10 Who Gmp Jobs

You will be responsible for overseeing the Quality Assurance department of the Pharmaceutical formulation unit. Your key responsibilities will include: - Demonstrating a minimum of 10 to 15 years of experience in QA within the Pharmaceutical industry - Possessing knowledge of Regulatory requirements and documentation such as water validation, process validation, etc. - Conducting training sessions for junior staff on incident management, change control, CAPA, and other relevant topics - Demonstrating expertise in WHO GMP / cGMP standards Your qualifications should include: - M.Pharm / B.Pharm / M.Sc. degree - Minimum of 10 to 15 years of experience in QA within the Pharmaceutical formulation...

Role & Responsibilities: Preparation of Analytical Method Validation (AMV) protocols, reports, and compilation of raw data. Execution of validation for compendial procedures as per USP General Chapter (1225). Performing validation of analytical procedures in accordance with ICH Q2(R1) guidelines. Conducting analytical method validation as per WHO GMP Volume-2 (Updated). Preparation and implementation of SOPs for Analytical Method Development and Validation. Preparation and execution of SOPs for Analytical Method Transfer. Ensuring all analytical activities comply with regulatory and quality standards. Performing analysis using analytical instruments such as HPLC, GC, FTIR, AAS, UV-Vis Spectr...

As a Quality Assurance Officer in the Pharma background, your role is crucial in maintaining the quality standards and regulatory compliance within the company. Your main responsibilities include: - Maintaining quality training requirements in compliance with FDA and other regulations. - Keeping up-to-date training records and updating training programs as necessary. - Designing training programs for both new and existing employees, from implementation to evaluation. - Proactively interacting with a wide range of employees to conduct training programs, support product launches, and enhance programs. Your skills should include: - Ensuring GMP & regulatory compliance, SOPs, and Change control....

Company Description AMN Life is a leading manufacturer and exporter of a wide range of formulations in various therapeutic segments including antibiotics, gastro, anti-inflammatories, cardiology, nephrology, CNS, and oncology. With facilities approved by EU, Health Canada, Brazil - Anvisa, and Philippines situated in Bhilad (Gujarat) and Kala Amb (Himachal Pradesh), AMN Life is equipped to handle large scale production and tech transfer projects. Headquartered in Bandra Kurla Complex, Mumbai, with offices in Singapore, UK, Australia, and Philippines, AMN Life excels in providing quality medicines at affordable prices globally. We are recognized for our strong global presence, innovative R&D,...

About the job About us/Company overview: mCaffeine is India's 1st caffeinated personal care brand with an exciting range of caffeinated products for young and aspiring millennials. We believe in confidence over all skin and body biases. Redefining age-old notions of beauty associated with colour, we never sell insecurities. We have vowed not to make fairness products. At mCaffeine, beauty has no colour or gender it's about you .You are a revolution, a culture, a routine, a high, and essentially now a lifestyle . You are Bold, Young, and Confident . Come, join the pack! Role Overview: We are looking for a Senior Executive QA & QC with strong experience in cosmetic manufacturing and a deep und...

We have been retained by a fast upcoming and highly reputed Pharma company to hire a "General Manager - Operations" to be based at Baddi (Himachal Pradesh). Details of the position are mentioned below: Company: Our client operates a WHO - GMP approved liquid oral manufacturing facility at Baadi (Himachal Pradesh). The company is a third party manufactures for Most of Top 50 Pharma companies in India. Designation: General Manager Operations Reporting to: Director Experience: 10 - 20 years of similar experience with a reputed Pharma company. Main Task: General Manager (GM) shall have responsibilities as enumerated below: To manage the manufacturing element of the organization ensuring high qua...

Oversee complete Production & Manufacturing operations at the Pharmaceutical Formulation Unit Ensure smooth execution of batch manufacturing for OSD (Tablets, Capsules, Dry Syrups) Ensure compliance with FDA regulations and GMP guidelines Monitor production efficiency, process optimization & manpower management Coordinate with QA, QC, and Regulatory teams for smooth operations Handle regulatory audits, validation, and documentation processes OSD Manufacturing Tablets, Capsules, Dry Syrups FDA Approval & Regulatory Compliance (WHO-GMP, Schedule M preferred) Production Planning & Process Optimization Team Leadership & Manpower Management

You should have a minimum of 10 to 15 years of experience in the QA department of Pharmaceutical formulation. Your responsibilities will include having knowledge of regulatory requirements and documentation such as water validation, process validation, incident management, change control, CAPA, etc. It is essential for you to be capable of providing training to junior staff. Familiarity with WHO GMP/cGMP is a requirement. The ideal candidate will hold an M.Pharm/B.Pharm/M.Sc. degree.,

You are invited to apply for the position of Quality Assurance Officer in the Pharma industry. This role specifically targets male candidates with a Pharma background. The Quality Assurance Officer will be based in Indore (Rajendra Nagar) and will be responsible for ensuring quality standards in compliance with regulatory requirements. Candidates with a qualification of B.com/B.pharma/B.tech and a minimum experience of 5 to 8 years in QA Pharma are preferred for this role. As a Quality Assurance Officer, your responsibilities will include maintaining quality training programs in adherence to FDA and other regulatory guidelines. This involves keeping training records up-to-date and revising p...

You should have a minimum of 5 years of experience in the packing department within the pharmaceutical, healthcare, or food processing industry. Your experience should include familiarity with Lean, OEE, and similar KPIs, as well as hands-on experience with UK MHRA or US FDA procedures. Additionally, you should have experience in equipment procurement, installation, startup, validation, and trial production run of a new WHO GMP compliant packing facility. As a part of your duties and responsibilities, you will be required to manage the packaging processes, ensure and control packaging activities, monitor yield losses during the packaging process, and ensure cost-effective packing material co...