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TS&D TECHNICIAN
TS&D TECHNICIAN
Interested candidates, kindly click HERE to submit your resume.
Date posted 14 Oct 2025
QC TECHNICIAN
QC TECHNICIAN
Responsibilities:
Conduct various analytical, bioassay and microbiological tests, including CE-SDS, cIEF, Karl Fischer titration, Total Organic Carbon (TOC) testing, UV-Vis spectrophotometry, FTIR, manual and automated titration, bioburden, container closure integrity testing (CCIT), and endotoxin testing
Conduct utility related sampling at utility system and environmental monitoring at manufacturing facilities.
Assist in analyzing and interpreting analytical, bioassay and microbiological results, maintaining accurate documentation.
Operate and maintain laboratory equipment and instruments.
Manage in-process, release stability sample, and reference standards
Qualifications:
Diploma and above in chemistry, biochemistry, microbiology, analytical chemistry, or related field.
Understanding of the drug development process preferred
In-depth knowledge of cGMP and compliance principles and a strong quality-focused mindset.
Strong attention to detail and ability to troubleshoot experimental challenges
Ability to work independently and as part of a collaborative team
Proficiency in English as a working language.
Career Development:
Comprehensive in-house training program (E-learning / OJT / Mentorship)
Dual career development tracks – Professional & Managerial Tracks
Opportunity for internal job rotation / Cross-BU transfer / Cross-country assignment
Cross cultural learning
GMP greenfield start-up experience
Interested candidates, kindly click HERE to submit your resume.
Date posted 15 Sep 2025
biologics GMP manufacturing technician
biologics GMP manufacturing technician
Job Summary:
The role includes material management, cleaning and sterilization, formulation, filling and lyophilization, capping, external washing, inspection and packaging, new plant construction, auditing, etc.
Responsibilities:
Responsible for the whole-process management of production materials, consumables, semi-finished products, and finished products, strictly adhering to GMP requirements.
Possess mastery of DP equipment principles and familiarity with the production process, enabling independent operation and basic maintenance of related equipment.
Draft and revise relevant operating procedures, batch production records, and related files in accordance with GMP requirements.
Strictly adhere to change control and deviation investigation processes, organize the drafting and implementation of changes, conduct deviation investigations, and establish corrective and preventive actions.
Analyze and resolve issues arising in the manufacturing process independently.
Continuously optimize production processes and workflows to ensure product quality and improve production efficiency.
Participate in the design and recommendation of new plants.
Participate in audits related to DP manufacturing.
Adhere to company compliance requirements.
Qualifications:
Diploma or higher in Pharmaceutical Manufacturing, Pharmaceutical Engineering, Pharmacy, Bioengineering, Biotechnology, Chemical Engineering, Microbiology, or related fields.
Knowledge of GMP is preferred, with expertise in aseptic production being an advantage.
Possess a solid foundation in pharmacy and biotechnology, with proficiency in Microsoft Office.
Strong English language skills and the ability to proactively analyze and solve problems that arise in the workplace.
Excellent hands-on operational skills, with careful and conscientious equipment operation and timely record-keeping.
Good communication and expression skills.
Effective team collaboration, efficient execution, and a strong sense of responsibility.
Interested candidates, kindly click HERE to submit your resume.
Date posted 15 Sep 2025
Technician 1, Quality Operation
Technician 1, Quality Operation
COMPANY OVERVIEW:
At Alcon, we are passionate about enhancing sight and helping people see brilliantly. With over 25,000 associates worldwide, we innovate fearlessly, champion progress, and act swiftly to improve global eye health. We foster an inclusive culture that values your contributions and supports your career growth. Join us and make a meaningful impact in the lives of our patients and customers.
POSITION SUMMARY:
This role is part of Alcon's Quality & Regulatory Affairs function, a team that ensures our products are in compliance with global, local, and internal regulations and meet the strictest standards of quality as we help people see brilliantly.
As a Technician, Quality Operations (Batch Review & QA Ops Oversight), is primarily responsible for handling technical tasks to support quality management in manufacturing and distribution. You will monitor product quality, resolve non-conformances, and maintain documentation while supporting daily operations and team efficiency.
In this role, a typical day will include:
Performing visual inspections of white stock and finished products to ensure quality standards are met.
Reviewing batch production records for compounding, filling, and packaging processes, ensuring all critical steps meet specifications prior to release.
Assessing autoclave reports for compounding and filling operations.
Conducting annual inspections of retention samples, including identification, segregation, and disposal, and maintaining the Retention/Reserve Sample Program.
Approving Engineering Change Notices (ECNs) and managing updates to the Bill of Materials (BOM).
Investigating and resolving deviations before batch release.
Coordinating the review of alarm reports and supporting impact assessments for critical alarms.
Supporting the preparation and administration of Master Documents such as SOPs, Forms, Templates and MBRs.
Assisting in the generation of Annual Product Quality Review (APQR) reports.
Setting up finished goods inspection plans for new products in SAP.
Tracking Master Batch Record (MBR) submissions and reporting weekly performance metrics.
Conducting aseptic audits of manufacturing processes and facilities.
Performing in-process checks and critical quality attributes during production shifts (e.g., IPC, IBA, line clearance approval).
Maintaining 5S standards and good housekeeping in the Lot Release area.
Monitoring key performance indicators (KPIs) and escalating issues as necessary.
Collaborating cross-functionally to support quality operations and continuous improvement.
Adhering to Alcon’s Quality Management System (QMS), GMP, GDP, and safety protocols.
WHAT YOU’LL BRING TO ALCON:
Minimum Diploma in Science, Engineering, or equivalent with at least 1-3 years of relevant experience in Quality Assurance within a manufacturing environment.
Experience in GMP/GDP-regulated industries, such as pharmaceuticals or medical devices.
Strong understanding of Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP).
Experience with cleanroom operations is an advantage.
Familiarity with MES and SAP systems is also preferred.
Strong analytical and problem-solving skills, with a keen eye for detail and a commitment to compliance.
Effective communication and collaboration skills to work cross-functionally and support continuous improvement.
Willingness to work rotational shift schedule across 3x shifts.
HOW YOU CAN THRIVE AT ALCON:
At Alcon, we are committed to fostering a work environment where our employees can grow, innovate, and excel. Here’s how you can thrive in your role with us:
Career Growth & Development – Gain access to continuous learning opportunities, leadership training, and career advancement programs to support your professional journey.
Collaborative Culture – Work alongside passionate and diverse teams in a dynamic and inclusive environment that encourages innovation and teamwork.
Impactful Work – Be part of a purpose-driven company that is improving lives by advancing eye care solutions worldwide.
Recognition & Rewards – Your contributions are valued and recognized through competitive compensation, performance incentives and career progression opportunities.
Global Exposure – Join a world-class organization with opportunities to collaborate across international teams and gain global industry insights.
Work-Life Balance & Well-Being – Enjoy employee wellness programs, flexible work arrangements and initiatives that support your well-being.
At Alcon, we empower our people to make a difference while growing their careers in an exciting and supportive environment. Join us and see brilliance in every opportunity!
📩 𝗛𝗼𝘄 𝘁𝗼 𝗔𝗽𝗽𝗹𝘆:
Send your 𝘂𝗽𝗱𝗮𝘁𝗲𝗱 𝗿𝗲𝘀𝘂𝗺𝗲 and 𝗲𝗮𝗿𝗹𝗶𝗲𝘀𝘁 𝗮𝘃𝗮𝗶𝗹𝗮𝗯𝗶𝗹𝗶𝘁𝘆 to: 𝗻𝗶𝗰𝗼𝗹𝗲.𝗳𝘂𝗻𝗴@𝗮𝗹𝗰𝗼𝗻.𝗰𝗼𝗺
Please indicate your 𝗽𝗿𝗲𝗳𝗲𝗿𝗿𝗲𝗱 𝗿𝗼𝗹𝗲 𝗶𝗻 𝘁𝗵𝗲 𝘀𝘂𝗯𝗷𝗲𝗰𝘁 line (e.g., Technician – Repair & Maintenance / Quality Operations, Associate I, Quality Operations )
SDAS EDM (for Student).pdfRegulatory Advisor
General Summary
The Regulatory Advisor will support the APAC Regulatory Affairs team by ensuring compliance of Michelman’s raw materials with applicable regulations. He/ she will also be responsible for liaising with customers and addressing their regulatory queries.
Primary Responsibilities
Raw Material Compliance:
Interface with the Procurement team and suppliers to collect and maintain regulatory information on raw materials (RM) and maintain the supplier contacts database.
Maintain integrity of Michelman’s RM regulatory information library such that the information is current, complete, accurate and easily retrievable. RM regulatory information includes SDSs, regulatory questionnaires, supplier compliance statements, compliance certificates, letters of guarantee, country of origin, etc.
Identify gaps and inefficiencies in the regulatory documentation program & resolve these with support from the Regulatory and Procurement teams.
Support the RM review process and participate in regulatory projects as assigned.
Interface with the R&D, Quality, EH&S organizations as required.
Chemical Registration & Compliance:
Oversee the pre-registration and registration of chemicals in Korea, Taiwan, and other Asian markets.
Ensure compliance with evolving regional chemical regulations in partnership with suppliers and third-party consultants
Customer Regulatory Requests:
Monitor and stay current on applicable regulations that are relevant to Michelman products.
Respond to internal/external customer requests for regulatory information on Michelman products.
Create and/ or revise customer response templates for new/ updated regulations and maintain database of response templates.
Other:
Provide support in other regulatory tasks and assist on projects as assigned
Critical Competencies, Knowledge, Skills, and Abilities:
General knowledge of chemical regulations relevant to Michelman products and applications in the region
Able to communicate concisely with internal and external customers.
Attention to detail and good record keeping skills.
Able to multi-task and work under time-constraints
Education and Experience:
Diploma or Bachelor of Science (or equivalent) in applicable field.
1-3 years’ experience with chemical regulations relevant to the region in question.
Experience with chemical registration in Korea, Taiwan, and other Asian markets will be an added advantage.
Interested candidates can send their resume to HR executive: Cerlyn
Date posted 14 April 2025
QC Associate
QC Associate
WuXi XDC
Job Summary
We are seeking a motivated and detail-oriented fresh graduate to join our team as an SG QC Scientist. In this entry-level role, you will support a range of testing and quality assurance activities essential to maintaining product quality in the pharmaceutical industry.
Responsibilities
Perform routine raw material testing, IPC, environmental monitoring, water testing, finished product testing, and expertise in HPLC and GC operations and troubleshooting.
Assist in developing and validating microbiological testing methods.
Analyze and interpret test results, ensuring documentation is accurate and thorough.
Support investigations into deviation and help implement corrective actions.
Qualifications
Diploma or above in Pharmacy, Chemistry, Biochemistry, Analytical Chemistry, or a related field.
A basic understanding of the drug development process is a plus.
Familiarity with cGMP compliance principles is beneficial.
Strong attention to detail and a quality-focused mindset.
Career Development
Comprehensive in-house training program (E-learning / OJT / Mentorship)
Dual career tracks — Professional & Managerial Tracks
Opportunity for internal job rotation / Cross-BU transfer / Cross-country assignment
Cross cultural learning
GMP greenfield start-up experience
Interested candidates can send their resume to: S29HR_JDEMB@wuxibiologics.com
Date posted 4 Dec 2024
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