606 Formulation Development Jobs

Manager Friction Formulation Developer Experience :- 10-15 yrs. Salary :- 20-25 Lac PA Qualification :- BE Metallurgy, M.Tech. Metallurgy Location :- Sonipat Only from Automotive Brakes Manufacturing Industries

TEAM LEADER - FORMULATION AND DEVELOPMENT INJECTABLE Activities and Responsibilities :- Coordinate with formulation scientists for day-to-day activities, designing formulation strategies, execution of laboratory trials and preparation of technical documents for sterile dosage forms. Coordinate with other technical staff responsible for testing new drug substances, excipients, pre-formulation samples, and formulation development samples. Ensure the timely completion of new product development of sterile dosage form. Interact with Manufacturing, Validation, and Materials Management teams to ensure smooth drug product development and transition to commercial-scale manufacturing. Manage all activities associated with registration batch manufacturing, including authoring, reviewing, and approving technical documents. To perform, review and interpret literature related to drug products, including patents, research articles, reference product details, drug substance information, and excipient details. Provide support in troubleshooting formulation and process-related issues for both sterile and sterile dosage forms. To perform various studies such as pre-formulation studies, API characterization study, excipient characterization study, excipient optimization studies, filter compatibility studies, tubing compatibility studies, bulk hold in SS vessels / SS compatibility studies, pH optimization studies, nitrogen requirement studies, photo stability studies, freeze-thaw studies, in-use studies, dilution compatibility studies, selection of sterilization methods, selection of packaging materials, stress studies, and scale-up operations. To perform all required activities, i.e., procurement of raw materials, packaging materials, and processing aids etc. for the initiation and execution of development batches, process validation/ exhibit batches and commercial batches of the drug product. To prepare and review product-specific risk assessments, QQ, Master Formulation Records (MFR), development batch Stability Protocols, Scale-up BMRs, Scale-up reports, Product Development Reports (PDR), etc. To propose and review finished product specifications to the Analytical Development Laboratory (ADL) based on dosage form requirements. To prepare and review of technical documents based on CTD required for dossier submission and handling all technical queries raised by all respected regulatory authority. Percolate the instruction and work assigned by Head R & D to Team members for timely completion of activities. To prepare and review Standard Operating Procedures (SOPs) and related documents, ensuring work is performed according to SOPs, Good Manufacturing Practices (GMP), and safety guidelines in the R&D department. To assist and support in the preparation and review of qualification and validation documents, change controls, deviations, investigations, and CAPAs. To visit LL sites and third-party sites for development batch trials or batch execution as required. To be responsible for coordination, execution, monitoring, and troubleshooting of scale-up batches, exhibit batches, process validation batches, and commercial batches at in-house manufacturing sites, CMO sites, TT sites, and LL sites. To co-ordination with Cross Functional Team to ensure timely completion of assigned activities. To perform any other task assigned by HOD / Management. THANKS YOU REGARDS MILAP RATHOD (7486829377) HR DEPARTMENT OPES HEALTHCARE PRIVATE LIMITED

Assist in formulation development and trial batch preparation. Conduct compatibility, stability, and dissolution studies. Maintain accurate documentation and support regulatory submissions. Participate in technology transfer and validation activities.

Job Summary: We are seeking a highly skilled and innovative R&D Manager to lead our product research and development efforts. Product Development & Innovation ,Research & Formulation

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Job Description: R&D Head (Cosmetics and Skincare) Job Title R&D Manager (Cosmetics and Skincare) Eligibility Criteria (Experience, Qualification, Skills)Qualification Advanced degree (Master's or Doctorate) in Ayurveda, Herbal Sciences, Chemistry, Chemical Engineering, Pharmaceutical Sciences, or related field Experience Minimum 12 years of in research and development, with significant exposure to cosmetics, homecare, or FMCG industries. Proven track record of leading successful product development projects and teams. Skills required Expertise in cosmetic chemistry, formulation techniques, and product innovation. In depth Knowledge of Cosmetics and homecare products and properties Leadership and strategic planning abilities. Communication and stakeholder management skills. Problem-solving and decision-making capabilities. Project management and organizational skills. Ability to inspire and motivate a multidisciplinary team. Market knowledge Job Location Jaipur Key Responsibilities Provide strategic leadership for setting the R&D vision Provide technical expertise and guidance to the Cosmetics and homecare R&D team Oversee all aspects of cosmetics and homecare product development Collaborate with internal (cross functional team) and external stakeholders Manage R&D budgets and resources effectively Ensure regulatory compliance and quality standards Establish KPIs metrics and benchmarks Drive continuous improvement and innovation Job description Provide vision, direction, and strategic guidance for the company's R&D efforts in cosmetics and homecare products Develop and implement R&D strategies aligned with business objectives, to address market needs and capitalize on emerging opportunities Lead, mentor, and inspire a multidisciplinary team of scientists, researchers, and technicians, fostering a culture of excellence, innovation, and collaboration. Oversee the entire product development lifecycle, from conceptualization and formulation to testing, validation, and commercialization. Drive collaborative research initiatives, joint ventures, and technology transfer agreements to enhance the company's R&D capabilities and accelerate innovation Ensure that all R&D activities comply with applicable regulatory requirements, quality standards, and industry best practices. Develop and manage the R&D budget, allocating resources effectively and efficiently to support priority projects and initiatives. Establish key performance indicators (KPIs), metrics, and benchmarks to monitor and evaluate the performance and impact of R&D initiatives. Stay abreast of market trends, consumer preferences, competitor activities, and technological advancements in the cosmetics and homecare segment.

1. Carry out literature search for upcoming products and accordingly plan for product development. 2. Preparation of product feasibility report. 3. Knowledge in the formulation development of Parenteral dosage forms. 4. Development flow for Parenteral dosage form. 5. Guidance to fellow colleagues regarding development flow. 6. Hands on experience in Formulation Development including pre-formulation study and Scale-up. 7. Initiation of Filter validation study with filter supplier. 8. To prepare Product development report (PDR). 9. Good hand at Compatibility studies for Finish product. 10. Visualize developmental needs of the product (i.e. API, Excipients, Packing materials). 11. Solve the problems and quires related to the development of the formulation and discuss with team members. 12. Transferring of new developed product to the Manufacturing site. 13. Understand/Familiarize with the problems faced during scale-up batches, trouble shooting. 14. Compilation and interpretation of routine analytical data. 15. Preparation of SOPS, MFR, Stability & Hold Time studies protocol, writing of Lab notebooks. 16. Preparation of in-process finished product specification and packing material specifications consulting with ADL personnel. 17. Have Sufficient Knowledge of regulatory guidelines (EU, ROW and US Markets). 18. To provide technical support for commercial batch manufactured. 19. To perform investigation of failures during exhibit batches/stability study. 20. Supporting role for OSD development including literature, documentation, and trial batches at FRD.

Job Title: Senior Executive / Executive FRD Non-Orals Business Unit: R&D1 Regulatory Affairs Job Grade G11B / G12A Location: Baroda At Sun Pharma, we commit to helping you Create your own sunshine by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community. Are You Ready to Create Your Own Sunshine? As you enter the Sun Pharma world, you ll find yourself becoming Better every day through continuous progress. Exhibit self-drive as you Take charge and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we Thrive together and support each other s journeys. Job Description 1. To prepare & execute metered dose inhaler (MDI) formulation development experiments 2. To design pre-formulation and prototype experiments and to monitor batches prepared for stability studies, method development & validation. 3. To prepare documents for import of API/Innovator sample and for manufacturing license for examination, testing & analysis of drug products. 4. To ensure procurement of raw material (API/Excipients), packing material & innovator samples in consultation with packing/Purchase department. 5. To evaluate Innovator pack details and review Innovator procurement quantity with justification. 6. To prepare product development protocol & report for different development studies. 8. To prepare test request for analysis of raw material (API/Excipients) & drug product. 9. To prepare stability protocol & report. 10. To prepare tech-transfer documents (e. g. sheet II, MF, RA, FMEA, stability plan, scale up report and SDS) 11. To support in execution of scale up /exhibit /clinical batches at plant/CMO 12. To prepare documents required for regulatory submission for all markets & to prepare/review technical reports/scientific justification to respond regulatory queries. 13. To prepare/review SOPs for laboratory equipment/instrument. 14. To prepare troubleshooting/investigational reports for failures/OOS/OOT. 15. To ensure compliance of internal quality system. Travel Estimate NA Job Requirements Educational Qualification M. Pharm Experience Tenure : 2-6 years Your Success Matters to Us At Sun Pharma, your success and well-being are our top priorities! We provide robust benefits and opportunities to foster personal and professional growth. Join us at Sun Pharma, where every day is an opportunity to grow, collaborate, and make a lasting impact. Let s create a brighter future together!

Job Title: Manager-2 - FR &D Non-Orals (Compliance group) Business Unit: R&D1 Regulatory Affairs Job Grade G11A Location : Baroda At Sun Pharma, we commit to helping you Create your own sunshine by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community. Are You Ready to Create Your Own Sunshine? As you enter the Sun Pharma world, you ll find yourself becoming Better every day through continuous progress. Exhibit self-drive as you Take charge and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we Thrive together and support each other s journeys. Job Description Review documents required for regulatory submissions across global markets, including product development reports and scientific justifications for responding to regulatory queries. Evaluate and review documents related to technology transfer to ensure accuracy and regulatory compliance. Review protocols and reports for various product development studies of Non-Oral products to ensure scientific soundness and regulatory alignment. Review documents required for drug-device combination products in accordance with applicable regulatory requirements. Review filter validation reports and conduct risk assessments for extractables and leachables, elemental impurities, and nitrosamine impurities. Prepare and review Standard Operating Procedures (SOPs) and internal guidelines to ensure system compliance. Review investigation reports related to failures, Out of Specification (OOS), and Out of Trend (OOT) results, and support root cause analysis. Ensure adherence to internal quality systems and regulatory standards & conduct SOP training. Travel Estimate NA Job Requirements Educational Qualification M Pharm Experience Tenure : 9-11 years Your Success Matters to Us At Sun Pharma, your success and well-being are our top priorities! We provide robust benefits and opportunities to foster personal and professional growth. Join us at Sun Pharma, where every day is an opportunity to grow, collaborate, and make a lasting impact. Let s create a brighter future together! Disclaimer: The preceding job description has been designed to indicate the general nature and level of work performed by employee within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities, and qualifications required of employees as assigned to this job. Nothing herein shall preclude the employer from changing these duties from time to time and assigning comparable duties or other duties commensurate with the experience and background of incumbent(s).

As a Product Development Manager, you will be responsible for developing new products and optimizing existing formulations for various dosage forms such as Tablets, Capsules, Solutions, Suspensions, Pellets, MUPS, etc. Your primary focus will be on regulated markets like the US, Europe, and ROW. Key Responsibilities: - Define project scope, activities, and timelines, and monitor progress to ensure timely completion. - Lead the development of new formulations by investigating API characteristics, safety, and compatibility with other ingredients, conducting necessary testing, and scaling up studies. - Identify resource requirements, including materials, manpower, and machinery, and utilize literature information effectively throughout development. - Develop R&D plans and experimental designs using QBD principles, analyze data, draw conclusions, and make recommendations for product development. - Coordinate lab scale-up and pilot BE batches, ensuring adherence to lab GMP practices. - Review lab experiment notebooks and technology transfer documents promptly. - Liaise with technology transfer and production teams for seamless technology transfer and review batch manufacturing and process validation documents. - Optimize existing product performance by researching API characteristics and formulas. - Monitor stability studies, interpret results, and advance product development accordingly. - Coordinate with various departments to ensure timely project completion. - Prepare departmental SOPs, manuals, and guidelines as required. - Monitor machine IQ, OQ, and PQ activities, ensuring proper functioning and maintenance. - Provide training to subordinates, technicians, and housekeeping personnel on equipment and systems. - Manage storage and destruction of raw materials and finished goods and maintain RLD samples inventory. - Participate in audits and ensure compliance with recommendations. - Stay updated with the latest developments in technology, conceptual thinking, and communication skills. Qualifications & Pre-Requisites: - Master's in Pharmacy (Pharmaceutics). - Must-Have Skills: Formulation development experience in Solid & Liquid Oral; Pellets project experience preferred. Additional Company Details: - The role may require working extended hours or shifts based on requirements. - Visits to manufacturing sites may be necessary. (Note: The additional notes section has been included as an "Additional Company Details" paragraph in the final JD),

Understand the project requirements & deliverables from supervisor/managerCarry out literature search by using SciFinder, Reaxys and other search engines.Comprehend and discuss the MSDS with supervisor/ team members.

Description Job Purpose Synthesis of vinyl acetate - ethylene VAE emulsions copolymers and terpolymers in lab and pilot scales Business Responsibility Areas Development of new emulsions based on VAE formulations - co- and terpolymersThorough knowledge of VAM emulsion polymerization and copolymerization chemistry such as conversion, reactivity ratio with different monomers, and viscosity managementIn depth knowledge of fundamentals of emulsion polymerization of different monomersUnderstanding of global developments and identifying new product ideas and timely commercialization of productsOversee development of emulsions to meet the defined product attributesMust have knowledge on key characterization parameters of emulsionsManaging long term product pipeline and new trends in exterior and interior segmentsHandling high pressure polymerization reactorsAttending customer complaints and providing solution to themSupport manufacturing units / plant for batch correction Corrective and preventive action to be taken post RCAGood information on competition benchmark productsGood teamwork with people development for effective productivityGetting in-depth knowledge of the relevant patent literature from VAE expert companies such as Wacker and CelaneseVery good Technical Report writing skills Qualifications Essential - PhD in polymer chemistry or Polymer science, followed by postdoctoral studies &/or a job stint in the polymers / coatings industry, preferably from Europe, USA, Singapore or Japan Previous Experience Essential: Minimum 5 years of experience in emulsion polymerization during PhD/ postdoctoral stint &/or in emulsion suppliers or organized paint manufacturing companyThorough knowledge and formulation skill of high pressure polymerization chemistry, along with exposure to Industrial customers for technical support Desired - Experience in hands-on VAM/VAE emulsion polymers in companies like Celanese, Wacker or Dairen will be preferred Also, prior experience in scale-up of emulsions from lab to shop floor is highly desired

Your Day-to-Day Tasks Include: 1. Initiating first level contact with Inbound and Outreach leads. 2. Creating and executing an outreach strategy in collaboration with the PDR Managers and PDR team leads.

Having 2 years experience of wet and dry emulsion adhesive batch process. From Initial charging to the final product. Knowledge of emulsion adhesive production operation and process method. Operate DCS system.

Excellent knowledge of products Manufacturing of Colour Cosmetics / personal care, Skincare, Cream, Shampoo, Hair Oil, Conditioner, Face Wash, Body Wash, Body Lotion and Foot Care ,Lipstick, Nail Polish Etc.

1. Understand the project requirements & deliverables from supervisor/manager 2. Carry out literature search by using SciFinder, Reaxys and other search engines Required Candidate profile 3. Comprehend and discuss the MSDS with supervisor/ team members.

JOB DUTIES AND RESPONSIBILITIES (Please Mention In Below Table) 1. Understand the project requirements & deliverables from supervisor/manager 2. Carry out literature search by using SciFinder, Reaxys and other search engines

Industry Pharma / R&D / Biotech Qualification M.Sc Key Skills Green Field Projects R&D Synthesis Agrochemical R&D Executive R&D Chemist M.Sc Chemistry Brownfield Chemical Research W

1.Understand the project requirements & deliverables from supervisor/manager 2.Carry out literature search by using SciFinder, Reaxys and other search engines 3.Comprehend and discuss the MSDS with supervisor/ team members.

R&D (Synthesis) -Agrochemical Industry-Saykha,Gujarat. Capital Placement Services Industry IT Software - Application Programming / Maintenance Qualification M.Sc Key Skills Green Field Projects UPLC Gujarat R&D (Synthesis) PDR R&D Develo

Dindayal Industries Limited, under the esteemed brand DINDAYAL AYURVEDA , is a leading organization in Ayurvedic Medicines, FMCG, and OTC Products , dedicated to delivering high-quality, natural health solutions. With a legacy built on trust and innovation, we continue to enhance wellness through our diversified product portfolio. Position: Production Manager Classical Ayurvedic Medicines Department: Manufacturing / Production Location: Ajmer & Bharatpur, Rajasthan Job Description: We are seeking an Ayurveda professional with hands-on experience in manufacturing classical Ayurvedic formulations including Asava–Arishta, Avaleha, Syrup, Churna, Rasavati, Guggulu, Swarna Yog, Ghrita, Taila, and related products. The candidate should have strong process knowledge, raw material understanding, and expertise in ensuring compliance with GMP and Ayurvedic pharmacopeial standards. Key Responsibilities: Having good knowledge of Drugs & Cosmetic Act , Licensing process, Labelling Protocols etc. Supervise production of classical Ayurvedic medicines in line with authentic procedures Ensure raw material selection, processing, and standardization as per classical texts Oversee formulation processes for Asava–Arishta, Avaleha, Syrup, Churna, Rasa Vati, Guggulu, Swarna Yog, Ghrita, Taila, etc. Monitor in-process quality checks and maintain compliance with GMP standards Collaborate with Quality Control and R&D teams for consistency and innovation Prepare and maintain production documentation as per regulatory requirements Key Requirements: Education: M.Pharm (Ayurveda) Experience: Minimum 3 years in Ayurvedic manufacturing/production Expertise in preparation of classical dosage forms (liquid, semi-solid, powder, and medicated oils/ghritas) Knowledge of raw materials, pharmacopeial standards, and traditional Ayurvedic formulations Employment Type: Full Time Compensation: As per industry standards How to Apply: Interested candidates may apply directly send their updated CV to hr@dindayalgroup.com

Dindayal Industries Limited, under the esteemed brand DINDAYAL AYURVEDA , is a leading organization in Ayurvedic Medicines and OTC Products , dedicated to delivering high-quality, natural health solutions. With a legacy built on trust and innovation, we continue to enhance wellness through our diversified product portfolio. Position: Manufacturing Chemist Ras Shastra Department: Manufacturing Location: Bharatpur, Rajasthan Job Description: We are looking for an Ayurveda professional specializing in Ras Shastra for our manufacturing units. The candidate should have hands-on experience in Bhasma-Pishti , Kupi pakwa rasayana , with strong knowledge of Ayurvedic formulations and production protocols. Key Responsibilities: Lead and oversee manufacturing of Bhasma-Pishti , Kupi pakwa rasayana . Ensure quality evaluation, sourcing, and utilization of raw materials Supervise formulation processes as per classical Ayurvedic texts and GMP standards Collaborate with R&D and Quality teams for new product development and standardization Maintain compliance with all statutory and regulatory requirements in Ayurvedic manufacturing Key Requirements: Education: MD (Ayurveda) Ras Shastra specialization Experience: Minimum 3 years in Ayurvedic manufacturing/production Proven expertise in medicated oils, Bhasma-Pishti , Kupi pakwa rasayana,. Knowledge of production planning, process compliance, and quality assurance Employment Type: Full Time Experience Level: Mid-Senior Level Compensation: As per industry standards How to Apply: Interested candidates may apply directly send their updated CV to hr@dindayalgroup.com

Dindayal Industries Limited, under the esteemed brand DINDAYAL AYURVEDA , is a leading organization in Ayurvedic Medicines, FMCG, and OTC Products , dedicated to delivering high-quality, natural health solutions. With a legacy built on trust and innovation, we continue to enhance wellness through our diversified product portfolio. Position: Manufacturing Chemist Panchkarma Specialist Department: Manufacturing Location: Bharatpur, Rajasthan Job Description: We are looking for an Ayurveda professional specializing in Panchkarma Specialist for our manufacturing units. The candidate should have hands-on experience in medicated oils and Panchkarma oils , with strong knowledge of Ayurvedic formulations and production protocols. Key Responsibilities: Lead and oversee manufacturing of Medicinal Oils, Ointments, Panchkarma Oils , Panchkarma churna, Kwath & other products. Ensure quality evaluation, sourcing, and utilization of raw materials Supervise formulation processes as per classical Ayurvedic texts and GMP standards Collaborate with R&D and Quality teams for new product development and standardization Maintain compliance with all statutory and regulatory requirements in Ayurvedic manufacturing Key Requirements: Education: MD (Ayurveda) – Panchkarma specialization Experience: Minimum 3 years in Ayurvedic manufacturing/production Proven expertise in Medicinal Oils, Ointments, Panchkarma Oils , Panchkarma churna, Kwath & other products Knowledge of production planning, process compliance, and quality assurance Employment Type: Full Time Experience Level: Mid-Senior Level Compensation: As per industry standards How to Apply: Interested candidates may apply directly send their updated CV to hr@dindayalgroup.com

Roles & Responsibilities - Supporting the management team to identify strategic R&D requirements in agronomy, farming system, soil and nutrition. - Ensure that strategic plans accurately capture the primary issues in each R & D fields and provide details required to build appropriate technical strategies. - Responsible for identifying communication opportunities and collaborating with grower team to work on productivity enhancement, cost minimization, Quality improvement and better reliability of production. - Develop SOP for crop production, nutrition and IPM for delivery of quality and standard product to market at lower cost of goods. - Develop SOP for Post-harvest management including sorting, grading, drying, packing, cold chain and till last mile logistics for quality and reliability of products and minimize wastage. - Train all the stake holders to ensure implementation of SOPs, Agronomic observations, practices, and documentation. - Sourcing, screening and grow out of new products to see robustness of the same for production and create a collaborative project with Seed suppliers and internal stakeholders for providing best Quality product with good Gross Margin. - Lead the current and future projects with R & D as approved by the Executive Committee to support business goals. - Determine and execute improved technologies used by suppliers, competitors, and customers. - Research design and evaluate materials, assemblies, process, and equipment. - Timely and accurate biochemical analysis and reporting of results for Quality decision making. - Proactively identify project issues and appropriately manage them to satisfaction of stakeholder''s business goals, monitor, and measure and report the performance of the field. - Manage the R & D infrastructure, plant and equipment as required. - Liaison with Government, Universities and regulatory agencies and private corporations to develop and commercialize new products and ensure its registrations as per regulations. - Liaison with government bodies like ICAR and leading agricultural universities and be aware of latest agronomical developments. - Manage the negotiation of overall price for contracts and that all projects are completed within set budget guidelines. - Plan and execute research on unlocking new varietals of the crops planned by the strategy team. - Advice the leadership and the RD lead on the crops to be taken up for RD. - Develop agronomical practices that ensure cost and time efficiencies while making sure of high- quality output with minimal time and effort required to implement the practices. - IP creation: Apply for patents to generate and protect IP that is permissible as per Indian laws - Collaboration with other teams and partnership with external bodies. - Advice farm ops team on deviant behaviour of the crops (like slower than expected growth, root development, deficiencies etc.) - Collaborate with farm operations team to train on new approved practices. - Document all phases of research and development and collaborate with IT team to prepare best-in-class tools to record, analyse and report the developments and outputs of the trials. - Partner with research teams of vendors for new age technologies to run trials. Education and Experience - Postgraduate in Agriculture with minimum 5 to 10 years of experience in Breeding, TD or PD of Vegetable or Nutraceuticals. - PhD in Vegetable Science or Nutraceuticals with 10 years of experience are preferred. Skill Requirements - Proven track record of managing multiple RD initiatives across multiple crops - Awareness of Indian Agri landscape weather, soil, varietals with an added advantage for the experience with new Agri technologies (like hydroponics) etc. - Demonstrated ability to effectively work on diverse teams and to actively participate in collaborative efforts. - Conducting Grow out test of different crop varieties of Field & Vegetable crops. - Good Breeding, Agronomy and Technology and Product Development skills. - Knowledge of Computer operating skill (MS Office, Excel & PPT etc.) - Knowledge of seed production field quality validation & monitoring skill of Field & Vegetable crops. - Ability for DOE, develop Hypotheses, data collection, analysis, interpretation, and logical conclusion. - Precise decision-making ability. - Ability to handle the large team of qualified professionals. - Good communication skill through mail, letter & verbal. - Good time management & leadership skill.

We are seeking an experienced in Production Manager to lead the end-to-end lifecycle of pharmaceutical / Nutraceutical .The candidate should possess hands-on experience in the manufacturing of Tablets, Capsules, Softgels, Sachets & Protein Powders. Required Candidate profile 1. Production Planning & Management , Quality Assurance & Compliance, Process Improvement & Cost Control, Equipment & Facility Management, Team Leadership, Compliance with Health & Safety Regulations