Assist with regulatory compliance tasks for the firm. Research and stay updated on relevant financial regulations. Review client documentation and ensure adherence to KYC/AML procedures. Prepare reports and presentations on compliance topics. Maintain accurate records of compliance activities. Skills Strong attention to detail and accuracy. Ability to understand and interpret complex regulations. Excellent research and problem-solving skills. Strong work ethic and commitment to ethical practices.

Inspect raw materials and finished products for quality Ensure consistent quality throughout the production process Perform quality & assist in equipment calibration Maintain inspection records & assist with quality reports Required Candidate profile Education:- Diploma or Bachelor’s in Printing Technology, Packaging, or related fields. Experience:- 0-2 years in Printing and Packaging Industry

Role & responsibilities Operation & Maintenance of ice cream packaging machinery like cone, cup, party pack, extruder, candy packaging lines and end of line equipment like taping machine, check weigher, metal detector, x ray, Homogenizer, mix plant etc., Provide strategic direction to Technicians to operate & maintain the machines to deliver best quality products in required quantity within the scheduled time. Minimize production downtime by ensuring that the maintenance staff are properly scheduled, trained, equipped, and motivated. Manage the preventative maintenance program and monitor critical spare stock. Co-ordinate with other departments like Utility, Production, Quality, Stores, etc., as per requirement. Ensure that maintenance activity is complying to GMPs / ISO:22000 and all related food safety practices. Contribute to continuous improvement in productivity, equipment efficiency, safety, quality, and cost optimization programs. Updating related documents & SAP (PM Module) on time. Academic Degree/ Diploma in Mechanical Engineering. Key Competencies: hands-on experience in food / Dairy / ice-cream packaging machinery operation & maintenance. Ability handles team of 10+ technical people and over 10 production / packaging lines. A disciplined team player who is willing to take initiative, passionate to learn, implement & train others. Good communicator (written & oral) with computer skills (MS Office / SAP PM Module).

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.

Role & responsibilities: Candidate should have core experience in the field of Technology Transfer. Should have in depth 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: 8 to 15 Years

1. To issue the Batch Manufacturing Record, Equipment cleaning record, Logbooks, Analytical Report for raw material, finish product and packing material. 2. Assistance in preparation of SOP of various departments/ preparation of draft SOPs. Required Candidate profile To review manufacturing, store, QC activity. To prepare approved vendor list and maintain vendor qualification. To Attend QR meeting as per schedule Call/ Whatsapp : 91-9327657730 / 9724346949

Roles and Responsibilities Responsible for Analytical Method Validation. Responsible for HPLC/GC instrument handling. Responsible for Daily review of Analytical balance and Daily Temperature monitoring. Responsible to follow analytical procedures and generate online raw data. Responsible for Stability Studies and Analysis. Responsible to operate and analyze of raw materials, In Process, cleaning samples, samples for vendor qualification, Stability samples, standard and Finish product Samples and instrumental method (HPLC / UPLC / GC) and to perform analysis of process validation. Responsible for Daily verification of analytical balance and daily temperature monitoring. Online entry in logbooks of instrument, column, working standard, chemical inventory whenever use. Responsible for in process data review in night shift. Finished product sample receive, entry taken in register and maintain daily status. Responsible to follow all the Standard operating procedures, to give Instructions for housekeeping, cleaning and maintaining the laboratory area. Responsible to follow all the analytical procedures and generates online raw data, Chromatograms, calculation sheets and charts with reviewer signature. Responsible to control and maintain records like protocols, Specification, Standard test procedure, Analytical work record, Standard operation procedure, In- process analysis records, usage log books and status labels during day to day Analysis. Responsible to perform calibration and maintain its records. Responsible to Prepare and maintain record of finished product. Responsible to maintain record of chemicals, glass wares and other lab items of department. Responsible for cleaning, maintenance, and daily calibration of specified instruments. Responsible to maintain records and qualification of primary standards, reference standards and working standards. Responsible for reporting to senior if any abnormality observed during analysis and perform for the out of specification and to investigate the OOS (Out of specification) or OOT (Out of trend)if found and Responsible for maintaining QMS related documents. Responsible to follow various EHS (Environment Health and safety) guideline and use appropriate PPEs (Personal protective equipments) . . Desired Candidate Profile Candidate Should be from Pharma background Candidate Should have excellent knowledge of ICH Guidelines Prefer Who can work in a shift and willing to relocate in Navsari, Gujarat Candidate should have Work Accuracy.

Team leader - Engineering is responsible to assist in the smooth and efficient running of the engineering department in support of all other operating departments. Job Description (a) To monitor fire Alarm / Life safety systems as necessary, to be fully informed of the system operation and to handle emergencies involving the systems. (b) Directing & Preforming maintenance activities in the guest room like plunging toilets, unclogging drains, repairing all types of hardware, electrical equipment including lamps, air conditioners / HVAC and AC ducts. (c) Check for new maintenance requests from the PMS ( Property Management System ) and update remarks once the task is completed. Update the maintenance work order form / Job card and file them. (d) Respond and attend to guest repair requests. Test, troubleshoot and perform basic repair on all types of equipment. Evaluates systems or facilities to determine maintenance or repairs that need to be performed. (e) Responsible to maintain the PM database and works with all team members to improve PM checklists on equipment. (f) Identify capital projects to improve production efficiencies, reduce material loss, improve quality, safety, housekeeping, GMP and other related KPI s. (g) Ensures work areas / the maintenance department is kept clean, tidy and in safe working condition at all times. All team members are responsible for minimizing both the Environmental and Health & Safety effects of the work that they perform (h) Performs other duties as assigned by engineering manager. (i) Ensure proper records are kept relating to all plant and equipment for the hotel including repair and service records. Ensure the proper use and periodic maintenance of all equipment.

Experience of 10+ years in Pharmaceutical / Biotech projects - Preferably Large scale Fermentation handling fully automated PLC/DCS based systems.

Assists in ensuring implementation of all aspects of Product Quality Assurance and Quality System Requirements Ensure production compliance with bottle and packaging specifications as per Alpla Standards Thorough knowledge in inspection and testing of Rigid Plastic Packaging products Complete understanding of testing equipments and procedures Ensure all quality policies, procedures, and work instructions are documented in a clear, simple and concise manner Review of exiting system procedures at regular intervals and fill the gaps. Ensure compliance with all quality programs, including GMP and FSMS Planning for the internal quality audit, Process audit, and Product audit Expert in managing customer complaint through root cause analysis - Hosts periodic customer visits, Interaction with customer and closure of complaints, Effective CAPA and closure of customer complaints, Manages customer complaint process What makes you great 8-10 years of experience B.Sc / B.Tech in Plastic Engg. / Diploma with 10+ yrs relevant background is preferable Computer literate (Excel, Minitab, Power point, Word) Ability to work well with other departments Able to handle multi-task environment with excellent organizational skills What you can expect working with us We facilitate a smooth start through individual and accurate training as well as professional guidance and support. We offer you a challenging task with a high degree of personal responsibility in an international working environment. Dynamic working style in a fast-growing region and a dynamic team

Candidate having 2 to 4 years of Experience in PET Preforms moulding. Candidate is having good material( PET) processing knowledge. Candidate must have good knowledge of handling Husky preform moulding machine. Candidate must have good knowledge of Resin Dryer like Piovan and Plastic system. Candidates have the ability to work independently and as part of a team. Knowledge of systems Like 5S, GMP and GDP. The candidate has good interpersonal and communication skills. What makes you great 1. Experience: 2 to 4 Yrs. 2. Qualification: Diploma - Electrical, Mechanical. Plastic-CIPET-PPT/DPT 3.Industry: Manufacturing 4. Gender: Male 5. Position: Tech -I/Tech -II 6.Salary: As per Industry Standards

The Purpose of the Specialist role is having expertise in Extractables and Leachables assessment, work in close collaboration with multiple functions such as MS&T, Supplier management, Regulatory, Toxicology, Procurement, Quality and Production. The individual plays a key role in support of Extractable and Leachable activities with a strong focus on data collection, Risk rating, assessments and evaluation. Job Description Location - Hyderabad Key Responsibilities: Extractable and Leachable (E&L) Expertise Understanding of Extractable and Leachable (E&L) risk assessment for materials based on supplier information and the ability to determine the risk level and update the Risk assessment. Building a comprehensive material library backed by corresponding E&L test data Managing the coordination for Extractables studies or product-specific leachable studies. Preparation of E&L Risk assessment, E&L testing Protocol and Report. Compile E&L data and provide the information to Toxicologist for assessment. Proficient in risk evaluation, decision matrix, Gap Analysis, and outcome understanding manufacturing materials. Comprehensive knowledge of the chemical and physical properties (leaching tendency) of MOC materials Skilled in defining the Original risk level, Mitigation factor, and Final risk level as part of the Risk Assessment process. Expertise in Extractable studies, their methodologies, analytical strategies, and design Expertise in setting the AET (Analytical Evaluation Threshold) and SCT (Safety concern threshold) for extractables and leachables detected during testing. Detailed understanding of E&L guidelines (SOPs, Pharmacopoeia and ICH standards) Proficient in identifying and assessing the Worst-case material representative approach. Collect the material list and data information from development centers and manufacturing sites. Active participation in E&L taskforce and network meetings. Also responsible for coordinating with the development, Supply management, QC, and Production department. Commitment to Diversity & Inclusion: : We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Essential Requirements: Preparation of process and cleaning validation documentation (Protocols, reports) as well as change evaluations for new product launches and Life cycle management activities. Ensure project tracking documentation/tools are updated according to plan Collaborate closely with the development organization (or sending site) for technical transfers and new product launches to ensure knowledge transfer, appropriate control strategies, risk analysis and control, and readiness for commercial process validation Ensure that data integrity checks are conducted to verify that all the data is complete, consistent, and free from errors before proceeding with any further analysis or reporting Coordination of documentation review with the site MS&T, QA, and QC, also Reg CMC where applicable Preparation, approval and life cycle management of Gxp documents Training Own the Training Curriculum for Own Job Profile Desirable Requirements: Bachelors degree in pharmacy, Pharmaceutical Technology, Chemical Engineering, Biotechnology, Chemistry, or equivalent science streams. Desirable MSc/MS. or equivalent experience. Min 5 years of experience in MS&T or in the manufacturing of pharmaceutical Drug substance and Product for Small and Large molecules. Should be familiar with regulatory guidance on ICH Q3,Validation, Product filing and Post approval changes. Proven project management experience in a cross-functional environment (e.g. multi-site, technical development, other functions). Expertise in reviewing and writing technical reports Good communication, Presentation and Interpersonal skills. Proficiency in English (oral and written) is required.

Officer/ Sr. officer Quality About Us Godrej Agrovet Limited (GAVL) is a diversified agribusiness company dedicated to improving the productivity of Indian farmers by innovating products and services that substantially increase crop and livestock yields. With FY 2023-24 sales of more than Rs.6300 Crore, GAVL has interests in Animal feed, Oil palm plantations, Agro-chemicals and Poultry processing. Godrej Agrovet has 62 manufacturing facilities across India with a network of ~20,000 rural distributors/dealers and over 3000 employees. About Godrej Industries Limited and Associate Companies (GILAC) GILAC is a holding company of the Godrej Group. We have significant interests in consumer goods, real estate, agriculture, chemicals, and financial services through our subsidiary and associate companies, across 18 countries. www.godrejindustries.com About Godrej Agrovet Limited (GAVL) Godrej Agrovet At Godrej Agrovet, a food and agriculture conglomerate, we are dedicated to improving the productivity of Indian farmers by innovating products and services that sustainably increase crop and livestock yields. https://www.godrejagrovet.com/ Animal Feed One of the largest organized players in the Compound Feed market in India, our Animal Feed business clocks over a million tonnes in annual sales. We have a diverse portfolio of products across cattle, broiler and layer feed. Our state-of-the-art manufacturing plants, equipped with quality assurance labs, help farmers improve farm productivity and profitability. We are also investing significantly in cutting-edge research and development to support our innovation pipeline. https://www.godrejagrovet.com/businesses/animal-feed Your Role Summary Verification and approval for Raw material, premix and finished goods analysis reports Handling of Lab Instruments and analytical procedure validation Upgradation of quality plan for Raw material and finished goods Complaint receiving, investigation and closing with feedback, RCA and CAPA Ensure lot wise analysis reports and batching accuracy for in process Raw material & Finished Product FIFO monitoring Monitoring of high value raw materials oxidation/heat generation Ensure forward and backward traceability system Pre-dispatch checking of finished goods before loading. Implementing and standardizing QC protocol (GMP, AOAC, AOCS and ISO methods) Validation and verification of CCPs (Critical Control Points) Preparation of Training Material as per need identification Internal audit plan and execution . Required Qualification: Qualification: B. Sc Chemistry, Post-Graduation: M. Sc (Science) Chemistry. Experience: 5 - 8 years' experience in Laboratory Analysis and control (Preferably from Feed/ Food / FMCG industry), Knowledge in SAP would be an added advantage Department: Quality Assurance/ Control. If this sounds like a role for you, apply now! We look forward to meeting you. Non-Disclosure Note: The intellectual property contained in this document is restricted between the intended recipient to whom the document has been forwarded and is deemed confidential and protected by law. contact-7483002795 Email-divyapomar05@gmail.com

Role & responsibilities JOB DESCRIPTION We are looking for a Food Technologist to manage production and quality control in our beverage manufacturing unit. The role involves overseeing daily production activities, ensuring product quality, conducting in-process checks, and maintaining compliance with FSSAI and food safety standards. The candidate should have experience in beverage production or food manufacturing with a strong understanding of GMP and HACCP guidelines. Key Responsibilities: Production Management: Supervise daily production activities to ensure smooth operations and timely completion of production targets. Coordinate with the team to maintain efficient workflow and minimize downtime. Quality Assurance & Control: Conduct in-process quality checks to ensure product consistency and compliance with FSSAI standards. Monitor raw material and finished product quality to meet established specifications. Compliance & Documentation: Ensure adherence to GMP, HACCP, and other food safety standards. Maintain detailed records of production processes, quality checks, and deviations. Process Improvement: Identify areas for process optimization to enhance product quality and production efficiency. Assist in implementing formulation changes or new product trials. Equipment & Hygiene Management: Oversee cleaning and sanitation of production equipment and ensure proper CIP (Cleaning in Place) protocols are followed. Team Coordination: Collaborate with cross-functional teams, including R&D and supply chain, to ensure smooth production planning and inventory management.

Role & responsibilities :- 1) Knowing HPLC/ GC, Dissolution, UV, FT-IR, Potentiometer Troubleshooting, Calibration, Method Validation and Method Development. 2) Perform the analysis individually for In process and stability samples as per plan. 3) Follow Good manufacturing practices, Good laboratory practices and Good documentation practices in ADL. 4) Method Development of new products for test like Cleaning, Assay, Residual solvent, Dissolution & organic impurities. 5) Preparation, storage and usage of Volumetric / Reagent / Standard / Indicator solution. 6) Perform the calibration and verification of all instrument / equipment as per calibration scheduled. Preferred candidate profile :- Post Graduation in M.Sc. Analytical Chemistry ./M. Pharma From Pharma Background Industry. Knowing GCMS, LCMS is added advantage Perks and benefits :- As per company

Role & responsibilities Responsible to receive, register and analyze batch samples and stability samples. Responsible to prepare reagents, buffers and test solutions as and when required. Responsible to operate, calibrate/ verify/ qualify HPLC, UPLC instruments. Responsible to execute the Analytical Method validations/verifications/Transfers Responsible to prepare SOPs, STPs, Protocols and other GMP documents Responsible to interpret and record the data / results accurately and contemporaneously. Responsible to report to superior any abnormalities found during routine activities Responsible to follow Hygiene, Safety, SOPs, GLP, GMP and GDP. Preferred candidate profile Adequate testing knowledge on Biologics/Monoclonal Antibodies Capillary Electrophoresis : CESDS-R, CESDS-NR HPLC : RP, SEC, Glycan, CEX, Ion exchange chromatography and Polysorbate 20 Maurice : charge variants by iCEF UPLC : Peptide mapping. Qualification and Experience : MSc Biotechnology/Biochemistry/Microbiology with 03-07 Years experience of Biosimilars/Biologics QC.

Job Description Company: GreenSignal Bio Pharma Pvt Ltd Location: Gummidipoondi, Chennai, Tamil Nadu Experience: 1-12 years above in production, preferably in the Bio-Pharmaceutical industry, specifically in vaccine manufacturing Educational Qualification: MSc Microbiology/Biotechnology/B. Pharm/B.Tech with more than 8 years of experience in vaccine biologicals and injectables Job Title: Senior Manager / Manager / Executive- Production Job Summary: The Senior Manager /Executive - Production will oversee daily vaccine manufacturing operations, ensure compliance with regulatory guidelines, manage production staff, and drive continuous improvement to enhance operational efficiency and product quality within the pharmaceutical industry. Key Responsibilities: Production Planning and Coordination: Plan, coordinate, and optimize end-to-end vaccine production activities to meet quality standards, timelines, and cost targets while ensuring resource availability. Oversee Manufacturing Operations: Supervise day-to-day manufacturing operations, including formulation, filling, packaging, and storage processes, ensuring efficient workflow and compliance with production protocols. Compliance: Ensure adherence to Standard Operating Procedures (SOPs), Good Manufacturing Practices (GMP), and regulatory guidelines (FDA, EMA, WHO). Issue Resolution: Troubleshoot and resolve production-related issues to minimize downtime and ensure batch integrity. Team Management: Lead and manage production staff, providing training on safety, quality, and operational protocols specific to vaccine manufacturing. Performance Monitoring: Track key production metrics, implement strategies to improve batch yields, and reduce material wastage. Safety Enforcement: Enforce workplace safety protocols to prevent accidents, contamination, and ensure bio-safety compliance. Risk Management: Identify risks in production processes, such as contamination risks or equipment failures, and develop contingency plans. Material Handling: Ensure safe handling, storage, and disposal of biological materials, vaccines, and hazardous chemicals following industry best practices. Process Improvement: Drive continuous improvement initiatives to enhance production efficiency and product quality. Equipment Management: Oversee the maintenance, calibration, and validation of production equipment to ensure optimal performance. Documentation and Reporting: Ensure accurate documentation of production activities and prepare reports for regulatory compliance and internal audits. Skills and Competencies: Strong leadership and team management abilities in vaccine manufacturing environments In-depth knowledge of GMP, regulatory compliance, and vaccine production protocols Proficient in production planning, batch processing, and process optimization Excellent problem-solving and troubleshooting skills within pharmaceutical production settings Strong communication and interpersonal skills for effective team coordination Risk assessment and mitigation capabilities specific to biological production Commitment to bio-safety, product quality, and continuous improvement About GreenSignal Bio Pharma Pvt Ltd: GreenSignal Bio Pharma Pvt Ltd is a leading pharmaceutical company dedicated to delivering quality healthcare solutions, with a strong focus on vaccine manufacturing and biological products. Our commitment to innovation, compliance, and operational excellence drives our success. For more information, please visit our website: www.gsbpl.com How to Apply: Interested candidates can apply at: hr@gsbpl.com Contact us at: 8778926365 Apply Now to join our team and contribute to impactful pharmaceutical and vaccine innovations!

• Responsible for planning, execution & commissioning of new projects within specific time frame. • Planning & execution various projects at plant level in regards with new facility development, Energy Management & other facility up gradations in regards with GMP & Safety. • Co-ordination with suppliers for Material and services as required for implementation of projects. • Responsible for preparing monthly and yearly budget for projects. • Responsible for implementing good engineering practices during project . • Responsible for implementing new technologies, cost and resource saving techniques and new innovation during projects for improvement and cost saving

Res. 4 overseeing the production of softgel capsules in a pharmaceutical Mfg. facility, ensuring the Qlty. & consistency of the final product by accurately measuring & mixing RMs & adhering to strict GMP regulations throughout the Mfg. process. Required Candidate profile BSc or related science field with Extensive Exp. of 1-2 Yrs in pharmaceutical Mfg., particularly softgel encapsulation. Knowledge of GMP regulations and quality control procedures.

Res. 4 ensuring that all MFG. processes & products adhere to established Qlty Stds. & regulatory reqs., by conducting audits, reviewing docs., investigating Qlty issues, & Impl. corrective actions to Mtg. the safety & efficacy of Pharma products. Required Candidate profile BSc or related science field with 1-2 Years of Relevant experience in the pharmaceutical industry, preferably in quality assurance.

Res. 4 overseeing QC processes within a Mfg. facility, ensuring that all products meet regulatory stds., & cGMP guidelines by managing doc., conducting IAs, & collaborating with Prod. teams to Mtg. product Qlty. throughout the Mfg. cycle. Required Candidate profile BSc or related science field with Exp.2-5 Yrs & Strong understanding of cGMP regulations & quality principles in pharmaceutical Mfg. & QA. Excellent analytical and problem-solving skills.

Responsible for overseeing all engineering aspects of a pharmaceutical manufacturing facility, including maintenance, project management, facility upgrades, and ensuring compliance with regulatory standards. Required Candidate profile BE or related science field with Extensive Exp. of 2-4 Yrs of Extensive Exp. in pharmaceutical Mfg.Engg. & Strong u/s of GMP regulations & Qlty. Stds. Expertise in project management methodologies

Job Title: Executive / Manager/Senior Manager Quality Control Department: Quality Control (QC) Company: Greensignal Bio Pharma Pvt Ltd Location: Gummidipoondi, SIPCOT, Chennai Position Overview: The Manager/Senior Manager of Quality Control (QC) at Greensignal Bio Pharma Pvt Ltd is responsible for developing, implementing, and managing quality control strategies and activities. This role ensures that all quality control processes are compliant with industry regulations and align with organizational goals. The individual will lead various quality control activities, such as sampling, testing, inspection, and documentation, while ensuring compliance with regulatory standards. Key Responsibilities: Develop and implement quality control strategies that align with organizational goals and regulatory standards (e.g., FDA, EU, WHO). Collaborate with cross-functional teams to ensure alignment of quality control objectives across departments. Oversee quality control activities, including sampling, testing, inspection, and documentation, ensuring compliance with internal and external standards. Ensure all quality control activities meet required regulatory standards (e.g., FDA, EU, WHO), and implement corrective actions when needed. Develop, maintain, and review quality control procedures, policies, and documentation to ensure consistency and compliance. Conduct internal audits to evaluate compliance with quality control procedures and identify areas for improvement. Collaborate with the regulatory affairs team to ensure timely and accurate submission of quality control documentation for regulatory filings. Provide training, guidance, and coaching to team members, ensuring they possess the necessary skills to perform quality control tasks effectively. Communicate quality control results, non-conformances, and corrective actions to cross-functional teams in a timely manner. Identify opportunities for continuous improvement in quality control processes and implement initiatives to improve efficiency and compliance. Minimal Qualifications: Education: Masters degree in Microbiology, Life Sciences, Pharmacy, or a related field (M.Sc. Microbiology preferred). Experience: Minimum of 8 years of experience in quality control, preferably in the pharmaceutical or biotechnology industry. Knowledge: Strong understanding of regulatory requirements (e.g., FDA, EU, WHO), microbiology, instrumentation, EMP, failure investigation, and related documentation. Skills: Excellent leadership and project management abilities. Strong written and verbal communication skills. Ability to collaborate effectively with cross-functional teams. Preferred Qualifications: Experience with global regulatory filings and compliance audits. Certification in Quality Management Systems (e.g., ISO 9001, Six Sigma). Expertise in advanced microbiological testing techniques. Personal Attributes: Strong problem-solving skills with keen attention to detail. Proactive and able to thrive in a fast-paced, dynamic environment. Ability to motivate, inspire, and develop team members. To Apply: Please submit your resume and cover letter detailing your qualifications and experience to the following contact details: Email: hr@gsbpl.com Mobile: 8778926365

• Responsible for analytical documents review, filing after approval for: • Batch Analysis • Method Validation and Method Transfers • OOS / OOT Investigations • Stability Protocols, Reports, Data • Certification of standards • Review of Specifications and Test Methods • Review of Calibration and Qualifications of Analytical Instruments • Audit trail review • Should understand all analytical instruments like HPLC, GC, Spectrophotometers, Other analytical instruments • Understanding of good laboratory practices in Quality control and Analytical Development and Validation • Understand 21CFR Part 11 requirements, Audit trail reviews, GMP requirements, ICH guidelines on Specifications, Method validations.

• Responsible for Operations of Quality control • Implementation of all Quality control procedures, Maintaining and Upgrading systems and processs in Quality control to meet most stringent regulatory requirements (GMP / GLP) • Handling all Regulatory audits, Client Audits, Internal Audits in QC • Planning and coordination for analysis and release of Input, Inprocess, Final products in time • Planning and management of resources for Quality control – Instruments, Chemicals and consumables, Manpower. • Providing all documentation and other necessary support for Regulatory for product registrations and life cycle management from Quality control