606 Formulation Development Jobs - Page 25

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.

Job Description: Department: Formulation R&D Experience: 3 - 7 Yrs. Qualification: M.Sc / M.Pharma Skills: Should have prior experience and knowledge of development of Soft Gelatin Capsules Technical Documentations - BOM / MFR stability study guidelines , QMS knowledge of pharmaceutical development Technology Transfer to commercial site Should have knowledge of development of other dosage forms (Solid Orals / Liquids /Semi-solids) Good to have knowledge on Nutra / Ayurvedic Regulations

Role & responsibilities Understanding the formulation strategy of competition products, designing approaches for novel skin care technology/formulations, prototype development, shelf-life studies, coordinating with evaluations team for various evaluations, working closely with IP team for patentability of formulations, documentation of technology and conducting technology transfer. Preferred candidate profile Qualifications B.Tech/M.Tech(CosmeticsTechnology) / M.Sc. Chemistry(Organic, Physical, Inorganic, Polymer, Industrial) / M.Sc.(Bio-Technology, Bio-Chemistry) Work Experience : Exposure to personal care product development as an employee 2-6 years of experience in personal care product development Skills : Experience in personal care product development, conducting stability studies, product evaluations, Scale up Good understanding about the physiology of skin, raw materials used in personal care products, their chemistry, interactions & compatibilities, Science of formulation development combined with knowledge of technology transfer, if any. Knowledge Formulation, emulsions, silicone chemistry, raw materials used in personal care products, latest developments in the field of cosmetics

Qualification: Post-graduate in Pharmacy or Pharmaceutical Engineering Experience: 15 to 20 years in sterile manufacturing plant operations, with a minimum of 10 years in a leadership role and at least 7 years in a regulated sterile manufacturing environment. About The Company Fresenius Kabi Oncology Limited, a wholly owned subsidiary of Fresenius Kabi, is a leading player in the oncology generics market with a broad portfolio that includes injectables, cytotoxic, and APIs. Its state-of-the-art production facility in Baddi features dedicated units for cytotoxic and non-cytotoxic products, including liquid and lyophilized injectables. The facility is approved by global regulatory authorities such as EMA, ANVISA, and Health Canada, and its products are registered in over 30 countries. About The Role As Site Head of the Baddi facility, you will oversee and be responsible for all aspects of site manufacturing operations. This leadership role is pivotal in ensuring operational excellence, regulatory compliance, and strategic alignment with the global oncology supply chain. You will be responsible for driving performance, fostering a culture of continuous improvement, and leading a cross-functional team toward sustainable and efficient operations. The potential candidates should be result-driven, resilient, collaborative and empathetic. About the Responsibilities Strategic Leadership: Lead the end-to-end operations of the sterile injectable plant, including production, quality, engineering, supply chain, and EHS functions. Regulatory Compliance: Ensure full compliance with internal and external regulatory standards (e.g., EU-GMP, WHO-GMP) and corporate SOPs. Operational Excellence: Drive continuous improvement in manufacturing efficiency, cost optimization, and product quality. Oversee the implementation of digitalisation, such as optical inspection and serialisation. People Management: Build and lead a high-performing cross-functional team. Foster a culture of accountability, safety, and innovation. Project Execution: Oversee capacity expansion, technology transfer, and commissioning of new lines (e.g., lyophilization, isolator-based filling systems). Stakeholder Engagement: Collaborate with corporate leadership, regulatory bodies, and cross-functional teams to align plant goals with organizational objectives.

JOB DESCRIPTION Job Title: Junior Analytical Development Scientist - Injectables Job Location: Bangalore Department : Analytical Development Drug Product About Syngene: Syngene ( www. syngeneintl. com ) is an innovation-led contract research, development and manufacturing organization offering integrated scientific services from early discovery to commercial supply. Mandatory expectation for all roles as per Syngene safety guidelines Overall adherence to safe practices and procedures of oneself and the teams aligned. Contributing to development of procedures, practices and systems that ensures safe operations and compliance to company s integrity quality standards. Driving a corporate culture that promotes environment, health, and safety (EHS) mindset and operational discipline at the workplace at all times. Ensuring safety of self, teams and lab/plant by adhering to safety protocols and following environment, health, and safety (EHS) requirements at all times in the workplace. Ensure all assigned mandatory trainings related to data integrity, health, and safety measures are completed on time by all members of the team including self Compliance to Syngene s quality standards at all times Core Purpose of the Role: Analytical development supporting Formulation development Routine analysis of samples Method development Instrument calibrations Documentation Report preparation Miscellaneous lab responsibilities Role Accountabilities: Candidate should have very good educational and theoretical background. Candidate should have knowledge of calibration, method development and troubleshooting using various instruments like Zetasizer, Mastersizer, Osmometer, KF auto titrator, dissolution (I, II IV), spectroscopic instruments e. g. UV spectrometer, IR and Chromatographic instruments e. g. HPLC/UPLC, GC, Liquid Particulate counter, etc. Knowledge of various regulatory guidelines w. r. t. method development, product development and documentation Knowledge of method development for injectable formulations w. r. t. tests like assay, degradation products, dissolutions, content uniformity, cleaning method, degradation products of liposomes/microspheres, free and bound API assay, etc. Knowledge of specification setting for parenteral dosage forms, in-process specifications as well as finished product specifications Knowledge and operating of instruments like LC-MS, GC-MS will be added advantage Good understanding of Documentation as per GxP requirements Online Lab notebook writing (ELN or any specific tools) Method development report preparation Assay, Degradation products, Dissolution, cleaning method, etc. Method of Analysis, Test report, SOP preparation Calibration documentation Review of documents generated by peers or juniors Should be able to search scientific literature on-line Leadership Capabilities: Not applicable Syngene Values All employees will consistently demonstrate alignment with our core values Excellence Integrity Professionalism Experience: More than 3 years up to 7 years Skills and Capabilities: Technical/functional Skills: Candidate should have good proficiency for MS-office tools Should be able to search scientific literature on-line Behavioral Skills: Strong commitment towards work, and a high level of dedication, enthusiasm, motivation, and persuasive ability in a team. Good speaking-listening-writing skills, attention to details, proactive self-starter. Ability to work successfully in a dynamic, ambiguous environment. Ability to meet tight deadlines and prioritize workloads. Ability to develop new ideas and creative solutions. Should be able to work in team and flexible for working in shifts. Should be a focused employee. Education: M. Pharm / M. Sc Equal Opportunity Employer .

ORGANISATIONAL OVERVIEW We, Lambda Therapeutic Research Limited are a leading global Clinical Research Organization (CRO) headquartered in Ahmedabad India, with facilities and operations in Mehsana (India), Warsaw (Poland), London (UK), Pittsburgh (USA), Las Vegas (USA) and Fargo (USA). Over 1500 employees are working across the globe in these facilities. Lambda offers Full-spectrum clinical trial solutions empowered by more than 20 years of service to the biopharmaceutical and generic industry. At Lambda, our gamut of services under the clinical research domain are executed with comprehensive efforts, to deliver positive results. Led by a management team of highly qualified & experienced industry leaders, we apply innovative technologies, therapeutic expertise, and a commitment to quality to help clients develop products safely, effectively, and quickly. Delivering the best accomplished by hiring the best. Employees are the pillars that hold up every quality promise that we make. That is why, we at Lambda are always looking for qualified and energetic individuals, with a desire for excellence, to join our team. JOB DETAILS The candidate should design and execute formulation development studies for drug product within the Process Sciences group. The role is critical to the delivery of a suitable formulation in the appropriate DP dosage form (liquid/lyo) and possessing desired physico chemical characteristics. KEY DELIVERABLES Provide technical leadership for DP formulation and lyophilization development and characterization. Strong understanding of design of formulation studies and selection of appropriate excipients for different dosage forms (liquid/lyo) and stability studies in order to design and develop suitable formulation in the appropriate DP dosage form (liquid/lyo) and possessing desired physico chemical characteristics. Perform studies for selection of primary packaging container and design/execute compatibility studies. Perform forced product degradation studies. Strong understanding of DP unit operations like freeze/thaw, filtration, filling, lyophilization Good collaboration skills with clients Responsible for authoring and reviewing technical reports related to drug product, and contribute to regulatory submissions and audits with health agencies. Contribute to publications/IP around formulations EXPERIENCE Strong understanding of design of formulation studies and appropriate excipients for different dosage forms (liquid/lyo) and stability studies Strong understanding of DP unit operations like freeze-thaw, filling, filtration, mixing, lyophilization, container closure integrity testing and packaging operations is desirable. Cross functional technical knowledge is highly desirable. Excellent oral and written communication and interpersonal skills will be desired. EDUCATIONAL QUALIFICATION Masters or Ph.D in Chemical/Biochemical Engineering or similar disciplines with 5+ years of work experience in drug product formulation development and manufacturing.