1,738 Cipla jobs in India

Job Title: Team Member - Technical Agreements

Division: Quality

Department: Corporate Quality Assurance

Sub Department: Commercial Compliance and Quality Systems

Accountabilities:

• To ensure logging of Quality Technical Agreement (QTA) requests (new / periodic / revision) in the excel sheet.

• To ensure QTAs related to outsourcing activities for Formulations, API and approved External Quality Control Testing Laboratories are prepared, reviewed and approved as per Customer / Company / Regulatory requirements.

• To ensure valid QTAs are available for Formulations, API and for approved External Quality Control Testing Laboratories.

• To prepare standard generic templates of QTAs and to carry out review / updation / customization of QTAs through mutual acceptance of partner(s) involved.

• To ensure that current version of generic template of QTAs are uploaded in server.

• Timely and effective coordination / follow-ups with cross functional teams / internal stake holders and relevant partner(s) for various inputs, review comments related to QTAs.

• Initial and reviewed by signatory for QTAs on behalf of Cipla Limited.

• To upload QTAs in SAP.

• Distribution of QTAs to the respective Manufacturing units, Regulatory Affairs, Business Development team, etc. and each of the partner(s).

• Maintenance of master hard and soft copies of QTAs.

• To perform the designated task through softwares like CipDox (Document Management System), TrackWise (Deviations, CAPA), SAP, etc. as per assigned roles and rights.

• To ensure the availability of updated list of QTAs for Formulations, API and External Quality Control Testing Laboratories.

• Providing timely updates and MIS report (Management Information System report) to the reporting manager.

Education Qualification: M. Sc/ B. Pharm

Excellent Opportunity

Analysts required in the QC department at Unison Pharmaceuticals Pvt Ltd, Moraiya.

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Company: Unison Pharmaceuticals Pvt Ltd

Experience: 1-7 Years

Qualification: Pharma

Location: Moriya, Ahmedabad

Job Role :

Physico Chemical (Analyst)- Friability / DT / Hardness / Thickness / UV

• Perform physical and chemical analysis for Raw material/ In process / Finished Product based on the test requirements like UV, friability, DT, hardness, thickness, moisture, average weight, and uniformity weight.
• Prepare documents for each analysis performed and get those checked by the reviewer.

HPLC Analyst:

• Carry out HPLC testing for assay, related substances, dissolution, and stability samples.
• Operate and maintain HPLC systems (Waters, Agilent, Shimadzu) with appropriate software (Empower/Chromeleon).
• Prepare standard and sample solutions as per SOPs and approved procedures.
• Document and report results with accuracy and clarity in analytical worksheets, logbooks, and LIMS (if applicable).
• Ensure compliance with GMP, GLP, and ALCOA+ data integrity principles.
• Perform regular calibration and maintenance of HPLC instruments.
• Support OOS/OOT investigation and participate in deviation handling and CAPA implementation.

Perks & Benefits

Dynamic work environment

Career development opportunities

Work-life balance

Free transportation

Canteen Facility

Free insurance coverage for self, spouse, and kids

Range of learning opportunities to help employees grow and thrive

If you are passionate about continuing to work in the pharmaceutical industry and possess the required skills, we encourage you to apply for this position.

Please submit your resume to to be considered for this role.

Join our team at Unison Pharmaceuticals and take the first step towards a rewarding career

Regards

Team HR

Unison Pharmaceuticals Pvt. Ltd.

We are expanding

You are invited to join one of the fastest growing pharma companies in India

About us: Unison Pharmaceuticals Private Limited (Formerly known as Unison Pharmaceuticals) was established in 1981 with a vision of providing quality and affordable medicines across the nation. With more than 4 decades of medical service to society, Unison is today one of the fastest-growing companies in Gujarat State. In addition to this, the company is ranked 82 among the top companies of India (Rupee wise sales) MAT March 2020. This makes Unison a distinguished company across the pharma industry.

Department: Quality Control

Section: HPLC Analysis & Chemical Analysis/ QC QMS

Experience: 2-7 years

Designation: Officer / Sr. Officer / Executive

Location: Moraiya, Ahmedabad.

No. of Openings:

HPLC Analysts: 5

Physico Chemical Analysts: 5

QC QMS: 2

Perks & Benefits:

• Dynamic work environment
• Career development opportunities
• Work-life balance
• Free transportation
• Canteen Facility
• Free insurance coverage for self, spouse, and kids
• Range of learning opportunities to help employees grow and thrive

If you are passionate about continuing to work in the pharmaceutical industry and possess the required skills & experience, we encourage you to apply for this position.

Regards,

HR Team

Unison Pharmaceuticals Pvt Ltd

Job Description - Quality Assurance / Control / Inspection (Textiles)

Location: Budhni, Madhya Pradesh

Experience Required: 3-7 Years

About Trident Group

Trident Group is a globally recognized leader in textiles, paper, and chemicals. With state-of-the-art manufacturing facilities and a focus on innovation, quality, and sustainability, we are seeking a Quality Assurance/Control/Inspection professional with a strong background in textiles to strengthen our quality operations at Budhni.

Role Overview

The Quality Assurance/Control/Inspection professional will be responsible for maintaining and improving quality standards across yarn, spinning, and textile production processes. The role involves quality checks, process monitoring, defect analysis, and ensuring compliance with industry standards.

Key Responsibilities

• Conduct quality inspections at all stages of yarn, spinning, and textile manufacturing.
• Implement and monitor quality control systems to ensure adherence to specifications.
• Test and analyze raw materials, in-process, and finished products for physical, chemical, and performance parameters.
• Identify defects, variations, and root causes, and recommend corrective actions.
• Collaborate with production teams to maintain process consistency and reduce rework/rejections.
• Maintain documentation of test results, inspection records, and quality reports.
• Support in quality audits, certifications, and customer compliance requirements.
• Drive continuous improvement initiatives in quality processes and standards.
• Ensure compliance with environmental, health, and safety norms within the quality domain.

Desired Skills & Qualifications

• B.Tech / M.Tech in Textiles from a reputed institute (mandatory).
• 3-7 years of experience in quality assurance/control/inspection in yarn, spinning, or textile manufacturing.
• Strong knowledge of textile testing standards (domestic & international).
• Familiarity with quality management systems (QMS) such as ISO, OEKO-TEX, or similar certifications.
• Analytical mindset with attention to detail and problem-solving abilities.
• Proficiency in MS Excel, ERP systems, and reporting.
• Good communication and coordination skills with cross-functional teams.

Why Join Us

• Opportunity to work with cutting-edge textile manufacturing facilities.
• Exposure to large-scale, export-oriented production processes.
• Competitive compensation and career growth opportunities.
• Be part of a quality-driven and innovation-led culture at Trident Group.

Job Location: Daman & Dahej

Qualification:- M.Sc. (Chemistry)/ B. Pharma/ M. Pharma

Experience:- 2-6 Years in (API or Solid Oral)

Required Candidate profile

* 2-6 years of experience into LCMS, HPLC, GC & Wet Chemical sections

* 2-6 years of experience into Analytical Validation, Finished Goods, Raw Material, Stability & GLP

Role & responsibilities

We are looking for a highly motivated and detail-oriented QC Microbiology Fresher to join our Quality Control team. As a QC Microbiology Fresher, you will be responsible for performing various microbiological testing, ensuring that products meet regulatory standards and maintaining the microbiology lab's cleanliness and safety protocols. The role offers a great opportunity for growth and learning in the pharmaceutical/biotech industry.

• Microbial Testing: Conduct sterility testing, endotoxin testing, and bioburden testing.

• Sample Handling:
  
  Collect and handle microbiological samples (raw materials, in-process materials, and finished products). Maintain accurate records of sample analysis.

• Media Preparation:
  
  Prepare and sterilize microbiological media, solutions, and reagents as per the standard operating procedures (SOPs).

• Lab Equipment Maintenance:
  
  Operate, maintain, and calibrate laboratory equipment, including autoclaves, incubators, and microscopes. Ensure equipment is functioning properly and troubleshoot as necessary.

• Documentation and Reporting:
  
  Document test results accurately and ensure that they are in compliance with company standards and regulatory requirements.

Assist in preparing microbiological reports and quality control documentation.

• Compliance:
  
  Follow Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP) in all lab operations. Ensure compliance with environmental health and safety guidelines within the lab.

• Quality Assurance Support:
  
  Assist in the preparation for audits by regulatory bodies (e.g., FDA, WHO). Participate in internal and external quality control audits.

Preferred candidate profile

• Strong attention to detail and accuracy.
• Good communication and interpersonal skills.
• Ability to work effectively both independently and as part of a team.
• Full-time position.
• Opportunity for career growth and advancement within the QC department.

Interested candidates can share their CV on

• Perform regular quality assessments on all incoming materials from vendors and outgoing products for shipping.
• Should have Diploma in Mechanical and working in ERP Software.
• Reject all products and materials that fail to meet quality expectations.
• Read blueprints, plans, and specifications to understand the requirements of products and services.
• Measure product dimensions, examine functionality, and compare the final product to the specifications.
• Recommend improvements to the production process to ensure quality control.
• Document inspection outcomes by completing detailed reports and performance records.
• Teach the production team about quality control concerns to improve product excellence.
• Supervise the production process.
• Resolve quality-related issues in a timely manner.

Job Types: Full-time, Permanent

Pay: From ₹15,000.00 per month

Ability to commute/relocate:

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

Experience:

• total work: 1 year (Preferred)

Work Location: In person

Responsible for day-to-day activities of Quality Control,

prepare and maintain documentation as per cGMP norms.

Working Experience on HPLC is must

Coordinate with other depart for smooth running of plant

Capable of handling external Audits

Required Candidate profile

Min Exp 2 to 10 years in Quality department of a reputed pharmaceutical Company

Knowledge of working in GMP Co. MS Office (MS Word & MS Excel) / ERP software.

and good time management skills

Perks and benefits

Performance linked incentive & annual bonus extra