Gujarat Pharmaceutical quality control Jobs – 199 Open Jobs Today

Quality Control Officer
CELOGEN PHARMA PVT LTD —Mahesana, Gujarat
- ₹20,000 - ₹25,000 a month
- Email
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Quick apply
Quality Control Officer
BHUMI PHARMACEUTICALS —Ajwa Road, Vadodara, Gujarat
- ₹15,000 - ₹25,000 a month
- B.Sc
- Master's degree
- Bachelor's degree
- Cell phone reimbursement
- Food provided
Quick apply
5h
Quality Assurance Officer
Noronic Pharmaceutical Pvt. Ltd. —Gota, Ahmedabad, Gujarat
- ₹1,80,000 - ₹3,60,000 a year
- Full-time
- Master's degree
- Bachelor's degree
- In-person
Quick apply
8d
Chemist / Officer - Quality Control
ACTYLIS —Ahmedabad, Gujarat
- B.Sc
- Master's degree
- Bachelor's degree
Executive - Quality Control, Pharma
Zentiva Group, a.s. —Ankleshwar, Gujarat
- Full-time
- Master's degree
- Analysis skills
Pharmaceutical Quality Assurance Analyst
HITECH ANALYTICAL LABORATORY LLP —Ahmedabad, Gujarat
- ₹15,000 - ₹35,000 a month
- Full-time
- Master's degree
- Bachelor's degree
- Organizational skills
Quick apply
Purchase Executive - Pharmaceutical Industry
VITAL CARE PVT LTD —Atladara, Vadodara, Gujarat
- ₹20,000 - ₹30,000 a month
- Full-time
- Oracle
- ERP systems
- Microsoft Office
Quick apply
3d
Pharmaceutical Quality Analyst
HITECH ANALYTICAL LABORATORY LLP —Ahmedabad, Gujarat
- ₹14,000 - ₹50,000 a month
- Full-time
- Laboratory experience
- Master's degree
- Bachelor's degree
Quick apply
Executive _Quality Control Microbiology
Amneal Pharmaceuticals —Ahmedabad, Gujarat
- Full-time
- Master's degree
Assistant Manager Quality Control - Reliance Rasayan - API WHO-GMP Facility
RELIANCE RASAYAN PVT LTD —Narol, Ahmedabad, Gujarat
- ₹45,000 - ₹50,000 a month
- Full-time
- Laboratory experience
- Master's degree
- APIs
Quick apply
7d
QA Officer Trainee (Pharmaceutical )
Briyosis Softcaps Pvt Ltd —Jarod, Gujarat
- ₹1,50,000 - ₹2,50,000 a year
- Full-time
- Microsoft Word
- B.Sc
- Master's degree
Quick apply
3d
CQA
Globela Pharma Pvt. Ltd. Unit-II —Sachin, Surat, Gujarat
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Quick apply
7d
Assistant Manager, Quality Control
Amneal Pharmaceuticals —Ahmedabad, Gujarat
- Full-time
- B.Sc
- Master's degree
- Bachelor's degree
Chemist
Sigachi Industries Limited —Dahej, Gujarat
- ₹12,000 - ₹40,000 a month
- Full-time
- B.Sc
- Laboratory experience
- Master's degree
- Paid time off
- Flexible schedule
Quick apply
1d
Deputy Manager, Quality Control
Amneal Pharmaceuticals —Ahmedabad, Gujarat
- Full-time
- Master's degree
QA Officer
Dadaji Lifescience Private Limited —Rajkot, Gujarat
- ₹20,000 - ₹25,000 a month
- Full-time
- B.Sc
- Master's degree
- Bachelor's degree
Quick apply
Research Associate
Cadila Pharmaceuticals Ltd —Dholka, Gujarat
- Full-time
- APIs
1d
Trainee Officer, Quality Control
Amneal Pharmaceuticals —Ahmedabad, Gujarat
- Full-time
- Bachelor's degree
4d
QA Officer
Asons Pharmaceuticals Pvt Ltd —Vejalpur, Gujarat
- From ₹14,000 a month
- Full-time
- Quality control
- In-person
- Manufacturing
Quick apply
Management Trainee
Cadila Pharmaceuticals Ltd —Dholka, Gujarat
- Full-time

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Quality Control Officer

CELOGEN PHARMA PVT LTD -
Mahesana, Gujarat

Quick apply

Job details

Full-time
₹20,000 - ₹25,000 a month

Qualifications

Microsoft Powerpoint
Microsoft Word
Six Sigma Certification
Microsoft Excel
Laboratory information management systems
Microsoft Office
Master's degree
Analysis skills
Bachelor's degree
Quality control
Pharmacy
Chemistry
Manufacturing
Communication skills
Lean manufacturing
Time management

Full job description

Job Title: Quality Control Officer

Location: Mehsana, Gujarat

About Celogen:

Celogen Pharma Pvt. Ltd. is a leading pharmaceutical formulations exporter/manufacturer based in India. The company provides it products and services in multiple countries globally including West Africa, East Africa, South Asia, South East Asia, the Middle East, South America & Europe. Apart from promoting our branded products in the retail sector, we also participate in a number of global tenders in a number of countries. The team comprises of a group of first generation marketing expats and some of the best technocrats in the field. The company has four manufacturing bases in India, manufacturing a variety of products.

This job posting is in a hormone formulation manufacturing division of Celogen Pharma.

Job Summary:

The Quality Control Officer will be a key member of our Quality Control team, responsible for ensuring the highest standards of quality for our pharmaceutical products, from raw materials to finished goods. This role involves the execution and oversight of various analytical tests, data review, documentation, and active participation in laboratory investigations and continuous improvement initiatives. The ideal candidate will have a strong background in pharmaceutical QC, excellent analytical skills, and a thorough understanding of cGLP guidelines.

Key Responsibilities:

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, GC, UV-Vis, FTIR, 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.

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.

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.

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.

Compliance & Audits:

Ensure strict adherence to current Good Manufacturing Practices (cGMP), Good Laboratory Practices (GLP), and other applicable regulatory guidelines (e.g., FDA, MHRA, WHO).
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.

Training & Mentorship:

May assist in training junior QC analysts on analytical techniques, instrument operation, and laboratory procedures.
Serve as a technical resource for other team members.

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.

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.

Educational Qualifications & Experience:

Education: Bachelor's or Master's degree in Pharmacy, Analytical Chemistry, Chemistry, or a related scientific discipline.
Experience: 1-2 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.
Experience with LIMS (Laboratory Information Management System) is highly desirable.
Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint).
In-depth knowledge of cGMP, 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.
Certification in Six Sigma or Lean Manufacturing is a plus.

To Apply:

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

Job Type: Full-time

Pay: ₹20,000.00 - ₹25,000.00 per month

Ability to commute/relocate:

Mahesana, Gujarat: Reliably commute or planning to relocate before starting work (Required)

Application Question(s):

Do you know how to operate an HPLC system ?

Work Location: In person

Quick apply

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