Ipqa - 156+ job offers

Sundyota Numandis Pharmaceuticals

IPQA Officer Department- QA Experience: - 1 to 2 years in OSD Pharmaceutical Industry Location - Ahmedabad Interested candidate share cv on- 8010601352 Required Candidate profile Role- 1)Handling In-Process Quality Assurance (IPQA) activities of dispensing, granulation, blending, compression, coatin

Nutralike Health Care

Roles and Responsibility Develop and implement comprehensive quality control processes to ensure compliance with regulatory requirements. Conduct regular audits and inspections to identify areas for improvement and implement corrective actions. Collaborate with cross-functional teams to resolve qual

USV

Line Clearance :–To give the line clearance for the different activity in their concern area like Dispensing, Granulation, Blending, Compression, Capsule, Coating and Packing as per their respective SOPs and batch records. Monitoring & Verifying of Records : – To monitor day to day activity in a

Amneal

Description Description: To ensure compliance with cGMP and regulatory requirements by performing in-process quality assurance activities on the manufacturing and packaging shop floor, including real-time monitoring, documentation review, sampling, and area/machine clearances, thereby supporting the

Growup Consultancy

₹25,000 - ₹50,000 /month

Responsibilities Conduct regular audits and inspections Ensure compliance with quality standards Collaborate with production team on improvement initiatives Monitor product quality during manufacturing process Call or whatsaap 8128793206 Perks and benefits Annual bonus, Provident fund

Quality HR India Pvt Ltd

Monitor manufacturing processes to ensure compliance with quality standards. Perform in-process inspections and record observations during production. Required Candidate profile Verify batch documentation, logbooks, and process parameters. Identify deviations, non-conformances, and initiate correcti

Quality HR India Pvt Ltd

IPQA (In-Process Quality Assurance) Monitoring -Supervise and monitor all IPQA activities in manufacturing areas. Ensure compliance with cGMP guidelines during production processes. Required Candidate profile Very good English written and verbal communication; preferably from medical device or Pharm

Natural Capsules

Qualification: BSc/Msc/B.Pharm Roles and Responsibilities: Experience: Freshner/ Experience 2-3 years. Having knowledge about IPQC inspections aware of rootcause analysis tools. Aware of CGMP practices ability to guide a team of 20 members Salary : Neogiatable based on their experience subject knowl

BDL - Beta Drugs Ltd.

Company Description Beta Drugs Ltd. (BDL) is a global leader in the field of oncology, committed to developing innovative products and advancing scientific knowledge. With a focus on delivering value to customers, BDL enhances the speed-to-market and effectiveness of its product launches. Backed by

Jairamdass Khushiram

₹16,667 - ₹29,167 /month

In-Process Monitoring,Line Clearance Activities,Documentation & Compliance,GMP & Hygiene Monitoring,Deviation & Investigation Support,Sampling & Verification,role involves line clearance, in-process checks, documentation verification, Required Candidate profile 1–5 years of experienc

Eurocrit Labs International Pvt Ltd

Line Clearance & Inspection: Conducting, verifying, and documenting line clearance before manufacturing and packaging to prevent cross-contamination. Aseptic Area Monitoring: Monitoring environmental conditions (temperature, humidity, pressure differentials) and adherence to aseptic gowning proc

GUFIC BIOSCIENCES LIMITED

₹25,000 - ₹41,667 /month

Key Responsibilities In-Process Quality Assurance (IPQA): Monitor and ensure compliance during manufacturing and packing operations. Conduct routine checks and validations to maintain product quality. Line Clearance Activities: Perform and document line clearance before batch initiation and between

Amneal Pharmaceuticals

Description JOB DESCRIPTION The role is responsible for ensuring day-to-day compliance with global GMP (Good Manufacturing Practices) during manufacturing, packing, and dispensing activities at the site. The role provides on-floor quality assurance support, ensuring operations are performed as per a

Amneal

Description Description: To ensure compliance with cGMP and regulatory requirements by performing in-process quality assurance activities on the manufacturing and packaging shop floor, including real-time monitoring, documentation review, sampling, and area/machine clearances, thereby supporting the

STL Digital Consulting

Job Description Role description Role Purpose: Oversees and plans quality control tests and analysis of software to meet or exceed specified standards and end user requirements Key Accountabilities: Bachelorãâ¢ãâãâs Degree in Computer Science 5+ years experience in a QA Certification in testing auto

Hanuchem Laboratories

Conduct thorough testing and validation of eye drops to ensure compliance with regulatory standards.Develop and implement effective quality control processes to prevent defects and improve product quality.Collaborate with cross-functional team Required Candidate profile Proven experience in quality

Umendra Life Sciences

Job Title: QA Officer IPQA (In-Process Quality Assurance) Company: Umendra Life Sciences Pvt. Ltd. Location: Bavla, Greater Ahmedabad, Gujarat (On-site | Manufacturing Plant) Experience: 13 Years Education: B.Sc / M.Sc / B.Pharm / M.Pharm Industry: Pharmaceuticals / Life Sciences Functional Area: Qu

NATURAL CAPSULES LTD.

Natural Capsules Limited provides excellent work and growth environment to people coming from diverse backgrounds. Each of these personnel possesses an extensive array of experience. The culture thrives on hard work, innovation, mutual respect, and a sense of accountability and responsibility. This

Job Description: Process Monitoring: Ensure production follows SOPs, HACCP plan, and quality standards. In-Process Checks: Conduct routine inspection/testing (moisture, weight, contamination, etc.). Line Clearance: Verify cleanliness, correct materials, and labeling before start-up. CCP verification

Flax Laboratories

Adhering to SOPs, GMP, and regulatory requirements. Sampling of Finished Product. Preparation of Annual Product Quality review. Plant round and ensure compliance status inline with regulatory requirement. Close monitoring of production processes.