244 Oot Jobs - Page 6

Unison Pharmaceuticals is seeking candidates for the role of Engineering QMS - Lead for our EU Approved Facility, Unit III Company : Unison Pharmaceuticals Ltd. Location : Moraiya, Ahmedabad - Unit III Designation : Upto Manager Job Role/Position: Engineering QMS - Lead Experience Required : 1015 Years (Pharma Industry OSD preferred) Key Responsibilities Preparation, review, and implementation of SOPs in line with GMP compliance . Review and control of daily operation logbooks and engineering documentation . Operation & Maintenance knowledge of utility equipment, HVAC, and water systems . Handling breakdown maintenance of utility and process equipment. Initiation, handling, and documentation...

Role & responsibilities To Handle batch release and stability testing of various biological products like GCSF, EPO, Vaccines Calibration and Performance Verification of Instruments Management of Reference Standard Review of the analytical data Management of Deviation, OOS & OOT, CAPA and Change control Validation of excel sheet Department training coordinator Management of Analyst Qualification Preparation of GMP documents such as Standard Test Procedure, Standard Operation Procedure, Performance verification protocol, Method Validation report, Data Recording Sheet, Specifications Quality softwares i.e. TIMS, LIMS

Skill Required 3 to 4 year Pharma background experience for FP , In process and PV samples. Roles and Responsibilites To analyze the samples of in process/FP/Process validation as per work allotted by section in charge/Designee. Preparation of report and submission of reports along with raw data to section in charge/Designee within time. Immediate reporting of any odd observation, incident, OOT and OOS result during analysis to section in charge/Designee. Qualification Required M.sc/B.pharm Relevant skills / Industry experience Should have 2 to 4 year experience. Relevant professional / Educational background M.sc/B.pharm

Roles and Responsibilites 1.In process Quality Assurance activity in Production and warehouse area 2.Provide line clearance as per SOP 3.Monitoring and QA rounds in production and Warehouse 4.Sample verification against TRF / BPCR 5.Carry out Semi-finished / finished product sampling for release, stability study and control samples 6.To send samples along with TRF to Quality control laboratory 7.Participate in media fill, process validation, cleaning validation activities as per requirement 8.Timely communication and co-ordination with all the stake holders 9.Participation in Change control, Deviation & Investigations as per requirement 10.Preparation / review of documents like; SOPs, risk a...

Excellent job opportunity for QA - AQA Specialist in Unison Pharmaceuticals Pvt Ltd, Moraiya, Ahmedabad About us: Unison Pharmaceuticals Private Limited (Formerly known as Unison Pharmaceuticals) was established in 1981 with a vision of providing quality and affordable medicines across the nation. With more than 4 decades of medical service to society, Unison is today one of the fastest-growing companies in Gujarat State. In addition to this, the company is ranked 82 among the top companies of India (Rupee wise sales) MAT March 2020. This makes Unison a distinguished company across the pharma industry. You are invited to join one of India's fastest growing pharma companies in India!! Experie...

This position is responsible for ensuring compliance with Herbalife requirements and adherence to global procedures in Quality assurance and control during the manufacturing, storage, and transportation of Herbalife raw and packing materials from RM Vendor to Contract manufacturing location in India. The role involves supervising Supplier Quality Assurance for Herbalife raw materials and Packing Material in Bangalore. Key responsibilities include monitoring vendor processes to ensure compliance with Herbalife Quality procedure requirements, conducting audits to maintain quality and hygiene standards, communicating with vendors for any changes impacting quality, handling rejections/complaints...

Dear All, We are conducting Walk-In Interview on 29th August 2025(Friday) for Quality Assurance and Quality Control( Formulations ) departments. Quality Assurance: Validations - 4-5 Years of experience in Process and Cleaning validations and equipment qualifications Quality Control: IPFP - 4-5 Years of experience in HPLC, GC, UV, Dissolution and RS. Stability - 4-6 Years of experience in Dissolution, GC, UV and Sample management Raw Materials - 2-3 Years of experience in sampling of Raw and Packing materials Analytical Method Validations - 3-5 Years of experience in Method validations, GC and Dissolution instruments GLP - 2-4 Years of experience in management of working and reference standar...

We are looking for QC - Manager profile with 15-20 years' experience in Quality Control of API Pharma. Specifically looking for candidates from Vizag or nearby locations. Job Description Responsible for all QC activities at OWN manufacturing site located at Vizag. Ensure timely completion of vendor samples, RM, In-process, cleaning samples, stability samples, FP analysis and miscellaneous samples. Plan and perform QC work such that production-related activities continue uninterrupted Identify training needs of QC personnel and provide job-related training to meet the GLP needs and skill upgradation. Maintain analytical instruments with suitable calibrations, preventive maintenance and suppor...

Tracking of all orders from the CFA / Warehouse Monitoring shipments to outstation locations and updating ETD. Maintaining a tracker for PODs and uploading PODs on SAP> Maintaining a working relationship with all E Comm/MT warehouse personal and Supply Chain co-ordinators at HO. Ensuring sufficient fleet/manpower at CFA to ensure appointments are met. Flagging any concerns at the CFA well in advance. Monitor stocks and flag potential OOS situations well in advance. Ensure FIFO at CFA.

Position : Executive Engineering QMS Qualification : BE Mechanical/ Electrical/ Instrumentation or B pharma preferably BE Experience : 6-7 years experience in handling engineering department GMP documentation activities and supporting engineering function as SME in QMS documentation Responsibilities : 1.Implementation of quality assurance standards, processes, controls and cGMP in warehouse. 2. Preparation of SOPs and ensure effective implementation. 3. should be well versed with deviation management SOP 4. Should be well versed with change control and CAPA management related to engineering department 5. Should be familiar with documentation like DQ, IQ, OQ and PQ. 6. To ensure that training...

Required QC Analyst exp 4-5 year, Finish Good HPLC salary -Hike on current salary Male only Location - Baddi Call at -9818040604

Ipca Laboratories Ltd, Wardha is as API plant we are looking for Production Manager with below mentioned JD To ensure weekly / monthly production schedules as per plans. Monitor shift wise production and provide feedback to HOD on daily basis. To ensure smooth running of the plant, co-ordinate effective with maintenance department for any break down, utility, services etc. To co-ordinates with Q.C., Store, R&D, Inprocess lab for production related jobs. To ensure that production norms as per laid down procedure are achieved. Through optimum use of resources & report to HOD about the area requiring improvement. To prepare daily logbook containing functioning of the plant in all respects, cove...

Led the qualification and validation of HVAC systems to ensure compliance with regulatory standards and maintain optimal environmental conditions for pharmaceutical manufacturing. Required Candidate profile Monitor the qualification process for water systems (e.g., purified water, WFI). Conducted performance testing, system validation, and routine monitoring to ensure the water quality meets.

Role & responsibilities Analytical QA Review the analytical documents which are generated after analysis of Drug Products. Preparation and Review of all Departmental SOP's for cGMP Compliance. Compilation and Review of the Batch Records, Certificate of Analysis, Analytical Protocol, etc which are required for release of Batches. Review and Approve SOPs, Change Controls, Deviations, Annual Product Quality Reviews, Incident Reports, Out of Calibrations, Out of Specifications, Out of Trends, Approve the Investigation Reports. Market Compliant, & manage Stability Samples etc. Review of Regulatory Requirements and its Compliance. Periodic review of all Quality functions and Procedure for appropri...

Hiring For QC AM For Formulation Co in Khambhat Location Qualification: BSc / MSc / B.Ph / M.Pharm Exp : 8 to 18 Years CTC: Good Salary Experience in Formulation Is Must Send CV on sdpbharuch@gmail.com with Subject: QC Khambhat Share with Friends Required Candidate profile SDP HR SOLUTION 611, Golden Square, Beside DMART, Near ABC Circle, Bholav, Bharuch - 392001 Free Jobs !!1 Share with Your Friends & Colleagues!!!

Job Title:- KMIL- Wholesale Banking- Risk Monitoring Analyst Grade:- M4/M5 Location:- Mumbai Track financial and project performance covenant: Monitoring financial and project performance against predefined convenants. Identify deviations and promptly communicate findings to relevant stakeholders. Project performance analysis: Conduct through analysis of project performance metrics. Provide insights and recommendations to mitigate risks. Track Compliances to sanctions conditions: Moniotor compliance with sanctions conditions imposed on credit facilities. Take proactive measures to address any non- compliance issue Site Visit: Conduct on site visit to assess the progress and status of project...

Designation - Manager - Quality Assurance Company - Leading Pharma Raw Material Mfg. Company Job Location - Dahej, Bharuch Qualification - B.Sc. / M.Sc. / B.E.- Chemical / B.Pharm Experience - Min. 8yrs. and above share with your friends Required Candidate profile company will provide transportation facility from Bharuch. Responsible for handling QA / GMP Related documentation QMS, Audit Preparation, Vendor Questionnaire, Market Compliant & Customer Compliance

Roles and Responsibilities Conduct analytical testing of finished products, including dissolution, UV-Vis, KF, FTIR, and GLP compliance. Develop and validate analytical methods for solid oral OSD products using techniques such as GC, HPLC, and UV spectroscopy. Perform method transfer and validation activities to ensure accuracy and reliability of test results. Collaborate with cross-functional teams to resolve OOS/OOT issues and implement corrective actions. Maintain accurate records of laboratory data, reports, and documentation in accordance with cGMP guidelines.

QA( AQA) To review the Audit Trial Report Review of SOPs pertaining to Quality Control (Chemical & Microbiology) Review of Stability protocols & Report Responsible for investigation and closure of OOL, OOT & OOS. To review the Equipment & usage log books of QC& microbiology. To review the calibration of QC & microbiology equipments Follow up for the closure of deviations/ change controls/CAPAs pertaining to QC area. To log OOS, OOT and OOLs and update the relevant databases and logbooks To Review the analytical method validation/other study Protocols, ROA and Reports Verification of Media Fill vials. Review of EMP, Water trends, specifications and testing Review of STPs & GTP materials/ Prod...

The primary purpose of this position is to ensure compliance with Herbalife requirements and adherence to HLF's global procedures in Quality assurance and control during the manufacturing and storage of Herbalife products at the Contract manufacturing location in India. As the Site QA lead at the CM (Indore) for Herbalife, you will be responsible for various QA activities on-site, including but not limited to: - Monitoring processes on set frequencies to ascertain compliance with Herbalife Quality procedure requirements - Conducting periodic audits of the facility and operations associated with Herbalife to help CM meet and improve quality and hygiene standards - Communicating with CM regula...

The position of Site Quality Assurance Lead at the Contract Manufacturing location in India for Herbalife involves ensuring compliance with Herbalife requirements and global procedures in Quality assurance and control during the manufacturing and storage of Herbalife products. The primary responsibility includes monitoring processes, conducting audits, and communicating with the Contract Manufacturer (CM) for quality improvement. The role also involves handling complaint resolution, conducting Root Cause Analysis (RCA), and implementing Corrective and Preventive Actions (CAPA). Regular training and coordination with the CM for dispatch approvals and validation of new products are essential t...

As an Analyst, you will be required to possess knowledge of various analytical instruments such as HPLC, UV, FTIR, GC, Polarimeter, KF, Auto titrator, and more. You will be responsible for the QCC-QMS Section, overseeing test procedures, handling OOS, OOAL, Deviation, Change Control Note, Incident, and preparing Investigation Reports. Additionally, you will review instrument logbooks, raw data of materials, in-process, finished products, and water analysis. Your skills and proficiency should include expertise in Analytical Instrumentation Handling, Good Laboratory Practices (GLP) & Documentation Accuracy, Data Integrity & Documentation, Regulatory Compliance, SOP Preparation & Revision, Inte...

As a Quality Control Technician III at TAPI, you will be an integral part of the leading international supplier of active pharmaceutical ingredients (APIs). TAPI boasts the industry's broadest portfolio, which includes over 350 API products. With a rich history spanning over 80 years, we are recognized as one of the most trusted API suppliers globally, catering to 80 PERCENT of the top 50 pharmaceutical companies. At TAPI, our commitment to excellence is driven by our experience, expertise, cutting-edge technologies, and unwavering dedication to exceptional customer service. Your primary responsibilities will include maintaining 24/7 audit readiness, possessing expertise in Wet Chemistry, an...

The responsibilities for this role include reviewing raw and finished product specifications, ensuring good laboratory practices in the Quality Control department, reviewing audit trial records, analyzing analytical records, reviewing instrument calibration and equipment qualification documents related to QC, validating analytical methods, verifying samples, handling reserve sample room, ensuring analyst qualification, reviewing working standards, managing deviations, change control, OOT, OOS, laboratory incidents, investigations, and annual trends, coordinating CAPA implementation verification and closure, reviewing instrument and equipment preventive maintenance, monitoring and recording t...

Role & responsibilities Roles and Responsibilities 1. Stability study documents compilation and its management. 2. Stability charging, withdrawal, trend and stability report preparation. 3. Review of DRS, Log book entry and related documentation to be make online. 4. Preparation of release COA and compilation of all related documents. 5. Provide training to new person or existing person for QC testing. 6. Preparation and review of Specification/STP/SOP/DRS/protocol/data recording sheet for QC documentation on routine basis. 7. Instrument and Equipment calibration activity. 8. QMS (change control/deviation/Incident/LIR etc.) related Activities. Desired Candidate Profile -Male Candidate Requir...