Qms -pharma Documentation

Post : Officer / Sr. Executive / Assi. Manager Experience : Min 2 Years / 6 Years/ 8 years. Qualification **:BSc / MSc (Microbiology / Biochemistry / Biotechnology)Or** **B Pharma**. Job Description: 1. Preparation and review of QA SOPs, 2. Preparation and review of other QA related documents such as Stability Protocol, VMP, SMF. 3. Preparation of...

Post : Executive Experience : Min 4 Years(**(Pharma Background)** (Experience in validation + Qualification of autoclave, LAF, HVAC) Job Description: 1. Review of SOP and other relevant documents of Engineering and HR. 2. Preparation and Review of Qualification & Validation Document of entire plant (PR, WH, EN,QC) 3. Execution of Qualification and...

Post : Executive Experience : Min. 4 Years **(Pharma - QC/Microbiology Background)** **Qualification : BSc / MSc (Microbiology / Biochemistry / Biotechnology)Or** **B Pharma.** **Job Description**: 1. Review of SOP, STPs, Specification, Analytical method Validation Protocol and reports and other relevant documents of QC (Chemical & Microbiology) 2....

Officer Level Experience : Min 2 Years ( **(Pharma Injectable Background).** **Qualification : BSc / MSc (Microbiology / Biochemistry / Biotechnology)** **Job Description**: 1. Review of SOPs & other relevant documents of Production, Packing and Warehouse department. 2. Review of Master as well as executed batch documents of Production and packing. 3....

Role & responsibilitiesHandling of QMS for drug substance of bacterial products. Should have good process understanding of upstream and downstream unit operations.Experience to handle QMS documents such as deviation, Change control, Investigations through Track-wise software.Should have experience on audit compliance, Regulatory guidelines and knowledge on...

QMS Implementation & MaintenanceEnsure compliance with ISO 9001:2015 requirements across all departments.Assist in preparing, reviewing, and controlling QMS documentation (SOPs, Work Instructions, Formats, Manuals).Coordinate Internal Audits, Management Review Meetings (MRM), and facilitate closure of NCs (non-conformities).Monitor effectiveness of processes...

We are looking for a QMS Engineer with knowledge of IATF 16949, ISO 9001, PPAP, FMEA, Control Plan, MSA, SPC, and related documentation.Responsibilities:Maintain and implement QMS as per IATF standardsPrepare and control quality documents (PPAP, FMEA, CP, etc.)Coordinate audits and ensure complianceSupport continual improvement...

Responsibilities:Ensure compliance with QMS protocols in production and packing areas.Review and maintain batch records, SOPs, and documentation as per USFDA standards.Support deviation investigations, CAPA, and change control processes.Coordinate with cross-functional teams to uphold GMP and regulatory requirements.Key Skills:Knowledge of QMS and GMP in...

About Company : Our client is a trusted global innovator of IT and business services. They help clients transform through consulting, industry solutions, business process services, digital & IT modernization and managed services. Our client enables them, as well as society, to move confidently into the digital future. We are committed to our clients...

Department: Production QMS Designation: Officer to Executive Experience: 3 to 6 Years Location: Bavla, Ahmedabad Key Responsibilities: ✅ Injectable Production Activities Carry out and monitor day-to-day manufacturing of injectable products (aseptic or terminal sterilized). Follow batch manufacturing records (BMRs) and SOPs during production. Coordinate...