196 Tablets Jobs - Page 8

Position : Section Head - Batch Release QA Functional Area: QA Reports to: QA Head Grade: G9B Department: Quality Location: Halol (OSD) POSITION SUMMARY Responsible for IPQA activity and strategy in line with Sun Pharma Compliance, Product Quality Management objectives and Regulatory requirements. Responsible for planning and arranging for internal and external departmental support of quality assurance activities as directed in approved protocols, quality systems or Procedures. Identify and implement solution for improving existing site quality assurance systems and processes Involvement in co-ordination of activities for software like SAP HANA at plant Responsible for review and Approval of Quality management/GMP records. Responsible to ensure and perform site data review of batch records for completeness of documentation, approval and rejection of materials per current good manufacturing procedures and escalation of quality incidences, Continuous process verification (CPV). Manage the batch release function at site wrt documentation, systems, approval and rejection of materials, products at the Site per current Good Manufacturing Practices requirements. The incumbent will assure individual compliance with the all concerned regulatory requirements, GxPs and applicable department programs, including training, documentation, Standard Operating Procedures, and Sun Pharma Global Quality Policies, Standards and Procedures. Key responsibilities: 1. Ensure compliance to regulatory requirements on product, process, equipment and release procedures. 2. Manage Batch release activities for commercial dispatch. 3. Escalate compliance concern to concern stakeholder. 4. Review, compliance of BPR and batch release for commercial dispatch. 5. Review and approve the investigations, CAPA, and effectiveness checks with adherence to timeline. 6. Execute change control and risk assessment whenever required. 7. Ensure Quality Metrics, Quarterly BPR report as per specify timeline. 8. Ensure timely Batch release through electronic system. 9. Planning and arranging for internal and external departmental support of Quality Assurance activities as directed in approved protocols, quality systems or Procedures. 10. Follow the EHS policy and maintain the compliance to GMP requirements. 11.Co-ordination with QPs and customers of different region for batch release. 12.Management of Technical agreement with QP and Customers. 13.Responsible for oversight in warehouse and BSR. 14.Management of retain sample storage , inspection and life cycle management. MINIMUM EDUCATION/EXPERIENCE REQUIREMENTS M.sc / M. Pharm/ B. Pharm 15 years with work experience preferred. REQUIRED SUCCESS ATTRIBUTE Knowledge of GxPs, cGMP and other regulatory requirements. Planning and Prioritization Collaboration Accountability Compliance Customer Service orientation Secondary Success Attributes People Connect Attention to detail Emotional control Effective Communication & Problem solving WORKING ENVIRONMENT/PHYSICAL REQUIREMENTS Incumbent performs work assignments in both normal office and non-aseptic manufacturing/packaging environments. Moderate to loud noise level is common in production rooms. The incumbent must be able to comply with the gowning requirements for entry into controlled non-aseptic manufacturing areas, and wear personal protective equipment as required. This job description is intended to describe the general nature and level of work being performed by the person assigned to this position. The primary duties and responsibilities are intended to describe those functions that are essential to the performance of this job. This job description does not state or imply that the above are the only duties and responsibilities assigned to this position. There are other duties and responsibilities that are considered incidental or secondary to the overall purpose of this job. Employees holding this position will be required to perform any other job-related duties as requested by management.

Roles and Responsibilities 1. Review of Technology data package and preparation of Gap analysis document. 2. Preparation of technology transfer protocol and report. 3. Co-ordination with FD for smooth Tech Transfer. 4. Monitoring of validation batches at production site. 5. Perform Feasibility trials, Product evaluation trials to understand critical process parameter for smooth transfer and process understanding. 6. Review of MPCR and protocol. 7. Planning for Execution of Process design, Process qualification batch. 8. Coordination with Production, Quality assurance, Quality control, Engineering, Regulatory Affairs, SCM and warehouse for the TT activities. 9. Should be part of handling deviation, change control and failure investigations. 10. Process manufacturing parameters for Qualification batches Vs Commercial batches. 11. Preparation and reviewing of intended batch documents for regulatory submission. 12. Trouble shooting of existing products and process improvement to increase output or to reduce processing time or to improve the quality of products.

Roles and Responsibilities Granulation: Operate and maintain granulation equipment (e.g., high shear mixers, fluid bed dryers). Perform wet and dry granulation processes, ensuring uniformity and consistency in batches. Monitor parameters like moisture content, particle size distribution, and granule flow properties. Compression: Operate tablet compression machines to produce solid dosage forms. Monitor compression parameters such as hardness, thickness, weight, and friability. Troubleshoot and adjust compression equipment to optimize production. Coating: Oversee the tablet and capsule coating processes, ensuring proper application of film coatings. Work with coating machines like pan coaters and fluid bed coaters. Monitor and control coating parameters such as spray rate, drying time, and temperature. Capsule Filling: Operate capsule filling machines to ensure accurate dosing of powder or pellets into capsules. Perform checks for capsule fill weight and ensure proper capsule sealing. Troubleshoot issues related to capsule filling, such as jammed capsules or weight discrepancies. General Responsibilities: Ensure all equipment is functioning properly and safely, adhering to preventive maintenance schedules. Maintain a clean and sterile environment in compliance with Good Manufacturing Practices (GMP). Perform in-process quality control checks to ensure that the products meet specifications. Document all activities, including batch records, machine logs, and quality checks in accordance with regulatory requirements. Collaborate with quality control and engineering teams to identify and resolve any production issues.onitor and control process parameters to ensure quality products meet specifications. Maintain accurate records of production data and perform routine maintenance tasks on equipment. Collaborate with team members to achieve daily targets and improve overall productivity. Ensure compliance with Good Manufacturing Practices (GMP) guidelines.

compliance with GMP and quality policie Approve RM/PM vendors and conduct regular quality audit validation, qualification, and batch release. GMP training $ support factory-wide implementation. Manage change control, deviation, and QMS execution.

Job Title: Senior Manager Formulation Development (Generic Finished Formulations) Department: Research & Development (R&D) Formulation Development Reports To: Head – Formulation Development / Vice President – R&D Job Purpose: To lead and manage the development of generic pharmaceutical finished dosage forms (oral solids, liquids, injectables, topical, etc.) from concept through scale-up, technology transfer, and regulatory submission. Responsible for ensuring robust, cost-effective, and regulatory-compliant formulations aligned with company strategy and market requirements. Key Responsibilities: Formulation Development & Optimization Lead the design and development of generic formulations for multiple dosage forms. Ensure development of stable, bioequivalent, and patient-friendly products. Drive pre-formulation studies, excipient compatibility, and optimization of manufacturing processes. Regulatory & Compliance Oversee preparation of product development reports, QbD documents, and regulatory submission modules (CTD/ANDA dossiers). Ensure compliance with CDSCO, USFDA, EMA, Health Canada, ENVISA and other global regulatory requirements. Provide technical support during regulatory audits and queries. Technology Transfer & Scale-up Lead pilot scale and exhibit batch manufacturing. Oversee technology transfer to manufacturing sites and ensure successful scale-up. Collaborate with Production, QA, and QC for smooth handover of products. Team Leadership & Project Management Manage and mentor formulation scientists and technical staff. Allocate resources, monitor project timelines, and ensure delivery as per business goals. Foster cross-functional collaboration with Analytical R&D, RA, Supply Chain, and BD teams. Innovation & Cost Optimization Identify and evaluate novel excipients, technologies, and platforms for product differentiation. Drive cost-effective formulation strategies without compromising quality and compliance. Monitor market trends, competitor products, and technological advancements. Key Skills & Competencies: Strong technical expertise in formulation science (solid oral dosage forms essential; additional knowledge of liquids, injectables preferred). Deep understanding of QbD, ICH guidelines, and global regulatory expectations. Proven experience in bioequivalence-oriented development. Strong leadership, people management, and project management skills. Excellent problem-solving, analytical, and decision-making abilities. Effective communication skills (written & verbal) for cross-functional and regulatory interactions. Education & Experience: M.Pharm / Ph.D. in Pharmaceutics / Pharmaceutical Technology. Minimum 10–15 years of experience in formulation development of generic finished dosage forms. Hands-on experience in developing products for regulated markets (US, EU, Canada). Proven track record of successful ANDA/NDA/MA submissions and approvals. Work Location: Ahmedabad, Gujarat Company Profile: Alpine Pharma Research is a group company of Alpine Health in USA which is a licensed pharmaceutical distributor based in Secaucus, New Jersey, USA that serves independent pharmacies across the US. Alpine Health offers a full range of generics, OTC's, diabetic supplies, vials and pharmacy supplies. Alpine Pharma Research in India is focused on developing high quality products for regulated and no-regulated healthcare markets including USA, India and ROW region. Based in Ahmedabad the company has its own manufacturing facility of medical plastics and is also developing OTC formulations for worldwide market. The company aims to have a portfolio of products that cater to pharmaceutical and healthcare industry across the globe.

B.Pharm / M.Pharm with 2 to 6 years of experience in Regulatory Affairs. To Review dossier prepared by executives & trainees & submit to client along with artworks for countries like ASIA, LATAM & ROW Market. Follow up with FRD & Microbiology Dept. Required Candidate profile Ensure that a company's products comply as per current ICH & Country Guidelines. To work on Renewals of Registration Certificate for countries. Courier of Legalized Documents such as COPP, FSC, POA. Perks and benefits Negotiable - Depending Upon Candidate & Experience

Interview For QA & QC Department for MNC Formulation Company in Navsari Qualification : Bsc / Msc Chemistry/ B.pharma/M.Pharma Experience : 3 to 8 Years CTC : Up to 8 LPA Send CV on sdpbharuch@gmail.com with Subject: Navsari QA & QC Navsari

We need a pharmacist to be based in our store for managing the orders and checking the same this would be a full time role The person needs to be responsible to manage daily inward and orders

Preferred candidate profile Qualification : B Pharma/M Pharma Year of Experience : 3 - 5 Yrs in shop floor management. Must have hands on experience in Compression/Coating Section. Having exposure of Audit facing internal and external party. Interested candidates may share profile at hr.plant@zuventus.com Job Location : Sikkim

Role & responsibilities 1. To ensure smooth third party Operation for all LL / TP location. 2. Responsible for third party process activities for OSD, solid oral dosage form. 3. To coordinate with LL / TP site for technical documents. 4. To be present and ensure production and packaging activities at LL/TP location. 5. To coordinate with PPMC / QA / QC / TP-LL location for smooth operation. 6. To prepare / review PIF (Product information form) and circulate with all stake holder, after approval timely share it with LL sites. 7. To ensure all activities to be done as per PIF. To maintain PIF file in soft and hard copy. 8. To maintain valid product and site license copy. 9. To prepare BMR / BPR for LL products and share it to LL site after final approval. 10. For ant changes / deviation ensure all should be handled through relevant QMS and its CAPA if any. 11. To ensure in-process at various stage of production and packaging and ensure its online documentation. 12. Before batch release ensure BMR and BPR and its relevant documents are reviewed and complied. 13. To ensure LL / TP site for readiness of audit. 14. To be present in process validation activities at LL/TP sites. 15. To coordinate with third party manufacturers for commercial products during technology transfer. To be present during technology transfer procedure at LL sites. 16. Identifying and executing continuous improvement opportunities at third party sites and communicate with TP and technical head. 17. To ensure products should be manufactured and packed and as per cGMPs, SOP's, relevant government regulations, and current industry standards. 18. To be part of audit team for RM vendor and LL-TP site. 19. Risk Management: • Identifying and assessing risks associated with third-party suppliers, including supply chain disruptions, quality issues, regulatory compliance and issues with CAPA. 20. Continuous Improvement: • Monitoring LL / TP site against key performance indicators (KPIs) and benchmarks. 21. Regulatory Compliance: • Ensuring that all third-party suppliers comply with relevant regulatory requirements, including Good Manufacturing Practices (GMP), Good Laboratory Practices, Good Distribution Practices (GDP), and other applicable regulations. Preferred candidate profile

Role & responsibilities: 1 Preparation of standard operating procedure with its annexure. 2 Preparation of Specification, standard test procedure of Raw Material, Packing Material, Finished product as per pharmacopeia and in-house methods. 3 Performing instrument qualification and calibration as per schedule. 4Sampling , analysis and review of raw water, purified water, raw material, packing material, finished product and in process sample, stability sample as per Specification with ERP entries 5 Preparation of COA of raw material, packing material, finished product and in process sample and stability study summary sheet ,trend analysis. 6 Maintenance of reference standard, primary standard and Preparation and maintenance of Working Standard. 7 Preparation and standardisation of Volumetric Solution and preparation of reagents. 8 Handling of all instruments and equipments in quality control. 9 Analysis of samples on HPLC,GC,IR and UV 10 Arrangement and maintenance of control sample and stability study sample 11 Sample send to public testing laboratory for analysis and coordination with laboratory for the same. 12 Monitoring the of chemicals and glassware received. 14 Monitoring the disposal of scrap, chemical and reagent waste and left over sample. 15 Calibration of Glassware 16 To follow the Good Documentation Practice and Good Laboratory Practice in the Laboratory. 17 To perform the analysis and Reporting of Water Validation, Method validation, Cleaning Validation and process validation 18 Any other task which is given to you by your senior in case of emergency. Knowledge Require 1. 2-6years of experience in Formulation Pharmaceutical Plant. 2. Relevant Experience in Pharma formulation plant. 3. Computer proficiency in MS Office, Excel, e-mail and internet function

Role & responsibilities : 1 To perform Operation activity of equipment and instruments as per SOP. 2. To affix the status label to equipments, instruments and IPC at each and every processing stage 3. To operate the equipment in safe and effective manner for production processing. 4. To follow and adhere to GDP and cGMP practices. 5.Inspect equipment to identify any replacement, and repairs. 6. Ensure that the equipment are maintained in good and safe working condition. 7. To Perform regular equipment maintenance to ensure production capacity and quality. 8. Identify and report unsafe operations and near misses to supervisor immediately. 9. Perform the activity as per SOP and instruction given in BMR and BPR. 10. To perform balance Calibration and instrument calibration as per SOP Preferred candidate profile: 1. 02- 07 years of experience in Formulation Pharmaceutical Plant. 2. Relevant Experience in Pharma formulation plant. 3. Computer proficiency in MS Office, Excel, e-mail and internet function.

F&D of Solid, Liquid and Topical dosage forms End-to-end formulation & development of Herbal Nutraceutical products Tech transfer and coordination - manufacturing, trial batches & troubleshooting Stay updated on FDA guidelines & industry practices

We're looking for an experienced professional to lead and drive innovative formulation strategies from development to regulatory submissions. Experience: 16-18 Years(Group Lead) Location: Hyderabad(Dulapally) Key Responsibilities: -Lead end-to-end formulation development of OSD products for regulated and semi-regulated markets -Oversee pre-formulation, technology transfer, scale-up, and exhibit batch manufacturing -Collaborate cross-functionally with QA, QC, RA, Production, and Project Management -Ensure timely completion of development milestones and regulatory documentation (CTD/ACTD) -Mentor and guide a team of formulation scientists -Strong knowledge of ICH guidelines, regulatory expectations, and QbD approach -Proven leadership and team management capabilities -Experience in regulated markets (US/EU) preferred Interested candidates can apply share their profile at raghuveera.vutla@aizant.com

We are looking for a highly skilled and experienced Formulation Development Professional with 1113 years of experience in oral solid dosage forms (OSD). Key Responsibilities: -Lead formulation development projects from R&D to commercial scale. -Design and execute formulation strategies for ANDA/CTD/ACTD submissions. -Conduct literature search, pre-formulation studies, and prototype development. -Troubleshoot formulation and process-related challenges. -Work closely with cross-functional teams Regulatory, ARD, QA, QC, and Manufacturing. -Prepare technical documents, development reports, and support dossier preparation. -Manage technology transfer and scale-up activities to manufacturing units. -Ensure adherence to cGMP, ICH, and regulatory guidelines. -Experience in regulated markets (US, EU) is preferred. If you are passionate about innovation in formulation and want to be part of a growing team, we would love to connect! Apply now or send your CV to raghuveera.vutla@aizant.com

Required Production Officer for a Reputed Pharmaceutical Company of Ahmedabad M. Pharma or MSc with 2 to 3 Years experience in Formulation Company. Apply or drop resume at 9879604156.

Roles and Responsibilities Develop new markets for pharmaceutical products through business development initiatives in ROW Market. Identify potential customers, build relationships, and negotiate deals to increase sales revenue. Conduct market research to stay updated on industry trends and competitor activity. Collaborate with cross-functional teams to launch new products in international markets. Manage export documentation and logistics for pharmaceuticals. Desired Candidate Profile 5-15 years of experience in International Business Development (IBD). Bachelor's degree in Pharmacy (B.Pharma) or Master's degree in Pharmacy (M.Pharma). Strong understanding of formulations, solid orals, tablets, and OSDs; knowledge of international market requirements preferred.

We're hiring a Plant Head – Manufacturing to lead our high-capacity TV facility. Must excel in P\&L, team leadership, quality, and large-format electronics assembly. Key focus on line balancing, KPIs, Lean practices, and end-to-end plant ops. Required Candidate profile B.E./B.Tech in EEE/IE with 15+ yrs in electronics mfg; TV preferred. Strong in P\&L, SMT, QA, team mgmt, compliance, CapEx & process ops. Mobile/laptop assembly exp also considered.

Sun Pharma is proud to announce the establishment of our world-class Technical Training Academies , a pioneering initiative in our industry. We invite passionate individuals with a zeal for coaching, and training to join us in this transformative journey. Seize this opportunity to enhance your career and shape the future of our organization. Joining our Technical Training Academies not only offers a chance to nurture your passion for coaching but also provides a platform to impact the industry at large. Its an opportunity to grow professionally while shaping the future of technical education in our field. Job Description: Location: Guwahati Technical Training Academy Head overseeing training initiatives across a cluster of pharmaceutical sites in India. As the Technical Training Academy Head, you will lead the development and execution of training programs across multiple pharmaceutical sites within a cluster. Your role is critical in enhancing employee skills, ensuring compliance, and driving operational excellence. Here are your key responsibilities: Understanding of the OSD Processes: In depth knowledge of OSD manufacturing methods Unit Operations Expertise: Knowledge & equipment proficiency in various unit operations related to OSD manufacturing - ranging from but not limited to - Granulation, Compression, Coating, Wurster Coating & Capsulation Strategic Planning : Collaborate with senior management to define the vision and strategy for technical training. Align training initiatives with business goals and industry best practices. Training Program Development : Design and curate training content for various roles (production, quality control, engineering, etc.). Develop comprehensive training modules covering technical skills, compliance, and safety. Training Delivery: Oversee training sessions, workshops, and webinars. Ensure effective knowledge transfer to employees at all levels. Quality and Compliance : Emphasize adherence to Good Manufacturing Practices (GMPs) and regulatory requirements. Monitor training effectiveness and address gaps. Resource Management : Allocate resources (trainers, facilities, materials) efficiently. Collaborate with site-specific training coordinators. Stakeholder Engagement : Work closely with HR, department heads, and site leaders. Understand specific training needs for each company. Continuous Improvement : Evaluate training outcomes and adjust programs as needed. Foster a culture of learning and skill development. Qualifications and Skills Experience : Proven track record in OSD manufacturing and unit operations, along with technical training or related roles. Leadership : Strong leadership skills to guide a team of trainers and coordinators. Communication : Excellent verbal and written communication. Industry Knowledge : Familiarity with pharmaceutical manufacturing processes. Adaptability : Ability to navigate diverse organizational cultures.

Hiring for Production Head for a leading Pharma Company near Chandigarh. Candidates with experience of working in MHRA site can apply

Production chemist required for a Nutraceuticals company at kundli, sonipat Qualification - any pharma or chemical Exp- min 10 yrs Salary - upto 70k Should have experience in oral and solid, powder all type of product