38 Jobs in Ankleshwar, Gujarat - Page 2

Position Title: Executive – Quality Control Qualification and Experience: M. Sc (Organic / Analytical Chemistry) / B. Pharm with 2 - 6 years of Experience as an analyst in the Pharmaceuticals / API industry. GMP & GLP knowledge Job overview: Implement quality control activities at Ankleshwar, adhering to regulatory/global quality Directives and HSE guidelines with optimum utilization of resources to ensure consistent good quality of products to meet customers’ requirements. Responsibilities: Analysis: Performing timely sampling and analysis of raw material, bulk product, intermediates, finished goods, and other samples. Performing analysis of Stability, process validation samples, and Cleaning Validation. Handling of sophisticated laboratory instruments viz., HPLC, GC, UV & IR spectrophotometer, Dissolution tester, auto-titrator, polarimeter, etc. Good Laboratory Practice Performing calibration & maintenance of the lab. Equipment and assistance for the qualification of laboratory equipment. Knowledge on the preparation of SOPs and Formats and Analytical Test records. Managing reference standards, working standards, laboratory reagents & chemicals. Arranging and observing Control Samples and maintaining the record. Participating in the Investigation of out-of-specification results. Maintaining laboratory raw data related to testing activity. Validation Performing Analytical Method validation, cleaning validation as per the protocol. Other Coordinating with production and the warehouse for analytical activities Compliance to HSE Requirements for QC laboratory. Identifying and correcting unsafe conditions or behaviours, and promptly reporting other potentially hazardous situations. Carrying out any other assignments or projects as per the instructions of the Department. Head to meet with the organizational objectives and priorities. Requirements GMP & GLP knowledge Good coordination & communication skills. Analytical ability Knowledge on LIMS & QMS What makes this position unique? This position will provide good exposure to work in GMP/ GLP environment. Location information: Ankleshwar, Gujarat, India

Department INFOTECH Job posted on May 23, 2025 Employment type P-P8-Probationer-HO Executive Title: CSV - IT Location: Gujarat Qualification: BCA / MCA Experience: 4+ years Key Responsibilities: Perform all Administration activities as mentioned in the user management SOP. Responsible for Activation/Reset/Change/Deactivation of User Access (24x7). Review, configure, and manage the Privilege Right Matrix. Prepare, create, and deactivate/update User Access Matrix. Provide access to service engineer user accounts and review service engineer audit trials. Prepare and update application-wise process steps for user management. Prepare and update the list of applications. Prepare and implement site SOPs and ensure their periodic updates. Prepare/Review qualification protocols and participate in all instrument and software qualification activities, including challenge tests with documentation. Handle all IT-related QMS activities (e.g., Change Control, Deviation, CAPA, Incident, Qualification documents, SOPs, etc.). Responsible for Backup and Restoration activities. Provide support during software assessment and mitigation plans. Provide support during software maintenance and network-related problems. Participate and ensure compliance with periodic reviews. Conduct periodic verification of GLP and desktop policies. Conduct risk-based network failure tests periodically. Explain the IT role in analytical applications and user management to internal/external auditors and regulators. Communicate effectively with middle/senior management. Capable of handling a team.

Female Candidates only. * B.Sc(Chemestry) is must.* Conduct market analysis. Collect and handle study data. Carry out fundamental administrative tasks, such as printing, emailing and obtaining office supplies. Collaborate and assist the team. Supporting the Front Office. Support with inventory management. Plan staff meetings and schedule updates. Process business invoices, bills and receipts. Aid in management. Office executive experience from prior employment. Outstanding organisational abilities. Understanding of Microsoft Office programs and computer operating systems. The capacity to cooperate in a group. Superior verbal and written communication abilities. Basic familiarity with accounting and financial software. Knowledge of market research methods. Job Type: Full-time Pay: ₹15,000.00 - ₹25,000.00 per month Benefits: Cell phone reimbursement Internet reimbursement Schedule: Day shift Morning shift Supplemental Pay: Commission pay Performance bonus Yearly bonus Ability to commute/relocate: Ankleshwar, Gujarat: Reliably commute or planning to relocate before starting work (Preferred) Application Question(s): Have you completed BSc(Chemistry)? Education: Bachelor's (Required) Language: English (Required) Work Location: In person Expected Start Date: 02/06/2025

Job Title: Junior Chemist – Agrochemical Industry Location: [Insert Location] Department: Quality Control / R&D / Production Lab Reports To: QC Manager / Lab Head / Plant Manager Experience Required: 0–2 years Employment Type: Full-time Job Summary: We are seeking a detail-oriented and enthusiastic Junior Chemist to join our agrochemical division. The role involves supporting the quality control and formulation teams by performing chemical tests on raw materials, technicals, and finished formulations under supervision. The candidate will work with common lab instruments and follow industry regulations and SOPs. Key Responsibilities: Assist in the analysis of technicals, formulations (EC, SC, WP, WG, etc.), and raw materials as per standard methods. Perform routine tests such as pH, specific gravity, viscosity, emulsion/stability, active ingredient content . Operate basic instruments like UV-Vis spectrophotometer, Karl Fischer, GC, HPLC (training will be provided if needed). Prepare reagents, standardize solutions, and maintain lab records as per SOPs. Ensure all samples are labeled, tested, and recorded accurately. Help with stability studies and maintain sample retention records. Support senior chemists in method development, pilot trials, and new formulation evaluations. Adhere to GLP, safety norms, and environmental standards during lab work. Required Qualifications & Skills: Education: B.Sc. / M.Sc. in Chemistry, Agrochemical Science, Industrial Chemistry, or related discipline. Experience: 0–2 years (freshers with internships in QC/R&D labs welcome). Skills: Basic knowledge of agrochemical formulations and testing procedures. Familiarity with laboratory safety and chemical handling. Willingness to learn analytical instruments and quality control documentation. Good observation, teamwork, and communication skills. Growth Opportunity: Exposure to QA/QC, R&D, regulatory documentation, and formulation technology . Hands-on training with industry-standard equipment and advanced lab techniques. Opportunity to grow into roles such as QC Chemist, Formulation Chemist, or Regulatory Analyst. Agrochemical Product Types You’ll Work With: Herbicides, Insecticides, Fungicides Liquid and Solid Formulations (EC, SC, WP, WG, SL, etc.) Job Type: Full-time Pay: ₹9,866.11 - ₹20,000.00 per month Benefits: Health insurance Paid sick time Schedule: Day shift Fixed shift Supplemental Pay: Yearly bonus Work Location: In person

Preferred Education Background: PhD Chemistry in Electrochemistry with >2 years of work experience. Role: · A bench scale chemist leads a team of chemists working on surfactant synthesis, polymer synthesis and its application testing for oil and gas and industries. Practical experience of electrochemistry. · Design and evaluate synthetic processes for the fine chemical market and for oil and gas industries application studies. Required Skill Set: · Good technical & working knowledge of standard laboratory techniques and modern analytic techniques and instrumentation. Deep technical knowledge of electrochemistry. · Must be able to optimize and scale up new products to pilot and full plant from gram to kilogram quantities in a cost-effective manner. · Strong communication skills (written and oral) including the ability to communicate effectively at all levels and able to report back results accurately and in a timely manner. · Good interpersonal, team-playing skills and the ability to operate in multi-disciplinary/cross-functional teams. · Ability to work in a team with dynamic multidisciplinary environment. · Ability to solve technical problems under one's own initiative, but with a willingness to seek expert assistance when required. · Ability to work unsupervised for shorter periods without losing touch with the aims of the team. Responsibilities: · Responsible for development, synthesis, full characterization, and evaluation of new and existing molecules. · Performs hands-on laboratory R&D on a routine basis to support projects and/or other technical activities. · Prepares results in a timely and accurate manner in the required format (written, verbal, formal presentation), summarizing all technical activities. · Writes, initiates, adapts and follows scientific procedures and protocols. · Effective communication with all team members, other chemists, production/plant staff, and team leaders to distribute results, problems and next step recommendations in a timely fashion. · Stays up to date with current developments in the areas of expertise. · Performs literature search. · Perform experiments along with a team. Accountability: · Safe working in accordance with safety policy and procedures. Performs safety, COSHH and risk assessments of all chemical processes. Contribute to evaluation of new target opportunities and understand and implement project Job Types: Full-time, Permanent Benefits: Cell phone reimbursement Health insurance Provident Fund Schedule: Day shift Work Location: In person

Job Description for Executive – Quality Assurance, Pharma Educational Qualification B. Pharm / M. Pharm from a reputed university Experience 3 to 5 years of similar experience in a regulatory-approved OSD manufacturing large unit. Quality Management/Continuous Improvement Line Clearance and shop floor compliance Assisting in Complaint Investigation system at site Assisting in Qualification and validation system, change control system, deviations Preparing & review the Annual Product Quality Review Review of Batch Manufacturing & Packing Records Coordination of cGMP Training activity. Compliance Ensure adherence to company Quality Standards, Local FDA MHRA regulations, by Understanding the requirements Performing the Gap analysis to find out the gaps in existing system Preparing a compliance plan for closure of gaps Execution of compliance plans Review of completion for compliance activity Validations & Qualifications: Ensure validated status of all equipment’s, manufacturing processes, and cleaning processes Review of protocols for qualification and validation of facility/ equipment / product / process Review of validation reports after execution of validation of facility /equipment / product / process Documentation Control: Preparation and Review of SOPs Controlled distribution and archival of documents & record Control of master documents Assuring quality of products by : Ensuring SOP compliance Review of Batch Manufacturing & Packing Records Ensuring implementation of Corrective actions/Preventive actions proposed in Deviations and Customer complaints Ensuring the effectiveness review of the implemented CAPA cGMP Training: To prepare training modules and organize training in GMP Execute the training program in coordination with all concerned departments Other: Review of maintenance and calibration program

WE REQUIRED ITI APPRENTICE FOR FOLLOWING TRADE 1. ITI AOCP 2. ITI ELECTRICIAN 3. ITI LACP 4. ITI FITTER Job Types: Full-time, Internship Contract length: 12 months Pay: ₹8,500.00 - ₹9,000.00 per month Schedule: Day shift Work Location: In person

* Company Name - Bhavna Roadways - website - bhavnaroadways.com * Location - Ankleswar, Gujarat region (1 Vacancy) * PF & ESIC Benefits wherever applicable Requirements Good Computer knowledge Good Communication & Interpersonal skills Candidates having experience in the Logistic / Cargo / Transportation Industry preferred. (Freshers can also apply) Reliable Must be deadline and goal-oriented Job Types: Full-time, Permanent Salary: Between ₹15,000.00 to ₹17,000.00 per month Schedule: Day shift Work Location: In person *Speak with the employer* +91 9322717032 or email us at hr@bhavnaroadways.com Expected Start Date: 21/05/2025 Job Type: Full-time Pay: ₹15,000.00 - ₹17,000.00 per month Benefits: Provident Fund Schedule: Day shift Supplemental Pay: Yearly bonus Education: Bachelor's (Preferred) Experience: Data entry: 1 year (Preferred) total work: 1 year (Preferred) Language: English (Preferred) Work Location: Remote Expected Start Date: 21/05/2025

Sales Executive position is open at Khushbu Auto Finance Ltd. in ANKLESHWAR . The role requires candidates who are skilled in building customer relationships, following up on leads, and maximizing sales opportunities. Identify prospects and develop sales strategies to drive business growth. The position offers an in-hand salary of ₹15000 - ₹20000 and prospects of growth. Key Responsibilities: Close sales through various methods like cold calling, presentations, and door-to-door visits. Build strong customer relationships and meet sales targets. Research and develop creative sales strategies to boost results. Report performance metrics and feedback to management regularly. Maintain and grow the client database effectively. Job Requirements: Candidates with 12th Pass and 0 - 1 years of experience in the sales field can apply for this role. Familiarity with different sales techniques is a must. Candidates should also have good communication, negotiation, and interpersonal skills. Proficiency in computer use and the ability to utilize technology effectively are essential. Job Type: Full-time Pay: ₹15,000.00 - ₹20,000.00 per month Benefits: Health insurance Paid time off Provident Fund Schedule: Day shift Work Location: In person

Job Description The Quality Assurance (QA) & Quality Control vendor approval process involves evaluating a supplier's ability to consistently provide products or services that meet quality standards, including physical audits, sample analysis, and review of documentation. This process ensures that only reliable vendors are used to maintain product quality and safety, often a critical requirement in industries like pharmaceuticals. Here's a more detailed breakdown of the QA vendor approval process: 1. Needs Assessment and Vendor Identification:  Determine Needs: The organization identifies the need for a new vendor and the specific requirements for the product or service.  Vendor Identification: Research and identify potential vendors who can meet the requirements. 2. Vendor Qualification:  Vendor Questionnaire: Potential vendors are typically asked to complete a questionnaire that gathers information about their capabilities, quality systems, and compliance.  Document Review: QA reviews the vendor's documentation, such as certificates of analysis (COAs), specifications, and method of analysis.  Sample Analysis: The vendor provides samples, which are tested by Quality Control (QC) to ensure they meet the required standards.  Site Audit: A physical audit of the vendor's manufacturing site is conducted to assess their quality control measures and overall compliance. 3. Vendor Evaluation and Approval:  Compliance Assessment: A evaluates the results of sample analysis and the site audit to determine if the vendor meets the required standards.  Risk Assessment: Vendors may be categorized by risk level, with those posing higher risks requiring more rigorous evaluation and monitoring.  Approval Decision: Based on the evaluation, QA makes a decision to approve or reject the vendor. 4. Ongoing Monitoring and Re-evaluation:  Performance Monitoring: Regularly monitor the vendor's performance on quality, timeliness, and other relevant factors.  Periodic Audits: Conduct periodic audits to ensure continued compliance and quality.  Re-evaluation: Periodically re-evaluate vendors to ensure they continue to meet the organization's standards. Job Types: Full-time, Permanent, Fresher Pay: ₹11,000.00 - ₹15,000.00 per month Benefits: Cell phone reimbursement Flexible schedule Internet reimbursement Leave encashment Paid sick time Provident Fund Schedule: Day shift Supplemental Pay: Performance bonus Yearly bonus Work Location: Remote Speak with the employer +91 9909004011 Expected Start Date: 15/05/2025

Job Description for Executive – Quality Assurance, Pharma Educational Qualification B. Pharm / M. Pharm from a reputed university Experience 1 to 4 years of similar experience in a regulatory-approved OSD manufacturing large unit. Quality Management/Continuous Improvement Line Clearance and shop floor compliance Assisting in Complaint Investigation system at site Assisting in Qualification and validation system, change control system, deviations Preparing & review the Annual Product Quality Review Review of Batch Manufacturing & Packing Records Coordination of cGMP Training activity. Compliance Ensure adherence to company Quality Standards, Local FDA MHRA regulations, by Understanding the requirements Performing the Gap analysis to find out the gaps in existing system Preparing a compliance plan for closure of gaps Execution of compliance plans Review of completion for compliance activity Validations & Qualifications: Ensure validated status of all equipment’s, manufacturing processes, and cleaning processes Review of protocols for qualification and validation of facility/ equipment / product / process Review of validation reports after execution of validation of facility /equipment / product / process Documentation Control: Preparation and Review of SOPs Controlled distribution and archival of documents & record Control of master documents Assuring quality of products by : Ensuring SOP compliance Review of Batch Manufacturing & Packing Records Ensuring implementation of Corrective actions/Preventive actions proposed in Deviations and Customer complaints Ensuring the effectiveness review of the implemented CAPA cGMP Training: To prepare training modules and organize training in GMP Execute the training program in coordination with all concerned departments Other: Review of maintenance and calibration program

Gautam Kucha 9638 9638 42 Apple Enterprise Plot No. 307/311-39 Rajat Pharma Ltd Near Ramdev Chowkdi GIDC Ankleshwar 393002 GST No. 24BOFPK0289H1ZZ Job Type: Full-time Pay: ₹8,500.00 - ₹35,000.00 per month Benefits: Cell phone reimbursement Schedule: Day shift Supplemental Pay: Performance bonus Language: English (Required) Work Location: In person

Gautam Kucha +91 99044 69115 Apple Enterprise Plot No. 307/311-39 Rajat Pharma LtdNear Ramdev ChowkdiGIDC Ankleshwar 393002GST No. 24BOFPK0289H1ZZ Job Type: Full-time Pay: ₹8,500.00 - ₹45,000.00 per month Benefits: Cell phone reimbursement Compensation Package: Performance bonus Schedule: Day shift Work Location: In person Speak with the employer +91 9904469115