1756 Gmp Jobs - Page 24

Responsibilities: Chromatographic techniques & System Handling Column Packing(BPG & Chromoflow) TFF System Centrifuge System Filtration, Filter Integrity, Buffer Preparation Expertise in Documentation, GMP Compliance

Participate in internal and external audits (USFDA, EDQM, WHO, MHRA, etc.),Ensure compliance with GMP, ICH, and regulatory guidelines in API manufacturing.Conduct in-process checks and ensure batch release activities are done per quality procedures. Required Candidate profile Experience of QMS software Exposure to regulatory audits and good Manufacturing practices. Strong communication and documentation skills. Sound knowledge of regulatory guidelines ICH, WHO, USFDA

Dear Applicants, Greeting from Biophore India pharmaceutical Pvt Ltd, We have opening for Formulation DQA Department Development Quality Assurance / Formulation Quality Assurance R&D: Handling of QMS documents and Ensure the SOP compliance Review of Formulation Analytical Development Documents & Formulation Product Development Documents. Method Validation and Transfer Protocols and Reports Product development with QbD approach Responsible for ensuring GMP/GLP/GDP compliance in the Formulation and Analytical areas as per the respective SOPs. Review of FRD activities (LNBs, BDRs, PDRs, MFRs and MPR’) SOP’s and Guidelines Preparation and Review and Approval of SOP’s. Responsible for conducting Internal Audits/External Audits for Cross functional Departments in Formulation Division and External Division. Conducting and Coordinating Employee Trainings. Responsible for Review and Approval of Vendor Qualification Should have experience in IPQA and Analytical QA (OSD/Injectable) Ref to Friends or colleagues. Interview Date on 12-07-2025 Company address Plot# 231, IDA Phase -II,, Pashamylaram, Biophore Road, Patancheru, Hyderabad, Telangana, India

Part of Technology Transfer Team (Under R&D vertical ) at Palli location Responsible for Preparation of Master BMR, BPRs and document management. Responsible for coordination with various departments like Regulatory Affairs, Manufacturing, Warehouse, Quality Assurance, Quality Control, Engineering for execution of Scale-up and Exhibit batches. Responsible for reviewing GMP related documents. Responsible to select Equipment at Facility. To facilitate the Change Controls to be logged for various reasons. To initiate the Change Controls due to revision in BMR / BPRs and other PD related changes. To study critical parameters during scale up batches to optimize the CPPs and CQAs. To provide the input related to batch size, process feasibility & process parameters to formulation scientist as per requirement. To monitor and ensure readiness for execution of scale-up / feasibility batches, Exhibit batches with respect to RM, PM & Miscellaneous items. Responsible for reviewing GMP related documents as applicable. To get actively involve in Scale-up and Exhibit batches. Activities other than the defined in the Job responsibility are to be done, as per the requirement of HOD, by following HOD s instruction and guidance. It will be advantage if candidate is having exposure of Infusion bag injectable dosage forms.

1) Analysis of raw material, Drug substance (API), Intermediates, by HPLC, GC, GC-MS, LC-MS, NMR, FT-NIR, UV-Visible Spectrophotometer Instruments. 2) Analytical method development for raw material and finished products (drug products) by HPLC, GC, GC-MS, LC-MS, NMR, FT-NIR, UV-Visible Spectrophotometer, Dissolution Instruments. 3) Preparation and maintenance of volumetric solutions, buffers, etc 4) Calibration of laboratory Instrument like UV-Visible Spectrophotometer, Balances, pH meter, KF Titrator, etc., as per calibration schedule 5) Experience in chemical analysis like, titration, moisture, LOD, sulphated ash, TLC IR, SOR, Clarity of solutions and quantitative solubility tests 6) Exposure of GMP / GLP / GDP in laboratory. 7) Knowledge of separation techniques in chemical separation in chromatography in Normal and reversed phase systems 8) Preparation of Standard operating procedures (SOP) for all the instruments, equipment and procedures. 9) Qualification of instruments

Responsible for ensuring utilities equipments are maintained to the highest level of safety and work to avoid lost time accidents, with immediate response and thorough investigations and corrective actions for all hazardous occurrences and accidents. Lead and Impliment Utility Excellence Program and Op Ex Tools / Op Ex Ways for driving continuous improvement initiatives in department. Responsible for Utility CIP Savings and leading division Engrgy effienceny goals Responsible for setting aggressive goals and targets for the departments functions and track the same by utilizing the KPIs to monitor and improve performance. Responsbile for putting in place preventive & pridiective maintenance programs and ensure that all equipments maintenance are carried out in effective manner. Responsible for ensuring continious engineering support, services and utilities to manufacturing operations and to the plant in general, to achieve plant goals. Lead and manage capital projects and Commission to meet KPIs. Anticipate crisis situations and implement necessary corrective actions at the earliest Collaborate with Regional / Divisional Teams for driving specific UEx initatives for the site. Responsible for encouraging knowledge sharing and the open exchange of ideas within the function. Collaborate with HR Department for recruitment and selection of personnel for the utility function. Responsible for ensuring that contractors working for department are in full compliance with all GMP EHS norms inclusive of local and corporate requirements. Responsible for ensuring all statutory compliances are in place for effective Waste Water Treatment Plant. Responsible for maitaining effective working relationship with Vendors, Statutory bodies as and when requiered. Participate in Internal / External and statutory audits/ inspections for department, also prepare corrective and preventive action plan for gaps if any. JOB FAMILY: Project Management DIVISION: ANSC Nutrition Supply Chain LOCATION: India > Jhagadia : Operation Support TRAVEL: Yes, 25 % of the Time t SIGNIFICANT WORK ACTIVITIES: Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day)

Job Description Executive IPQA M. Pharma/ B. Pharma. Minimum 5 Years Experience in solid dosage form- Tablets (Hormone) Person shall be well versed with manufacturing and packaging operations, Compression Machines, Isolators, Blenders, Bulk packing lines, & Process Validation. Person with Experience in Hormone Facility shall be preferred. Followings will be the responsibilities of the position holder: Ensure compliance to cGMP Regulations, established SOPs, FO/MI and PO/PI and for all operational activities, area and equipment. Perform QA review of executed batch production records and ensure the submission of Batch production record in the document cell. Calibration & maintaining documentation of In-process Quality Assurance (IPQA) instruments. Data back-up activities of IPQA instruments as per defined SOP frequency. Monitor the environmental conditions mentioned in the batch production record and SOP. Certification of batch production records for compliance and stage-wise compliance. Reporting any GMP related discrepancies, non-conformances and deviations to superiors immediately. Collection and entry of data for APR preparation. Line Clearance: Ensure physically that the area and equipment to be used for manufacturing and packaging of next product/batch are free from any material/remnants of previous product. Ensure to prevent mix up and cross contamination. Check for proper environmental conditions with respect to temperature, Relative humidity, differential pressure etc. Ensure that the Batch Production record is completed up to the previous stage. Verify the material with respect to the container labels and quantity from the batch production record. In-Process Checks: Ensure the calibration of instruments for in-process checks. In-process checks as per the approved manufacturing and packaging instructions. Enclose all the printouts generated during in-process checks along with the batch production record. All printouts shall be duly signed after checking. Inform the production manager, supervisor and quality assurance manager about the in-process failure observed during in-process checks. To record all the observations in the Batch Production Record Inspection: Inspection of the Tablets/Capsules as per SOP. Inspection of the Finished Goods as per SOP and clearance of Transfer Ticket by ensuring the quantity and batch details. Sampling: Ensure for usage of appropriate sampling tool for sampling. Ensure sampling device cleaning prior to the sampling. Sampling procedure to be followed as per SOP No. SOP019995 (Sampling of intermediates, finished product and stability samples) & SOP020059 (Collection and shipment of Analytical samples of EU market). Ensure sampling of in-process finished product, process validation, cleaning validation, control samples, EU Lab testing samples & stability samples, Reference & Retention sample as per SOP. Approval: Approval of coding pattern on immediate pack and secondary pack to be verified as per the approved packaging instructions / written procedures. JOB FAMILY: Operations Quality t

Actylis is a global solutions provider with over 75 years of experience, specializing in streamlining the management of critical ingredients and raw materials for our business partners. We offer both sourcing and manufacturing solutions tailored to meet diverse and evolving needs, ensuring a reliable, agile, and secure supply network. Our commitment to customization allows us to create flexible solutions, whether it s a unique specification, custom packaging, or tailored logistics strategies. With deep expertise in quality and regulatory compliance, sourcing and logistics management, analytical services, and R&D support, we reduce complexities and mitigate risks, empowering our partners to focus on growing their business. In furtherance of that goal, Actylis is seeking new members of the team. This expansion, coupled with a comprehensive benefits package, and opportunities for challenge and growth, make Actylis the ideal place to work and thrive. We hope you ll consider joining us! Location: Actylis Ahmedabad Position summary: The Quality Service Specialist primarily supports commercial and customer quality document requests. Key Responsibilities: Develop Goals and Motivations for Excellence in Quality Support Services: Place the interests of the Commercial Team and the Customer first; our success depends on their success. Be highly responsive and timely to the Commercial Team and Customer Key Accounts. Meet deadlines; communicate status and delays to the Team and customers proactively. Pursue an unrelenting quest for quality; use speed and simplicity to achieve goals. Communicate pleasantly and effectively. Demonstrate professional etiquette and courtesy when interfacing with customers. Conduct oneself with the highest level of integrity and business ethics. Commit to teamwork; seek out and use the ideas and skills of all colleagues. Reach for the highest standards of performance; show a passion for winning. Commercial Team Support Function: Curate any and all Commercial Team and direct Customer Requests: Process information received from Commercial Team personnel via SFDC or the shared email inbox. Manage and prioritize information to ensure timely delivery as per the established SLAs. Organize and maintain documentation received in the Quality sharepoint and/or MasterControl and conduct follow-up, as applicable. Liaise with internal and external stakeholders to resolve customer requests. Complies with and adheres to all regulatory compliance areas, policies and procedures. Identifies and implements best practices in Quality Services. Keep all document logs and SFDC task queue up-to-date. Review weekly tasks and responsibilities with direct supervisor. Coordinate the review and signature of CDA/NDAs and QAAs. Coordinate the completion of customer questionnaires, declarations and statements. Update Actylis Statements, Declaration and documents including but not limited to: TSE/BSE, Elemental Impurities, Residual Solvents, GMO, Allergens, Melamine, Prop 65, etc. Respond to Product Information Requests including but not limited to: Specifications, Typical COAs, Certificate of Origin, Test Methods, Shelf-Life Letter, Manufacturer and Supply Chain Information, Packaging Specification/Information, Storage Conditions Statement, Stability Statement, Stability Data, Example Label, etc. Manage product Information packages based on ICH and/or IPEC guidelines. Act as liaison in organizing the timing and set-up of customer audits Qualifications & Experience: Bachelor of Science in Chemistry or related field Quality Systems Knowledge (ISO and GMP) - 2 years experience Industry knowledge preferred Strong communication (oral and written) Accurately apply due dates Meet deadlines Complete tasks Sense of urgency Ability to make sound decisions Ability to multi-tasks Ability to read, understand and apply complex instructions/regulations Stress-management Computer literate Self-motivated, have initiative Analytical Ability to work independently Time-management Attention to detail SUPERVISORY RESPONSIBILITIES: N/A Actylis is an Equal Opportunity Employer. Actylis does not discriminate on the basis of race, religion, color, sex, gender identity or expression, sexual orientation, age, non-disqualifying physical or mental disability, national origin, veteran status or any other basis covered by appropriate law. All employment is decided based on qualifications, merit, and business need.

To Support developing strategies to enter the market for the products in EU , Canada, Australia, Brazil etc. Independent supervision of all regulatory activities regarding dossier review, compilation, submission, approval and lifecycle management of the assigned products. Compilation and maintenance of regulatory documents in the supported business areas; Representation of Regulatory Affairs for SRA countries especially with regard to the regulatory requirements; Co-ordination with the CFT (QA/QC/RND/BD) team members to align the requirements and get it work done smoothly. Problem solving and strategic planning mindset are essential skills for this role with project management skills for collaborating with the BDMs in an entrepreneurial, fast-paced company environment Total Experience : 12 to 15 Yrs preferably in injectable, SOD with a knowledge of GMP. Extensive knowledge of regulatory requirements, but also GMP guidelines, enable to find constructive solutions for sometimes complex issues Characterized by high quality awareness paired with practicality and solution-oriented thinking, as well as flexibility and perseverance Exposure in Regulatory approved companies from EU, Health Canada, TGA ANVISA, WHO, FDA etc. Expected Output (Quantitative/Qualitative) from the role in current or next 1 year Master Dossier compilation, Query resolution Support Business development team by getting on time registrations

Job Description Planning /Analysis (Routine and stability and QBD analysis) of ongoing projects by performing analysis of various tests (e.g. Dissolution, assay, Related substances test, or as per requirement) within given Time. Analytical Method development as per current SOP/guideline wherever required. Regulatory query/Plant Query related analysis for different products. To follow Good Laboratories practice while working. Documentation and compliance and review of data generated on all analytical activities as per the GLP/GMP norms and to keep working place neat and clean. Method transfer at plant. Method equivalency, method verification, pharmaceutical equivalency analysis of Pharmacopeial method. Preparation/review of various documents like method transfer waiver, method equivalency report, cleaning validation report SOP, T-STP/FP STP etc. Coordination with team members, superiors and subordinates within the group and across all relevant groups (customers) to achieve target timelines. Procuring of columns, reagents and miscellaneous items for analytical product development/support. Whenever required give training to subordinates/colleagues to upgrade their knowledge and current requirements. Work Experience 3 to 5 years of experience Education Masters in Analytical Chemistry or Analytical Chemistry Post Graduation in Pharmacy or Analytical Chemistry Competencies

To perform Machine and area clearance during dispensing, manufacturing and packaging operation. To perform sampling of blend, finished product, reserve sample, stability sample, hold time samples and other in-process samples and to manage sampling aids. To carry out in-process checks, AQL and ANSI Sampling as per respective documents viz. protocol,BMR, BPR, SOPs and other GxP documents. To ensure GMP practices at manufacturing shop floor. To verify raw material dispensing activity. To approve batch coding details during packaging operation. Review of executed batch records and release for next processing stage. Preparation and review of CPV data trend. To perform impact assessment of breakdown memo. To initiate change control, unplanned and planned deviation where ever required. To review area, equipment and cleaning log and to ensure proper labelling. To review environmental monitoring record, calibration records and executed Batch Manufacturing and packaging Records and respective electronic records. To perform calibration of IPQA instruments. To ensure appropriate labelling during manufacturing and packaging. Storage, handling and dispensing of printed packing materials. To review and approve packaging artworks, proofs and shade cards. To archive executed documents like BMR, BPR, Hold time Protocol etc. To review and approve the Quality Notification (Viz Change control and Deviation) during Batch Manufacturing/packaging. To monitor and record the environmental condition of label control room. To prepare and revise functional SOPs, wherever required. Activities other than defined in the Job Responsibility are to be done, as per the requirement of HOD, by following HODS instructions and guidance.

Instrumentation Engineer Automated Dairy Plant Department: Engineering & Maintenance Reports to: Maintenance Manager Location: Melmaruvathur Industry: Dairy Job Summary: The Instrumentation Engineer is responsible for ensuring the optimal performance, calibration, maintenance, and integration of all instrumentation and control systems in the automated dairy processing plant. This role supports process automation, ensures compliance with food safety standards, and minimizes downtime. Key Responsibilities: Instrumentation Management: Install, calibrate, troubleshoot, and maintain sensors, flow meters, pressure gauges, transmitters, PLCs, HMIs, SCADA systems, and other control instruments. Ensure all process instruments are calibrated as per preventive maintenance schedules. Automation Support: Work closely with automation and electrical teams to maintain PLC/DCS/SCADA systems (Siemens, Allen Bradley, Schneider, etc.). Assist in programming and modifying logic for process optimization. Monitor and analyze control system performance and suggest improvements. Preventive and Predictive Maintenance: Develop and implement preventive maintenance schedules for all instrumentation and control equipment. Conduct root cause analysis for repetitive failures and implement corrective actions. Compliance and Documentation: Ensure instrumentation and control systems comply with FSSAI, ISO 22000, HACCP, and other dairy industry norms. Maintain documentation of calibration records, loop diagrams, P&IDs, and change management logs. Project Execution: Support new equipment commissioning and automation upgrades. Participate in CAPEX projects related to instrumentation and controls. Team Coordination & Training: Coordinate with production, quality, and maintenance teams for operational excellence. Train technicians and operators on instrumentation handling and basic troubleshooting. Key Skills and Competencies: Strong understanding of process instrumentation and automation in dairy/food industries. Hands-on experience with PLCs, SCADA, VFDs, PID control loops. Familiarity with utility instrumentation boilers, ammonia compressors, pasteurizers, CIP/SIP systems. Analytical thinking, troubleshooting skills, and attention to detail. Knowledge of safety protocols and GMP. Qualifications: B.E./B.Tech in Instrumentation, Electronics & Communication, or related discipline. 1 6 years of experience in a dairy or food manufacturing environment, especially automated plants.

About HCP Wellness At HCP Wellness Private Limited , we are committed to delivering safe, effective, and high-quality skin care, cosmetic, and oral care products. Our culture thrives on scientific excellence, GMP compliance, and sustainable innovation. We believe in empowering our team to lead quality-focused solutions that help build trusted personal care brands. Job Overview We are looking for a Microbiologist to join our Quality & R&D division in Ahmedabad. The ideal candidate will be responsible for ensuring microbiological safety and compliance of all raw materials, bulk, and finished goods used in cosmetic and personal care product manufacturing. Your insights will directly impact product integrity, consumer safety, and regulatory compliance. Key Responsibilities Perform microbiological testing of raw materials, in-process samples, water systems, packaging, and finished goods. Conduct environmental monitoring of cleanrooms and production areas (air, surface, and personnel hygiene). Validate disinfectants, preservative efficacy, and microbial limits as per pharmacopeial standards (IP/BP/USP). Maintain and calibrate laboratory equipment and ensure proper documentation (SOPs, logbooks, test records). Support product stability studies, contamination investigations, and root cause analysis. Coordinate with QA and R&D for batch release, deviation handling, and process improvements. Ensure adherence to GMP, ISO, and regulatory compliance for cosmetic and oral care formulations. Qualifications & Skills Education / Certifications: B.Sc / M.Sc in Microbiology, Biotechnology, or Life Sciences Hard Skills: Expertise in microbial testing techniques (TPC, Yeast & Mold, Pathogens) Hands-on experience with colony counters, autoclaves, incubators, and laminar airflow Familiarity with preservative efficacy testing (PET), D-value & Z-value analysis Knowledge of regulatory guidelines BIS, FDA, ISO, and cosmetic-specific standards Soft Skills: Detail-oriented and accurate in documentation and reporting Strong analytical and problem-solving skills Team player with good communication across departments Ability to handle audits and provide scientific justifications Preferred Experience: 3+ years of hands-on experience in microbiology testing within a cosmetics, pharma, or personal care manufacturing setup Why Join Us? Be part of a growing and future-focused company where your scientific contributions directly shape the quality and safety of consumer products. We offer a collaborative and innovation-driven work culture, aligned with global best practices in personal care manufacturing. Apply Now WhatsApp Apply Now WhatsApp Job Location : Bavla On Call Assistance: HCP HR Talent Acquisition +91 7600217962 +91 9998962424 Email hr@hcpwellness.in career@hcpwellness.in info@hcpwellness.in Job Type: Full-time Perks: Team Outings Cafeteria Soft Skill Training Job Training Health Insurance Office cab/shuttle

About HCP Wellness Private Limited: HCP Wellness is a GMP-certified, innovation-led contract manufacturer specializing in skin care, cosmetic, and oral care products. We believe in quality, consistency, and customer satisfaction fueled by science, safety, and sustainability. Join a growing team where quality meets innovation. Job Overview: We are seeking an experienced QC Microbiologist to support our quality control operations by performing microbiological testing on raw materials, bulk, and finished goods. The ideal candidate will ensure that all products meet regulatory, safety, and quality standards. Key Responsibilities: Conduct routine microbiological testing (TPC, yeast & mold, pathogens) on raw materials, in-process, and finished products. Perform environmental monitoring and maintain hygiene compliance across production areas. Validate sterilization methods and efficacy of preservatives in formulations. Calibrate and maintain laboratory instruments and microbial media as per SOPs. Document and report results accurately in line with cGMP and regulatory requirements. Coordinate with QA, production, and R&D teams for troubleshooting and investigations. Participate in internal audits and assist in regulatory inspections as needed. Required Qualifications: Education: B.Sc./M.Sc. in Microbiology or Biotechnology Hard Skills: Microbial limit testing, preservative efficacy testing, and identification techniques Use of laboratory instruments like autoclaves, incubators, laminar airflow cabinets Knowledge of pharmacopeial methods (IP, USP, BP) Proficient in documentation as per cGMP and SOP protocols Soft Skills: Detail-oriented with strong analytical and observational skills Team collaboration and good communication across departments Ability to manage lab timelines and troubleshoot independently Strong organizational and reporting ability Preferred Experience: Minimum 3 years of hands-on experience in a microbiology laboratory, preferably within a cosmetic, personal care, or pharmaceutical manufacturing setup. Why Join Us? Be part of an R&D-driven, future-focused manufacturing company Collaborative culture that values quality, innovation, and personal growth Competitive compensation, learning opportunities, and a cleanroom-grade work environment Apply Now WhatsApp Apply Now WhatsApp Job Location : Bavla On Call Assistance: HCP HR Talent Acquisition +91 7600217962 +91 9998962424 Email hr@hcpwellness.in career@hcpwellness.in info@hcpwellness.in Job Type: Full-time Perks: Team Outings Cafeteria Soft Skill Training Job Training Health Insurance Office cab/shuttle

About HCP Wellness Private Limited At HCP Wellness , we are committed to delivering high-quality, innovative, and safe cosmetic and personal care products. Rooted in scientific excellence and a customer-first approach, we combine tradition and technology to craft skincare, oral care, and cosmetic solutions that people trust. Our culture is built on integrity, continuous learning, and a passion for wellness. Job Overview We are seeking a detail-oriented and quality-focused Microbiologist to join our dynamic Quality Assurance & R&D team. The ideal candidate will play a vital role in ensuring microbiological safety and compliance of our cosmetic and oral care products, supporting regulatory requirements and brand integrity. Key Responsibilities Perform microbiological testing on raw materials, in-process samples, and finished goods (TPC, Yeast & Mold, Pathogens etc.) Maintain and calibrate microbiology lab instruments and ensure timely documentation. Prepare and standardize culture media as per ISO, BIS, and GMP standards. Conduct environmental monitoring (air sampling, surface swabs, personnel hygiene monitoring). Investigate microbial contamination and implement corrective & preventive actions (CAPA). Work collaboratively with QA/QC, production, and R&D teams to ensure product safety and compliance. Stay up to date with relevant cosmetic microbiology standards and regulatory guidelines (e.g., IS 14648, ISO 22716, FDA, BIS). Qualifications & Skills Hard Skills Strong knowledge of microbiological testing methods and GMP/GLP practices. Proficiency in working with microbiological instruments (Incubators, Autoclaves, Laminar Flow, etc.). Understanding of regulatory requirements specific to cosmetics and personal care manufacturing. Ability to handle and interpret microbial limit tests (MLT), preservative efficacy test (PET), etc. Soft Skills High attention to detail and accuracy. Strong analytical and problem-solving skills. Excellent communication and documentation skills. Team-oriented, self-motivated, and adaptable to a fast-paced environment. Education & Certifications B.Sc. / M.Sc. in Microbiology or related Life Sciences field. Preferred Experience 3+ years of hands-on experience in a microbiology role within a cosmetic, pharmaceutical, or personal care manufacturing environment. Why Join HCP Wellness? Be part of an innovative and ethical company committed to wellness and sustainability. Work in a GMP & ISO-certified facility with a strong quality-centric culture. Grow with a team that values integrity, scientific rigor, and continuous improvement. Apply Now WhatsApp Apply Now WhatsApp Job Location : Bavla On Call Assistance: HCP HR Talent Acquisition +91 7600217962 +91 9998962424 Email hr@hcpwellness.in career@hcpwellness.in info@hcpwellness.in Job Type: Full-time Perks: Team Outings Cafeteria Soft Skill Training Job Training Health Insurance Office cab/shuttle

Research Associate, Cell Culture and Bioassays About Mynvax Mynvax is a clinical-stage vaccine biotechnology company headquartered in Bangalore, India, developing novel, recombinant, and thermostable vaccines against respiratory viral infections, including influenza and RSV. With a pipeline of promising candidates and multiple ongoing collaborations, Mynvax offers a unique opportunity to work at the cutting edge of vaccine development. Role Maintain and passage mammalian cell lines under sterile conditions. Support in vitro bioassays such as ELISA, virus neutralization assays, and cytopathic effect-based assays. Perform RNA isolation, cDNA synthesis, and qPCR for viral load estimation. Assist in the preparation and handling of BSL-2 viruses under appropriate biosafety protocols. Process animal sera or tissue samples for immunological analysis. Maintain laboratory notebooks and electronic records with high attention to detail. Assist with assay optimization, reagent preparation, and documentation for preclinical studies. Ensure compliance with biosafety and quality standards during laboratory operations. Required Qualifications M.Sc. or M. Tech in biotechnology, microbiology, immunology, or related life science fields. 0-3 years of hands-on laboratory experience in academic or industrial settings. Familiarity with mammalian cell culture, ELISA, and virus-based neutralization assays. Knowledge of BSL-2 biosafety practices and handling of infectious materials. Good understanding of basic laboratory techniques and experimental design. Desirable Skills Experience with in vivo sample collection or processing from preclinical models. Exposure to data analysis tools and statistical interpretation of assay results. Prior work in a regulated or GLP/GMP-compliant environment. What Mynvax offers: A dynamic research environment with exposure to cutting-edge vaccine development. Training and mentorship in immunology, virology, and preclinical research. Collaborative environment with growth opportunities and skill development. Competitive salary and full-time employment benefits.

About Us: At HCP Wellness Private Limited , we are committed to delivering premium-quality skincare, cosmetic, and oral care products through innovation, safety, and compliance. Our values emphasize integrity, scientific excellence, and customer-centric solutions across every aspect of manufacturing. We are currently seeking a QC Microbiologist to join our Skin Care & Oral Care Division and ensure our products meet the highest microbiological standards. Role Overview: The QC Microbiologist will play a critical role in maintaining microbiological quality standards across the production of skin care and oral care products. This includes routine sampling, microbial testing, environmental monitoring, and compliance with GMP standards. The ideal candidate will have hands-on lab experience and a proactive approach to product safety and process hygiene. Key Responsibilities: Conduct microbiological testing of raw materials, bulk, and finished products (e.g., TVC, yeast & mold, pathogen testing) Perform environmental monitoring (air sampling, surface swabs, water testing) in production and QC areas Validate and maintain aseptic techniques and microbial limits Investigate microbial contamination and assist in root cause analysis and CAPA implementation Maintain detailed documentation and test records in compliance with GMP and GLP Ensure all QC microbiological equipment is calibrated and maintained Collaborate with QA, production, and R&D teams for continuous improvement in quality standards Stay updated with regulatory guidelines such as BIS, ISO 22716 (GMP for Cosmetics), and FDA Required Qualifications: Education: B.Sc. / M.Sc. in Microbiology, Biotechnology, or related life sciences field Hard Skills: Proficiency in microbial testing (TVC, MPN, Pathogen Detection, etc.) Experience with autoclaves, laminar flow hoods, incubators, and related lab equipment Familiarity with regulatory documentation and SOPs Working knowledge of ISO, GMP, and microbiological quality systems Soft Skills: Attention to detail and strong observational skills Effective communication and reporting skills Analytical thinking and problem-solving attitude Team player with a quality-first mindset Preferred Experience: 3 to 4 years of hands-on experience in QC Microbiology in the cosmetics, skin care, or oral care industry Prior exposure to contract manufacturing or third-party testing labs is a plus Why Join HCP Wellness? Work in a GMP-certified, innovation-driven facility Be part of a growing cosmetic manufacturing leader in India Opportunity to grow with a culture that fosters scientific excellence and quality leadership Apply Now WhatsApp Apply Now WhatsApp Job Location : Bavla On Call Assistance: HCP HR Talent Acquisition +91 7600217962 +91 9998962424 Email hr@hcpwellness.in career@hcpwellness.in info@hcpwellness.in Job Type: Full-time Perks: Team Outings Cafeteria Soft Skill Training Job Training Health Insurance Office cab/shuttle

About Us: HCP Wellness Private Limited is a leading name in the manufacturing of high-quality skincare, cosmetics, and oral care products. As a GMP-certified and innovation-driven company, we are committed to product safety, quality, and excellence. Our work culture promotes integrity, collaboration, and continuous improvement. Position Overview: We are seeking a detail-oriented and quality-focused Microbiologist to support our Quality Control and R&D teams. The ideal candidate will ensure all cosmetic and personal care products meet microbiological safety and compliance standards in line with national and international regulatory guidelines. Key Responsibilities: Perform microbiological testing of raw materials, bulk, and finished cosmetic products. Conduct environmental monitoring of production and packaging areas. Validate and monitor water systems (RO/DM/Water for Injection) for microbial contamination. Prepare and maintain microbiological documentation, reports, and SOPs. Carry out microbial limit tests (MLT), preservative efficacy testing (PET), and pathogen identification. Ensure adherence to GMP, ISO, and cosmetic regulatory norms. Support QA/QC investigations in case of non-compliance or contamination. Coordinate with the R&D and production teams for product formulation safety. Required Qualifications: Education: B.Sc./M.Sc. in Microbiology, Biotechnology, or related life sciences field. Experience: Minimum 3 to 4 years in microbiological testing within cosmetics, personal care, or pharmaceutical manufacturing. Hard Skills: Strong knowledge of microbial limit tests, preservative efficacy testing, and aseptic techniques. Proficient in operating microbiology lab equipment (incubators, autoclaves, laminar flow, etc.). Familiar with regulatory standards (GMP, ISO 22716, BIS, FDA guidelines). Technical writing and documentation skills for lab reports and audits. Soft Skills: Attention to detail with strong analytical thinking. Good communication and team collaboration abilities. Problem-solving mindset with a focus on root cause analysis. Ability to work under pressure and meet tight deadlines. Why Join HCP Wellness? Opportunity to work with a leading third-party cosmetic manufacturer. Culture of innovation, integrity, and continuous learning. Safe and compliant work environment with career growth opportunities. Apply Now WhatsApp Apply Now WhatsApp Job Location : Bavla On Call Assistance: HCP HR Talent Acquisition +91 7600217962 +91 9998962424 Email hr@hcpwellness.in career@hcpwellness.in info@hcpwellness.in Job Type: Full-time Perks: Team Outings Cafeteria Soft Skill Training Job Training Health Insurance Office cab/shuttle

We are looking for a skilled Associate Process Manager to join our team at eClerx Services Ltd. The ideal candidate will have a strong background in IT Services & Consulting and 7-10 years of experience. Roles and Responsibility Manage and oversee the implementation of new processes and procedures. Analyze and improve existing processes to increase efficiency and productivity. Collaborate with cross-functional teams to identify areas for improvement. Develop and maintain process documentation and standard operating procedures. Ensure compliance with industry standards and regulatory requirements. Identify and mitigate risks associated with process improvements. Job Requirements Strong understanding of IT Services & Consulting principles and practices. Excellent analytical and problem-solving skills. Ability to work collaboratively with cross-functional teams. Strong communication and interpersonal skills. Experience with process improvement methodologies. Ability to adapt to changing priorities and deadlines.

We are looking for a skilled Associate Process Manager to join our team at eClerx Services Ltd. The ideal candidate will have a strong background in IT Services & Consulting and 7-10 years of experience. Roles and Responsibility Manage and oversee the implementation of new processes and procedures. Analyze and improve existing processes to increase efficiency and productivity. Collaborate with cross-functional teams to identify areas for improvement. Develop and maintain process documentation and standard operating procedures. Ensure compliance with industry standards and regulatory requirements. Identify and mitigate risks associated with process improvements. Job Requirements Strong understanding of IT Services & Consulting principles and practices. Excellent analytical and problem-solving skills. Ability to work effectively in a fast-paced environment and prioritize tasks. Strong communication and interpersonal skills. Experience with process management tools and technologies. Ability to lead and motivate teams to achieve process goals.

Walk-in at Matoda Were currently recruiting for multiple positions at our SANAND manufacturing facility. If any role aligns with your experience, please bring your updated resume and walk in during the scheduled drive. Please find our current job requirements and venue details mentioned. Requirement : Injectable Manufacturing & Visual Inspection Aseptic operations/ QMS / SKID / Multi-vessel / SVP / Visual Inspector (Senior Officer / Officer / Associate) Experience - 01 to 05 Years Qualification - B. Pharmacy/ M Pharmacy / Msc /Bsc / Diploma / ITI Time and Venue : 12th June 2025, 09:30 Hrs to 14:00 Hrs SATURDAY ______________________________________________________ INTAS, Matoda facility Plot No. 457, 458 Sarkhej Bavla Highway, Matoda Village, Sanand, Taluka, Ahmedabad, Gujarat 382210 ______________________________________________________ We would be pleased if you forward or refer any of your colleagues matching the desired job roles. *Having relevant qualification only can attend the scheduled walk-in.

Walk-in at Matoda Were currently recruiting for multiple positions at our SANAND manufacturing facility. If any role aligns with your experience, please bring your updated resume and walk in during the scheduled drive. Please find our current job requirements and venue details mentioned. Requirement : Injectable Manufacturing & Visual Inspection Aseptic operations/ QMS / SKID / Multi-vessel / SVP / Visual Inspector (Senior Officer / Officer / Associate) Experience - 01 to 05 Years Qualification - B. Pharmacy/ M Pharmacy / Msc /Bsc / Diploma / ITI Time and Venue : 12th JULY 2025, 09:30 Hrs to 14:00 Hrs SATURDAY ______________________________________________________ INTAS, Matoda facility Plot No. 457, 458 Sarkhej Bavla Highway, Matoda Village, Sanand, Taluka, Ahmedabad, Gujarat 382210 ______________________________________________________ We would be pleased if you forward or refer any of your colleagues matching the desired job roles. *Having relevant qualification only can attend the scheduled walk-in.

Proven Experience of working in GMP/GLP and scientific environment. Basic knowledge of Spectroscopic and Biophysical techniques, Peptide chemistry, peptide and peptide characterization (Expertise in any one of the subject). Experience in related compound method development and method validation for Peptide drug product using LC-UV and Amino acid analyzer. Hands on Experience of using SEC-UV SEC-MALS, SV-AUC, CE and data interpretation (Expertise in any one of the techniques and data interpretation). Experience in preparation and review of method development, method validation reports. Knowledge of ICH guidelines and regulatory requirement for peptide product. Team player. Willing to work at different job location as per the team requirement. knowledge of scientific writing will be plus.

Role & responsibilities To plan and procure, evaluate and control on the inventories of Raw materials/Packaging materials as per production requirements. To co-ordinate with purchase department for ensuring timely availability of materials. To co-ordinate with Quality control for timely release of materials as per production requirements. To prepare/review and implementation of SOPs in department. To train the down line personnel for departmental SOP and updates. To ensure adherence to SOPs and cGMP during operation in the department. To prepare and provide MIS reports as per the requirement. To verify and ensure for maintenance and integrity of all cGMP and statutory records. To ensure materials receipt/storage/dispensing are done as per defined procedures with refer to respective MSDS and follow safety requirements. To ensure rejected materials returning/destruction are done as per defined procedures with refer to respective MSDS. To ensure the weighing balances verification/calibration is done as per respective SOP. To ensure environment condition of designated area as per respective SOP. To co-ordinate with engineering department for execution of departmental equipment maintenance as per the preventive maintenance plan. To ensure standard weights/balances/instruments to be calibrated on or before due date of calibration. To ensure defined safety measures are followed by the team during operation. To monitor the receipt/storage/issuance of engineering/misc. materials are done as per defined procedures. To prepare protocol/report for equipment qualification in help of engineering department, Participate to perform the qualification studies. To prepare protocol/report for temperature mapping in area, Participate to perform the mapping study. To ensure in time dispatch of finished goods to the customer with proper documents. To ensure areas are upkeep. To take a lead for initiate/evaluate and timely closer of the change control/deviation. To face the audits. To comply the queries observed during the

Job Title: Consultant / Senior Consultant / Deputy Manager Calc Analyst Experience: 3-8 Years Location: Mumbai, Pune, Gurgaon Role Overview: We are looking for skilled Calc Analysts with strong technical and domain expertise to join a fast-growing team supporting pension and insurance clients in the UK. The ideal candidate will be hands-on with VBA, Excel Macros , and have a solid understanding of Defined Benefit (DB) pension schemes . Key Responsibilities: Design and build calculators based on UK pension/insurance requirements. Write and maintain detailed specification documents for calculator logic. Develop and enhance tools using VBA and Excel Macros . Collaborate with cross-functional teams to deliver high-quality actuarial and analytical solutions. Required Skills: Strong hands-on experience in VBA and Excel Macros (mandatory). Prior experience in UK DB Pension/Insurance domain (mandatory). Ability to interpret actuarial calculations and specifications. Strong documentation and communication skills. Work Model: 5 days a week from office (Mumbai, Pune, or Gurgaon).