Quality control chemist jobs in San Diego, CaliforniaCreate job alerts

SUMMARY: Seeking an experienced analytical chemist to join our Analytical Development & Quality Control (ADQC) group at the Research Associate II level. The ideal candidate will be familiar with HPLC and other chemistry techniques, possess a strong work ethic and strong technical background, demonstrate excellent oral and written communication skills, and have experience working in a GMP environment. The successful candidate will be able to perform the following responsibilities with a high degree of independence and attention to detail. RESPONSIBILITIES: • Conduct routine and non-routine analysis of Raw and Starting material samples, • Review analytical data for compliance to SOPs, • Assemble and document data for quality review, • Present and participate in internal and external scientific meetings, • Revise and update SOPs as needed (e.g., analytical methods, equipment procedures, and material specifications), • Conducts analytical investigations, • Applies knowledge of cGMP and GLP, • May develop and/or optimize analytical methods, • May author sections of scientific reports REQUIREMENTS: • BS or MS degree in Chemistry or related field, • 2+ years of experience in analytical development and quality control role, • Practical knowledge of HPLC, MS, and GC, including operation of instrumentation, • Familiarity with GMP requirements, with hands-on GMP experience preferred, • Experience following SOPs and recording data in laboratory notebooks or data collection forms, • Ability to interpret experimental results and demonstrate good judgement in resolving issues / making recommendations, • Detail oriented with strong organizational skills, • Excellent written and verbal communication skills, • Ability to manage priorities and maintain aggressive timelines for multiple projects

The Quality Control Chemist I conducts various analytical testing of raw materials, semi-finished intermediates, finished products, and new compounds/products in various stages of design and development to characterize and determine quality. Position: Quality Control Chemist I. Provide timely and hi

BS in Chemistry, Biochemistry, or related field. If you are a detail-oriented chemist looking to grow your career in a GMP environment, we encourage you to apply. We are seeking a Quality Control Chemist to perform analytical testing and ensure our products meet the highest GMP and quality standards

Degree in Chemistry, Engineering, or Life Science. The Quality Control Chemist I conducts various analytical testing of raw materials, semi-finished intermediates, finished products, and new compounds/products in various stages of design and development to characterize and determine quality. Degree

BS in Chemistry, Biochemistry, or related field. If you are a detail-oriented chemist looking to grow your career in a GMP environment, we encourage you to apply. Department Quality Control Role QC Chemist I Locations San Diego.

The Quality Control Chemist I conducts various analytical testing of raw materials, semi-finished intermediates, finished products, and new compounds/products in various stages of design and development to characterize and determine quality. Degree in Chemistry, Engineering, or Life Science, minimum

Job Title - Quality Control Chemist. Degree in Chemistry, Engineering, or Life Science. The Quality Control Chemist I conducts various analytical testing of raw materials, semi-finished intermediates, finished products, and new compounds/products in various stages of design and development to charac

My name is Nick Davis and I am with InstantServe LLC. We're currently recruiting for a role that we think would be a great fit for someone with your skills and experience. Would you be open to learning more about this? I have included a brief job description below to help you better understand the qualifications we are looking for: Our company places a high value on employee referrals, and we are willing to offer a generous referral bonus to anyone who successfully recommends a candidate that we end up hiring. If you know of anyone who you believe would be a great fit for this role, I would greatly appreciate it if you could provide a recommendation. Job Title: Associate Director / Director, Chemical Development Location: San Diego, CA Job type: Full time Permanent Shift: Full-time 8 hours a day 40 hours a week Pay Range: USD $180 - $210k Yearly/Annually + target bonus, long-term-incentives, 401k + Benefits Must-Haves 1minimum 9 years industry experience (NOT including postdoc) 2must be a process chemist with strong synthetic chemistry skills 3must be based in San Diego or willing to relocate to San Diego Nice-To-Haves 1big pharma experience (Merck, Janssen, AbbVie, Gilead, Amgen) Job Description Company Overview: We prize scientific excellence, creativity, team players and we are committed to continued innovation. We have worked hard to create a collaborative and dynamic work culture where your ideas and discoveries are valued and will have an impact. We are growing and there are opportunities for mentorship and career progression. Job Summary: The Associate Director / Director of Chemical Development will successfully develop robust synthetic processes and deliver non-GMP & GMP material on multi-kilogram scale in a safe, environmentally conscious, and efficient manner. This individual will be responsible for implementing strategies to progress compounds from preclinical development through commercialization with specific focus on delivering drug substance to support clinical and commercial needs for all small molecule programs. Essential Duties and Responsibilities: • Lead a team of external scientist(s) to conduct synthetic route scalability assessment, route scouting (as necessary), route selection, and route optimization to deliver non-GMP & GMP material on multi-kilogram scale., • Proactively work with CDMO partners to manage process development and manufacturing of intermediates and API; management of API/retain inventory., • Represent Chemical Development on CMC subteams., • Responsible for phase appropriate synthetic route design and implementation of control strategies for regulatory starting materials and drug substance., • Lead fate and purge studies and genotoxic impurity evaluation., • Lead technical transfers of intermediate/API processes and support external manufacturing activities by acting as PIP (person in plant)., • Work cross-functionally to communicate Chemical Development timelines/objectives., • Contribute to quarterly updates of Chemical Development budget & resource allocation., • Author and review the relevant CMC sections for US and ex-US regulatory filings., • Work with quality assurance (QA) to manage the release of GMP drug substance and resolve technical issues or deviations., • Review and approve master batch records, validation protocols/reports, and specifications required for drug substance manufacturing, as well as author development reports., • Monitor compounds in preclinical development and develop synthetic routes to key cores for advanced leads., • Work with Medicinal Chemistry to ensure that synthetic route, final solid form, and compound properties are suitable for development., • Support PAR, DOE studies, and validation activities for drug substance. Educational and Experience Requirements: Ph.D. with 9+ years of experience or BS/MS with 15+ years of experience in organic chemistry, chemical engineering, pharmaceutical sciences or closely related discipline with relevant small molecule development experience. Knowledge and implementation of ICH Guidelines and current Good Manufacturing Practices (cGMPs). Knowledge of API solid state properties and the potential impact to drug product manufacturing and performance. Ability to manage multiple projects spanning all phases of development and rapidly adapt to changing program needs. Strong track record in process chemistry development, CDMO management and multi-kilogram scale manufacturing. Excellent written and verbal communication skills. Ability to effectively organize and prioritize tasks to achieve deadlines. Ability to effectively manage and develop a high functioning team. Recruit, develop and retain top Chemical Development talent to drive the organizational strategy, next generation manufacturing teams, and lifecycle management.

The University of California prohibits smoking and tobacco use at all of its university-controlled properties.

Serve as a trusted internal partner, offering guidance, feedback and hands-on support to elevate planning quality across the firm. An ideal candidate will be motivated by our mission to empower families to take control of their financial lives, live their values with clarity and peace of mind and ac

Balance standardization with flexibility to ensure advisors can deliver both high-quality and highly personalized advice. Serve as a trusted internal partner, offering guidance, feedback and hands-on support to elevate planning quality across the firm. An ideal candidate will be motivated by our mis

Quality Control Administrative Position. We're looking for someone organized, detail-oriented, and proactive to join our Quality Control team. At Lloyd Pest Control, we're a family-owned company that values doing the right thing, supporting our team, and creating opportunities for growth.

A Taste of What You'll Do Looking for an exciting seasonal opportunity in the worlds of wine and chemistry? Come join GALLO's Turner Road Vintners Quality Assurance team! We are hiring seasonal Lab Technicians for the 2026 season. With the guidance of our experienced team, you will observe the depar

A leading staffing and recruiting firm in San Diego is seeking a skilled Hardware Process Engineer for a remote role.The ideal candidate will have at least 5 years of hardware engineering experience and expertise in regulatory standards.This position involves developing hardware design documentation

Raytheon - 8650 Balboa Avenue - Responsibilities: Conduct in-process and final inspections of electronic assemblies to determine product quality and acceptability of inspected items; Identify and report defects, deviations, and non-conformities; Collaborate with engineering and production teams to r

A leading medical device company is seeking a Staff Process Engineer (Hardware) for a remote position based in San Diego, CA.The role involves defining and implementing hardware design processes while ensuring compliance with regulatory standards.The ideal candidate should have at least 5 years of e

Research Administration Business Development AssociateJob Type: Full-timeWorkWork from Home / Remote / some travel may be required post-pandemic.Hours: 8:00 AM – 5:00 PM (Monday-Friday).Candidates must be somewhat flexible, as working hours may vary depending upon geographic location/time zone.Ove

In-vivo procedures, blood/tissue collection.Clean & maintain lab equipment.Conduct sample collection & testing – record test data/results.Follow GLPs & SOPs and ensure overall compliance.Perform other duties as needed.Bachelor's degree in Life Sciences or similar.Good verbal & writ

Assist with analyzing process data and critical quality parameters for control of the manufacturing process. A pioneer in soft chemistry, SNF has long been present on all continents, employing 8,150 people, including more than 2,300 in the USA. The process engineer will be expected to perform proces

Proficiency with Six Sigma/Lean, statistical tools, and manufacturing execution documentation (pFMEA, control plans, sampling plans). Meet The TeamWe are seeking a Principal Data Analytics Engineer to serve as a technical authority for advanced data analysis in support of engineering, manufacturing,

Location : San Diego, CA (Hybrid 1 day/week).Reports to : Associate Director Clinical Trial Management.Polaris Pharmaceuticals, part of Polaris Group, is a multinational biotechnology company focused on the discovery, development, and manufacturing of innovative therapies, with a primary focus on on

Experience with maintaining, tuning, scripting and programming motion control equipment.

Eligibilities and Qualifications.

Participate/perform the prescribed Quality Control (QC)/College of American Pathology (CAP) programs. Perform clinical laboratory tests in any one or a combination of areas as described in following sections of the laboratory: hematology, chemistry, urinalysis, serology, microbiology and blood bank.

Outstanding organizational talents and attention to detail, particularly in quality control and documentation practices. Conduct routine and complex clinical lab tests-covering chemistry, hematology, immunology, and beyond-adhering to established protocols. Meticulously document all procedures, ment

Firestorm is seeking a Quality Inspector to play a critical role in ensuring the quality, reliability, and performance of next-generation aerospace and defense hardware. Partner with manufacturing, engineering, and quality teams to resolve quality issues and improve processes. This role will work ha

Conducts examinations and quality control inspections on products, materials and components at various stages of the production process to ensure compliance with established quality and reliability standards. The Quality Inspector inspects a range of components, parts and/or products for the area as

Work closely with machinists and manufacturing teams to resolve quality issues and improve product quality. Assist with the completion and maintenance of inspection reports and quality documentation. Provide guidance to production personnel regarding quality standards and inspection expectations.

Interface with Engineering, Production, Planning, Quality Engineering and Customers.

This role supports quality conformance, documentation, and inspection activities in a fast?paced, safety?critical industrial environment. The Quality Assurance Inspector I is responsible for conducting in?process and final inspections to verify compliance with applicable technical requirements, draw

Nice to haves (in descending order): experience in Inspection in a biotech or pharma business, other quality assurance experience in biotech or pharma, manufacturing experience in biotech/pharma. Review dilution, bottling & packaging processes to ensure all finished products meet specifications prio

May monitor and verify quality in accordance with statistical process or other control procedures. Under general direction this position is responsible for inspecting cables, parts, assemblies, tooling fixtures and material to ensure compliance with customer requirements, company specifications, and

Interface with Engineering, Production, Planning, Quality Engineering and Customers.

Participates in establishing quality standards for life cycle maintenance, documentation, development methods, and testing. Documents and analyzes test results, and makes recommendations to improve overall quality. May provide quality-related training.

Now Hiring: Quality Assurance Inspector I. This role supports quality conformance, documentation, and inspection activities in a fast?paced, safety?critical industrial environment. The Quality Assurance Inspector I is responsible for conducting in?process and final inspections to verify compliance w

Quality Assurance (QA) Inspector II[14419]. Review dilution, bottling & packaging processes to ensure all finished products meet specifications prior to releasing products to Finished Goods Inventory or Inventory Control for bottled components. The QA Inspector II will also be responsible for suppor

For example, that convergent microRNA repression of key targets, independent of transcriptional change, controls critical developmental transitions and drives neuronal subtype diversification (Du et al. RNA binding sites) that control gene dosage of haploinsufficient NDD genes, with direct translati

Conducts examinations and quality control inspections on products, materials and components at various stages of the production process to ensure compliance with established quality and reliability standards. Identifies moderately difficult quality issues in design, process or other inefficiencies t

Reports to Supervisor or Manager of Quality Assurance. Actively participates in implementing and monitoring continuous improvement initiatives to improve safety, improve quality, reduce cycle time, and reduce costs. Performs other Quality Assurance tasks as assigned by supervisor/manager.

Quality Technician 2 - Metrology Inspector. Applied Composites (AC) is seeking a Quality Technician 2 - Metrology Inspector.

Conducts examinations and quality control inspections on products, materials and components at various stages of the production process to ensure compliance with established quality and reliability standards.