qc chemist

<div>Site Name: Saudi Arabia - Jeddah 
Posted Date: Oct 22 2025 
Job Description
GSK Saudi Arabia is committed to supporting Vision 2030 and the Saudi Arabian National Agenda including Saudization in line with the hiring and the training and development of Saudi National capability.
Are you a Quality professional who is energized by the challenge of being part of one of the leading pharmaceutical companies worldwide? If so, this role QC Chemist is the one for you to explore.
As QC Chemist you will be responsible to perform QC chemical and microbiology testing, to comply with GSK and local regulatory requirements 
This role will provide YOU the opportunity to lead key activities to progress YOUR career, these responsibilities include some of the following&hellip;
Key Responsibilities
<ul><li>Following all EHS guidelines in the analytical laboratory and on the entire facility</li><li>
Compliance with all GMP, QMS and data integrity requirements, as well as regulatory expectations.</li><li>
Perform the sampling activity for Microbiology, Materials and Finished goods, in compliance to GMP requirements.</li><li>
Perform the chemical and microbiological testing for stability samples, finished product and raw materials.</li><li>
Perform and execute the utilities and cross contamination testing plan.</li><li>
Test to be comply with local methods and specification as per SOP, BARs &amp; RMA or RMS methods.</li><li>
Preparation of all required documentation for testing, including BARs, stability protocols and reports.</li><li>
Preparation of all required reagents for testing.</li><li>
Perform calibration and maintenance of certain laboratory equipment as assigned.</li><li>
Inventory check and ordering of chemical and glassware as required.</li><li>
On time complete training curricula assigned in My-Learning or QMS training and provide the training to the staff where it is required.</li><li>
Maintain the Data record and entree in all QC related documents and files.</li><li>
Adhering to the OOS procedure and documenting investigations as required.</li><li>
To provide support to PPR by providing trend results for critical product (release) parameters, OOS investigation reports, providing laboratory equipment validation status and analytical method status.</li><li>
Identify any risk and escalate to the line manager, where applicable.</li><li>
Following and sustaining GPS standards for all lab activities.</li><li>
Supervisor, develop, implement and monitor chemical laboratory procedures (SOP/ BAR/ RMA/ BPS) against regulatory, QMS, CAPs and pharmacopoeia requirements, and ensuring compliance of laboratory activities with local SOPs. And provide the training to the analyst and technicians as required.</li><li>
Perform and supervisor analytical method validation or transfer as required, cleaning validation, analytical equipments validation (IQ, OQ &amp; PQ), Calibration and maintenance with related scheduled.</li><li>
Checking / verifying the entire chemical lab result and submit to QC manager for final approval, execute OOS investigations when required and ensure trending of critical product parameters are trended, reviewed and available for PPR.</li><li>
Maintain the Data record and entree in all QC related documents and files.</li><li>
Monitoring the lab inventory of the lab wear, consumables materials, chemicals and reference standard.</li><li>
Promote safe-working and laboratory environment that complies with company EHS requirements.</li><li>
Identify any risk and escalate to the line manager,</li><li>
Adhere to Safety, Quality and GPS standards and sustain the relevant QA &amp; EHS KPI metrics to achieve Zero Accident, Zero Defect, Zero Waste and continues improvements.</li></ul>
Why you?
Basic Qualifications:
We are looking for professionals with these required skills to achieve our goals:<ul><li>
Bachelor&rsquo;s degree with majors in Chemistry, Biochemistry or Pharmacy.</li><li>
2 - 4 years of experience in similar role.</li><li>
Good level of English in terms of speaking, writing and reading.</li><li>
Knowledge of EHS, GMP and GLP.</li><li>
Computer Skills (Word, Excel &amp; Power point).</li><li>
Time management skills.</li><li>
Good analytical and problem-solving skills.</li></ul>
Why GSK? 
Uniting science, technology and talent to get ahead of disease together.
GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases &ndash; to impact health at scale.
People and patients around the world count on the medicines and vaccines we make, so we&rsquo;re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.
Contact information: 
You may apply for this position online by selecting the Apply now button.
Important notice to Employment businesses/ Agencies
GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.</div>

QC Chemist

<div>
 
 Site Name:
 
 Saudi Arabia - Jeddah
 
 
 
 Posted Date:
 
 Oct 22 2025
 
 
 
 Job Description
 
 
 
 
 GSK Saudi Arabia is committed to supporting Vision 2030 and the Saudi Arabian National Agenda including Saudization in line with the hiring and the training and development of Saudi National capability.
 
 
 
 Are you a
 
 Quality professional
 
 who is energized by the challenge of being part of one of the leading pharmaceutical companies worldwide? If so, this role
 
 QC Chemist
 
 is the one for you to explore.
 
 
 As
 
 QC Chemist
 
 you will be responsible to perform QC chemical and microbiology testing, to comply with GSK and local regulatory requirements
 
 
 This role will provide YOU the opportunity to lead key activities to progress YOUR career, these responsibilities include some of the following&hellip;
 
 
 
 Key Responsibilities
 
 
 
 
 <ul>
 <li>
 Following all EHS guidelines in the analytical laboratory and on the entire facility
 </li>
 <li>
 Compliance with all GMP, QMS and data integrity requirements, as well as regulatory expectations.
 </li>
 <li>
 Perform the sampling activity for Microbiology, Materials and Finished goods, in compliance to GMP requirements.
 </li>
 <li>
 Perform the chemical and microbiological testing for stability samples, finished product and raw materials.
 </li>
 <li>
 Perform and execute the utilities and cross contamination testing plan.
 </li>
 <li>
 Test to be comply with local methods and specification as per SOP, BARs &amp; RMA or RMS methods.
 </li>
 <li>
 Preparation of all required documentation for testing, including BARs, stability protocols and reports.
 </li>
 <li>
 Preparation of all required reagents for testing.
 </li>
 <li>
 Perform calibration and maintenance of certain laboratory equipment as assigned.
 </li>
 <li>
 Inventory check and ordering of chemical and glassware as required.
 </li>
 <li>
 On time complete training curricula assigned in My-Learning or QMS training and provide the training to the staff where it is required.
 </li>
 <li>
 Maintain the Data record and entree in all QC related documents and files.
 </li>
 <li>
 Adhering to the OOS procedure and documenting investigations as required.
 </li>
 <li>
 To provide support to PPR by providing trend results for critical product (release) parameters, OOS investigation reports, providing laboratory equipment validation status and analytical method status.
 </li>
 <li>
 Identify any risk and escalate to the line manager, where applicable.
 </li>
 <li>
 Following and sustaining GPS standards for all lab activities.
 </li>
 <li>
 Supervisor, develop, implement and monitor chemical laboratory procedures (SOP/ BAR/ RMA/ BPS) against regulatory, QMS, CAPs and pharmacopoeia requirements, and ensuring compliance of laboratory activities with local SOPs. And provide the training to the analyst and technicians as required.
 </li>
 <li>
 Perform and supervisor analytical method validation or transfer as required, cleaning validation, analytical equipments validation (IQ, OQ &amp; PQ), Calibration and maintenance with related scheduled.
 </li>
 <li>
 Checking / verifying the entire chemical lab result and submit to QC manager for final approval, execute OOS investigations when required and ensure trending of critical product parameters are trended, reviewed and available for PPR.
 </li>
 <li>
 Maintain the Data record and entree in all QC related documents and files.
 </li>
 <li>
 Monitoring the lab inventory of the lab wear, consumables materials, chemicals and reference standard.
 </li>
 <li>
 Promote safe-working and laboratory environment that complies with company EHS requirements.
 </li>
 <li>
 Identify any risk and escalate to the line manager,
 </li>
 <li>
 Adhere to Safety, Quality and GPS standards and sustain the relevant QA &amp; EHS KPI metrics to achieve Zero Accident, Zero Defect, Zero Waste and continues improvements.
 
 
 
 </li>
 </ul>
 
 
 Why you?
 
 
 
 
 
 
 Basic Qualifications:
 
 
 
 
 We are looking for professionals with these required skills to achieve our goals:
 
 
 
 <ul>
 <li>
 Bachelor&rsquo;s degree with majors in Chemistry, Biochemistry or Pharmacy.
 </li>
 <li>
 2 - 4 years of experience in similar role.
 </li>
 <li>
 Good level of English in terms of speaking, writing and reading.
 </li>
 <li>
 Knowledge of EHS, GMP and GLP.
 </li>
 <li>
 Computer Skills (Word, Excel &amp; Power point).
 </li>
 <li>
 Time management skills.
 </li>
 <li>
 Good analytical and problem-solving skills.
 
 
 
 </li>
 </ul>
 
 Why GSK?
 
 
 Uniting science, technology and talent to get ahead of disease together.
 
 
 
 GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases &ndash; to impact health at scale.
 
 
 People and patients around the world count on the medicines and vaccines we make, so we&rsquo;re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.
 
 
 
 Contact information:
 
 
 
 You may apply for this position online by selecting the
 
 Apply now
 
 button.
 
 
 
 Important notice to Employment businesses/ Agencies
 
 
 
 GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.
</div>

Randstad USA

<div>
 
 Job Summary
 
 
 
 A prominent manufacturing plant in the Jessup, MD area is seeking an R&amp;D Chemist. The Chemist will conduct research and development toward new product development of technical foams. The position will include hands on lab work, data analysis, project management, and reporting to Sr Management. This is a high-priority search, salaried in the $80K+ range!
 
 
 location: Baltimore, Maryland
 
 
 job type: Permanent
 
 
 salary: $75,000 - 90,000 per year
 
 
 work hours: 8am to 4pm
 
 
 education: Bachelors
 
 
 
 Responsibilities
 
 
 
 <ul>
 <li>
 Develop an understanding of the mechanical and technical aspects of polyurethane foam chemistry and manufacturing to support R&amp;D activities
 </li>
 <li>
 Interfacing with multiple departments to understand project goals and performance requirements
 </li>
 <li>
 Researching scientific literature in support of R&amp;D activities
 
 
 </li>
 </ul>
 
 Qualifications
 
 
 
 <ul>
 <li>
 Experience level: Entry Level
 </li>
 <li>
 Education: Bachelors
 
 
 </li>
 </ul>
 
 Skills
 
 
 
 <ul>
 <li>
 Research &amp; Development
 
 
 </li>
 </ul>
 Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.
 
 
 At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com.
 
 
 Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&amp;D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility).
 
 
 This posting is open for thirty (30) days.
</div>

Piramal Pharma Solutions

<div>
 
 
 POSITION SUMMARY:
 
 Piramal Pharma Solutions&rsquo; HPAPI Research and Manufacturing facility, located in Riverview, Michigan, is seeking a qualified Quality Control Chemist to join our Quality Control team. The Quality Control Chemist is responsible for providing analytical chemistry support for the facility.
 
 
 
 
 
 
 
 To perform this position 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:
 
 
 
 
 
 
 <ul>
 <li>
 Shall adhere to all applicable regulatory requirements, including FDA, EPA, OSHA, and related safety, health and environmental procedures, policies and practices.
 </li>
 <li>
 Consistent support and practice of all Piramal Pharma Solutions mission, vision, and values.
 </li>
 <li>
 Identify and protect the original technical information as part of the company property.
 </li>
 </ul>
 
 
 
 
 
 KEY RESPONSIBILITIES:
 
 
 <ul>
 <li>
 Support manufacturing operations through the testing of raw materials and starting materials as required to meet production timelines.
 </li>
 <li>
 Perform cleaning verifications on multi-use equipment using approved methods.
 </li>
 <li>
 Test reference standards and stability samples.
 </li>
 <li>
 Document sample preparation, equipment set-up, and test results in laboratory notebooks or other appropriate test record forms. Verify data with second quality team member as required. Maintain all records as required to maintain compliance.
 </li>
 <li>
 As required, test intermediates and final products to meet production timelines/client requirements.
 </li>
 <li>
 Assist in the revision of documentation as required.
 </li>
 <li>
 Participate in quality unit projects, including but not limited to supplier certification, methods development, methods validation and training of both quality unit members as appropriate.
 </li>
 <li>
 Provide support in the maintenance and calibration of laboratory analytical instrumentation.
 </li>
 <li>
 Assist in the maintenance of the QC laboratory through routine housekeeping, as well as keeping personal bench area and desk organized.
 </li>
 <li>
 As required, perform routine testing on the water system (DI, ice, potable, and QC water), and prepare reports as needed.
 </li>
 </ul>
 
 
 
 
 
 EDUCATION/EXPERIENCE:
 
 
 <ul>
 <li>
 Bachelor&rsquo;s degree in Chemistry or Biochemistry or equivalent.
 </li>
 <li>
 One (1) year of experience in pharmaceutical quality control or equivalent is preferred
 </li>
 <li>
 Familiarity with analytical testing and instrumentation.
 </li>
 </ul>
 
 
 
 
 
 JOB COMPENTENCIES:
 
 
 <ul>
 <li>
 Excellent organizational and planning skills.
 </li>
 <li>
 Strong written, verbal, and interpersonal communication skills.
 </li>
 <li>
 High attention to detail.
 </li>
 <li>
 Demonstrated strong analytical skills, and the ability to work independently against multiple deadlines.
 </li>
 </ul>
 
 
</div>

Quality Control Chemist

USAntibiotics

<div>
 
 
 POSITION SUMMARY
 
 
 
 
 
 
 The Chemist will provide analytical support for QC testing of antibiotic products which include raw materials, in-process samples, stability samples, validation samples, product surveillance, and finished products according to Quality Assurance standard procedures, as assigned. Assist with development and validation of chemical assays. Assist with installing, validating, and trouble-shooting new and existing equipment, including automated systems, as assigned. Accurately generate and document all analytical test results per written procedures and corporate policies and support management in the evaluation and review of all test results and investigations as needed.
 
 
 
 
 
 
 ROLES &amp; RESPONSIBILITIES:
 
 
 
 
 
 <ul>
 <li>
 Maintains the QC laboratories to comply with cGMP and US Antibiotics standards of safety, quality, and cleanliness.
 </li>
 <li>
 Follows all safety precautions and guidance from training sessions, chemical hygiene plan, MSDSs (Material Safety Data Sheets), and other technical literature and resources.
 </li>
 <li>
 Performs efficient and reliable analytical tests following validated procedures for raw material, in process, validation, product surveillance, finished product, stability, water, and environmental samples, as assigned.
 </li>
 <li>
 Documents all results in accordance with cGMPs and written procedures.
 </li>
 <li>
 Troubleshoots and solves problems with assays and laboratory equipment and reports all observations.
 </li>
 <li>
 Strictly follows written procedures to minimize analytical variability. Recommends any potential improvements or changes to methods and lab operations (changes implemented via the change control process).
 </li>
 <li>
 Interprets analytical results correctly, notifying supervision promptly of any situation that indicates analytical issues or product issues.
 </li>
 <li>
 Participates in analytical method validations or transfers as required.
 </li>
 <li>
 Performs satisfactorily on all analyst qualification studies, indicating technical proficiency.
 </li>
 <li>
 Plans, performs, and documents non-routine tests (or special studies) and investigations under the direction of supervisor and/or manager.
 </li>
 <li>
 Evaluates and utilizes state-of-the-art equipment, including automated systems and computerized systems to perform and document testing and meet the goals of improved performance, including reliability and efficiency.
 </li>
 <li>
 Maintains and improves proficiency of technical skills through training.
 </li>
 <li>
 Conducts special studies in accordance with protocols and direction of management. Prepares well-documented reports of results.
 </li>
 <li>
 Carries out other departmental duties as deemed appropriate by supervisor/manager.
 </li>
 <li>
 Reviews (i.e., validates) analytical test results for other laboratory personnel, as required.
 </li>
 <li>
 Assists supervision in conducting analytical failure investigations, as required, following all procedures.
 </li>
 <li>
 Calibrates and maintains assigned laboratory equipment as needed according to schedules and procedures, documenting all results.
 </li>
 <li>
 Assists with equipment qualification testing as required by management.
 </li>
 <li>
 Assists with sampling tasks as required.
 </li>
 <li>
 Ensures that testing of products manufactured at the facility is performed per approved procedures and appropriate regulations and those lab operations conform to company standards for safety and performance.
 </li>
 <li>
 Reports all test results and any concerns with accuracy of analytical data and/or any issues that may impact product quality, efficacy, safety, or purity.
 </li>
 <li>
 Supports production needs by efficient laboratory turnaround of samples with right-first-time testing.
 </li>
 <li>
 Evaluates test results versus established test criteria and/or product specifications.
 </li>
 <li>
 Must be able to follow procedures for investigative analytical results as required.
 </li>
 <li>
 Advises, in a technical role, less-experienced staff, notifying supervisor or manager of problems/issues or additional training needs.
 </li>
 <li>
 Initiates ideas for operational changes and continuous improvement in laboratory, within constraints of policies and procedures to improve cGMP compliance, efficiency, cost, and performance.
 </li>
 <li>
 Must be able to assure the accuracy and integrity of analytical results/documentation generated. Exercises careful attention to testing procedures, and sampling handling and preparation as to avoid known degradation failure modes for materials under test, and to documentation.
 </li>
 </ul>
 
 
 
 
 
 EDUCATION, WORK EXPERIENCE, CERTIFICATIONS:
 
 
 <ul>
 <li>
 BS/BA degree in Chemistry (or related science) or equivalent related analytical experience.
 </li>
 <li>
 Minimum of 0-5 years of analytical experience in pharmaceutical industry and/or other scientific experience.
 </li>
 <li>
 Strong knowledge/experience of cGMPs in areas beyond QC laboratory.
 </li>
 </ul>
 
 
 
 
 
 KNOWLEDGE, SKILLS, AND ABILITIES:
 
 
 
 
 Skills/Abilities:
 
 
 <ul>
 <li>
 Demonstrate ability to perform a wide variety of chemical, instrumental, and chromatographic analyses in an efficient, reliable, and safety conscious manner.
 </li>
 <li>
 Advanced computer skills.
 </li>
 <li>
 Appropriate interpersonal and leadership skills
 </li>
 <li>
 Strong verbal communication skills and technical writing skills.
 </li>
 <li>
 Ability to prioritize and decide appropriate course of actions for routine issues.
 </li>
 <li>
 Ability to recognize possible compliance, technical, or safety-related issues and notify supervisor or manager promptly.
 </li>
 <li>
 Ability to suggest appropriate corrective and/or preventive action(s) and assist with implementation.
 </li>
 <li>
 Ability to work in a multi-disciplinary team environment
 </li>
 <li>
 Demonstrate visual acuity per SOP requirements
 </li>
 </ul>
 
 
 Required Knowledge:
 
 
 <ul>
 <li>
 Understanding of analytical techniques, test methodology, method development, method validation and reporting for data integrity.
 </li>
 <li>
 Comprehensive skills related to chemical, instrumental, chromatographic analysis, Operational Excellence, statistical applications and tools
 </li>
 <li>
 Understanding of equipment installation, validation, calibration, and troubleshooting, etc.
 </li>
 <li>
 Strong knowledge of cGMPs, USP and FDA&rsquo;s laboratory related requirements.
 </li>
 </ul>
 
 
</div>

Chemist

kuwait shop

Chemist needed for cosmetic production factory in Kuwait1- A production chemistMust have experience in the field of cosmetics and personal care products.Good in English and computer skills.Good knowledge of water desalination system.2- Research and Development (R&amp;D) ChemistExperience in cosmetics and personal care is required .Good in English and computer skills .Ability to develop and innovate new products .3- QC Quality Control chemistBachelor's degree in Chemistry or a related fieldExperience in the pharmaceutical or cosmetics analysisGood knowledge of (HPLC, UV, IR instruments.)Good knowledge of the GMP in pharmaceutical industries.Good in English and computer skills .Accommodation is available - Residence and annual renewal fees are coveredPlease send your CV tojob@kuwaitshop1.comOr what's app: 0096551781180Salary range: $1000 to $1600Job Type: Full-timeJob Type: Full-timePay: KD300.000 - KD500.000 per month

chemical engineer

Krete

<div>
 
 Krete Industries is looking for a Formulation Chemist/Scientist with a strong product development history and experience with chemicals commonly used in construction chemicals, industrial &amp; institutional cleaning, and paints &amp; coatings.
 
 
 
 
 
 This position will be responsible for developing and refining formulations, conducting wet chemistry/laboratory bench work (e.g. QC, raw material evaluation, alternative material approvals, etc.), and maintaining rigorous quality control standards through testing and parameter management. The role also encompasses project management and research initiatives to support innovation and product advancement.
 
 
 
 
 
 The Formulation Chemist will work closely with the Applications Lab, contributing to concrete testing and providing chemical insights to enhance performance and improve outcomes. The Formulation Chemist will also work closely with Production to ensure to quality and successful scale-up of new products and processes.
 
 
 
 
 
 
 About Krete Industries:
 
 
 
 Established in 1990 in Brookfield, WI, Krete Industries provides high-quality concrete admixtures and service solutions to the concrete industry. We believe in solving problems, sharing knowledge, and making the highest quality products. We are authentic, thorough, adaptable, and personable in everything we do.
 
 
 
 
 
 
 Tasks:
 
 
 
 &bull; Quality control of raw materials and finished goods
 
 
 &bull; Perform chemical lab activities to assist with production, R&amp;D, and customer support
 
 
 o pH
 
 
 o Specific gravity
 
 
 o FTIR analysis
 
 
 o Develop and produce new product concepts
 
 
 o Other lab-related tasks as required to support teams
 
 
 &bull; Perform, review, edit, and create (when necessary) chemical laboratory procedures and standards
 
 
 &bull; Create and deliver reports for quality control and R&amp;D purposes
 
 
 &bull; Identify the composition of chemicals and chemical compounds
 
 
 &bull; Maintain a clean and safe laboratory environment
 
 
 &bull; Source/vet raw materials and alternatives
 
 
 &bull; Maintain production batch tickets, certificate of analysis, safety data sheets, Raws Database, and QC Database
 
 
 &bull; Collaborate with the Applications Lab and Production teams to lead new product development initiatives from concept through scale-up and commercialization
 
 
 &bull; Technical troubleshooting (internal and external)
 
 
 
 
 
 
 Responsibilities:
 
 
 
 &bull; Maintain product formulas, improving/optimizing current or creating new ones as needed
 
 
 &bull; Initiate and/or manage R&amp;D projects
 
 
 &bull; Maintain laboratory instruments and equipment
 
 
 &bull; Maintain raw material documentation (CoA, SDS, database, etc.)
 
 
 &bull; Maintain finished good documentation (CoA, SDS, database, etc.)
 
 
 &bull; Perform quality control activities for raw material and finished goods
 
 
 &bull; Formulate/develop products and provide input on scaling production feasibility
 
 
 &bull; Improve efficiency and efficacy of laboratory procedures
 
 
 &bull; Work with production to ensure efficient batching and troubleshoot as necessary
 
 
 &bull; Provide technical support (internal and external) when needed
 
 
 &bull; Become a &ldquo;technical&rdquo; Subject Matter Expert (SME)
 
 
 
 
 
 
 Skills:
 
 
 
 &bull; Computer (Microsoft Office, Google Calendar, Slack, Fishbowl, general)
 
 
 &bull; Communication and presentation
 
 
 &bull; Self-starter
 
 
 &bull; SME/mentor
 
 
 &bull; Professional/technical writing
 
 
 &bull; Data/record keeping practices
 
 
 &bull; SDS management
 
 
 
 
 
 
 Resources Provided:
 
 
 
 &bull; Basic/minimal computer training
 
 
 &bull; All PPE
 
 
 &bull; Relevant SOPs for operations/testing
 
 
 &bull; On the job training
 
 
 o Concrete Basics
 
 
 o Admixture/Chemical Basics
 
 
 o ASTM/NCMA testing
 
 
 o Lab equipment
 
 
 o Safety/OSHA
 
 
 &bull; Necessary laboratory equipment for expected responsibilities and tasks
 
 
 
 
 
 
 Required:
 
 
 
 &bull; Minimum of 5 years of experience in similar roles
 
 
 &bull; Minimum of 1 full development cycle of a product
 
 
 &bull; Comfortable being a Subject Matter Expert (SME)
 
 
 &bull; Understanding of chemical blending production, process, and interactions
 
 
 &bull; Understanding of chemical laboratory equipment/instrumentation and maintenance
 
 
 &bull; Strong formulation skills
 
 
 &bull; Strong foundation in wet chemistry procedures
 
 
 &bull; BSc in Chemistry or relevant field
 
 
 &bull; FTIR experience
 
 
 
 
 
 
 Preferred:
 
 
 
 &bull; Advanced Microsoft Excel user
 
 
 &bull; Experience with Microsoft Access/maintaining databases
 
 
 &bull; Understanding of statistics and how to set upper and lower control limits for QC and production
 
 
 &bull; Experience in Concrete Admixtures, Industrial and Institutional Cleaning, Paints and Coatings, or related industries
 
 
 &bull; SDS writing experience
 
 
 
 
 
 
 Benefits offered:
 
 
 
 &bull; Health, dental, and vision insurance
 
 
 &bull; Paid time off (PTO)
 
 
 &bull; A 401(k)-retirement plan with company match (available after 1 year)
 
 
 
</div>

Formulation Chemist

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