Trabajos chemist en Chula Vista, CaliforniaCrear alertas

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, • 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, • 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 Job Title: Manufacturing Chemist Job Description The Manufacturing Chemist synthesizes and manufactures complex organic molecules in a regulated laboratory environment, using established protocols and advanced chromatographic techniques. This role performs HPLC purification and analytical testing, supports commercial-scale manufacturing processes, and ensures all activities comply with GMP, ISO, and Quality Management System requirements. The position offers hands-on experience with complex molecules, regulated systems, and cross-functional collaboration in a safety-driven, process-focused culture. Responsibilities • Synthesize and manufacture complex organic molecules by following established synthetic organic chemistry protocols., • Perform HPLC purification and analytical testing, including instrument setup, method execution, and data analysis., • Execute daily laboratory activities with minimal supervision after completing training., • Follow all Standard Operating Procedures (SOPs), Work Instructions, and Quality Management System (QMS) requirements., • Generate, analyze, and document experimental and manufacturing data to support process and product decisions., • Maintain accurate and compliant records in accordance with Good Documentation Practices (GDP) in GMP and ISO-regulated environments., • Complete inventory management activities, including labeling, tracking, and performing computerized inventory transactions., • Process manufacturing work orders using ERP and/or Manufacturing Execution Systems (MES)., • Maintain laboratory equipment, including routine cleaning, basic troubleshooting, and supporting calibration and upkeep activities., • Collaborate cross-functionally with R&D, Quality, Environmental Health & Safety (EH&S), and Manufacturing Engineering teams., • Perform safety and quality inspections as part of an established 6S program and support continuous improvement initiatives., • Adhere to all safety, regulatory, and compliance requirements in all laboratory and manufacturing activities., • Handle chemicals, reagents, and lab equipment safely and responsibly in a manufacturing or regulated lab environment., • Hands-on bench experience synthesizing organic molecules using established synthetic organic chemistry protocols., • Ability to execute chemical reactions safely, accurately, and reproducibly in a manufacturing or regulated laboratory environment., • Experience with purification and analysis using HPLC systems, including Reverse Phase and/or Ion Exchange chromatography., • Ability to prepare samples, run HPLC sequences, and interpret chromatographic data using systems such as Agilent OpenLab and GE AKTA., • Proven ability to follow SOPs and Work Instructions and operate within GMP and ISO-regulated environments., • Strong Good Documentation Practices (GDP) and experience generating and maintaining accurate laboratory and manufacturing records., • Proficiency with standard laboratory instrumentation, including HPLC/UPLC, reactors, rotary evaporators (rotavaps), UV/Vis spectrophotometers, and pH meters., • Bachelor’s degree in Chemistry, Biochemistry, or Biology., • 0–2 years of hands-on laboratory experience in synthetic chemistry or chemical manufacturing., • Strong written and verbal communication skills., • High attention to detail, strong organization skills, and commitment to data integrity., • Experience working in GMP manufacturing environments and familiarity with lean manufacturing principles., • Knowledge of chromatography beyond HPLC, including general chromatographic techniques and purification strategies., • Experience using ERP and/or MES systems to process manufacturing work orders and manage inventory., • Familiarity with laboratory quality systems and QMS processes in a regulated environment., • Background or coursework in chemistry, biochemistry, or biology that supports understanding of complex organic molecules and analytical methods., • Comfort working with 6S or similar continuous improvement and workplace organization programs., • Ability to collaborate effectively with cross-functional teams such as R&D, Quality, EH&S, and Manufacturing Engineering. This role is based in an onsite laboratory environment at a corporate headquarters facility. The position follows standard business hours, typically around 8:00 AM to 5:00 PM, with flexibility within a 7:00 AM to 5:00 PM window, for a full-time, non-exempt schedule of approximately 40 hours per week. The work environment includes routine use of laboratory instrumentation such as HPLC/UPLC systems, reactors, rotary evaporators, UV/Vis spectrophotometers, pH meters, and chromatography systems including Agilent OpenLab and GE AKTA. The culture is collaborative, safety-driven, and process-focused, emphasizing GMP and ISO compliance, 6S practices, and continuous improvement. Team members work closely with R&D, Quality, EH&S, and Manufacturing Engineering in a highly regulated, quality-oriented setting that supports commercial-scale life sciences manufacturing. Job Type & Location This is a Contract position based out of San Diego, CA. Pay and Benefits The pay range for this position is $27.50 - $34.50/hr. 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 • Hiring diverse talent, • Maintaining an inclusive environment through persistent self-reflection, • Building a culture of care, engagement, and recognition with clear outcomes Our Bangalore, Hyderabad, Pune, and Chennai delivery centers are hubs of engineering expertise, with core capabilities in mechanical and electrical engineering, systems and software, and manufacturing engineering. Our teams deliver work across multiple industries including transportation, consumer and industrial products, and life sciences. We serve more than 4,500 clients, including many Fortune 500 brands. Learn more about how we can work together at actalentservices.com.

About Mercor’s talent network Join our Chemist Expert Network to connect with leading AI labs and companies seeking your expertise. About Mercor projects Experts in our network contribute to: - Training and evaluating AI models in Chemistry - Creating tasks and deliverables based on real-world

Facility: Coronado Hospital City Coronado Department Job Status Regular Shift Variable FTE 1 Shift Start Time Shift End Time California Clinical Laboratory Scientist (CLS) Generalist license - CA Department of Public Health; Other Hours : Shift Start Time: Variable Shift End Time: Variable AWS Hours Requirement: 8/40 - 8 Hour Shift Additional Shift Information: Weekend Requirements: As Needed On-Call Required: No Hourly Pay Range (Minimum - Midpoint - Maximum): $57.740 - $74.490 - $83.440 The stated pay scale reflects the range that Sharp reasonably expects to pay for this position. The actual pay rate and pay grade for this position will be dependent on a variety of factors, including an applicant's years of experience, unique skills and abilities, education, alignment with similar internal candidates, marketplace factors, other requirements for the position, and employer business practices. What You Will Do Provides the technical knowledge, expertise and judgment required to support the Sharp HealthCare (SHC) mission and scope of laboratory services. Required Qualifications * Other : Education required for CA State CLS. * 5 Years experience in a Clinical Laboratory as a CLS required; including competency and expertise in one or more clinical departments. * California Clinical Laboratory Scientist (CLS) Generalist license - CA Department of Public Health OR California Clinical Chemist Scientist License - CA Department of Public Health OR California Clinical Microbiologist Scientist License - CA Department of Public Health OR California Clinical Toxicologist Scientist License - CA Department of Public Health OR California Clinical Histocompatability Scientist License - CA Department of Public Health OR California Clinical Genetic Molecular Biologist Scientist License - CA Department of Public Health OR California Clinical Cytogeneticist Scientist License - CA Department of Public Health -REQUIRED Other Qualification Requirements Communication and TeamworkProactively initiates communication and works cooperatively with others to successfully complete work assignments.Demonstrates positive verbal and non-verbal communication skills.Completes documentation legibly, accurately, and timely.Stays informed through staff meetings, electronic communication, in-services, and educational opportunities.Establishes effective working relationships between internal and external customers.Seeks opportunities for feedback to improve effectiveness of own communication.Validates messages by clarifying expectations and verifying understanding of agreements/action plans and utilizing communication tools, such as Closed Loop and SBAR. * Demonstrates flexibility and AdaptabilityUses time effectively and actively sets priorities.Demonstrates flexibility in work practices and adjusts to unscheduled situations.Cooperates with initiatives to improve work processes.Tries new ideas and new ways of doing thingsPositively embraces and is receptive to change and actively participates in the process. * Equipment Use, Testing and DocumentationUtilizes all equipment (including phone, copier, fax, etc.), instruments, products, and other tools per manufacturer's and training instructions and according to established procedures; facilitates issue resolution.Reports, documents and resolves or facilitates resolution of equipment/analyzers/tool/reagent issues and failures in a timely and efficient manner.Removes defective equipment from use, documents problem, and notifies appropriate personnel for repair; verifies equipment inspections are up-to-date. Follows through on problem resolution and validates equipment/analyzers performance post repair.Participates in analyzer and test methodology, evaluation, selection and validation, and provides input in decision-making processes.Demonstrates competency and efficient use of all tool applications (IT, PC, other system/software) and equipment to produce the end product. Demonstrates advanced competency of current software applications, including troubleshooting middleware issues, validating Auto-verification criteria, and working with vendor and IT to resolve software issues.Performs required preventive and corrective maintenance on equipment/analyzers/tools, including comprehensive validation of accuracy, complete documentation of work orders/issues and scheduled review of data/logs/reports as required by CLIA, CA State, CAP and other regulatory agencies.Actively manages inventory and demonstrates ability to evaluate consumables (reagent/supply) inventory to prevent shortages; alerts ordering personnel and proactively resolves immediate issues/shortages. With lab leadership approval, works with vendors to make appropriate changes to standing orders to meet business needs.Supervises and uses equipment and related applications in completing testing and documentation processes. * LeadershipCollaborates with and advises Directors, Managers, Sr. Specialists, Leads and section staff in maintaining and enhancing technical, managerial, and financial performances.Assists in the development and enhancement of laboratory services through collaboration with patient care and support services to provide optimal patient care.Develops and institutes policies and procedures to facilitate application of SHC corporate commitment to compliance guidelines.Acts as Technical Consultant regarding abnormal or unusual orders or results: interacts with staff and physicians to solve problems and provide interpretation of lab procedures and processes; may include oversight of near patient testing; performs technical lead duties.Apprises Senior Specialists, Lab Managers or Pathologists of conditions or situations that may be or are compromising quality of care.Supports and provides input for development, revisions, and implementation of policies and procedures to provide consistent quality lab services to all customers; participates in annual review of policies and procedures.Conducts regularly scheduled section meetings/huddles providing updates and communication to assigned staff; holds 4-5 section meetings and directs at least 6 subgroup meetings annually.Performs or provides input for performance appraisals and corrective action of assigned staff to Lab Manager/Director; completes performance appraisals within 30 days of anniversary date.Conducts or facilitates core and technical competency development and assessment of all assigned staff members.Adjusts for changes in workload and shifting of staff and skill mix; makes recommendations for staff utilization, development, and section process optimization.Reviews patient results with appropriate actions or coaching of staff when problems are found; assists Lab Manager/Director with personnel problem solving activities; including documentation and coaching with resolution, follow through, and prevention.Assists in maintaining CAP, JCAHO, CA State, AABB, FDA, and other accreditation and regulatory agency standards and regulations.Demonstrates emotional intelligence, critical thinking, and logical decision-making, especially under critical and stressful situations, to reach acceptable resolutions. * Test Processes by evaluating quality control systems, data and outcomesSupervises and performs pre-analytical, analytical, and post-analytical tests and processes by evaluating quality control systems, data, and outcomes.Completes and assesses QC performance, proficiency testing, test validation/calibration/linearity with indicated corrective action and resolution as needed, including scheduled review.Coordinates and completes processes to meet standards established to maintain quality testing, including collaboration and engagement in continuous improvement of processes.Has knowledge of and reviews and monitors compliance of quality assurance indicators; works with the laboratory team to meet/exceed the established thresholds. Maintains expected goals and implements action plans as needed.Completes, validates and monitors daily position tasks within expected timeframes to meet QA indicator goal expectations.Identifies errors and follows-through with investigation, correction, documentation, coaching and notification to appropriate caregiver and lab leadership. * Test Processes relative to diagnosis, assessment and treatmentSupervises and performs pre-analytical, analytical and post-analytical test processes and evaluates results produced relative to the diagnosis, assessment, and treatment of disease.SHC corporate commitments to compliance training principles are correctly and appropriately utilized when performing assigned procedures as written.Completes testing procedures without error using written policies, procedures and other appropriate resources; identifies issues in and submits necessary revisions to policies and procedures.Performs new procedures and policies within acceptable training time intervals; meets/exceeds department turnaround time goals.Documents activities and results consistently, thoroughly and legibly; proof reads and double checks work in assigned section to achieve zero defects and zero harm.Reviews operational reports for possible clerical and analytical errors and make correction as necessary.Evaluates data for accuracy and verifies any questionable finding with thorough investigation and appropriate follow-through.Supervises and performs pre-analytical (patient reception, sample collection, processing) and analytical procedures and demonstrates assessment of testing factors with regard to patient age and population specific groups. Sharp HealthCare is an equal opportunity/affirmative action employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, gender, gender identity, sexual orientation, age, status as a protected veteran, among other things, or status as a qualified individual with disability or any other protected class

Industry laboratory experience (synthetic organic chemistry preferred over biochemistry/bio but willing to review all laboratory resumes). The Production Chemist I supports the manufacture, analysis, and processing of polymers from raw material, intermediate, to finished goods inventory. Degree in C

Position : Production Chemist II (Strong Chemist Exp is Required). Industry laboratory experience (prefer chemistry over biochemistry/bio but willing to review all laboratory resumes). Chemistry with a minimum of 2 years of experience in an industry synthetic chemistry lab or a B.

A leading AI solutions company is seeking a skilled computational chemist to join their AI Simulation team focused on drug discovery.

A leading biotechnology company in San Diego seeks an experienced Associate Principal or Principal Scientist in Computational Chemistry.