We have been retained by a highly reputed and fast growing Pharma Company to Hire a "Senior Manager / DGM - Maintenance (Engineering Head ) for their formulation unit Located at Aurangabad. Details of the position are mentioned below: Company: Our Client is a state-of-the-art Pharmaceutical Organisation involved in Research, Manufacturing, Marketing, Sales and Distribution of Medicinal Formulations and Products. Designation: Senior Manager / DGM - Maintenance (Head Engineering). State of the Art Plant manufacturing Oral Solids, Liquid Orals & Injectables Job Location: Aurangabad Educational Qualification: B.E. / B.Tech - Mechanical Engineering Experience: Minimum of 12 years of experience of managing Utilities and Machinery of a Formulation Unit of a reputed Pharma Company. Please Note that the candidate must be currently working as Manager Engineering / Maintenance of a formulation Unit. CTC: 10 - 14 Lakh Per Annum Those of you whose profile matches the above mentioned description and would like to apply for this position shall forward their updated resume to sudhirvinayak@gmail.com In case of a query, please feel free to speak to the undersigned: Sudhir Vinayak, Director, Pharma Placements Inc. Mobile: 9820234987
We have been retained by a highly progressive and fast growing Pharma company to hire an " Executive / Assistant Manager - HR" to be based at their manufacturing plant based at Aurangabad. Company's HO is located at Mumbai. Details of the position are mentioned below: Company: Our client is a highly reputed and fast growing pharma with a substantial domestic and international presence. Designation: Executive / Assistant Manager - HR. Job Location: Aurangabad Role & responsibilities: Lead and manage the HR Department, ensuring effective and efficient operations. To provide a comprehensive HR advisory service to the Company. Manage the recruitment process. Support present and future company demands through growing, involving, inspiring, and preserving human capital. Stay abreast of industry trends and best practices to continuously improve HR processes. Monitor and ensure the company's compliance with state, and local employment laws and regulations, recommend best practices; review and accordingly modify policies on a timely basis to maintain compliance. Conduct training and development programs as and when required in manufacturing plant. Responsible for handling HR Audit with the support of HR team. Preferred candidate profile : 5 - 10 years of experience in the relevant field, preferably in a pharmaceutical company of high repute Knowledge of computers Excellent verbal and written communication skills In-depth knowledge of HR best practices, employment laws and regulations. Those of you whose profile matches the above mentioned description and will like to apply for this position shall forward their updated profile to director.ppi@gmail.com In case of a query, please feel free to speak to the undersigned: Kanika Vinayak, Director, Pharma Placements Inc. Mobile No: 98202 29398
We have been hired by a highly reputed and fast growing Pharma company to hire a "DGM - Formulation & Development' to be based at their plant located at Aurangabad . Details of the position are mentioned below: Role & responsibilities: Literature search/study and to prepare development trials strategies. Pre formulation study execution. Market/Innovator/reference product characterization. Execution and documentation of trial batches for prototype formulation development. Execution and monitoring of development stability studies. Execution of process optimization/scale-up batches. Technology transfer activities at site. Preparation/review of documents like BOM, MFR, compatibility study protocol & report, stability study protocol and report, PDR, etc as per requirements. Co-ordination with production, other relevant cross-functional departments/teams. Having experience/exposure of formulation development of solid oral, liquid, dry syrup, etc dosage forms aimed for ROW and domestic market. Should possess experience in handling various equipment like RMG, FBD/FBP, compression machine, roller compactor, coating machine, etc. Preferred candidate profile : Educational Qualification: M. Pharm Experience: 12 - 20 Years of relevant experience in a leading Pharma Company. Good Communication & Presentation skills Those of you whose profile matches the above mentioned description and would like to apply for this position shall forward their updated CV to sudhirvinayak@gmail.com In case of a query, please feel free to speak to the undersigned: Sudhir Vinayak Director, Pharma Placements Inc. Mobile number: 98202 34987
We have been retained by a fast upcoming and highly reputed Pharma company to hire a "General Manager - Operations" to be based at Baddi (Himachal Pradesh). Details of the position are mentioned below: Company: Our client operates a WHO - GMP approved liquid oral manufacturing facility at Baadi (Himachal Pradesh). The company is a third party manufactures for Most of Top 50 Pharma companies in India. Designation: General Manager Operations Reporting to: Director Experience: 10 - 20 years of similar experience with a reputed Pharma company. Main Task: General Manager (GM) shall have responsibilities as enumerated below: To manage the manufacturing element of the organization ensuring high quality business activities with maximum efficiency, service and profitability for the organization. Ensuring that the team understands that the organizations profits and achievements are reflected in all its operations and activities including relationships and risk management. To maintain overall organization responsibility for performing all duties in compliance with related manufacturing legal/statutory regulations, professional duties, responsibilities and obligations and insert as applicable e.g. Current Good Manufacturing Practices (cGMP), Best Practice Guidelines & WHO-GMP certification. To manage, direct and monitor the overall performance of the organization. To design and set up the Quality Management System. To maintain and improve mechanisms for manufacturing and all organization activities, including surveying and measuring the manufacturing operations, process, outcomes and profitability and disseminate feedback to the appropriate internal entities. Accountable for day to day activity of manufacturing and testing. To support all other departments in matters related to manufacturing, e.g. procurement of materials (RM & PM). To lead preapproval inspections and final inspections of all Regulatory authorities. Work allocation of all department heads and monitoring of their work. To discuss all observation with dept. heads and to plan the actions accordingly. To initiate the cGMP compliance norms. To conduct internal audits/self-inspection periodically, to ensure strict quality standards. To ensure SOP`s compliance by HODs on continuous basis. To set an example for team members of commitment, manufacturing process expertise, work ethics and habits and personal character. To interact and co-operate with all members of the organization, its suppliers and customers Authorizing authority for specification of equipments, instruments, systems to be procured. Liaison with FDA Authorities. Training to all subordinates. Authorization of all documents concerned to Production, Maintenance, Quality Control, Quality Assurance & other process. To ensure implementation & compliance of Quality Standards in every stage of manufacturing. cGMP documents Control & Monitoring. To ensure timely release of finished goods. Interaction with manufacturers, suppliers and vendors. To oversee validation and responsible for supervising, monitoring and ensuring all the matters related to validation. To ensure authorization & certification of all the validation documents. To provide the Price List based on mail received from party. Evaluation and introduction of new product. Other Task: Approving of vendor credentials of qualifications, professional competence, solvency, market standings etc. Ensure quality systems through management. Attending to market complaints through proper investigation & sorting out matters. To get actively involved in the design and construction of pharmaceutical manufacturing facility to comply with the regulatory agencies. To interact with external consultants/agencies. Preparation for inspection by external bodies. You are responsible for your allocated workload and must meet all targets as agreed with your Line Manager. You must contribute towards the smooth running of the organization generally. Any Other Work Assigned : Any other task assigned by the Director from time to time. Those of you whose profile matches the above mentioned description and would like to apply for this position shall forward their updated resumes to sudhirvinayak@gmail.com In case of a query, please feel free to speak to the undersigned Sudhir Vinayak, Director, Pharma Placements Inc. Mobile no.: 98202 34987
Position Regulatory Consultant Company Information Our client is a reputed Pharmaceutical Consulting firm working in the area of GMP and Global Regulatory Affairs. They have their head office in Mumbai and subsidiaries in Singapore, Malaysia, Australia and in Europe. The company has been providing high quality & timely consulting service to the Pharmaceutical Industry in India and internationally. The company has a young and committed team of GMP and Regulatory Experts. The company is inviting applications for the role of Regulatory Consultant and are looking for dynamic, driven individuals with strong initiative who can thrive in the entrepreneurial environment at our firm. Role & Responsibilities The person will be responsible for Regulatory consulting services at the firm. The responsibilities of this position include, but are not limited to, the following: Ownership for assigned regulatory projects including dossier writing, submissions, approval tracking, query resolution across Developed markets (EU,US, UK & Australia) and Emerging markets Ensure regulatory compliance, accuracy, timely completion, version control & adherence to internal SOPs Providing strategic input to the Management and Partners on regulatory projects Keep abreast of new developments in regulations across all critical health authorities Experience & Qualifications Regulatory affairs experience in small molecules for a minimum of 6-8 years is mandatory Must be well versed with ICH CTD guidelines and other regulatory guidelines from developed markets (US, EU, Australia/ UK). Must have hands-on experience in regulatory submissions pertaining to generics/ small molecules in US/ EU/Australia/ UK Computer and technical skills (including eCTD software knowledge) Strong & Flawless communication skills. Accuracy and attention to detail. Those of you whose profile matches the above mentioned description and would like to apply for this position shall forward their updated resume to sudhirvinayak@gmail.com In case of a query, please feel free to speak to the undersigned: Sudhir Vinayak, Director, Pharma Placements Inc. Mobile: 98202 34987