Job Title: Marketing and Research Intern Department: Marketing and Research Company: Macsen Laboratories Location: Udaipur Duration: 3 months (In office) Company Description Macsen Laboratories, a pharmaceutical and chemical manufacturing organization with its origin dating back to 1952, is engaged in manufacturing niche Active Pharmaceutical Ingredients, pharmaceutical application dyes, compounds of precious and rare earth metals, and other specialty inorganic compounds. Macsen has also started new verticals of Pharmaceutical Analytical Services, Contract Research, and Custom Synthesis. Headquartered in the city of Lakes, Udaipur (Rajasthan, India), Macsen presently has various manufacturing units in Udaipur. Qualifications - Any Graduate Bachelor's in Marketing, Business, and Science - Knowledge of basic Microsoft Office tools and email. - Good written and verbal communication. Key Responsibilities: ● Research potential new products in the chemical and pharmaceutical sectors. ● Product Research for our e-commerce store. ● Source and evaluate suppliers for materials required for product development. ● Support in organizing product data and maintaining supplier databases ● Provide support in day-to-day marketing and research operations Note- "This is a 3-month internship with the possibility of a Pre-Placement Offer (PPO) based on performance Perks and Benefits - Gain practical exposure in marketing fields. - Stipend and recommendation letter. Show more Show less

Job Title: Purchase Officer Department: Purchase Required Experience: 2 to 3 years Location- Udaipur, Rajasthan Job Overview: As a Purchase Officer, you will play a vital role in ensuring the efficient procurement of goods and services necessary for our operations. Your responsibilities will include sourcing suppliers, negotiating contracts, managing vendor relationships, and maintaining accurate records of purchases. You will work closely with various departments to understand their procurement needs and ensure the timely delivery of materials while adhering to company policies and regulatory requirements. Qualifications: B.Tech in Mechanical Engineering. A Master's degree is preferred in Supply Chain Management. Minimum of 2-3 years of experience in procurement or purchasing, preferably in the pharmaceutical industry. Strong negotiation skills with the ability to build and maintain effective relationships with suppliers. Excellent communication and interpersonal skills, with the ability to collaborate effectively with internal stakeholders and external partners. Proficient in using procurement software and MS Office applications, including Excel, Word, and PowerPoint. Key Responsibilities: Source suppliers and vendors for pharmaceutical raw materials, packaging materials, equipment, and other goods and services required by the company. Evaluate suppliers based on price, quality, reliability, and other factors to ensure the best value for the company. Negotiate contracts, terms, and pricing agreements with suppliers to obtain favorable terms and conditions. Coordinate with internal stakeholders, including store, Engineering, Maintenance, production, quality assurance, and finance departments, to understand their procurement requirements and timelines. Generate purchase orders, review purchase requisitions, and ensure accuracy of orders placed. Monitor and track order status to ensure timely delivery of materials and services, resolving any issues or delays that may arise. Maintain accurate records of purchases, including prices, quantities, and delivery dates, using appropriate documentation and systems. Manage relationships with suppliers, addressing any concerns or issues that may arise, and working collaboratively to resolve them. Stay informed about industry trends, market conditions, and regulatory requirements related to procurement and supply chain management in the pharmaceutical sector. • Implement cost-saving initiatives and process improvements to optimize procurement operations and achieve greater efficiency. Why Join Us? Opportunity to work with a dynamic and supportive team. Exposure to diverse technical challenges and growth opportunities. Competitive salary package and professional growth prospects. How to Apply: Send your updated resume to hrd@macsenlab.com.

Job Description: Head of Quality Experience: 15 Years or more Location: Udaipur About Macsen Drugs: Macsen Drugs is a USFDA registered, WHO-GMP certified, TGA GMP certified, and EU GMP (Written Confirmation) certified manufacturer of active pharmaceutical ingredients or bulk drugs for varied therapeutic applications like antidote, urinary antiseptic, topical antiseptic, ophthalmic diagnostic, anti-dandruff, anti-acne, and several other applications. Job Overview: We are seeking an experienced and detail-oriented individual to perform research activities as designing and conducting scientific experiments, analyzing and interpreting results, leading to significant value to the process development. Efficient contribution to the overall success of the research & development team performance according to objectives and targets set by the Management. Responsibilities: 1. Quality Assurance (QA) Develop and implement a comprehensive Quality Management System (QMS) compliant with cGMP and ICH guidelines. Review and approve quality documents such as SOPs, batch records, deviations, and CAPA reports. Ensure the site is prepared for regulatory audits and inspections from the USFDA, EMA, WHO, and other agencies. Conduct internal audits and self-inspections to maintain quality standards. 2. Quality Control (QC) Oversee laboratory operations, ensuring raw materials, intermediates, and finished products meet established quality specifications. Manage analytical method validations and stability studies. Monitor calibration and maintenance of laboratory instruments. 3. Regulatory Affairs Prepare and submit regulatory documents, including DMFs, for US and international markets. Address regulatory queries and implement corrective actions for observations from audits or inspections. Stay updated on global regulatory trends and ensure compliance with evolving requirements. 4. Production Oversight Collaborate with production teams to ensure manufacturing processes align with quality standards. Oversee cleaning and process validation for a multi-product facility to prevent cross-contamination. Troubleshoot production and analytical challenges in coordination with R&D. 5. Data Integrity and Security Ensure compliance with 21 CFR Part 11 for electronic records, signatures, and data integrity. Establish protocols for data security and governance across all quality operations. 6. Cross-Functional Coordination Work with R&D and Analytical Development Labs for seamless technology transfer and method development. Collaborate with Stores and Maintenance teams to ensure proper inventory management and equipment validation. Coordinate training programs for team members to maintain high-quality standards. 7. Leadership Lead and mentor teams across QA, QC, Regulatory, Production, and Maintenance departments. • Foster a culture of quality, accountability, and continuous improvement. 1. Educational Qualifications Bachelor's or Master's degree in Pharmacy, Chemistry, Biotechnology, or a related scientific field. Additional certifications in Quality Management Systems (e.g., ISO 9001, Six Sigma) are preferred. 2. Experience Requirements Minimum 15 years of experience in API manufacturing, with at least 5 years in a leadership role managing QA, QC, and Regulatory Affairs. Proven experience in handling audits and inspections by regulatory agencies such as USFDA, EMA, WHO, or PICS. Hands-on experience in managing multi-product facilities with cleaning and process validation expertise. How to Apply: Send your updated resume to hrd@macsenlab.com

Job Description: Sales & Marketing Associate Location : Macsen Labs 305, Nirmal Corporate Centre, Near Nirmal Lifestyle, LBS, Mulund West, Mumbai-400080, India. About Macsen Laboratories: Macsen Laboratories, a pharmaceutical and chemical manufacturing organization with its origin dating back to 1952, is engaged in the manufacturing of niche Active Pharmaceutical Ingredients, pharmaceutical application dyes, compounds of precious and rare earth metals, and other specialty inorganic compounds. Macsen has also started new verticals of Pharmaceutical Analytical Services, Contract Research, and Custom Synthesis. Headquartered in the city of lakes, Udaipur (Rajasthan, India), Macsen presently has various manufacturing units in and around Udaipur. Job Overview : We are seeking a dynamic and motivated Sales & Marketing Associate to join our team. The ideal candidate will play a crucial role in driving sales, developing marketing strategies, and strengthening customer relationships. Roles & Responsibilities: Generate qualified leads in intended geographies for all products and services being offered by Macsen Laboratories. Initiate conversations with prospective customers through outbound campaigns such as tele-calling, emails, etc., to build a pipeline of new customers. Understand the products and services offered by Macsen Laboratories to be able to meaningfully communicate their benefits to targeted customers. Identify prospective customers and lucrative geographies to expand Macsens' reach through market and competitor research. Route qualified opportunities to the appropriate sales executives for further development and closure. Drive other marketing campaigns through emails, content writing, etc. Ensure compliance with all legal, regulatory, and safety requirements on the site. Qualification & Skills: Graduate or post-graduate in any discipline (Preferably from a Science Background). Should have excellent written and verbal communication skills. Self-motivated, enthusiastic individual with a high level of integrity and work ethic. Should be flexible with attending to clients as per the time zones in different countries to which they belong. Why Join Us? Opportunity to work with a dynamic and supportive team. Exposure to diverse technical challenges and growth opportunities. Competitive salary package and professional growth prospects. How to Apply: Send your updated resume to hrd@macsenlab.com.

Job Description: Head of Quality Experience: 15 Years or more Location: Udaipur About Macsen Drugs: Macsen Drugs is a USFDA registered, WHO-GMP certified, TGA GMP certified, and EU GMP (Written Confirmation) certified manufacturer of active pharmaceutical ingredients or bulk drugs for varied therapeutic applications like antidote, urinary antiseptic, topical antiseptic, ophthalmic diagnostic, anti-dandruff, anti-acne, and several other applications. Job Overview: The Head of Quality is responsible for ensuring that all products and processes comply with internal and external quality standards, regulatory requirements, and customer expectations. This role will lead the Quality Assurance (QA), Quality Control (QC), and Compliance functions, while driving continuous improvement across operations. Responsibilities: 1. Quality Assurance (QA) • Develop and implement a comprehensive Quality Management System (QMS) compliant with cGMP and ICH guidelines. • Review and approve quality documents such as SOPs, batch records, deviations, and CAPA reports. • Ensure the site is prepared for regulatory audits and inspections from USFDA, EMA, WHO, and other agencies. • Conduct internal audits and self-inspections to maintain quality standards. 2. Quality Control (QC) • Oversee laboratory operations, ensuring raw materials, intermediates, and finished products meet established quality specifications. • Manage analytical method validations and stability studies. • Monitor calibration and maintenance of laboratory instruments. 3. Regulatory Affairs • Prepare and submit regulatory documents, including DMFs, for US and international markets. • Address regulatory queries and implement corrective actions for observations from audits or inspections. • Stay updated on global regulatory trends and ensure compliance with evolving requirements. 4. Production Oversight • Collaborate with production teams to ensure manufacturing processes align with quality standards. • Oversee cleaning and process validation for a multi-product facility to prevent cross-contamination. • Troubleshoot production and analytical challenges in coordination with R&D. 5. Data Integrity and Security • Ensure compliance with 21 CFR Part 11 for electronic records, signatures, and data integrity. • Establish protocols for data security and governance across all quality operations. 6. Cross-Functional Coordination • Work with R&D and Analytical Development Labs for seamless technology transfer and method development. • Collaborate with Stores and Maintenance teams to ensure proper inventory management and equipment validation. • Coordinate training programs for team members to maintain high-quality standards. 7. Leadership • Lead and mentor teams across QA, QC, Regulatory, Production, and Maintenance departments. • Foster a culture of quality, accountability, and continuous improvement. 1. Educational Qualifications • Bachelor’s or Master’s degree in Pharmacy, Chemistry, Biotechnology, or a related scientific field. • Additional certifications in Quality Management Systems (e.g., ISO 9001, Six Sigma) are preferred. 2. Experience Requirements • Minimum 15 years of experience in API manufacturing, with at least 5 years in a leadership role managing QA, QC, and Regulatory Affairs. • Proven experience in handling audits and inspections by regulatory agencies such as USFDA, EMA, WHO, or PICS. • Hands-on experience in managing multi-product facilities with cleaning and process validation expertise. How to Apply: Send your updated resume to hrd@macsenlab.com

Job Title: Purchase Officer Department: Purchase Required Experience: 2 to 3 years Location : Udaipur, Rajasthan Job Overview: As a Purchase Officer, you will play a vital role in ensuring the efficient procurement of goods and services necessary for our operations. Your responsibilities will include sourcing suppliers, negotiating contracts, managing vendor relationships, and maintaining accurate records of purchases. You will work closely with various departments to understand their procurement needs and ensure timely delivery of materials while adhering to company policies and regulatory requirements. Qualifications: • B-tech in Mechanical Engineering. A Master's degree is preferred in Supply Chain Management. • Minimum of 2-3 years of experience in procurement or purchasing, preferably in the pharmaceutical industry. • Strong negotiation skills with the ability to build and maintain effective relationships with suppliers. • Excellent communication and interpersonal skills, with the ability to collaborate effectively with internal stakeholders and external partners. • Proficient in using procurement software and MS Office applications, including Excel, Word, and PowerPoint. Key Responsibilities: • Source suppliers and vendors for pharmaceutical raw materials, packaging materials, equipments, and other goods and services required by the company. • Evaluate suppliers based on price, quality, reliability, and other factors to ensure the best value for the company. • Negotiate contracts, terms, and pricing agreements with suppliers to obtain favorable terms and conditions. • Coordinate with internal stakeholders, including store, Engineering, Maintenance, production, quality assurance, and finance departments, to understand their procurement requirements and timelines. • Generate purchase orders, review purchase requisitions, and ensure accuracy of orders placed. • Monitor and track order status to ensure timely delivery of materials and services, resolving any issues or delays that may arise. • Maintain accurate records of purchases, including prices, quantities, and delivery dates, using appropriate documentation and systems. • Manage relationships with suppliers, addressing any concerns or issues that may arise, and working collaboratively to resolve them. • Stay informed about industry trends, market conditions, and regulatory requirements related to procurement and supply chain management in the pharmaceutical sector. • Implement cost-saving initiatives and process improvements to optimize procurement operations and achieve greater efficiency.

Job Title: ARD Chemist / Scientist Location: Udaipur Job Summary: We are seeking a motivated and detail-oriented individual to join our ARD team. The candidate will be responsible for method development and validation, impurity profiling, and instrumental analysis to support our Synthesis R&D and quality operations. Key Responsibilities: 1 Method Development & Validation Develop HPLC, GC, and LC-MS analytical methods for monitoring in-process reaction samples from the Synthesis R&D team. Develop and validate HPLC methods suitable for AMV (Analytical Method Validation) and transfer to QC. 2 Impurity Profiling & Characterization Perform impurity profiling of APIs and intermediates. Identify and characterize impurities using advanced techniques like mass spectrometry. 3 Instrument Handling & Calibration Ensure all analytical instruments (HPLC, GC, LC-MS, etc.) are maintained in optimal working condition. Perform regular calibration and documentation of analytical instruments. 4 Documentation & Compliance Maintain proper records as per regulatory and internal quality standards. Support preparation of SOPs, protocols, and technical reports. Key Skills Required: Strong knowledge of HPLC, GC, and LC-MS techniques Experience in method development and impurity profiling Familiarity with ICH guidelines and regulatory requirements Proficiency in analytical software like Empower/Chromeleon Good documentation and communication skills

Job Title: Marketing and Research Intern Department: Marketing and Research Company: Macsen Laboratories Location: Udaipur Duration: 3 months (In office) Qualifications - Any Graduate Bachelor's in Marketing, Business, and Science - Knowledge of basic Microsoft Office tools and email. - Good written and verbal communication. Key Responsibilities: Research potential new products in the chemical and pharmaceutical sectors. Product Research for our e-commerce store. Source and evaluate suppliers for materials required for product development. Support in organizing product data and maintaining supplier databases Provide support in day-to-day marketing and research operations Note- This is a 3-month internship with the possibility of a Pre-Placement Offer (PPO) based on performance.

Marketing & Research Intern Job Role Research potential new products in the chemical & pharma sector. Source and evaluate suppliers for materials required for product development. Support in organizing product data & maintaining supplier database

JOB ROLE AND RESPONSIBILITIES ELECTRICAL MANAGER 1. Complete the Brownfield Projects in time. In the future, complete the entire Electrical project of the ongoing Greenfield Project. 2. Prepare BOQ for individual activities; Identify material required as per BOQ; raise an indent; and construct the Projects after procuring the same. Assist Commercial Dept. in vendor finalization and release of PO by proper comparison of the proposals from vendors. 3. Monitor Electrical Projects for proper progress and, after verification of the bills, recommend them for payment. 4. Attend electrical maintenance of the P&M, -PM (preventive)/ Breakdown. 5. Maintaining of necessary critical electrical spares to prevent production downtime. 6. AMC of electrical equipment. 7. Electrical expansion, modification, and erection work as demanded by business growth. 8. Liaise with the Rajasthan EB and SE office related work. 9. Power/Energy saving initiatives. 10 . Electrical equipment yearly testing with reports. 11. Electrical drawings approval, addition/deletion works.

We are seeking a dedicated & skilled Production Officer to join our team. The ideal candidate should have experience in a regulatory-approved manufacturing plant with experience in handling critical production equipment & knowledge of cGMP standards.

Job Description: Store Officer Location: Udaipur About Macsen Drugs: Macsen Drugs is a USFDA registered, WHO-GMP certified, TGA GMP certified and EU GMP (Written Confirmation) certified manufacturer of active pharmaceutical ingredients or bulk drugs for varied therapeutic applications like antidote, urinary antiseptic, topical antiseptic, ophthalmic diagnostic, anti-dandruff, anti-acne, and several other applications. Job Overview: We are seeking a highly organized and detail-oriented Store In-Charge to manage inventory, oversee daily store operations, and ensure smooth material handling. The ideal candidate should have experience in store management, stock control, and coordination with various departments. Key Responsibilities: Manage the overall store operations, including material receipt, storage, and issuance. Maintain accurate records of inventory levels and conduct periodic stock audits. Ensure proper documentation of incoming and outgoing materials. Coordinate with the procurement and production teams for stock requirements. Monitor and maintain stock levels to prevent shortages or overstocking. Implement and oversee store safety measures and housekeeping standards. Identify slow-moving and obsolete stock and suggest corrective actions. Maintain proper labeling, stacking, and storage of materials to ensure easy retrieval. Ensure compliance with company policies and standard operating procedures. Generate and submit reports related to stock, consumption, and wastage. Develop and maintain a database of scientific resources, references, and publications for easy access. Monitor regulatory changes and advancements relevant to the company's research areas. Required Skills & Attributes: Strong knowledge of inventory management and stock control. Proficiency in MS Excel. Good organizational and problem-solving skills. Ability to coordinate with different departments effectively. Attention to detail and accuracy in record-keeping. Who Can Apply? Education: Graduate or Diploma in Logistics, Supply Chain, or a related field. Experience: 3-5 years in store management, preferably in the manufacturing or pharmaceutical industry. If you are a proactive and responsible individual with expertise in store operations, we invite you to apply and be part of our growing team!

As an ARD Chemist / Scientist at our Udaipur location, you will be a key member of our ARD team, responsible for method development and validation, impurity profiling, and instrumental analysis to support our Synthesis R&D and quality operations. Your primary responsibilities will include developing and validating HPLC, GC, and LC-MS analytical methods for monitoring in-process reaction samples, as well as developing HPLC methods suitable for Analytical Method Validation (AMV) and transfer to QC. You will also be tasked with performing impurity profiling of APIs and intermediates, identifying and characterizing impurities using advanced techniques like mass spectrometry, and ensuring that all analytical instruments are maintained in optimal working condition through regular calibration and documentation. In addition, you will play a crucial role in maintaining proper records as per regulatory and internal quality standards, supporting the preparation of SOPs, protocols, and technical reports, and ensuring compliance with ICH guidelines and regulatory requirements. To excel in this role, you must possess a strong knowledge of HPLC, GC, and LC-MS techniques, along with experience in method development and impurity profiling. Familiarity with analytical software such as Empower/Chromeleon, good documentation, and communication skills are also essential for success in this position.,

You will be joining our ARD team in Udaipur as an ARD Chemist / Scientist. Your main responsibilities will include method development and validation, impurity profiling, and instrumental analysis to assist our Synthesis R&D and quality operations. Your key responsibilities will include developing HPLC, GC, and LC-MS analytical methods for monitoring in-process reaction samples, validating HPLC methods suitable for AMV, performing impurity profiling of APIs and intermediates, identifying and characterizing impurities using advanced techniques like mass spectrometry, ensuring all analytical instruments are well-maintained, performing regular calibration and documentation of analytical instruments, maintaining proper records as per regulatory and internal quality standards, and supporting the preparation of SOPs, protocols, and technical reports. To excel in this role, you should possess a strong knowledge of HPLC, GC, and LC-MS techniques, have experience in method development and impurity profiling, be familiar with ICH guidelines and regulatory requirements, be proficient in analytical software like Empower/Chromeleon, and have good documentation and communication skills.,

Job Title: Marketing and Research Intern Department: Marketing and Research Company: Macsen Laboratories Location: Udaipur Duration: 3 months (In office) Company Description Macsen Laboratories, a pharmaceutical and chemical manufacturing organization with its origin dating back to 1952, is engaged in manufacturing niche Active Pharmaceutical Ingredients, pharmaceutical application dyes, compounds of precious and rare earth metals, and other specialty inorganic compounds. Macsen has also started new verticals of Pharmaceutical Analytical Services, Contract Research, and Custom Synthesis. Headquartered in the city of Lakes, Udaipur (Rajasthan, India), Macsen presently has various manufacturing units in Udaipur. Qualifications - Any Graduate Bachelor's in Marketing, Business, and Science - Knowledge of basic Microsoft Office tools and email. - Good written and verbal communication. Key Responsibilities: ● Research potential new products in the chemical and pharmaceutical sectors. ● Product Research for our e-commerce store. ● Source and evaluate suppliers for materials required for product development. ● Support in organizing product data and maintaining supplier databases ● Provide support in day-to-day marketing and research operations Note - This is a 3-month internship with the possibility of a Pre-Placement Offer (PPO) based on performance. Perks and Benefits - Gain practical exposure in marketing fields. - Stipend and recommendation letter.