95 Job openings found

Job Description: We are seeking a skilled and experienced microbiology professional to lead microbial testing and environmental monitoring activities in an API manufacturing setup. The Assistant Manager will ensure compliance with regulatory standards, supervise microbiological operations, and support quality systems in the microbiology lab. Key Responsibilities: Oversee routine microbiological testing of raw materials, ...

1. Adhere to cGMP and GDP practices and perform activities as per SOP.   2. Verify documents and ensure all activities, activities are performed as per SOP.   3. Final Quality Check & Approval of the finished products (Components, assemblies/2D/3D bags/liners).   4. Execute shift production as per planning and verify Integrity report and sealing parameters   5. ...

Job Descripation 1. Responsible for Checking & distribution of approved artwork.2. Responsible for colour approval of the shade card.3. Responsible for the Allocation & Verification of the Pharma code.4. Responsible for the Allocation & Verification of GTIN numbers as per GS1 guidelines.5. Artwork management as per the product brief.6. To verify ...

Experience: 10+ years of experience including team handling experience in similar domain Location: Ahmedabad, Gujarat   Summary of Profile specifications:   Incumbent should have sound knowledge of domestic regulatory functions with ref to DBT-RCGM, CDSCO and state FDA regulations.  He/she should be a seasoned professional with leadership qualities, have knowledge about NDCT rules, Biosimilar guidelines, cGMP ...

Job Title: Quality Head (Biosimilars, Insulin & Dry Powder Formulations) Department: Quality Assurance Location: Bhopal Reports To: Plant Head / Corporate QA Head   Position Summary: Eris Lifesciences is looking for a seasoned Head – Quality Assurance to lead QA operations for its biotech and sterile manufacturing unit, specializing in biosimilars, insulin, vaccines, monoclonal antibodies (MABs), and ...

6.1 Over all responsibility of Quality Assurance Department. 6.2 Vendors approval for RM & PM. 6.3 Periodical Quality Audit. 6.4 Activities related to Drug Control Authorities. 6.5 Evaluation of Product Complaints & Product Recall. 6.6 Validation and Qualification. 6.7 GMP Training to Staff. 6.8 GMP Implementation in the factory. 6.9 Co-ordination with various departments to implement cGMP in ...

Position:         QC Officer  Location:        Daman Experience:     4 - 5 Years Industries:      Pharma  Responsibilities: Individually handling department & manpower. Strong leadership skills to guide, supervise work activities, and help team members develop their skills. Work allocation / Planning and Review of documents. Preparation of SOP, Specification, Standard Test Procedures (STP), ...

The job description is as below: • Monitor team metrics and objectives ensuring meeting of goals. • Maintain all technical document of all phases of research and development. • Assess the scope of projects and ensure that they are on time and within budget. • Maintain the BOM and review the changes or modifications ...

Job Title: Plant Head - Pharma Pellet Manufacturing Facility Location: SB Organics, Chandapur Village, Hathnoora Mandal, Sangareddy District, Telangana Company Overview:SB Organics is a WHO-GMP accredited pharmaceutical pellet manufacturing facility dedicated to producinghigh-quality medicines. We are committed to adhering to the highest standards in manufacturing, ensuring the safety,efficacy, and compliance of our ...

DISCIPLINE / DEPARTMENT VALIDATION & QUALIFICATION / GMPPOSITION EXECUTIVE (FEMALE CANDIDATE ONLY)EXPERIENCE REQUIRED MIN. 2-6 YEARSCTC DEPENDING UPON CANDIDATE’S KNOWLEDGE AND EXPERIENCEQUALIFICATION B. PHARMA / M. PHARMA / M.SC. LIFE SCIENCES JOB DESCRIPTION:• Comprehensive understanding of complete validation life cycle, risk-based qualificationmethodology• Experience in pharmaceutical OSD facility / Sterile facility or ...