Home Jobs QC Support Expert
Back to Jobs

QC Support Expert - Job Opportunity at AVENTIS PHARMA MANUFACTURING PTE LTD

Singapore, Singapore
Full-time
Mid-level
Posted: August 8, 2025
On-site
SGD 4,800 - 7,000 per month

Benefits

Comprehensive health and wellbeing benefits package providing extensive medical coverage and family support beyond standard industry offerings
Thoughtfully designed rewards and recognition program that acknowledges individual contributions and amplifies career impact through performance-based incentives
Global career development opportunities including international assignments and cross-functional mobility to accelerate professional growth
Future-focused work environment with cutting-edge technology and innovation-driven projects in life-saving pharmaceutical manufacturing
Supportive team culture emphasizing collaboration and knowledge sharing within a mission-driven organization focused on global health impact

Key Responsibilities

Drive strategic quality control initiatives across global communities of practice, representing site operations and ensuring seamless knowledge transfer between local and international teams
Lead comprehensive validation master planning and equipment lifecycle management, directly impacting manufacturing compliance and regulatory readiness across GXP laboratory operations
Spearhead analytical method performance optimization through trend analysis and continuous improvement initiatives, ensuring product quality standards exceed regulatory expectations
Oversee critical digital transformation projects for QC laboratory systems, managing core model implementation and ensuring data integrity across all quality control processes
Execute strategic equipment lifecycle management programs, including obsolescence risk mitigation and capacity planning to support future manufacturing growth
Lead regulatory compliance initiatives and serve as primary technical expert during inspections, ensuring adherence to global quality standards and company reputation protection
Drive continuous improvement culture through metrics-driven performance monitoring and cross-functional collaboration to enhance operational excellence
Provide technical leadership for major laboratory projects and system implementations, ensuring successful delivery of business-critical quality control capabilities

Requirements

Education

University Degree in relevant scientific discipline; Diploma holders with relevant working experience can be considered

Experience

Ideally 5 years of experience in quality control within pharmaceutical with knowledge of Good Manufacturing Practices (GMP), regulatory requirements and expertise on lab instruments

Required Skills

Strong interpersonal relationships to establish the partnerships necessary for the development of the Quality culture Independent, discipline and assertiveness in decision-making and execution in laboratory activities Good communication skills to advocate QC positions with other functions, including during inspections Continuous improvement mindset Knowledge of regulations and standards of the pharmaceutical industry, Global Quality policies and Data Integrity Requirements Knowledge of the quality systems and associated technologies Ability to analyze complex data and laboratory results to make informed decisions and identify areas for improvement Keen attention to detail to ensure accuracy in testing, reporting, and compliance with regulatory requirements Proficiency in identifying issues and implementing effective solutions to resolve quality control problems Good understanding of good laboratory practices, good documentation practice and data integrity requirements Experienced in analytical method continuous monitoring requirements
Advertisement
Ad Space

Sauge AI Market Intelligence

Industry Trends

The pharmaceutical industry is experiencing unprecedented digital transformation in quality control operations, with increasing adoption of AI-powered analytics, automated testing systems, and integrated LIMS platforms to enhance efficiency and compliance. Companies are investing heavily in digital quality management systems to streamline regulatory submissions and improve real-time monitoring capabilities. Regulatory agencies worldwide are implementing stricter data integrity requirements and enhanced GMP guidelines, creating high demand for professionals who can navigate complex compliance landscapes. The focus on continuous process verification and risk-based approaches to quality management is reshaping traditional QC roles. Post-pandemic supply chain resilience has become critical, driving pharmaceutical companies to establish regional manufacturing hubs and strengthen local quality control capabilities. Singapore's position as a biopharmaceutical hub in Asia-Pacific is attracting significant investment in advanced manufacturing and quality infrastructure. The industry is moving toward predictive quality management using advanced analytics and IoT-enabled laboratory equipment. This trend is creating opportunities for QC professionals who can bridge traditional laboratory practices with modern data science and digital technologies.

Salary Evaluation

The offered salary range of SGD 4,800-7,000 monthly (approximately USD 43,200-63,000 annually) appears competitive for Singapore's pharmaceutical sector, particularly considering the mid-level nature of the role and comprehensive benefits package. This range aligns well with regional market standards for experienced QC professionals in multinational pharmaceutical companies, though it may be slightly below premium ranges offered by some global leaders for similar roles requiring extensive LIMS expertise and regulatory leadership responsibilities.

Role Significance

Typically oversees a cross-functional team of 5-12 laboratory technicians, equipment specialists, and validation personnel, while collaborating extensively with global quality teams, regulatory affairs, and manufacturing operations. The role involves matrix management responsibilities and serves as a key liaison between site operations and corporate quality functions.
This role represents a senior technical specialist position with significant cross-functional influence and regulatory responsibility. While not at director level, the incumbent serves as a subject matter expert with decision-making authority over critical quality control processes, equipment management, and regulatory compliance initiatives. The position requires independent judgment and strategic thinking, indicating substantial professional autonomy and organizational trust.

Key Projects

Implementation of next-generation LIMS systems and digital quality management platforms requiring technical leadership and change management expertise Regulatory readiness initiatives for FDA, EMA, and local health authority inspections, including documentation modernization and compliance gap remediation Equipment modernization and capacity expansion projects supporting new product launches and manufacturing scale-up initiatives Analytical method validation and transfer projects for new therapeutic products and biosimilars entering the manufacturing pipeline

Success Factors

Deep technical expertise in pharmaceutical analytical methods combined with strong regulatory knowledge enables successful navigation of complex compliance requirements and inspection preparedness Exceptional project management and cross-functional collaboration skills are essential for leading digital transformation initiatives and managing multiple stakeholder expectations across global matrix organizations Proactive risk management mindset and attention to detail are critical for identifying potential compliance issues before they impact manufacturing operations or regulatory standing Strong communication and influence skills enable effective advocacy for quality positions during regulatory interactions and cross-functional decision-making processes Continuous learning agility is essential for staying current with evolving regulatory requirements, new analytical technologies, and industry best practices in an rapidly changing pharmaceutical landscape

Market Demand

High demand exists for experienced QC professionals in Singapore's thriving pharmaceutical manufacturing sector, particularly those with expertise in digital laboratory systems, regulatory compliance, and equipment lifecycle management. The combination of technical skills, regulatory knowledge, and leadership capabilities required for this role creates a relatively specialized talent pool, giving candidates significant negotiating power in the current market.

Important Skills

Critical Skills

LIMS (Laboratory Information Management Systems) expertise is absolutely essential as pharmaceutical companies increasingly rely on integrated digital platforms for quality data management, regulatory reporting, and operational efficiency. Proficiency in Labware LIMS specifically mentioned indicates the critical importance of hands-on system administration and optimization capabilities. GMP (Good Manufacturing Practice) knowledge and regulatory compliance expertise are fundamental requirements that directly impact company operations, regulatory standing, and market access. Deep understanding of global regulatory requirements enables effective navigation of complex compliance landscapes and inspection preparedness. Analytical method validation and equipment qualification experience are core technical competencies that ensure product quality, regulatory compliance, and manufacturing reliability. These skills directly impact patient safety and commercial success of pharmaceutical products. Data integrity and documentation practices are increasingly critical as regulatory agencies intensify focus on data reliability and traceability. Strong capabilities in this area protect companies from regulatory action and support sustainable business operations.

Beneficial Skills

Digital transformation and change management skills are becoming increasingly valuable as pharmaceutical companies modernize laboratory operations and implement Industry 4.0 technologies throughout their quality systems Cross-cultural communication and global collaboration abilities enhance effectiveness in matrix organizations and support career advancement in multinational pharmaceutical companies operating across diverse markets Project management certification and leadership development training provide competitive advantages for career progression into management roles and complex initiative leadership responsibilities Statistical analysis and data science capabilities are increasingly important as pharmaceutical companies adopt advanced analytics for predictive quality management and continuous process improvement initiatives

Unique Aspects

The role combines traditional pharmaceutical quality control expertise with cutting-edge digital laboratory management, requiring both deep technical knowledge and modern technology adoption capabilities
Global community of practice participation provides unique exposure to international best practices and cross-cultural collaboration opportunities rare in purely regional pharmaceutical roles
Direct involvement in regulatory inspection support and documentation provides valuable experience in high-stakes compliance environments and regulatory relationship management
Comprehensive equipment lifecycle management responsibility offers unique technical leadership experience spanning from strategic planning through operational execution
Integration of HSE (Health, Safety, Environment) responsibilities with quality oversight creates broader operational perspective and leadership development opportunities

Career Growth

Career progression to management roles typically occurs within 3-5 years for high-performing individuals, with advancement opportunities accelerated by successful project leadership, regulatory expertise demonstration, and cross-functional collaboration success. International assignment opportunities may provide faster progression paths within global pharmaceutical organizations.

Potential Next Roles

Quality Control Manager or Laboratory Manager positions overseeing broader operational responsibilities and larger teams within pharmaceutical manufacturing organizations Regulatory Affairs Manager roles focusing on CMC (Chemistry, Manufacturing, and Controls) submissions and regulatory strategy for product development programs Validation Manager positions leading company-wide validation programs and equipment qualification initiatives across multiple manufacturing sites Technical Operations Manager roles combining quality oversight with manufacturing operations responsibility in integrated pharmaceutical production environments

Company Overview

AVENTIS PHARMA MANUFACTURING PTE LTD

Aventis Pharma Manufacturing represents the manufacturing arm of a major global pharmaceutical organization, operating as part of an integrated network serving 4.3 billion healthcare solutions annually. The company maintains significant manufacturing capabilities in Singapore, supporting both regional distribution and global supply chain requirements for critical therapeutic products.

As part of a leading global pharmaceutical enterprise, Aventis operates with substantial market presence and regulatory credibility across multiple therapeutic areas. The Singapore facility likely serves as a key regional manufacturing hub supporting Asia-Pacific operations while maintaining global quality standards and regulatory compliance.
Singapore operations represent a strategic manufacturing and quality control center serving the rapidly growing Asia-Pacific pharmaceutical market. The location provides access to skilled technical talent, modern infrastructure, and favorable regulatory environment supporting both regional supply and export manufacturing capabilities.
The organization emphasizes mission-driven work culture focused on patient impact and global health outcomes, creating meaningful career purpose for quality professionals. The company appears to prioritize professional development, international collaboration, and continuous improvement, fostering an environment of technical excellence and regulatory leadership.
Advertisement
Ad Space
Apply Now

Data Sources & Analysis Information

Job Listings Data

The job listings displayed on this platform are sourced through BrightData's comprehensive API, ensuring up-to-date and accurate job market information.

Sauge AI Market Intelligence

Our advanced AI system analyzes each job listing to provide valuable insights including:

  • Industry trends and market dynamics
  • Salary estimates and market demand analysis
  • Role significance and career growth potential
  • Critical success factors and key skills
  • Unique aspects of each position

This integration of reliable job data with AI-powered analysis helps provide you with comprehensive insights for making informed career decisions.