243 Batch Manufacturing Jobs - Page 2

Hiring for one of the Largest Acrylic Emulsion Manufacturer in India supplying Adhesives & Emulsions all over India & Exports Experience:1 + Years CTC: Upto 3.5 LPA Roles and Responsibility Experience in emulsion / resins / adhesives reactor batch processing & basic trouble shooting. Able to run the reactors independently both in auto (SCADA / DCS) & manual mode. Able to manage team (at helpers level) & being a team player in the shifts. Others : SAP User experience, Quality Safety protocols inclined person. Taking batches as per the production planning with minimum batch cycle time. Timely escalation to shift in-charge and higher authorities in case of any machine related issue and cannot be resolved at individual level. Run batches as per the Production Plan within the SOPs and Quality parameters and benchmark yield. Ensure to check the correct raw material and correct quantity as per the SOP, before charging into the vessel. Responsible for all the operations with respect to the reactor, from ensuring utility, timely availability of raw material, ET preparation, charging of raw material, reactor processing as per SOP and downing. To take all batches by using Automation (except instructed for manual operation) and report any issue faced. Ensure to adhere and follow records as per QMS, Responsible Care and Zero-Defect norms. Maintain yield loss as per the forecast. Ensure to check the correct line-up of process fluids and utility (cooling & DM Hot & Cold, Stream, Stream, Air etc.) and double check that other reactor valves are in closed condition. Ensure that the generation and consumption of white water are recorded and fully consumed as per compatibility. Ensure safety of self and that of the co-workers. Always use and ensure usage of PPEs and maintain safe working environment. Report any unsafe act or condition to the shift in-charge. Ensure housekeeping and make sure that the Production area is well maintained. Immediately raise any issue that may lead to production loss to the shift in-charge. Implement and sustain 5S initiatives on the shop floor and support the team leader to set culture of compliances with regular checks and audits. Provide ideas for improvement/ innovation. Preferred candidate profile ***Candidates from nearby locations such as Uthukottai, Palavakam, Pariyapalayam, Janapachatram, Ponneri, and Kavarapetai can apply or refer suitable candidates for this position *NO CAB *NO ACCOMODATION To apply Send mail to hrconnect@apmcindia.in or Whatsapp 9787836999

Position: Production Officer Chemical Location: Kanpur (Rania), Uttar Pradesh Experience Required: 23 years in chemical manufacturing (adhesives, emulsions, resins, solvents, construction chemicals) with shift handling experience Salary Budget: 35,000 per month (Annual CTC: 4.20 Lakhs) Job Description: Astral Limited is hiring a Production Officer Chemical to manage shift operations at our chemical manufacturing facility in Kanpur (Rania). The ideal candidate should have hands-on experience in production processes related to adhesives, emulsions, resins, solvents, or construction chemicals, and should be capable of independently handling shift responsibilities. Key Responsibilities: Manage and monitor daily production activities during assigned shifts. Operate and supervise chemical process equipment such as reactors, mixers, blenders, and distillation units. Ensure adherence to production plans, quality standards, and safety protocols. Coordinate with maintenance, quality, and warehouse teams for smooth operations. Maintain process parameters and ensure timely reporting of deviations. Lead shift manpower and ensure discipline, productivity, and safety. Maintain batch records, production logs, and shift reports. Ensure proper handling of raw materials, solvents, and finished goods. Implement 5S, GMP, and safety practices across the production floor. Troubleshoot process issues and escalate critical problems to senior management. Key Skills & Attributes: Hands-on experience in chemical production processes (adhesive, emulsion, resin, solvent, etc.). Knowledge of process control, safety standards, and chemical handling. Ability to lead shift teams and coordinate with cross-functional departments. Good understanding of SOPs, batch documentation, and quality compliance. Strong problem-solving and decision-making skills. Familiarity with ISO, GMP, and EHS standards. Preferred Qualifications: Diploma/B.Tech in Chemical Engineering. Candidates with shift handling experience in chemical manufacturing will be preferred. Preferred Industry Experience: Adhesives, emulsions, resins, construction chemicals, solvents, or similar chemical process industries. Experience in batch or continuous process operations will be an added advantage. Why Join Astral? Astral offers a dynamic and growth-oriented work environment focused on innovation, safety, and operational excellence. Be a part of our Kanpur (Rania) team and contribute to the production of high-quality chemical products. How to Apply: Interested candidates with relevant experience are invited to apply with their updated resume at ramesh.chaudhary@astralltd.com or via WhatsApp at 8353912032 .

Working Hours - 8 Hrs Role & responsibilities Dispensing, Manufacturing, Packaging and Dispatch activities. -Review and control of SOPs, BPR Issuance,Cleaning Validation,Line Clearance. -Master Formulae and records. -Good Documentation as per GLP,Preparation. -Review of process validation protocols and reports. -Familiar with Production machinery, Production floor working, pH meter, Refractometer, and GLP.

Job Description Key Responsibilities 1. Monitoring of IPQA activities in all functional departments. 2. Responsible for BMR correction/ quantity verification before batch execution along with QC. 3. Responsible for area and line clearance in production area. 4. Responsible for BMR verification for the completion and online inspection of batch execution at site. 5. Responsible for dispatch verification along with dispatch checklist, BMR, labels (at site and godown) 6. Site inspection for any abnormalities with respect to Raw materials, Packing materials, Products, labels, BMR, Dispatch. 7. Responsible for implementation of 5S at site. 8. Handling of Deviations, failure investigation, Change management and customer compliant. Skills Required 1. Through knowledge about the methodologies of quality assurance and its standard 2. Effective communication, coordination, Multitasking and time management 3. Through knowledge about Quality Management System and Integration Management system. 4. Proficiency in MSOffice Application (Word, Excel, PowerPoint, Outlook) Technical/Functional Proficiency Required 1. Expertise in Manufacturing process flow and Control method, process inspection, compliance and Root Cause Analysis. 2. The training imparting technique to the shop floor peoples.

Looking for Production Chemist for Vasai Location, daily production of colour cosmetics quality control and batch consistency formulation and process improvements understanding of manufacturing processes

HE should be able to implement Pharmaceutical SOP for Production department with help of Manpower and Materials, Shift wise produciton as per schedule . Implementaton SOP on ground level under guildelines -SOP of GMP /FDI in various Produciton lines Required Candidate profile HE should be able to implement Pharmaceutical SOP for Production department with help of Manpower and Materials, Shift wise produciton as per schedule under guildelines of GMP-FDI for production

You will be working as a Production Executive at ACRYNOVA INDUSTRIES (P) LTD, a renowned company in India with 45 years of experience in producing acrylic emulsions for various applications such as textile printing, paint, adhesive, leather, and paper coating. Your primary responsibility will be to oversee the emulsion production process. Your key responsibilities will include following instructions from the production head, ensuring that the Standard Operating Procedures (SOPs) for batch manufacturing are strictly adhered to, verifying raw material inputs before starting the batch, and strictly following the time cycle of the batch process. You will be required to effectively supervise and manage the officers and casual workers in the shift, ensuring that all necessary documents are filled out correctly before the end of the shift. Additionally, you will need to ensure that all subordinates in the shifts are wearing Personal Protective Equipment (PPE) at all times. Any deviations from the standard procedures must be promptly reported to the Head of Department (HOD) or Works Manager (WM). You will also be responsible for attending mandatory trainings, performing safety coordinator activities as required, and overseeing the overall plant operations during your shifts. Furthermore, you will play a crucial role in ensuring that all utilities are operated as needed to minimize costs. Candidates with a stable career history and experience in emulsion production work are preferred for this role. The position is based in Boisar, India, and candidates must be willing to relocate with their families. If you are passionate about production management and have the required qualifications, this role offers an exciting opportunity to contribute to the success of a leading acrylic emulsions producer.,

Responsible for API Plant shift Oprn like batch charging,Reaction, extraction etc, Planning& Scheduling Prodn activities, maintain parameters as SOPs, Ensure GMP regulatory/EHS & ISO compliance, troubleshooting, documentation, SAP Entry, Manpower mgt Required Candidate profile BE-Chemical with 4 to 8 yrs relevant working exp in API plant. Should be well Conversant with API mfg conversion reaction & unit operation like filtration, drying, Batch/Continuous Distillation Column Perks and benefits Negotiable

Responsible for handling of production activities in shift ensuring minimal deviation, Monitoring process parameters, resolving production issues, manpower Mgt, compliance of SOP & EHS /ISO norms, Co-ord’n with service depts, Production report etc. Required Candidate profile B.E./B.Tech.(Chem) with 7 to 10 years relevant experience preferably in continuous batch process chemical plant having DCS system. Perks and benefits Negotiable

JOB DESCRIPTION (Sr. Officer) Supervision of manufacturing, processing, packaging and holding of drug product as per define and approved procedures for stability batches and commercial batches. Maintaining the area and equipment in orderly manner as per cGMP requirements in a good state of repair and sanitized condition. To perform online documentation with respect to departmental procedures as per good documentation. To impart training of operation and cleaning related SOP to all subordinates and operators. Co-ordination for IQ / OQ for any new equipments / system. To perform PQ for any new equipments / system. To follow all concern departmental SOPs for day to day operation and cleaning. To handle and manage material movement as per defined procedure and approved Batch Manufacturing Record / Batch Packing Record. Review, execution and implementation of Batch Manufacturing Records, Batch Packaging Records, Process Study Protocols, Process Study Reports and all relevant Documents. To follow all safety rules and departmental general instructions. To perform work other than defined in the Job responsibility are to be done, as per the requirement of HOD, by following HODs instruction and guidance.

Role & responsibilities Manufacturing of cell line/cell culture based AG for FG Cell culture operations, including inoculation and observatory monolayer work Compilation of all commercial batch data and BMR filling RM/PM issuance, sterilization, and monitoring of all supportive data Maintaining procell-related modules, areas, and utility fixed assets Receiving NPD from R&D and scaling up for commercialization Areas, equipment validation, and maintenance Cell bank passage history maintenance and reconciliation Preferred candidate profile Throughout knowledge of cell line/primary culture Propagation of cell line & maintenance Aseptic handling Sound knowledge of QMS Sound knowledge of cGMP, GDP

Supervisor (- B. Pharm / M. Pharm) having the experience with 2 to 6 years for Supervising in Aseptic Area. Exposure of machine qualification activity will be added advantage. •Plant Operator (Autoclave, Filling, Compounding, Washing/Tunnel/Capping & Lyophilizer) D. Pharm/ITI with 1 to 6 Years of relevant experience in operating production machines like Vial Filling, PFS Filling, Autoclave, Vial washer & Depyrogenation tunnel.

*Operate and monitor injectable (DPI)production equipment in compliance with cGMP standards. *Execute manufacturing processes compounding, aseptic filling, vial washing, autoclaving, and lyophilization. *Maintain (BMR) and related documentation. Required Candidate profile *Ensure adherence to safety, hygiene, & quality standards during production activities. *Familiarity with regulatory guidelines (USFDA, MHRA, WHO, etc.). *Good documentation and communication skills.

Interview for SVP & Injectable Pharma Plant in Bharuch on Permanent Payroll for QA, QC & Microbiologist on 07-09-2025 Exp: 3 to 8 yrs CTC: As per industry Location: Dahej Send CV on sdpbharuch@gmail.com with Subject: SVP Bharuch & Call 9727755486 Required Candidate profile No of Openings QC : 10 QA : 15 Microbiologist : 5 Exp in SVP / Injectable Plant is Must Share with Your Colleagues & Seniors No Interview & Joining Charges Project Expansion on going

Interview for SVP & Injectable Pharma Plant in Bharuch on Permanent Payroll for QA, QC & Microbiologist on 07-09-2025 Exp: 3 to 8 yrs CTC: As per industry Location: Dahej Send CV on sdpbharuch@gmail.com with Subject: SVP Bharuch & Call 9727755486 Required Candidate profile No of Openings QC : 10 QA : 15 Microbiologist : 5 Exp in SVP / Injectable Plant is Must Share with Your Colleagues & Seniors No Interview & Joining Charges Project Expansion on going

You will be responsible for strictly adhering to cGMP, Safety, and Environmental Practices while working in the manufacturing plant. Your duties will include filling Batch Manufacturing records, cleaning equipment, following Good Manufacturing practices, maintaining Good Housekeeping, wearing proper personnel protective equipment, and planning for Raw Material availability for daily production as per the production plan. Additionally, you will be required to maintain documents like Issue and dispensing register, carry out processes as per Batch Manufacturing Record (BMR) without any deviation, and ensure adherence to data integrity in online documentation. Hazardous operations should be handled safely, and resources like Utility, Men, and Machine should be effectively utilized. To qualify for this role, you should hold a B.E/B.Tech degree in a relevant field such as Chemical or Chemistry. The ability to work collaboratively in a team-oriented environment and strong communication skills, both verbal and written, are essential. Piramal Group, with three decades of existence, follows a growth strategy of both organic and inorganic methods. The group is committed to inclusive growth while upholding ethical and values-driven practices. Equal employment opportunity is a fundamental principle where employment decisions are based on merit, qualifications, skills, and achievements, ensuring equal opportunities for all applicants and employees. Piramal Pharma Solutions (PPS) is a Contract Development and Manufacturing Organization (CDMO) providing end-to-end solutions across the drug life cycle. Your role will be in API Production at Piramal Enterprises Limited in Chennai, Tamil Nadu. The company offers a wide range of services, including drug discovery solutions, process & pharmaceutical development services, clinical trial supplies, commercial supply of APIs, and finished dosage forms. Specialized services like the development and manufacture of highly potent APIs, antibody-drug conjugations, sterile fill/finish, peptide products & services, and potent solid oral drug products are also available. Services for biologics such as vaccines, gene therapies, and monoclonal antibodies are offered through investment in Yapan Bio Private Limited. With a proven track record, PPS is a trusted partner for innovators and generic companies worldwide. This is a full-time position requiring a Master's Degree, and the job identification number is 8465.,

Job Title: Projects & Engineering - Process Engineer Business Unit: Sun Global Operations Job Grade G9A/ G9B -Senior Manager Location : Green Field Project Site At Sun Pharma, we commit to helping you Create your own sunshine by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community. Are You Ready to Create Your Own Sunshine? As you enter the Sun Pharma world, you ll find yourself becoming Better every day through continuous progress. Exhibit self-drive as you Take charge and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we Thrive together and support each other s journeys. Key responsibilities: Expertise in operation of below process and equipment s: To handle aseptic and lyophilisation area. To handle process like filtration, filling, Lyophilizer loading and unloading, lyophilisation process, capping, leak test and X ray inspection. To handle the process equipment s like vial washing, tunnel sterilizer, filling machine, capping machine, Lyophilizer loading and unloading system, Lyophilizer, filtration skid, and isolators, VHP passbox etc. To handle indenting to procurement of new equipment s of aseptic area and lyophilizer area as mentioned above. To handle preparation and execution of qualification protocol of new equipment like, User requirement specification, Design qualification, Installation qualification, operational qualification and performance qualification . To prepare new standard operating procedure for process and equipment s. Experience for preparation of batch manufacturing records. To handle the QMS documents like change control, CAPA, risk assessment, deviation etc. To handle communication with vendor and procurement team on procurement to design parts of new equipment s. To ensure compliance to cGMP and documentation for various production activities. Ensure proper planning and execution of the qualification activity in accordance with the plan and allocation of man power. Travel Estimate As Required Job Requirements Educational Qualification BE Mechanical / Electrical Experience Tenure : 10 to 15 Years of experience in relevant field in Pharmaceutical Industry Your Success Matters to Us At Sun Pharma, your success and well-being are our top priorities! We provide robust benefits and opportunities to foster personal and professional growth. Join us at Sun Pharma, where every day is an opportunity to grow, collaborate, and make a lasting impact. Let s create a brighter future together! Disclaimer: The preceding job description has been designed to indicate the general nature and level of work performed by employee within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities, and qualifications required of employees as assigned to this job. Nothing herein shall preclude the employer from changing these duties from time to time and assigning comparable duties or other duties commensurate with the experience and background of incumbent(s).

Job Title: PROJECTS & ENGINEERING - Process Equip Mfg Business Unit: Sun Global Operations Job Grade G10 - Manager 1 Location : New green field site (Pithampur - Indore) At Sun Pharma, we commit to helping you Create your own sunshine by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community. Are You Ready to Create Your Own Sunshine? As you enter the Sun Pharma world, you ll find yourself becoming Better every day through continuous progress. Exhibit self-drive as you Take charge and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we Thrive together and support each other s journeys. Key responsibilities: To handle manufacturing and component washing and sterilization area. To handle process like manufacturing of liquid product including media, complex injectable and suspension manufacturing. To handle the process equipment s in manufacturing like manufacturing skid, filtration skid, suspension manufacturing skid, CIP SIP skid for manufacturing and filtration equipment s, dispensing isolators, manufacturing isolators, pH meter, DO meter, integrity tester etc. To handle component washing and sterilization area and its equipment s like Autoclave, Terminal sterilizer, ultrasonication machine, GMP washer, VHP pass box, external washing machine, leak test and X ray inspection machine etc. To handle indenting to procurement of new manufacturing equipment s as well as component washing and sterilization equipment s as mentioned above. To ensure compliance to cGMP and documentation for various production activities Experience for preparation and execution of qualification protocol of new equipment like, User requirement specification, Design qualification, Installation qualification, operational qualification and performance qualification. To prepare of new standard operating procedure for process and equipment s. Experience for preparation of batch manufacturing records. To handle the QMS documents like change control, CAPA, risk assessment, deviation etc. To handle communication with vendor and procurement team on procurement to design parts of new equipment s Ensure proper planning and execution of the qualification activity in accordance with the plan and allocation of man power. Travel Estimate Job Requirements Educational Qualification B. Pharmacy, M. Pharmacy Experience Tenure : 5 to 10 Years of experience in relevant field in Pharmaceutical Industry Your Success Matters to Us At Sun Pharma, your success and well-being are our top priorities! We provide robust benefits and opportunities to foster personal and professional growth. Join us at Sun Pharma, where every day is an opportunity to grow, collaborate, and make a lasting impact. Let s create a brighter future together! Disclaimer: The preceding job description has been designed to indicate the general nature and level of work performed by employee within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities, and qualifications required of employees as assigned to this job. Nothing herein shall preclude the employer from changing these duties from time to time and assigning comparable duties or other duties commensurate with the experience and background of incumbent(s).

Production Chemist / Senior Production Chemist /Production Executive Dear Candidate, We have an exciting opportunity for candidates who are interested to pursue their career as a Production Chemist / Sr Production Chemist / Production Executive's in Pharmaceutical / Nutraceutical Industry. Experience: 2-10yrs. Education: B.Sc. / M.Sc. Chemistry / BE/ B TECH / Diploma in Chemical Engineering. Shifts: Should have willingness to work in Rotational Shifts. Job Location: Hassan / Kunigal / Dobaspet. Gender: Only Males. Roles and Responsibilities : Manage and execute production processing activities. Work on Production Plan to achieve the dispatch commitment. Ensure the team to achieve "ZERO ACCIDENT" work environment. Ensure adherence to standard operating procedures (SOPs) and batch manufacturing records for smooth production operations and regulatory compliance. Operate, monitor, and maintain processing equipment and other related machinery. Assist in troubleshooting and optimizing processes to enhance yield, purity, and overall process efficiency. Maintain detailed and accurate production records, including deviations, equipment logs, and batch reports, in compliance with cGMP guidelines. Collaborate with quality assurance and control teams to ensure that all activities meet regulatory and product quality standards. Monitor and manage raw materials, consumables, and reagents required for processing activities. Ensure adherence to safety protocols and regulatory requirements, including environmental and biosafety standards, during production. Ensuring data integrity. Handling Solvent recovery. Responsible for physical inspection during dispatch. ****** ONLY MALES ARE PREFERRED FOR THESE POSITIONS*******

We are hiring Production Officer for pharma intermediate manufacturing Unit. Requirement:- Qualification :-B.Sc/M.Sc Experience :- 2 to 3 years in pharma industry. Benefits:- PF & Bonus Salary isn't a constrain for right candidates.

Role & responsibilities Handling of QMS for drug substance of bacterial products. Should have good process understanding of upstream and downstream unit operations. Experience to handle QMS documents such as deviation, Change control, Investigations through Track-wise software. Should have experience on audit compliance, Regulatory guidelines and knowledge on documentation such as SOP, BMR preparation. 5-8 years of experience on QMS and compliance, Documentation role along with good understanding about manufacturing process operations of bacterial and recombinant vaccine and biological therapeutics. Preferred candidate profile

As a team member at Biocon Biologics Limited, a subsidiary of Biocon Limited, you will be part of a fully integrated global biosimilars organization dedicated to leveraging cutting-edge science and innovative tech platforms to enhance healthcare outcomes. With a strong research pipeline focusing on biosimilar molecules for diabetes, oncology, immunology, and other non-communicable diseases, we are committed to making treatment more accessible and affordable for patients worldwide. Your responsibilities will include performing line clearance for various manufacturing activities such as formulation, washing, filling, sealing, and others in designated areas. You will also be responsible for reviewing and approving execution reports across different stages of the manufacturing process, including sterilization, filtration, integrity testing, and more. Additionally, you will play a key role in collecting and submitting samples for in-process checks, finished product analysis, and process validation. In this role, you will be expected to review batch manufacturing records, protocols, and other GMP documents to ensure compliance with regulatory standards. You will also be involved in the review and approval of validation/study protocols, reports, master batch records, and SOPs. Furthermore, you will be responsible for investigating complaints, deviations, out-of-specifications issues, and overseeing practices related to media fill, aseptic techniques, microbial monitoring, and clean room maintenance. As part of your duties, you will gain an overview of manufacturing and filling equipment, including utilities such as the water system, HVAC, compressed air, and steam plant. Your attention to detail and adherence to quality standards will be crucial in maintaining the integrity of our manufacturing processes and ensuring the delivery of high-quality healthcare products to our global customer base.,

Job Description Required for IPQA acitities. Required for Batch manufacturing record review. Required for line clearnace and other shop floor related activity of QA. Work Experience 3 to 8 years. Education Graduation in Pharmacy Competencies

Perform in-process quality checks during manufacturing and packaging stages Ensure compliance with GMP, ISO, and regulatory standards Review and verify batch manufacturing and packing records Identify and report non-conformances, and implement corrective and preventive actions (CAPA) Conduct line clearance, sampling, and documentation as per SOPs Coordinate with production, QC, and warehouse departments to ensure product quality Maintain documentation for internal audits and regulatory inspections Provide on-the-floor training to production staff on quality protocols Help maintain quality-related documents and SOPs. Support in internal audits and regulatory inspections.

Seeking a IPQA Executive to ensure skincare products meet regulatory, safety & quality standards. Work closely with manufacturing, R&D, and QC teams. Requirement: 2+ years of QA experience, preferably in cosmetics or pharma manufacturing. Required Candidate profile Skincare manufacturing & QC expertise Knowledge of FDA, GMP, ISO regulations Attention to detail & procedural compliance Strong analytical, problem-solving & com skills Ability to work with GMP proces