
Senior Software Engineer: Leading Expertise in Computerized System Validation
4 days ago
As a senior software engineer, you will contribute to the development of cutting-edge Life Science projects for esteemed clients. Your expertise in computerized system validation and compliance with GXP standards will be instrumental in ensuring seamless project execution.
">Required Skills and Qualifications:">- Proven experience in software development and validation, with a strong understanding of GXP regulations
- Excellent problem-solving skills and ability to work independently
- Strong communication and collaboration skills, with the ability to work effectively in cross-functional teams
We offer a competitive compensation package, including opportunities for professional growth and development. Our dynamic work environment is ideal for individuals who thrive in fast-paced settings and are passionate about delivering exceptional results.
">Others:">You will have the opportunity to lead and contribute to various projects, collaborating with a talented team of professionals. We value diversity and promote a culture of inclusion, encouraging our employees to share their ideas and perspectives.
"],-
Computerized System Validation
2 days ago
Singapore VALINA SERVICES PTE. LTD. Full timeAs a CSV Engineer, you will be working for our clients in the respect of the applicable regulations and quality procedures. Main assignments: - To be responsible for preparing and/or executing validation activities and documentation for Computerized Systems, under respected regulations or guidelines: 21 CFR Part 11, 21 CFR Part 820, ISO 13485, GAMP 5,...
-
Computer System Validation Consultant
3 days ago
Singapore PHARMENG TECHNOLOGY PTE. LTD. Full time**Responsibilities**: - Create and refine validation protocols for GxP critical reports, focusing on Computerized Equipment Validation within the QC lab. - Configure static Master Data for validated/GMP-compliant LabWare LIMS (version 6), specifically emphasizing Computerized Equipment. - Actively participate in executing, reviewing, and approving...
-
Computer System Validation Consultant
1 week ago
Singapore PharmEng Technology Pte Ltd Full time $90,000 - $120,000 per year**Responsibilities**: - Create and refine validation protocols for GxP critical reports, focusing on Computerized Equipment Validation within the QC lab. - Configure static Master Data for validated/GMP-compliant LabWare LIMS (version 6), specifically emphasizing Computerized Equipment. - Actively participate in executing, reviewing, and approving...
-
Validation Professional
2 weeks ago
Singapore beBeeValidation Full time $80,000 - $120,000Job Title: Validation Professional - Software System CheckerAbout the Role:We are seeking an experienced Validation Contractor to join our team in the QC Laboratory. The successful candidate will be responsible for planning and executing validation activities associated with software system upgrades and decommissioning of legacy systems in a GMP-regulated...
-
Analytical System Validator
4 days ago
Singapore beBeeValidation Full time $90,000 - $120,000Join us in shaping the future of pharmaceutical solutions.We are seeking a skilled Validation Specialist to support key validation activities within the Quality Control (QC) Laboratory. This role involves both software upgrade validation and the decommissioning of legacy computerized systems in a Good Manufacturing Practices (GMP)-regulated laboratory...
-
QA Validation Engineer
2 days ago
Singapore No deviation Pte Ltd Full timeAbout Nd Incorporated in 2007, we are a patient-centric solution provider for the pharmaceutical industry. We are experts in engineering consultancy, commissioning, qualification and validation services, and regulatory quality/compliance in Asia and Europe. We offer personalized focused solutions for the pharmaceutical industry in engineering consultancy...
-
Validation Engineer
2 weeks ago
Singapore ANTER CONSULTING PTE. LTD. Full time**Responsibilities**: - Develop and execute Commissioning, Qualification, and Validation (CQV) protocols (IQ/OQ/PQ) for pharmaceutical manufacturing facilities, equipment, and systems. - Collaborate with project teams to ensure compliance with regulatory standards (e.g., FDA, EMA, GMP). - Perform risk assessments, gap analysis, and prepare validation...
-
Pharmaceutical Validation Engineer
4 days ago
Singapore beBeeQuality Full time $90,000 - $120,000Job OverviewWe are seeking a skilled Validation Specialist to support key validation activities within our Quality Control (QC) Laboratory. This role involves both software upgrade validation and the decommissioning of legacy computerized systems in a Good Manufacturing Practice (GMP)-regulated environment.Key Responsibilities:Plan and execute validation...
-
QC CSV Validation Engineer
2 weeks ago
Singapore No deviation Full timeOverview Join to apply for the QC CSV Validation Engineer role at No deviation . This range is provided by No deviation. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more. Base pay range About No Deviation At No deviation, we are dedicated to delivering patient-centric solutions that revolutionize the...
-
Qc Csv Validation Engineer
4 days ago
Singapore No deviation Pte Ltd Full time**About No deviation** At No deviation, we are dedicated to delivering patient-centric solutions that revolutionize the pharmaceutical landscape. As a dynamic expert in engineering consultancy, Commissioning Qualification Validation (CQV), and Quality, Compliance, and Regulatory services, we are looking for individuals who are excited to contribute to...