116 Job openings found

Major Responsibilities: Ø  Quality Management System Implementation and Modification control. Ø  Document Control. Ø  Approval for batch release. Ø  Review and approval of Qualification Document. Ø  Review and approval of Calibration and Validation document. Ø  Planning, execution and compliance of both internal and external audits. Ø  Preparation of audit compliance report.   Job description Minor Responsibilities:   Ø  Review and approval of SMF, VMP and Quality manual. Ø  Review and approval of ...

Position:        QA Officer Location:        Vapi Experience:    2 - 5 Years Industries:     Pharma   Responsibilities:         Documentation & Record Review: Review specifications, sampling instructions, test methods, and analytical reports. Review and approval of Batch Manufacturing Record (BMR), Batch Packing Record (BPR), Master Formula Record (MFR), and Equipment Qualification Records. Review completed Batch ...

Position:         Sr. Officer/Executive - QC Location:        Vapi Experience:     3 - 5 Years Industries:      Pharma  Responsibilities: Individually handling department & manpower. Strong leadership skills to guide, supervise work activities, and help team members develop their skills. Work allocation / Planning and Review of documents. Preparation of SOP, Specification, Standard Test Procedures (STP), ...

Role & responsibilities 1. Handling Deviations / Change Control / CAPA / Incidence Reports / Training Records. 2. Handling MFR / BMR / BPR preparation and Review 3. Handling preparation of SOPs / Protocols / QMS. 4. Handling Documentation Control. 5.. Handling of SMF /VMP / Qualification 6. Should be able to handle audit compliance and ...

Job Description:1. Analysis1.1  Raw material / packing material analysis at the time of incoming1.2  In process analysis time to time1.3  Finished product analysis and compare to require specification compliance2. Manage QC lab2.1  Method validation – Set test methods as pharmacopoeia and GMP requirement.2.2  Instrument calibration: Prepare calibration Schedule and calibration ...

Job Description:1. Analysis1.1  Raw material / packing material analysis at the time of incoming1.2  In process analysis time to time1.3  Finished product analysis and compare to require specification compliance2. Manage QC lab2.1  Method validation – Set test methods as pharmacopoeia and GMP requirement.2.2  Instrument calibration: Prepare calibration Schedule and calibration ...

Job Description:1. Analysis1.1  Raw material / packing material analysis at the time of incoming1.2  In process analysis time to time1.3  Finished product analysis and compare to require specification compliance2. Manage QC lab2.1  Method validation – Set test methods as pharmacopoeia and GMP requirement.2.2  Instrument calibration: Prepare calibration Schedule and calibration ...

Hiring for Quality Executive in Glucose & Starch Powder Manufacturing Industry Position: Quality Executive 02 Education – BSC Chemistry Experience:  Min 3 Years in Quality Assurance, Documentation & Audit Skill: COPA, Audit, etc Job responsibility: Handling of Change Control. Data compilation of annual product review report. Batch Release Co-ordination and participation in validation activities. Logbook issuance and retrieval. Participation in line ...

Position:          Production Officer Location:         Vapi Experience:      5 - 8 Years Industries:       Pharma - API Responsibilities. Handling of QAMS, DMS activities Prepare SOP, BMR, ECR and all related docs. as per CGMP TO maintain & review all document like change control, Incident with compliance report Involvement in the ...

Good Knowledge of USFDA/ EDQM /ANVISA / and all other regulatory & CGMP awareness. Strategic oversight and leadership: Develop and implement the company's quality management system (QMS) and strategy, aligning it with business objectives. This includes overseeing all aspects of quality operations and managing the QA and QC departments. Regulatory compliance: Ensure ...