Huskur Gate Karnataka Pharmaceutical Jobs – 554 Open Jobs Today

Senior Associate QA
CELEGENCE —Bengaluru, Karnataka
- Hybrid work
- Master's degree
- Project management
- Communication skills
8d
Wastewater Design Engineer
Wock-Oliver Global —JP Nagar, Bengaluru, Karnataka
- ₹65,000 - ₹1,10,000 a month
- Full-time
- AutoCAD
- Master's degree
- Programmable logic controllers
Quick apply
Senior Drug Safety Associate
Accenture —Bengaluru, Karnataka
- Full-time
- Master's degree
- Bachelor's degree
- Data entry
Job Description - Senior Scientist - Insilico
Quantumzyme —Bengaluru, Karnataka
- Doctoral degree
- C++
- Leadership
Healthcare Research & Data Analyst
Clarivate —Bengaluru Urban District, Karnataka
- Full-time
- Hybrid work
- Microsoft Excel
- Doctoral degree
- Research
8d
Scientific Officer
Cadila Pharmaceuticals Ltd —Bengaluru, Karnataka
- Full-time
- Analysis skills
- Leadership
- Communication skills
Quality Specialist (QMS, Documentation)
Merck KGaA —Bengaluru, Karnataka
- Master's degree
- Communication skills
Associate Medical Data Review Manager
IQVIA —Bengaluru, Karnataka
- Full-time
- Medicine
- Anatomy knowledge
- Customer service
Medical Representative (Pharma Sales)
Jolly Healthcare —Bangalore City, Bengaluru, Karnataka
- ₹18,000 - ₹40,000 a month
- Full-time
- Sales
- B.Sc
- Bachelor's degree
- Health insurance
- Paid time off
Quick apply
CEO - Pharma
Benaka Healthcare —Bengaluru, Karnataka
- ₹4,00,000 - ₹10,00,000 a month
- Full-time
- Microsoft Powerpoint
- Microsoft Excel
- Management
Quick apply
Associate Study Coordinator
Labcorp —Bengaluru, Karnataka
- Full-time
- Microsoft Word
- Microsoft Excel
- Microsoft Outlook
Medical Representative
Cadila Pharmaceuticals Limited —Bangalore City, Bengaluru, Karnataka
- ₹3,00,000 a year
- Sales
- Master's degree
- Bachelor's degree
Quick apply
Assistant Sales Manager-Medical/Pharma
Mindful TMS Neurocare —Bengaluru, Karnataka
- ₹40,000 - ₹45,000 a month
- Full-time
- In-person
- Health insurance
- Life insurance
Quick apply
14d
Sr. Interior Designer (Healthcare/Laboratories/Diagnostic Centres/Clinics)
Creencia Technologies Private Limited —Bengaluru, Karnataka
- From ₹80,000 a month
- Full-time
- AutoCAD
- Hospitality
- Microsoft Office
Quick apply
QC Engineer
ABS FUJITSU GENERAL PRIVATE LIMITED —Bangalore City, Bengaluru, Karnataka
- ₹35,000 - ₹50,000 a month
- Full-time
- Microsoft Powerpoint
- Bachelor's degree
- Quality control
- Health insurance
- Cell phone reimbursement
Quick apply
Senior Analyst (Tableau developer+ Pharma)
EVERSANA —Bengaluru, Karnataka
- Full-time
- Microsoft Powerpoint
- Sales
- Master's degree
Quick apply
Senior Drug Safety Scientist
Accenture —Bengaluru, Karnataka
- Full-time
- Medicine
- Bachelor's degree
- Data entry
Real-World Evidence Analyst
Mango Sciences —Bengaluru, Karnataka
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Consultant, Regulatory Operations
Syner-G —Bengaluru, Karnataka
- Remote
- Bachelor's degree
- Communication skills
Quick apply
2d
Medical Representative
Cadila Pharmaceuticals —Bangalore City, Bengaluru, Karnataka
- Full-time
- B.Sc
- Master's degree
- Bachelor's degree
- Flexible schedule
- Paid sick time
Quick apply

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Senior Associate QA

CELEGENCE
Bengaluru, Karnataka

Apply Now

Job details

8 days ago

Qualifications

Quality management
ISO 9001
Master's degree
Project management
M.Pharma
Document management
Communication skills

Full job description

Global Opportunities to Join the Celegence Team At Celegence, you have the opportunity to shine and truly make a difference. We have a growing organization where your inputs will be valued. We have roles for all levels; both recent graduates and experienced professionals. We are currently looking for applicants with the following backgrounds. Celegence offers competitive compensation and benefits, growth opportunities, and a supportive work environment. Celegence is an Equal Employment Opportunity Employer All employment decisions at Celegence are made without regard to age, race, creed, colour, religion, sex, national origin, ancestry, disability status, veteran status, sexual orientation, gender identity or expression, genetic information, marital status, citizenship status or any other basis as protected by federal, state, or local law. Celegence is committed to providing a positive work environment as a part of the core Organizational value and is free from discrimination and harassment, and we will not tolerate any form of unlawful discrimination or harassment. Why work at Celegence? Be a part of a remarkable journey! Collaborative Team Here at Celegence, you get a great team that always stands by you. Supportive Manager A supportive Manager who makes sure you are absolutely comfortable with the work you’re doing. HR team An amazing HR team who is always working up different ways to keep the employees motivated (also by sending lovely goodies every now and then). Leadership Team Here you get the best leadership team that is equally concerned about employee’s career growth as they are about the development of this organization.

Senior Associate QA

Bangalore
Onsite, Hybrid
Reporting to Associate Director - QA

About Celegence

Celegence LLC is a privately owned consulting organization headquartered in Chicago, Illinois (USA), with offices across the UK, Europe and India. The company specializes in Regulatory Affairs consulting services and technology solutions for the global Life Sciences industry.

Our experienced professionals support organizations in managing day-to-day regulatory operations by ensuring global compliance, applying deep industry expertise and leveraging technology and automation to improve operational efficiency.

Our vision is to become the premier niche provider of regulatory services and innovative solutions, enabling life science organizations to deliver exceptional patient value through end-to-end regulatory excellence.

Job Requirement

Qualification

M.Sc. or M. Pharma

Experience

7 to 10 Years

Technical Skills

ISO 9001:2015 Standards
QMS Document Management
Audit Management
Change Management
CAPA Management
Vendor Management

Soft Skills

Strong communication skills (verbal and written)
Analytical thinking and problem-solving ability
Effective stakeholder collaboration and teamwork
Time management with the ability to handle multiple priorities

Competencies

Strong knowledge of ISO 9001:2015 standards and Quality Management System (QMS) processes.
Audit Management including planning, execution and closure.
Corrective and Preventive Action (CAPA) Management.
Document Control and Change Management within the Quality Management System.

Personal Traits

Integrity

High level of integrity with a strong ethical mindset.

Ownership

Strong ownership, accountability and commitment to quality.

Detail-Oriented

Focused on quality, compliance and continuous attention to detail.

Continuous Improvement

Proactive attitude with a continuous improvement mindset and willingness to innovate.

Roles & Responsibilities

Document Control & Management
- Maintain and update QMS documents including creation, review and revision in line with ISO standards.
- Manage complete document lifecycle including version control and archival.
- Review SOPs, Policies, Manuals and Work Instructions for accuracy and compliance.
- Ensure periodic review and timely revision of documents.
- Prepare and publish quarterly QMS reports with key metrics and insights.

Audit & Compliance
- Schedule and coordinate internal audits as per the approved audit plan.
- Conduct internal audits and document findings.
- Share audit outcomes with Project Managers and Delivery Heads.
- Support external audit preparation and readiness activities.
- Track and ensure timely closure of audit findings.

Project Management Support
- Maintain and update the Global Project Tracker.
- Ensure project documentation remains complete and audit ready.
- Verify project-specific risk assessments.
- Track mitigation and contingency plans.
- Support adherence to customer-specific QMS requirements.

Change Management
- Coordinate with Cross Functional Teams to manage Change Requests.
- Track Change Request lifecycle and closure.
- Review Change Requests for completeness, risk and impact assessment.
- Ensure proper risk analysis before approvals.

Vendor & Risk Management
- Maintain and update the Approved Vendor List.
- Ensure vendor documentation is complete and available.
- Track vendor evaluation and re-evaluation activities.
- Maintain department risk assessment trackers.
- Support mitigation and contingency planning.

CFT Support & Training
- Ensure adherence to QMS processes across functions.
- Track action items and follow up for timely closure.
- Conduct monthly QA discussions with functional teams.
- Provide QMS training and awareness sessions.
- Promote collaboration between QA and Cross Functional Teams.

Continuous Improvement & Innovation
- Drive adoption of QMS tools and workflow automation.
- Reduce manual dependency and improve data accuracy.
- Track quality, efficiency and compliance improvement metrics.
- Identify process improvement opportunities.
- Promote continuous improvement and operational excellence.
- Improve document control efficiency and traceability using automation tools.

Apply Now

Refine Your Search

pharmaceutical jobs in huskur gate karnataka

Senior Associate QA

Wastewater Design Engineer

Senior Drug Safety Associate

Job Description - Senior Scientist - Insilico

Healthcare Research & Data Analyst

Scientific Officer

Quality Specialist (QMS, Documentation)

Associate Medical Data Review Manager

Medical Representative (Pharma Sales)

CEO - Pharma

Associate Study Coordinator

Medical Representative

Assistant Sales Manager-Medical/Pharma

Sr. Interior Designer (Healthcare/Laboratories/Diagnostic Centres/Clinics)

QC Engineer

Senior Analyst (Tableau developer+ Pharma)

Senior Drug Safety Scientist

Real-World Evidence Analyst

Consultant, Regulatory Operations

Medical Representative

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Senior Associate QA

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