System Audit

Location :Ankleshwar, Gujrat:Always adhere to technical procedures and Good Manufacturing Processes(GMP).Assist with stores organization /stock control.Attend to breakdowns onsite ensuring that there is always a rapidresponse, and that plant equipment and machinery breakdown time isminimized. Always endeavour to reduce downtime of site plant andmachinery;...

University education (pharmacy, chemistry, pharma technology, biology etc.) English language in writing and speaking, other language is the advantage (Czech is not mandatory) Microsoft Office Excel, Word, Outlook Experience in pharma industry or quality lag is a must Experience as the GMP / GDP auditor at least two years Experience with TrackWise is the...

Education: Graduate/ Post Graduate in Pharmacy Experience: 03 years in Pharma industry with awareness of Quality management systems, manufacturing activities, process validation, Qualification, Regulatory requirements Quality Management/Continuous Improvement Release/rejection of Finished Products Working as a key user for management of SAP Athena QM module....

Responsibilities : Good knowledge of Safety Management with Legal Requirements and capability to meet Legal Compliances. Implementation, Updating, Review and Auditing of the Company HSE Systems. Ensure that necessary monitoring and measurement of HSE performance parameters is carried out Appropriate investigation and reporting of OH&S (Occupational...

Responsibilities:Good knowledge of Safety Management with Legal Requirements and capability to meet Legal Compliances.Implementation, Updating, Review and Auditing of the Company HSE Systems.Ensure that necessary monitoring and measurement of HSE performance parameters is carried out Appropriate investigation and reporting of OH&S (Occupational hazards and...

Responsibilities : Preparation, Review and Issuance of Departmental Sops, Guidelines and Policies. LNB's and Logbooks Issuance and Checking for daily entries in Logbooks. To Review various Documents like Change controls, Incident Reports, CAPA, OOS Results, Deviations, Issuance Records and Internal Audit Reports. Prepare, Review and Maintain...

LocationIndia, Ankleshwar, IndeBusiness ControllerAt Dormer Pramet, our purpose is to build on the company's heritage and success to innovate our way into the future. By keeping a long-term focus in everything we do, we can support our ambitions to grow manufacturing and prosperity for all. This brings jobs, with opportunities for both growth and security....

Opening: 1 Nos Job ID:Employment Type:Full Time- Reference:Work Experience: 6.0 Year(s)To 8.0 Year(s)- CTC Salary: 4.00 LPA TO 5.00 LPA- Function: Production / Quality / Maintenance- Industry: Chemicals/PetroChemical- Qualification: B.Sc - Chemistry; M.Sc - Chemistry- Location: AnkleshwarPosted On: 07th Aug, 2023**Position: Quality ExecutiveLocation:...

Position – QA executive.Experience – 4 or 5 years only pharma line (API experience )CTC:5LPAStrong knowledge of QMSLocation – AnkleshwarRESPONSIBILITIES:To issue the Batch Manufacturing Record, Equipment cleaning record, Logbooks, Analytical Report for raw material, finish product and packing material.Assistance in preparation of SOP of various...

Position – QA executive.Experience – 4 or 5 years only pharma line (API experience )CTC: 5LPAStrong knowledge of QMSLocation – AnkleshwarRESPONSIBILITIES:To issue the Batch Manufacturing Record, Equipment cleaning record, Logbooks, Analytical Report for raw material, finish product and packing material.Assistance in preparation of SOP of various...

Job Description: Education : B. E Chemical Experience: 7-9 yrs. experience in Chemical/ API production Technical skills & Competencies / Language : Know-how of API Production , plant processes and technological updates, SAP Knowledge, data analysis, cGMP & HSE knowhow Behavioral Competencies: Fast, Lean, Inclusive ,Creative, Connected,...

Education: Graduate / Post Graduate in Pharmacy or Chemistry Experience:years in Pharma industry with awareness of Quality management systems, manufacturing activities, process validation, Qualification, Regulatory requirements Quality Management/Continuous Improvement Handling of Deviations & CAPA Handling of Product Technical Complaints Review of Master...

JOB PURPOSE_GenericPurpose of this job is to co-ordinate and organize API manufacturing activities in shifts adhering to cGMP / HSE norms/ standards with optimum utilization of man / machines and facilities in compliance with regulatory requirements, living Group's Values and Code of EthicsSpecific additions (if needed)N/AKEY ACCOUNTABILITIESSpecificHave...

Tax ProfessionalAt Dormer Pramet, our purpose is to build on the company's heritage and success to innovate our way into the future. By keeping a long-term focus in everything we do, we can support our ambitions to grow manufacturing and prosperity for all. This brings jobs, with opportunities for both growth and security. It is what we care for, and what...

Job Description: Internal Job Description Education / Experience M.Sc. Analytical/Organic Chemistry/Inorganic Chemistry  Min. 5 years’ Experience in a Quality Control/Analysis laboratory in a cGMP/ISO environment, with exposure to method development and validation activities  Technical skills &   Competencies /...

**Location : Ankleshwar, Gujrat**: 1. Always adhere to technical procedures and Good Manufacturing Processes (GMP). 2. Assist with stores organization /stock control. 3. Attend to breakdowns onsite ensuring that there is always a rapid response, and that plant equipment and machinery breakdown time is minimized. Always endeavour to reduce downtime of site...

**Location : Ankleshwar, Gujrat.**: (a) Responsible for all reactive and proactive maintenance work, whilst making sure it is carried out to the highest possible standards across the whole of the site. (b) Expected to carry out all maintenance across the plant, in both a low care and high care environment. (c) Attend to breakdowns onsite ensuring that there...

University education (pharmacy, chemistry, pharma technology, biology etc.) - English language in writing and speaking, other language is the advantage (Czech is not mandatory) - Microsoft Office - Excel, Word, Outlook - Experience in pharma industry or quality lag is a must - Experience as the GMP / GDP auditor at least two years - Experience with TrackWise...

**Education**: - Graduate/ Post Graduate in Pharmacy - Experience: - 0-3 years in Pharma industry with awareness of Quality management systems, manufacturing activities, process validation, Qualification, Regulatory requirements - Quality Management/Continuous Improvement - Release/rejection of Finished Products - Working as a key user for management of...

Responsibilities : Good knowledge of Safety Management with Legal Requirements and capability to meet Legal Compliances. Implementation, Updating, Review and Auditing of the Company HSE Systems. Ensure that necessary monitoring and measurement of HSE performance parameters is carried out Appropriate investigation and reporting of OH&S...

Responsibilities : Good knowledge of Safety Management with Legal Requirements and capability to meet Legal Compliances. Implementation, Updating, Review and Auditing of the Company HSE Systems. Ensure that necessary monitoring and measurement of HSE performance parameters is carried out Appropriate investigation and reporting of OH&S...

Opening: 1 Nos.- Job ID: 65654- Employment Type: Full Time- Reference: - Work Experience: 6.0 Year(s) To 8.0 Year(s)- CTC Salary: 4.00 LPA TO 5.00 LPA- Function: Production / Quality / Maintenance- Industry: Chemicals/PetroChemical- Qualification: B.Sc - Chemistry; M.Sc - Chemistry- Location: - Ankleshwar Posted On: 07th Aug, 2023 **Position: Quality...

Key profile requirements:M.Pharm/B.Pharm/MSC with min 12 years of experience Pharmaceutical manufacturing (API) (Preference M.Pharm/B.Pharm)Sound knowledge of API manufacturing operationsExperience of all the profiles of Pharmaceutical Quality management system (QMS)Leading investigationsLeading Inspection and customer audit (Direct exposure of USFDA, EDQM,...

Responsibilities:Good knowledge of Safety Management with Legal Requirements and capability to meet Legal Compliances.Implementation, Updating, Review and Auditing of the Company HSE Systems.Ensure that necessary monitoring and measurement of HSE performance parameters is carried out Appropriate investigation and reporting of OH&S (Occupational hazards and...

Opening: 1 Nos.- Job ID: 57580- Employment Type: Full Time- Reference: - Work Experience: 3.0 Year(s) To 5.0 Year(s)- CTC Salary: 4.00 LPA TO 5.00 LPA- Function: Production / Quality / Maintenance- Industry: Chemicals/PetroChemical- Qualification: B.Sc - Chemistry; M.Sc / MS Science - Chemistry- Location: - Ankleshwar Posted On: 06th Apr, 2023 **Position:...

Ø Installing and configuring computer hardware, software, systems, networks, printers and scanners Ø Considering smooth working of staff due to IT Ø Manitaining server room Ø Assisting staffs Ø Monitoring and maintaining computer systems and networks Ø Responding in a timely manner to service issues and requests Ø Providing technical support...

Location India, Ankleshwar, Inde Business Controller At Dormer Pramet, our purpose is to build on the company’s heritage and success to innovate our way into the future. By keeping a long-term focus in everything we do, we can support our ambitions to grow manufacturing and prosperity for all. This brings jobs, with opportunities for both growth and...

Responsibilities : Preparation, Review and Issuance of Departmental Sops, Guidelines and Policies. LNB's and Logbooks Issuance and Checking for daily entries in Logbooks. To Review various Documents like Change controls, Incident Reports, CAPA, OOS Results, Deviations, Issuance Records and Internal Audit Reports. Prepare, Review and Maintain...

Responsibilities : Preparation, Review and Issuance of Departmental Sops, Guidelines and Policies. LNB's and Logbooks Issuance and Checking for daily entries in Logbooks. To Review various Documents like Change controls, Incident Reports, CAPA, OOS Results, Deviations, Issuance Records and Internal Audit Reports. Prepare, Review and Maintain...

Job Description: ? Accountable for the end-to-end HR activities of company? Plan, organize and keep organization structure current? Managing and monitoring contractors, labour attendance & payroll system.? Do HRP (human resource planning) for new positions, and set budget for the position as permarket standards? Managing recruiter and be...

Key profile requirements: M.Pharm/B.Pharm/MSC with min 12 years of experience Pharmaceutical manufacturing (API) (Preference M.Pharm/B.Pharm) Sound knowledge of API manufacturing operations Experience of all the profiles of Pharmaceutical Quality management system (QMS) Leading investigations Leading Inspection and customer audit (Direct...

Key profile requirements: M.Pharm/B.Pharm/MSC with min 12 years of experience Pharmaceutical manufacturing (API) (Preference M.Pharm/B.Pharm) Sound knowledge of API manufacturing operations Experience of all the profiles of Pharmaceutical Quality management system (QMS) Leading investigations Leading Inspection and customer audit (Direct...

Key profile requirements: M.Pharm/B.Pharm/MSC with min 12 years of experience Pharmaceutical manufacturing (API) (Preference M.Pharm/B.Pharm) Sound knowledge of API manufacturing operations Experience of all the profiles of Pharmaceutical Quality management system (QMS) Leading investigations Leading Inspection and customer audit...

2-3 years Ankleshwar 350000 (INR) - 475000 (INR) Job Description 1) Responsible for maintaining and improving Safety, Health and environment in plant operations. 2) Maintaining ISO 9001:2015, ISO 14001:2015, ISO 45001:2018 management systems. 3) Investigation of accidents/incidents and taking appropriate corrective and preventive action. 4) Maintaining...