Title: Production chemist. Company : Sinterx Pharma Private Limited Location : Valigonda, Choutuppal. Job Description for Production Chemist. Searching for a reliable and highly skilled Production chemist (2 to 5 years) for an emerging Pharmaceutical Manufacturing company called Sinterx Pharma Pvt Ltd. Based out of Hyderabad, Sinterx is a rising company in the industry with deep relations with various high-stakes players in this industry and a dedicated and motivated team. Responsibilities: Assist in the Preparation and execution of chemical Production Batches, following standard operating procedures (SOPs) to ensure accurate and consistent product quality. Safely manage pyrophoric reagents, Raney nickel, and operate pressure reactors (autoclave) in line with company policies Perform the filtration of low-melting solids and ensure optimal filtration techniques are applied. Report any deviations from specifications and work with the senior chemist to troubleshoot and rectify issues. Maintain accurate records of production activities, Including Batch records, test results, and any deviations from standard procedures. Generate reports and summaries as required by the production and quality control teams. Adhere to safety protocols and guidelines to ensure a secure working environment. Identify and report any safety hazards or concerns promptly. Operate production equipment such as reactors, mixers, and Filters. Perform routine maintenance on equipment to ensure functionality. Work closely with cross-functional teams, including production, quality control, and research and development. Communicate effectively with team members to ensure a smooth production process. Actively participate in process improvement initiatives to enhance efficiency and Product quality. Propose ideas for optimizing production workflows. Qualifications and work experience required: Candidates with an undergraduate or postgraduate degree in chemistry [B. Sc (Chemistry)/ M. Sc (Chemistry)] from a reputed university with high academic achievements may apply. Individuals with up to 5+years of experience in the pharmaceutical Production sector. Strong willingness to learn, adapt, and work effectively as part of a team. A desire to gain experience in leading and contributing to Production. Excellent communication skills, with the ability to present complex scientific concepts to both technical and non-technical audiences. Strong problem-solving abilities and a creative mindset to drive innovation and overcome scientific challenges. Physical demand/Factors: • While executing the responsibilities of this role, the employee must meticulously monitor the production processes undertaken or delegated to them, keenly observing any deviations in the chemical reactions or equipment performance. This necessitates strong visual acuity to detect subtle changes in processes, fine motor skills for precise operation and adjustment of production equipment, and the ability to sustain focus for extended periods. Additionally, the employee should possess the physical endurance to stand or move across the production floor for prolonged durations, handling machinery and monitoring production activities. Adherence to safety protocols, including the appropriate use of personal protective equipment, is imperative due to potential exposure to hazardous chemicals and heavy machinery during production operations. • The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. This job description is not all-inclusive. It acts as a guideline and is subject to change over time. Additional duties may be assigned based on business needs. If you are Interested in the job Position, forward your resume to hr@sinterxpahrma.co
You are invited to join Sinterx Pharma Private Limited as a Production Chemist where you will play a crucial role in the manufacturing of pharmaceutical products. Sinterx Pharma Pvt Ltd is an emerging company based in Hyderabad, with a dedicated team and strong industry connections. **Responsibilities:** - Assist in the preparation and execution of chemical production batches following standard operating procedures (SOPs) to maintain product quality. - Safely handle pyrophoric reagents, Raney nickel, and operate pressure reactors (autoclave) in accordance with company policies. - Conduct filtration of low-melting solids using optimal techniques. - Report any deviations from specifications and collaborate with senior chemists to troubleshoot and resolve issues. - Maintain accurate records of production activities, including batch records, test results, and deviations. - Generate required reports and summaries for production and quality control teams. - Adhere to safety protocols and guidelines to ensure a secure working environment. - Operate production equipment such as reactors, mixers, and filters. - Perform routine maintenance on equipment to ensure functionality. - Collaborate with cross-functional teams for smooth production processes. - Participate in process improvement initiatives to enhance efficiency and product quality. - Share ideas for optimizing production workflows. **Qualifications and work experience required:** - Bachelor's or Master's degree in chemistry (B. Sc (Chemistry)/ M. Sc (Chemistry)) from a reputed university. - Minimum 2-5 years of experience in pharmaceutical production. - Strong willingness to learn, adapt, and work effectively in a team. - Excellent communication skills for technical and non-technical audiences. - Strong problem-solving abilities and a creative mindset for innovation. **Physical demand/Factors:** - Meticulously monitor production processes, observe deviations, and adjust equipment. - Strong visual acuity, fine motor skills, and ability to sustain focus for extended periods. - Physical endurance to stand or move across the production floor for prolonged durations. - Adherence to safety protocols and proper use of personal protective equipment. This job description serves as a guideline and may be subject to change over time. If you are interested in this position, kindly forward your resume to hr@sinterxpahrma.co.,
Title: QC- Chemist Company : Sinterx Pharma Private Limited Location : Valigonda, Choutuppal. Position Description: The QC Chemist with 5 to 8 years of experience is responsible for leading and executing complex analytical testing of API intermediates to ensure compliance with predefined quality standards and regulatory guidelines. This role includes conducting advanced testing, reviewing analytical data, supporting investigations, mentoring junior analysts, and contributing to continual improvement initiatives. The QC Chemist plays a key role in maintaining product quality throughout the production lifecycle by collaborating closely with Quality Assurance, Production, and R&D teams. Educational Background: Bachelor’s or Master’s Degree in Chemistry , Pharmaceutical Sciences , or Life Sciences Work Experience: 5 to 8 years of experience in Quality Control within the API or API Intermediate manufacturing industry Hands-on experience in instrumental analysis (HPLC, GC, UV, IR, KF, etc.) and wet chemistry techniques Strong understanding of regulatory guidelines (GMP, ICH, FDA, etc.) and data integrity practices Key Responsibilities: Perform routine and non-routine analysis of raw materials, intermediates, and in-process samples using validated methods and instruments. Conduct instrumental analysis using HPLC, GC, UV, FTIR, KF , and ensure proper calibration and maintenance. Review and interpret analytical data, ensure compliance with internal specifications and regulatory standards. Identify and investigate deviations, OOS/OOT results , and support CAPA implementation in collaboration with QA. Lead or assist in method validation, method transfer , and stability studies for intermediates. Ensure strict adherence to GMP, GLP, and ALCOA+ principles in all documentation and laboratory practices. Maintain and review laboratory documentation including test records, logbooks, equipment usage logs , and analytical reports . Support internal and external audits by preparing necessary documentation and responding to audit findings. Provide technical support and training to junior analysts , ensuring adherence to safety, quality, and compliance standards. Collaborate with Production, QA, AR&D, and Regulatory Affairs for continuous improvement and troubleshooting. Required Skills: Advanced analytical and problem-solving skills Proficiency in handling and troubleshooting analytical instruments (HPLC, GC, etc.) In-depth knowledge of ICH guidelines , GMP regulations , and data integrity principles Strong documentation and reporting abilities Ability to work independently and as part of a cross-functional team Experience in investigation and risk assessment processes Familiarity with LIMS, Empower, or similar laboratory data systems (preferred) Key Attributes: Detail-oriented with a focus on data accuracy and compliance Good communication and interpersonal skills Ability to handle multiple tasks and meet deadlines in a fast-paced environment Commitment to continuous learning and process improvement If you are Interested in the job Position, forward your resume to hr@sinterxpahrma.co
Position Title: QA Chemist (Team Member) Company Name: Sinterx Pharma Private Limited Location: Valigonda, Choutuppal. Description: The QA Chemist with 5 to 8 years of experience is responsible for ensuring that all API intermediate manufacturing operations comply with established quality standards, GMP requirements, and regulatory guidelines. This role involves reviewing and approving GMP documentation, overseeing batch records, managing deviations and CAPA, conducting internal audits, and ensuring continuous compliance across the production lifecycle. The QA Chemist will collaborate with cross-functional teams including Production, QC, and R&D to maintain quality excellence and support regulatory inspections. Educational Background: Bachelor’s or Master’s Degree in Chemistry, Pharmaceutical Sciences, or Life Sciences Work Experience: 5 to 8 years of experience in Quality Assurance within the API or API Intermediate manufacturing industry Hands-on experience in preparing and reviewing GMP documentation such as BMRs, BPRs, and SOPs Strong understanding of regulatory guidelines (GMP, ICH, FDA, etc.) and data integrity practices Key Responsibilities: Review and approve batch manufacturing records (BMRs), batch packaging records (BPRs), change controls, deviations, and CAPAs. Ensure compliance with cGMP, ICH, FDA, and other applicable regulatory guidelines across all operations. Perform in-process quality checks, line clearance, and review of raw material and intermediate usage. Prepare and Manage documentation systems including SOPs, validation protocols, and logbooks, ensuring adherence to ALCOA+ principles. Support internal audits, vendor audits, and regulatory inspections by preparing and reviewing necessary documentation. Review and approve analytical and stability reports from QC to ensure accuracy and compliance. Monitor and support training programs to ensure employees follow quality procedures and standards. Lead or support quality risk assessments and provide QA input during technology transfer, scale-up, and commercial manufacturing. Actively participate in investigation of deviations, OOS/OOT results, and ensure effective CAPA closure. Collaborate with Production, QC, AR&D, and Regulatory Affairs to maintain a culture of quality and continuous improvement. Required Skills: Strong knowledge of GMP regulations, ICH guidelines, and data integrity practices Proficiency in reviewing and managing GMP documentation (BMR, BPR, SOPs, validation protocols) Strong analytical, problem-solving, and decision-making abilities Experience in handling deviations, CAPA, and risk assessments Familiarity with QMS software, LIMS, or other quality management systems (preferred) Excellent organizational and reporting skills Key Attributes: High attention to detail and commitment to compliance Strong communication and interpersonal skills Ability to multitask and manage priorities in a dynamic environment Proactive approach to continuous improvement and regulatory readiness Interested candidates can share their profiles at Hr@sinterxpharma.co
As a QA Chemist at Sinterx Pharma Private Limited, you will play a crucial role in ensuring that all API intermediate manufacturing operations adhere to established quality standards, GMP requirements, and regulatory guidelines. Your responsibilities will include: - Reviewing and approving GMP documentation such as BMRs, BPRs, SOPs - Overseeing batch records, managing deviations, and CAPA - Conducting internal audits and ensuring compliance throughout the production lifecycle Qualifications required for this role include: - Bachelor's or Master's Degree in Chemistry, Pharmaceutical Sciences, or Life Sciences - 5 to 8 years of experience in Quality Assurance within the API or API Intermediate manufacturing industry - Hands-on experience in preparing and reviewing GMP documentation - Strong understanding of regulatory guidelines (GMP, ICH, FDA, etc.) and data integrity practices In this role, you will need to: - Review and approve batch manufacturing records, change controls, deviations, and CAPAs - Ensure compliance with cGMP, ICH, FDA, and other regulatory guidelines - Perform in-process quality checks and review raw material and intermediate usage You will also be responsible for: - Managing documentation systems including SOPs, validation protocols, and logbooks - Supporting internal audits, vendor audits, and regulatory inspections - Collaborating with cross-functional teams to maintain quality excellence and support regulatory inspections Key skills required for this role: - Strong knowledge of GMP regulations, ICH guidelines, and data integrity practices - Proficiency in reviewing and managing GMP documentation - Strong analytical, problem-solving, and decision-making abilities - Experience in handling deviations, CAPA, and risk assessments Key attributes we are looking for in a candidate: - High attention to detail and commitment to compliance - Strong communication and interpersonal skills - Ability to multitask and manage priorities effectively - Proactive approach to continuous improvement and regulatory readiness If you are interested in this opportunity, please share your profile at Hr@sinterxpharma.co.,
As a QC Chemist with 5 to 8 years of experience at Sinterx Pharma Private Limited, your role involves leading and executing complex analytical testing of API intermediates to ensure compliance with quality standards and regulatory guidelines. You will conduct advanced testing, review analytical data, support investigations, mentor junior analysts, and contribute to continual improvement initiatives. Collaboration with Quality Assurance, Production, and R&D teams is essential to maintain product quality throughout the production lifecycle. **Key Responsibilities:** - Perform routine and non-routine analysis of raw materials, intermediates, and in-process samples using validated methods and instruments. - Conduct instrumental analysis using HPLC, GC, UV, FTIR, KF, and ensure proper calibration and maintenance. - Review and interpret analytical data, ensuring compliance with internal specifications and regulatory standards. - Identify and investigate deviations, OOS/OOT results, and support CAPA implementation in collaboration with QA. - Lead or assist in method validation, method transfer, and stability studies for intermediates. - Maintain strict adherence to GMP, GLP, and ALCOA+ principles in all documentation and laboratory practices. - Review laboratory documentation including test records, logbooks, equipment usage logs, and analytical reports. - Provide technical support and training to junior analysts, ensuring adherence to safety, quality, and compliance standards. - Collaborate with Production, QA, AR&D, and Regulatory Affairs for continuous improvement and troubleshooting. **Qualification Required:** - Bachelors or Masters Degree in Chemistry, Pharmaceutical Sciences, or Life Sciences - 5 to 8 years of experience in Quality Control within the API or API Intermediate manufacturing industry - Hands-on experience in instrumental analysis (HPLC, GC, UV, IR, KF, etc.) - Strong understanding of regulatory guidelines (GMP, ICH, FDA, etc.) and data integrity practices If you are detail-oriented with a focus on data accuracy and compliance, possess good communication skills, and have the ability to work in a fast-paced environment while meeting deadlines, this QC Chemist position at Sinterx Pharma Private Limited might be the right fit for you. If you are interested in this job opportunity, kindly forward your resume to hr@sinterxpharma.co.,