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5.0 - 10.0 years

4 - 8 Lacs

kolkata

Work from Office

JOB PROFILE OF SR. TECHNICAL OFFICER-QUALITY ASSURANCE MENDINE PHARMACEUTICALS PVT LTD Job Title / Designation- SENIOR TECHNICAL OFFICER - QA Qualifications- M.PHARM Experience- 5 to 10 years experience in QUALITY ASSURANCE Job Objective- The ideal candidate will be responsible for implementing and maintaining quality systems, ensuring compliance with cGMP guidelines, conducting internal audits, reviewing batch records, and supporting regulatory inspections. This role demands strong documentation skills, a sound understanding of pharmaceutical quality standards, and the ability to work collaboratively across departments to uphold product integrity and safety throughout the manufacturing proc...

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10.0 - 20.0 years

8 - 13 Lacs

vadodara

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Title: QA Manager Business Unit: CQC (Complaints) Job Grade: G11A / Manager 2 Location : Tandalja, Vadodara Educational Qualification: B.Pharma / M.Sc (Life Sciences) Experience: 10 to 14 Years Position Summary Review of Product Quality Complaint Investigation Reports (Drug Products). Coordinate with other stakeholders involved in the complaint handling process. Monitor the progress of Filed Alert Reports, Recalls & Product Quality Complaint closure etc. Logging of Product Quality Complaints (PQC) in the database (TrackWise). Acknowledge the complaints to the complainants. Providing the response letter to the complainant. Reconciliation of received Product Quality Complaint. Note: 1) Candida...

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6.0 - 10.0 years

17 - 22 Lacs

noida

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Manager Data Services Consulting for UKG is an integral member of a dynamic organization responsible for managing a team of skilled data consultants of our Human Capital Management products. The team is accountable for delivering high-quality data consulting services to our customers and is responsible for accurately converting data from customers source system(s) into UKG Ready. Skills essential to this role are strong analysis, change control, consulting, organization, written and verbal communication. Functional and technical knowledge of HCM and Payroll systems strongly desired. The individual guides the internal team members and as well assists customers with the extraction and transfor...

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6.0 - 11.0 years

18 - 22 Lacs

mumbai

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Role Description The Group Audit (GA) function comprises c. 880 staff who take a proactive, risk based and independent approach to assist the Bank's business and infrastructure functions to identify key control weaknesses. GA prides itself in ensuring the highest standard in professional delivery. Being DB's 'third line of defense GA have a high internal profile, acting as an independent and forward-looking challenger and adviser to Senior Management. We are strongly rem/lied upon by the Regulators. We are a diverse and inclusive global division where culture is at the core of our team dynamic; GA is inextricably linked to promoting strong corporate and ethical governance, a philosophy that ...

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9.0 - 14.0 years

8 - 12 Lacs

bharuch, ankleshwar

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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

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5.0 - 7.0 years

0 Lacs

pune, maharashtra, india

Remote

Entity: Finance Job Family Group: Project Management Group Job Description: We are a global energy business involved in every aspect of the energy system. We are working towards delivering light, heat, and mobility to millions of people every day. We are one of the very few companies equipped to solve some of the big complex challenges that matter for the future. We have a real contribution to make to the world&aposs ambition of a low-carbon future. Join us and be part of what we can accomplish together. You can participate in our new ambition to become a net zero company by 2050 or sooner and help the world get to net zero. Would you like to discover how our diverse, hardworking people are ...

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0.0 - 5.0 years

2 - 7 Lacs

pune

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Enhance images by correcting resolution and composition, cropping images and adjusting tone, color, saturation and brightness. Adding or removing objects from an image or inserting text. Smoothen skin, remove big creases, general tidy up, clean up floor, sharpen clothing better where it looks too big, remove flyaway/loose hair strands Have an eye for art and composition as they relate to whats typically desirable in a photographic image. To present your designs and ideas when required to all levels up to and including managers & clients. To constantly review competitor sites and make recommendations to maintain client s position as market leader, ensure client s on-line content continues to ...

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2.0 - 5.0 years

2 - 6 Lacs

gurugram

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Culture holidays India Pvt. Ltd. is looking for Senior Executive to join our dynamic team and embark on a rewarding career journey Leading the full audit cycle by checking tax compliance, verifying financial records, and inspecting accounts. Analyzing the results of the audit and presenting possible solutions for ineffective financial practices to management. Evaluating company accounting procedures, payroll, inventory, and tax statements to guide financial policymaking. Conducting risk assessments to recommend aversion measures and cost savings. Following up with management to ensure remediations are implemented into the company's financial practices. Supervising junior auditing personnel a...

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1.0 - 3.0 years

4 - 5 Lacs

noida

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Key Responsibilities: Administer and maintain SQL Server databases, ensuring high availability (HA) and optimizing performance. Perform regular database backups, monitoring, and auditing to maintain data integrity and security. Utilize PowerShell scripting to automate routine database tasks, streamline processes, and improve operational efficiency. Perform performance tuning to optimize database systems for improved speed and responsiveness. Monitor and troubleshoot database-related issues, ensuring quick resolution of any operational problems. Implement and maintain disaster recovery procedures to ensure data availability and minimal downtime. Collaborate with other IT teams to ensure datab...

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3.0 - 8.0 years

3 - 5 Lacs

bengaluru

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Key Responsibilities: Administer and maintain SQL Server databases, ensuring high availability (HA) and optimizing performance. Perform regular database backups, monitoring, and auditing to maintain data integrity and security. Utilize PowerShell scripting to automate routine database tasks, streamline processes, and improve operational efficiency. Perform performance tuning to optimize database systems for improved speed and responsiveness. Monitor and troubleshoot database-related issues, ensuring quick resolution of any operational problems. Implement and maintain disaster recovery procedures to ensure data availability and minimal downtime. Collaborate with other IT teams to ensure datab...

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6.0 - 10.0 years

15 - 19 Lacs

pune

Work from Office

Key Responsibilities Develop and maintain supply chain analytics to monitor operational performance and trends. Lead and participate in Six Sigma and supply chain improvement initiatives. Ensure data integrity and consistency across all analytics and reporting platforms. Design and implement reporting solutions for key supply chain KPIs. Analyze KPIs to identify improvement opportunities and develop actionable insights. Build and maintain repeatable, scalable analytics using business systems and BI tools. Conduct scenario modeling and internal/external benchmarking. Provide financial analysis to support supply chain decisions. Collaborate with global stakeholders to understand requirements a...

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0.0 - 2.0 years

8 - 12 Lacs

pune

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Job Purpose: Assist QHSE - Marine superintendents/ Managers with Maintain and control the Division filing system. Maintain and control Controlled and uncontrolled documentation to and from vessels. Prepare documents specific for voyages to US, Canada, (e.g., VGP, COFR). Reports To : Assistant Manager (QHSE) / Marine Superintendent (QHSE) Qualifications: Graduate Experience: Sailing Experience 2nd Officer/ 3rd officer/ Science graduate with experience. Graduates who are interested in ship management industry. Skills Required: Good Communication Skills Good Knowledge of Microsoft office Responsibilities: Assisting QHSE Superintendents in: Conducting office internal audits Arranging for MLC aud...

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2.0 - 6.0 years

0 - 3 Lacs

dahej

Work from Office

Role & responsibilities: Outline the day-to-day responsibilities for this role. Preferred candidate profile: Specify required role expertise, previous job experience, or relevant certifications.

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12.0 - 18.0 years

12 - 18 Lacs

sonipat

Work from Office

QMS and it's implementation Review and approval of NCs, CAPA, Change Controls, Validation Master Plan, SMF, BMR, BPR, Quality Manual, Vendor qualification. Lead and manage internal/ external audits, QA compliance, continuous improvement, MRM data Required Candidate profile Bachelor’s/Master’s in Mechanical/ Biomedical 10+ years of exp. QA & QMS in the medical devices Strong knowledge of QMS, GMP, regulatory guidelines (ISO, USFDA, CE, WHO),handling audits, QA practices.

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2.0 - 5.0 years

4 - 5 Lacs

bengaluru

Work from Office

Issuance & retrieval of BPCRs/ ECRs/ formats/ log books etc. Preparation of QA SOPs and list of SOPs. Follow-up cross functional team for periodic review and review of other departmental SOPs as and when required. Distribution of controlled documents e.g. SOPs, specification etc. QC Analytical Raw data and sampling and review checklist Issued. Ensure all the activities comply with EHS regulations and policies. Ensure Zero accident / Incident at work place Ensure all the activities / documentation as per the cGMP guideline

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1.0 - 2.0 years

1 - 4 Lacs

gurugram

Work from Office

Requisition for Executive for the implementation and monitoring of GLP in TIC. Skills Required : Good Laboratory Practice, Quality Assurance, MS Office Package, Communication Skills Roles and Responsibilities : Preparation of documents related to applying GLP (Good Laboratory Practices). Ensure the upkeep and maintenance of the laboratory by implementing GLP. Ensure compliance with GLP standards. Logbook management, sample management, SOP management, and other document management related to GLP. Any other work related to Quality assurance assigned by the manager. GLP-trained person or experience working in GLP labs. Must have good verbal and written skills.

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12.0 - 15.0 years

12 - 15 Lacs

vapi

Work from Office

Designation - Manager - Production Location - Vapi - Gujrat Salary - Upto 15 LPA Experience - 12-15 Years Qualification - M.Sc. (Chemistry) or B.E. (Chemical) Job Description - 1 Overall responsible for planning and maintenance of optimum inventory of raw materials, in process and finished goods. 2.To ensure the products are manufactured and stored according to pre-approved instructions to obtain required quality. 3.Implementation of procedures related to intermediates or APIs manufacturing processing production areas. 4.Regular review & evaluation of production record for- quality and yields and completeness prior to submission in Quality Assurance. 5.To ensure required initial and continui...

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2.0 - 4.0 years

2 - 4 Lacs

vapi

Work from Office

Role & responsibilities Handling the Change Control Programme and functional Change Control Coordinator. Handling of Deviation and Market Compliant. Preparation and review of Annual Product Quality Review. Preparation, maintenance, reviews of all other QMS documentation. Handling of RM/PM rejection documents. Preparation and issuance of SOP's. Preparation, Review and Execution of Process Validation Protocol and Report. To Collect and send sample to QC for analysis. To release the product for next stage after receiving QC release report. To maintain logbook and document control. Issuance of format. Reviewing of BMR / BPR. Ensure the implementation and compliance with cGMP aspects. Ensure comp...

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3.0 - 6.0 years

3 - 6 Lacs

bharuch, dahej

Work from Office

Responsible for QA functions-legal documentation, Compliance of QA/ISO/EHS systems/insecticides rules, Analysis, Timely, accurate & cost effective analytical support to plant, preparing SOP/Verification of testing methods, Instruments calibration etc Required Candidate profile M.Sc.with 3 to 6 yrs relevant exp in Agrochemical industry. Knowledge of quality systems, in house calibration of lab instruments , handling of QA lab Instruments , Root Cause Analysis Techniques etc.

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2.0 - 5.0 years

2 - 6 Lacs

hyderabad

Work from Office

Roles and Responsibilities Conduct quality reviews of documents, including CAPAs, change controls, and 21 CFR compliance. Ensure adherence to company policies and procedures through document review. Develop and maintain a thorough understanding of regulatory requirements for pharmaceuticals. Provide feedback on document quality and suggest improvements where necessary. Collaborate with cross-functional teams to resolve issues related to document control.

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1.0 - 4.0 years

2 - 7 Lacs

ahmedabad

Work from Office

Ensure compliance with GMP & regulatory standards, oversee quality systems, audits & validations, manage QA team, review batch records, handle deviations/CAPA, support regulatory inspections, ensure product quality & safety across manufacturing.

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6.0 - 11.0 years

22 - 27 Lacs

bengaluru

Work from Office

As a member of the Consulting organization, you are responsible for ensuring that a quality, integrated software solution is delivered in a timely manner, at budget, and to our client's satisfaction. This involves working closely with the client to understand and manage their expectations, as well as working closely with Oracle and third-party vendors to ensure delivery. Responsibilities Experienced in managing large-scale and complex Oracle Cloud implementation and transformation projects from initiation to completion. Create and lead comprehensive project plans covering budget, structure, scheduling, staffing models, and resourcing while ensuring alignment with Oracles compliance, security...

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1.0 - 8.0 years

8 - 11 Lacs

kolkata, west bengal, india

On-site

Project Planning Scheduling: Develop detailed project plans and schedules using Microsoft Project (MSP) . Monitor and update the master construction schedule, ensuring it aligns with agreements made with contractors. Develop schedules at both macro and micro levels, categorizing tasks into overall programs, tender schedules, and individual work categories. Manage sequencing of activities, ensuring that timelines and project phases are met according to the plan. Project Governance Coordination: Establish effective project governance, processes, and systems to ensure smooth execution. Manage the change control process to ensure adherence to project scope and minimize scope creep. Ensure consis...

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3.0 - 7.0 years

8 - 11 Lacs

chennai, tamil nadu, india

On-site

Project Planning Scheduling: Develop detailed project plans and schedules using Microsoft Project (MSP) . Monitor and update the master construction schedule, ensuring it aligns with agreements made with contractors. Develop schedules at both macro and micro levels, categorizing tasks into overall programs, tender schedules, and individual work categories. Manage sequencing of activities, ensuring that timelines and project phases are met according to the plan. Project Governance Coordination: Establish effective project governance, processes, and systems to ensure smooth execution. Manage the change control process to ensure adherence to project scope and minimize scope creep. Ensure consis...

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3.0 - 7.0 years

0 Lacs

rajasthan

On-site

As a Qualified Person (QP) at PCI, you will play a crucial role in certifying investigational medicinal products in compliance with the requirements of the Investigational Medicinal Product Dossier (IMPD) and Product Specification File (PSF). Your responsibilities include ensuring the compliance of all batches to EU Directives, Annex 16, and Detailed Commission Guidelines related to Investigational Medicinal Products (IMPs). You will provide direct support and guidance to the Quality management team to ensure that Quality operations meet the necessary site safety, quality, and cGMP requirements. Additionally, you will participate in cross-functional teams to offer consultative support on qua...

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