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6 Laboratory Practices Jobs

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1.0 - 5.0 years

0 Lacs

gujarat

On-site

You will conduct routine quality control tests on raw materials, in-process products, and finished goods to ensure adherence to internal and external quality standards and regulations. You will be responsible for analyzing test results, maintaining accurate records of quality control activities, and collaborating with the production and R&D teams to troubleshoot quality issues and implement corrective actions. Your role will involve assisting in the development and validation of new testing methods and protocols, monitoring quality metrics and trends, and recommending improvements as necessary. In this position, you will also participate in internal and external audits related to quality control, provide training and support to staff on quality control procedures, and ensure proper calibration and maintenance of laboratory equipment. Your familiarity with regulatory standards and laboratory accreditation processes, such as ISO and GMP, will be essential in this role. Additionally, you will need to have a strong knowledge of quality control methodologies and laboratory practices, as well as proficiency in using laboratory instruments and software for data analysis. The role requires a Bachelor's or Master's degree in Chemistry and at least 1 year of experience in quality control, compliance management, laboratory testing, and working as a chemist. Strong attention to detail, problem-solving skills, communication abilities, and teamwork skills are also important for this position. This is a full-time, permanent role in the Ion Exchange Resins, Chemicals, Water Treatment, and Wastewater Treatment industry, based in Sanand, Gujarat. Health insurance benefits are provided, and reliable commuting or willingness to relocate to the work location is required.,

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2.0 - 6.0 years

0 Lacs

koppal, karnataka

On-site

You are a dedicated and passionate Physics Teacher, responsible for inspiring students to explore the fascinating world of physics through engaging lessons and hands-on experiments. Your role involves developing curriculum, providing academic support, and fostering a positive learning environment that encourages critical thinking and scientific inquiry. Your responsibilities include developing and implementing comprehensive lesson plans that cater to diverse learning styles, teaching physics concepts effectively using various instructional strategies, and providing mentoring and academic advising to guide students in their academic pursuits. You will conduct assessments to evaluate student understanding, facilitate laboratory experiments and demonstrations, and collaborate with colleagues on interdisciplinary projects. As a Physics Teacher, you must hold a Bachelor's degree in Physics, Education, or a related field, with teaching certification preferred. You should have a strong knowledge of physics concepts and principles, the ability to convey complex ideas in an accessible manner, and experience in lesson planning, tutoring, or mentoring students. Familiarity with scientific research methodologies, laboratory practices, and technology integration in the classroom is a plus. Your excellent communication skills, both verbal and written, along with a passion for teaching and inspiring students, are essential for this role. Your commitment to fostering an inclusive classroom environment that supports all learners is crucial. If you are enthusiastic about teaching physics and making a difference in students" lives, this full-time opportunity is for you. Food and Provident Fund benefits are provided, and the work location is in person. Apply now to be a part of this rewarding journey in education!,

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5.0 - 9.0 years

0 Lacs

vadodara, gujarat

On-site

As an Analytical Scientist in our team, you will be responsible for developing and validating robust HPLC methods for the characterization and quantification of biological products such as monoclonal antibodies and recombinant proteins. Your role will involve performing method optimization, robustness studies, and transfer protocols following ICH guidelines. You will also be conducting routine and stability testing by analyzing in-process, release, and stability samples using various techniques including HPLC/UPLC, Capillary and Gel Electrophoresis, UV spectrophotometric methods, Host Cell DNA quantification, and immunoassays like HCP ELISA. In addition, you will be in charge of operating and maintaining analytical instruments such as HPLC, electrophoresis systems, spectrophotometers, and ELISA readers, ensuring their proper calibration, troubleshooting, and performance verification. Your responsibilities will also include preparing and reviewing SOPs, STPs, protocols, reports, and analytical records to comply with regulatory requirements. You will need to maintain accurate documentation in laboratory notebooks and electronic systems. Furthermore, you will participate in internal and external audits and provide analytical data to support regulatory submissions. Collaboration with cross-functional teams including R&D, Quality Control, and Regulatory Affairs will be essential in supporting product development and lifecycle management. You will offer technical support during investigations, deviations, and CAPAs, as well as train junior analysts and new team members on analytical techniques and laboratory practices. To excel in this role, you should hold an M.Sc. / M.Tech / M.Pharm in Biotechnology, Biochemistry, or a related life sciences discipline, along with 4-8 years of relevant experience in analytical development or QC of biopharmaceuticals. Hands-on experience with HPLC method development and ELISA-based techniques is required, as well as familiarity with regulatory guidelines such as ICH, FDA, and EMA, and quality systems. Key skills for this position include strong analytical and problem-solving abilities, attention to detail and data integrity, excellent documentation and communication skills, proficiency in software tools like Empower, Chromeleon, SoftMax Pro, and the capability to manage multiple projects and meet deadlines.,

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3.0 - 7.0 years

0 Lacs

karnataka

On-site

Job Description: As a QMS Project Reviewer at Syngene International Limited in Bengaluru, you will play a vital role in drug substance development and manufacturing processes. Syngene is an innovation-led contract research, development, and manufacturing organization that offers integrated scientific services from early discovery to commercial supply. Safety is a top priority at Syngene, and you will be expected to adhere to safety guidelines, procedures, and SOPs to ensure a safe working environment for yourself, your team, and the lab/plant. Your core responsibilities will include following GMP, GDP, and GLP procedures, creating/revising/reviewing procedures such as SOPs and protocols, reviewing and approving Master BMR and PDR, and ensuring compliance. You will also be responsible for verifying product details, conducting assessments, investigating deviations, and handling returned products and product recalls. This role presents an exciting opportunity to interact with clients globally, collaborate with cross-functional departments, and gain exposure to various aspects of product development and commercial manufacturing. You will be expected to demonstrate expertise in handling QMS activities, reviewing Master Batch Record and Analytical Documents, and maintaining good communication and coordination skills among cross-functional teams. To be successful in this role, you should have 3-6 years of experience in project-related QMS activities, experience in client handling, and a strong educational background with an MSc in Chemistry. Additionally, you should possess good knowledge of Good Documentation and laboratory practices, as well as excellent skills in reviewing specifications and methods of analysis. At Syngene, we value excellence, integrity, and professionalism, and we are committed to providing equal opportunities for all employees. Join us at Syngene and be a part of our mission to deliver high-quality scientific services while maintaining a strong focus on safety and compliance.,

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7.0 - 11.0 years

0 Lacs

hyderabad, telangana

On-site

As a member of the Chemistry Solutions Department based in Hyderabad, India, your primary responsibility will be to manage and nurture client relationships. You will be expected to oversee the efficient delivery of projects, ensuring that project costs are managed effectively and resources are utilized efficiently. It will also be your duty to promote a culture of safety and good laboratory practices, while safeguarding records, data integrity, and intellectual property confidentiality. Additionally, you will play a crucial role in maintaining high morale within the team and fostering their skill development. Effective management of both internal and external stakeholders will be a key aspect of your role. To qualify for this position, you must hold a Ph.D. or a PDF in Organic or Medicinal Chemistry and possess 7 to 11 years of relevant experience in the field. Furthermore, you will be tasked with reporting team structures and designations within the department. Candidates with preferred educational qualifications are encouraged to apply, with a focus on specific categories, field specializations, degrees, academic scores, and institution tiers. Required certifications, trainings, and work experiences within the industry and role will be crucial for success in this position. Your performance will be measured based on key performance indicators and competencies relevant to the role. A deep understanding of the required knowledge and skills, along with specific abilities, will be necessary to excel in this dynamic work environment. The role may involve travel and require a valid work permit and access to a vehicle. Understanding of contract types, time constraints, compliance issues, and union affiliations will also be essential for successful performance in this role.,

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7.0 - 11.0 years

0 Lacs

karnataka

On-site

The job is based in Bangalore, India within the Chemistry Solutions department. As part of your role, you will be responsible for managing and enhancing client relationships, ensuring timely project delivery, monitoring project costs and resource utilization, promoting a culture of safety and good laboratory practices, maintaining records and confidentiality of intellectual property, fostering team morale and skill development, as well as managing internal and external stakeholders effectively. To be eligible for this position, you should possess a Ph.D. or PDF in Organic or Medicinal Chemistry along with 7 to 11 years of relevant experience.,

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