What Jobs are available for Analytical Chemist in Bahrain?

• Lead and mentor a team of analytical chemists, fostering a collaborative and high-performance environment.
• Develop, validate, and implement analytical methods for the characterization and quality control of raw materials, intermediates, and finished pharmaceutical products using techniques such as HPLC, GC, MS, UV-Vis, IR, and titration.
• Oversee the execution of routine and non-routine analytical testing according to established protocols and regulatory guidelines (e.g., GMP, ICH).
• Troubleshoot and resolve analytical challenges, ensuring the accuracy and reliability of test results.
• Review and approve analytical data, reports, and validation documentation.
• Collaborate with formulation scientists, process development teams, and quality assurance to support product development and manufacturing.
• Ensure laboratory equipment is properly maintained, calibrated, and qualified.
• Stay current with regulatory requirements and industry best practices in analytical chemistry.
• Manage analytical project timelines and resources effectively.
• Contribute to regulatory submissions by providing comprehensive analytical data and justifications.

• Develop, validate, and implement analytical methods for raw materials, in-process samples, and finished products.
• Perform routine and non-routine chemical testing using a variety of analytical instruments (e.g., HPLC, GC, Spectroscopy, Titration).
• Analyze test results, interpret data, and generate comprehensive reports.
• Investigate out-of-specification (OOS) results and implement corrective and preventive actions (CAPA).
• Maintain laboratory equipment, ensuring calibration and proper functioning.
• Ensure compliance with all relevant quality standards, regulatory requirements, and company policies.
• Collaborate with R&D and production teams to address quality-related issues and support product development.
• Prepare and maintain detailed laboratory notebooks and documentation.
• Train junior laboratory personnel on analytical techniques and quality procedures.
• Contribute to the continuous improvement of quality control processes and laboratory operations.
• Monitor and manage inventory of laboratory chemicals and consumables.

• Bachelor's degree or Master's degree in Chemistry, Analytical Chemistry, or a related science field.
• Minimum of 5 years of experience in a quality control laboratory setting, preferably within the manufacturing sector.
• Extensive hands-on experience with analytical instrumentation (HPLC, GC, UV-Vis, IR spectroscopy, etc.).
• Strong understanding of quality management systems (e.g., ISO 9001) and relevant regulatory guidelines.
• Proficiency in data analysis and interpretation, with excellent attention to detail.
• Excellent written and verbal communication skills.
• Ability to work independently and as part of a team in a hybrid work environment.
• Experience with method development and validation is highly desirable.
• Knowledge of GMP/GLP principles is an advantage.

• Ph.D. or Master's degree in Analytical Chemistry, Biochemistry, Pharmaceutical Sciences, or a related field.
• Minimum of 7 years of experience in bio-analytical method development and validation.
• Extensive hands-on experience with LC-MS/MS, HPLC, and GC.
• Proficiency in data analysis and interpretation using relevant software (e.g., MassHunter, Analyst, Empower).
• Strong understanding of GLP regulations and their application in bio-analytical testing.
• Experience with small molecule and/or large molecule analysis.
• Excellent written and verbal communication skills.
• Proven ability to work effectively in a remote, collaborative environment.

• Perform routine and non-routine chemical analyses on raw materials, intermediates, and finished pharmaceutical products using techniques such as HPLC, GC, UV-Vis, FT-IR, and titration.
• Develop, validate, and transfer analytical methods according to ICH guidelines and regulatory requirements.
• Investigate out-of-specification (OOS) results, identify root causes, and implement corrective and preventive actions (CAPAs).
• Maintain and calibrate laboratory equipment to ensure accurate and reliable results.
• Prepare and review analytical reports, test records, and validation documents.
• Ensure compliance with GMP, ISO, and other relevant quality standards and regulations.
• Participate in internal and external audits as a subject matter expert.
• Collaborate with R&D, manufacturing, and regulatory affairs departments on product development and troubleshooting.
• Maintain a safe laboratory environment and adhere to all safety protocols.
• Train and mentor junior QC chemists and technicians.

• Master's degree or Ph.D. in Chemistry, Pharmaceutical Sciences, or a related field.
• Minimum of 6 years of hands-on experience in pharmaceutical quality control, with a strong focus on analytical chemistry.
• Extensive experience with analytical instrumentation such as HPLC, GC, Mass Spectrometry, and dissolution testers.
• In-depth knowledge of GMP, pharmacopeias (USP, EP, BP), and regulatory guidelines (ICH).
• Proven experience in method development and validation.
• Strong problem-solving skills and the ability to troubleshoot analytical issues effectively.
• Excellent documentation skills and attention to detail.
• Proficiency in data analysis and interpretation.
• Ability to work independently and as part of a team in a fast-paced environment.
• Good written and verbal communication skills.

• Perform analytical testing on raw materials, intermediates, and finished pharmaceutical products.
• Develop, validate, and transfer analytical methods according to regulatory guidelines.
• Operate and maintain analytical instrumentation such as HPLC, GC, UV-Vis, and FTIR.
• Analyze and interpret complex analytical data, ensuring accuracy and compliance.
• Conduct stability studies and analyze results to determine shelf-life.
• Investigate out-of-specification (OOS) results and implement corrective actions.
• Prepare detailed analytical reports and maintain accurate laboratory documentation.
• Collaborate with R&D, manufacturing, and regulatory affairs teams on quality-related issues.
• Ensure all activities comply with Good Manufacturing Practices (GMP) and relevant regulatory standards.
• Contribute to process improvements and the optimization of quality control procedures.

• Bachelor's or Master's degree in Chemistry, Pharmaceutical Sciences, or a related field.
• Minimum of 5 years of experience in pharmaceutical Quality Control (QC).
• Extensive experience with analytical techniques such as HPLC, GC, UV-Vis, FTIR.
• Proficiency in method development, validation, and stability testing.
• Strong understanding of GMP regulations and ICH guidelines.
• Excellent analytical, problem-solving, and critical thinking skills.
• Ability to work independently and manage workload effectively in a remote environment.
• Strong written and verbal communication skills for clear documentation and reporting.
• Experience with laboratory information management systems (LIMS) is a plus.

• Developing, validating, and transferring analytical methods for raw materials, intermediates, and finished drug products.
• Performing routine and non-routine analytical testing using a range of instrumentation (e.g., HPLC, UPLC, GC, LC-MS, GC-MS, ICP-MS, UV-Vis, FTIR, NMR).
• Troubleshooting analytical instrumentation and resolving method-related issues.
• Characterizing unknown impurities and degradation products.
• Conducting stability studies and analyzing stability data.
• Interpreting analytical results and preparing comprehensive reports.
• Collaborating with R&D teams to provide analytical support for new product development.
• Ensuring compliance with Good Laboratory Practices (GLP) and regulatory guidelines (e.g., FDA, EMA).
• Mentoring junior analytical chemists and providing technical guidance.
• Maintaining laboratory equipment and ensuring proper calibration and maintenance.
• Contributing to the optimization of analytical processes and workflows.
• Reviewing and approving analytical data and documentation.

Company Description

Shafiq Glass, founded in 2005, has become a leading provider of high-quality aluminium and glass products in Bahrain. The company's modern fabrication plant meets international standards, emphasizing their commitment to quality and excellence. Specializing in doors, windows, storefronts, entrances, and more, Shafiq Glass is renowned for completing reputable projects across Bahrain. Their aluminum division offers a comprehensive selection of profiles for doors and windows, alongside the supply and installation of ACP for facades. Shafiq Glass consistently exceeds client expectations with high-quality products and services that meet industry standards.

Role Description

This is a full-time on-site role for a Quality Control Engineer, located in Al-Hidd. The Quality Control Engineer will be responsible for inspecting and assessing the quality of aluminium and glass products, ensuring they meet company and industry standards. Daily tasks include conducting tests, documenting quality issues, suggesting improvements, and collaborating with other departments to resolve quality-related problems. The role also involves maintaining quality control documentation and updating quality management systems.

Qualifications

• Skills in Quality Control and Quality Assurance
• Strong Analytical Skills for problem identification and resolution
• Effective Communication skills
• Experience in Quality Management processes and systems
• Excellent attention to detail and commitment to quality
• Relevant experience in the glass and aluminium industry is a plus
• Bachelor's degree in Engineering

Job Description:

We are seeking an experienced Quality Control Manager to oversee project quality assurance and contract management in compliance with U.S. Government standards.

Requirements (Mandatory):

• Valid Construction Quality Management (CQM) for Contractors Certificate issued by USACE or U.S. Navy (must be current and verifiable).
• Minimum 5 years of experience working on U.S. Government construction projects in a QC role.

Responsibilities:

• Implement and manage the Quality Control (QC) program in full compliance with USACE/U.S. Navy requirements.
• Conduct inspections, prepare reports, and ensure all work conforms to contract requirements, specifications, and applicable standards.
• Lead and document the three-phase QC inspections (Preparatory, Initial, and Follow-up).
• Ensure compliance with safety, environmental, and labor regulations on U.S. Government projects.
• Manage the contract in general, including coordination with project managers, subcontractors, and U.S. Government representatives to ensure timely and compliant delivery of all obligations.

Application Instructions:

Only candidates who meet the above requirements are eligible. Please submit your CV along with a copy of your valid USACE/U.S. Navy CQM Certificate. Applications without the required certificate and experience will not be considered.

Job Type: Full-time