GMP Jobs

Urgent opening for Senior Quality in Beverages Company @ AmbalaExperience - 4+ Years of experience within the beverage industry, focusing on QA/QC.Salary - 6 to 7 Lakh paTypical QualificationsEducation: Bachelor's degree in Food Technology, Food Science, Engineering, or a related field.Skills: Strong knowledge of HACCP, GMP, sensory evaluation, and proficiency in MS Office for reporting.An Assistant Manager of Quality in the beverage industry ensures that products meet strict safety, regulatory, and company standards, with an average salary ranging from 6.4 Lakhs to over 9.8 Lakhs per year depending on experience. Key responsibilities include conducting audits, ensuring ISO 22000 compliance, and monitoring production quality.+3Key Responsibilities & Account abilitiesQuality Assurance & Compliance: Ensure 100% compliance with food safety regulations, regulatory norms, and ISO 22000 standards in manufacturing plants.Auditing: Conduct regular audits of manufacturing facilities, vendors, warehouses, and cold storage, often requiring at least 25-30 audits per month.Production Monitoring: Oversee daily quality control checks, sensory evaluations, and monitor the temperature of raw materials and finished goods in logistics.Reporting & Improvement: Analyze audit findings to prepare monthly reports, implementing corrective and preventive actions (CAPA) to improve processes.Training: Train production staff on quality standards and food safety practices.

Key Responsibilities Sample Analysis: o Conduct chemical and physical analysis of raw materials, intermediates, and finished products using standard laboratory techniques. Perform stability studies and report observations. Documentation: o Maintain accurate and detailed laboratory records as per Good Documentation Practices (GDP). o Prepare and review analytical reports, COAs (Certificates of Analysis), and lab protocols. Compliance & Safety: o Ensure compliance with Good Manufacturing Practices (GMP), Standard Operating Procedures (SOPs), and regulatory guidelines. o Follow laboratory safety protocols and maintain a clean and organized workspace. Equipment Maintenance: o Calibrate and maintain laboratory instruments and troubleshoot issues as needed. o Ensure timely preventive maintenance of equipment. Quality Assurance: o Identify and report out-of-specification (OOS) results and participate in root cause investigations. o Assist in preparing for internal and external audits. Continuous Improvement: o Participate in validation activities and method development as required. o Contribute to process improvements in QC procedures.

QUALIFIED MICROBIOLOGIST required urgently for API (Pharma mfg co.Suitablly qualified & experienced candidates must apply immediately with following details...1. Latest Resume2. Present/ last salary3. Ready to travel to Taloja4. Joining dateMail details to shobana@rankandfileindia.com OR whatsapp to 9820824647Call/ contact urgentlySHOBANARank & File consultants9820824647________________________________________________________________ MICROBIOLOGIST required urgently @TALOJA for established API PHARMA co.Company: MARVEL DRUGS PVT LTDProducts: Veterinary API / IntermediatesLocation: Taloja MIDCSalary: Rs 25000 to 30000 pm IN HANDWeekly off FridaysGood work environmentREQUIREDBSc/MSc in MicrobiologyMin. 3 years of experience in API/ pharma industryResident of Navi Mumbai, Willing to travel to TalojaGood knowledge of water, RM, FG analysisKnowledge of GMP procedures

We are seeking dedicated API Plant Operators for our facility in Nandesari GIDC, Vadodara. The ideal candidates will support manufacturing operations, ensuring strict adherence to GMP and SOP guidelines. This full-time position involves operating various equipment, monitoring process parameters, and maintaining accurate documentation. It's an excellent opportunity for junior and trainee operators, as well as freshers with relevant qualifications. Join our team to kickstart a rewarding career in the API and pharmaceutical industry

Hiring Alert: ISO Coordinator (Manufacturing Industry Nagpur)Location: Nagpur, MaharashtraDepartment: Quality / OperationsExperience: 25 yearsQualification: Bachelors degree in Engineering, Business, or related fieldKey Responsibilities:A) ISO CoordinationDevelop, implement, and monitor Quality Management Systems (QMS).Maintain documentation and records as per ISO 9001 standards.Coordinate and support internal & external audits for ISO compliance.Conduct employee training on ISO procedures and corrective actions.Manage supplier audits and maintain approved vendor lists.B) MIS Data Creation & ManagementPrepare and maintain daily, weekly & monthly MIS reports.Build dashboards and performance tracking tools (Google Sheets / Excel).Analyze shop floor KPIs and drive process improvements.Automate repetitive reporting tasks to enhance accuracy & efficiency.Present visual reports and insights to management teams.C) Shop Floor CoordinationCollaborate with Production & Quality teams to capture real-time data.Monitor Plan vs Actual status and identify process bottlenecks.Track dispatch and monthly revenue reports.Required Skills:Hands-on experience with ISO standards & audit process.Certification in ISO 9001 / Quality Management Systems preferred.Advanced Excel / Google Sheets skills (Pivot, VLOOKUP, automation).Familiarity with Google Data Studio or Power BI is an advantage.Strong analytical, coordination, and communication abilities.Salary: Based on experience & interviewJoining: Immediate preferred

Salary: Take home / net - Rs 50000 to 75000 pm plus bonus, leave encashment and PFGood work environment_________________________________Candidates can mail (rankandfile94@yahoo.co.in) or whatsapp (97 6996 4647) following details 1. Resume2. Present Salary3. Notice period_________________________________Required:Diploma/ BE - Mech/ Production Engg with minimum 12 years experience in Projects/ Engineering/ Maintenance in API / Bulk Drugs / Intermediates industry;Good knowledge of basic chemistry and chemical processesMust be familiar with cGMP protocols/ procedures with respect to maintenance functionExperience of handling Jr Engr / maintenance technicians desirableAge profile: 35 to 50 yearsCall/ contact urgentlySHOBANARank & File consultantsBrief job profile:Independently responsible for maintenance of Plant & Utility equipments such as rotating and static equipmentAssist in other engg activities like expansion, modification, project activitiesCoordinate with mechanical, electrical & civil contractors for routine & project activities_________________________________About the Organisation:Our client is an established SSI unit manufacturing niche API & intermediate products for export/ global markets;It has a modern manufacturing unit at Taloja;The co has ambitious growth plans and has developed new molecules through in-house R&D which will be marketed in domestic and global markets;

Job Title: Production Shift In-charge Location: Nandesari, VadodaraPositions: 2 Education: B.Sc. / M.Sc. / Diploma in Chemical Engineering.Experience: 5-10 years of working experience in an API (Active Pharmaceutical Ingredient) and intermediate plant, with a strong understanding and practical application of GMP (Good Manufacturing Practices)Job Summary:We are seeking a highly motivated and experienced Production Shift In-charge to join our team for Pharmaceutical Company. The successful candidate will be responsible for overseeing and managing all production activities during their assigned shift, ensuring efficient operation, adherence to quality standards, and compliance with all safety and regulatory requirements. This role requires a strong leader with proven experience in pharmaceutical manufacturing, specifically in API and intermediate production.Key Responsibilities:Shift Management: Lead and supervise a team of production operators and technicians during the assigned shift. Plan and organize daily production activities to meet targets and schedules. Allocate tasks and responsibilities to team members effectively. Monitor production processes and troubleshoot any issues that arise. Ensure smooth shift transitions and effective communication with incoming/outgoing shifts.Production Operations: Oversee the manufacturing of APIs and intermediates, ensuring processes are followed according to batch production records and standard operating procedures (SOPs). Monitor raw material consumption, in-process parameters, and finished product quality. Optimize production efficiency and minimize waste. Coordinate with other departments such as Quality Control, Quality Assurance, Maintenance, and Stores to ensure seamless operations.Quality and Compliance (GMP): Ensure strict adherence to Good Manufacturing Practices (GMP) and other relevant regulatory guidelines. Oversee the accurate and timely completion of all production documentation, including batch records, logbooks, and deviation reports. Identify and report any deviations, non-conformances, or quality incidents, and participate in investigations. Implement corrective and preventive actions (CAPA) as required. Ensure equipment and facility are maintained in a state of readiness and compliance.Safety and Environment: Promote and enforce a strong safety culture within the production area. Ensure all team members follow safety procedures and use appropriate personal protective equipment (PPE). Report any safety hazards or incidents promptly. Ensure compliance with environmental regulations.Team Development: Provide training and guidance to production operators and technicians. Foster a positive and productive working environment. Conduct performance evaluations and provide feedback to team members.Reporting: Prepare daily, weekly, and monthly production reports. Communicate production status, challenges, and achievements to management.Skills and Qualifications: Proven leadership and supervisory skills in a manufacturing environment. In-depth knowledge of API and intermediate manufacturing processes. Strong understanding and practical application of GMP, GLP, and other relevant pharmaceutical regulations. Excellent problem-solving and decision-making abilities. Strong communication (verbal and written) and interpersonal skills. Ability to work effectively in a fast-paced, dynamic environment. Proficiency in using relevant computer software for data entry and reporting. Ability to work flexible shifts, including nights, weekends, and holidays, as required.

An R&D Product Development Executive in the food industry researches, creates, and improves food products, recipes, and packaging from concept to commercialization. Key responsibilities include conducting lab/pilot trials, ensuring regulatory compliance (FSSAI), improving quality, and collaborating with cross-functional teams to drive innovation. Location - Baddi Himachal PradeshRequired Qualifications & SkillsEducation: Bachelors or Masters degree in Food Technology, Food Science, or a related field.Experience: 15+ years of experience in food R&D, NPD, or quality assurance.Technical Skills: Strong knowledge of food chemistry, microbiology, ingredients functionality, and food processing techniques.Soft Skills: Excellent project management, problem-solving, communication, and teamwork skills. Key ResponsibilitiesProduct Development: Develop new food products (NPD) and improve existing formulations to enhance quality, taste, and shelf-life.Trials & Scaling: Execute lab-scale experiments and pilot plant trials, ensuring smooth technology transfer to production.Regulatory & Safety: Ensure compliance with FSSAI, FDA, or other local food safety regulations (GMPs, GHPs).Documentation: Maintain detailed records of formulations, ingredients, and processing parameters.Sensory Evaluation: Conduct sensory tests to refine products based on consumer feedback.Vendor Management: Collaborate with vendors for ingredient sourcing and material specifications.

A Quality Chemist for a CSD (Carbonated Soft Drink) line ensures product safety, quality compliance (HACCP, GMP, FSSAI), and adherence to standards during beverage production. Key responsibilities include online physical/chemical testing, monitoring syrup/water treatment, and filler performance. They calibrate equipment like Carbo QC and seam testers, and maintain, analyze, and document production quality.Key Requirements Education: Master's or Bachelor's degree in Food Science, Chemistry, or relevant field.Experience: Experience in beverage production (CSD, Hotfill) is preferred, often requiring 1-2+ years.Salary - 4.5 Lacs paLocation - Lucknow UPSkills: Strong analytical, troubleshooting, and documentation skills. Industry ContextQuality Chemist positions are common in major beverage companies (e.g., Coca-Cola bottlers) and in companies like Jain Irrigation Systems for Hotfill/CSD lines.Core Responsibilities & TasksOnline Monitoring: Performing,, and documenting physical and chemical tests directly on the production line to ensure adherence to standards.Quality Assurance: Maintaining compliance with HACCP (Hazard Analysis Critical Control Point), Good Manufacturing Practices (GMP), and Food Safety and Standards Authority of India (FSSAI) guidelines.Process Control: Monitoring water treatment plants (WTP) and beverage bottling processes.Laboratory Analysis: Testing for parameters like brix, carbonation levels, acidity, and pH.Equipment Calibration: Maintaining and calibrating lab equipment such as Carbo QC and Seam Testers to ensure testing accuracy.

Urgent opening for Quality Executive in Beverages Company @ AmbalaExperience - 2 to 3 Years in Beverage QualitySalary - 35,000 to 40,000 Per Month(M.Sc./B.Sc.) and focus on quality control (QC),Quality Executives in the beverage industry, notably at companies like Varun Beverages Ltd (VBL) and Hindustan Coca Cola Beverages (HCCB), are responsible for ensuring production standards, food safety, and compliance with regulations. Roles often require a background in science (M.Sc./B.Sc.) and focus on quality control (QC), Good Manufacturing Practices (GMP), and product testing. Key Aspects of the Role & Industry:Top Employers: Varun Beverages (PepsiCo bottler), Hindustan Coca Cola Beverages (HCCB), Kandhari Beverages, and (bottlers) are major hirers.Responsibilities: Ensuring product quality from raw material to finished goods, maintaining GMP, and adhering to regulatory, safety, and quality standards.Qualifications: Typically requires a degree in Science (Chemistry, Microbiology, Food Science) and 07+ years of experience.with top performers eKey Skills: Knowledge of beverage manufacturing, quality control testing, and food safety standards. Common Challenges & Experience:Work-Life Balance: Some reviews mention long hours and challenging work-life balance due to fluctuating production schedules.Environment: Fast-paced manufacturing settings, which can be intense but offer good learning opportunities for production quality.