Vapi, Gj Quality control head Jobs – 20 Open Jobs Today

Quality Control Head
CELOGEN PHARMA PVT LTD —Daman, Daman and Diu
- ₹35,000 - ₹80,000 a month
- Email
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Quick apply
QC Head
Avik Pharmaceuticals Ltd —Vapi, Gujarat
- ₹10,00,000 - ₹15,00,000 a year
- Full-time
- Quality control
- APIs
- In-person
Quick apply
9d
Senior Operations Coordinator
HR Group & Company —Daman, Daman and Diu
- ₹9,60,000 - ₹12,00,000 a year
- Full-time
- Assembly
- Bachelor's degree
- In-person
Quick apply
Deputy General HR Manager
activity next business solutions —Daman, Daman and Diu
- ₹4,79,037.90 - ₹20,00,000.00 a year
- Full-time
- Management
- English
- Master's degree
Quick apply
Manager / Sr. Manager - HR & Admin- Manufacturing
Ananta Resource Management —Pardi, Gujarat
- ₹15,00,000 - ₹20,00,000 a year
- Full-time
- Analysis skills
- Bachelor's degree
- Conflict management
- Paid time off
- Paid sick time
Quick apply
Plant Head – Plastic Injection Molding
HR Group & Company —Daman, Daman and Diu
- ₹12,00,000 - ₹15,00,000 a year
- Full-time
- Analysis skills
- Project management
- Bachelor's degree
Quick apply
11d
Officer Quality Assurance
Bhageria Industries Limited —Vapi, Gujarat
- ₹20,000 - ₹30,000 a month
- Full-time
- Quality control
- In-person
- Manufacturing
Quick apply
2d
Block Head
Vital Laboratories —Vapi, Gujarat
- Email
- English
- Cleaning
General Manager
Jaros Industries Pvt. Ltd —Vapi, Gujarat
- ₹7,00,000 - ₹12,00,000 a year
- Full-time
- Management
- Master's degree
- Assembly
- Cell phone reimbursement
Quick apply
12d
QA Head
Vital Laboratories —Vapi, Gujarat
- Email
- APIs
Manufacturing head (IMM, IBM, ISBM, and EBM )
Talent Vision Services —Silvassa, Daman and Diu
- ₹17,00,000 a year
- Full-time
- Management
- Master's degree
- Bachelor's degree
Quick apply
STORES INCHARGE
HR Group & Company —Daman, Daman and Diu
- ₹3,00,000 - ₹4,20,000 a year
- Full-time
- Bachelor's degree
- In-person
- Manufacturing
Quick apply
QC Head
Vital Laboratories —Vapi, Gujarat
- Email
Production Sub Lead
STL - Sterlite Technologies Limited —Dadra, Daman and Diu
- Microsoft Excel
- Management
- Bachelor's degree
Project Coordinator
HR Creations —Vapi, Gujarat
- ₹10,00,000.17 - ₹15,00,000.91 a year
- Full-time
- Civil engineering
- Bachelor's degree
- Construction
Quick apply
Manager Costing
Ananta Resource Management —Pardi, Gujarat
- ₹12,00,000 - ₹15,00,000 a year
- Full-time
- Inventory control
- Inventory management
- English
- Paid time off
- Paid sick time
Quick apply
Store Supervisor
STRONGWIRE INDUSTRIES —Vapi, Gujarat
- ₹15,000 - ₹22,000 a month
- Full-time
- Analysis skills
- Bachelor's degree
- Typing
Quick apply
TOOL ROOM MANAGER
Mehta Tubes Ltd. (Unit:II) —Umargam, Gujarat
- ₹15,000.00 - ₹70,137.10 a month
- Full-time
- Bachelor's degree
- In-person
- Diploma
- Food provided
Quick apply
Tool Room Manager
Nobtech Enterpries —Umargam, Gujarat
- ₹35,000 - ₹45,000 a month
- Full-time
- Bachelor's degree
- In-person
- Diploma
- Commuter assistance
- Cell phone reimbursement
Quick apply
Design Engineer - NPD
STL - Sterlite Technologies Limited —Dadra, Daman and Diu
- CAD
- Engineering
- Master's degree

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Quality Control Head

CELOGEN PHARMA PVT LTD -
Daman, Daman and Diu

Quick apply

Job details

Full-time
₹35,000 - ₹80,000 a month

Qualifications

Microsoft Powerpoint
Microsoft Word
Microsoft Excel
Microsoft Office
Master's degree
Quality assurance
Bachelor's degree
Quality control
Chemistry
Manufacturing
Leadership
Communication skills
Time management

Full job description

Job Title: Quality Control Head

Location: Daman, Daman and Diu

Job Summary:

The Head of Quality Control (QC) is a senior leadership position responsible for directing all laboratory operations related to the testing of raw materials, packaging materials, in-process materials, and finished pharmaceutical products. This role ensures that all quality control activities are conducted in strict compliance with current Good Laboratory Practices (GLP), and all applicable national and international regulatory standards . The successful candidate will drive the strategic direction of the QC function, ensuring high-quality, timely analytical support for manufacturing and product release.

Responsibilities:

1. Analytical Testing:

· Perform routine and non-routine analytical testing of raw materials, in-process samples, finished products, stability samples, and packaging materials using various analytical techniques (e.g., HPLC, KF, Dissolution, Titration, Physical testing).

· Ensure all testing is conducted in accordance with approved pharmacopoeial methods and in-house specifications.

· Operate, calibrate, and maintain analytical instruments, ensuring their optimal performance and readiness for testing.

2. Data Review & Documentation:

· Thoroughly review analytical data, raw data, and laboratory notebooks for accuracy, completeness, and compliance with established procedures and regulatory requirements.

· Prepare and review Certificates of Analysis (COAs) and other relevant quality documents.

· Ensure timely and accurate documentation of all testing activities, results, and observations.

· Maintain detailed and organized laboratory records.

3. Investigations & Deviations:

· Participate in Out-of-Specification (OOS) and Out-of-Trend (OOT) investigations, identifying root causes and recommending corrective and preventive actions (CAPAs).

· Document and investigate laboratory deviations, ensuring adherence to established procedures.

· Support the implementation and verification of CAPAs.

4. Method Development & Validation Support:

· Assist in the development, transfer, and validation of analytical methods as per regulatory guidelines.

· Conduct feasibility studies and provide technical input for method optimization.

5. Compliance & Audits:

· Ensure strict adherence to current Good Manufacturing Practices (cGMP), Good Laboratory Practices (GLP), and other applicable regulatory guidelines

· Participate in internal and external audits (e.g., regulatory inspections, customer audits) by providing necessary documentation and technical support.

· Address audit observations and implement corrective actions.

6. Training & Mentorship:

· Train junior QC analysts on analytical techniques, instrument operation, and laboratory procedures.

· Serve as a technical resource for other team members.

7. Safety & Housekeeping:

· Comply with all laboratory safety procedures and guidelines.

· Maintain a clean, organized, and safe working environment.

· Manage laboratory waste in accordance with environmental regulations.

8. Continuous Improvement:

· Identify opportunities for process improvements and efficiency enhancements within the QC laboratory.

· Contribute to the revision and creation of Standard Operating Procedures (SOPs) and other quality documents.

9. Strategic Leadership & Management

Establish Strategic Direction: Develop and execute the long-term strategy for the QC department, aligning it with the company’s overall business and quality objectives.
Team Leadership: Lead, mentor, and manage the QC team, fostering a culture of quality, compliance, and continuous improvement. Manage department budget, resources, and personnel development.
Laboratory Oversight: Oversee the daily operations of the QC laboratory, including scheduling, resource allocation, and maintaining laboratory infrastructure, instrumentation, and environment.

10. Regulatory Compliance & Quality Systems

Compliance Assurance: Ensure all QC testing, documentation, investigations, and releases comply with cGMP, GLP, Pharmacopoeial requirements (e.g., USP, EP, JP), and regulatory filings.
Audit Management: Serve as the primary QC representative during regulatory inspections (e.g., FDA, MHRA, EMA) and internal/external audits. Ensure timely and effective closure of all QC-related audit observations and CAPAs.
Documentation Control: Review and approve critical QC documentation, including Standard Operating Procedures (SOPs), test methods, specifications, method validation/transfer protocols and reports, and stability protocols.

11. Analytical Operations & Data Integrity

Testing & Release: Direct the accurate and timely testing of all materials (Raw, In-Process, Finished Product, Stability) and authorize the release or rejection of products based on analytical results.
Investigations: Oversee and approve all QC investigations, including Out-of-Specification (OOS), Out-of-Trend (OOT), and deviation reports, ensuring thorough root cause analysis and effective corrective and preventive actions (CAPA).
Method Life Cycle Management: Direct the development, validation, transfer, and routine monitoring of analytical test methods to ensure they are phase-appropriate and robust.
Data Integrity: Champion data integrity practices within the QC laboratory, ensuring all electronic and paper records are accurate, complete, and attributable.

12. Cross-functional Collaboration

Internal Partnering: Collaborate closely with Manufacturing, Quality Assurance (QA), Regulatory Affairs, and Research & Development (R&D) to resolve quality issues, support process improvements, and meet production deadlines.
Supplier Quality: Coordinate with QA to evaluate and monitor the quality of materials received from suppliers.

Qualifications:

· Education: Bachelor's or Master's degree in Analytical Chemistry, Organic Chemistry

· Experience: 8-10 years of progressive experience in Quality Control within a pharmaceutical manufacturing environment.

Skills & Competencies:

· Proficient in operating and troubleshooting a wide range of analytical instruments (HPLC, GC, UV-Vis, FTIR, KF, Dissolution apparatus, etc.).

· Strong understanding of analytical method validation and transfer principles.

· Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint).

· In-depth knowledge of GLP, and regulatory requirements (e.g., ICH guidelines).

· Excellent analytical, problem-solving, and critical thinking skills.

· Strong attention to detail and accuracy.

· Ability to work independently and as part of a team in a fast-paced environment.

· Excellent written and verbal communication skills.

· Strong organizational and time management skills.

· Experience with specific pharmaceutical dosage forms (e.g., tablets, capsules, injectables, liquids).

· Familiarity with Data Integrity principles.

To Apply:

Interested candidates are invited to submit their resume and cover letter to [email protected]

Job Type: Full-time

Pay: ₹35,000.00 - ₹80,000.00 per month

Work Location: In person

Quick apply

Refine Your Search

quality control head jobs in vapi, gj

Quality Control Head

QC Head

Senior Operations Coordinator

Deputy General HR Manager

Manager / Sr. Manager - HR & Admin- Manufacturing

Plant Head – Plastic Injection Molding

Officer Quality Assurance

Block Head

General Manager

QA Head

Manufacturing head (IMM, IBM, ISBM, and EBM )

STORES INCHARGE

QC Head

Production Sub Lead

Project Coordinator

Manager Costing

Store Supervisor

TOOL ROOM MANAGER

Tool Room Manager

Design Engineer - NPD

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