pharmaceutical analyst

SAJA Pharmaceuticals

<div>
 
 
 Position:
 
 Analytical Research Analyst
 
 
 
 Department:
 
 Research &amp; Development
 
 
 
 Location:
 
 Plant, Jeddah, Saudi Arabia
 
 
 
 
 
 
 Job Summary:
 
 
 
 We are seeking a skilled and motivated Analytical Research Analyst to join our Research &amp; Development team. The ideal candidate will be responsible for performing advanced analytical testing, method validation, and supporting the development of new pharmaceutical products in compliance with international standards.
 
 
 
 
 
 
 Key Responsibilities:
 
 
 <ul>
 <li>
 Conduct chemical and physical analysis of raw materials, intermediates, and finished products.
 </li>
 <li>
 Perform method validation and verification activities according to ICH guidelines.
 </li>
 <li>
 Operate and maintain analytical instruments such as HPLC, UPLC, and other laboratory equipment.
 </li>
 <li>
 Develop and validate analytical methods and ensure compliance with pharmacopeial standards (USP, BP, EP).
 </li>
 <li>
 Perform calibration, troubleshooting, and preventive maintenance of laboratory instruments.
 </li>
 <li>
 Prepare, document, and review analytical data in accordance with GMP and data integrity principles.
 </li>
 <li>
 Ensure laboratory activities adhere to safety, health, and environmental regulations.
 </li>
 <li>
 Support continuous improvement initiatives and collaborate effectively within cross-functional R&amp;D teams.
 </li>
 </ul>
 
 
 
 
 
 Qualifications and Experience:
 
 
 <ul>
 <li>
 Bachelor&rsquo;s degree in Pharmacy, Chemistry, or a related scientific field.
 </li>
 <li>
 2 to 5 years of experience in R&amp;D analytical laboratories (pharmaceutical industry preferred).
 </li>
 <li>
 Hands-on experience with HPLC/UPLC and other analytical instruments.
 </li>
 <li>
 Solid understanding of method validation, ICH guidelines, and pharmacopeial procedures.
 </li>
 <li>
 Strong skills in data documentation, integrity, and analysis.
 </li>
 <li>
 Excellent problem-solving and troubleshooting abilities.
 </li>
 <li>
 Ability to work independently, under pressure, and meet deadlines.
 </li>
 </ul>
 
 
 
 
 
 Language Skills:
 
 
 <ul>
 <li>
 
 English:
 
 Excellent (required)
 </li>
 <li>
 
 Arabic:
 
 Advantageous
 </li>
 </ul>
 
 
</div>

Analytical Research Analyst

Luminol Biopharma Pvt Ltd

Job Title: Junior/Mid-Level Analyst &ndash; HPLC, UV, Dissolution, Assay, RS, and Method Validation Company: KMS Healthcare Pvt. Ltd. Department: Quality Control / Analytical R&amp;D Experience: 2-10 years in pharmaceutical analysisJob Summary:We are seeking an experienced Analyst with expertise in HPLC, UV-Vis spectroscopy, dissolution testing, assay, related substances (RS), and method validation as per ICH guidelines. The candidate will be responsible for conducting analytical testing, preparing protocols/reports, and ensuring compliance with regulatory standards.Key Responsibilities:1. Analytical Testing &amp; Instrumentation:<ul><li>Perform routine and non-routine analysis using HPLC, UV-Vis, dissolution apparatus, and other lab instruments.</li><li>Conduct assay, related substances (RS), dissolution, and stability testing as per pharmacopeial methods (USP/EP/BP/IP).</li><li>Troubleshoot and maintain analytical instruments (HPLC, UV spectrophotometer, dissolution apparatus).</li></ul>2. Method Validation &amp; Transfer:<ul><li>Prepare and execute method validation/verification protocols (Accuracy, Precision, Linearity, Specificity, LOD/LOQ, Robustness) as per ICH Q2(R1).</li><li>Support method transfer activities between labs or sites.</li></ul>3. Documentation &amp; Compliance:<ul><li>Prepare analytical reports, validation protocols, and reports in compliance with GMP/GLP.</li><li>Review and ensure data integrity (ALCOA+ principles).</li><li>Follow SOPs, pharmacopeial guidelines (USP/EP), and ICH requirements.</li></ul>4. Regulatory &amp; Audits:<ul><li>Support regulatory submissions (ANDAs, DMFs) with analytical data.</li><li>Participate in internal/external audits (FDA, WHO, MHRA).</li></ul>5. Cross-Functional Collaboration:<ul><li>Work with QA, R&amp;D, and production teams for investigations (OOS/OOT, deviations).</li><li>Train junior analysts on analytical techniques and compliance.</li></ul>Qualifications &amp; Skills:<ul><li>Education: Bio Technology/ M.Sc./B.Pharm/M.Pharm in Chemistry/Pharmaceutical Sciences.</li><li>Experience: 2-10 years in pharmaceutical QC/ADL labs, with hands-on experience in:</li><li>HPLC/UPLC (Method development/validation preferred).</li><li>UV-Vis spectroscopy, dissolution testing (Apparatus I/II).</li><li>Assay, RS, forced degradation studies.</li><li>Regulatory Knowledge: ICH, USFDA, GMP, GLP.</li><li>Software: Empower, LabSolutions, Dissolution software.</li><li>Soft Skills: Detail-oriented, problem-solving, teamwork.</li></ul>Preferred:<ul><li>Experience in oral solid dosages (tablets/capsules).</li><li>Knowledge of impurity profiling, stability studies (ICH Q1A).</li></ul>Why Join Us?<ul><li>Opportunity to work in a GMP-compliant lab with advanced instrumentation.</li><li>Career growth in analytical development/validation.</li><li>Exposure to global regulatory standards.</li></ul>Job Type: Full-timeLocation:Door No.6, Kamarajar St, East Tambaram, Selaiyur, Chennai, Tamil Nadu 600059Note:&middot; Experience in the relevant/same field.Please Share resume Mobile # +91 9500112999 (WhatsApp)Job Types: Full-time, PermanentPay: &#8377;35,000.00 - &#8377;70,000.00 per monthBenefits:<ul><li>Provident Fund</li></ul>Work Location: In person

Analytical Scientist

Abdi Ibrahim Pharmaceuticals

<div>
 
 
 Abdi &Idot;brahim,
 
 founded in 1912, has the largest product portfolio in the sector and is the largest employer in the Turkish pharmaceutical industry with 5.500 employees. Abdi &Idot;brahim has been the leader of Turkey&rsquo;s pharmaceutical industry since 2002 with its powerful vision.
 
 
 
 
 
 Today, Abdi &Idot;brahim operates in 17 countries outside T&uuml;rkiye, exports to more than 70 countries ranging from Canada to European Union member states, from North Africa to Asia. As a corporate citizen working towards creating a better world and a better future, adhering to its mission in the sector and to the requirements of societal priorities, Abdi &Idot;brahim focuses on sustainability in all its business processes.
 
 
 
 
 
 Its vision for 2025 - apart from maintaining its status as a wholly local company - is to become "one of the top 100 pharmaceutical companies in the world.
 
 
 
 
 
 We are looking for an "
 
 
 Analytical Development Analyst/Specialist
 
 
 " to join our R&amp;D Center located in Esenyurt.
 
 
 
 
 
 
 Qualifications
 
 
 
 
 
 <ul>
 <li>
 Graduated from Chemistry or Chemical Engineering departments,
 </li>
 <li>
 Preferably holding or currently pursuing a Master&rsquo;s degree in Analytical Chemistry or Pharmaceutical Chemistry,
 </li>
 <li>
 Minimum 2 years of analytical experience is required for the specialist role,
 </li>
 <li>
 Excellent command of English (both written and verbal),
 </li>
 <li>
 Strong teamwork and communication skills,
 </li>
 <li>
 Knowledge and hands-on experience in analytical method development, method validation, and stability studies,
 </li>
 <li>
 Ability to follow up-to-date scientific publications and regulatory guidelines in English,
 </li>
 <li>
 Analytical thinker with strong problem-solving orientation.
 </li>
 </ul>
 
 
 
 
 
 Job Description
 
 
 
 
 
 <ul>
 <li>
 Conduct literature research for raw materials and finished products related to newly approved product development projects,
 </li>
 <li>
 Perform analytical method development, validation, and required testing activities, and prepare corresponding reports in compliance with applicable requirements,
 </li>
 <li>
 Carry out stability analyses for new products, prepare and evaluate stability reports in line with regulations,
 </li>
 <li>
 Prepare analytical documentation sections of registration dossiers in CTD format for submission to the Ministry of Health.
 </li>
 </ul>
 
 
</div>

R&D Analytical Development Analyst/Specialist

STEM Healthcare

<div>Job purpose:

We are looking for a highly analytical and data-driven graduate to join us in the business analysis team. The role will help you to develop a solid understanding of the pharmaceutical industry, strong quantitative and qualitative analytical skills, and to gain a unique insight into best practices across the industry.

As a member of the analysis team, you will have great visibility and exposure to senior directors in the company and the opportunity to take on a high level of responsibility for project delivery early-on in your career. You will be supported by an experienced analyst team through your development and training and be expected to collaborate and offer new insight within a close-knit team environment.

Key Responsibilities:
<ul>
<li>Managing multiple LIVE projects and their timelines to meet both internal and client's deadlines.</li>
<li>Collaborating with Project leaders/Lead Analysts to interpret data and formulate action plans and recommendations for clients.</li>
<li>Analyzing data from multi-sources using quantitative and qualitative methods to derive</li>
<li>Pressure testing data and identifying areas for investigation and training.</li>
<li>Building and maintaining MS Excel databases from source data.</li>
<li>Produce high quality presentations and other deliverables for clients using PowerPoint.</li>
<li>Supporting members in the analysis team to meet client deadlines and drive development and efficiencies within the team both locally and on international projects.</li>
</ul>
Essential Requirements:
<ul>
<li>The ideal candidate must have an Science/Analytics based degree in subjects with numerical emphasis (such as Chemistry, Physics, Mathematics, biotechnology, Engineering etc.)</li>
<li>A few years of experience in a similar analysis or sales job within the pharmaceutical industry is preferable.</li>
<li>Strong communication and multi-tasking skills to handle multiple projects with different stakeholders.</li>
<li>Advanced Level experience in using Excel and PowerPoint.</li>
<li>Proactive individual with drive and ambition, a strong work ethic to grow in a dynamic environment with good opportunities to help develop and further the business as a whole.</li>
</ul><div>
Don't meet every job requirement? That's okay! Our company is dedicated to building a diverse, inclusive, and authentic workplace. If you're excited about this role, but your experience doesn't perfectly fit every qualification, we encourage you to apply anyway. You may be just the right person for this role or others.</div></div>

Business Analyst

Star Laboratories (Pvt.) Ltd.

Education &amp; Experience:<ul><li>MSc (Chemistry) or Pharm-D (Doctor of Pharmacy) from HEC-recognized institution.</li><li>Minimum Experience 3 to 4 years</li><li>Candidates with pharmaceutical experience preferred; must not be currently enrolled in studies</li></ul>Responsibilities:<ul><li>Responsible for CTD dossier preparation, method validation and verification, and ensuring compliance with QC protocols and regulatory standards in pharmaceutical analysis.</li><li>Also responsible about CTD Dossiers and Reports</li></ul>Job Locations: Multan Road, Chung LahoreJob Type: Full-timeWork Location: In person

Sr. QC Analyst (Validation)

Dr. Reddy's Laboratories

<div>
 
 Dr. Reddy&rsquo;s Laboratories Ltd. is a leading multinational pharmaceutical company based across global locations. Each of our 24,000 plus employees comes to work every day for one collective purpose: to accelerate access to affordable and innovative medicines because
 
 Good Health Can&rsquo;t Wait
 
 .
 
 
 
 
 We started in 1984 with a modest investment, 20 employees and a bold vision. Today, we have research and development centres, manufacturing facilities or a commercial presence in 66 countries.
 
 
 
 
 For nearly four decades, we have stood for access, affordability and innovation based on the bedrock of deep science, progressive people practices and robust corporate governance. As the pharmaceutical industry evolves and undergoes disruption, we see an opportunity &ndash; to strengthen our core further (the next steps) and to build the future (the new bets).
 
 
 
 
 &lsquo;The Next and the New&rsquo; is how we aim to continue to be the partner of choice &ndash; purpose-driven, future-ready and sustainable. Our aim is to reach over 1.5 Bn+ patients across the world by 2030 by growing our core businesses and building for the future with sustainability at the core of our purpose and strategy. Sustainability for us means operating in a manner that respects people, planet and purpose &ndash; helping us conserve precious resources, serve our patients, create value for stakeholders, give back to society, fulfil our potential and maintain our integrity and transparency
 
 
 
 
 Dr Reddy&rsquo;s maintains a work environment, free from discrimination and is an equal opportunity employer. We are committed to employ &amp; nurture all qualified diverse workforce without regard to race, colour religion, nationality, sex, age, disability status, genetics, sexual orientation, gender expression, citizenship or any other characteristic or classification protected by applicable law(s) of the country we operate in. We treasure every talent, and recognize merit and diversity in our organization.
 
 
 
 
 
 
 Job Description
 
 
 
 
 
 Job Summary
 
 
 
 We are seeking a dynamic and experienced Analytical Specialist in Active Pharmaceutical Ingredient (API) MSc business for employing advanced analytical techniques to characterize and elucidate the structure and properties of various materials at a molecular and atomic level. You will play a crucial role in driving research and development initiatives by providing in-depth insights into complex materials through the application of cutting-edge analytical methodologies.
 
 
 
 
 
 
 
 Roles &amp; Responsibilities
 
 
 
 &bull; You will be responsible for working on new product development, addressing regulatory deficiency queries, and leveraging filings. Your role involves ensuring the qualification of reference/working standards, developing analytical methods, conducting validations, and transferring methods to QC.
 
 
 &bull; You will be responsible for developing and validating analytical methods, preparing method development and validation reports, and conducting online sample analysis for product development. Your role includes compiling forced degradation studies and identifying unknown impurities.
 
 
 &bull; You will compile stability data for completed projects, analyse product strategy, efficiency, and cross-functional issues in Analytical Research and Development (AR&amp;D). Your role involves visualizing developmental needs, understanding process scalability, and ensuring the procurement of necessary laboratory supplies.
 
 
 &bull; You will be responsible for maintaining lab equipment according to Good Laboratory Practices (GLP), investigating abnormal results in collaboration with group leaders, and ensuring calibration of instruments as per the schedule. Your role includes adhering to safety and environmental protocols, keeping the work area clean, and maintaining well-organized documentation.
 
 
 &bull; You will be responsible to employ advanced analytical techniques such as spectroscopy Nuclear Magnetic Resonance (NMR), Fourier Transform Infrared Spectroscopy (FTIR), Ultraviolet- Visible Spectroscopy (UV-Vis), mass spectrometry, Gas chromatography (GC), high-performance liquid chromatography HPLC), electron microscopy transmission electron microscope (TEM) and the scanning electron microscope (SEM), X-ray diffraction, and other specialized techniques to analyse and characterize materials.
 
 
 &bull; You will be responsible for trouble shooting for products from lab development stage to plant scale up using various analytical techniques.
 
 
 &bull; You will be Supporting complex generic projects by generating knowledge of Reference listed Drug (RLD) through reverse engineering and develop strategy to prove pharmaceutical sameness.
 
 
 &bull; You will be responsible for Coaching, Mentoring and training the scientists and members of the team.
 
 
 
 
 
 
 Qualifications
 
 
 
 
 
 Educational qualification:
 
 MS in Pharmaceutical Analysis/Post Graduation in Pharma/Physics
 
 
 
 Minimum work experience:
 
 5-10 years of experience
 
 
 
 Skills &amp; attributes:
 
 
 
 
 Technical Skills
 
 
 
 &bull; Hands on experience in Reverse Engineering of drug products
 
 
 &bull; Experience in Nuclear Magnetic Resonance (NMR), Fourier Transform Infrared Spectroscopy (FTIR), Ultraviolet- Visible Spectroscopy (UV-Vis).
 
 
 &bull; Knowledge on Morphology Analysis, Image Analysis and Optical Microscopy.
 
 
 &bull; Understanding and experience on Gas chromatography (GC) or high-performance liquid chromatography HPLC) method development and method validations.
 
 
 &bull; Hands on experience in liquid chromatography mass spectrometry (LCMS)/ liquid chromatography-high resolution mass spectrometry (LC-HRMS)
 
 
 &bull; Experience in electron microscopy, Transmission Electron Microscope (TEM) and the Scanning Electron Microscope (SEM)
 
 
 &bull; Knowledge on competitive strategies for technology innovation and Analytical Equipment.
 
 
 &bull; Proficiency in data analysis, interpretation, and statistical tools.
 
 
 
 
 
 
 
 Behavioral Skills
 
 
 
 &bull; Excellent communication and interpersonal skills.
 
 
 &bull; Ability to work with cross functional teams.
 
 
 &bull; Strong analytical and problem-solving abilities.
 
 
 &bull; Leadership skills to motivate and mentor the team.
 
 
 
 
 
 
 Additional Information
 
 
 
 
 
 About the Department
 
 
 
 
 
 
 Integrated Product Development Organisation
 
 
 
 
 
 We integrate our deep science capabilities and cutting-edge technology to develop innovative, accessible and affordable therapies for patients worldwide. We are a science-driven, innovation-focused pharmaceutical company committed to accelerating access to healthcare solutions to patients around the world. We have End to end capabilities in API, Formulations, Clinical, Intellectual Property and Regulatory Affairs. We are serving 55+ markets including USA, Canada, Europe, China, LATAM, ASEAN and all Emerging Markets with innovative and generic products ranging from Active pharmaceutical ingredients (API), Oral formulations, Parenteral (Injectables, Opthalmics) &amp; Other dosages
 
 
 Our product development efforts drive a portfolio of more than 1,000 products Enabled by our robust R&amp;D team consisting of more 200 scientists and functional experts and more than 150 doctorates, we have filed 1,071 patents and also published over 1,000 papers for peer review over the years.
 
 
 
 
 
 Benefits Offered
 
 
 
 At Dr. Reddy&rsquo;s we actively help to catalyse your career growth and professional development through personalised learning programs.
 
 
 The benefits you will enjoy at Dr. Reddy&rsquo;s are on par with the best industry standards. They include, among other things and other essential equipment, joining &amp; relocation support, family support (Maternity &amp; Paternity benefits), learning and development opportunities, medical coverage for yourself and your family, life coverage for yourself.
 
 
 
 
 
 Our Work Culture
 
 
 
 Ask any employee at Dr. Reddy&rsquo;s why they come to work every day and they&rsquo;ll say, because Good Health Can&rsquo;t Wait. This is our credo as well as the guiding principle behind all our actions. We see healthcare solutions not only as scientific formulations, but as a means to help patients lead healthier lives, and we&rsquo;re always attuned to the new and the next to empower people to stay fit. And to do this, we foster a culture of empathy and dynamism. People are at the core of our journey over the last few decades. They have been supported by an enabling environment that buoys individual ability while fostering teamwork and shared success. We believe that when people with diverse skills are bound together by a common purpose and value system, they can make magic.
 
 
 For more details, please visit our career website at
 
 https://careers.drreddys.com/#!/
 
 
</div>

Haleon

<div>
 
 About Haleon:
 
 
 
 Hello. We&rsquo;re Haleon. A new world-leading consumer company. Shaped by all of us. Together, we&rsquo;re improving everyday health for millions of people. By growing and innovating our global portfolio of category-leading brands &ndash; including Sensodyne, Panadol, Advil, Voltaren, Theraflu, Otrivin, and Centrum &ndash; through a unique combination of deep human understanding and trusted science. What&rsquo;s more, we&rsquo;re achieving it in a company that we&rsquo;re building together. In an environment that we&rsquo;re co-creating. And a culture that&rsquo;s uniquely ours. Care to join us. It isn&rsquo;t a question.
 
 
 
 Job Purpose:
 
 
 
 Analysis of FG, Validation, cleaning validation leading to timely approval of respective products/batches
 
 
 
 Key Responsibilities:
 
 
 
 <ul>
 <li>
 Analysis of Semi-finished/finished products for timely approval, NPI batches, process validation, cleaning validation testing of products.
 </li>
 <li>
 To receive the lab samples &amp; maintain records
 </li>
 <li>
 Timely complete and maintained all related documents like LIMS reports, logbook etc. keeping in the view of data integrity principal ALCOA plus
 </li>
 <li>
 To maintain 5S in lab related to lab glassware
 </li>
 <li>
 Timely report any OOT OOS, Atypical, events and deviation
 </li>
 <li>
 To ensure proper disposal of waste
 </li>
 <li>
 To check &amp; maintain the cleaning of lab glassware
 </li>
 <li>
 To maintain the lab reagents according to their compatibility
 </li>
 <li>
 Support in Audit preparation activities with reporting manager
 </li>
 <li>
 Comply and ensure compliance to GMP (Good Manufacturing practices), quality and other related policies, guidelines and requirements as applicable by law and company corporate guidelines
 </li>
 <li>
 Comply and ensure compliance to environment health and safety policies, guidelines and requirements as applicable by law and company corporate guidelines.
 </li>
 <li>
 Any other responsibility assigned from time to time as per business requirements
 
 
 
 </li>
 </ul>
 
 Skills and Competencies:
 
 
 
 <ul>
 <li>
 B.S/M.Sc. (Chemistry)/Pharm D
 </li>
 <li>
 Fresh or Analyst 1-2 Year
 </li>
 <li>
 Good analytical skills and knowledge of pharmaceutical company or relevant company
 
 
 
 </li>
 </ul>
 Please save a copy of the job description, as this may be helpful to refer to once the advert closes.
 
 
 
 Why Join Us?
 
 
 
 The future of everyday health is changing. And we&rsquo;re the people changing it. In front of us is an incredible opportunity to go beyond what any of us have done before. And make everyday health more achievable, more inclusive and more sustainable. For more and more people.
 
 
 So join us, as we build one of the world&rsquo;s leading consumer companies. Join us to innovate our category-leading brands. To better understand people&rsquo;s everyday health needs. To tackle the biggest barriers that stand in their way. To change individual and societal behavior.
 
 
 In our efforts to further tackle barriers that may be standing in our way, we have implemented what we call a Hybrid Working model, known as Home office. Home office in the country of employment is permitted for all employees whose position allows it. The employee and the manager agree on the circumstances in which working from the office is required and in which the employee can work remotely or specific local arrangements. This helps us with ensuring that we maintain a healthy work-life balance, and give our best to our people.
 
 
 Join us to work with colleagues who share your restless energy. To explore your interests. To stretch yourself to do the best work of your career. And join us, as together we build a working experience that encourages us all to lead happier, healthier, more productive lives.
 
 
 The way we see it, every day is an opportunity for better. And we&rsquo;re going all in to realize it.
 
 
 Care to join us. Find out what life at Haleon is really like www.haleon.com/careers/
 
 
 At Haleon we embrace our diverse workforce by creating an inclusive environment that celebrates our unique perspectives, generates curiosity to create unmatched understanding of each other, and promotes fair and equitable outcomes for everyone. We're striving to create a climate where we celebrate our diversity in all forms by treating each other with respect, listening to different viewpoints, supporting our communities, and creating a workplace where your authentic self belongs and thrives. We believe in an agile working culture for all our roles. If flexibility is important to you, we encourage you to explore with our hiring team what the opportunities are.
 
 
 As you apply, we will ask you to share some personal information, which is entirely voluntary. We want to have an opportunity to consider a diverse pool of qualified candidates and this information will assist us in meeting that objective and in understanding how well we are doing against our inclusion and diversity ambitions. We would really appreciate it if you could take a few moments to complete it. Rest assured, Hiring Managers do not have access to this information and we will treat your information confidentially.
 
 
 Haleon is an Equal Opportunity Employer. All qualified applicants will receive equal consideration for employment without regard to race, color, national origin, religion, sex, pregnancy, marital status, sexual orientation, gender identity/expression, age, disability, genetic information, military service, covered/protected veteran status or any other federal, state or local protected class.
 
 
 Accommodation Requests
 
 
 If you require a reasonable accommodation or other assistance to apply for a job at Haleon at any stage of the application process, please let your recruiter know by providing them with a description of specific accommodations you are requesting. We&rsquo;ll provide all reasonable accommodations to support you throughout the recruitment process and treat all information you provide us in confidence.
</div>

Quality Control Analyst

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