Duties & Responsibilities:

• Develop resin formulations for CCL (copper clad laminate) applications
• Researching new methods and raw materials to develop new products and improve existing products in both quality and cost
• Lead R&D projects through various stage of development to the commercialization
• Collaborate with R&D counterpart in US and Japan on R&D projects
• Sourcing alternative raw materials for existing products. Carry out evaluation and qualification
• Calculating and analysing test results and preparing detailed reports with recommendations and conclusions
• Estimate the cost, resources and time required to conduct one or more research projects and monitor the performance of these projects to ensure targets are met
• Provide technical support to production, QA, technical service and other departments when required (such as troubleshooting and failure analysis, etc.)
• Support new product and process transfer from other BUs
• Perform any other reasonable duties as required by Management from time to time

Requirements:

• At least a Bachelor's Degree in Polymer, Chemistry or related
• 3 to 5 years’ experience in formulation is preferred
• Good communication and interpersonal skills
• Mature, tactful, resourceful, positive attitude and self-motivated

Essential Duties and Responsibilities:

• Learns to conduct routine analyses in compliance with applicable methods, protocols, SOPs, and regulatory agency guidelines.
• Learns how to document work and maintain study documentation and laboratory records.
• Learns how to use laboratory equipment and software appropriate for assigned tasks.
• Learns to carry out testing on all aspects of work and calibration of equipment in the respective section when necessary.
• Learns to highlight abnormalities and discrepancies in the testing, calibration and results.
• Learns to perform the duties of a Quality Officer for the section
• Attends and participates in project meetings.
• Learns to perform peer review of data.
• Learns to highlight abnormalities and discrepancies in the testing, calibration and results.
• Contributes to a cohesive team environment. Plans individual workload in coordination with team members.
• General laboratory work like sample receipt and registration, preparation of sample bottles and helping to maintain cleanliness of laboratory, equipment and apparatus.
• Maintains a clean and safe laboratory work environment.
• Conducts all activities in a safe and efficient manner
• Assist the Lab Manager/Senior Chemist in all aspects of work in the respective section.
• Demonstrate and promotes the company vision.
• Regular attendance and punctuality.
• Performs other duties as assigned.

Core Responsibilities:

• Performs various chemical analyses
• Maintain of lab stocks / consumables / standards / documents
• Take charge of and maintains instrumentation such as ICP-OES, GC-FID
• Generates reports for tests done
• Method validation / development as required

Requirement:

• Diploma or a Degree in Chemical / Biochemical studies
• Relevant experience is preferred
• Experiences in laboratory analysis, including ICP-OES, GC-MS preferred
• Good working attitude and able to work under pressure
• Possess a valid Class 3 driving licence will be an added advantage
• Able to work as a team

Core Responsibilities:

• Performs various chemical analyses
• Maintain of lab stocks / consumables / standards / documents
• Take charge of and maintains instrumentation such as ICP-OES, GC-FID
• Generates reports for tests done
• Method validation / development as required

Requirement:

• Diploma or a Degree in Chemical / Biochemical studies
• Relevant experience is preferred
• Experiences in laboratory analysis, including ICP-OES, GC-MS preferred
• Good working attitude and able to work under pressure
• Possess a valid Class 3 driving licence will be an added advantage
• Able to work as a team

No Deviation is a provider of patient-centric solutions for the pharmaceutical industry, and we are currently seeking individuals who are passionate about joining our team.

Our areas of expertise include engineering consultancy, Commissioning Qualification Validation (CQV), as well as Quality, Compliance, and Regulatory services.

We strongly uphold our core values of Empathy, Integrity, and Transparency, and we strive to create a collaborative, innovative, and inclusive work environment that fosters personal growth and development.

We are seeking an experienced Senior QC Chemist to join our quality control team on a 1-year contract. The ideal candidate will have a minimum of 6 years of experience in quality control within the pharmaceutical or biopharmaceutical industry. This role requires advanced expertise in analytical methods, strong problem-solving skills, and an ability to work independently while collaborating closely with cross-functional teams.

Key Responsibilities

• Analytical Testing: Perform analytical testing on raw materials, in-process materials, and finished products in line with established protocols and cGMP standards. Utilize advanced techniques such as HPLC, GC, UV-Vis, and FTIR to ensure product quality.
• Data Review and Reporting: Analyze test results, compile comprehensive reports, and ensure accurate documentation of data in compliance with regulatory requirements. Conduct peer reviews of laboratory results generated by junior chemists.
• Troubleshooting and Process Improvement: Identify and troubleshoot analytical challenges and equipment issues, implementing corrective actions where necessary. Participate in continuous improvement initiatives to enhance testing processes and efficiencies.
• Compliance and Audit Preparation: Ensure adherence to SOPs, GLP, and cGMP regulations. Support internal and external audits by preparing documentation and providing subject matter expertise in QC processes.
• Method Development and Validation: Lead efforts in developing and validating analytical methods as required, ensuring they meet industry standards and regulatory guidelines.
• Training and Mentorship: Provide guidance and training to junior QC Chemists, promoting best practices in quality control and laboratory safety.

Requirements

• Education: Bachelor’s degree in Chemistry, Biochemistry, or a related field. A master’s degree is a plus.
• Experience: Minimum of 6 years in a QC role within a regulated environment, preferably in the pharmaceutical or biopharmaceutical industry.
• Technical Skills: Proficiency in advanced analytical techniques and experience with laboratory information management systems (LIMS).
• Regulatory Knowledge: Strong understanding of regulatory standards, including cGMP, GLP, and ICH guidelines.
• Attention to Detail: High level of accuracy and attention to detail, with strong organizational and documentation skills.
• Contract Duration: 1 year (with possibility of extension based on project needs and performance)

Essential Duties and Responsibilities:

• Learns to conduct routine analyses in compliance with applicable methods, protocols, SOPs, and regulatory agency guidelines.
• Learns how to document work and maintain study documentation and laboratory records.
• Learns how to use laboratory equipment and software appropriate for assigned tasks.
• Learns to carry out testing on all aspects of work and calibration of equipment in the respective section when necessary.
• Learns to highlight abnormalities and discrepancies in the testing, calibration and results.
• Learns to perform the duties of a Quality Officer for the section
• Attends and participates in project meetings.
• Learns to perform peer review of data.
• Learns to highlight abnormalities and discrepancies in the testing, calibration and results.
• Contributes to a cohesive team environment. Plans individual workload in coordination with team members.
• General laboratory work like sample receipt and registration, preparation of sample bottles and helping to maintain cleanliness of laboratory, equipment and apparatus.
• Maintains a clean and safe laboratory work environment.
• Conducts all activities in a safe and efficient manner
• Assist the Lab Manager/Senior Chemist in all aspects of work in the respective section.
• Demonstrate and promotes the company vision.
• Regular attendance and punctuality.
• Performs other duties as assigned.

Essential Duties and Responsibilities:

• Demonstrates and promotes the company vision
• Regular attendance and punctuality
• Applies GMP/GLP in all areas of responsibility, as appropriate
• Learns to conduct routine analyses in compliance with applicable methods, protocols, SOPs, and regulatory agency guidelines.
• Learns how to document work and maintain study documentation and laboratory records.
• Learns how to use laboratory equipment and software appropriate for assigned tasks.
• Attends and participates in project meetings.
• Learns to perform peer review of data.
• Learns to plan assigned workload on a daily basis and effectively schedule multiple assignments.
• Contributes to a cohesive team environment.  Plans individual workload in coordination with team members.
• Maintains a clean and safe laboratory work environment.
• Conducts all activities in a safe and efficient manner
• Performs other duties as assigned

Responsibilities:

Supports operations in the areas of process, troubleshooting and process improvements to improve reliability and increase capacity. Develops process improvement proposals for project implementation and execution. Monitors process trends and product quality to ensure product quality conformance. Provide up-to-date process status and liaise with production to ensure operation smooth production. Continuously review performance of material/product and take necessary actions for improvements. The job will involves R&D production, process control, new projects and trouble shooting exercises. Other ad-hoc relating duties as assigned from time to time.