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....

QMS DocumentationCAPADeviationChange ControlHandling of Deviations related to procedure and equipment functioning through detailed  investigation tools.   Handling of CAPA based on investigation and proactive actions.   Preparation and Review of Quality Risk Assessment/ Impact Assessment related to  engineering and cross functional teams....

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....

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...

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...

Non- QM Underwriter The Underwriter is responsible for assessing the risk of a borrower being able to repay their mortgage to the lender, decision the loan adhering to the regulatory guidelines and company policy & procedures. Job Duties: Underwrite and decision Non-QM loans to comply with all applicable regulations. Should be able to underwrite all Tiers,...

Non- QM Underwriter The Underwriter is responsible for assessing the risk of a borrower being able to repay their mortgage to the lender, decision the loan adhering to the regulatory guidelines and company policy & procedures. Job Duties: Underwrite and decision Non-QM loans to comply with all applicable regulations. Should be able to underwrite all Tiers,...