Validation QA Senior
7 days ago
Job Description –Validation QA Job Summary Responsible for overseeing manufacturing, testing, validation and NPI activities, ensuring compliance with internal procedures and regulatory requirements. Responsibilities Provide quality oversight for validation and re-qualification engineering activities, ensuring validation status is consistently maintained for related facilities and systems. Review and approve GMP manufacturing and testing-related documents. Authorize the release of facilities, utilities, equipment, instruments and automation systems for GMP production use. Oversee routine on-site GMP production, NPI related activities and testing, ensuring all GMP processes are executed in strict adherence to company procedures. Contribute to the establishment of an effective quality system and ensure its efficient operation across all GMP functions and processes in daily operations. Manage quality events, including deviations, change controls, CAPA, and lab investigations etc. Support both internal and external audits. Carry out additional tasks as assigned by leadership. Qualifications Bachelor's degree or higher in Biologics, Pharmacy, Pharmaceutical Engineering, Bioengineering, or other relevant fields. 8-10 years of relevant QA experience in Biopharma or Pharmaceuticals industry Familiar with FDA, EMEA, and PICS GMP requirements. Knowledgeable in biological product manufacturing and related quality control requirements. Experience with a new site start-up is preferred. ADC manufacturing and quality management experience is a plus. Proficient in English listening, speaking, reading, and writing. Skilled in Microsoft Word, Excel, PowerPoint, etc. Strong learning ability. Excellent cross-functional communication and collaboration skills. Strong logical thinking and conflict management abilities. Demonstrates strong ownership. #J-18808-Ljbffr
-
Validation QA Senior
15 minutes ago
Singapur, Singapore Wuxixdc Full timeSenior TA Specialist of the Bioconjugate Leader Job Description – Validation QA Job Summary Responsible for overseeing manufacturing, testing, validation and NPI activities, ensuring compliance with internal procedures and regulatory requirements. Responsibilities Provide quality oversight for validation and re-qualification engineering activities,...
-
Validation QA Senior
3 weeks ago
Singapur, Singapore WUXI XDC SINGAPORE PRIVATE LIMITED Full timeJob Description –Validation QA Job Summary Responsible for overseeing manufacturing, testing, validation and NPI activities, ensuring compliance with internal procedures and regulatory requirements. Responsibilities Provide quality oversight for validation and re-qualification engineering activities, ensuring validation status is consistently maintained...
-
Senior Validation QA Lead – GMP Quality
15 minutes ago
Singapur, Singapore Wuxixdc Full timeA leading pharmaceutical company in Singapore is seeking a qualified Senior TA Specialist to oversee manufacturing, testing, and validation activities. Responsible for ensuring compliance with internal procedures and regulatory requirements, the ideal candidate will have a Bachelor's degree and 8-10 years of QA experience in the Biopharma industry....
-
Senior Validation QA — GMP Compliance
7 days ago
Singapur, Singapore WuXi XDC Full timeA global biopharmaceutical company in Singapore is hiring a Validation QA responsible for overseeing manufacturing, testing, and validation activities. The role requires 8-10 years of QA experience in the Biopharma industry, with a strong knowledge of GMP requirements. Candidates must possess a relevant degree and demonstrate excellent communication, logical...
-
Senior Validation QA Lead – Biopharma Compliance
3 weeks ago
Singapur, Singapore WUXI XDC SINGAPORE PRIVATE LIMITED Full timeA leading biopharmaceutical company in Singapore is seeking a Validation QA professional. The successful candidate will be responsible for overseeing quality assurance in manufacturing, testing, and validation processes, ensuring compliance with regulatory standards. You need to have 8-10 years of relevant experience in the biopharma industry and familiarity...
-
Senior QA Lead
14 minutes ago
Singapur, Singapore Hyphen Connect Full timeAbout the Company We are hiring for one of our clients. They are a fast-growing Web3 startup rethinking how digital identity and reputation work online. They’re building privacy-first infrastructure that lets users prove who they are and what they’ve done—without giving up personal data. Backed by strong ecosystem partners and a passionate founding...
-
Senior QA Engineer
3 weeks ago
Singapur, Singapore Robert Walters Full timeAbout the Role Our client is seeking a Senior QA Automation Engineer to design, enhance, and manage our automated testing ecosystem. You will own the automation framework, ensure high‑quality releases through robust testing strategies, and lead the QA team in delivering consistent and reliable results. This role combines hands‑on automation work, team...
-
Senior Compliance
1 week ago
Singapur, Singapore Lonza Biologics Porriño SLU Full timeA leading biopharmaceutical company in Singapore is seeking a Senior Specialist in Compliance for Audit Management within their QA team. This role involves overseeing Quality Assurance activities, ensuring compliance with regulatory standards, and facilitating audits. Candidates should have a bachelor's degree and extensive experience in Validation and...
-
Validation Officer
3 weeks ago
Singapur, Singapore GMP Technologies Full timeValidation Officer (1 year contract) | Pharma MNC | West Job Openings Validation Officer (1 year contract) | Pharma MNC | West About the job Validation Officer (1 year contract) | Pharma MNC | West Purpose: Support validation and quality activities to ensure manufacturing processes, equipment, and systems comply with GMP and regulatory requirements, under...
-
Validation Officer
3 weeks ago
Singapur, Singapore GMP TECHNOLOGIES (S) PTE LTD Full timeJob Purpose To ensure manufacturing facilities, processes, analytical methods, and systems are validated in compliance with cGMP and regulatory requirements , ensuring consistent product quality in accordance with established specifications. Key Responsibilities Participate in and/or lead GMP audits of equipment, systems, processes, and cross-functional...