Biopharma - QA Operations Engineer

Responsible for overseeing manufacturing, testing and validation activities, ensuring compliance with internal procedures and regulatory requirements.Responsibilities:Oversee routine quality control for on-site GMP production and testing, ensuring all GMP activities are executed in strict adherence to company procedures.Contribute to the establishment of an...

QA Consultant – Supplier Qualification & AuditsOther information:Type of contract: fixed-term (6 months)Years of exp: 3-5 yrsLocation: Tuas AreaAre you ready to join a world leader in the exciting and dynamic fields of the Pharmaceutical and Medical Device industries ? PQE Group has been at the forefront of these industries since 1998 , with 40...

**Responsibilities**: - Coordinate with suppliers and verify supplier quality standards are in accordance to the requirements - Track and qualify or disqualify suppliers according to standards - Liaise with suppliers or support the senior supplier qual specialist to support documentation compilation and GMP/GDP review per procedural requirements - Monitor...

**QA Consultant - Supplier Qualification & Audits** **Other information**: Type of contract: fixed-term (6 months) Years of exp: 3-5 yrs Location: Tuas Area Are you ready to join a **world leader**in the exciting and dynamic fields of the **Pharmaceutical and Medical Device industries**? **PQE Group**has been at the forefront of these industries **since...

Provide validation strategy and QA oversight on computer system validation (lab equipment, process equipment, IT, automation system - DeltaV, PEMS, AMS) and equipment/system validation (vessels, fermenter, washing machine, washing cabinet, chambers, Isolator) and SIP - Review and approve validation protocols and reports including validation lifecycle...

**Responsibilities: - Main responsibilities include overseeing batch record review and incoming material quality audit. - Provide quality oversight of GMP manufacturing and manufacturing support, including technical operations, engineering, QC laboratory and supply chain activities. - Review completed incoming material inspection packages, Batch Records,...

Quality Operations Associate must assist site management to oversee the quality system execution on the manufacturing and production areas at all times. The personnel are required to observe, document, discuss, and report quality adverse events related to the manufacturing of the product and are responsible to ensure highest quality and compliance of...

**Responsibilities**: - Support QA Manager to maintain Quality system - Perform internal audit and ensure that quality system is in place at all times. - Initiate root cause analysis and continuous improvement - Maintain and conduct regular reviews of calibration and PM for instruments and equipment - Responsible for the Corrective and Preventive Action...

Company Prestige BioPharma limited Designation Intern (CMC & Bioanalysis Quality) Date Listed 22 Oct 2025 Job Type Entry Level / Junior Executive - Intern/TS Job Period Immediate Start, For At Least 6 Months Profession Healthcare / Pharmaceutical / Sports Industry Manufacturing General / Biomedical / Pharmaceutical Location Name 21 Biopolis...

Senior Process Package Engineers-BioPharma Get AI-powered advice on this job and more exclusive features. Direct message the job poster from Process Engineering Specialists Consulting Manager at PES-Providing PMC/Client Side Rep Solutions to the #LifeSciences and #MissionCritical industry PES is an international services company providing Project Management,...