Total 94 chemist job vacancies in Hong Kong

• Perform biochemistry, analytical testing of raw material, in-process control samples and final product 

• Perform Quality Tag Out for laboratory equipments such as freezer, water bath

• Implement and maintain cGMP 

• Effectively perform various laboratory techniques

• Ensure all equipment is used and maintained in GMP environment 

Requirements: 

• Minimum  Degree in Chemistry, Biochemistry or related scientific degree

• 1-3 years relevant experience in the Bio-Pharmaceutical / Pharmaceutical industry

• Comfortable to do shift work

• Familiar with GMP / GLP environment

• Able to start immediate or within short notice period 

If you meet the requirements of this role, please email a detailed resume in Word document to Cindy Wong

CEI Registration No.: R2095121

Email: cindywong@recruitexpress.com.sg

*All information will be treated with strictest confidence. We regret that only short-listed applicants will be notified.

EA License No: 99C4599

EA Personnel No: R2095121

EA Personnel Name: Cindy Wong Xin Yi

Perform testing and analysis in accordance with the standard/in-house methods and to comply with QA/QC procedures.

· To ensure timeliness, precision and accuracy of analytical results to meet turnaround time.

· Effective implementation and maintenance of MS ISO/IEC 17025 as well as Group Quality System.

· Adhere to group HSE safety procedures.

· Ensure that information from the clients is kept as strictly confidential and never revealed to the third party.

· Ensure all analytical equipment, apparatus etc are maintained and calibrated as per the required schedule.

· Ensure root-cause of all non-conformities or customer complaints are to be investigated and identified with appropriate corrective and preventive actions.

· To treat proficiency Testing Programmed or Round Robin seriously and make sure the result obtained is most accurate and precise.

· To train, supervise and monitor lab technicians /Junior Staff with assigned test methods and procedures.

· To ensure all controlled quality procedures, test methods and document are kept confidentially and restricted within SGS premise.

· Practice Good Housekeeping and Good Laboratory practice.

· Adherence to SGS Health, Safety and Environment (HSE) Policy by uphold a good safety behavior and exercising necessary standard and process when carry out your responsibilities at all times to ensure compliance to the HSE requirements.

· Perform any other responsibilities as assigned by your reporting manager and/or Senior Management

Perform testing and analysis in accordance with the standard/in-house methods and to comply with QA/QC procedures.

· To ensure timeliness, precision and accuracy of analytical results to meet turnaround time.

· Effective implementation and maintenance of MS ISO/IEC 17025 as well as Group Quality System.

· Adhere to group HSE safety procedures.

· Ensure that information from the clients is kept as strictly confidential and never revealed to the third party.

· Ensure all analytical equipment, apparatus etc are maintained and calibrated as per the required schedule.

· Ensure root-cause of all non-conformities or customer complaints are to be investigated and identified with appropriate corrective and preventive actions.

· To treat proficiency Testing Programmed or Round Robin seriously and make sure the result obtained is most accurate and precise.

· To train, supervise and monitor lab technicians /Junior Staff with assigned test methods and procedures.

· To ensure all controlled quality procedures, test methods and document are kept confidentially and restricted within SGS premise.

· Practice Good Housekeeping and Good Laboratory practice.

· Adherence to SGS Health, Safety and Environment (HSE) Policy by uphold a good safety behavior and exercising necessary standard and process when carry out your responsibilities at all times to ensure compliance to the HSE requirements.

· Perform any other responsibilities as assigned by your reporting manager and/or Senior Management

Responsibilities

• Perform laboratory tests on samples in accordance to standards
• Ensure accurate and reliable analytical results
• Responsible for training and supervising junior staff in technical matters
• Assist in maintaining and improving our laboratory quality system
• To maintain and upkeep quality system as per SAC-Singlas requirement
• Ensure proper equipment performance and test data reliability by carrying out routine QA/QC protocols and scheduled Preventive Maintenance as needed
• Participate in planning and work distribution
• Other ad-hoc duties assigned

Job Requirements:

• Minimum Degree - Chemistry related faculty
• Minimum 1 year work experience in relevant field
• Basic Chemistry and analytical skills
• Good communication
• Team Player

Key Responsibilities

1.     To ensure that all manufactured products conform with specified standards before products are released / sold to customers.

2.     To supervise and ensure smooth QC routine raw material &work-in-progress testing.

3.    Issuing COA, COC or any other documentations upon customer's request.

4.    Collecting data and study trend analysis for improving current product application performance.

5.    Participate in assessing and qualifying new raw materials for potential use.

6.     Work with procurement to ensure that raw materials purchased are within specifications.

7.     Maintain and manage retention samples keeping &disposal.

8.     Investigate customer’s complaint, correction actions and preventive actions taken are documented.

9.     Proper isolation and disposition of non-conformance materials and products.

10. Involves in product development initiatives, lab trial sample preparation, performs formulation adjustments, conducts stability monitoring and maintain proper record and documentation.

11.  To assist the Company’s Workplace Safety and Health committee.

12.  Compile and analyze customer’s complaints to establish trends and alert Management / Sales Customer Service / Production / Procurement for concerted effort to pre-empt and eradicate issues.

13. Knowledge of ISO management systems and experience with Halal certification applications or renewals would be an advantage.

14.  Prepare technical reports for management information.

Other Duties:

The duties listed are not exhaustive and may be varied from time to time as dictated by the changing needs of the organisation.

The post holder will be expected to undertake other duties as appropriate and as requested by his/her manager.

This position will support Hard Coat and Anti Fog Product Development projects to build a commercially viable functional coating product pipeline in alignment with SDC business goals.

Responsibilities:

• Lead or assist projects in product development milestone attainment including competitive benchmarking, product formulation and optimization, establishment of manufacturing control plan for scale-up and production
• Screen and qualify alternative key raw materials to facilitate sustained supply of functional coating and film products
• Generate ideas and proofs-of-concept for new technologies for proprietary product and intellectual property development
• Leverage new and innovative building blocks to accelerate development of proprietary value-added functional coatings
• Provide support for development of new equipment, formulas, processes, and methods for solution of technical problems.
• Provide investigation support on newly developed and scale-up manufactured products to improve quality by research into composition, structure, properties, relationships, and reactions of matter
• Confer with Vendors, Scientists and Engineers regarding product development
• Prepare standards and specifications for processes, instruments, products and tests
• Document and communicate effectively internally with cross-functional teams

Requirements:

• Bachelor’s degree in chemistry or related field and minimum two years Coatings and Specialty Chemicals industry experience, or equivalent combination of education and experience
• Familiarity with a variety of Chemical Coatings Industry’s concepts, practices, and procedures
• Stay current with outside growth of technology, including new coating building blocks and processes
• Highly self-motivated with good presentation skills
• Proficient in Microsoft Word, Power Point, and Excel
• Willing to work at Tuas South

• Initiate, perform and support key developments of products, materials, processes, technology modules and methods within the framework of feasibility studies, business cases and/or projects, incl. experimental work and coordination of lab, pilot or production trials.
• Continuously ensure and drive the development of knowledge within specific sub technology field (width & depth).
• Contribute to and initiate invention disclosures.
• Perform literature and patent searches in consultation with the related responsible persons, support FTO analysis from a technological perspective. 
• Provide input to the relevant Technology Roadmap(s) while making investment recommendations for technology development.
• Actively build up and maintain internal and external networks, with the focus on technological aspects incl. scouting and screening of new raw materials (e.g. suppliers, institutions, academia).
• Support recruiting and technical guidance of students or apprentices.

Qualification

1. Educational level & Certifications

• PhD degree in Science or Engineering discipline or Master degree or Degree in Science or Engineering or in discipline with at least 3 years of experience.

2. Experiences

• Experience in manufacturing processes of polymeric films and functional layers (e.g. organic solutions and dispersions).
• Work with solvents and flammable and toxic materials.
• Work in chemical labs (preferably in clean room environment).
• Use of analytical lab equipment for material property determination (e.g. rheology and microscopy).
• Preferably work experience with adhesives or pressure sensitive adhesives.

Interested candidates please send in your resume to:
Topaz Liang Huimin (CEI No. R1104500), email to: topaz@recruitexpress.com.sg

EA License No: 99C4599

• To conduct testing according to SOP, QA/QC procedures in accordance to ISO/IEC 17025 and meeting turnaround time (TAT).
• To adhere to group HSE safety procedures.
• To establish and review laboratory operating procedures.
• Ensure all quality manual and procedures are appropriately documented and followed.
• Ensuring all results / test reports / certificates are reviewed and issued professionally.
• To review, check and make sure results accuracy of Proficiency Testing Programme or Round Robin prior submitting to the PT organizer.
• Ensure Good Housekeeping and Good Laboratory Practice (GLP) in the laboratory.
• To comply with all Health, Safety and Environmental (HSE) local regulation (Occupational Safety and Health Act 1996, Factory and Machinery Act 1967, Environmental Quality Act 1974).
• To report any hazard / risk, near-miss and incident in Crystal system.
• Ensure that all Operational Integrity Management System (OIMS) requirements are met.

• Perform biochemistry, analytical and raw material of in-process and marketed products for lot release in accordance with quality standards and procedures.
• Responsible for housekeeping duties in the lab
• Perform Quality Tag Out for laboratory equipments such as freezer, water bath and etc.
• Support laboratory operations including but not limited to method transfer, equipment qualification, calibration, cleaning and maintenance, purchase and receipt of reagents and consumables, waste management, reagent and media preparation, critical reagent management and document management.
• Review lot release data, identify testing discrepancies and participate in laboratory investigations.
• Participate in inspection and ensure that the laboratory and documents are in a constant state of regulatory compliance and inspection readiness.
• To assist in writing SOP documents, Change plan or change records (document revisions) supporting continuous improvement of test procedures and assay sheet design.
• To carry out completion and review of GMP Documentation of data sheets or LIMS software.

Qualifications:

• Min Bachelor of Science majoring in Chemistry, Biochemistry or related scientific degree
• At least 1-3 years relevant experience depending on qualification, preferably in the bio-pharmaceutical / Pharmaceutical industry mailto:jalenetan@recruitexpress.com.sg
  

Interested candidates, please forward your resume to jalenetan@recruitexpress.com.sgmailto:jalenetan@recruitexpress.com.sg

Consultant: Jalene Tan (R26160390)
Recruit Express Pte Ltd (99C4599)

To provide an effective testing and analytical service to the plant ensuring that products manufactured are tested to specification on time and plant quality and safety goals are met.

Ensure that all raw material, in-process and finished product testing and method transfer testing is carried out per schedule and per GMP. Ensure that records are maintained to appropriate requirements.

Responsibilities:

• Perform biochemistry, analytical and raw material of in-process and marketed products for lot release in accordance with quality standards and procedures
• Responsible for housekeeping duties in the lab. Perform Quality Tag Out for laboratory equipment such as freezer, water bath, etc.
• Support laboratory operations including but not limited to method transfer, equipment qualification, calibration, cleaning and maintenance, purchase and receipt of reagents and consumables, waste management, reagent and media preparation, critical reagent management and document management
• Review lot release data, identify testing discrepancies and participate in laboratory investigations
• Participate in inspection and ensure that the laboratory and documents are in a constant state of regulatory compliance and inspection readiness
• To assist in writing SOP documents, change plan or change records (document revisions) supporting continuous improvement of test procedures and assay sheet design
• To carry out completion and review of GMP Documentation of data sheets or LIMS software
• To carry out QC sample receipt, assay and release procedures
• Support Audit preparation and any audit related activity
• Reading and understanding the test procedure and the requirements per USP, JP and EP

About You:

• Bachelor of Science majoring in Chemistry, Biochemistry or related scientific degree
• At least 1-3 years relevant experience depending on qualification, preferably in the bio-pharmaceutical / Pharmaceutical industry
• Good working knowledge of cGMP and regulatory requirements related to Quality is preferred 
• Problem-solving and troubleshooting skills
• Highly motivated and independent
• Possess good interpersonal and communication skills
• Knowledge of cGLP / cGMP, FDA, EMA and ICH guidance and industry standards for analytical development and characterization
• Must be able to do rotating 12-hour shift work (day and night shifts)

1 year contract, subject to extension     

As a Vita Coco Chemist / Associate Chemist, you will perform all tasks associated with the analytical lab operations, including chemical analysis, equipment calibration/maintenance, OOS investigation, method validation and other related tasks as assigned.

Responsibilities:

• Perform chemical and physical analysis of raw materials, in-process samples, finished products, stability samples, and non-routine samples.

• Conduct sensory sessions and packaging integrity checks.

• Manage calibration, maintenance and qualification of laboratory equipment.

• Participate in R&D activities such as formulation, shelf-life and homogeneity study.

• Responsible for ISO 17025 accreditation processes.

• Responsible for procurement and monitoring of lab inventory, liaising with vendors for equipment troubleshooting and maintenance.

• Draft, review and maintain operating procedures for laboratory equipment and processes.

• Render scientific assistance to our partners across the globe.

• Responsible for method validation and verification.

• Participate in project meetings.

• Assist in driving continuous improvement activities in the laboratory.

• Coordinate/participate in 6S activities for the analytical lab.

• Maintain housekeeping standards & observe safety requirements and Good Laboratory practices in the laboratory.

Additional Chemist Responsibilities:

• Assist in providing training for new hires/ interns.

• Provide technical expertise and guidance to Associate Chemists and interns.

• Assist in developing newly identified tests.

• Highlight unusual results to Senior Chemist.

Requirements:

• Diploma/Degree in Chemistry/Food Science-related field.

• Prior experience in ISO/IEC 17025 would be advantageous.

• Prior experience in QC/testing laboratory would be advantageous.

• Proficiency in MS Office tools, such as Word, Excel etc.

Expectations:

• Chemistry knowledge: To have a thorough understanding of chemistry procedures and principles, e.g. safe use and disposal of chemicals.

• Analytical skills: Be able to perform chemical analysis.

• Detailed-oriented: Maintains accurate records of data and processes.

• Computer skills: Proficient in MS Excel, Word for data entries, reports and data trending.

• Teamwork: To be able to work well with the team and collaborate with other teams.

• Problem solving skills: Able to analyze data, identify issues, troubleshooting.

• Good conduct/attitude: Adhere to company policies and behave professionally.

Job summary

As an Chemist at Vita Coco, you will test products, support research and help keep quality and safety standards high.

Primary Goals/Objectives:

To provide an effective testing and analytical service to the plant ensuring that products manufactured are tested to specification on time and plant quality and safety goals are met.

Ensure that all raw material, in-process and finished product testing and method transfer testing is carried out per schedule and per GMP. Ensure that records are maintained to appropriate requirements.

Major Responsibilities:

• Perform biochemistry, analytical and raw material of in-process and marketed products for lot release in accordance with quality standards and procedures.
• Responsible for housekeeping duties in the lab. Perform Quality Tag Out for laboratory equipment such as freezer, water bath and etc.
• Support laboratory operations including but not limited to method transfer, equipment qualification, calibration, cleaning and maintenance, purchase and receipt of reagents and consumables, waste management, reagent and media preparation, critical reagent management and document management.
• Review lot release data, identify testing discrepancies and participate in laboratory investigations.
• Participate in inspection and ensure that the laboratory and documents are in a constant state of regulatory compliance and inspection readiness.
• To assist in writing SOP documents, Change plan or change records (document revisions) supporting continuous improvement of test procedures and assay sheet design.
• To carry out completion and review of GMP Documentation of data sheets or LIMS software.
• To carry out QC sample receipt, assay and release procedures.
• Support Audit preparation and any audit related activity
• Reading and understanding the test procedure and the requirements per USP, JP and EP.

Requirements:

• min. Bachelor Degree in Biochemistry and above
• Possess 2-3 years of prior lab analyst experience in bio-chemistry related functions
• Able to do 12 hour rotating day and night shift

Interested candidates please send your updated resume in MS word format to:

kate.leau@recruitexpress.com.sg
Subject: QC Chemist (Bio)


EA Personnel: Kate Leau Wei Xuan (R1552331)
Company Registration No.: 99C4599

• Perform biochemistry, analytical and raw material of in-process and marketed products for lot release in accordance with quality standards and procedures.
• Responsible for housekeeping duties in the lab
• Perform Quality Tag Out for laboratory equipments such as freezer, water bath and etc.
• Support laboratory operations including but not limited to method transfer, equipment qualification, calibration, cleaning and maintenance, purchase and receipt of reagents and consumables, waste management, reagent and media preparation, critical reagent management and document management.
• Review lot release data, identify testing discrepancies and participate in laboratory investigations.
• Participate in inspection and ensure that the laboratory and documents are in a constant state of regulatory compliance and inspection readiness.
• To assist in writing SOP documents, Change plan or change records (document revisions) supporting continuous improvement of test procedures and assay sheet design.
• To carry out completion and review of GMP Documentation of data sheets or LIMS software.

Qualifications:

• Min Bachelor of Science majoring in Chemistry, Biochemistry or related scientific degree
• At least 1-3 years relevant experience depending on qualification, preferably in the bio-pharmaceutical / Pharmaceutical industry mailto:jalenetan@recruitexpress.com.sg
  

Interested candidates, please forward your resume to jalenetan@recruitexpress.com.sgmailto:jalenetan@recruitexpress.com.sg

Consultant: Jalene Tan (R26160390)
Recruit Express Pte Ltd (99C4599)

Opening for Pharmaceutical MNC Company in the West (Company transport provided)

1. Biotechnologist - 1 year contract, renewable

• Perform biochemistry, analytical testing of raw material, in-process control samples and final product 

• Perform Quality Tag Out for laboratory equipment such as freezer, water bath

• Implement and maintain cGMP 

• Effectively perform various laboratory techniques

• Ensure all equipment is used and maintained in GMP environment 

Requirements: 

• Minimum  Degree in Chemistry, Biochemistry or related scientific degree
• 1-3 years relevant experience in the Bio-Pharmaceutical / Pharmaceutical industry
• Familiar with GMP / GLP environmentAble to start immediate or within short notice period 
• Able to do 12-hour rotating day & night shift

Interested candidates please send your updated resume in MS Word Format:

kate.leau@recruitexpress.com.sg

Subject: QC Chemist (Bio)


EA Personnel: Kate Leau Wei Xuan (R1552331)
Company Registration No.: 99C4599