17 Pharmaceutical Chemistry Jobs

Aster MIMS Kannur is seeking a dedicated and detail-oriented Pharmacist to join our team. The ideal candidate will play a crucial role in ensuring the safe and effective use of medications for our patients. This position is open to candidates with 0-5 years of experience in the pharmacy field. Responsibilities Dispensing medications accurately and safely to patients. Providing information and advice on the safe use of prescriptions and over-the-counter medications. Monitoring patient health and progress to ensure the effectiveness of medications. Collaborating with healthcare professionals to optimize patient care. Maintaining accurate patient records and medication inventories. Counseling patients on lifestyle changes and health management. Ensuring compliance with regulatory and safety standards. Skills and Qualifications Bachelor of Pharmacy (B.Pharm) or Doctor of Pharmacy (Pharm.D) degree. Valid pharmacist license in India. Strong knowledge of pharmacology and pharmaceutical care. Excellent communication and interpersonal skills. Ability to work in a fast-paced environment and manage time effectively. Attention to detail and strong organizational skills. Familiarity with pharmacy management software and electronic health records.

Eurofins Scientific is an international life sciences company that provides a wide range of analytical testing services to clients across multiple industries. From food and pharmaceuticals to environmental and cosmetic products, Eurofins ensures safety, authenticity, and accuracy. With a global presence and over 900 laboratories, Eurofins is a leader in food, environmental, pharmaceutical and cosmetic product testing, as well as in genomics, clinical studies support, and other specialized diagnostic testing. Applies GMP/GLP in all areas of responsibility, as appropriate Demonstrate and promote the company vision Regular attendance and punctuality Read and understand analytical procedures Review documentation, generated data, calculated results, and final reports according to departmental, corporate, and client SOPs Gain a technical understanding of the techniques in which review is being performed Use MS Windows applications such as EXCEL, Word, Access, Outlook email Conducts all activities in a safe and efficient manner Performs other duties as assigned Qualifications M.Pharm (Pharmaceutical Analysis) / M.Sc Chemistry Additional Information Experience level : 0 - 2 years in Bio/Pharmaceutical Analysis Key Candidate Attributes: Self-motivation; excellent quality of work and attention to detail Ability to communicate effectively with coworkers and internal/external clients Ability to learn new tasks quickly and to move easily from task to task Ability to handle prioritization and multiple tasks simultaneously Ability to use a personal computer and learn necessary programs Good communication skills (oral and written) Organizational ability and good judgement Science background/education and/or laboratory experience

Eurofins Scientific is an international life sciences company that provides a wide range of analytical testing services to clients across multiple industries. From food and pharmaceuticals to environmental and cosmetic products, Eurofins ensures safety, authenticity, and accuracy. With a global presence and over 900 laboratories, Eurofins is a leader in food, environmental, pharmaceutical and cosmetic product testing, as well as in genomics, clinical studies support, and other specialized diagnostic testing. Position Summary: Ensuring that the client receives quality data by reviewing laboratory data for accuracy, clarity, and adherence to GMP and/or GLP regulations Essential Duties and Responsibilities: Exercise discretion and independent judgment with respect to matters of significance directly related to the management or general business operations through the data review process Perform review of scientific data, including, but not limited to standard preparation, calibrations, methodology, QC, sample data, compound evaluation and other subjective review based on testing performed; perform complex calculations to verify results Verify the data is of sound quality and determine if data is compliant and defendable based on industry regulations and methodology May serve as technical advisor for analysts with regard to QA/QC of data Diagnose problems; solve simple problems, and suggest solution to complete problems in professional area Keep oneself and peers abreast of current developments and trends in professional area by reading and understanding internal procedures, attending/providing training sessions, by writing/revising SOPs (as required), and by assisting Group Leader / Principal Specialists in training new and existing employees Use MS Windows applications such as Excel, Word, Access, Outlook email; create complex Excel worksheets and formulas Communicate with internal clients to discuss any findings and notify them of any necessary rework or compliance/regulatory concerns Conducts all activities in a safe and efficient manner Attention to details Works in collaboration Performs other duties as assigned Applies GMP/GLP in all areas of responsibility, as appropriate Demonstrate and promote the company vision Regular attendance and punctuality Read and understand analytical procedures Qualifications Education/Experience (BMQ: Masters degree in a science-related field with 6-10 years of experience in Bio/Pharmaceutical Chemistry drug product/substance testing with knowledge of regulatory requirements. Theoretical / Practical experience with analytical techniques such as Ligand binding assays, ELISA, Gel electrophoresis, Proteomics, Flow Cytometry, TEM, PCR, cell culture and cell-based assays (such as reporter gene, cell signaling, and cell proliferation). etc. Knowledge of USP/EP compendia, and laboratory software applications such as LIMS, Electronic Notebook is preferred. Additional Information Key Candidate Attributes: Self-motivation; excellent quality of work and attention to detail Ability to communicate effectively with coworkers and internal/external clients Ability to learn new tasks quickly and to move easily from task to task Ability to handle prioritization and multiple tasks simultaneously Ability to use a personal computer and learn necessary programs Good communication skills (oral and written) Organizational ability and good judgement Science background/education and/or laboratory experience Strong Math Skills Logical Thinking, Good Reasoning Ability Motivation to excel Coaching/mentoring of peers

Eurofins Scientific is an international life sciences company that provides a wide range of analytical testing services to clients across multiple industries. From food and pharmaceuticals to environmental and cosmetic products, Eurofins ensures safety, authenticity, and accuracy. With a global presence and over 900 laboratories, Eurofins is a leader in food, environmental, pharmaceutical and cosmetic product testing, as well as in genomics, clinical studies support, and other specialized diagnostic testing. Position Summary: Ensure the client receives quality data in a timely manner by reviewing laboratory documentation, generated data, calculated results, and final reports for accuracy, clarity, and adherence to GMP and/or GLP regulations, and evaluating problems/system failures to achieve efficiency gains Essential Duties and Responsibilities: Applies GMP/GLP in all areas of responsibility, as appropriate Demonstrate and promote the company vision Regular attendance and punctuality Review simple and complex routine and non-routine data (for 3 or more areas) according to departmental, corporate, and client SOPs; read and understand analytical procedures; make sure all work is performed according to GLP/GMP requirements; perform complex calculations Communication in writing and in person with laboratory personnel in an intelligent and clear manner Exercise discretion and independent judgment with respect to matters of significance directly related to the management or general business operations through the data review process Perform review of scientific data, including, but not limited to standard preparation, calibrations, methodology, QC, sample data, integration review, compound evaluation, chemical identification, and other subjective review based on testing performed; perform complex calculations to verify results Verify the data is of sound quality and determine if data is compliant and defendable based on industry regulations and methodology May serve as technical advisor for analysts with regard to QA/QC of data Diagnose problems; solve simple problems, and suggest solution to complete problems in professional area Keep oneself and peers abreast of current developments and trends in professional area by reading and understanding internal procedures, attending/providing training sessions, by writing/revising SOPs (as required), and by assisting Group Leader / Principal Specialists in training new and existing employees Use MS Windows applications such as Excel, Word, Access, Outlook email; create complex Excel worksheets and formulas Communicate with internal clients to discuss any findings and notify them of any necessary rework or compliance/regulatory concerns Conducts all activities in a safe and efficient manner Performs other duties as assigned Qualifications M.Pharm (Pharmaceutical Analysis) Additional Information Experience level :5 - 8 years in Bio/Pharmaceutical AnalysisExperience with analytical techniques such as pH meter, Spectroscopy (UV, IR, NMR), Chromatography (HPLC/UPLC, GC, ICetc.) and LC-MS/MS, knowledge of USP/EP compendia, and laboratory software applications such as Waters Empower software, LIMS, Electronic Notebook is preferred. Key Candidate Attributes: Self-motivation; excellent quality of work and attention to detail Ability to communicate effectively with coworkers and internal/external clients Ability to learn new tasks quickly and to move easily from task to task Ability to handle prioritization and multiple tasks simultaneously Ability to use a personal computer and learn necessary programs Good communication skills (oral and written) Organizational ability and good judgement Science background/education and/or laboratory experience

Eurofins Scientific is an international life sciences company that provides a wide range of analytical testing services to clients across multiple industries. From food and pharmaceuticals to environmental and cosmetic products, Eurofins ensures safety, authenticity, and accuracy. With a global presence and over 900 laboratories, Eurofins is a leader in food, environmental, pharmaceutical and cosmetic product testing, as well as in genomics, clinical studies support, and other specialized diagnostic testing. Applies GMP/GLP in all areas of responsibility, as appropriate Demonstrate and promote the company vision Regular attendance and punctuality Read and understand analytical procedures Review documentation, generated data, calculated results, and final reports according to departmental, corporate, and client SOPs Gain a technical understanding of the techniques in which review is being performed Use MS Windows applications such as EXCEL, Word, Access, Outlook email Conducts all activities in a safe and efficient manner Performs other duties as assigned Qualifications Masters degree in a science-related field with 0-2 years of experience in Bio/Pharmaceutical Chemistry drug product/substance testing with knowledge of regulatory requirements. Theoretical / Practical experience with analytical techniques such as Ligand binding assays, ELISA, RIA, etc. Knowledge of USP/EP compendia, and laboratory software applications such as LIMS, Electronic Notebook is preferred..

Eurofins Scientific is an international life sciences company that provides a wide range of analytical testing services to clients across multiple industries. From food and pharmaceuticals to environmental and cosmetic products, Eurofins ensures safety, authenticity, and accuracy. With a global presence and over 900 laboratories, Eurofins is a leader in food, environmental, pharmaceutical and cosmetic product testing, as well as in genomics, clinical studies support, and other specialized diagnostic testing. The Project Manager Assistant (PMA) position is an administrative role working directly with a group of Project Managers, focusing on a specific area of the business. This role requires the use of technical functions to navigate Eurofins Lancaster Labs (ELLI) information systems, construct and develop relationships with ELLIs internal scientific and support departments, and assist project managers with a variety of tasks to allow the PMs to focus on client communication. Please note that this position does require direct client interaction. This is a great role if you also aspire to move into a PM position in the future. Employee Responsibilities: Support Sample and Project Management in building and maintaining studies including entering and review of material items, study start and end dates, and generating project plans for the PM teams. Managing incoming and in house Reference Standards by reaching out to the client for updated CoAs when expirations are approaching. Working with Pricing and Analytical Definition to generate quotes and build templates for sample entry of incoming samples. Track financial aspects of projects including purchase order and invoice management. This may also include generating Change Orders, special invoice requests and potentially End of Month billing for clients that qualify. Support Project Managers in an administrative capacity with a variety of other assignments Qualifications M. Pharm / M.Sc, Analyitical Chemistry PMP certification would be an additional advantage Additional Information Experience Level : 5 - 7 years in Bio/Pharmaceutical Analysis Key Candidate Attributes: Possesses excellent communication skills both oral and written Has a strong organization and attention to detail Computer skills Experience utilizing MS Office and MS Project or other project organization tools. Experience navigating a LIMS or equivalent is a plus Ability to learn new techniques, perform and prioritize multiple tasks simultaneously, keep accurate records, follow instructions, and comply with agency and company policies (GMP knowledge is a plus) Ability to work both independently and as part of a team, be self-motivated, adaptable, and maintain a positive attitude, even with critical deadlines Initiative/ Self-Starter proactively seek out work and training opportunities, offer to assist others, strive for high productivity and output in a fast-paced environment

Eurofins Scientific is an international life sciences company that provides a wide range of analytical testing services to clients across multiple industries. From food and pharmaceuticals to environmental and cosmetic products, Eurofins ensures safety, authenticity, and accuracy. With a global presence and over 900 laboratories, Eurofins is a leader in food, environmental, pharmaceutical and cosmetic product testing, as well as in genomics, clinical studies support, and other specialized diagnostic testing. Support processing of incoming samples by accurate and timely entry and review of sample information in LIMS. Employee Responsibilities: Audit sample information, including the formal review of all protocols, specifications, methods, and other documents submitted by the client or used by the project within a LIMS system. Manage technical information within a LIMS system relating to Sample Management. Send entry instructions to the sample administration regarding incoming samples. Direct client interaction via email Communicate with Project Management, Inside/Outside Business Development, and Technical groups as necessary to complete assignments Communicate regular status updates to supervisor Qualifications M.Pharm/M.Sc Additional Information Experience level : 3 - 5 years in Bio/Pharmaceutical Analysis Key Candidate Attributes: Self-motivation; excellent quality of work and attention to detail Ability to communicate effectively with coworkers and internal/external clients Ability to learn new tasks quickly and to move easily from task to task Ability to handle prioritization and multiple tasks simultaneously Ability to use a personal computer and learn necessary programs Good communication skills (oral and written) Organizational ability and good judgement Science background/education and/or laboratory experience

Method development and validation processes. Ability to plan, coordinate, and execute projects from initiation to completion, Commitment to maintaining Good Laboratory Practices (GLP) Maintenance and preventive maintenance of instruments. Required Candidate profile supervising, mentoring, and guiding both junior and senior research associates. Prep HPLC as part of the overall industry experience. Proven hands-on experience with HPLC and LC-MS techniques.

Method development and validation processes. Ability to plan, coordinate, and execute projects from initiation to completion, Commitment to maintaining Good Laboratory Practices (GLP) Maintenance and preventive maintenance of instruments. Required Candidate profile supervising, mentoring, and guiding both junior and senior research associates. Prep HPLC as part of the overall industry experience. Proven hands-on experience with HPLC and LC-MS techniques.

Method development and validation processes. Ability to plan, coordinate, and execute projects from initiation to completion, Commitment to maintaining Good Laboratory Practices (GLP) Maintenance and preventive maintenance of instruments. Required Candidate profile supervising, mentoring, and guiding both junior and senior research associates. Prep HPLC as part of the overall industry experience. Proven hands-on experience with HPLC and LC-MS techniques.

We are looking for an Assistant Professor in Pharmaceutical Chemistry who will be responsible for teaching and mentoring pharmacy students, developing educational content, and participating in research activities related to Pharmaceutical Chemistry.

Job Title : Associate Professor / Professor Department : College of Pharmaceutical Sciences Institution : Rama University , Kanpur Location : Mandhana , Kanpur Position Type : Full-Time role Position Summary The College of Pharmaceutical Sciences at Rama University seeks a dynamic and dedicated individual for the position of Associate Professor/Professor in the Department of Pharmaceutical Sciences. The successful candidate will have a strong academic background, a passion for teaching, and an active research agenda that will contribute to the growth of the department. This is an exciting opportunity to work in a highly collaborative environment with world-class faculty and contribute to advancing pharmaceutical science education, research, and practice. Key Responsibilities Teaching and Curriculum Development : Teach undergraduate, graduate, and professional courses in Pharmaceutical Sciences, including but not limited to pharmacology, pharmaceutics, medicinal chemistry, and pharmaceutical biotechnology. Develop, implement, and evaluate course content, lecture materials, and assessments. Mentor and advise students, including supervising graduate students in their research projects and theses. Participate in curriculum development and improvement within the department to ensure the program meets the latest advancements in pharmaceutical sciences. Research and Scholarship : Establish and maintain an active research program in an area of pharmaceutical sciences. Publish research findings in peer-reviewed journals and present at national and international conferences. Seek external funding through grants and partnerships to support research initiatives. Collaborate with colleagues within the department and across disciplines to foster research innovation and advancement. Service and Leadership : Contribute to the development of the departments goals, strategic plans, and initiatives. Serve on departmental, college, and university committees as assigned. Participate in professional organizations and activities related to pharmaceutical sciences. Provide leadership in service learning and outreach activities within the community and the profession. Administrative and Professional Development : Participate in academic advising and student recruitment. Attend departmental meetings and contribute to the administrative responsibilities of the department. Engage in ongoing professional development to stay current in the field and contribute to the advancement of pharmaceutical sciences. Required Qualifications Ph.D. in Pharmaceutical Sciences, Pharmacology, Medicinal Chemistry, Pharmaceutics, or a closely related field from an accredited institution. For Associate Professor: A minimum of [X] years of post-doctoral academic and/or professional experience, with a strong track record in teaching, research, and service. For Professor: A minimum of [X] years of post-doctoral academic and/or professional experience, with demonstrated leadership in research, teaching, and professional service. Demonstrated expertise in one or more areas of pharmaceutical sciences (e.g., drug development, pharmacology, medicinal chemistry, clinical pharmacology, pharmaceutics, etc.). A strong record of peer-reviewed publications and external research funding. Experience in teaching at the undergraduate or graduate level, including course development and delivery. Strong communication skills and the ability to mentor students and collaborate with colleagues. Preferred Qualifications Post-doctoral experience in a relevant area of pharmaceutical sciences. Experience in obtaining federal, industry, or foundation research funding. Evidence of leadership in professional organizations, research teams, or educational initiatives. Experience in interdisciplinary collaboration and industry partnerships.

We are seeking highly motivated individuals to join our esteemed institution as Principal in the Era College of Pharmacy a unit associated with ERA University . An ideal applicant for this position will have a strong commitment and aptitude Students & Staff. As a Principal you will play a pivotal role in shaping the future of aspiring technocrats and contribute to the academic excellence of our institution. Role & responsibilities To perform all the duties and responsibilities of the College and Department Preferred candidate profile Candidate must have relevant Qualification and Experience as per norms of PCI from a reputed institution. Salary Negotiable If you meet the above-mentioned qualifications and are excited about the prospect of joining our dynamic team at Era University & Medical College, Lucknow. We invite you to apply by submitting your updated resume with details of your relevant experience and salary expectations to Email: stuti.kumar@erauniversity.in or Whatsapp: +919236481374.

This is a full-time on-site role for a Professor at Yalamarty Colleges in Visakhapatnam. The Professor will be responsible for delivering lectures, conducting research, developing curriculum, grading assignments, and mentoring students.

Job Title : Associate Professor / Professor Department : College of Pharmaceutical Sciences Institution : Rama University , Kanpur Location : Mandhana , Kanpur Position Type : Full-Time role Position Summary The College of Pharmaceutical Sciences at Rama University seeks a dynamic and dedicated individual for the position of Associate Professor/Professor in the Department of Pharmaceutical Sciences. The successful candidate will have a strong academic background, a passion for teaching, and an active research agenda that will contribute to the growth of the department. This is an exciting opportunity to work in a highly collaborative environment with world-class faculty and contribute to advancing pharmaceutical science education, research, and practice. Key Responsibilities Teaching and Curriculum Development : Teach undergraduate, graduate, and professional courses in Pharmaceutical Sciences, including but not limited to pharmacology, pharmaceutics, medicinal chemistry, and pharmaceutical biotechnology. Develop, implement, and evaluate course content, lecture materials, and assessments. Mentor and advise students, including supervising graduate students in their research projects and theses. Participate in curriculum development and improvement within the department to ensure the program meets the latest advancements in pharmaceutical sciences. Research and Scholarship : Establish and maintain an active research program in an area of pharmaceutical sciences. Publish research findings in peer-reviewed journals and present at national and international conferences. Seek external funding through grants and partnerships to support research initiatives. Collaborate with colleagues within the department and across disciplines to foster research innovation and advancement. Service and Leadership : Contribute to the development of the departments goals, strategic plans, and initiatives. Serve on departmental, college, and university committees as assigned. Participate in professional organizations and activities related to pharmaceutical sciences. Provide leadership in service learning and outreach activities within the community and the profession. Administrative and Professional Development : Participate in academic advising and student recruitment. Attend departmental meetings and contribute to the administrative responsibilities of the department. Engage in ongoing professional development to stay current in the field and contribute to the advancement of pharmaceutical sciences. Required Qualifications Ph.D. in Pharmaceutical Sciences, Pharmacology, Medicinal Chemistry, Pharmaceutics, or a closely related field from an accredited institution. For Associate Professor: A minimum of [X] years of post-doctoral academic and/or professional experience, with a strong track record in teaching, research, and service. For Professor: A minimum of [X] years of post-doctoral academic and/or professional experience, with demonstrated leadership in research, teaching, and professional service. Demonstrated expertise in one or more areas of pharmaceutical sciences (e.g., drug development, pharmacology, medicinal chemistry, clinical pharmacology, pharmaceutics, etc.). A strong record of peer-reviewed publications and external research funding. Experience in teaching at the undergraduate or graduate level, including course development and delivery. Strong communication skills and the ability to mentor students and collaborate with colleagues. Preferred Qualifications Post-doctoral experience in a relevant area of pharmaceutical sciences. Experience in obtaining federal, industry, or foundation research funding. Evidence of leadership in professional organizations, research teams, or educational initiatives. Experience in interdisciplinary collaboration and industry partnerships.

Conduct in-depth research on nutraceutical ingredients, formulations, and processes. Identify trends in the nutraceutical industry and propose innovative product ideas. Evaluate raw materials, including testing for quality, safety, and efficacy Required Candidate profile Minimum 2-4 years of experience in R&D within the Nutraceutical or Pharmaceutical Hands-on experience in formulation development and stability testing.

Conduct in-depth research on nutraceutical ingredients, formulations, and processes. Identify trends in the nutraceutical industry and propose innovative product ideas. Evaluate raw materials, including testing for quality, safety, and efficacy. Required Candidate profile Minimum 2-4 years of experience in R&D within the Nutraceutical or Pharmaceutical Hands-on experience in formulation development and stability testing.