Role & responsibilities - Coordinating with statutory, tax auditors - GST Reconcillation - Return Filing under Income Tax & GST - Fixed Assets Register Management - Quarterly TDS Returns - Experienced with subsidiary accounting and preparation of consolidated financial statements - Must be proficient in Excel and should be able to perform advanced Excel functions such as Vlookup, Mail Merge, Pivot Tables Preferred candidate profile - Must be a chartered accountant with an experience of 3-5 years Perks and benefits - Leave Salary, Bonus
Key Responsibilities: Perform routine microbiological testing of water, raw materials, in-process samples, and finished products. Conduct environmental monitoring of clean rooms and production areas. Execute microbial limit tests, sterility testing, endotoxin testing, and identification of microorganisms. Validate and monitor sterilization processes Maintain microbiology lab equipment and ensure proper calibration. Maintain accurate documentation and data entry in compliance with cGMP and GLP standards. Support regulatory audits and inspections by providing required data and records. Collaborate with Quality Assurance and Production teams to investigate and resolve microbial contamination issues. Develop SOPs, protocols, and reports for microbiological activities. Qualifications: B.Sc. / M.Sc. in Microbiology or related life sciences field. Experience in a pharmaceutical microbiology lab preferred (Freshers with strong academic background may also be considered). Sound knowledge of microbiological techniques and relevant pharmacopeial standards (USP, IP, BP). Familiarity with cGMP, GLP, and other regulatory guidelines. Strong documentation, analytical, and communication skills. Desired Attributes: Attention to detail and commitment to accuracy Ability to work independently and as part of a team Problem-solving mindset and proactive approach Willingness to work in shifts, if required
We are seeking a detail-oriented Excel & Documentation Specialist with strong English fluency to support our team with data management, reconciliation, documentation, and professional communication . The ideal candidate should be proficient in Excel , be willing to assist in documentation , and drafting business letters and reports . Roles and Responsibilities Excellent knowledge of Word and Excel. Strong Excel skills (Pivot Tables, VLOOKUP, INDEX-MATCH, data validation) Excellent English proficiency (written and spoken) for documentation and communication. Desired Candidate Profile Knowledge of MS Office / other software Extremely Computer Savy Languages: English (Fluent); Strong Verbal and Written Communication. Job Benefits & Perks Bonus
Key Responsibilities Production Oversight Monitor routine activities in sterile manufacturing and filling areas. Ensure adherence to batch manufacturing records (BMR) and SOPs during production. Assist in line clearance before starting new batches. Compliance & Documentation Maintain accurate in-process records and logbooks. Ensure compliance with cGMP, WHO, and regulatory requirements. Support in documentation during in-process checks. Equipment & Facility Management Check cleanliness, calibration, and readiness of equipment. Coordinate with maintenance for breakdowns or preventive maintenance. People & Process Support Supervise operators and contract staff to ensure correct procedure execution. Provide basic on-the-job training to floor staff. Quality & Safety Monitor environmental control parameters in aseptic areas. Report any deviations, breakdowns, or non-compliance to the senior supervisor/manager. Follow and enforce safety protocols and PPE usage. Qualifications & Skills Education: B.Sc. / M.Sc. (Chemistry, Microbiology) or B.Pharm / M.Pharm. Experience: 03 years in sterile/aseptic manufacturing preferred (freshers with strong academic background may be considered). Skills: Basic knowledge of aseptic techniques and cleanroom operations. Understanding of BMR, SOPs, and documentation practices. Ability to work in a team and follow instructions. Attention to detail and good communication skills.
Overview We are looking for a Personal Assistant with a strong background in Accounts & Finance , excellent English writing and drafting skills , and high proficiency in Excel and computer applications . The role will involve handling accounts, drafting professional correspondence, preparing reports, and supporting in GST return filing and compliance . Knowledge of Excel Macros (VBA) will be an added advantage. Key Responsibilities Maintain accurate books of accounts, ledgers, and reconciliations . Prepare MIS reports, financial statements, and cash flow summaries . Handle GST return filing and support in statutory compliance. Assist in audit preparation, taxation, and regulatory requirements . Draft and review letters, notices, and professional correspondence in English. Create and maintain Excel-based reports and dashboards (Pivot, VLOOKUP, Power Query). (Preferred) Automate reports and repetitive tasks using Excel Macros/VBA . Maintain organized documentation and filing systems (digital & physical). Ensure confidentiality and accuracy in all financial and business information. Required Skills Strong command over English writing, drafting, and communication . Advanced Excel proficiency (Pivot Tables, formulas, Power Query). Familiarity with Excel Macros/VBA preferred. Hands-on knowledge of GST return filing and related compliance. Experience with accounting software (Tally/ERP or similar). High attention to detail, accuracy, and integrity. Ability to work independently and manage multiple tasks effectively. Qualifications CA (preferred) / Semi-qualified CA / M.Com / MBA (Finance). 2-4 years experience in accounts, audit, taxation, or GST compliance . Prior exposure to letter drafting and business correspondence will be an added advantage. Compensation Competitive salary, aligned with qualifications and experience.
Key Responsibilities Supervise day-to-day production activities for Capsules and Dry Syrup sections. Ensure adherence to Batch Manufacturing Records (BMR/BPR), SOPs, and cGMP practices. Coordinate with QA, QC, Stores, and Maintenance to ensure smooth operations. Plan and monitor production schedules, manpower allocation, and material availability. Maintain accurate documentation, in-process checks, and production records. Ensure equipment calibration, cleaning validation, and line clearance before batches. Identify process deviations and support investigation and CAPA implementation. Support in regulatory audits, internal audits, and documentation readiness. Train and supervise operators, ensuring safety and hygiene in the production area. Support scale-up and technology transfer of new products in coordination with R&D. Required Skills & Competencies Strong technical knowledge of capsule filling, dry syrup formulation, and granulation processes. Understanding of WHO-GMP / Schedule M compliance requirements. Proficiency in documentation, SOP writing, and deviation handling. Excellent coordination and team management skills. Analytical mindset with attention to detail and process optimization. Qualifications & Experience B.Pharm / M.Pharm / B.Sc / M.Sc in Pharmaceutical Sciences or related field. 5–8 years of experience in OSD production (Capsules/Dry Syrup) in a WHO-GMP compliant facility. Experience in regulatory audits (WHO, State FDA, etc.) preferred.
Role & responsibilities Job Title: Quality Control / Quality Assurance Executive (Fresher) Industry: Pharmaceuticals Manufacturing Department: Quality Control (QC) / Quality Assurance (QA) Company: Vivek Pharmaceuticals Pvt Ltd Location: Jammu Employment Type: Full Time Experience: 0 2 Years Qualification: B.Pharm / M.Pharm / B.Sc / M.Sc (Chemistry, Microbiology, Biotechnology or related field) Job Summary: We are looking for passionate and detail-oriented candidates to join our Quality team. The selected candidates will be part of controlling product quality, compliance with regulatory requirements, and in all quality operations. Key Responsibilities: Quality Control (QC): Conduct routine tests using instruments like HPLC, GC, UV, IR, Dissolution Apparatus, etc. Maintain laboratory records and documentation as per cGMP standards. Ensure timely calibration and maintenance of lab instruments. Support stability studies and preparation of analytical reports. Quality Assurance (QA): Review batch manufacturing and packaging records. Participate in internal audits, change control, deviation handling, and CAPA activities. Assist in documentation control SOPs, specifications, validation protocols, and reports, batch manufacturing records. Support training and quality systems across departments. Skills & Competencies: Strong understanding of GMP, GLP, and regulatory guidelines. Good communication and documentation skills. Basic knowledge of analytical techniques and instruments. Keen attention to detail and commitment to quality. How to Apply: Email your Resume: recruiter.vpj@gmail.com Contact Number: 95414 20147 Preferred candidate profile
Role & responsibilities - Coordinating with statutory, tax auditors - GST Reconcillation - Return Filing under Income Tax & GST - Fixed Assets Register Management - Quarterly TDS Returns - Experienced with subsidiary accounting and preparation of consolidated financial statements - Must be proficient in Excel and should be able to perform advanced Excel functions such as Vlookup, Mail Merge, Pivot Tables Preferred candidate profile - Must be a chartered accountant with an experience of 3-5 years Perks and benefits - Leave Salary, Bonus