analytical scientist

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>

Analytical Scientist

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

Veranova L P

<div>Discover Veranova
At Veranova, we believe people are our most important asset, and we are dedicated to building the most talented workforce in our industry. Our commitment to uncompromising focuses on quality, compliance, safety, and excellence in delivery shapes everything we do. We are not just looking for skills; we are seeking innovative individuals who have a mindset open to learning and growth, and a desire to make a difference.
Veranova is a global leader in the development and manufacturing of complex active pharmaceutical ingredients (APIs) for pharma and biotech customers. With deep technical expertise and impressive flexibility, we develop solutions and processes that support and accelerate innovation.
Join us on our mission to enable current and next-generation therapeutics to improve and save the lives of patients.
Role Overview:
We are seeking a highly motivated and skilled Analytical Scientist to join our Analytical team in New England. The successful candidate will have expertise in LCMS (Liquid Chromatography-Mass Spectrometry) based characterization of complex bioconjugates, with a strong understanding of ADC structure and stability.
Core Responsibilities:<ul><li>
Exercise technical judgment in the planning, implementation, and analysis of experiments related to method development, validation, reference standard creation and qualification, forced degradation, product characterization, and compatibility studies in accordance with pertinent ICH regulatory guidelines.</li><li>
Develop and optimize LCMS methods for qualitative and quantitative analysis of ADCs. Develop and validate quantitative LCMS methods such as:<ul><li>
Drug-to-Antibody Ratio (DAR) determination.</li><li>
Payload quantification (free and conjugated forms).</li><li>
Linker stability and degradation profiling.</li><li>
Site-specific conjugation analysis.</li></ul></li><li>
Perform intact mass analysis, peptide mapping, drug-to-antibody ratio (DAR) determination, and payload identification.</li><li>
Characterize ADCs for critical quality attributes including conjugation sites, linker stability, and degradation products.</li><li>
Author test methods, protocols, reports, and regulatory documents as needed.</li><li>
Provide support for development and cGMP manufacturing campaigns, ensuring compliance with regulatory requirements and documentation standards - including both in-process and release samples.</li><li>
Adhere to safety and quality standards.</li><li>
Communicate technical findings and results to both internal and external stakeholders, including clients and regulatory bodies.</li><li>
Collaborate with chemistry development scientists, quality control and regulatory affairs teams to ensure successful project delivery.</li><li>
Mentor and develop scientific staff. Ensure continued technical and professional growth of department members, encourage efforts towards excellence and knowledge sharing.</li><li>
Possess strong communication (oral, written), organizational, and leadership skills.</li><li>
Maintain and troubleshoot LCMS instrumentation (e.g., Orbitrap, Q-TOF, Triple Quad).</li></ul>
Qualifications:
Required<ul><li>
Ph.D., M.S., or B.S. in Analytical Chemistry, Biochemistry, Chemistry, Chemical/Biomedical Engineering, or other related scientific discipline.</li><li>
Relevant experience in analytical method development, validation and characterization of bioconjugates. (PhD with 4+ years, MS with 6+ years, BS with 8 + years of experience.</li><li>
4+ years of hands-on experience in LCMS analysis of biologics, preferably ADCs.</li><li>
Strong knowledge of protein chemistry, conjugation technologies, and biotherapeutic development.</li><li>
Proficiency in any of the software tools for MS data analysis (e.g., Xcalibur, MassHunter, Skyline, Biopharma Finder).</li><li>
Well organized with good problem-solving skills, a high level of attention to detail and have a passion for delivering high quality data in a fast-paced environment.</li></ul>
Preferred<ul><li>
Experience with regulatory submissions and GMP/GLP environments.</li><li>
Experience with various techniques used in the characterization of ADC&rsquo;s such as capillary electrophoresis (CE-SDS) for ADC purity and size analysis, hydrophobic interaction chromatography (HIC) for DAR profiling, size-exclusion chromatography (SEC) for aggregation and stability studies, UV-Vis spectroscopy and fluorescence-based assays for payload quantification, and immunoassays (ELISA, ECL) for antibody detection.</li></ul>
Our Commitment:<ul><li>
Health &amp; Wellness: Comprehensive health &amp; Wellness benefits. Access to mental health resources and wellness programs. Generous PTO and holiday pay policies.</li><li>
Financial Wellness: Comprehensive total compensation package that includes competitive base salary, Defined Contribution Pension program, eligibility for performance-based bonuses, and attractive 401(k) Plan with company match.</li><li>
Professional Development: Opportunities for continuous learning through LinkedIn Learning, workshops, conferences, and mentorship. Tuition Assistance for Undergraduate and Graduate degree programs.</li><li>
Inclusive Culture: At Veranova, an inclusive culture is integral to our values. We are committed to ensuring that everyone can bring their full self to work and thrive in their career.</li></ul>
How to Apply:
At Veranova, we are on a misson to meet people that believe in our values and can contribute to the team in a variety of ways. Please visit www.veranova.com to view all open roles and join our Talent Community to stay connected and learn about opportunities as they arise.
We value a range of experiences and perspectives. If you want to be part of improving and saving the lives of patients, we encourage you to apply regardless of whether you meet every qualification listed.
For applicants who may require a reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email to talentacquisition@veranova.com in order to confirm your request for an accommodation. Please include the job number, title, and location of role. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Veranova employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.
Additional Information:
Applicants for this role must be authorized to work in the United States without further employer sponsorship.
Agency and Search Firm Representatives: Veranova does not accept unsolicited resumes from agencies and/or search firms for this job posting.
Important Notice Regarding Recruitment Scams: Veranova is committed to providing professional and secure recruitment experience for all applicants. Unfortunately, fraudulent job postings and recruitment scams are becoming more prevalent. We want to ensure that all candidates are aware of potential scams. Please see our notice here.<ul><li>
Legitimate communications from Veranova will only come from official email addresses using our domain: veranova.com.</li><li>
Legitimate LinkedIn communications will only come from active Veranova employees.</li><li>
Veranova will never ask candidates for sensitive personal information during the application process (e.g., bank account details or social security number).</li><li>
Veranova will never ask candidates for payment (e.g., for equipment, training, or background checks).</li></ul>
All your information will be kept confidential according to EEO guidelines.
Veranova is an Equal Opportunity Employer. It is the policy of Veranova to provide equal employment access and opportunity to all persons regardless of age, race, color, national origin, religion, sex, sexual orientation, gender identity and/or expression, physical or mental disability, genetic information, citizenship, marital status, veteran status, or any other characteristic protected by federal, state, or local law.
All applications are carefully considered, and your details will be stored on our secure Application Management System. This is used throughout Veranova for the selection of suitable candidates for our vacancies as they arise. Veranova respects your privacy and is committed to protecting your personal information. For more information about how your personal data is used please view our privacy notice.
#LI-Onsite</div>

Analytical Scientist - Anti Body Drug Conjugates

Syngene International Limited

<div>
 Date: 14 Oct 2025
 
 
 Location:
 
 
 IN
 
 
 Division: Discovery Services
 
 
 
 Job Title: Junior Analytical Development Scientist - OSD
 
 
 
 
 Job Location: Bengaluru
 
 
 
 
 Department: DPA &ndash; FD
 
 
 
 
 About Syngene :
 
 Syngene (www.syngeneintl.com) is an innovation-led contract research, development and manufacturing organization offering integrated scientific services from early discovery to commercial supply.
 
 
 At Syngene, safety is at the heart of everything we do personally and professionally. Syngene has placed safety at par with business performance with shared responsibility and accountability, including following safety guidelines, procedures and SOPs, in letter and spirit
 
 
 
 Mandatory expectation for all roles as per Syngene safety guidelines
 
 
 
 <ul>
 <li>
 Overall adherence to safe practices and procedures of oneself and the teams aligned
 </li>
 <li>
 Contributing to development of procedures, practices and systems that ensures safe operations and compliance to company&rsquo;s integrity &amp; quality standards
 </li>
 <li>
 Driving a corporate culture that promotes environment, health, and safety (EHS) mindset and operational discipline at the workplace at all times.
 </li>
 <li>
 Ensuring safety of self, teams and lab/plant by adhering to safety protocols and following environment, health, and safety (EHS) requirements at all times in the workplace.
 </li>
 <li>
 Ensure all assigned mandatory trainings related to data integrity, health, and safety measures are completed on time by all members of the team including self
 </li>
 <li>
 Compliance to Syngene&rsquo; s quality standards at all times
 </li>
 <li>
 Hold self and their teams accountable for the achievement of safety goals
 </li>
 <li>
 Govern and Review safety metrics from time to time
 
 
 </li>
 </ul>
 
 Core Purpose Of The Role
 
 
 
 <ul>
 <li>
 Analytical development supporting Formulation development
 </li>
 <li>
 Routine analysis of samples
 </li>
 <li>
 Method development
 </li>
 <li>
 Instrument calibrations
 </li>
 <li>
 Documentation
 </li>
 <li>
 Report preparation
 </li>
 <li>
 Miscellaneous lab responsibilities
 
 
 </li>
 </ul>
 
 Role Accountabilities
 
 
 
 <ul>
 <li>
 Candidate should have very good educational and theoretical background.
 </li>
 <li>
 Candidate should have knowledge of calibration, method development and troubleshooting using various instruments like KF auto titrator, dissolution (I, II &amp; IV), spectroscopic instruments e.g. UV spectrometer, IR and Chromatographic instruments e.g. HPLC, GC
 </li>
 <li>
 Knowledge of various regulatory guidelines w.r.t. method development, product development and documentation
 </li>
 <li>
 Knowledge of method development for oral dosage forms w.r.t. tests like assay, degradation products, dissolutions, blend uniformity, content uniformity, cleaning method, etc.
 </li>
 <li>
 Knowledge of specification setting for oral dosage forms, in-process specifications as well as product specifications
 </li>
 <li>
 Knowledge and operating of instruments like LC-MS, GC-MS will be added advantage
 </li>
 <li>
 Good understanding of Documentation as per GxP requirements
 </li>
 <li>
 Online Lab notebook writing
 </li>
 <li>
 Method development report preparation &ndash; Assay, Degradation products, Dissolution, cleaning method, etc.
 </li>
 <li>
 Method of Analysis, Test report, SOP preparation
 </li>
 <li>
 Calibration documentation
 </li>
 <li>
 Review of documents generated by peers or juniors
 </li>
 <li>
 Should be able to search scientific literature on-line
 </li>
 <li>
 Should be a team player and able to coach juniors technically
 
 
 </li>
 </ul>
 
 Syngene Values
 
 
 
 All employees will consistently demonstrate alignment with our core values
 
 
 Excellence
 
 
 Integrity
 
 
 Professionalism
 
 
 
 Experience:
 
 More than 5 years up to 8 years
 
 
 
 Skills And Capabilities
 
 
 
 Candidate should have good proficiency for MS-office tools
 
 
 Should be able to search scientific literature on-line
 
 
 
 Behavioral Skills
 
 
 
 Strong commitment towards work, and a high level of dedication, enthusiasm, motivation, and persuasive ability in a team.
 
 
 Good speaking-listening-writing skills, attention to details, proactive self-starter.
 
 
 Ability to work successfully in a dynamic, ambiguous environment.
 
 
 Ability to meet tight deadlines and prioritize workloads.
 
 
 Ability to develop new ideas and creative solutions.
 
 
 Should be able to work in team and flexible for working in shifts.
 
 
 Should be a focused employee.
 
 
 
 Education:
 
 M.Pharm / M.Sc
 
 
 
 Equal Opportunity Employer
 
 
 
 It is the policy of Syngene to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by applicable legislation or local law. In addition, Syngene will provide reasonable accommodations for qualified individuals with disabilities.
</div>

Junior Analytical Development Scientist - OSD

Tap Growth ai

<div>
 
 🌟 We're Hiring: Scientist! 🌟
 
 
 
 We are seeking a dedicated and analytical Scientist to join our research team and contribute to groundbreaking scientific discoveries. The ideal candidate will have a strong foundation in scientific methodology, data analysis, and research techniques to support our innovative projects and drive scientific excellence.
 
 
 
 📍 Location:
 
 Durham, United States
 
 
 
 ⏰ Work Mode:
 
 Work From Office
 
 
 
 💼 Role:
 
 Scientist
 
 
 
 Pay Scale:
 
 Up to $98, 404.80 (Dependent on Experience)
 
 
 
 What You'll Do
 
 
 
 Laboratory Data Review:
 
 
 <ul>
 <li>
 Scientific data review of laboratory documentation and data to appropriate standards (GMPs, SOPs, protocols, methods).
 </li>
 <li>
 Good understanding of data integrity and ALCOA+ (Attributable, Legible, Contemporaneous, Original, and Accurate) principles.
 </li>
 <li>
 Peer review of results and documentation of product development studies including statistical data reports (JMP).
 </li>
 <li>
 Peer review of method validations and analytical technical transfers.
 </li>
 <li>
 Transcription checking of regulatory submissions, reports, and / or JMP tables / plots.
 
 
 </li>
 </ul>
 
 What We're Looking For
 
 
 
 <ul>
 <li>
 BS or MS in Chemistry, Pharmaceutical Sciences, or a similar applicable discipline.
 </li>
 <li>
 Experience with HPLC in a GMP / QC setting, Empower software preferred.
 </li>
 <li>
 Experience with Inhalation testing products, large and small molecule preferred.
 </li>
 <li>
 Strong understanding of GMP and FDA guidelines for pharmaceutical manufacturing and validation.
 </li>
 <li>
 Strong organizational skills for managing multiple priorities.
 </li>
 <li>
 Effective communication and interpersonal skills for coordination with lab personnel, and management.
 
 
 </li>
 </ul>
 
 
 Ready to advance science? 🚀 Apply now and let's innovate together!
 
 
</div>

Scientist

LanceSoft, Inc.

<div>
 
 
 Job Title: Analytical Chemist
 
 
 
 
 Location: Andover, MA 01810
 
 
 
 
 Duration: 18 Months
 
 
 
 M-F, onsite Andover, 1st shift
 
 
 
 
 
 
 Skill
 
 
 
 
 Last Used
 
 
 
 
 No. of Years of Experience
 
 
 
 
 Capillary electrophoresis
 
 
 
 
 GC - MS
 
 
 
 
 Method qualification
 
 
 
 
 UHPLC
 
 
 
 
 
 
 
 
 Job Description (Required):
 
 
 <ul>
 <li>
 This opportunity provides analytical support to internal process development groups. The position will work with a number of different analytical techniques that will include UPLC, HPLC, GC, and CE.
 </li>
 <li>
 If applicable, analytical research and development activities will include literature searches, analytical method development, test procedure writing, analytical method qualification and method transfer.
 </li>
 <li>
 Analyzes early-stage lab samples, pilot plant samples, production samples, in=process samples and CRO samples.
 </li>
 <li>
 Possesses extensive knowledge of various laboratory instruments like U/HPLC, GC, and CE.
 </li>
 <li>
 BSc with at least 5+ years relevant experience
 </li>
 <li>
 MSc with at least 2+ years relevant experience
 </li>
 </ul>
 
 
 
 
 
 Notes:
 
 
 
 Scientist
 
 <ul>
 <li>
 looking for someone to jump right in, hands on exp.
 </li>
 </ul>
 
 looking for someone very familiar and comfortable with HPLC, GC
 
 <ul>
 <li>
 M-F, onsite Andover, 1st shift
 </li>
 <li>
 Pharma preferred, Mix of academic and industry is good too
 </li>
 </ul>
 
 
 
 
 
 Interview: Onsite
 
 
</div>

Analytical Chemist

Medasource

<div>
 
 
 Title:
 
 Associate Scientist I
 
 
 
 Duration:
 
 Contract through June 2026
 
 
 
 Schedule:
 
 M-F 8-5 Onsite
 
 
 
 Occupational Summary
 
 
 
 The Associate Scientist I will support the development, qualification, and execution of analytical methods to
 
 
 enable optimization of processes, formulations and characterization of vaccine products. This incumbent in this
 
 
 position will be involved in pharmaceutical and analytical development for GMP production of vaccine products
 
 
 and therapeutics.
 
 
 
 Work Performed
 
 
 
 &bull; Perform pharmaceutical development and successful GMP release including:
 
 
 o Analytical development
 
 
 o Develop product specific release and characterization methods
 
 
 &bull; Quality methods for product release and complete comprehensive characterization of clinical lots
 
 
 &bull; Complete GMP testing in line with OCH and regulatory guidance
 
 
 &bull; Formulation development - developing formulations to stabilize vaccine products
 
 
 &bull; Employ analytical characterization tools to inform product formulation design
 
 
 &bull; Lead formulation &amp; filling of vaccine products including tech transfer &amp; production under GMP
 
 
 conditions
 
 
 &bull; Execute and document development and GMP actitivites in compliance with regulatory requirements
 
 
 &bull; Collaborate closely with other development teams to provide support for development activities and will
 
 
 work diligently with other development functions to understand how the production process changes
 
 
 impact product quality
 
 
 &bull; Compile data and perform analysis and interpretation and draw conclusions regarding progress and
 
 
 results of work, utilizing the data in appropriate decision making; summarize date, present results and
 
 
 propose next steps to advance development
 
 
 &bull; Write and review development reports; writes procols for tech transfer and SOPs for GMP production,
 
 
 and present data to project teams and larger settings
 
 
 
 Required Qualifications
 
 
 
 &bull; Knowledge and hands on classwork with analytical methods and/or product formulation
 
 
 &bull; Hands on experience with specific analytical methods (HPLC, immunoassays, biochemical methods),
 
 
 molecular or pharmaceutical product formulation (buffer &amp; excipient screening, thermal stability
 
 
 evaluation, biophysical methods) is preferred.
 
 
 &bull; GMP experience huge plus
 
 
 &bull; Must have the ability to work independently with guidance from senior scientists/managers
 
 
 &bull; Demonstrated ability in solving moderately complex analytical problems with guidance from senior
 
 
 development scientists
 
 
 &bull; Strong oral and written communication skills
 
</div>

Associate Scientist

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