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analytical chemist

Germer International - Pharmaceutical Recruiting

<div>
 
 Our pharmaceutical client is looking for a chemist to join their growing organization! If you are someone who wants to be a part of a highly technical team, this may be the role for you!
 
 
 
 
 
 The Chemist II/III will conduct release and stability testing for pharmaceutical products with specific focus on LC and GC chromatographic analyses as well as dissolution testing.
 
 
 This position involves conducting various analytical tests to ensure the quality and performance of solid dosage forms while maintaining a high level of laboratory safety and compliance.
 
 
 
 
 
 
 Key Responsibilities
 
 :
 
 
 
 
 <ul>
 <li>
 Prepare solid dosage samples for analysis by accurately weighing, blending, and homogenizing materials to ensure representative samples for testing.
 </li>
 <li>
 Conduct dissolution testing of solid oral drug products using USP Apparatus I and Apparatus II.
 </li>
 <li>
 Perform HPLC assays for the quantitative analysis of pharmaceutical components, including potency, purity, and samples from dissolution testing.
 </li>
 <li>
 Ensure analytical instrumentation is properly maintained.
 </li>
 <li>
 Ensure that all laboratory work complies with Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP), following established Standard Operating Procedures (SOPs).
 </li>
 <li>
 Maintain accurate and detailed records of experiments, results, and procedures in laboratory notebooks and electronic systems, ensuring data integrity.
 </li>
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 Adhere to safety protocols and participate in laboratory safety initiatives, ensuring a safe and compliant work environment.
 </li>
 </ul>
 
 
 
 
 
 Minimum Qualifications
 
 :
 
 
 
 
 <ul>
 <li>
 Bachelor&rsquo;s degree in chemistry with at least two (2) years of experience in the pharmaceutical industry.
 </li>
 <li>
 Hands-on experience with HPLC, GC, Dissolution, and use of Empower software
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 <li>
 Strong analytical and problem-solving skills.
 </li>
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 Excellent communication and teamwork skills.
 </li>
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 Attention to detail and commitment to maintaining data integrity.
 </li>
 </ul>
 
 
</div>

Analytical Chemist

LanceSoft, Inc.

<div>
 
 
 Job title: Analytical Chemist
 
 
 
 
 Location: Lincoln NE, 68462
 
 
 
 
 Duration: 12 months
 
 
 
 
 
 
 Description:
 
 
 <ul>
 <li>
 Develops knowledge of Analytical Science &amp; Technology policies and procedures.
 </li>
 <li>
 Develops an understanding of applicable, current Good Manufacturing Practices (cGMP) requirements, laboratory processes and procedures, data integrity and utilization of good documentation practices.
 </li>
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 Conduct experiments using common analytical techniques in support of analytical method development and validation in a GxP laboratory.
 </li>
 <li>
 Develops proficiency using analytical techniques to support upper-level scientists and assigned projects.
 </li>
 <li>
 Responsible for preparation of solvents, standards, mobile phases, and samples required for analytical testing in support of assigned project expectations.
 </li>
 <li>
 Management and testing of stability study samples.
 </li>
 <li>
 Demonstrates proficiency using instrumentation to support work based upon assigned projects. This may include, but is not limited to: UPLC, HPLC, LC/MS and GC.
 </li>
 <li>
 Understands established internal and external expectations and maintains effective communication pathways.
 </li>
 <li>
 Working knowledge of Microsoft Word, Microsoft Excel and Laboratory Information System (eLN).
 </li>
 </ul>
 
 
</div>

Discover International

<div>
 
 Hi Network,
 
 
 We are seeking a skilled Analytical Chemist with strong expertise in pharmaceutical analysis to join our team in the Rockford area. The ideal candidate will bring hands-on experience in chromatographic techniques and drug release testing to support product development and quality initiatives.
 
 
 
 Responsibilities:
 
 
 <ul>
 <li>
 Perform analytical testing using HPLC and GC to support pharmaceutical product development and manufacturing.
 </li>
 <li>
 Conduct drug release and dissolution testing in compliance with regulatory guidelines.
 </li>
 <li>
 Develop, validate, and troubleshoot analytical methods for raw materials, intermediates, and finished products.
 </li>
 <li>
 Generate, review, and interpret analytical data, ensuring accuracy and adherence to cGMP standards.
 </li>
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 Prepare technical reports, SOPs, and documentation to support regulatory submissions and internal quality systems.
 </li>
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 Collaborate with cross-functional teams, including formulation, process development, and quality assurance.
 </li>
 <li>
 Ensure laboratory equipment is calibrated, maintained, and operated in compliance with safety and quality procedures.
 </li>
 <li>
 Contribute to continuous improvement initiatives by identifying opportunities to enhance laboratory efficiency and reliability.
 </li>
 </ul>
 
 If you have the experience mentioned above, please send me your resume.
 
 
 Thanks,
 
 
 Nabil.
 
 
 
</div>

Mindlance

<div>
 
 
 Job Title: Chemist II
 
 
 
 
 Location: Cambridge, MA
 
 
 
 
 Duration: 12+ months with possible extension
 
 
 
 
 
 
 Job Description:
 
 
 &bull; Plan and execute assigned laboratory tasks utilizing standard procedures and technical understanding of various techniques to complete assigned tasks.
 
 
 &bull; Independently generate precise, reliable and reproducible data in a timely manner. Document the experimentation per the regulatory requirements.
 
 
 &bull; Demonstrate experimental precision and strong data interpretation skills and should possess understanding of core scientific discipline.
 
 
 &bull; Develop protocols for more complex tests or experiments performed with less defined assays and parameters.
 
 
 &bull; Ensures safety requirements are met when performing tasks.
 
 
 &bull; Ensures timely delivery of high-quality precise data.
 
 
 &bull; Applies basic computer skills including word processing, spreadsheets, and instrument related systems.
 
 
 &bull; Presents findings of defined experiments to larger audiences.
 
 
 Requirements/Qualifications
 
 
 &bull; BS/BA in Chemistry, Chemical Engineer, Biochemistry, Medical Technology, Biology or related field with minimum 5 yrs lab experience (pharmaceutical industry preferred) or master&rsquo;s degree with 0- 2 yrs lab experience (pharmaceutical industry preferred).
 
 
 &bull; Experienced use of analytical instruments including HPLC, GC, dissolution, KF and chromatography data systems (i.e., Empower, Openlab, or Chromeleon).
 
 
 &bull; Strong documentation skills and familiarity of GMP, GLP. Able to present experimental findings to larger groups. Strong communication skills.
 
 
 
 
 
 EEO:
 
 
 
 
 &ldquo;Mindlance is an Equal Opportunity Employer and does not discriminate in employment on the basis of &ndash; Minority/Gender/Disability/Religion/LGBTQI/Age/Veterans.&rdquo;
 
</div>

ARL Bio Pharma

<div>
 Chemist I - Analytical
 
 
 Position Summary
 
 
 Join a company where you can make a difference from day one and help make the world a better and safer place. ARL Bio Pharma provides analytical and microbiological testing for the pharmaceutical industry. Our laboratory works with pharmaceutical companies, compounding and hospital pharmacies, drug manufacturers, and raw material suppliers bringing excellence to pharmaceutical sciences and making pharmaceuticals safer. This position is a fantastic stepping-stone for those with some basic experience looking to expand their career in the interesting world of the pharmaceutical industry. The Chemist I is responsible for utilizing established methods and standard lab equipment/instrumentation (HPLC, IC) to qualitatively and quantitatively analyze routine pharmaceutical substances and formulations.
 
 
 
 Some highlights...
 
 
 
 <ul>
 <li>
 Paid Training
 </li>
 <li>
 Work in a comfortable office setting with casual dress code
 </li>
 <li>
 Have your own workspace where you can work largely independently
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 <li>
 Free Medical and Dental insurance
 </li>
 <li>
 401K Retirement with Company Match
 </li>
 <li>
 Excellent Work/Life Balance
 
 
 </li>
 </ul>
 This is a full-time role with a great benefits package.
 
 
 
 Work Schedule:
 
 7:00 am - 4:30pm
 
 
 
 Restrictions:
 
 Because of vital nature of this work, we do not allow medical marijuana cards and we do random drug testing on all of our employees.
 
 
 
 Essential Functions
 
 
 
 <ul>
 <li>
 Adhere to Quality Management System (QMS)
 </li>
 <li>
 Follow prescribed safety rules and regulations in performing all assigned duties
 </li>
 <li>
 Follow written and oral instruction
 </li>
 <li>
 Prepare reagents and solutions required for testing
 </li>
 <li>
 Perform laboratory testing and record results in compliance with cGMP&rsquo;s (if applicable) and internal QMS
 </li>
 <li>
 Work and think independently, yet share ideas and work towards team goals
 </li>
 <li>
 Use a personal computer including word processing, spreadsheets, email and database applications
 </li>
 <li>
 Express thoughts in a clear concise manner both orally and written
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 <li>
 Work to establish the ability to effectively prioritize and plan multiple work activities with varying deadlines and complexities
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 <li>
 Adherence to all ARL safety standards, protocols, policies and procedures
 
 
 </li>
 </ul>
 
 Position Requirements...
 
 
 
 <ul>
 <li>
 An associate degree in chemistry or related science with 2+ years industrial experience OR...
 </li>
 <li>
 Bachelor&rsquo;s degree in chemistry or related science with 1-2 years&rsquo; experience in the Pharmaceutical industry.
 </li>
 <li>
 Communication Proficiency
 </li>
 <li>
 Problem Solving/Analysis
 </li>
 <li>
 Organization/Multi-tasking
 </li>
 <li>
 Collaboration Skills
 </li>
 <li>
 Thoroughness
 
 
 </li>
 </ul>
 
 Work Environment...
 
 
 
 This job operates in a laboratory environment.
 
 
 
 Physical Demands...
 
 
 
 The role requires standing for prolonged periods of time; dexterity in fingers and hands to perform complex and precise manipulations; ability to walk and stoop; ability to lift and move up to 50 pounds; see in the normal visual range including the ability to distinguish colors and shades and hear in the normal audio range with or without correction.
 
 
 AAP/EEO Statement
 
 
 ARL Bio Pharma, Inc. provides equal employment opportunity to all individuals regardless of their race, color, creed, religion, gender, age, sexual orientation, gender identity, national origin, disability, veteran status, genetics or any other characteristic protected by state, federal, or local law. ARL Bio Pharma, Inc. expressly prohibits any form of workplace harassment based on race, color, creed, religion, gender, age, sexual orientation, gender identity, national origin, disability, veteran status, genetics or any other characteristic protected by state, federal, or local law. Improper interference with the ability of ARL Bio Pharma, Inc. employees to perform their job duties may result in discipline up to and including discharge. Further, the company takes affirmative action to ensure that applicants and employees are treated without regard to any of these characteristics.
 
 
 Employment Type: Full Time
 
 
 Years Experience: 1 - 3 years
 
 
 Salary: $24 - $30 Hourly
 
 
 Bonus/Commission: No
 
 
</div>

Kelly

<div>
 
 Kelly&reg; Science &amp; Clinical is seeking Analytical Chemists for a 3-month contract opportunity with a leading CDMO in Boulder, CO. If you are driven by the prospect of translating cutting-edge scientific discoveries into tangible advancements and are poised to advance your career, join us as we pioneer progress in the biotechnology and medical device industries.
 
 
 
 
 
 
 Workplace:
 
 Onsite in Boulder, CO
 
 
 
 
 
 
 Position Title:
 
 Analytical Chemist
 
 
 
 
 
 
 Position Type:
 
 3-month contract
 
 
 
 
 
 
 Pay rate:
 
 $36-50 per hour.
 
 
 
 
 
 
 Company:
 
 Kelly&reg; Science &amp; Clinical
 
 
 
 
 
 
 Client Overview
 
 
 
 A premier Contract Development and Manufacturing Organization (CDMO) specializing in the development and production of active pharmaceutical ingredients (APIs), excipients, drug products, and packaging solutions, is seeking an experienced Analytical Research &amp; Development Scientist. With an international network spanning Europe and the U.S. and a team of thousands, this organization partners with top pharmaceutical and biotech companies to deliver therapies that improve lives worldwide.
 
 
 
 
 
 Operating across six advanced technology platforms&mdash;Peptides, Lipids &amp; Carbohydrates, Injectables, Highly Potent &amp; Oncology, Small Molecules, and Oligonucleotides&mdash;the company offers tailored solutions from early development through commercial manufacturing.
 
 
 Play a pivotal role in developing innovative analytical methods and optimizing manufacturing processes, ensuring world-class quality and supporting regulatory compliance throughout the product lifecycle.
 
 
 
 
 
 
 Key Responsibilities
 
 
 <ul>
 <li>
 Develop, implement, and validate robust analytical methods for manufacturing, quality assurance, and regulatory submissions
 </li>
 <li>
 Drive innovation in analytical methodologies and manage seamless technology transfers across global facilities
 </li>
 <li>
 Plan and execute research proposals, identifying project goals, resource needs, and practical applications
 </li>
 <li>
 Conduct analytical testing on drug substances, intermediates, and raw materials for clinical and registration purposes
 </li>
 <li>
 Ensure meticulous documentation and compliance with ICH and internal stability guidelines
 </li>
 <li>
 Troubleshoot and resolve analytical challenges in manufacturing environments
 </li>
 <li>
 Support stability programs and uphold QEH&amp;S principles
 </li>
 <li>
 Manage hazardous and non-hazardous waste according to environmental and safety standards
 </li>
 <li>
 Adapt to flexible working hours to support production and validation demands
 </li>
 </ul>
 
 
 
 
 
 
 
 
 Qualifications
 
 
 <ul>
 <li>
 Bachelor&rsquo;s degree in Chemistry or a related field, with a minimum of 3 years&rsquo; relevant experience in the pharmaceutical sector
 </li>
 <li>
 Strong analytical chemistry expertise with proven proficiency in method development and GMP compliance
 </li>
 <li>
 Excellent verbal and written communication skills, with the ability to engage stakeholders at every level
 </li>
 <li>
 Advanced skills in mathematical analysis and statistical concepts
 </li>
 <li>
 Willingness to travel both domestically and internationally as required
 </li>
 </ul>
 
 
 
 
 
 Why Join Us:
 
 
 <ul>
 <li>
 Competitive compensation package and potential for permanent placement following the temporary period.
 </li>
 <li>
 Opportunity to work at the forefront of biotechnology innovation in a collaborative and dynamic environment.
 </li>
 <li>
 Access to ongoing career development and networking opportunities through Kelly&reg; Science &amp; Clinical's expansive network of industry experts and recruiters.
 </li>
 </ul>
 
 
 
 
 If your qualifications align with the requirements of this role, we invite you to apply and take the next step in your career journey. Rest assured, even if this opportunity isn't the perfect match, your profile will remain within our network, ensuring you're connected to a wealth of future opportunities in the field of science and clinical research.
 
</div>

Catalent

<div>
 
 Position Summary
 
 
 
 Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, manufacture, and supply products that help people live better and healthier lives. Catalent is dedicated to delivering unparalleled service to pharma, biotech, and consumer health customers, supporting product development, launch, and full life-cycle supply. With time-tested experience in development sciences, delivery technologies, and multi-modality manufacturing, Catalent supports the acceleration of development programs and the launch of more than a hundred new products every year. Powered by thousands of scientists and technicians and the latest technology platforms at more than 40 global sites, Catalent supplies billions of doses of life-enhancing and life-saving treatments for patients annually. Catalent is committed to a Patient First culture through excellence in quality and compliance, and to the safety of every patient, consumer and Catalent employee.
 
 
 The Analytical Chemist II client compounds following client guidelines, CMTI procedures, policies, and cGMPs to ensure timely flow and completion of in-process micronization and milling and external analytical testing jobs. The Analytical Chemist II will also be responsible for technical review of peer data. Testing includes (but is not limited to) characterization of drug substance physical properties (particle size analysis, x-ray powder diffraction, surface area analysis etc.) and chemical testing of drug substance and drug product samples (HPLC, GC, Karl Fisher etc.), stability testing, release testing etc.
 
 
 This position is 100% on-site at the Malvern site.
 
 
 Shift: Monday - Thursday 12:00 pm - 10:30 pm
 
 
 
 The Role
 
 
 
 
 <ul>
 <li>
 Carry out the analytical testing activities of pharmaceutical actives and excipients according to client specific test methods, CMTI test methods, or USP tests.
 </li>
 <li>
 Verify cleaning of processing equipment through analytical testing procedures.
 </li>
 <li>
 Technical support and assistance in training of analytical chemist I (i.e. test methods, Documentation, etc).
 </li>
 <li>
 Support Management by communicating directly with clients regarding new projects, on-going projects, etc.
 </li>
 <li>
 Provide analytical support to CMTI Operations group, with emphasis on in-process particle size analysis, ID testing, controlled supply testing, cleaning verification etc. Communicate in-process testing results to operations personnel in a timely manner.
 </li>
 <li>
 Document all testing, deviations, investigations etc. as per cGMP and CMTI guidelines.
 </li>
 <li>
 Perform routine maintenance and conduct performance verification testing on analytical equipment.
 </li>
 <li>
 Maintain a clean, safe working environment. Responsibilities may include: glassware cleaning, solvent/sample disposal etc.
 </li>
 <li>
 All other duties as assigned.
 
 
 
 </li>
 </ul>
 
 The Candidate
 
 
 
 
 <ul>
 <li>
 Bachelor of Science in a scientific discipline; 2+ years' experience preferred.
 </li>
 <li>
 1+ years GMP Laboratory or equivalent experience.
 </li>
 <li>
 Ability to stand or walk for up to 8 hours per day, climb steps and ladders, and lift up to 40 pounds as needed.
 </li>
 <li>
 Ability to wear safety shoes when applicable.
 
 
 
 </li>
 </ul>
 
 Why You Should Join Catalent
 
 
 
 
 <ul>
 <li>
 Competitive medical benefits and 401K
 </li>
 <li>
 152 hours of PTO + 8 Paid Holidays
 </li>
 <li>
 Dynamic, fast-paced work environment
 </li>
 <li>
 Opportunity to work on Continuous Improvement Processes
 
 
 
 </li>
 </ul>
 
 Catalent offers rewarding opportunities to further your career!
 
 Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.
 
 
 personal initiative. dynamic pace. meaningful work.
 
 
 Visit Catalent Careers to explore career opportunities.
 
 
 Catalent is an Equal Opportunity Employer, including disability and veterans.
 
 
 If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to DisabilityAccommodations@catalent.com. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.
 
 
 Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written &amp; signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.
 
 
 Important Security Notice to U.S. Job Seekers:
 
 
 Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond&mdash; it is a fraudulent request. Please forward such requests to spam@catalent.com for us to investigate with local authorities.
 
 
 California Job Seekers can find our California Job Applicant Notice HERE.
</div>

Analytical Chemist II

Explore 2064+ Analytical chemist in United States this September. Find roles across top companies and apply now to boost your career.

2064 analytical chemist jobs IN United States

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Analytical Chemist II