700 Oos Jobs - Page 5

The ideal candidate brings 1-6 Years and a strong record of GMP/cGMP compliance within regulated pharma, chemicals or biotech environments Key responsibilities include ownership of day-to-day operations, documentation integrity, SOP creation/review, deviation/OOS handling, CAPA and change control management, audit readiness, cross-functional coordination with Production, QC, Engineering and Supply Chain, and proactive risk assessment to protect product quality and patient safety The role requires hands-on problem solving, stakeholder communication, coaching junior staff, and contribution to continuous improvement (5S/Lean/Kaizen) Lead microbiology practices including EM, MLT, sterility assur...

Chief Manager Township Administration (MP 25/13) based in Narmada, Gujarat. The ideal candidate brings 15-20 years and a strong record of GMP/cGMP compliance within regulated pharma, chemicals or biotech environments. Key responsibilities include ownership of day-to-day operations, documentation integrity, SOP creation/review, deviation/OOS handling, CAPA and change control management, audit readiness, cross-functional coordination with Production, QC, Engineering and Supply Chain, and proactive risk assessment to protect product quality and patient safety. The role requires hands-on problem solving, stakeholder communication, coaching junior staff, and contribution to continuous improvement...

HPLC Operator (01 Position) based in Vapi, Gujarat. The ideal candidate brings 5 to 10 years and a strong record of GMP/cGMP compliance within regulated pharma, chemicals or biotech environments. Key responsibilities include ownership of day-to-day operations, documentation integrity, SOP creation/review, deviation/OOS handling, CAPA and change control management, audit readiness, cross-functional coordination with Production, QC, Engineering and Supply Chain, and proactive risk assessment to protect product quality and patient safety. The role requires hands-on problem solving, stakeholder communication, coaching junior staff, and contribution to continuous improvement (5S/Lean/Kaizen). Ope...

Role & responsibilities: Preparation and Review of documents such as SOP, BMR, BPR, Analytical Reports, SMF, VMP, APQR, MFR validation protocols/report and qualification protocols/report. To maintain, destruction records and ensure safe destruction of obsolete records. Execution and evaluation of qualification and validation studies. Participation in technology transfer process from F & D and other manufacturing site. To review the change control proposed and to ensure closure of the change controls, post implementation after conducting impact assessment. Investigate deviations, non-conformances, and out-of-specification (OOS) results. Implement and track Corrective and Preventive Actions (C...

Chemveda is hiring for Quality Assurance Assistant Manager Position Experience - 8-12 years Qualification - M.Sc Chemistry /M.Pharma Designation - Executive Job Responsibilities :- 1. To design, develop, and implement a controlled document system for projects in Process Research & Development, Analytical Research & Development, Development Quality Assurance, and other relevant departments. 2. To define, implement, and monitor the Quality Systems for their effective implementation and compliance during the development of projects at PR&D and AR&D. 3. To be part of Quality management systems during or after project execution. 4. Responsible for receiving, reviewing, and archiving all records r...

Walk-In Interview Date : 18th, 19th & 20th November 2025 (Tuesday ,Wednesday & Thursday) Timing : 9:00 AM to 4:00 PM Venue : Umedica Laboratories Pvt, Ltd. Plot No 221,221/1 II Phase GIDC Nr Morarji Circle, Vapi 396195. 1. Tablet Packing Department: To Operate Blister Pack Machine ELMACH 3015 PDA machine/ IC 150C / WKH100 Cartonator machine/ Track and Trace machine with Temper Evident., CVC Primary & Secondary) Position: Technical Associates (Operator) Qualification: ITI / Diploma /BSC Experience: 2 to 5 years No. of Vacant Position: 20 2. Quality Control Department: Candidates having educational qualification of BSc/MSc with specialization in Chemistry. Organic chemistry/Analytical chemcist...

Ensure adherence to safety practices and procedures for self and the team. Contribute to the development of systems and practices that comply with company integrity and EHSS standards. Drive a corporate culture that promotes environment, health, and safety (EHS) in the workplace. Ensure safety compliance by following safety protocols and EHS requirements at all times. Ensure timely completion of mandatory safety and data integrity training for all team members. Uphold Syngene s quality standards in all operations. Hold self and teams accountable for achieving safety goals. Review and track safety metrics periodically. Assist with Emergency Management System and Contractor Management. Strengt...

Overall adherence to safe practices and procedures of oneself and the teams aligned Contributing to development of procedures, practices and systems that ensures safe operations and compliance to company s integrity & quality standards Driving a corporate culture that promotes environment, health, and safety (EHS) mindset and operational discipline at the workplace at all times. Ensuring safety of self, teams, and lab/plant by adhering to safety protocols and following environment, health, and safety (EHS) requirements at all times in the workplace. Ensure all assigned mandatory trainings related to data integrity, health, and safety measures are completed on time by all members of the team ...

Helps to analyze Installed Base data to identify discrepancies, trends, and potential issues, making recommendations for data integrity improvements. Adheres to data governance policies and procedures, ensuring that Installed Base records are managed and updated in compliance with company standards. Collects and consolidates data from various sources to ensure the completeness and accuracy of Installed Base records, facilitating effective decision-making. Ensures that all changes to the Installed Base records are accurately captured and reflected in the system in a timely manner, minimizing data inaccuracies. Handles complex data correction tasks by investigating root causes of errors, coord...

Support the technical transfer activity for a multi-phase and multi-year project to transfer programs into a third-party contract manufacturing facility in India. Provide Technical direction and support for third party manufacturing activities including coordination of activities with cross-functional roles from Quality, Regulatory, Development, Project Management, Supply Chain, Procurement and Validation. Be involved in the full project life cycle - successful project completion will include full implementation from initiation to deployment for multiple products, including equipment setup validation, manufacturing process transfer and validation, Test method transfer and validation, and pos...

Job Title: Deputy Manager- Formulation Location: Govandi, Mumbai Working Days: Monday to Saturday(2nd and 4th Saturday off, 1st,3rd and 5th Saturday operational) Department: Corporate Quality Assurance Qualification, Experience and Technical Competency: 1. Masters Degree in Pharmacy or Science or equivalent scientific field. 2. Minimum 10 years experience in Pharmaceutical Industry (Strong background of Formulation industry with 2 to 3 years experience in Quality Control.) 3. Work experience in Regulatory Sites (USFDA, MHRA, EU GMP) 4. Knowledge of current Good Manyfacturing Practices (cGMP), Quality Management Systems (QMS) and regulatory guidelines. Key Requirements: Responsible for Qualit...

Laxmi Organic Industries Limited. We are chemical manufacturing industry, looking for candidates interested in Technical Associate - QA Officer for Dahej. Job Title: Technical Associate-Quality (QA) Department: Quality Control/ Quality Assurance Reporting to: Sr.Manager-Quality (QA) Functional Area: Quality Assurance Type of Job: Permanent Location: Dahej, Site IV Job Purpose Execution, implementation and review of QA procedures. Role and Responsibilities Operational: - Online plant round for inspection of finished product packing and to identify gap as per IMS system. - Area / Equipment cleaning visual inspection and packing clearance. - Review of BMR & MFR for QA head approval. Its master ...

Line Clearance for Dispensing, Manufacturing & Packing activities Dispensing of RM/PM for batch Mfg Monitoring of IPQA activities (Granulation, Blending, Capsulation, Compression, Coating, Packing Sampling of IP and FP Samples Batch documents review

Job Description of Executive QC (Reviewer) : Review raw data, analytical reports, stability study documentation, and other records to ensure data integrity (following ALCOA+ principles) and consistency against source documents. Confirm all documentation is complete, meets company quality standards, and adheres to relevant internal and external (FDA, WHO, etc.) regulatory guidelines and Standard Operating Procedures (SOPs). Spot errors, deviations, non-conformances, or out-of-specification (OOS) results, and ensure they are thoroughly investigated. Provide training and mentorship to junior QC staff and other relevant team members on compliance and quality standards. Stay updated with regulato...

Job Title - Lab Assistant - Probability and Statistics Location - Vellore, Tamil Nadu, India Job Description SUMMARY Keeps laboratory supplies ready by inventorying stock; placing orders; verifying receipts. Keeps equipment operating by following operating instructions; troubleshooting breakdowns; maintaining supplies; performing preventive maintenance; calling for repairs. Documents information by maintaining daily logs and equipment record books. Resolves problems by examining and evaluating data; selecting corrective steps. Enhances laboratory and organization reputation by accepting ownership for accomplishing new and different requests; exploring opportunities to add value to job accomp...

Prepare, review of Annual Product Quality Review trend data, report. Handling of Change Control proposal. Validation batches monitoring, sampling Co-ordination Internal Audit and Non schedule Audit. QA Analysis of sterile pharma products. Required Candidate profile 1. Candidate must have min 4 yrs of experience at managerial level 2. Candidate must have sterile manufacturing experience.

Role & responsibilities Timely investigation and resolution of OOT/OOS test results. Follow GXP and Review COA, Documents. Assess and ensure compliance to QC regulatory requirements. Effectively manage the site Quality Control activities Ensure AMV/AMT at site. Design, implement and reviews with QC section heads for compliance related to SOPs, policies, standards and quality systems. Design and execute continuous improvement initiatives in the site to enhance compliance, drive efficiencies and cost effectiveness. Facilitate arrangement of all the resources required to QC laboratory to achieve desired productivity, SLA defined as per KPI by continual improving the process excellence. Develop ...

GLP & review of analytical data of raw material, finished product & stability sample analysis Knowledge of RCA & CAPA,Change control,Deviation,OOS,Failures,Incident,APQR,batch records,market complaint,line clearance,in-process checks & AQL procedures Required Candidate profile Must have good experience in quality assurance - cosmetics or Pharma industry Must have independently handled the QA documentation wrork Must be sincere and smart Can set new processes

• To maintain and adherence of the GLP and safety procedures in laboratory. • To raise the request for issuance of work data sheet / protocols. • To perform the analysis as per work allocation and records the results in work sheet / protocol and maintain on line documentation. • To maintain the CFR 21 part -11 compliance by following laid down procedures. • To perform all the HPLC related analysis of In-process, finished products & returned goods / Hold time / Stability study /reference / working standard analysis as per laid down specification & test procedures , SOPs, as per work allocation and report the analysis data in LIMS modules and report to Section – Head. • To ensure that every sp...

• To maintain and adherence of the GLP and safety procedures in laboratory. • To perform the analysis as per work allocation and records the results in work sheet (Protocols) for raw material / packing materials/intermediates /APIs/ Stability and etc.. as per current specification and method of analysis. • To work as Analyst and maintain the CFR 21 part -11 compliance by following laid down procedures. • To perform all the HPLC related analysis and perform the online documentation for In-process, intermediate, finished products & returned goods / raw materials Hold time / Stability study / working standard analysis as per laid down specification & test procedures , SOPs, as per work allocati...

Dear Applicants, Greeting from Biophore India pharmaceutical Pvt Ltd, We have opening for Formulation - DQA Department(OSD/Injectable) Job Description: Handling of QMS documents and Ensure the SOP compliance Review of Formulation Analytical Development Documents & Formulation Product Development Documents. Method Validation and Transfer Protocols and Reports Product development with QbD approach Responsible for ensuring GMP/GLP/GDP compliance in the Formulation and Analytical areas as per the respective SOPs. Review of FRD activities (LNBs, BDR’s, PDR’s, MFR’s and MPR’) SOP’s and Guidelines Preparation and Review and Approval of SOP’s. Responsible for conducting Internal Audits/External Audi...

1. Managing the quality documents and conducting internal Audit & data review etc. 2. Maintaining all records and documentation as per 17025:20053. 3. Maintaining regularly and tracked calibration and standard log books, 4. Directing all quality activities for the laboratory such as ILC, IQC, Training, etc. 5. Preparing compliance report for the audit or for the closure of various shortcomings or NCs.

Production - Senior Officer -Fermentation upstream opertor. Should have experience in Aseptic practices, Handling of Fermenter, Process vessels, Homogenizer, TFF systems, Filtration, Biosafety cabinet. Microbial fermentation experience. Manufacturing activities according to effective SOPs. Batch related documents in manufacturing area. Readiness related to batch manufacturing. Execution of activities in compliance to cGMP. Execution of activities during campaign change. Decontamination and disposable of bio waste. Preparation of URS for the equipment. Preparation of MCB/WCB. Automated or manual CIP of all the equipment in the manufacturing area. Follow safety norms in the manufacturing depar...

Qualification :MSc in Chemistry, Organic Chemistry, Molecular Chemistry 5 to 7 years in API Manufacturing (Active Pharmaceutical Ingredients) Job Role :- Assist in development, implementation, and maintenance o

Job Description You will be responsible for overseeing quality assurance processes as a Manager - Quality Assurance (QA) at ZIM Laboratories Limited located in Nagpur. Your role will involve ensuring adherence to regulatory and compliance standards, implementing strategies to maintain product quality, reviewing and approving quality documentation, managing QA audits, supervising quality control operations, and coordinating with R&D and production teams to uphold quality benchmarks. Key Responsibilities - Oversee quality assurance processes - Ensure adherence to regulatory and compliance standards - Implement strategies to maintain product quality - Review and approve quality documentation - ...