Deutsche Hausverwaltung Plus

Oversee and manage QMS processes including Deviation Management CAPA Change Control Risk Management and Product Quality Reviews (PQRs).Lead Quality investigations and root cause analysis for process deviations and quality events.Ensure timely closure of audit observations and effectiv المزيد...

The Production Trainee/Apprentice will be responsible for assisting in various production activities under the guidance of senior operators and supervisors.Key duties include learning equipment operation following GMP guidelines maintaining production records and ensuring adherence to المزيد...

Manufacturing Process: Assist in the granulation compression coating filling and packaging of pharmaceutical formulations. Machine Handling: Support in operating cleaning and maintaining manufacturing equipment such as RMG FBD Compression Blenders Coating Machines and Capsule Fillers المزيد...

check the proper status labeling during production.2. To check the preventive maintenance of equipment and calibration of instruments in production department.3. To issue additional material from warehouse department.4. To check that equipment instrument are clean and operate as per المزيد...

In process activity in production and packing areaPerform Line clearances activities as per defined instruction in SOPContinuous monitoring of GMP and cGMP compliance at shop floorPerform calibration of IPQA instrument on time.Issuance review and control the change management activiti المزيد...

Analytical Method Validation (AMV): Perform method validation verification and transfer for pharmaceutical products as per ICH guidelines. Instrument Handling & Calibration: Operate and maintain HPLC GC UV FTIR and dissolution apparatus ensuring compliance with calibration and sy المزيد...

Critical Operator1. Responsible for performing packing operations as per respective BPR.2. Responsible for per forming the calibration of equipment like weighing balances as per schedule and to maintain records for it.3. To label and arrange the in process materials finish product as المزيد...

Role Objective: Collaborate with Site Leadership Team support and participate in effective implementation and sustenance of PACT (Productivity Alignment Compliance Transparency) program. Contribute in fostering a culture of openness collaboration and ownership under PACT guidelines to المزيد...

OOS OOT & Deviation Investigation: Conduct detailed investigations for Out of Specification (OOS) Out of Trend (OOT) and deviations identifying root causes and corrective actions. CAPA Implementation: Develop and implement Corrective and Preventive Actions (CAPA) to prevent recur المزيد...

Analytical Method Validation (AMV): Perform method validation verification and transfer for pharmaceutical products as per ICH guidelines. Instrument Handling & Calibration: Operate and maintain HPLC GC UV FTIR and dissolution apparatus ensuring compliance with calibration and sy المزيد...

InProcess Quality Monitoring: Conduct realtime IPQA checks in granulation compression coating and packaging areas to ensure product quality. Process Validation & Sampling: Perform inprocess sampling environmental monitoring and validation activities to ensure regulatory complianc المزيد...

IPQA Monitoring: Conduct inprocess checks during compounding filtration filling lyophilization and sealing to ensure sterility assurance. Environmental Monitoring: Perform viable and nonviable particle monitoring gowning qualification and cleanroom validation as per SOPs. Process Val المزيد...

Documentation Management: Maintain review and update SOPs protocols test reports and validation documents as per GMP GLP and data integrity guidelines. Regulatory Compliance: Ensure all microbiology documentation meets the requirements of USFDA MHRA WHO and EUGMP regulatory agencies. المزيد...

Conduct Analytical Testing: Perform routine analytical tests including HPLC UV and titrations on raw materials inprocess samples and finished products ensuring adherence to standard operating procedures.Follow GMP & GLP Guidelines: Ensure compliance with Good Manufacturing Practic المزيد...

Sterile Packing Operations: Supervise vial ampoule and prefilled syringe packing ensuring smooth operations and adherence to packaging protocols. Regulatory Compliance: Ensure compliance with GMP USFDA MHRA WHO and EUGMP guidelines maintaining sterility assurance during packaging. Pr المزيد...

InProcess Quality Monitoring: Conduct realtime IPQA checks in granulation compression coating and packaging areas to ensure product quality. Process Validation & Sampling: Perform inprocess sampling environmental monitoring and validation activities to ensure regulatory complianc المزيد...

InProcess Monitoring: Assist in monitoring critical process steps during manufacturing and packaging to ensure adherence to batch manufacturing records (BMRs/BPRs). Line Clearance & Verification: Support line clearance activities for dispensing manufacturing and packaging ensurin المزيد...

Machine Operation: Operate and monitor BQS blister packing machines ensuring smooth and efficient production. Setup & Changeover: Perform machine setup format changeover and adjustments to accommodate different product specifications. InProcess Quality Checks: Conduct leak test المزيد...

1. To coordinate and cooperate with DDRL DDRLTT SCM PPC ProductionQA QC and other related departments for smooth technology receiving & transfer to production and troubleshooting of Bio/Scale up/Assessment/Exhibit/PPQ Batches.2. To evaluate Critical Quality Attribute (CQA) & C المزيد...

Provide Market Feedback to Managers Marketing Team (P)Attend induction CTP Cycle meetings to understand campaigns and other processesEnsure effective delivery of communication/messages inside the clinicPrepare Campaign customers list asper the strategy.Prepare SVL of right Drs STP MTP المزيد...