120 Contract Manufacturing Jobs - Page 4

This role is responsible for Responsibilities Supervision & Control Managing Team Brand growth Prescription Growth Prescribers growth Market Share Ensuring ROI Development of subordinates Relationships around the role Key External Stakeholder(s) Doctors, Stockiest, Retailers, CFA staff, Fellow professionals, Institutional administrators Key Internal Stakeholder(s) Superiors, Subordinates , PMT, HR & Sales Admin Competencies critical for the role Scientific/ Technical Competencies Proficiency level Proven Leadership qualities Good communicator Proven track records Ambitious Behavioral Analytical ability

Responsibilities Achievement of set targets. Maintaining set call Average/coverage. Complete use of allotted resources. Increasing prescriber base Focus on target customers. Maintaining call average and customer coverage Increasing PCPM. Timely reporting. Ensuring ROI Relationships around the role Competencies critical for the role Scientific/ Technical Competencies Proficiency level Convincing ability Presentation Selling Communication Behavioral Analytical ability PR Skills

Responsibilities Achievement of set targets. Maintaining set call Average/coverage. Complete use of allotted resources. Increasing prescriber base Focus on target customers. Maintaining call average and customer coverage Increasing PCPM. Timely reporting. Ensuring ROI Relationships around the role Competencies critical for the role Scientific/ Technical Competencies Proficiency level Convincing ability Presentation Selling Communication Behavioral Analytical ability PR Skills

The candidate coming into this role is expected to drive the licensing strategy to expand our portfolio of pharmaceutical products under the most competitive terms, identify global business development opportunities, identify the strategy that grants the quickest access to the market, and negotiation of offers along with the license and supply, distribution, co-development and contract manufacturing agreements. Key Responsibilities: Prior Experience Required: Why should a candidate want to take up this opportunity? Propose & execute strategies to expand our portfolio through In-licensing in Europe, Canada, and Australia. Identify partners and negotiate in-licensing, distribution, technology transfer,r or collaboration agreements. Enhance our business development efforts in the ROW/Emerging markets and maintain profitability of the business. Coordinate with a team of internal and external stakeholders to enrich our portfolio, explore new product technologies, and expand our footprint. Collaborate with internal teams such as R&D, Production, and Supply Chain to align business development efforts with product development and availability. Develop and maintain effective relationships with internal and external customers, regulators, and other stakeholders. 15-20 years of experience with at least 5 years leading the ROW markets sales portfolio for a similarly sized or larger company. Must have a good understanding of the way the key pharma industrys drivers influences the launch of products. Must have a strong grasp on regulated and advance market regulatory guidelines and market intel in markets in Europe, Canada and Australia. Must possess deep knowledge of the relevant players on the retail distribution and on the pharmaceutical client in-licensing side to deal with in these markets. Experience in negotiation & deal closure. Experience of working across multiple time zones and in global business cultures.

Role & responsibilities 1. Identify and pursue new business opportunities in the LATAM market by developing strategies for B2B Out-Licensing, CMO, and CDMO services. 2. Establish long-term relationships with potential clients, partners, and distributors in the region to drive business growth. 3. Lead negotiations and close deals related to contract manufacturing, development services, and out-licensing agreements. 4. Work closely with senior management to develop and execute tailored business strategies for the LATAM market. 5. Represent Anthea at key industry trade shows, exhibitions, and conferences in LATAM, promoting the companys services and fostering new business relationships. 6. Conduct comprehensive market research to understand industry trends, competitors, and customer needs within the LATAM region. 7. Regular travel to LATAM for client meetings, business development activities, and networking opportunities. 8. Collaborate with Anthea's internal teams, including R&D and Operations, to align business development efforts with the companys broader goals. As the Business Development Lead for the LATAM market, Manager primary responsibility will be to identify and engage with potential partners, clients, and stakeholders, to promote Antheas products and services. Lead will be expected to develop strategies to penetrate the market, build a strong network, and maximize business opportunities within the region. Preferred candidate profile 10+ years of experience in business development within the finished dosage sector, preferably in injectables, with a focus on B2B out-licensing, CMO, or CDMO services. Proven understanding of the LATAM pharmaceutical market and its key players, trends, and regulatory environment. Strong negotiation, communication, and interpersonal skills. Perks and benefits

Job Description Tata Consumer Products Ltd. About the Job: Manager PM Procurement, Beverages Function: Product Supply Organization Location: Bengaluru Reporting To: , Beverages At Tata Consumer Products Ltd, we stand #Forbetter Planet, Sourcing, Nutrition, Communities. And #ForBetter Opportunities . Here s an exciting one! How does this Job align to our Strategy At the core of Tata Consumer Products business approach lie six strategic pillars that serve as the foundation for its growth and success: Strengthening Accelerating our Core Business, Driving Digital and Innovation, Unlocking Synergies, Creating a Future Ready Organization, Exploring New Opportunities and Embedding Sustainability. This job opportunity closely aligns with one of these key strategic pillars, which is driving Strengthening Accelerating our Core Business . The role involves development, implementation and ongoing management of procurement processes and strategies for flexibles packaging materials for Beverages category. MD CEO Where do you come in as VP Procurement Packaging, Materials Services Executive Director COO Associate Director Packaging Material, Beverages Associate Manager Packaging Material, Beverages This job is at N 4 level (N corresponds to CEO s level) Top dimensions: Geography : India Direct reports: Complexity of the role (Optional): Matrix Reports: NA Type of Role: NA Primary Stakeholders (Optional): External Stakeholders Vendors, artwork agencies etc. Internal Stakeholders PSO Production SOP, Marketing, Finance Quality What are the Key Deliverables in this role Financial Outcomes Timely delivery of Packing material requirements at optimal costs at optimal inventory levels would be the primary responsibility of the role. Implement strategies, initiatives procurement plans. Management of cost models, budgets LE. Customer Service Improved service levels, OTIF, quality levels, improved vendor performance partnership scores. Meet Quality Marketing expectations on product shelf throw and quality parameters optimize inventory holding days. Internal Processes Supporting the development of processes and policies to ensure full compliance to internal standards. LE MIS reporting Inventory, SLOB, SOB, Weekly Monthly PM availability, Rejections, Disputes etc.. Delivering procurement best practices. To support implementation of strategies on digitization to mitigate risks on redundancies. Innovation and Learning Challenging the status quo and finding innovative solutions to business challenges. Demonstrating creativity and initiative in the identification and delivery of cost savings and added value. What are the Critical success factors for the Role Graduate with 6 8 years work experience in packaging material procurement in FMCG industry. Knowledge prior experience in category strategy formulation, Spend Analysis Procurement Strategy and Review, Contract Manufacturing meeting Statutory Compliances Knowledge in SAP MS Excel What are the Desirable success factors for the Role Good team working, multi tasking and prioritization skills, with the ability to perform under pressure. Knowledge on commercial negotiations, Subject matter packaging material and relevant markets. Ability to manage multiple stakeholders and manage complex and ambiguous scenarios. TCPL Growth Mindset and Behaviors We are obsessed about keeping Consumers Customers first in our hearts that s why we are here ! We are trailblazers in executing with Excellence Together as One Team ! We take Ownership of our business delivering value for our Stakeholders .. no Compromises ! We are Open to Continuously improving Continuously innovating For Better ! We live breathe our Tata Code of Conduct

" Jubilant Pharma Limited is a global integrated pharmaceutical company offering a wide range of products and services to its customers across geographies. We organise our business into two segments, namely, Specialty Pharmaceuticals, comprising Radiopharmaceuticals (including Radio pharmacies), Contract Manufacturing of Sterile Injectable, Non-sterile Allergy Therapy Products, and Generics APIs, comprising Solid Dosage Formulations Active Pharmaceutical Ingredients. Jubilant Generics (JGL) is a wholly - owned subsidiary of Jubilant Pharma. JGL in India has Research Development units at Noida and Mysore. It has two manufacturing facilities one at Mysore, Karnataka and another at Roorkee, Uttarakhand, engaged in APIs and Dosage manufacturing, respectively. The manufacturing location at Mysore is spread over 69 acres and it s a USFDA approved site engaged in manufacturing of APIs, and caters to the sales worldwide. API portfolio focusses on Lifestyle driven Therapeutic Areas (CVS, CNS) and targets complex and newly approved molecules. The company is the market leader in four APIs and is amongst the top three players for another three APIs in its portfolio helping it maintain a high contribution margin. The manufacturing location at Roorkee, Uttarakhand is state of the art facility and is audited and approved by USFDA, Japan PMDA, UK MHRA, TGA, WHO and Brazil ANVISA. This business focusses on B2B model for EU, Canada and emerging markets. Both manufacturing units are backward- integrated and are supported by around 500 research and development professionals based at Noida and Mysore. RD works on Development of new products in API, Solid Dosage Formulations of Oral Solid, Sterile Injectable, Semi-Solids Ointments, Creams and Liquids. All BA/BE studies are done In house at our 80 Bed facility which is inspected and having approvals /certifications from The Drugs Controller General (India) and has global regulatory accreditations including USFDA, EMEA, ANVISA (Brazil), INFRAMED (Portugal Authority), NPRA(Malaysia), AGES MEA (Austria) for GCP and NABL, CAP accreditations for Path lab services. JGL s full-fledged Regulatory Affairs IPR professionals ensures unique portfolio of patents and product filings in regulatory and non-regulatory market. Revenue of Jubilant Pharma is constantly increasing and during the Financial Year 2018 -19 it was INR 53,240 Million as compared to INR 39,950 Million during the Financial Year 2017-18. Kindly refer www.jubilantpharma.com for more information about organization. ",

Job Location : Bavla About Us: HCP Wellness Private Limited is a leading private label skin care, cosmetics, and oral care manufacturing company in India . We are committed to innovation, quality, and excellence in beauty and personal care product manufacturing. Our values focus on precision, teamwork, and continuous improvement, making us a trusted partner for global brands. Job Overview: We are looking for a skilled Machine Operator to join our manufacturing team in Ahmedabad, Bavla. The ideal candidate will operate and maintain production machinery to ensure efficient and high-quality manufacturing of skin care, cosmetics, and oral care products. Key Responsibilities: Operate, monitor, and maintain production machines for skin care, cosmetic, and oral care product manufacturing. Ensure machine efficiency, safety, and smooth operations while maintaining production targets. Perform routine checks, troubleshooting, and minor repairs to minimize downtime. Monitor product quality and adherence to manufacturing standards. Follow Good Manufacturing Practices (GMP) and Standard Operating Procedures (SOPs). Work closely with the quality control and production team to maintain product consistency. Maintain accurate production logs and reports. Required Qualifications Skills: Hard Skills: Knowledge of cosmetic, skincare, and oral care manufacturing machinery. Experience with mixing, filling, and packaging machines. Understanding of GMP, safety protocols, and quality control processes. Ability to read and interpret machine manuals and technical documents. Soft Skills: Strong attention to detail and problem-solving skills. Ability to work in a fast-paced environment with minimal supervision. Good communication and teamwork skills. Commitment to quality and continuous improvement. Education Certifications: ITI/Diploma in Mechanical, Electrical, or a related field is preferred. Certification in Machine Operations or Manufacturing Processes is a plus. Preferred Experience: 1-3 years of experience in machine operation within the cosmetics, skin care, or oral care industry. Prior experience in a private label or contract manufacturing setup is advantageous. Why Join HCP Wellness Private Limited Work with a leading private label manufacturer in the personal care industry. Opportunity for career growth and skill development. Competitive salary and a positive, team-oriented work environment. Company-provided transport with pick-up and drop-off services. Experienced professionals from companies like Nivea, Colgate, and PG can apply. Location Advantage: Our Bavla plant is easily accessible from Changodar, Moraiya, Sarkhej, Bhayla, Sanand GIDC, and Ahmedabad, making it a great opportunity for candidates from nearby industrial areas.

Profile: The role involves managing business development co-ordination for new and existing products/clients. Additionally, the role requires effective customer relationship management, re-engaging lost clients, and expanding the client base through referrals Negotiate pricing and customizations to maintain business Coordinate with stakeholders to ensure timely product delivery Track competitors and market trends to inform strategy Plan sales forecasting, budgeting, and marketing activities Good at maintaining the sales MIS Candidate Profile: B.Pharma with minimum 2 years experience as a sales/business coordinator Preferred background in contract manufacturing for Allopathic and Nutraceuticals Strong verbal and written communication skills Someone who can join in 15-20 days Office Working: Monday to Friday [5 days]

" Jubilant Life Sciences Limited is one of the Indias leading corporate and a highly treasured brand throughout the world. The organization has a presence in the fields of Pharma and Life Sciences, Agri & Performance Polymers, Food & Retail, Oil & Gas and Services. Jubilant Life Sciences Limited is an integrated global pharmaceutical and life sciences Company engaged in Pharmaceuticals, Life Science Ingredients and Other businesses including Drug Discovery Solutions and India Branded Pharmaceuticals. The Pharmaceuticals segment, through its wholly owned subsidiary Jubilant Pharma Limited, is engaged in manufacturing and supply of APIs, Solid Dosage Formulations, Radiopharmaceuticals, Allergy Therapy Products and Contract Manufacturing of Sterile Injectable and Non-sterile products through 6 USFDA approved manufacturing facilities in the US, Canada and India and a network of over 50 radio-pharmacies in the US. The Life Science Ingredients segment, is engaged in Specialty Intermediates, Nutritional Products and Life Science Chemicals through 5 manufacturing facilities in India. The Drug Discovery Solutions business, provides proprietary in-house innovation & collaborative research and partnership for out-licensing through 2 world class research centers in India. Jubilant Life Sciences Limited has a team of around 7,700 multicultural people across the globe and is committed to deliver value to its customers across over 100 countries. The Company is well recognized as a Partner of Choice by leading pharmaceuticals and life sciences companies globally. Ranked No. 6 amongst top 10 Global Pharmaceutical outsourcing players as per UNCTAD World Investment Report 2011 Reputed and High Quality relationships with 19 out of the top 20 Pharmaceutical companies, and 6 out of the top 10 Agrochemical companies globally Vision To acquire and maintain global leadership position in chosen areas of businesses To continuously create new opportunities for growth in our strategic businesses To be among the top 10 most admired companies to work for To continuously achieve a return on invested capital of at least 10 points higher than the cost of capital. Our Promise We will, with utmost care for the environment and society, continue to enhance value for our customer by providing innovative products and economically efficient solutions; and for our stakeholders through growth, cost effectiveness and wise investment of resources. Kindly refer www.jubl.com for more information about organization. Position Production Chemist Business Unit / Function 3 Cyano Pyridine Location Bharuch Reports to Shift In Charge Summary of Job To ensure the shift plant operation as per SOP s and work instructions. Key Responsibilities (Performance Indicators) To maintain the logbook and shift report. To operate the plant as per SOPs. To note down all the plant readings regularly and record in log sheet. Loading & unloading of the materials from drums, tanks & receivers as per the SOP. Maintaining alertness & keeping Shift in-charge posted about any abnormality in the plant. To make use of all the personnel protective equipment and maintain proper housekeeping in plant. Planned transfer/unloading of raw materials and dispatch of the finish goods. To analyze all process samples as per the quality plan to control process parameters. To collect the all process samples as per instruction of Shift In-charge along with all necessary safety precautions. To transfer the raw materials as per requirements. In addition to the above jobs, the management may assign any other responsibility as and when required. Awareness about responsible care (Environment, Health, Safety and Security ) No. of Reportees Nil Qualification & Experience Diploma Chemical Engineer or B.Sc. in Chemistry 3 5 years of experience in Continuous chemical process / batch process plant. Key Competencies (Technical, Functional & Behavioral) Operating knowledge of Continuous chemical process / batch process. Working knowledge of Reactors, filters, centrifuges in the batch process. Adherence to quality / Safety norms. Knowledge of DCS / PLC based plant operation. Knowledge of distillation operation. Material handling (Toxic / hazardous). ",

" Jubilant Life Sciences Limited is one of the Indias leading corporate and a highly treasured brand throughout the world. The organization has a presence in the fields of Pharma and Life Sciences, Agri & Performance Polymers, Food & Retail, Oil & Gas and Services. Jubilant Life Sciences Limited is an integrated global pharmaceutical and life sciences Company engaged in Pharmaceuticals, Life Science Ingredients and Other businesses including Drug Discovery Solutions and India Branded Pharmaceuticals. The Pharmaceuticals segment, through its wholly owned subsidiary Jubilant Pharma Limited, is engaged in manufacturing and supply of APIs, Solid Dosage Formulations, Radiopharmaceuticals, Allergy Therapy Products and Contract Manufacturing of Sterile Injectable and Non-sterile products through 6 USFDA approved manufacturing facilities in the US, Canada and India and a network of over 50 radio-pharmacies in the US. The Life Science Ingredients segment, is engaged in Specialty Intermediates, Nutritional Products and Life Science Chemicals through 5 manufacturing facilities in India. The Drug Discovery Solutions business, provides proprietary in-house innovation & collaborative research and partnership for out-licensing through 2 world class research centers in India. Jubilant Life Sciences Limited has a team of around 7,700 multicultural people across the globe and is committed to deliver value to its customers across over 100 countries. The Company is well recognized as a Partner of Choice by leading pharmaceuticals and life sciences companies globally. Ranked No. 6 amongst top 10 Global Pharmaceutical outsourcing players as per UNCTAD World Investment Report 2011 Reputed and High Quality relationships with 19 out of the top 20 Pharmaceutical companies, and 6 out of the top 10 Agrochemical companies globally Vision To acquire and maintain global leadership position in chosen areas of businesses To continuously create new opportunities for growth in our strategic businesses To be among the top 10 most admired companies to work for To continuously achieve a return on invested capital of at least 10 points higher than the cost of capital. Our Promise We will, with utmost care for the environment and society, continue to enhance value for our customer by providing innovative products and economically efficient solutions; and for our stakeholders through growth, cost effectiveness and wise investment of resources. Kindly refer www.jubl.com for more information about organization. Position Production Chemist (Continuous / Batch) Grade - A2 Business Unit / Function Department Niacinamide Location Bharuch Reports to Shift In-charge Summary of Job (Purpose/ objective of the job Department organogram to be enclosed) To ensure the shift plant operation as per SOP s and work instructions. Key Responsibilities (Performance Indicators) Operating the plant as per the instruction of the SIC. Operation and cleaning of equipment s used in the process area. On line monitoring of the environment conditions in process area. To note down all the plant reading regularly. To maintain online BPRs and GMP documents regularly. Taking raw material transfer. Loading / unloading of the material from drums, tanks and receives as per the instructions. Collecting all the process samples as per instructions of shift in-charge along with all necessary safety precautions. Safety of man and machine and housekeeping of the plant. Ensuring strict adherence to the permit system. Report the deviation from the standard practices. Perform packing, labeling activities as per SO Tomaintain TPMand WCM in the plant. To maintain 5S in plant Awareness about responsible care (Environment, Health, Safety and Security) No. of Reportees NA Qualification & Experience Diploma Chemical Engineer or B.Sc. or M. Sc with 3 5 years of experience in Continuous chemical process / batch process plant. Key Competencies ( Technical, Functional & Behavioral) Operating knowledge of Continuous chemical process / batch process. Working knowledge of Reactors, filters, centrifuges in the batch process. Adherence to quality / Safety norms. Knowledge of DCS / PLC based plant operation. Knowledge of distillation operation. Material handling (Toxic / hazardous). Knowledge of MSDS. ",

" Jubilant Pharma Limited is a global integrated pharmaceutical company offering a wide range of products and services to its customers across geographies. We organise our business into two segments, namely, Specialty Pharmaceuticals, comprising Radiopharmaceuticals (including Radio pharmacies), Contract Manufacturing of Sterile Injectable, Non-sterile & Allergy Therapy Products, and Generics & APIs, comprising Solid Dosage Formulations & Active Pharmaceutical Ingredients. Jubilant Generics (JGL) is a wholly - owned subsidiary of Jubilant Pharma. JGL in India has Research & Development units at Noida and Mysore. It has two manufacturing facilities one at Mysore, Karnataka and another at Roorkee, Uttarakhand, engaged in APIs and Dosage manufacturing, respectively. The manufacturing location at Mysore is spread over 69 acres and it s a USFDA approved site engaged in manufacturing of APIs, and caters to the sales worldwide. API portfolio focusses on Lifestyle driven Therapeutic Areas (CVS, CNS) and targets complex and newly approved molecules. The company is the market leader in four APIs and is amongst the top three players for another three APIs in its portfolio helping it maintain a high contribution margin. The manufacturing location at Roorkee, Uttarakhand is state of the art facility and is audited and approved by USFDA, Japan PMDA, UK MHRA, TGA, WHO and Brazil ANVISA. This business focusses on B2B model for EU, Canada and emerging markets. Both manufacturing units are backward- integrated and are supported by around 500 research and development professionals based at Noida and Mysore. R&D works on Development of new products in API, Solid Dosage Formulations of Oral Solid, Sterile Injectable, Semi-Solids Ointments, Creams and Liquids. All BA/BE studies are done In house at our 80 Bed facility which is inspected and having approvals /certifications from The Drugs Controller General (India) and has global regulatory accreditations including USFDA, EMEA, ANVISA (Brazil), INFRAMED (Portugal Authority), NPRA(Malaysia), AGES MEA (Austria) for GCP and NABL, CAP accreditations for Path lab services. JGL s full-fledged Regulatory Affairs & IPR professionals ensures unique portfolio of patents and product filings in regulatory and non-regulatory market. Revenue of Jubilant Pharma is constantly increasing and during the Financial Year 2018 -19 it was INR 53,240 Million as compared to INR 39,950 Million during the Financial Year 2017-18. Kindly refer www.jubilantpharma.com for more information about organization. ",

Vision To acquire and maintain global leadership position in chosen areas of businesses To continuously create new opportunities for growth in our strategic businesses To be among the top 10 most admired companies to work for To continuously achieve a return on invested capital of at least 10 points higher than the cost of capital. Key Responsibilities (Performance Indicators) Knowledge about IMS system (ISO 9001:2015, ISO 14001:2015 OHSAS 18001:2007, and cGMP, USFDA, FSSC 22000, NABL . Analytical skill for QC instrument, i.e. GLC, HPLC, UV-Visible, FTIR, ICP, K/F, Melting point etc. Regularize the QC activities as per cGMP requirements. RM, PKG, In-process and FG sampling & Analysis. Co-ordination with QC staff, R&D, Commercial and production for quality & dispatch related activities for on time dispatches. Day to day monitoring and execution online all IPQC and FG analysis activities. Resolve the trouble shooting related to QC activities. Knowledge about 21 CFR Part 211, 111 with data integrity (Part-11) Awareness about responsible care (Environment, Health, Safety and Security) Qualification & Experience M.Sc. (Chemistry) with 2 - 6 yrs. Key Competencies (Technical, Functional & Behavioral) Handling, Calibration and Hand-on experience of all QC instruments. Compliance of 21 CFR Part-11. Troubleshooting related to QC analytical instrument ",

" Jubilant Life Sciences Limited is one of the Indias leading corporate and a highly treasured brand throughout the world. The organization has a presence in the fields of Pharma and Life Sciences, Agri & Performance Polymers, Food & Retail, Oil & Gas and Services. Jubilant Life Sciences Limited is an integrated global pharmaceutical and life sciences Company engaged in Pharmaceuticals, Life Science Ingredients and Other businesses including Drug Discovery Solutions and India Branded Pharmaceuticals. The Pharmaceuticals segment, through its wholly owned subsidiary Jubilant Pharma Limited, is engaged in manufacturing and supply of APIs, Solid Dosage Formulations, Radiopharmaceuticals, Allergy Therapy Products and Contract Manufacturing of Sterile Injectable and Non-sterile products through 6 USFDA approved manufacturing facilities in the US, Canada and India and a network of over 50 radio-pharmacies in the US. The Life Science Ingredients segment, is engaged in Specialty Intermediates, Nutritional Products and Life Science Chemicals through 5 manufacturing facilities in India. The Drug Discovery Solutions business, provides proprietary in-house innovation & collaborative research and partnership for out-licensing through 2 world class research centers in India. Jubilant Life Sciences Limited has a team of around 7,700 multicultural people across the globe and is committed to deliver value to its customers across over 100 countries. The Company is well recognized as a Partner of Choice by leading pharmaceuticals and life sciences companies globally. Ranked No. 6 amongst top 10 Global Pharmaceutical outsourcing players as per UNCTAD World Investment Report 2011 Reputed and High Quality relationships with 19 out of the top 20 Pharmaceutical companies, and 6 out of the top 10 Agrochemical companies globally Vision To acquire and maintain global leadership position in chosen areas of businesses To continuously create new opportunities for growth in our strategic businesses To be among the top 10 most admired companies to work for To continuously achieve a return on invested capital of at least 10 points higher than the cost of capital. Our Promise We will, with utmost care for the environment and society, continue to enhance value for our customer by providing innovative products and economically efficient solutions; and for our stakeholders through growth, cost effectiveness and wise investment of resources. Kindly refer www.jubl.com for more information about organization. Designation / Position: - Boiler and CPP Shift In-charge Band / Grade / Level: - A4 Location : - Bharuch Job Summary (Optional): - Operation & maintain of AFBC Boiler, Coal & Ash handling plant & Turbine. To ensure uninterrupted Power and steam generation and other utilities and to optimize it s cost. To achieve Zero -break down, Zero - defect, Zero - accident, Zero - wastage and Zero abnormality. Reporting Manager: - Sr Manager/Section Manager Direct Reports (Optional): - None Team Size (Optional): - Matrix Relationship (Optional): - Key Responsibilities Efficient and effective operation and maintenance of utilities: Coal fired process Boiler and BOP, WTP, DM Plant, Air Compressors, Incinerator and to maintain all norms wrt to quality, cost and delivery. Reduction in steam generation cost by continuous improvement in O&M. Maintain optimal stock of coal stock & other chemicals. Daily Utility report. To implement of 5S in plant and office. Awareness about responsible care (Environment, Health, Safety and Security ) Qualifications & Experience: - Diploma/B.E. Mechanical 3 to 5 years of experience operations and maintenance of Coal Fired Boiler & Utilities Key Competencies (Technical, Functional & Behavioural) Boiler Proficiency engineer Operation & maintenance of Coal Fired Boiler & Utilities. Well versed with IBR regulations and applicable standards, Protection & Safety Interlocks for Boiler. ",

Preparation and review the system based SOP`s. Preparation, Evaluation and closer of change controls, CAPA, Market complaint & deviations Running the plan as per written SOP/WI. Batch entry in ERP (SAP / BAAN) Preparation of the daily production report and commercial report. Compliance with company quality policy in all aspects. Review raw material, intermediate, finished product specifications. Generate, review, and approve GMP documentation such as Standard Operating Procedures, non-conformance reports, Out of specification results. Participate in daily activities, ensuring cleaning, environmental monitoring and maintenance schedules are up to date and maintained to GMP standards. Area and equipment logbooks completed. Implements the manufacturing plan and establishes procedures for maintaining high standards of manufacturing operations to ensure that all products confirm to established customer and company quality standards. Sound Knowledge in Equipment qualification & Process Validation Safety of man and machine and housekeeping of the plant. Avoiding any abnormality in the plant by frequent checks. Ensure the required quality and safety standards are achieved and maintained with respect to cGMP operating procedures, all cGMP batch manufacturing documentation, area housekeeping in cGMP suites, SHE (Safety, Health & Environment), and compliance with the relevant regulatory (ICH Guidelines/MHRA). Training and development of team members. To implement ISO 9001, ISO-14001, SMS -45001, TPM. To implement 5S+1S in plant and office. Qualification & Experience B. Tech (Chemical Engineering) with 3-5 years or B.Sc. (Organic) with 6-7 of experience in Fine Chemical/ Bulk drug / API Plant. Key Competencies ( Technical, Functional & Behavioral) Knowledge of Fine Chemical/ batch chemical process. Practical experience in handling reactors, centrifuges, filters used in API / Bulk drug / Batch chemical plants. Exposure in ERP or like software. Computer proficiency Technical knowledge.

Vision To acquire and maintain global leadership position in chosen areas of businesses Key Responsibilities (Performance Indicators) Controlling all operating parameters for smooth running of the plant in the shifts. Maintaining logbook and shift report. Running the plant as per written SOP / WI. Preparation of the daily production report and commercial report. Compliance with company EHS policy in all aspects of production during the shift operations. Safety of man and machine and housekeeping of the plant. Avoiding any abnormality in the plant by frequent checks. Ensuring strict adherence to permit system. To implement ISO 9000, ISO-14000, OHSAS -18000, TPM and WCM in the plant. Job allocation to technician and monitoring the work done. Training and development of team members. To implement 5S in plant Qualification & Experience B.E / B. Tech Chemical Engineer with 3-5 of experience in continuous chemical process. Key Competencies ( Technical, Functional & Behavioral) Knowledge of Continuous chemical process. Working Knowledge of operation of pumps, compressors, blowers, safety valves and control valves. Exposure in preparing SOP s and WI s of the concerned area. Strong skills in adherence to quality / safety norms. Understanding and experience of manpower handling. Exposure to WCM activities and TPM / TQM concepts. Experience in DCS / PLC based control systems in plants. Approval HoD / CoD Unit HR

" Jubilant Life Sciences Limited is one of the Indias leading corporate and a highly treasured brand throughout the world. The organization has a presence in the fields of Pharma and Life Sciences, Agri & Performance Polymers, Food & Retail, Oil & Gas and Services. Jubilant Life Sciences Limited is an integrated global pharmaceutical and life sciences Company engaged in Pharmaceuticals, Life Science Ingredients and Other businesses including Drug Discovery Solutions and India Branded Pharmaceuticals. The Pharmaceuticals segment, through its wholly owned subsidiary Jubilant Pharma Limited, is engaged in manufacturing and supply of APIs, Solid Dosage Formulations, Radiopharmaceuticals, Allergy Therapy Products and Contract Manufacturing of Sterile Injectable and Non-sterile products through 6 USFDA approved manufacturing facilities in the US, Canada and India and a network of over 50 radio-pharmacies in the US. The Life Science Ingredients segment, is engaged in Specialty Intermediates, Nutritional Products and Life Science Chemicals through 5 manufacturing facilities in India. The Drug Discovery Solutions business, provides proprietary in-house innovation & collaborative research and partnership for out-licensing through 2 world class research centers in India. Jubilant Life Sciences Limited has a team of around 7,700 multicultural people across the globe and is committed to deliver value to its customers across over 100 countries. The Company is well recognized as a Partner of Choice by leading pharmaceuticals and life sciences companies globally. Ranked No. 6 amongst top 10 Global Pharmaceutical outsourcing players as per UNCTAD World Investment Report 2011 Reputed and High Quality relationships with 19 out of the top 20 Pharmaceutical companies, and 6 out of the top 10 Agrochemical companies globally Vision To acquire and maintain global leadership position in chosen areas of businesses To continuously create new opportunities for growth in our strategic businesses To be among the top 10 most admired companies to work for To continuously achieve a return on invested capital of at least 10 points higher than the cost of capital. Our Promise We will, with utmost care for the environment and society, continue to enhance value for our customer by providing innovative products and economically efficient solutions; and for our stakeholders through growth, cost effectiveness and wise investment of resources. Kindly refer www.jubl.com for more information about organization. Position Manager- Electrical Grade L3 Business Unit / Function Department Engineering Location Bharuch Reports to Head of Department Summary of Job (Purpose/ objective of the job Department organogram to be enclosed) To ensure smooth functioning of electrical installations through effective & efficient maintenance management of Power Generation, transmission, distribution System. Key Responsibilities (Performance Indicators) Monitor and Prepare power consumption report Prepare Preventative maintenance schedule of Electrical Report Monitoring of PCC / MCC Panel for any abnormality Monitoring of preventative maintenance execution as per schedule Coordinate with service provider / vendor for timely servicing / maintenance of equipment Preparation of IMS and EnMS related documents Participation in safety improvement schemes Motivate team members for good work Providing Training on Technical / Safety Topics to the team members Inventory management of spares and critical items. Monitoring of maintenance budget and prepare variance report Preparation of department MIS Reports Calibration of Electrical Equipment Coordinate with Govt. Agencies Suggest and Implementation of energy saving schemes Preparation of breakdown report Execution of unsafe condition observed by other team members Maintain Housekeeping in respective area. No. of Reportees 10-12 Qualification & Experience B.E / B.Tech Electrical with 10-15 years of experience in the electrical maintenance of large industrial complex. Key Competencies ( Technical, Functional & Behavioral) Technical: Knowledge & experience in projects and maintenance of HT & LT Electrical Systems like Alternators, Transformers, Motors, and Protection relays etc. Well versed with Legal & Statutory requirement for HT/LT Elect. System with desired Protection & Safety Standards applicable for Chemical & Power Plants. Have practiced modern Electrical maintenance techniques for better efficiency of the electrical installations. Good communication and Inter-personnel skills

Job Description: Outsourcing Manager (Aerospace & Defence Industry) Location: Pune Company: Senwell Exports Private Limited Company Overview: Senwell Exports Private Limited specializes in precision machining of aerospace and defence components as per customer specifications. The company primarily serves clients in the Aerospace & Defence sector, focusing on high-precision machining, special processes, and stringent quality standards. exporting majorly to international and domestic levels. Roles and responsibilities: Drive organization and departmental KPIs/objectives specific to aerospace and defense outsourcing. Identify and evaluate potential suppliers for precision machining and special processes such as heat treatment, anodizing, plating, coating, and NDT (Non-Destructive Testing). Strong knowledge of aerospace-grade manufacturing processes, material selection, and special processes required for aerospace components. Negotiate with suppliers for cost optimization and ensure on-time delivery with AS9100D Work in collaboration with cross-functional teams (CFT) to ensure on-time delivery (OTD) to customers. Hands-on experience in supplier resourcing, capacity planning analysis, and aerospace supply chain development programs. Implement cost-reduction projects while maintaining strict adherence to aerospace standards. Inventory management (system stock vs. physical stock) to optimize procurement strategies. Monitor and liquidate non-moving inventory efficiently. Work closely with suppliers to resolve quality complaints, driving CAPA (corrective and preventive actions) as per aerospace industry standards. Familiarity with QMS, AS9100, NADCAP, APQP, PPAP, DFMEA, PFMEA, and industry trends & innovations in Aerospace & Defence manufacturing. Strong skills in ERP and MS Office (Word, Excel, PowerPoint) for supplier and inventory tracking. Problem-solving and conflict resolution skills with the ability to make informed decisions in a fast-paced aerospace supply chain environment. Qualification & Experience: Engineering Graduate with 10-15 years of experience in Sourcing/Outsourcing for precision machining components.

Sales for contract manufacturing for new business development for Alpla India Region. Identify and target new business opportunities through market research, networking, and industry events. Add new clients to existing business Develop and implement strategic plans to achieve sales targets and expand the customer base. Build and maintain a robust sales pipeline to ensure a steady flow of potential clients. Establish and nurture relationships with key decision-makers and stakeholders in target organizations. Understand client needs and provide tailored solutions to meet their business objectives. Ensure high levels of client satisfaction through effective communication and problem-solving. Develop and execute sales strategies to drive revenue growth and market penetration. Conduct sales presentations, negotiations, and contract discussions with potential clients. Collaborate with internal teams, including marketing, product development, and customer support, to align efforts and achieve business goals. Stay informed about industry trends, competitive landscape, and market conditions. Willing to travel. What makes you great Bachelors / Masters degree in Business, Marketing, or a related field (MBA preferred). Proven experience in sales and business development, preferably in CM industries. Strong understanding of sales principles, techniques, and tools. Excellent communication, negotiation, and presentation skills. Ability to build and maintain long-term client relationships. Strong analytical and problem-solving abilities. Ability to work independently and as part of a team in a fast-paced environment What you can expect working with us We facilitate a smooth start through individual and accurate training as well as professional guidance and support. We offer you a challenging task with a high degree of personal responsibility in an international working environment. Dynamic working style in a fast-growing region and a dynamic team

The role involves managing business development for new and existing products by acquiring prospective clients and generating leads through referrals, social media, and networking at conferences and trade fairs. Additionally, the role requires effective customer relationship management, re-engaging lost clients, and expanding the client base through referrals. Job Type: Work from Office Location: Noida, Sector 65 Work Timings: 9:00 AM - 5:30 PM (Alternate Saturdays off) Key Responsibilities: Business Development: Develop client base via social media, referrals, cold calls, trade fairs, and conferences. Contact decision-makers, screen opportunities, and lead sales efforts following SOPs. Convert inquiries into active discussions by understanding client requirements. Negotiate pricing and customizations to maintain profit margins. Coordinate with stakeholders to ensure timely product delivery. Track competitors and market trends to inform strategy. Plan sales forecasting, budgeting, and marketing activities. Sustain and revive sales with new, existing, and inactive clients. Customer Relationship Management: Address customer queries on product specs, pricing, and delivery. Ensure compliance with regulatory standards (FSSAI, AYUSH). Record and analyze client feedback for continuous improvement. Maintain post-sales connections to identify and address gaps. Analysis & Reporting: Maintain a prospect database and provide weekly progress reports. Report monthly on market trends, competitor activities, and new opportunities. Candidate Profile: Familiar with market trends and lead generation in the domestic market. Preferred background in contract manufacturing. B.Pharma (MBA in Marketing preferred). Strong verbal and written communication skills. Proficient in MS Office and PowerPoint.

Ensures that the review of CMC documentation is completed in timely compliant manner as per Teva CORP standards and related Guidance s. Review of Method Development/Validation Protocols Reports, Stability Protocols Reports received from various Teva contracting sites, RD units, Method Development Stability Testing Centres. Review of Instrument/Equipment Qualification records. Review of BMR. Ensures that the Product Quality Reviews / Annual Product Reviews for Teva products are completed in a timely and compliant manner as per Teva s CORP Quality Management systems. PQR/APR compilation and approval must be well associated with the Teva Manufacturing Sites, Global Quality Units and Commercial affiliates to meet the targets and ensure compliance. Compilation of high quality Annual Product Reviews (APRs) / Product Quality Reviews (PQRs) for products manufactured at various manufacturing sites and retrieve data from the Quality and regulatory databases and system Liaising with third party contract manufacturers and QA/QC/Technical support personnel located globally for data collection and arranging responses. Recommend actions and professionally communicate to sites/ Quality units for continuous improvement in quality of products Receives guidance from Supervisor, Group Leader, Manager Global Quality Services, Associate Director Global Quality GBS, other Managers in Quality Strategy Shared Services, EMSO Quality affiliates, Commercial Quality EU IM, TGO sites How you ll spend your day Review of CMC Documentation - The owner of the function Review of Method Development / Validation protocols reports. Review of Stability Study protocol, reports grids. Review of Instrument / Equipment Qualification records. Review of Batch Manufacturing Records. Liaising with contracting Teva units and QA/QC personnels located globally for arranging required documents and query responses. Escalation of issues to Supervisor, Group Leader, Manager Global Quality GBS. Contemporaneous updation of SharePoint data base Data requesting and Compilation of PQR s The owner of the function Compilation of high quality Annual Product Reviews (APRs) / Product Quality Reviews (PQRs) for products manufactured at various manufacturing sites and retrieve data from the Quality and regulatory databases and systems Liaising with third party contract manufacturers and QA personnel located globally for data collection required for compilation of APRs/ PQRs. Follow up with the CMO s for the receipt of data within time. Check quotation received from CMO and initiate PR/PO for QP s approval. Once the data is received responsible for filling the PQR receipt checklist and scheduling the PQR in SharePoint. Escalation of PQR issues to Supervisor, Group Leader, Manager PQR Centre. Contemporaneous updation of SharePoint data base Quality Management Systems The owner of the function Initiate the process of change controls and deviations Preparation of local SOP s and its related documents. Participate in self-inspection process Performance Management Participate in continuous process improvement projects to improve efficiency of the unit Your experience and qualifications 2 to 8 years of experience in QA / QC function in the pharmaceutical industry Master s Degree in Pharmacy or other natural sciences or Bachelor Degree in Pharmacy or other natural sciences Basic knowledge on worldwide cGxP regulations Good English language skills, other language skills could be helpful Good communication skills Basic knowledge of Computerised Systems. Knowledge of Systems in TEVA s IT landscape (TrackWise, SAP, LIMS, Global Insights, Glorya etc.) would be of advantage Basic understanding of manufacturing, QC and Contract manufacturing processes Engagement to drive improvements and ability to manage complexity Hands-on experience on Analytical Method development, Method Validation for API and FP of different analytical methods (e.g. Assay, impurities, dissolution etc.) Stability Studies. Hands-on experience on Review of Instrument/Equipment qualification records. Basic knowledge / hands on experience of review of BMR. Basic knowledge / hands on experience on Product Quality Reviews

Review of Method Development / Validation protocols reports. Review of Stability Study protocol, reports grids. Review of Instrument / Equipment Qualification records. Review of Batch Manufacturing Records. Liaising with contracting Teva units and QA/QC personnels located globally for arranging required documents and query responses. Escalation of issues to Supervisor, Group Leader, Manager Global Quality GBS. Contemporaneous updation of SharePoint data base Data requesting and Compilation of PQR s The owner of the function Compilation of high quality Annual Product Reviews (APRs) / Product Quality Reviews (PQRs) for products manufactured at various manufacturing sites and retrieve data from the Quality and regulatory databases and systems Liaising with third party contract manufacturers and QA personnel located globally for data collection required for compilation of APRs/ PQRs. Follow up with the CMO s for the receipt of data within time. Check quotation received from CMO and initiate PR/PO for QP s approval. Once the data is received responsible for filling the PQR receipt checklist and scheduling the PQR in SharePoint. Escalation of PQR issues to Supervisor, Group Leader, Manager PQR Centre. Contemporaneous updation of SharePoint data base Quality Management Systems The owner of the function Initiate the process of change controls and deviations Preparation of local SOP s and its related documents. Participate in self-inspection process Performance Management Participate in continuous process improvement projects to improve efficiency of the unit Your experience and qualifications 2 to 8 years of experience in QA / QC function in the pharmaceutical industry Master s Degree in Pharmacy or other natural sciences or Bachelor Degree in Pharmacy or other natural sciences Basic knowledge on worldwide cGxP regulations Good English language skills, other language skills could be helpful Good communication skills Basic knowledge of Computerised Systems. Knowledge of Systems in TEVA s IT landscape (TrackWise, SAP, LIMS, Global Insights, Glorya etc.) would be of advantage Basic understanding of manufacturing, QC and Contract manufacturing processes Engagement to drive improvements and ability to manage complexity Hands-on experience on Analytical Method development, Method Validation for API and FP of different analytical methods (e.g. Assay, impurities, dissolution etc.) Stability Studies. Hands-on experience on Review of Instrument/Equipment qualification records. Basic knowledge / hands on experience of review of BMR. Basic knowledge / hands on experience on Product Quality Reviews.

The Asst Manager- QA/AC plays a critical role in maintaining the quality of new pharmaceutical products within the organization. This position requires a detail-oriented individual with a strong understanding of GMP practices, Quality, and legal compliances, and pharma regulations. The Asst Manager- QA/QC will collaborate with cross-functional teams and internal and external stakeholders, coordinate project activities, and ensure adherence to timelines and quality standards, and compliances for new product development in the organization. Responsibilities: Evaluate the various manufacturing facilities by conducting the facility GMP audits/inspections as per regulatory guidelines and approve the facility post proper due diligence and publish an audit report for compliance if required. Evaluate the tech pack (Quality documents/dossier) of the shortlisted finished formulations across various dosage forms manufactured by the manufacturer to ensure the pre-requisite quality requirements to approve the product. Ensure the compliance of pharmaceutical jurisprudence i.e. acts and rules for the new products like Drugs and Cosmetics Acts and rules, DPCO Act, NDPS Act and Drugs and Magic Remedies (Objectionable Advertisement) Act, etc. Handle contract manufacturing Facilities by carrying out their periodic Facility and Product Audits and timely revert to the Manufacturing Vendors on Audit findings and closures. Identify Non-Conformances and work towards closure with RCA and CAPA . Review the quality documents received from the contract manufacturer relating to manufacturing new batches and ensure necessary regulatory and quality Compliance. Ensure Internal Quality reports reviews on a monthly basis and share the findings with the respective stakeholders and perform CAPA if required. Coordination with Contract/Public Testing Labs to ensure the products are being tested at regular intervals in order to ensure the product quality. Log and investigate market complaints with customers and manufacturing sites, for RCA and closure with appropriate CAPA. Manage / Implement corporate quality management system through SOPs, and documentation throughout contract manufacturing sites. Desired Skills and Expertise: An expert in the understanding of manufacturing stages and critical processing stages of Oral Solid Dosage Form, Oral Liquid Dosage Form & Injectables / Parenteral, and various other dosage forms . Good knowledge and assessment capabilities of manufacturing sites with respect to GMP and GLP . Experience in Auditing WHO or EU - GMP Facilities. Good understanding of Pharmacopoeia, WHO - GMP, Schedule M & ICH Guidelines Good understanding of the Drug and Cosmetic Act from regulatory and artwork Management standpoint. Good knowledge of investigation tools for RCA and CAPA. Understanding of vendor management (Product and Facility Audit) Good written and verbal communication skills Self-driven and motivated Willing to work in a fast pace, challenging environment in a Start-up Hands-on experience with Excel. Qualifications Required: Degree in pharmaceutical sciences or pharmacy. Minimum 5 years of experience in Corporate Quality Functions including experience in site auditing and compliance. Minimum 1 year of experience on the manufacturing floor.

Ensures that the review of CMC documentation is completed in timely compliant manner as per Teva CORP standards and related Guidance s. Review of Method Development/Validation Protocols Reports, Stability Protocols Reports received from various Teva contracting sites, RD units, Method Development Stability Testing Centres. Review of Instrument/Equipment Qualification records. Review of BMR. Ensures that the Product Quality Reviews / Annual Product Reviews for Teva products are completed in a timely and compliant manner as per Teva s CORP Quality Management systems. PQR/APR compilation and approval must be well associated with the Teva Manufacturing Sites, Global Quality Units and Commercial affiliates to meet the targets and ensure compliance. Compilation of high quality Annual Product Reviews (APRs) / Product Quality Reviews (PQRs) for products manufactured at various manufacturing sites and retrieve data from the Quality and regulatory databases and system Liaising with third party contract manufacturers and QA/QC/Technical support personnel located globally for data collection and arranging responses. Recommend actions and professionally communicate to sites/ Quality units for continuous improvement in quality of products Receives guidance from Supervisor, Group Leader, Manager Global Quality Services, Associate Director Global Quality GBS, other Managers in Quality Strategy Shared Services, EMSO Quality affiliates, Commercial Quality EU IM, TGO sites How you ll spend your day Review of CMC Documentation Review of Method Development / Validation protocols reports. Review of Stability Study protocol, reports grids. Review of Instrument / Equipment Qualification records. Review of Batch Manufacturing Records. Liaising with contracting Teva units and QA/QC personnels located globally for arranging required documents and query responses. Escalation of issues to Supervisor, Group Leader, Manager Global Quality GBS. Contemporaneous updation of SharePoint data base Data requesting and Compilation of PQR s Compilation of high-quality Annual Product Reviews (APRs) / Product Quality Reviews (PQRs) for products manufactured at various manufacturing sites and retrieve data from the Quality and regulatory databases and systems Liaising with third party contract manufacturers and QA personnel located globally for data collection required for compilation of APRs/ PQRs. Follow up with the CMO s for the receipt of data within time. Check quotation received from CMO and initiate PR/PO for QP s approval. Once the data is received responsible for filling the PQR receipt checklist and scheduling the PQR in SharePoint. Escalation of PQR issues to Supervisor, Group Leader, Manager PQR Centre. Contemporaneous updation of SharePoint data base Quality Management Systems Initiate the process of change controls and deviations Preparation of local SOP s and its related documents. Participate in self-inspection process Performance Management Participate in continuous process improvement projects to improve efficiency of the unit Training Prepare the Training Materials for GMP training and on the job training. Imparts training on procedures as needed. Miscellaneous Support Any other tasks assigned by the management for smooth functioning of the team Your experience and qualifications 2 to 8 years of experience in QA / QC function in the pharmaceutical industry Master s Degree in Pharmacy or other natural sciences or Bachelor Degree in Pharmacy or other natural sciences Basic knowledge on worldwide cGxP regulations Good English language skills, other language skills could be helpful Good communication skills Basic knowledge of Computerised Systems. Knowledge of Systems in TEVA s IT landscape (TrackWise, SAP, LIMS, Global Insights, Glorya etc.) would be of advantage Basic understanding of manufacturing, QC and Contract manufacturing processes Engagement to drive improvements and ability to manage complexity Hands-on experience on Analytical Method development, Method Validation for API and FP of different analytical methods (e.g. Assay, impurities, dissolution etc.) Stability Studies. Hands-on experience on Review of Instrument/Equipment qualification records. Basic knowledge / hands on experience of review of BMR. Basic knowledge / hands on experience on Product Quality Reviews.

Acts as first line proxy for Associate. Dir. PQRs Global Quality GBS, India RD Quality Ensures that the APR/PQR for Teva products and review/approval of RD Documents are completed in a timely and compliant manner as per Teva s CORP Quality Management systems. PQR/APR compilation and approval must be well associated with the Teva Manufacturing Sites, Global Quality Units and Commercial affiliates to meet the targets and ensure compliance. Defines team operating standards and ensures essential CORP local procedures are followed based on knowledge of own discipline. Manages and supervises a team of 20 professional employees consisting of authors, reviewers, optional approvers and Group Leaders heading different Quality oversights. Is accountable for the performance and results of the team under his/her responsibility within the function Global Quality GBS. Creates and adapts departmental plans and priorities to address resource and operational challenges for PQR compilation, review, approval and for review, release of RD documents. Ensures that decisions are guided by CORP policies, procedures and Global Quality s business plan. Receives guidance from Associate Director Global Quality- GBS India and RD Quality, Sen. Dir. Quality Strategy and Shared Services and Global Head RD Quality, other Managers in Global Quality GBS and GBS, Global IT, EMSO Quality affiliates, Commercial Quality EU IM, TGO and RD Quality Provides technical guidance and training to employees, colleagues/related managers and/or TEVA internal customers. acts as escalation point within the interaction between the Team and external suppliers or internal stakeholders. Participates in Quality councils and delivers input for the performance of the team/teams under his/her responsibility. Is responsible for employee performance objectives in the team, conducts performance reviews and recommends pay actions. Supports modernization by use of relevant IT Tools. Ensures continuous improvement of efficiency and compliance by establishing and monitoring relevant KPIs (OPEX). How you ll spend your day Job responsibilities A) Approval of PQR s The owner of the function Approve Annual Product Reviews (APRs) / Product Quality Reviews (PQRs) which do not require approval step by any other TEVA /non-TEVA stakeholder like QPs, RPs or FvPs. Recommend actions and communicate to internal and external stakeholders for identified actions as part of the Approval process to improve quality of products (CAPA) Support and guide in escalation of PQR issues and initiate and conduct meetings / telecons if required on priority. Escalate the issues of the team to higher management for non-responsive CMO s and TEVA s internal stake holders B) Supervisor RD Quality Provide oversight for execution of activities within the RD Quality Shared Services unit including but not limited to: Review/Approval of RD documents including analytical methods, validation protocols and reports, study protocols and reports, specifications, and executed batch records. Release of Materials Provision of Inspection Readiness support Provision of support for generation and maintenance of QTA s Performance of Corporate Gap Assessments against RD site SOP s Creation/revision of RD site SOP s Review/Approval of Equipment/Instrument qualification, calibration, and maintenance documents. Review/approval of Computer Systems Validations documents Management and trending of RD Quality kpi s Preparation of presentations for RD site s Quality Council meetings Data reviews C) Quality Management Systems The owner of the function Ensures that the local quality management system is maintained in the team under his/her responsibility Ensures that the local Quality Management System is compliant with respective regulatory guidelines and TEVA s CORP QMS (Gap Assessments) Approves process of change controls and deviations Writes or approves local SOP s and its related templates. Monitors self-inspections and related CAPA of the team under his/her responsibility as per timelines and verification of compliance report. JD to be contd.. D) Performance Management Monitors and compiles the KPI scores of the team under his/her responsibility and supports the team to improve their efficiency. Participates in the customers council meetings and supports the effectiveness of the councils Participates in the Monthly Quality Council of the PQR-Center and enhances the effectiveness and efficiency of it by suitable reports/metrics and continuous improvement. Writes or evaluates the monthly reports as needed by various stakeholders. Proactively initiates and leads continuous process improvement projects to improve efficiency groups across the team. E) Training The incumbent Performs GMP training and on the job training. Imparts training on procedures as needed. Reviews the training status of the team and regularly verifies that training was performed in time and successfully. F) Miscellaneous Support The owner of the function is responsible for Maintaining Employee Central and other relevant Master Data Responsible for approval of PO s related to purchase of PQR s Review the invoicing cost involved with respect to the status. Approval of POs in SAP- for hiring and other requests like purchase orders for costs involved in updation of software Write or Review monthly report to be presented to higher management Approve various access levels for all reportees for various software on an annual basis Monitor HC justification for every approval Maintain CAPA reports and Risk Assessments on the performance of the department in cases those are requested by health authorities Support the maintenance of the IC QTA with current updates Ensures the robust handover procedure in case of exits Your experience and qualifications Bachelor s degree in pharmacy or Natural Sciences, master s degree in pharmacy or Natural Sciences More than 12 years of experience in QA / QC, RD function in the pharmaceutical industry. More than 5 years of experience in a managerial role. Well-founded knowledge on worldwide cGxP regulations. Excellent English language skills, other language skills could be helpful incl. local Indian Languages Very Good communication skills and ability to work in a matrix structure. Very good knowledge of Computerised Systems in TEVA s IT landscape (Trac-Wise, SAP, LIMS, Global Insights, Hot Dog Glorya, Veeva etc.) Good understanding of manufacturing, QC, RD and Contract manufacturing processes Engagement to drive improvements and ability to manage complexity Ability to guide a team and influence other stakeholders Ability to work as manager in a matrix organization (GBS) and act properly on conflicting interests Mobility required