Supply Chain Manager

SMARTT PRECISION MFG PTE. LTD.; Singapore; On-site; SGD 60,000 - 80,000; Full time

Job summary

A leading manufacturing company in Singapore is seeking a QC S&T Analyst for a contract role. You will support laboratory operations and ensure compliance with regulatory requirements. The ideal candidate has a degree in a science-related discipline and experience in quality control within the pharmaceutical industry. This role offers a competitive salary of $3,000 - $5,000 a month and the opportunity to extend the contract based on performance.

Qualifications

• Minimum 1 - 3 years of pharmaceutical experience in a Quality Control Function.
• Experienced in Regulatory/Pharmaceutical requirements.
• Basic GMP knowledge/Experience on QC Lab Equipment and Method transfer.

Responsibilities

• Supports laboratory operation and infrastructure.
• Participates in managing laboratory equipment and computerized systems.
• Supports preparation and participates in internal/external audits.

Skills

Analytical thinking

Good communication skills

Ability to work in cross-functional teams

Motivated and independent

Education

University Degree in Science related discipline

Tools

Empower

LIMS

SAP

Job description

Overview

• Author and execute qualification and equipment qualification documentation / method transfer (e.g.: Reports, Protocol, change control, related quality documents…)
• Knowledge of clinical trials - Knowledge of clinical trial conduct, and skill in applying applicable clinical research regulatory requirements
• 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…
• Conduct daily inspection on receiving raw materials, production, deliveries with regulatory requirement including Halal.
• Assist in ensuring the products are traceable.
• Functional responsibilities include ensuring that product was made according to the procedure and regulatory requirements as well as accurate and timely…
• Perform data profiling and quality checks to ensure compliance with enterprise and regulatory standards.
• We provide risk transformation, data and modeling…

QC S&T Analyst (Pharma/Biotech) - job post

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Job details

Pay

$3,000 - $5,000 a month

Job type

Contract

Location

Based in Tuas

Full job description

Responsibilities:

• Supports team task to support laboratory operation and infrastructure in the areas of examples: Equipment, Data Systems, Method) needs
• Participates in the management of laboratory equipment and computerized systems in QC laboratory to ensure business continuity and system data maintenance e.g., Empower, LIMS, SAP and equipment maintenance/calibration is in a state of compliance
• Participates in method technology transfer and laboratory equipment technological refresh/introduction activities into QC Laboratory within project timeline
• Participates in QC laboratory long range planning to ensure laboratory infrastructure needs is secured and Data integrity plan is in place to support business and laboratory compliance
• Author and execute qualification and equipment qualification documentation / method transfer (E.g.: Reports, Protocol, change control, related quality documents or procedures) are in cGMP compliance to corporate/site or regulatory requirements
• Supports and ensure timely escalation/handling of lab events or related quality actions. (E.g.: NCR, Lab Investigation, CAPA)
• Supports preparation and participate in internal/external audit, audit responses, to enable a successful audit outcome
• Participate in EHS, Business Compliance, cGMP and all other compliance-related matters, where applicable. Lead/supports CI initiatives to enable laboratory performance metrics
• Carry out any other task as assigned by Line manager

About You:

• University Degree in Science related discipline (e.g.: Chemistry, biology, pharmaceutical sciences, or equivalent experiences)
• Minimum 1 - 3 years of pharmaceutical experience in a Quality Control Function
• Experienced in Regulatory/ Pharmaceutical requirements
• Analytical thinking with basic problem solving and writing skills
• Motivated and independent
• Basic GMP knowledge/Experience on QC Lab Equipment and Method transfer
• Good communication skills and Strong ability to work cross functional teams
• Ability to work towards timeline
• Based in Tuas

Job Type: Contract

Contract length: 12 months. Option to extend/convert subject to performance review.