214 Api Production Jobs - Page 8

Role: Chemist / Sr Chemist Department: Production Location: Bidar About Us: Sai Life Sciences is one of the fastest-growing Contract Research, Development, and Manufacturing Organizations (CRDMOs). As a pure-play, full-service partner, we collaborate with over 300 global innovator pharma and biotech companies to accelerate the discovery, development, and commercialization of their NCE programs. We have over 3000 employees across our facilities in India, the UK, and the USA, working together to deliver scientific excellence and customer success. We are a Great Place to Work certified organization with a culture of openness, mutual respect, and inclusivity. We embrace diversity and follow equa...

Hi Greetings from Avani consulting , We have job opportunities with (pharma company) for the production department in mysore location NOTE :- We are going to conduct a Walk-in interview in Mysore on 21-june- 2025(Saturday) Whom ever are interested they can join for interview just share updated resume Job Description for Production-Associate Position- Associate Work Experience Min 3-12 yrs in API Drive Location : Banglore Work Location: Mysore ( Nanjangud) Gender Any Qualification- B.Tech Chemical Engineering/M Sc and Bsc Chemistry /Diploma in chemical Engg Roles & Responsibility 1. Responsible for appropriate production planning & execution of batches in line with targeted commitments comply...

Qualifications: M.Sc./ B.E - B.Tech (Chemical Engg.) 2 to 5 years of experience. Experience in handling critical equipment like reactor, centrifuge, blender, sifter, multi-mill, etc. Job Responsibilities: Ensure that the products are manufactured as per the cGMP. Maintain documentation as per regulatory authorities requirements like change control, and deviations. Highlight technical problems and take corrective actions. •

Qualifications: M.Sc./ B.E - B.Tech (Chemical Engg.) •1 to 4 years of experience. •Experience in handling critical equipment like reactor, centrifuge, blender, sifter, multi-mill, etc. • • Job Responsibilities: Ensure that the products are manufactured as per the cGMP. Maintain documentation as per regulatory authorities requirements like change control, and deviations. Highlight technical problems and take corrective actions. •

Role & responsibilities Work Experience required (Chemical/Pharma Experience only) M.Sc. 2 years plus Diploma/B.Sc. 5 years plus Report to : Shift in charge Production Supervisor Job Purpose: To manage the shift operation and all direct staff. To ensure the smooth running of the process. To ensure that all process to be run as per standard operating procedure To ensure comply with the companys Environment Health and Safety procedures along with that all direct staff Key Responsibilities Knowledge of operation & maintenance of chemical process and plant equipment. Familiar with unit operations and unit processes Experience of supervising and handling of hazardous chemicals and waste. To take ...

Roles and Responsibilities Monitor and maintain accurate records of production processes, including batch tracking and inventory management. Collaborate with cross-functional teams to resolve issues related to productivity, yield improvement, and equipment maintenance.

Roles and Responsibilities Ensure smooth operation of production activities, including API (Active Pharmaceutical Ingredient) manufacturing, bulk drugs, and pharmaceutical production. Maintain accurate records of production data, inventory management, and batch documentation.

Business: PPL Digwal Department: PTS Job Overview: To perform Production actives as per GMP & Safety Travel Requirements: NA Reporting Structure: Reports to Research Scientist - R&D (Service) Key Stakeholders: Internal: QC, QA, SCM & Safety External: NA Experience: 4--8 Year Experience in manufacturing (API) as per Pharma Manufacturing GMP requirements. Responsibilities for Internal Candidates Key Roles & Responsibilities 1. Design the scheme of experiments. 2. Plant trouble shooting, investigation and root cause analysis. 3. IUT support for vendor qualification and plant batches. 4. Carry out experiments during the feasibility and optimization stage. 5. Visualize the development needs of th...

Hi Greetings from Avani consulting , We have job opportunities with (pharma company) for the production department in mysore location NOTE :- We are going to conduct a Walk-in interview in Mysore on 14-june- 2025(Saturday) Who ever are interested they can join for interview just share updated resume Job Description for Production-Associate Position- Associate Work Experience Min 3-12 yrs in API Location Mysore ( Nanjangud) Gender – Any Qualification- B.Tech Chemical Engineering/M Sc and Bsc Chemistry /Diploma in chemical Engg Roles & Responsibility 1. Responsible for appropriate production planning & execution of batches in line with targeted commitments complying cGMP& Safety requirements. ...

Hi Greetings from Avani consulting , We have job opportunities with (pharma company) for the production department in mysore location NOTE :- We are going to conduct a Walk-in interview in Mysore on 14-june- 2025(Saturday) Who ever are interested they can join for interview just share updated resume Job Description for Production-Associate Position- Associate Work Experience Min 3-12 yrs in API Location – Mysore ( Nanjangud) Gender – Any Qualification- B.Tech Chemical Engineering/M Sc and Bsc Chemistry /Diploma in chemical Engg Roles & Responsibility 1. Responsible for appropriate production planning & execution of batches in line with targeted commitments complying cGMP& Safety requirements...

Hi, Greetings Walk in Invitation: We are having face to face interview on 14th June Saturday in Mysore.- Single Round Company : A leading Pharma API Unit - in Mysore Position - Production Department Associate Work Experience Min 3 yrs in API in current Salary 20% to 25 % hike on current CTC. Note: No Charges If interested drop your CV to Priyanka Palit [ 9518220852 || priyanka@avaniconsulting.com ] Thanks & Regards Priyanka Palit

Recruiter Mohaneswara Reddy https://www.linkedin.com/in/mohaneswarareddy Role & responsibilities The responsibilities are Operations, Control and Monitoring 1. Improving, continuous reviewing and up gradation of existing production SOPs and work systems to ensure their strict implementation in respective block. 2. Resolution and identification of maintenance related activities of equipment and facility and making sure those are closed appropriately 3. Executing proposed changes in product, process or equipment and facility. 4. Preparing production plan and supervising the API and Intermediate batches as per production plan. 5. Ensure facility upkeep is maintained all the time. 6. Any other a...

This role involves following cGMP, safety, and environmental standards. The ideal candidate will have experience in API manufacturing, knowledge of regulatory guidelines, and a focus on quality and safety. Description: Strictly following cGMP, Safety and Environmental Practices. Filling of Batch Manufacturing record and equipment cleaning record. Following Good Manufacturing practices during operation. Ensuring Good Housekeeping in the respective plant area and its equipment. Usage of Proper personnel protective equipment as per requirement. Planning and ensuring RM availability for daily production as per production plan. Maintaining the documents like Issue and dispensing register. Carryin...

Hii, Greetings from Avaniconsulting ! We are hiring for Production associate for a leading Pharma API Manufacturing company Position- Associate Work Experience Min 3-10 yrs in API Location - Mysore Gender - Any Qualification- B.Tech in Chemical Engineering /Msc Chemistry/Diploma Chemical/BSC Chemistry Roles & Responsibility 1. Responsible for appropriate production planning & execution of batches in line with targeted commitments complying cGMP& Safety requirements. 2. To ensure gowning practices, entry / exit procedures, usage of PPEs are followed by team while in the department. 3. To ensure adherence of process instructions as per Batch Manufacturing Record and respective departmental pro...

Role & responsibilities GurZac Biz Solutions Private Limited is assisting a renowned company in hiring for the position of Purchase Executive in an API manufacturing company to assist in the the procurement of raw materials, components, and other supplies needed for production . The role involves sourcing, negotiating prices, and ensuring the timely delivery of high-quality materials while adhering to regulatory standards. Sourcing & Supplier Management. Negotiation & Procurement Quality Control Cost Reduction Inventory Mangement Compliance Management Preferred candidate profile Must have minimum 2 years experience in purchase for API Manufacturing Company. Must be proficient in computers. C...

Roles and Responsibilities Prepare and review batch records for API production runs to ensure compliance with regulatory requirements. Collaborate with cross-functional teams to resolve issues related to product quality and process optimization. Develop and maintain knowledge of current Good Manufacturing Practices (cGMP) guidelines and industry standards.

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Job Title: Site Head API Manufacturing Location: Dahej Reporting to: Head of Operations / Managing Director Job Summary: The Site Head will lead and oversee the entire operations of the API manufacturing facility, ensuring compliance with cGMP and regulatory standards while achieving operational excellence, cost-effectiveness, and timely delivery. This role is responsible for managing production, quality, EHS, engineering, supply chain, HR, and finance at the site level. Key Responsibilities: Strategic and Operational Leadership Provide leadership to all departments within the site to achieve strategic goals. Develop and implement operational strategies that align with business objectives. D...

Role & responsibilities Preferred candidate profile

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

Role & responsibilities JD Of Officer production : Having exposure in batch process handling in API manufacturing. Hydrogenation block work experience OR shift in charge role will be an added advantage. Recording QMS documents as per cGMP guidelines Having knowledge on safety measures in batch operations execution. Following shift operation as per the production plan with safe and cGMP environment and responsible for maintaining good housekeeping of plants Shall submit the in process / intermediate sample to QC lab for analysis as per the batch instruction. JD Of Jr.officer production : To receive operating instructions for the shift from Production Executive. Ensure batch processing is carr...

Accountable to develop, implement and communicate the regulatory strategies to support registration activities for all Products for all global markets such as US, EU, Canada, Gulf and ROW Market. Lead, manage and develop leading edge regulatory strategies leading to successful regulatory filings and approvals for Generics for Global markets. implement changes required to comply with new regulatory requirements and to effectively lead and direct the creation of required data packages and facilitate knowledge for drug development. Collaborate with development and other cross functional teams during the product development activities to provide appropriate CMC as well as regulatory strategies. ...

Roles and Responsibilities Ensure compliance with cGMP guidelines during API production processes. Conduct BPR review meetings to ensure quality control standards are met. Oversee bulk drug manufacturing operations, including packaging and labeling. Collaborate with cross-functional teams to resolve issues related to production scheduling and inventory management. Maintain accurate records of production activities, batches, and equipment maintenance. Desired Candidate Profile 0-5 years of experience in API production or pharmaceutical industry. Strong understanding of BPR review procedures and regulations (cGMP). Excellent communication skills for effective collaboration with team members. P...

Role & responsibilities In process / Intermediate / Raw Material test limits preparation as per MPR • Receive and safeguard Batch Production Record (BPR) from QA • Follow the appropriate Good Manufacturing Practices • Ensure that entire operations are being carried out in a prescribed manner • Handle the Non-Confirming product as per the Shift-In charge • Follow the transfers of intermediates/ Final Product/ finished product to appropriate storage area • Record any deviation or abnormality in the batch production records during the process and inform the same to Shift-In charge • Prepare the deviation report for standard time deviations and deviation of BPR operations during the process • Re...

Role & responsibilities 1. To procure Raw materials from Ware house 2. Carry out the manufacturing operations according to the BPCR provided by QA department 3. Perform the Operations in accordance to the established SOPs and cGMP and capture the data in relevant documents. 4. To maintain for Good documentation practise at work place ( ALCOA) 5. To ensure the entry of batch related details in ERP. 6. To execute batches every day as per the Production planning schedule.