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Job DescriptionAnalytical Chemist II Location: San Diego, CA (Onsite) Position Overview We are seeking an experienced Analytical Chemist II to join our Analytical Method Development & Transfer team in San Diego. In this role, you will support the development, qualification, validation, and transfer of analytical methods for oligonucleotides, raw materials, and reagent consumables used in advanced genomics and sequencing applications. The ideal candidate brings strong hands-on experience with HPLC/UHPLC, LC-MS, and analytical method development in a regulated environment. This position offers the opportunity to work with cutting-edge technologies, collaborate across manufacturing, quality, and development teams, and directly contribute to product quality and manufacturing success. Key Responsibilities • Develop, optimize, qualify, validate, and transfer analytical methods for oligonucleotides, raw materials, and reagent consumables., • Operate, troubleshoot, and maintain analytical instrumentation, including HPLC/UHPLC and LC-MS systems., • Support oligonucleotide synthesis, release testing, quality testing, and analytical characterization activities., • Utilize UV-Vis, FTIR, and NMR techniques for material characterization and routine testing., • Analyze complex datasets and provide scientifically sound conclusions and recommendations., • Investigate analytical issues, perform root cause analysis, and implement corrective actions., • Author and review technical documents including protocols, validation reports, transfer reports, SOPs, and work instructions., • Ensure compliance with GMP, GDP, FDA cGMP, ICH, and USP requirements., • Partner with Manufacturing, Quality, and R&D teams to support multiple projects and timelines., • Contribute to continuous improvement initiatives that enhance analytical methods, laboratory efficiency, and product quality.Required Qualifications, • Bachelor's, Master's, or PhD in Chemistry, Analytical Chemistry, Biochemistry, Molecular Biology, or a related scientific discipline., • 3+ years of analytical method development experience in a regulated laboratory environment., • Experience with analytical method qualification, validation, and transfer., • Strong hands-on expertise with HPLC/UHPLC operation, troubleshooting, and data interpretation., • Experience with LC-MS instrumentation and analytical data analysis., • Knowledge of oligonucleotide testing, characterization, and quality control processes., • Experience using analytical techniques such as UV-Vis, FTIR, and NMR., • Strong technical writing skills with experience preparing protocols, reports, SOPs, and related documentation., • Working knowledge of FDA cGMP, ICH, USP, GMP, and GDP requirements., • Ability to manage multiple priorities in a fast-paced environment while working independently and collaboratively.Preferred Qualifications, • Experience in Analytical Method Development and Transfer groups., • GMP experience within biotechnology, life sciences, pharmaceutical, or manufacturing environments., • Familiarity with genomics, sequencing technologies, or nucleic acid-based products., • Strong problem-solving skills with the ability to troubleshoot complex analytical challenges., • Continuous improvement mindset and commitment to operational excellence.Why Join Us?, • Work with innovative genomics and sequencing technologies., • Collaborate with highly skilled cross-functional teams., • Gain exposure to advanced analytical instrumentation and methodologies., • Make a direct impact on product quality and manufacturing success., • Opportunities for professional growth and long-term career development.Work Environment This is a full-time, onsite laboratory position based in San Diego, CA. The role follows a typical Monday-Friday daytime schedule and involves hands-on work with advanced analytical instruments including HPLC/UHPLC, LC-MS, UV-Vis, FTIR, and NMR. The environment is collaborative, fast-paced, and focused on delivering high-quality scientific results in support of commercial manufacturing and product development. Job Type & Location This is a Contract position based out of San Diego, CA. Pay and Benefits The pay range for this position is $36.00 - $45.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in San Diego,CA. Application Deadline This position is anticipated to close on Sep 18, 2026. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service. The company is an equal opportunity employer and will consider all applications withoutregard to race, sex, age, color, religion, national origin, veteran status, disability,sexual orientation, gender identity, genetic information or any characteristic protectedby law. If you would like to request a reasonable accommodation, such as the modification oradjustment of the job application process or interviewing process due to a disability,please email actalentaccommodation@actalentservices.com for other accommodation options. San Francisco Fair Chance Ordinance:Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in thecity and county of San Francisco, we will consider for employment qualified applicantswith arrest and conviction records. Massachusetts Lie Detector:It is unlawful in Massachusetts to require or administer a lie detector test as acondition of employment or continued employment. An employer who violates this lawshall be subject to criminal penalties and civil liability. Use of Artificial Intelligence (AI):We may use Artificial Intelligence (AI) to support parts of our hiring process,including sourcing, screening, and evaluating candidates. AI helps assess applicationsand qualifications, but final decisions are made by our hiring team. By applying, youacknowledge and agree that your application may be reviewed using AI tools.

Job Description Location: San Diego, CA Job Type: Full-Time Salary Range: $150,000 - $160,000 Position Overview We are seeking a Staff Surface Process Engineer / Surface Chemist to develop and scale surface chemistry processes. This role combines deep expertise in precision substrate processing, process equipment engineering and surface chemistry with hands-on laboratory work in a fast-paced, multidisciplinary environment. The successful candidate will drive development of surface chemistry processes including cleaning, coating and surface functionalization and other processes. This role requires experience with equipment used to manufacture and characterize these surfaces. Key Responsibilities • Develop surface processing methods including cleaning, deposition, coating, curing, and QC., • Develop robust vapor-phase deposition processes including silanization and other surface modification techniques, with emphasis on process uniformity, reproducibility, and manufacturability., • Lead development, optimization, qualification, and troubleshooting of plasma cleaning processes., • Specify, develop, optimize, and troubleshoot process equipment including vapor deposition systems, plasma tools, ovens, wet processing tools, and related automation., • Establish process windows, critical process parameters, and statistical process controls for surface treatments., • Design and execute statistically rigorous experiments (DOE) to understand process interactions and optimize surface performance., • Characterize processed surfaces using techniques such as ellipsometry, contact angle, AFM, optical microscopy, fluorescence imaging, profilometry, XPS, SEM, and related analytical methods., • Translate laboratory processes into scalable manufacturing methods with high yield and reproducibility., • Drive equipment selection, installation, qualification, and process transfer to manufacturing., • Mentor junior scientists and engineers while fostering rigorous experimental design, scientific curiosity, and rapid technical iteration. Qualifications Required: • M.S. (+8 years of relevant industrial experience) or Ph.D. (+ 4 years) in Mechanical Engineering, Chemistry, Chemical Engineering, Materials Science, Biomedical Engineering, or a related discipline., • Demonstrated expertise in surface processing and process development., • Extensive experience in one or more of the following:, • Coating methods including spin coating and dunk coating, • Plasma cleaning equipment, • Chemical mechanical polishing (CMP), surface planarization, • Vapor-phase surface deposition processes and equipment, • Wet chemical cleaning and substrate preparation, • Strong understanding of process development for glass, silicon, metal oxide, and other semiconductor-related materials., • Experience developing manufacturing-ready surface processes with an emphasis on spatial uniformity, repeatability, process capability, and yield., • Experience selecting, operating, qualifying, and troubleshooting process equipment., • Experience with statistical experimental design (DOE), process optimization, and statistical analysis tools (JMP, Python, R, etc.)., • Experience using surface characterization techniques including ellipsometry, contact angle, AFM, profilometry, fluorescence microscopy, SEM, XPS, or related methods., • Strong written and verbal communication skills., • Comfortable working in a fast-moving, highly collaborative environment., • Hands-on willingness to develop and troubleshoot processes in the laboratory. Preferred: • Experience with biotechnological device manufacturing., • Experience integrating surface chemistry with photolithography, nanoimprint lithography, or other advanced fabrication techniques., • Experience transferring laboratory processes into pilot or high-volume manufacturing., • Experience supporting manufacturing equipment qualification and process validation. Why Join Us • Work with a multidisciplinary team spanning chemistry, engineering, optics, biology and manufacturing., • Play a central role in developing scalable processes from research through commercialization., • Competitive compensation, equity, comprehensive benefits, and flexibility to support work-life integration. We are an equal opportunity employer. We thrive on diversity and collaboration

Job DescriptionCompany Description Consider joining Lancaster Laboratories where people are the most important element in our chemistry. Celebrating 50 years of service, Lancaster Laboratories is a leading contract lab providing testing and research services in the environmental, pharmaceutical, and biopharmaceutical sciences to clients worldwide. Job Description Eurofins PSS in San Diego is looking to expand its capabilities in protein generation and analytical characterizations within Protein Biosciences group. The overall responsibility of the individual will be to assist in protein and other discovery reagents expression and purification, analytical assays of purified proteins, and other related lab tasks to support reagent generation. Key Objectives/Deliverables: • Proficient in routine antibody purification using established platform process, • Assist protein reagents purification using various column separation techniques, • Independently conduct antibody/protein analysis using HPLC and other related methods for protein characterization, • Assistance in general lab tasks to support analytical biochemistry and biophysical techniques, including sample preparation, data collection and data analysis, • Appropriate documentation of all experimental results, and the sharing and presentation of obtained results, • Highly detail-oriented, eager to learn new techniques, and maintains high precision in daily lab operationsQualifications, • Authorization to work in the United States indefinitely without restriction or sponsorship, • Bachelor’s degree in biology, biochemistry, chemistry, or similar discipline, • Experience in protein purification and analytical characterizations. Additional Information What we offer: • Excellent full time benefits including comprehensive medical coverage, dental, and vision options, • Life and disability insurance, • 401(k) with company match, • Paid vacation and holidays, • Career Development and continuing education opportunities, • Compensation Range: $52,000 - $57,000/yr Position is full-time, 8am - 5pm with occasional overtime required. Eurofins Lancaster Laboratories Professional Scientific Services® (PSS) is a global, award-winning insourcing solution that places our people at our clients’ site dedicated to running and managing laboratory services while eliminating headcount, co-employment and project-management worries. We infuse our 55-year track record of scientific and laboratory operations expertise, as well as HR and great place to work best practices, to recruit, hire, train and manage highly qualified scientists to perform laboratory services using our client’s quality systems and equipment. Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Job Description Beloteca, Inc. is a generic pharmaceutical development company specializing in the development of injectable products. It is desirable that the candidate have past practical experience and education in handling chemicals, operating laboratory equipment, generating and manipulating data, as well as computer database and word-processing skills. Job Description: • Independent execution of various standard laboratory techniques, including but not limited to H/UPLC, GC, water content analysis per USP, appearance assessment, water activity per USP, • May participate in qualification/verification of assays, • Assay and documentation review and report writing, • Responsible for exhibiting professional behavior with both internal and external business associates that reflects positively on the company and is consistent with the company’s policies and practices., • Execution of more advanced analytical techniques with assistance such as LC/MS, DSC, and TGA, • Independent preparation of samples, solutions, instrument set-up and breakdown, • Independent preparation of data packets and creation of stability data sheets and Certificates of Analysis to summarize analytical testing, • Assisted participation in Out of Specification investigations and the documentation of analytical deviations along with Qualified Investigators and management, • Understand and apply ICH and FDA guidance Basic Qualifications: • BS in Biology, Chemistry and/or related science discipline., • Computer literacy in Windows applications and the MS Office., • Excellent oral and written communication skills are essential., • Minimum of 3 years experience with HPLC, UPLC, GC, Karl Fisher, pH, • Maintain a safe working environment for all employees, ensuring compliance to all local, state, and federal codes and regulations. Preferred Qualifications: • Ability and willingness to work flexible hours., • Great attention to detail, quality, and a desire for success., • Self-motivated individual with the ability to learn, lead and strengthen the Beloteca, Inc. team.

Job Description Analytical Scientist, Ph.D. Location: San Diego, CA Job Type: Full-Time, Onsite About Us We are an innovative, stealth-mode biotech focused on developing best-in-class delivery for in vivo gene editing. Job Summary We are seeking a highly skilled Analytical Scientist to join our team in a hands-on, lab-based role. The successful candidate will be responsible for developing, validating, and executing analytical methods for the characterization of proteins, RNA, and lipids, central to our lipid nanoparticle (LNP) gene editing platform. This role requires deep expertise in LC/MS and complementary analytical techniques, with the ability to independently design experiments, troubleshoot complex analytical challenges, and deliver high-quality data to support research, process development, and regulatory submissions. The Analytical Scientist will serve as a subject matter expert across the organization on bioanalytical methodologies. Title and salary will be commensurate with experience. Responsibilities • Design, develop, optimize, and validate analytical methods for the characterization of proteins (e.g., Cas9, antibody constructs), mRNA, gRNA, and lipid components using LC/MS (intact mass, peptide mapping, oligonucleotide analysis, lipidomics)., • Perform routine and non-routine hands-on analyses in the laboratory; operate, maintain, and troubleshoot LC/MS instrumentation (e.g., Q-TOF, Orbitrap, triple quadrupole) and associated sample preparation workflows., • Develop and execute orthogonal analytical methods including but not limited to HPLC/UPLC (RP, SEC, IEX, HILIC), capillary electrophoresis, UV/Vis spectrophotometry, and fluorescence-based assays., • Characterize LNP drug product attributes including lipid composition and ratios, encapsulation efficiency, RNA integrity, protein identity and purity, and post-translational or chemical modifications., • Support formulation development, process development, and stability studies by providing timely, high-quality analytical data and interpretation., • Author and review analytical methods, protocols, technical reports, and SOPs to support research activities and future regulatory filings., • Analyze and interpret complex mass spectrometry datasets; present findings to cross-functional teams and contribute to program-level decision-making., • Evaluate and implement new analytical technologies, software tools, and workflows to improve throughput, sensitivity, and data quality., • Collaborate closely with formulation scientists, biologists, process development, and CMC teams to ensure analytical needs are met across programs., • Maintain laboratory equipment, consumable inventories, and ensure compliance with safety and data integrity standards. Qualifications • Ph.D. in Analytical Chemistry, Biochemistry, Chemistry, Pharmaceutical Sciences, or a related field., • 3+ years of industry or postdoctoral experience in bioanalytical method development and characterization of biopharmaceuticals, nucleic acids, or lipid-based drug products., • Extensive hands-on experience with LC/MS platforms (Q-TOF, Orbitrap, or triple quadrupole) for protein, oligonucleotide, and/or lipid analysis., • Proficiency in chromatographic techniques (RP-HPLC, SEC, IEX, HILIC) and associated data analysis software (e.g., MassLynx, Xcalibur, Empower, BioPharma Finder, UNIFI)., • Strong understanding of protein characterization (intact mass, peptide mapping, glycosylation, disulfide mapping) and/or nucleic acid analysis (RNA integrity, modification mapping, sequence confirmation)., • Demonstrated ability to independently design experiments, interpret complex datasets, and communicate results clearly in written and oral formats., • Strong problem-solving skills and ability to manage multiple projects in a fast-paced environment. Preferred Qualifications • Experience with lipid nanoparticle characterization and/or lipidomics by LC/MS., • Familiarity with mRNA and guide RNA analytical characterization (e.g., capillary electrophoresis, IP-RP-HPLC, LC/MS-based modification analysis)., • Experience supporting GMP or GLP analytical activities, method validation per ICH guidelines (Q2/Q14), or contributing to regulatory submissions., • Knowledge of gene therapy or gene editing product development and associated analytical expectations., • Experience with mass spectrometry-based quantitative assays (e.g., MRM/SRM for lipid or protein quantitation). Benefits • Competitive salary, equity, and comprehensive benefits package., • Opportunities for professional growth and leadership development., • Fast-paced, collaborative, and innovative work environment., • We offer an exceptional benefits package to include Medical, Dental, Vision, Life, Disability, a 401k Match of 4%, Paid Time Off and Equity. How to Apply Interested candidates should submit their resume and a cover letter detailing relevant experience. To be considered for the role, applicants must be: • Eligible to work in the United States for any employer without current or future sponsorship., • Able to work onsite in our San Diego, CA lab., • Direct candidates only and not from a third party, i.e., staffing agency. Equal Opportunity Employer We are an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. All employment decisions are based on business needs, job requirements, and individual qualifications, without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran, or disability status. Salary Range $110,000 - $140,000

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