
 
 These are the specific areas of knowledge, skill and ability that are important for successful job performance. They must be job related and consistent with business necessity.
 
 
 <ul>
 <li>
 Presentation and persuasion skills
 </li>
 <li>
 Developed written and verbal communication skills
 
 
 </li>
 </ul>
 
 SALARY
 
 
 
 Actual pay will be based on your skills and experience.
 
 
 
 Benefits
 
 
 
 <ul>
 <li>
 401(k) matching - Corden Pharma will contribute 100% of the first 6% - 100% vested after 2 years of service
 </li>
 <li>
 Accident Plan
 </li>
 <li>
 Critical Illness Insurance
 </li>
 <li>
 Dental Insurance
 </li>
 <li>
 Disability Insurance
 </li>
 <li>
 Employee Assistance Program
 </li>
 <li>
 Flexible Spending Account
 </li>
 <li>
 Health Insurance PPO/HSA
 </li>
 <li>
 Hospital Indemnity Plan
 </li>
 <li>
 ID Theft Protection
 </li>
 <li>
 Life Insurance
 </li>
 <li>
 Paid Maternity/Paternity Leave
 </li>
 <li>
 Tuition Reimbursement
 </li>
 <li>
 Wellness Program
 </li>
 <li>
 Vacation &ndash; Three Weeks 1st Year
 </li>
 <li>
 Vision Insurance
 
 
 </li>
 </ul>
 
 EQUAL OPPORTUNITY EMPLOYER
 
 
 
 Corden Pharma provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws. Corden Pharma embraces fair hiring practices.
 
 
 
 This posting will expire on Dec 22, 2025 but may be extended.
 
</div>

Integrated Resources, Inc ( IRI )

<div>
 
 
 Essential Job Functions and Responsibilities:
 
 
 <ul>
 <li>
 Testing experience: IR, pH, TLC-plates, Solubility, other wet chemistry analysis
 </li>
 <li>
 Instrument experience: HPLC
 </li>
 <li>
 Complete a peer review of analytical data
 </li>
 <li>
 Draft/Execute Validation Protocols
 </li>
 <li>
 Write Reports for executed Protocols
 </li>
 <li>
 Act as technical review for Protocols and Reports
 </li>
 <li>
 Proficient in following Compendial testing methods (USP/EP/JP)
 </li>
 <li>
 Utilize written procedures to perform testing.
 </li>
 <li>
 Demonstrate strong planning &amp; organizational skills.
 </li>
 <li>
 Solution focused when faced with any problems or setbacks.
 </li>
 <li>
 Highly self-motivated.
 </li>
 <li>
 Strong initiative and drive.
 </li>
 <li>
 Demonstrated critical thinking skills.
 </li>
 <li>
 Demonstrate the ability to manage larger projects/process with minimal oversight.
 </li>
 <li>
 Utilize written procedures to perform testing.
 </li>
 <li>
 Able to recognize out-of-spec (OOS) results and work through an investigation with minimal guidance to determine root cause with appropriate corrective actions, where applicable to QC.
 </li>
 <li>
 Perform needed instrument or titrant verification/calibration during scheduled time.
 </li>
 <li>
 Demonstrates Good Documentation Practices (GDP) and Data Integrity Principles.
 </li>
 <li>
 Pays attention to detail and brings issues to supervision&rsquo;s attention.
 </li>
 <li>
 Demonstrated ability to work effectively in a team environment.
 </li>
 <li>
 Knowledge of basic computer software (Microsoft Office and Microsoft 365).
 </li>
 <li>
 Demonstrate the ability to work independently and take initiative to perform daily job functions along with special projects.
 </li>
 <li>
 Work in accordance with current procedures and demonstrate proper laboratory safety and housekeeping practices.
 </li>
 </ul>
 
 
 
 
 
 Additional Responsibilities:
 
 
 <ul>
 <li>
 Demonstrates our Core Values &ndash; Courage, Respect, Achievement, Integrity, Responsibility, Transparency.
 </li>
 <li>
 Follows all policies and procedures as defined from Corporate and Site.
 </li>
 <li>
 Develops and/or assist in the implementation of process improvement, safety, quality, and 5S ideas.
 </li>
 <li>
 Organizes and maintains a clean and orderly work area in accordance with the administrative General Housekeeping policy/procedures.
 </li>
 <li>
 Performs all functions in a safe and timely manner in accordance with OSHA standards and general rules and regulations governing the workplace.
 </li>
 <li>
 Responsible for following general personal protective equipment (PPE) requirements as established by company policy.
 </li>
 <li>
 Demonstrates professional working behavior when working with all staff and visitors.
 </li>
 <li>
 Follow trained requirement to IPEC cGMP/ISO9001/14001/45001 Management Systems, if appropriate.
 </li>
 <li>
 Seeks guidance from Supervisor as needed to ensure the above
 </li>
 </ul>
 
 
 
 
 
 Education, Qualifications, Experience:
 
 
 <ul>
 <li>
 Bachelors&rsquo; degree in Chemistry or Life Science field with a Minimum 5 years of laboratory experience
 </li>
 <li>
 Associate degree in Chemistry or other Life Science field with a Minimum of 10 years of experience outside of academic laboratories.
 </li>
 <li>
 Method Validation
 </li>
 <li>
 Compendial Testing (USP/EP/JP)
 </li>
 <li>
 GMP laboratory
 </li>
 </ul>
</div>

Fragorium LLC

Job SummaryWe are looking for a GC-MS Analyst/Chemist at our facility in Dubai to operate, maintain, and troubleshoot GC-MS instruments for routine and advanced analytical testing, ensuring accurate identification and quantification of raw materials, fragrance ingredients and finished products according to industry standards.Key Responsibilities<ul><li>Perform qualitative and quantitative analysis of samples using GC-MS (e.g., volatile compounds, essential oils, aroma chemicals, solvents)</li><li>Develop, optimize, and validate GC-MS methods to improve accuracy, sensitivity, and run efficiency</li><li>Interpret mass spectra, chromatograms, and fragmentation patterns for component identification</li><li>Monitor instrument performance, conduct calibration, and run daily QC checks.</li><li>Prepare standards, reagents, and sample dilutions with strict adherence to laboratory protocols</li><li>Ensure accurate record-keeping of results, methods, and instrument parameters in LIMS or laboratory notebooks</li><li>Prepare analytical reports and communicate findings to QC, R&amp;D, and Production teams</li><li>Maintain compliance with ISO/IEC 17025, Good Laboratory Practices (GLP), and internal SOPs</li><li>Conduct routine preventive maintenance on GC-MS instruments (column installation, injector maintenance, ion source cleaning)</li><li>Troubleshoot instrument issues and coordinate service visits when required.</li><li>Maintain inventory of consumables and critical spares</li><li>Perform method verification, system suitability tests, and instrument qualification (IQ/OQ/PQ)</li><li>Ensure all tests are performed within specified timelines to support production requirements</li><li>Follow all laboratory safety guidelines, chemical handling procedures, and waste disposal protocols.</li></ul>Requirements<ul><li>Minimum 2 to 4 years of experience operating GC-MS (Agilent, Shimadzu, Thermo, or equivalent).</li><li>Bachelor&rsquo;s or Master&rsquo;s degree in Chemistry, Analytical Chemistry, or related field</li><li>Strong understanding of gas chromatography principles and mass spectrometry</li><li>Experience in fragrance, flavour, essential oils, cosmetics, or chemical manufacturing is an advantage</li><li>Proficiency in MS data interpretation and library matching (NIST, Wiley, etc.)</li><li>Ability to develop and troubleshoot analytical methods</li><li>Knowledge of additional analytical techniques (GC-FID, HPLC, FTIR, Karl Fischer) is a plus</li><li>Strong attention to detail and analytical mindset</li><li>Excellent documentation and reporting skills</li><li>Ability to work independently and in a multi-disciplinary team</li><li>Good time management and ability to handle multiple tasks</li></ul>Job Types: Full-time, PermanentPay: AED4,000.00 - AED6,000.00 per monthEducation:<ul><li>Master's (Preferred)</li></ul>Experience:<ul><li>GC-MS Analyst/Chemist (Fragrance Industry): 2 years (Preferred)</li></ul>Location:<ul><li>Dubai (Preferred)</li></ul>

GC-MS Analyst/Chemist

Wood

<div>
 
 Job Description
 
 
 
 Wood is recruiting for a Senior Chemist / Lab Expert to join its Projects team in Sohar, Oman with relevant experience in Petroleum Refinery in handling PQC&amp; PQA of Gases , Hydrocarbons , Utility and environmental samples by Sophisticated Analytical Techniques and complex analysers and well familiar in ASTM/UOP/APHA/SMS/IP/SMS Testing methods and has the capability to deliver below requirements,
 
 
 
 Responsibilities
 
 
 
 
 Designing the future. Transforming the world
 
 
 
 Candidates with relevant experience in Petroleum Refinery
 
 
 
 What We Can Offer
 
 
 
 <ul>
 <li>
 Meaningful and interesting projects delivered to leaders of industry across oil and gas and emerging energy sectors
 </li>
 <li>
 Commitment to Diversity and Inclusion; we are an organisation actively committed to diversity and inclusion across our busiess with employee networks committed to giving all employees a voice
 </li>
 <li>
 Competitive salary with regular salary reviews to ensure we are rewarding at the right level in line with the market
 </li>
 <li>
 Medical Insurance: Ensures inpatient and outpatient care is available should you require treatment. Cover limits apply, please refer to the terms of benefit and network list for further details.
 </li>
 <li>
 Workmen&rsquo;s Compensation: Provides payment of 3 x Annual Wage (up to a maximum of 5000 OMR) upon death or permanent disability.
 </li>
 <li>
 Employee Assistance Programme: Allows you to feel comfortable knowing that you or your immediate family members can confidentially discuss any work or personal issues that are an inevitable part of life. The programme helps support your mental, physical, social &amp; financial well-being.
 
 
 </li>
 </ul>
 
 Senior Chemist/Lab Expert Will Be Responsible
 
 
 
 <ul>
 <li>
 Identify and recommend Online analysers that can measure in real time critical quality properties dependable enough to reduce sampling and laboratory testing.
 </li>
 <li>
 Provides specialized analytical solution to upgrade the laboratory&rsquo;s capability to measure asset integrity related parameters critical to plant Reliability improvement.
 </li>
 <li>
 Upgrade the laboratory visual dashboard to include critical tracking data related to IOW/POW, relevant KPI associated with Asset Reliability and Asset management.
 </li>
 <li>
 Provide technical support and interpretation including hands on for Studies and Test Runs pertained to CDU , Merox , RFCC Revamp Projects for maximization of process units output.
 </li>
 <li>
 Provide analytical techniques and data interpretation of Flare Gases and environmental samples
 </li>
 <li>
 Interprets complex and specialized data analysis to advise PES and Operation in process troubleshooting
 </li>
 <li>
 Work closely with other departments within the refinery, such as engineering or production, to troubleshoot problems or identify opportunities for process improvement
 </li>
 <li>
 Provide inputs to Lab management for OPEX and CAPEX Optimizations and Lab Equipment reliability Index and back up methods creation in support of Test Run.
 
 
 </li>
 </ul>
 
 Qualifications
 
 
 
 <ul>
 <li>
 Bachelor&rsquo;s degree in chemistry
 </li>
 <li>
 Minimum 8 years of experience
 </li>
 <li>
 Experience in Petroleum Refinery
 
 
 </li>
 </ul>
 
 About Us
 
 
 
 Wood is a global leader in consulting and engineering, helping to unlock solutions to critical challenges in energy and materials markets. We provide consulting, projects and operations solutions in 60 countries, employing around 35,000 people. www.woodplc.com
 
 
 
 Diversity Statement
 
 
 
 We are an equal opportunity employer that recognises the value of a diverse workforce. All suitably qualified applicants will receive consideration for employment on the basis of objective criteria and without regard to the following (which is a non-exhaustive list): race, colour, age, religion, gender, national origin, disability, sexual orientation, gender identity, protected veteran status, or other characteristics in accordance with the relevant governing laws.
</div>

Senior Chemist / Lab Expert

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