associate scientist

Adecco

Quality Control Associate Scientist (Temporary - until February 2026) Basingstoke, UK Full-time, Temporary Contract Are you an experienced Quality Control professional looking to make an impact in a leading life sciences organisation? We have an exciting opportunity for a Quality Control Associate Scientist to join our team in Basingstoke on a temporary basis until February 2026. About the Role As a Quality Control Associate Scientist, you will play a key role in ensuring our products meet the highest standards of quality and compliance. You will carry out a range of QC testing activities in accordance with Oxoid test specifications and methods, supporting the timely and accurate release of products. Key Responsibilities <ul> <li> Perform Quality Control testing in line with Oxoid test specifications, including Level 1, 2, and 3 testing methods. </li><li> Prepare media and manage the use of autoclaves. </li><li> Complete Out of Specification (OOS) reports and assist with investigations. </li><li> Maintain accurate and up-to-date training records. </li><li> Plan, track, and control the progress of products under test, providing reliable availability dates to Planning and Customer Services. </li><li> Proactively alert the QC Team Leader to any potential issues or failures and support follow-up investigations. </li><li> Record all test results within the SAP Quality Management module. </li><li> Conduct equipment checks, cleaning, and audits to ensure compliance with quality standards. </li><li> Manage waste disposal and replenish consumables as required. </li></ul> About You We're looking for someone with: <ul> <li> Previous experience in a Quality Control or laboratory environment (ideally within life sciences, microbiology, or pharmaceuticals). </li><li> Strong attention to detail and a proactive approach to problem-solving. </li><li> Familiarity with SAP Quality Management or similar systems (desirable). </li><li> Excellent organisational and communication skills. </li><li> The ability to work effectively in a fast-paced, team-oriented environment. </li></ul> Contract Details <ul> <li> Location: Basingstoke </li><li> Contract type: Temporary (until February 2026) </li><li> Hours: Full-time </li></ul> Join a team dedicated to maintaining the highest standards of product quality and safety - and help us deliver excellence every day. Adecco acts as an employment agency for permanent recruitment and an employment business for the supply of temporary workers. The Adecco Group UK & Ireland is an Equal Opportunities Employer. By applying for this role your details will be submitted to Adecco. Our Candidate Privacy Information Statement explaining how we will use your information is available on our website.

QC Associate Scientist

Syngene International Limited

<div>
 Date: 23 Dec 2025
 
 
 Location:
 
 
 Bangalore, KA, IN, 560099
 
 
 Division: Dedicated Centre
 
 
 
 Job Description
 
 
 
 Designation: Associate Scientist (8-I)
 
 
 Job Location: Bangalore
 
 
 Department: BBRC PD ARD &ndash; GMP
 
 
 
 About Syngene
 
 
 
 Incorporated in 1993, Syngene International Ltd. is an innovation-focused global discovery, development, and manufacturing organization providing integrated scientific services to the pharmaceutical, biotechnology, nutrition, animal health, consumer goods, and specialty chemical industries worldwide. Syngene&rsquo;s clientele includes world leaders such as Bristol-Myers Squibb, Baxter, Amgen, GSK, Merck KGaA, and Herbalife. Its innovative culture is driven by the passion of its 4240- a strong team of scientists who work with clients from around the world to solve their scientific problems, improve R&amp;D productivity, speed up time to market, and lower the cost of innovation.
 
 
 Job Purpose (1-2 Lines): Analytical Research and Development working on Analytical GMP testing (AGT), and Syngene BMS Laboratory (SBL) stability programs
 
 
 
 Key Responsibilities
 
 
 
 <ul>
 <li>
 Routine testing of stability samples using chromatographic, dissolution, and wet analytical techniques under a GMP environment following all cGMP practices
 </li>
 <li>
 Performing instrument calibration, method validation, and method transfers
 </li>
 <li>
 Troubleshooting HPLC and dissolution apparatus
 </li>
 <li>
 Interpretation of stability data and results trending
 </li>
 <li>
 Investigation of OOS/OOT and other laboratory events
 </li>
 <li>
 Deliver analytical results within the established windows and as per applicable guidelines
 </li>
 <li>
 Compliance &amp; implementation of quality systems
 </li>
 <li>
 Follow environment, health, and safety (EHS) requirements at all times in the workplace ensuring individual and lab/plant safety
 </li>
 <li>
 Electronic lab notebook documentation
 </li>
 <li>
 Miscellaneous lab responsibilities
 
 
 </li>
 </ul>
 Educational Qualifications: M.Sc. Chemistry or M. Pharm
 
 
 
 Technical/Functional Skills
 
 
 
 <ul>
 <li>
 The candidate should have a good educational and theoretical, analytical chemistry background
 </li>
 <li>
 Good knowledge of analytical techniques
 </li>
 <li>
 The candidate should understand instrument calibration, method validation, and routine analysis
 </li>
 <li>
 Good understanding of documentation as per GxP requirements (electronic notebook)
 </li>
 <li>
 The candidate should have good proficiency in MS office tools
 </li>
 <li>
 Experience in stability samples testing and good knowledge of ICH guidelines &amp; cGMP regulatory requirements
 </li>
 <li>
 Must have worked in a cGMP-regulated environment, exposure to regulatory inspections like US FDA, MHRA, etc. is preferred
 
 
 </li>
 </ul>
 
 Behavioral Skills
 
 
 
 <ul>
 <li>
 Strong commitment toward work and a high level of dedication, enthusiasm, and motivation
 </li>
 <li>
 Good speaking-listening-writing skills, attention to detail, proactive self-starter
 </li>
 <li>
 Ability to work successfully in a dynamic environment
 </li>
 <li>
 Should be able to work in a team and flexible for working in shifts.
 </li>
 <li>
 Ability to meet tight deadlines and prioritize workloads.
 
 
 </li>
 </ul>
 
 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>

Associate Scientist

Intas Pharmaceuticals

<div>
 
 About Intas
 
 
 
 
 Recruitment Fraud Disclaimer:
 
 
 
 
 Intas Pharmaceuticals does not request or accept any fees during recruitment. If someone asks for payment on our behalf, it is a scam. Please report the incident to the local police or cybercrime unit. Your trust and safety are important to us.
 
 
 
 Intas is a leading global pharmaceutical company specializing in the development, manufacturing, and marketing of pharmaceutical formulations. The mission of the company is to address unmet medical and societal needs through a fully integrated pharmaceutical value chain spanning across the world.
 
 
 Through its subsidiaries, the International presence of Intas includes the following countries: over 85 worldwide, with some of the more important global markets like North America, Europe, Latin America, and the Asia-Pacific under the well-known brand name Accord Healthcare. The rapid expansion has been due to organic growth and strategic acquisitions alone, vindicating its position in some of the important major pharmaceutical markets across the world.
 
 
 Intas follows high standards of quality, as reflected by products approved for leading global regulatory agencies including USFDA, MHRA, and EMA. Substantial in-house R&amp;D capability, along with the beginning of a focus on highly advanced areas like Biosimilars and New Chemical Entities-Intas continues to push the frontiers of excellence in healthcare.
 
 
 At Intas, our success is fundamentally built on the strength of our people. Our ongoing commitment is to attract and retain the best talent in the industry while fostering an empowering environment that encourages innovation and excellence. This approach ensures that every employee plays a meaningful role in driving both the company&rsquo;s growth and advancements in global healthcare.
 
 
 Job Title: Associate Scientist - DPD
 
 
 Job Requisitions No.: 15797
 
 
 
 Job Description
 
 
 
 Competencies
 
 
 Intas - Problem Solving
 
 
 Intas - Action Oriented
 
 
 Intas - Dealing with Ambiguity
 
 
 Intas - Customer Focus
 
 
 Intas - Time Management
 
 
 Purpose of Job
 
 
 Skill Required
 
 
 Roles and Responsibilites
 
 
 <ul>
 <li>
 To support in planning, executing, &amp; performing various drug product development studies and bio-similarity studies.
 </li>
 <li>
 Writing protocols and reports for various drug product development studies
 </li>
 <li>
 To support in process and technology transfer related documentations.
 </li>
 <li>
 To support in executing the stability studies and preparing reports for same.
 </li>
 <li>
 Getting trained on batch manufacturing procedure for drug product and do related documentation.
 </li>
 <li>
 To get trained on HPLC and CE techniques and perform analysis of stability samples.
 </li>
 <li>
 Response to DQA observations and closure of reports.
 </li>
 <li>
 Preparing and updating of SOPs.
 </li>
 <li>
 Ensuring the calibration of the equipment as per the schedules.
 </li>
 <li>
 Attending necessary trainings and following compliance.
 </li>
 <li>
 To follow &lsquo;Good Documentation Practices and Data Integrity&rsquo; requirements during any GxP Operation and recording at site.
 </li>
 <li>
 To take responsibility that application of Data Integrity requirements and potential consequences for not following it are understood and followed.
 </li>
 <li>
 To review in the perspective of compliance to Data Integrity requirements while reviewing any GxP data (Records, Reports) specific to Job description.
 
 
 </li>
 </ul>
 Qualification Required
 
 
 
 Relevant Skills / Industry Experience
 
 
 
 Relevant professional / Educational background
 
 
 
 Any Other Requirements (If Any)
 
 
 
 Compensation / Reward
 
 
 Location:
 
 
 Biotech, Ahmedabad, GJ, IN, 382213
 
 
 Travel: 0%
 
 
 Life at Intas Pharmaceuticals
 
 
 For over three decades, Intas has thrived due to the exceptional talent of its people. Our growth is fueled by a dynamic environment that nurtures individual potential while fostering collaboration and collective success. We believe that when diverse skills and perspectives unite under a shared purpose and value system, we can achieve remarkable outcomes, driving innovation and excellence across the pharmaceutical landscape.
 
 
 Date: 26 Dec 2025
</div>

Associate Scientist - DPD

Mount Sinai Health System

<div>Description
The Associate Scientist is experienced in the conduct of research involving the understanding of human diseases and improvement of human health. May assist in the operation of the clinical laboratory. Engages in clinical investigation or other research, production, technical writing, and related activities, and may mentor less senior scientist and Associate Researcher staff. 
Responsibilities<ul><li>
Conducts research to develop methodologies, instrumentation and procedures for medical application, analyzing data and presenting findings.</li><li>
Designs and conducts complex clinical research studies requiring the determination and evaluation of alternative methods, computational modeling, diagnosis and treatment.</li><li>
Plans and directs studies to investigate human or animal disease, preventive methods, and treatments for disease.</li><li>
May assist in clinical laboratory operations.</li><li>
Follows strict safety procedures when handling materials to avoid contamination.</li><li>
Teaches principles of medicine and medical and laboratory procedures to physicians, residents, students, and research staff.</li><li>
Confers with health departments, industry personnel, physicians, and others to develop health safety standards and public health improvement programs.</li><li>
Develops treatments and designs research tools and techniques.</li><li>
Explores subject area and defines scope and selection of problems for investigation through conceptually related studies.</li><li>
Develops hypotheses to be tested and methodology for evaluating results.</li><li>
Examines the results of clinical trials and adjusts the dosage levels to reduce negative side effects or to induce better results.</li><li>
Communicates research results to the scientific community via published papers.</li><li>
Develops new proposals for research and obtain support for new and/ or continuing research activities.</li><li>
Makes recommendations that have a major impact on extensive scientific research activities.</li><li>
Performs other related duties.</li></ul> 

Qualifications<ul><li>
Ph.D. in Biological Science or related field</li><li>
Three years experience</li></ul> 
Employer Description
Strength through Unity and Inclusion

The Mount Sinai Health System is committed to fostering an environment where everyone can contribute to excellence. We share a common dedication to delivering outstanding patient care. When you join us, you become part of Mount Sinai&rsquo;s unparalleled legacy of achievement, education, and innovation as we work together to transform healthcare. We encourage all team members to actively participate in creating a culture that ensures fair access to opportunities, promotes inclusive practices, and supports the success of every individual.

At Mount Sinai, our leaders are committed to fostering a workplace where all employees feel valued, respected, and empowered to grow. We strive to create an environment where collaboration, fairness, and continuous learning drive positive change, improving the well-being of our staff, patients, and organization. Our leaders are expected to challenge outdated practices, promote a culture of respect, and work toward meaningful improvements that enhance patient care and workplace experiences. We are dedicated to building a supportive and welcoming environment where everyone has the opportunity to thrive and advance professionally. Explore this opportunity and be part of the next chapter in our history.

About the Mount Sinai Health System:

Mount Sinai Health System is one of the largest academic medical systems in the New York metro area, with more than 48,000 employees working across eight hospitals, more than 400 outpatient practices, more than 300 labs, a school of nursing, and a leading school of medicine and graduate education. Mount Sinai advances health for all people, everywhere, by taking on the most complex health care challenges of our time &mdash; discovering and applying new scientific learning and knowledge; developing safer, more effective treatments; educating the next generation of medical leaders and innovators; and supporting local communities by delivering high-quality care to all who need it. Through the integration of its hospitals, labs, and schools, Mount Sinai offers comprehensive health care solutions from birth through geriatrics, leveraging innovative approaches such as artificial intelligence and informatics while keeping patients&rsquo; medical and emotional needs at the center of all treatment. The Health System includes more than 9,000 primary and specialty care physicians; 13 joint-venture outpatient surgery centers throughout the five boroughs of New York City, Westchester, Long Island, and Florida; and more than 30 affiliated community health centers. We are consistently ranked by U.S. News &amp; World Report's Best Hospitals, receiving high &quot;Honor Roll&quot; status, and are highly ranked: No. 1 in Geriatrics, top 5 in Cardiology/Heart Surgery, and top 20 in Diabetes/Endocrinology, Gastroenterology/GI Surgery, Neurology/Neurosurgery, Orthopedics, Pulmonology/Lung Surgery, Rehabilitation, and Urology. New York Eye and Ear Infirmary of Mount Sinai is ranked No. 12 in Ophthalmology. U.S. News &amp; World Report&rsquo;s &ldquo;Best Children&rsquo;s Hospitals&rdquo; ranks Mount Sinai Kravis Children's Hospital among the country&rsquo;s best in several pediatric specialties. The Icahn School of Medicine at Mount Sinai is ranked No. 11 nationwide in National Institutes of Health funding and in the 99th percentile in research dollars per investigator according to the Association of American Medical Colleges. Newsweek&rsquo;s &ldquo;The World&rsquo;s Best Smart Hospitals&rdquo; ranks The Mount Sinai Hospital as No. 1 in New York and in the top five globally, and Mount Sinai Morningside in the top 20 globally.

Equal Opportunity Employer

The Mount Sinai Health System is an equal opportunity employer, complying with all applicable federal civil rights laws. We do not discriminate, exclude, or treat individuals differently based on race, color, national origin, age, religion, disability, sex, sexual orientation, gender, veteran status, or any other characteristic protected by law. We are deeply committed to fostering an environment where all faculty, staff, students, trainees, patients, visitors, and the communities we serve feel respected and supported. Our goal is to create a healthcare and learning institution that actively works to remove barriers, address challenges, and promote fairness in all aspects of our organization. 
Compensation
The Mount Sinai Health System (MSHS) provides salary ranges that comply with the New York City Law on Salary Transparency in Job Advertisements. The salary range for the role is $58661 - $110000 Annually. Actual salaries depend on a variety of factors, including experience, education, and operational need. The salary range or contractual rate listed does not include bonuses/incentive, differential pay or other forms of compensation or benefits.</div>

Associate Scientist - Endocrinology

Aditi Consulting

<div>
 
 
 
 
 Payrate:
 
 
 
 $29.00 - $31.00/hr.
 
 
 &nbsp;
 
 
 
 Summary:
 
 
 
 
 This role involves performing experiments, organizing data, and analyzing results with minimal supervision. The position requires planning, conducting, and monitoring experiments, ensuring data integrity, and compliance with protocols and applicable regulations.
 
 
 &nbsp;
 
 
 
 Responsibilities:
 
 
 
 <ul>
 <li>
 
 
 Monitor or follow established experimental designs and protocols to perform routine tasks and studies
 
 
 </li>
 <li>
 
 
 Plan, conduct, analyze, and record experiments; provide interpretation of data
 
 
 </li>
 <li>
 
 
 Transfer experimental methods from literature to the lab and modify as needed
 
 
 </li>
 <li>
 
 
 Develop and implement new protocols with moderate review
 
 
 </li>
 <li>
 
 
 Engage coworkers in scientific discussions
 
 
 </li>
 <li>
 
 
 Communicate data and interpretations to the work group
 
 
 </li>
 <li>
 
 
 Develop systems to ensure quality data
 
 
 </li>
 <li>
 
 
 Operate standard laboratory equipment and major instruments/techniques
 
 
 </li>
 <li>
 
 
 Troubleshoot equipment and experimental issues effectively
 
 
 </li>
 <li>
 
 
 Contribute to internal/external reports, presentations, regulatory documents, invention disclosures, and/or patents
 
 
 </li>
 <li>
 
 
 Participate in department-wide support efforts such as safety, recruiting, and committees
 
 
 </li>
 <li>
 
 
 Train staff and/or supervise others as needed
 
 
 </li>
 <li>
 
 
 Coordinate and organize resources to complete tasks
 
 
 </li>
 <li>
 
 
 Demonstrate sound judgment and know when to seek input versus acting independently
 
 
 </li>
 <li>
 
 
 Oversee the general operations of the NMR facility and provide hands-on new user instrument training to chemists.
 
 
 </li>
 <li>
 
 
 Maintain the lab&rsquo;s NMR spectrometers and all associated equipment, performing or organizing all necessary calibrations, repairs and upgrades.
 
 
 </li>
 <li>
 
 
 Acquire NMR data for quality control of small molecule drugs, intermediates, and starting materials.
 
 
 </li>
 <li>
 
 
 Collaborate and communicate effectively with a team of chemists and separation scientists.
 
 
 </li>
 </ul>
 
 &nbsp;
 
 
 
 Qualifications:
 
 
 
 <ul>
 <li>
 
 
 Degree in Organic Chemistry, Physical Chemistry, Pharmaceutical Sciences, or a related field.
 
 
 </li>
 <li>
 
 
 General instrumentation experience with the ability to set up Client experiments and calibrate NMR and LC-MS instruments.
 
 
 </li>
 <li>
 
 
 Experience with the operation, troubleshooting, and maintenance of Bruker NMR spectrometers, HPLC and MS equipment (Agilent, Waters).
 
 
 </li>
 <li>
 
 
 Experience using 1D (1H, 13C, 19F, 31P, etc.) and 2D (COSY, TOCSY, NOESY, HSQC, HMBC, etc.) multinuclear solution-state NMR experiments for structure confirmation.
 
 
 </li>
 <li>
 
 
 Ability to run automated acquisition and analysis software programs such as Bruker Topspin or Agilent MassHunter.
 
 
 </li>
 <li>
 
 
 Experience with NMR and LC-MS data analysis packages such as ACD/Spectrus or Mestre Nova.
 
 
 </li>
 <li>
 
 
 Familiarity with the principles of organic chemistry, analytical and separation sciences, and automated liquid handling systems.
 
 
 </li>
 </ul>
 
 &nbsp;
 
 
 
 Pay Transparency:
 
 
 
 
 The typical base pay for this role across the U.S. is:
 
 $29.00 - $31.00 /hour
 
 . Non-exempt positions are eligible for overtime at a rate of 1.5 times the base hourly rate for all hours worked in excess of 40 in a work week, or as required by state or local law. Final offer amounts, within the base pay set forth above, are determined by factors including your relevant skills, education and experience. Full-time employees are eligible to select from different benefits packages. Packages may include medical, dental, and vision benefits, health savings accounts with qualified medical plan enrollment, 10 paid days off, 3 days paid bereavement leave, 401(k) plan participation with employer match,&nbsp; life and disability insurance, commuter benefits, dependent care flexible spending account, accident insurance, critical illness insurance, hospital indemnity insurance, accommodations and reimbursement for work travel, and discretionary performance or recognition bonus. Sick leave and mobile phone reimbursement provided based on state or local law.&nbsp;
 
 
 
 &nbsp;
 
 
 
 
 Consent to Communication and Use of AI Technology:
 
 
 
 
 
 By submitting your application for this position and providing your email address(es) and/or phone number(s), you consent to receive text (SMS), email, and/or voice communication whether automated (including auto telephone dialing systems or automatic text messaging systems), pre-recorded, AI-assisted, or individually initiated from Aditi Consulting, our agents, representatives, or affiliates at the phone number and/or email address you have provided. These communications may include information about potential opportunities and information. Message and data rates may apply. Message frequency may vary.
 
 
 
 
 
 You represent and warrant that the email address(es) and/or telephone number(s) you provided to us belong to you and that you are permitted to receive calls, text (SMS) messages, and/or emails at these contacts. You also acknowledge and agree to Aditi Consulting LLC&rsquo;s use of AI technology during the sourcing process, including calls from an AI Voice Recruiter. AI is used solely to gather data and does not replace human-based decision-making in employment decisions.  Calls may be recorded.
 
 
 
 &nbsp;
 
 
 
 Consent is not a condition of purchasing any property, goods, or services. You may revoke your consent at any time by replying &ldquo;STOP&rdquo; to messages or by contacting
 
 
 
 
 privacy@aditiconsulting.com
 
 
 
 
 .
 
 
 
 
 
 For information about our collection, use, and disclosure of applicant's personal information as well as applicants' rights over their personal information, please see our
 
 
 
 
 Privacy Policy
 
 
 
 
 .
 
 
 
 &nbsp;
 
 
 
 #AditiConsulting
 
 # 25 - 23191
 
 
 
 
</div>

GenScript

<div>
 
 
 About GenScript
 
 
 
 
 GenScript Biotech Corporation (Stock Code: 1548.HK) is a global biotechnology group. Founded in 2002, GenScript has an established global presence across North America, Europe, the Greater China, and Asia Pacific. GenScript's businesses encompass four major categories based on its leading gene synthesis technology, including operation as a Life Science CRO, enzyme and synthetic biology products, biologics development and manufacturing, and cell therapy.
 
 
 
 GenScript is committed to striving towards its vision of being the most reliable biotech company in the world to make humans and nature healthier through biotechnology.
 
 
 
 
 About ProBio
 
 
 
 
 ProBio proactively provides end-to-end CDMO service from drug discovery to commercialization with proactive strategies, professional solutions and efficient processes in cell and gene therapy, vaccine, biologics discovery and antibody protein drug to accelerate drug development for customers. ProBio&rsquo;s total cell and gene therapy solution covers CMC of plasmid and virus for IND filing as well as clinical manufacturing and commercial manufacturing.&nbsp;
 
 
 
 
 Job Summary:
 
 
 
 We are seeking a detail-oriented and proactive
 
 Analytical Associate Scientist or Scientist
 
 to join our US Protein Department. This role involves performing analytical testing and characterization of protein products to support research, development, and production activities. The ideal candidate will have a strong background in analytical chemistry, biochemistry, or biotechnology, with practical laboratory experience and familiarity with regulatory standards.
 
 
 
 Key Responsibilities:
 
 
 <ol>
 <li>
 Perform routine and non-routine analytical testing on protein samples using techniques such as HPLC, SDS-PAGE, ELISA, UV-Vis spectroscopy, and others as required.
 </li>
 <li>
 Prepare reagents, standards, and samples according to established protocols.
 </li>
 <li>
 Record, analyze, and interpret data with accuracy and integrity; prepare detailed reports and documentation.
 </li>
 <li>
 Maintain and calibrate laboratory instruments and ensure compliance with quality standards and safety regulations.
 </li>
 <li>
 Assist in method development, validation, and troubleshooting of analytical procedures.
 </li>
 <li>
 Collaborate with cross-functional teams to support project timelines and deliverables.
 </li>
 <li>
 Participate in the review and update of SOPs, batch records, and other quality documentation.
 </li>
 <li>
 Support continuous improvement initiatives and additional tasks as assigned by the supervisor.
 </li>
 </ol>
 
 
 Qualifications:
 
 
 <ol>
 <li>
 BS/MS in analytical chemistry, biochemistry, biotechnology, or related with 2+ years of relevant experience in protein purification/characterization.
 </li>
 <li>
 Hands-on experience with analytical instruments such as HPLC, SDS-PAGE, ELISA, UV-Vis, or similar is preferred.
 </li>
 <li>
 Strong attention to detail, organizational skills, and commitment to data integrity.
 </li>
 <li>
 Ability to work independently and collaboratively in a fast-paced team environment.
 </li>
 <li>
 Good communication skills and the ability to clearly document and present data.
 </li>
 <li>
 Experience working in a CRO or CDMO setting is an advantage.
 </li>
 </ol>
 
 &nbsp;
 
 
 
 #GS
 
 
 
 &nbsp;
 
 
 
 GenScript USA Inc/ProBio Inc. is a proud equal opportunity/affirmative action employer committed to attracting, retaining, and maximizing the performance of a diverse and inclusive workforce. It is the Company's policy to ensure equal employment opportunity without discrimination or harassment based on race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity or expression, age, disability, national origin, marital or domestic/civil partnership status, genetic information, citizenship status, uniformed service member or veteran status, or any other characteristic protected by law.
 
 
 
 
 GenScript USA Inc./ProBio Inc. maintains a drug-free workplace.
 
 
 
 &nbsp;
 
 
 
 
 Please note: Genscript USA Inc./ProBio Inc. will only contact candidates through verified application sources. GenScript/Probio does not request personal information from candidates through individual email or any other platform.&nbsp;
 
 
 
</div>

Analytical Associate Scientist/Scientist

ClinLab Solutions Group

<div>
 
 The qualified candidate will take an active role in supporting drug development by applying a variety of analytical methodologies to support physical and chemical characterization of drug substances (including raw materials and intermediates) and drug products. Working knowledge of analytical (e.g., HPLC-UV, HPLC-MS, GC-MS, spectroscopy) and physical chemical techniques (e.g., particle size, dissolution) used for the characterization of pharmaceutical substances and products is desired. Hand-on experience in HPLC method development is highly desired. Position level varies from bench chemist to principle scientist, depending on experience.
 
 
 
 Principal Responsibilities:
 
 
 
 The individual will be responsible for performing laboratory work in support of analytical testing of pharmaceutical projects, and relevant experience with the following analytical methodologies: chromatography, dissolution, KF, particle size will be desirable. Job responsibilities may include analytical method development and validation; stability and release testing; testing to support pharmaceutical development efforts; direct interaction with project team members, including presentation of data; critical review of data; preparation of technical reports; and evaluation of new instrumentation or analytical techniques. The candidate must be able to interact effectively with peers and leaders as part of a multi-disciplinary team and work in a fast-paced environment. Attention to detail, strong organizational skills, the ability to multitask, and effective interpersonal and communication skills are required.
 
 
 
 Qualifications
 
 
 
 The position requires a B.S, M.S. in Pharmaceutical Chemistry, Analytical Chemistry, Chemistry, or Pharmaceutical Sciences with relevant working experience in pharmaceutical industry.
 
 
 Working knowledge in analytical method development and validation under cGMP environment.
 
 
 Experience with a wide-variety of software and information systems (e.g. Empower, ChemStation, or LIMS).
 
 
 Experience in problem-solving skills and instrument trouble-shooting.
 
 
 Good oral and written communication skills and the ability to write and review technical reports and scientific papers are desired.
 
 
 Working knowledge of pharmaceutical product development, CMC regulatory requirements, project management; and capability to collaborate with colleagues.
 
</div>

Associate Scientist-Analytical R&D

Search 4028+ Associate scientist jobs near you this January. New roles added regularly across leading industries. Apply today.

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