448 Formulation Jobs - Page 14

Responsibilities : The JRA would be responsible for planning, coordinating andexecuting product claims substantiation activities through methods andtechniques in Microbiology, Biotechnology and Consumer research acrossdifferent categories and brands within Personal Care R&D, basis definedtimelines. The JRA would be required to network and coordinate studieswith various external labs/CROs and analyse data received and draw conclusionsfor claims suitability. He/She is required to align and establish processes,methods and bioassays for Microbiology / Biotechnology, Product evaluationsthrough Consumer / Clinical research and participate in the creation of noveland differentiated product claims and consumer demonstrations. Job responsibilities: Assist in product evaluations andclaim substantiation through methods in wet lab research [Microbiology/Cell-Culture/ Bioassays etc], Dry lab research, Consumer / Clinical researchetc. in defined timelines. Actively engage with Stakeholders[formulation teams, Brand teams] to understand the requirement and suggestappropriate testing approaches, timely execution of the evaluations and communicationof result as per the set schedules Actively engage with Consumers todraw insights on product performance and acceptance, Consumer behavior andpreferences. Ensure documentation thoroughnessof all the assigned projects. Work independently and in teams (withinteam and with cross-functional teams) to enable timely decisions on assignedprojects. Operate and maintain advancedInstruments (instruments used for in vivo and in vitro product evaluations) Participate in ideation andtroubleshooting activities within the group. Learn and develop existingprocesses in lab and documentation etc. Learnand develop new methods, new capabilities for continuous skill enhancement. Requirements Qualifications : M.Sc.Microbiology / M.Sc. Microbiology + Biotechnology Biotechnology disciplines/skills likeHuman/Animal Cell culture techniques would be a plus. Knowledge/experiencein Personal Care and Home Care product evaluations (Consumers skin/hair etc.,Surfaces, lab-methods), Basic appreciation of Statistics. Work Experience : 1-5 years experience in Microbiology, Cell culture, Cell Biology, PersonalCare product testing in FMCG or allied Industries Experience in Personal Care and Home Careproduct evaluations (Consumers skin/hair etc., Surfaces, lab-methods), Basicappreciation of Statistics. Skills : Microbiology laboratory testing skillse.g. aseptic and sterile techniques, optical microscopy, bacterial staining, culturing,isolation, enumeration and identification, use of biological safety cabinets,media and buffer preparation, diagnostic biochemical tests for microbes,antimicrobial bioassays etc.). Self-Initiator, Strong, Clear andOpen Communication Skills, Sound Analytical Mindset, Inclination to learn andoperate advanced instruments and research methodology employed in productefficacy assessments. Networking skills to coordinate studieswith various external labs / CROs and analyse data received and drawconclusions for product claims suitability. Biotechnologyskills like Human/Animal Cell culture, cryo-preservation, MTT Assay, celllysate preparation, RNA/DNA extraction, cDNA and qPCR etc. Instrumentand Lab maintenance with experience on audits in core domain and ISO 14001,17025 etc. Networkingabilities, ability to connect with people and openly communicate LanguageProficiency: Kannada, Tamil/ Telugu, Hindi Knowledge MS Excel, MS Word, MS-Powerpoint,Basic Statistics tools. Fair understanding on PersonalCare and Home Care products and Market Anabove average understanding of Skin and Hair Biology and basic methods inevaluating product efficacies in Personal Care and Home Care domain.

The Manager ProductDevelopment is a senior position in the Foods Business mandated to design,develop and supervise the implementation of the Categories Product developmentstrategy. Principal Accountabilities Actively collaborate with cross-functional teams to drive PD projects from concept to commercialization with focused, agile and speedy execution. Drive expansion into new range of offerings as per business plan to develop competitively superior product portfolio. Focus on upgrading and updating product quality parameters and systems for existing products ensuring that consumer feedback feeds into the quality and manufacturing systems so that consistent quality is maintained in the market. Develop scientific building blocks for future innovation and portfolio building Ensure scientific backing for meaningful product claims and applying for IP in relevant cases. Responsible for onboarding vendors, quality system/documentation to ensure consistent quality in seasoning and regulatory compliance for all the product development & manufacturing Develop team members to enhance their skill sets and technical capabilities Requirements Expertise in Food sciences, Processing technologies and must have contributed in developing and launching the products (from pilot to commercial scale) in previous organizations. Experience of leading a team, Technical Knowledge and experience of: Product Formulation, chemical composition, ingredient properties and functions, techniques of processing/manufacturing & storage Food analysis instrumentation & procedures Food related statutory compliances Microbiology, food safety, food chemistry, food preservation and shelf-life study Manufacturing and quality systems such as HACCP, GMP, ISO, TPM, Six-sigma and Lean Design of experiments, Statistical analysis and interpretation of data Claim substantiation and IP Product costing and contributions

Roles and Responsibilities Ensure primary packaging material meets quality standards. Perform blister packing operations according to SOPs. Conduct bottling activities with precision and efficiency. Manage secondary packaging processes effectively. Maintain accurate records of production data.

You are accountable for the teams performance, compliance, and audit readiness, managing product return and replacement processes, and partnering with global colleagues to resolve issues. You will ensure the team is trained and proficient, support the development of training programs, and promote quality risk management. Leading the surveillance team, you will generate complaint metrics and monitor KPIs to improve processes. You will also support Product Surety/Corporate Security and Serialization activities, manage employee-related activities, and foster a collaborative and empowered team environment. Key Responsibilities As Hyderabad Product Quality Complaints (PQC) Team lead, you are accountable for the delivery performance and quality of service provided by the HYD PQC team. Reporting to the HYD Global Quality Lead, you will work closely with the Global Process Owner for Product Quality Complaints to deliver compliant, accurate, timely and efficient services for the management of Product Quality Complaints and associated data, systems and processes for BMS products. Leading the Hyderabad Product Quality Complaints (PQCs) team members to deliver robust and timely processing of Product Quality Complaints (PQCs) to meet enterprise and global regulatory requirements Leading the Hyderabad PQC surveillance team to collect, manage and analyze PQC data, highlighting trends, signals and risks and focus areas to PQC Management and Quality Councils supporting effective decision making to protect the organization and our patients and to optimise PQC performance Leading the Hyderabad PQC digital team to design, deliver and maintain digital solutions to optimize PQC processes, deliver efficiencies in PQC process performance and optimize system interfaces Communicates continuously and effectively with management (Global Quality Lead, Hyderabad, Senior/ Director Product Quality Complaints, Site Quality & Compliance Leadership as appropriate) and key PQC stakeholders on PQC related matters Accountable for HYD PQC team delivery of performance and compliance requirements, in alignment with HYD Global Quality Lead, and Senior Director Product Quality Complaints Accountable through your HYD team for daily case processing of incoming PQCs while adhering to triage timelines and ensuring compliance to global Health Authority reporting (eg Field Alert Reports, Medical Device Reports, etc) Accountable through your HYD team for delivering comprehensive, timely and compliant PQC reports and records for closure to designated Quality approvers across the network Accountable for the continuous audit-ready state of the HYD team Manage the product return and product replacement processes required for PQC investigation Partner with global PQC US/EU colleagues and/or market Quality colleagues and/or network sites and/or third parties to ensure timely resolution to PQC sample return and/or product replacement issues Partner with PQC Management, and key stakeholders (intake teams, Medical Information, Safety, Third Parties, PQC Local Process Owners and Investigation sites to optimize the intake & processing of Product Quality Complaints Escalate system performance issues to PQC Systems Support for expedited resolution Accountable through the HYD team for the optimum performance of digital tools (BOTs, dashboards, Sharepoints, flash reports etc) Develop trusting, open and collaborative partnerships while ensuring stakeholders have a clear understanding of BMSs PQC procedural requirements Support the development and implementation of PQC training programs including new product launch trainings Ensure the local HYD PQC team are adequately trained and proficient to complete required PQC-related actions, in line with BMS policies, procedures and regulatory expectations Provide experienced based training and mentoring to PQC HYD team and external personnel supporting PQC processing to ensure compliance with regulations Assist in the establishment of quality risk management for complaint handling and promote the understanding of risk management for product quality complaints Leading the HYD surveillance team, accountable for complaint metrics generation as well as monitoring of Key Performance Indicators (KPls) to facilitate improvements for end-to-end complaint process Support Product Surety/Corporate Security and Serialization activities as necessary Grows, develops, engages and empowers team Manage employee related activities for the department (hires, trains, appraises, mentors, motivates, disciplines) The roles, responsibilities and duties prescribed in this job description are descriptive but may not be all inclusive. Qualifications & Experience Bachelor of Science in Life Sciences (Chemistry, Biology) or Health Sciences. Post-graduate qualification preferred. A minimum of 7 years of pharmaceutical industry GMP experience and demonstrated leadership in Quality and/or Compliance discipline with in-depth knowledge of global health authorities regulations and requirements. Experience in a senior role with product quality complaints involving global teams and globally distributed products is required. A minimum of 3 years experience in a people management role is required. Prior employment on a pharmaceutical manufacturing site in a Quality or operations role is an advantage. Fluent in English, with proven professional working proficiency in English for reading, writing and speaking Excellent communication with management, peers, and other functional areas Subject matter expertise in global regulatory requirements and expectations for management of PQCs is required Excellent understanding of product formulation* & presentation* types, defect categories applicable to each, and the inherent risk that defect types pose to patient safety *(Solid Oral Dose, Device/Combination, Topical, Liquid / Suspension / Powder / Freeze-Dried Parenteral etc) Ability to apply critical thinking in a high-volume, fast-paced environment, in the knowledge that decisions taken support patient safety Strong people management expertise and ability to focus on execution of strategic decisions while balance conflicting priorities Ability to effectively lead teams to thrive in a fast-paced, highly regulated environment Strong communication (written and verbal), leadership, influencing & negotiating and collaboration skills Demonstrated ability to influence areas not under direct control to achieve objectives and effectively communicate challenging goals & objectives Demonstrated ability to make and act on decisions while balancing speed, quality and risk Ability to work in a matrix environment and build strong relationships by being transparent, reliable and delivering on commitments A continuous improvement mindset Ability to build and maintain collaborative relationships with stakeholders in multiple geographic locations by engaging transparently, performing reliably, and delivering on commitments Customer and partner focus, including the ability to listen and incorporate feedback from key stakeholders Strong analytical skills and ability to deliver meaningful messaging from data analysis Financial acumen to meet budget for PQC processing Strong working knowledge in software and applications relevant to the role (eQMS eg VEEVA Infinity, ERP eg SAP, artwork eg BAMS, regulatory eg Verity, MS Office - Word, Excel, Powerpoint, Sharepoint) Commitment to Quality

We are hiring for Multiple position in Microbiology Department ; Contact person Mr. Srinivasa M, those who are unable to attend the interview are requested to forward their resumes to email id: naveenkumarp@microlabs.in, jonesnaveenrajp@microlabs.in Candidates are requested to carry their copies of Resume, Mark Sheets, Experience Certificates, Latest salary certificate, pay slips of three months and one photographs. Date & Time: 23rd March,2025 (Sunday). Time: 9.00 AM TO 5.00 PM. Venue: Papaya Tree Hotel A.B. Road, Indore Mega City Circle, Indore, Madhya Pradesh - 453331. MICROBIOLOGY: Position: Sr. Officer/ Executive / Sr. Executive ( Only for male candidates) Vacancy: 15 Qualification : B.Sc/ M.Sc- Microbiology/ BioTech Experience: 2-8 years experience in Sterile Manufacturing facility. Job Profile: Microbiology Analytical Activities (MLT, BET, Stability), Environmental monitoring, QMS activities in sterile manufacturing facility.

Job Description 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. 2-5 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

Role & responsibilities Batch manufacturing must have worked in Beta and cepha section Preferred candidate profile 3years+ experience in OSD-Beta and cepha section face to face interview preferred

Job Summary: The R&D Executive will take care of the research activities for the Agrochemical segment, managing the development of surfactant formulations for the currently popular pesticide active Technical molecules, conduct the performance testing of the products in the Application Laboratory and introduce the new products to suit the customer requirements Key Responsibilities: Manage the agrochemical surfactants preparation and formulation development to cater to the requirements of the pesticide formulation industry Should have knowledge of the basic chemistry of surfactants Should have knowledge of the various commercial surfactants and polymers that go into agro formulations and their key attributes Should have knowledge of the various pesticide Technicals currently in use in the industry and the various types of formulations that are available in the market for these Technicals Should have knowledge of the type of surfactants required to get stable emulsions and dispersions of the active ingredients Understanding of the parameters for testing of formulations as per accepted industry specifications Prepare and introduce surfactants and blends to provide solutions for EC, SC, WP, WDG, OD, SL and other current formulations produced by the agro industry Prepare Recommendation Charts for our range, listing our suitable products against the various agro pesticide technicals, with formulation types Should be able to jointly demonstrate the product performance at the customers end Work closely with the team in developing new products & applications for agro industry Serve as the technical lead in customer meetings Collaborate with the Marketing team to define product performance requirements and manage projects to customer validation. Collaborate with the Marketing team to develop effective sales presentations Partner closely with Marketing team to develop innovative products and explore new business opportunities Initiate projects to explore new opportunities Ensure successful scale-up of new products from lab & pilot plant to full-scale production. Expected Expertise: Experience and knowledge of chemistry of various anionic and nonionic surfactants, ethoxylates, propoxylates, polymeric surfactants and other materials used in agro formulations Hands-on experience in developing and testing of formulations Requirements: B. Sc. / M. Sc. in Organic Chemistry At least 2-3 years of experience in surfactants for agro industry Experience in developing R&D projects, from formulation to commercialization. Excellent communication and project management skills. R&D, Research, Agrochemicals

We are looking for Mid-level energetic, dynamic, task and target oriented Business development person having 8-10 years experiences in business development of Pre-clinical drug Discovery CRO services for NCEs/Peptide/Protac etc. who has very good track record to achieve target and bring revenues for the company within a definite time frame. Location: Bengaluru For this job position CRO experiences for business development is mandatory. We are looking for Mid-level energetic, dynamic, task and target oriented Business development person having 8-10 years experiences in business development of Formulation CRO services in the area of injectable/Semi-solid/Liquid/Gel etc. for Pharma/Herbal/Nutraceuticals/Cosmetic/Personal care products who has very good track record to achieve target and bring revenues for the company within a definite time frame. Location: Bengaluru For this job position CRO experiences for business development is mandatory.

- Manufacturing planning - Monitoring of preparation of BASE & SHADES for Nail Polish - Updating all daily production records - Dispensing of RM & making batch as per SOP . Required Candidate profile - A degree in life sciences, chemistry, pharmacy, or a related field - Familiarity with laboratory equipment and testing methods used in production (e.g., viscosity testers, stability chambers)

Greetings from Elico !! We are hiring for Chemist Freshers and experienced candidates for Hyderabad Location . Please go through the below job description. Type of interview - Only Walk-in interviews ( Face to Face) Role: Chemist Department: QA Division: Instrumentation Division(Manufacturing) Qualification: B.Sc & M.Sc. (Chemistry / Analytical Chemistry)up to 2023. Experience: 0 - 2 yrs only Males Specifications: *Should have good oral and Written communication. *Should have good typing skills. *Willing to Travel. *Should be an energetic and enthusiastic team player. *Good Knowledge on computer. *Ready to give commitment for 2 Years (If Freshers) / 1 Year ( If Experienced). *Certificates are Mandatory Responsibilities: *Demonstrations to the customers. *QA Testing. *Water Testing (no of parameters based on the requirement). Note : Interested candidates walk-in to below address Along with your Resume & Marks sheet xerox copies. we have only walk-in interviews & please don't call to us. Elico Limited B-90, C-56, A.P.I.E, Gate No. 6, Jinkalawada Road Sanathnagar, Hyderabad, Telangana - 500018 Contact : Ravi Teja / 9866005442 / Whats app Land Mark: Near Sanath Nagar Railway station. Google maps - https://goo.gl/maps/2oUHDhVzuhmVF57r5 Regards HR Team

To handle the niche category core customers To provide Clinical Facilitation for the upcoming aesthetic Drs To revive the previous prescribers as well as create new customers To conduct Grow Hands-on workshops in clinic & institutions for Basic & Advance indications along with Complication management To achieve primary and secondary sales targets and growth objectives assigned for his / her territory. Prepare monthly, quarterly sales forecasts and chase it with meticulous planning and Account Management. Establish productive and professional relationships with all the stake holders of his / her territory such as HCPs, Stockists, Pharmacies, Purchase department of different accounts and support staff of the account to name a few. Implement effective sales strategies for his territory under the guidance of the National Head and with the help of Brand promotion, Strategies Implementation and Execution effectively to achieve his territorys budget. Identify the key accounts for negotiation and closing the business agreements. Provide timely feedback and suggestions to the National Head on his / her territorys clients needs. Ensure implementation of CRM and KOL engagement plans in his / her territory in conjunction with marketing and medical affairs team. Identify new potential customers and new market opportunities from his territory. Accountable for his / her territorys Collections / Management of accounts receivables. Prepare & participate in periodic sales review of his territory by the National Head and suggest way-forward to surpass his / her territory revenue targets. Critical Competencies, Skills, Knowledge & attributes: Should be a peoples person with Strong team work attitude. Should possess Professional manners and etiquettes. Self-motivated with a results-driven approach excellent with negotiation skills. Enthusiastic with strong interpersonal skills. High achievement orientation Effective communication skills Should be learning Agile and passionate about sales. Good at using MS Office / EXCEL. Education and Work Experience Requirements: Science Graduate , minimum 4 Years of experience in Derma cosmetics and preferably in Pharma Aesthetic Injectable Sales / Speciality divisions Desirable: MBA / Diploma in Sales & Marketing.

Onesource is looking for IPQA executive/ Sr Executives. Pls find the JD as below. Roles and Responsibilities Perform IPQA activities during formulation development, including batch manufacturing process validation. Conduct BMR reviews for injectable products, ensuring compliance with regulatory requirements. Collaborate with cross-functional teams to resolve quality issues and implement corrective actions. Maintain accurate records of all QA activities, reports, and documentation.

1. Good Documentation Practices, Compliance for Standard Operating Procedures, Quality Management Systems shall be followed. 2. Review and understanding of product related technicalities for smooth transfer of products to Internal Manufacturing facility of Strides or External Facility. 3. Co-ordination and collection of technical documents from internal sites. 4. Review of Tech pack documents and sharing (MFR, MPR, Spec/STP, BMR, BPR, Tool drawings layouts etc.) to Internal or external manufacturing sites. 5. Review of Master documents before initiating validation batches at Internal or external manufacturing sites. 6. Handling of Investigation related to OOS/OOT/Deviation occurred/reported for New Products and Site Transfer Projects. 7. Conducting/Monitoring of Feasibility trials/ Scale up trials at R&D or Manufacturing site. 8. To be involved in cost improvement program for identified product, to change the formula and improvise the process as required. 9. Handling of Product Robustness Projects and related activities like conducting the trials at R&D, Execution and Monitoring of Optimization batches and Registration/Commercial batches for PR projects. 10. Handling of Trouble shooting to improve the product quality attributes. 11. Review of APQR, RCI, CAPAs, PDR and other related documents. 12. Handling of QMS events (CC/Deviations) in Trackwise. 13. Ensure Test license availability at R&D & Plant. 14. Ensuring Toolings and RMs availability for execution of lab trial batches, PO/PE/Scale up batches and monitoring the batches during execution. 15. Preparation and Review of Trial Reports, and Investigational Summary Reports. 16. Preparation and Review of Documents i.e. MFRs, BMRs, BPRs, Protocols/Reports, QRM for Trial/Feasibility, PO and New Products, various batch sizes and subsequent revisions of all kinds. 17. Review & Approval of PVP & PVR. 18. Preparation and review of stability protocol for experimental batches. 19. Initiation/approval of the test request for the analysis. 20. Process optimization activities for internal/external products as identified and assigned. 21. GMP, GDP, Quality Management systems and SOP shall be followed to ensure the continuous compliance.

Dear All, We are seeking a highly motivated and talented Formulation R&D Scientist to join our innovative team. The ideal candidate will have a strong foundation in formulation development and you will play a crucial role in developing new and improved formulations, ensuring product quality, and meeting regulatory requirements. Location: Hyderabad(Dulapally) Required Experience: 6-8 Years Job Responsibilities: 1. Plan and execute Pre-formulation and formulation activities and ensure the timely execution of project related tasks in coordination with team members. 2. Actively participate in the literature search and preparation of formulation development strategy. 3. Coordinate with QA department for getting forms and logbooks 4. Follow good laboratory practices, good documentation practices (online LNB writing) and maintain the logbooks and forms for equipment/instruments 5. Coordination and participation of internal department audits / sponsor or client audits 6. Coordination with purchase/sourcing department for procurement of materials 7. Participation in qualification of equipments/instrument pertaining to the department 8. Compilation, interpretation and review of analytical results and stability data 9. Submission of documents and coordination with liaison personnel for procuring required licenses for carrying out the development work 10. To initiate the project and allot the product identification codes 11. Preparation of Master formula card (MFC), scale up BMR, process evaluation plan, exhibit batch protocols, stability protocol, Dissolution profiling report, Assessment report, Tablet sub division study summary report and all documents related to Formulation development. 12. To drive all concerned documents from formulation development to exhibit batches and then to commercialization through document management system. 13. Coordinate to prepare the specifications for raw materials, in-process and finished product. 14. Preparation of product development reports (PDR) 15. Preparation of summary reports for exhibit and process evaluation batches. 16. Initiation of Change controls. 17. Initiation of document/ mandatory revision/withdrawal control form. 18. Initiation of departmental incidents. 19. Conducting departmental trainings. 20. Calibration of instrument/equipment pertaining to the department. 21. Preparation and processing of department SOPs/Guidelines/Operating instructions. 22. Preparation of summary reports for exhibit and process evaluation batches Note: Interested candidates can share their resumes to raghuveera.vutla@aizant.com and Immediate joiners are more preferable

Roles and Responsibilities Manage process engineering activities for OSD (Oral Solid Dose) injectable products, ensuring compliance with regulatory requirements. Lead a team of engineers to design, develop, test, and commission electrical systems for sterile manufacturing facilities. Collaborate with cross-functional teams to ensure smooth operation of production lines and maintain high-quality standards. Develop and implement process improvements to increase efficiency, reduce costs, and enhance productivity. Ensure effective communication among team members, stakeholders, and senior management.

Cross-Functional Collaboration: Collaborate with R&D, manufacturing, and marketing teams to integrate regulatory considerations into the product development and commercialization processes. Regulatory Submissions: Oversee the preparation and submission of all necessary regulatory new dossier filings, and variations, to relevant health authorities in the targeted regions. Market Intelligence: Monitor and analyze evolving regulatory landscapes and market trends to proactively identify opportunities and challenges. Stakeholder Engagement: Build and maintain strong relationships with regulatory agencies, industry associations, and key stakeholders to facilitate smooth regulatory processes. Team Leadership: Lead and mentor a diverse team of regulatory professionals, promoting a culture of excellence, compliance, and continuous improvement. Compliance Oversight: Ensure all regulatory activities adhere to internal policies and external regulations, managing audits and inspections effectively.

Role & responsibilities: Candidate should have core experience in the field of Technology Transfer. Should have knowledge about documentation, exhibit, scale up, OSD, coating, granulation and compression. Preferred candidate profile: Candidates should have experience in Pharmaceutical background. Qualification: M. PHARM. Experience: 3 to 8 Years

He is responsible for Maintenance Planning ,Scheduling, Team Management, Troubleshooting , Problem Solving ,Break down Maintaince /Analyisis,• Resolve machine breakdowns and execute preventive maintenance Equipment maintenance, Safety compliance Required Candidate profile Resolve machine breakdowns and execute preventive maintenance Equipment maintenance, Safety compliance

Role & responsibilities Preferred candidate profile Perks and benefits

JD – Prepare/Review Design Drawings as project deliverables. Prepare Documents as project deliverables. Knowledge and understanding of relevant Design Guidelines & Statutory Requirements Formulation Projects (Pharma Industry) Required Candidate profile Executive – Projects Qualification – B.E / B.Tech in Mechanical/ Chemical Experience – 5 plus years in Formulation Projects (Pharma Industry) Location – Thane

Preferred candidate profile The candidate MUST BE PROFICIENT IN HPLC & GC HANDLING AND ANALYSIS, as THIS IS A CRUCIAL CRITERIA FOR SELECTION." FDA Approved Candidates will be given preference. Experience In Pharma formulation or External Preparation. Must be excellent in written and spoken English; net savvy and adept at computer skills. Good in communication.

Roles and Responsibilities Develop and implement training programs to enhance employee skills and performance. Conduct Training Needs Identification (TNI) and Gap Analysis to identify skill gaps in employees. Design and deliver soft skills training sessions, including communication, leadership, teamwork, time management, etc. Collaborate with stakeholders to develop customized learning solutions for specific business needs. Monitor the effectiveness of training programs through evaluation metrics such as ROI analysis.

Role & responsibilities Troubleshooting: Leads troubleshooting efforts for mechanical issues, identifying root causes and implementing corrective actions. Preventive Maintenance: Develops and implements preventive maintenance programs to minimize mechanical equipment failures. Also Coordinating with operations teams to minimize downtime. Mechanical Integrity: Ensures mechanical equipment is properly installed, maintained, and repaired to maintain mechanical integrity. Should have experience in Formulation plant and have very good knowledge of handling process and packing equipment like blending, Sifting, milling RMG, FBD, Tablet Compression, coating Bulk counting, cartonating, labelling Root Cause Analysis: Conducts root cause analysis for equipment failures, implementing corrective actions to prevent recurrence. Maintenance Planning: Develops and implements maintenance plans, schedules, and budgets for mechanical equipment. Documentation and Reporting: Maintains accurate records of mechanical maintenance activities, writing reports and presenting findings to management. Continuous Improvement: Stays up to date with industrys best practices. implementing improvements to mechanical maintenance procedures and standards. Should have good knowledge on GMP and GDP. Experience in preparation and facing regulatory audits. Ensuring compliance with safety regulations and Implementing energy efficiency improvements and to perform any other job assigned by the management from time to time. Preferred candidate profile Diploma/bachelors degree in mechanical with relevant 2-4 years of Engineering maintenance experience in organized Pharma/FMCG company. Candidates should have good communication and interpersonal skills.

Role & responsibilities 1. Prepare the validation schedules for new projects, revalidation schedules for existing equipment/utilities as per respective procedures 2. Execute and review of all the qualification/re-qualification protocols and reports pertaining to equipment, utilities, instruments and facilities 3. Responsible to update or review Qualification, Production and engineering related procedures which are compliant to current GXP regulatory norms 4. Responsible for preparation of Validation master plan/Site master file Responsible for reviewing and ensuring all the scheduled activities for Preventive maintenance, filter cleaning, filter replacements, calibrations, Alarm/audit trail reports etc are performed as per the respective procedures within specified time Preferred candidate profile B Pharmacy/Msc Education qualification with 03 to 09 years experiance Perks and benefits Best in industry