8 Calibrations Jobs

You will be responsible for performing chemical and instrumentation analysis on various materials including in-process, raw materials, packing materials, intermediates, and finished products. Your primary goal will be to ensure compliance with dispatch timelines as per the monthly schedule provided by PPL. Your duties will include conducting instrumentation analysis using ICP-MS and LC-MS for the mentioned materials to meet dispatch timelines. Additionally, you will be involved in analytical method developments, validations, transfers, and verifications using ICP-MS and LC-MS/MS. You will be required to prepare and review protocols, worksheets, and reports for method developments, validations, verifications, and transfers. Allotting work to chemists within the section, calibrating instruments, maintaining documentation online, and ensuring minimum stock levels for various materials and standards will also be part of your responsibilities. Monitoring and reviewing analytical data, calibration data, and qualification data, as well as ensuring instruments are calibrated and maintained in working condition, will be crucial tasks. You will also play a key role in reducing lab incidences, implementing CAPA, and maintaining safe working conditions. Collaboration with QA, Production, PPIC, Warehouse, and TSD for smooth dispatches, as well as training employees on GLP/GMP and coordinating with external laboratories, will be essential aspects of your role. Your commitment to data integrity, timely analysis and release of batches, cost control, and adherence to safety practices will contribute to the overall success of the team. This position requires a Bachelor's degree and offers an opportunity to work with Piramal Pharma Solutions (PPS), a Contract Development and Manufacturing Organization (CDMO) known for its end-to-end development and manufacturing solutions across the drug life cycle. PPAs serves customers globally and provides a wide range of services, making it a preferred partner for innovators and generic companies.,

The Engineering Department at Zydus Biotech Park in Changodar, Ahmedabad is looking for a qualified candidate for the position of Executive/Senior Executive - Instrumentation. The ideal candidate should hold a B.E. degree in Instrumentation and Control with 3 to 5 years of relevant experience. As an Executive/Senior Executive - Instrumentation, your primary responsibilities will include conducting preventive maintenance of plant/process equipment, performing calibrations, and ensuring the qualification of equipment and SCADA systems in compliance with 21 CFR guidelines. You will also be responsible for troubleshooting SCADA, PLC, and instruments as needed. Additionally, you will be in charge of maintaining Quality Management System (QMS) and Good Manufacturing Practices (GMP) documentation such as log books, records, status labels, preventive maintenance records, deviations, change control, and Corrective and Preventive Actions (CAPA) reports. The ideal candidate should possess knowledge of various process equipment including Autoclaves, Bio-reactors, fermenters, and Lyophilizers. Experience in implementing safety procedures and practices such as Lockout-Tagout (LOTO), proper use of Personal Protective Equipment (PPEs), and work permits system is essential for this role.,

As a Supervisor at Sigachi located in Dahej, you will play a crucial role in ensuring the smooth production operations in line with GMP standards. Sigachi, a renowned manufacturer of Excipients for Pharma, Nutra, and food industries, has been a key player in the market since its inception in 1989. With multiple facilities in Telangana and Gujarat, Sigachi has solidified its position as a leading producer of Microcrystalline Cellulose globally. Operating under various certifications like EXCiPACT GMP, SGMP, HACCP, EDQM CEP, and ISO 9001:2015, Sigachi has built a reputation for delivering high-quality products across continents. Your primary responsibilities will include planning and organizing production schedules to meet targets for output, quality, and yield. You will oversee all production operations to ensure compliance with SOPs and GMP standards. Collaborating closely with the Quality Control department, you will focus on continuous improvement and effective resource utilization to maintain quality parameters. Additionally, you will coordinate with cross-functional teams, particularly the Engineering Department, to ensure the production of top-notch quality products. It will be your duty to provide on-the-job training for production staff and maintain updated training records. You will be responsible for reporting deviations, conducting investigations, and implementing corrective and preventive actions as necessary. Moreover, your role will involve coordinating with QA for batch release, investigating non-conforming batches, and ensuring batch identification and traceability. Maintaining equipment/instruments calibration, practicing good housekeeping, and adhering to gowning procedures are also part of your responsibilities. In terms of qualifications, we are looking for candidates preferably with a B.Sc, M.Sc, B.Pharm, M.Pharm, or B.Tech (Chemical) degree. An experience of 8 - 10 years in the Pharma Industry or Excipient Manufacturing sector will be highly advantageous for this role. If you are a self-driven professional with a keen eye for detail and a strong background in production operations, this position at Sigachi offers a challenging yet rewarding opportunity to showcase your expertise and contribute to the company's commitment to excellence.,

As a Production Associate at PPL Digwal, your primary responsibility will be to perform production activities in compliance with GMP and Safety standards. You will report directly to the Manager of Production and collaborate with internal stakeholders such as QC, QA, SCM, and Safety departments. With 4-8 years of experience in manufacturing (API) according to Pharma Manufacturing GMP requirements, you will play a crucial role in ensuring EHS continual improvement by participating in activities like emergency mock drills, training sessions, and permit to work procedures. It is essential to follow all site safety requirements, exhibit positive behavior in safety culture transformation, and use necessary Personal Protective Equipment (PPE) during shop-floor operations. Your responsibilities will also include identifying unsafe conditions or acts, reporting safety-related incidents promptly, following instructions from previous shifts or managers diligently, and reviewing/updating shop-floor documents in a timely manner. Additionally, you will be responsible for maintaining cleanliness, ensuring good housekeeping in designated areas, and coordinating with relevant departments for equipment maintenance, calibration, and batch execution. To qualify for this role, you should hold a B.Sc/M.Sc in Chemistry or B.Tech in Chemical Engineering. The job is a full-time position based at Piramal Enterprises Limited in Digwal, Medak, Telangana. Don't miss the opportunity to apply for this position with Job ID 5381 before the deadline on 07/22/2025, 04:31 AM.,

Requirements & Eligibility: Good communication skills (verbal and written). Must be willing to work a 9-hour rotational shift anytime between 7:00 a.m. to 10:00 p.m. (Sunday working required). Ability to handle pressure and adapt to work requirements. The candidate should be available to work from office. The Key Responsibility Areas will be: Call Monitoring Providing feedback for monitored calls. Preparing reports on quality and variance in calibrations Performing activities such as live audits, side-by-side barging, and floor walks to monitor the process and identify areas for improvement. Conducting sessions such as tape reviews, briefings, and calibrations for standardization. Initiating process improvement initiatives. Completing assignments given by the team. Receive and document customer complaints through various channels (phone, email, online platforms). Investigate the nature of each complaint to understand the issues raised. Analyze complaint data to identify trends, patterns, and root causes. Collaborate with relevant departments to gather information and insights. Maintain detailed records of customer complaints, investigations, and resolutions. Prepare and submit reports to management highlighting key findings and recommendations. Communicate with customers to acknowledge their complaints and provide updates on the investigation and resolution process. Collaborate with internal teams to facilitate effective communication and resolution. Work with relevant departments to develop and implement solutions to address identified issues. Ensure timely resolution of complaints while adhering to organizational policies and procedures. Identify opportunities for process improvement based on recurring complaints. Collaborate with teams to implement changes that prevent future complaints. Ensure compliance with industry regulations and standards in handling and resolving customer complaints. Monitor and evaluate customer satisfaction levels through feedback and follow-up surveys. Implement measures to enhance overall customer satisfaction and loyalty. Prepare regular reports for management summarizing complaint data, trends, and resolutions. Provide training to staff on effective complaint resolution techniques. Promote a customer-focused culture within the organization. You can share your resume on, WhatsApp 8779797282 Anjali Maurya Mail amaurya1@europ-assistance.in

Role & responsibilities Conduct Temperature Mapping for equipment and controlled environments as per regulatory standards. Perform Validation of PLCs / HMIs to ensure system functionality and compliance. Handle SCADA System Qualification, Troubleshooting, and Support , ensuring smooth operations and minimal downtime. Manage Calibration of all critical instruments used in the API manufacturing process, maintaining accuracy and compliance. Maintain calibration records, schedules, and ensure timely execution of calibration and validation activities. Coordinate with cross-functional teams for effective implementation of instrumentation projects and modifications. Ensure compliance with cGMP, regulatory, and safety guidelines in all instrumentation activities. Provide technical support during regulatory audits and inspections. Preferred candidate profile Minimum 3 to 9 years of relevant experience in instrumentation within the API or pharmaceutical industry . Sound knowledge of PLCs, HMIs, SCADA systems, temperature mapping techniques, and calibration standards. Strong troubleshooting and documentation skills. Ability to work in cross-functional teams and manage multiple tasks efficiently.

Mainly focus on IN PROCESS QUALITY, REJECTION CONTROL, REJECTION ANALYSIS, ZERO REJECTION at CUSTOMER END, CALIBRATION of RECEIVING GAUGES by CMM, SUB ASSEMBLY SETUP APPROVAL, CHILD PARTS INSPECTION, SUB ASSEMBLY, IN-HOUSE VALIDATION of PARTS et Required Candidate profile DME/BE/CIPET 10+yrs exp with any AUTOMOTIVE PLASTIC / IM Unit into INPROCESS QUALITY / IPQC handling LINE QA, REJECTION CONTROL, CHILD PARTS QAAPPROVAL etc Exposure in WIRING HARNESS / IM is a plus Perks and benefits Excellent Perks. Send CV cv.ch2@adonisstaff.in

Lead INPROCESS QA / IPQC handling QA PROCESSES, REJECTION ANALYSIS, QUALITY COSTING, CALIBRATIONS, PROCESS AUDIT, PRODUCT AUDIT, LAYOUT INSPECTION, FINAL INSPECTION, QUALITY COMPLIANCES, CQA, IPQC, FINAL QUALITY CHECKS, CUSTOMER COMPLAINTS HANDLING.. Required Candidate profile DME/BE/CIPET 10-20yrs exp with any AUTOMOTIVE PLASTIC / IM Unit into QA having 5+yrs of strong exposure in INPROCESS QUALITY / IPQC must Apply only if u hv exp in AUTOMOTIVE INJECTION MOLDING unit Perks and benefits Excellent Perks. Send CV cv.ch2@adonisstaff.in