Role & responsibilities Develop and implement the engineering strategy in alignment with the companys overall goals and objectives.Lead the engineering team to drive innovation, efficiency, and continuous improvement in manufacturing processes and facilities.Oversee the design, development, and optimization of manufacturing systems and processes.Ensure engineering projects are completed on time, within scope, and within budget.Monitor and manage engineering KPIs and performance metrics to ensure operational excellence.Ensure all engineering activities comply with industry regulations, standards, and company policies, including USFDA, MHRA, EUGMP and cGMP guidelines.Handling of regulatory audits of USFDA, MHRA and EUGMP and its compliances.Hands on experience of Safety, EHS and statutory compliance.Lead engineering efforts to prepare for and support regulatory inspections and audits.Manage engineering projects from concept through execution, including new facility builds, equipment upgrades, and process improvements.Coordinate with cross-functional teams like quality assurance, and production, to support project goals.Develop and manage the engineering departments budget.Identify cost-saving opportunities and ensure efficient allocation of resources.Drive the adoption of new technologies and engineering practices to enhance productivity and product quality.Evaluate and implement best practices and emerging trends in pharmaceutical engineering.Communicate engineering strategies, progress, and issues effectively to senior management and other stakeholders.Collaborate with external partners, vendors, and consultants as needed.Preferred candidate profile API and Regulatory experience and audit complianceStrong leadership and team management skills.Excellent project management abilities.Proven ability to drive process improvements and innovation.Effective communication and interpersonal skills.Strong problem-solving and analytical skills Perks and benefits

Role & responsibilities 1. To identify new vendors for KSM, Solvent, Raw materials and packaging material.2. To communicate with vendor for material procurement as well as timely delivery of material.3. To maintain approved supplies and vendor list.4. To calculate vendor Q Score on annual basis. 5. Responsible to prepare MOP data of purchase department for ISO/ EHS6. Responsible for preparation, changes and release Purchase order for Raw material, Packing material, Import material, Lab chemicals. 7. Responsible for preparation of Purchase related SOPs & related documents.8. Responsible for reviewing and maintaining of all the documents like SOP, Control formats and data as per requirement of ISO-9001:2015, 14001:2015 and OHSAS 45001:2018. 9. Initiate & Implement action plan to achieve department objectives.11. Responsible for vendor development, monitoring of vendor performance.12. To handle electronic system like SAP, eDMS, eQMS, and LMSPreferred candidate profile Candidate should have experience in the API pharmaceuticals industry Perks and benefits

Role & responsibilities Analytical Test data review in software as well as in hard copy format.knowledge of eQMS and eDMS, LIMSInvestigation review of incidence and OOS and OOTCoordinate with QA related QMSPreferred candidate profile Candidate should from API pharma background Ready to work in all shift (Shift working duty)Perks and benefits

Role & responsibilities Receipt and Issuance activities.Dispensing activities,eDMS and eQMS knowledge SAP Knowledge Preferred candidate profile API experience mustready to work in all shift (Shift working duty)Perks and benefits

Role & responsibilities Analytical Data Review for chromatography and non-chromatography instrument .Handling of QMS activities like OOS, OOT, Incidence, Change Control, deviation and related investigations activities.Handling of LIMS Software,Handling of eQMS and eDMS software.Preferred candidate profile API pharmaceutical experience is mustReady to work in all shift (Shift working duty)Perks and benefits

Role & responsibilities Analytical Chemical TestingHPLC Analysis, GC AnalysisWet Lab AnalysisReady to work in all shift (Shift working duty)Preferred candidate profile Candidate will be preferred from API PharmaPerks and benefits