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Job DescriptionQUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and enthusiastic to join our team. In this role, you’ll work with a highly enthusiastic team, contributing in a world-class manufacturing industry in Puerto Rico & USA. Responsibilities: • Set-up and breakdown of various manufacturing equipment., • Performing in-process sampling of equipment and operating analytical equipment., • Following documents (SOPs, Batch Records) with strict adherence to safety and compliance., • Maintaining an organized and clean workspace., • Working in a non-clean room mfg environment wearing safety shoes, lab frock, and safety glasses., • Identifying, recommending, and implementing improvements related to routine functions., • Performing activities that include periods of rigorous, repetitive work., • Movement of heavy equipment on casters., • Bachelor’s degree in Biology and/or Life Sciences, • Recent college graduates are welcome to apply, • Chromatography Experience - At least 1 year experience preferred, • Biotech Process Development or Manufacturing experience, • Large Scale processing, buffer prep or media prep experience, • Able to take direction well, follow documents and policies at all times, • Able to regularly lift up to 35lbs, push and pull objects that require up to 50lbs of force, and work on your feet for long durations., • Able to perform the list of physical movements that may be necessary to perform daily functions on the production floor: bending, reaching above the head, climbing, kneeling, squatting, stooping, walking upstairs, and standing on portable stairs or ladders up to 6 feet off of the ground., • Available to work multiple shifts (days and swings, 5 x 8hrs) on a 3-month rotational basis:, • Swing shift: 2:30pm - 11:30PM Powered by JazzHR xEiWBa51De

Job Description Position: Associate Director to Director, Biostatistics Department: Global Medical-Biometrics and Quantitative Sciences Location: Remote (PST Zone) with up to 20% global and domestic travel Reports To: Executive Director, Biometrics Position Summary This position will report to the Executive Director of Biometrics and will provide statistical leadership across programs and trials from early- to late-phase development. The role will contribute strategically to project decisions and study operations, apply innovative statistical approaches (e.g., modeling and simulation, adaptive design, Bayesian methods), support and defend analyses and interpretations in internal cross-functional meetings, and prepare and communicate responses to regulatory agency inquiries. Responsibilities • Serve as lead statistician on project teams, providing strategic and operational expertise for all stages of clinical development programs and support of other functions, • Write or review protocols, SAP, CSR and other related documents to ensure scientific integrity of the applied statistical methodology, • Adhere to company standards, and all applicable regulations and guidelines, • Perform or oversee statistical analyses and interpretation of study results. Direct vendors to perform all statistical related tasks, • Collaborate cross-functionally on study design, data standards, and reporting, • Supply statistical input for regulatory submissions and in response to agency queries., • Collaborate on interdepartmental and scientific activities, • Provide support for investigator publications, • Ensure compliance with departmental and company goals, • Effectively communicates timely and relevant updates to all team members involved, • Demonstrated sound knowledge of applied statistics and biostatistics and relevant experience in the application of statistics to medical trials, • Previous experience with all phases of clinical research and NDA, • Applies judgment and professional expertise independently, • Ability to prioritize and multitask, • Ph.D in Biostatistics or closely related discipline with a minimum of 8 years' experience in pharmaceutical and biotech industry; or, • M.S in Biostatistics or equivalent with a minimum of 11 years' experience in pharmaceutical and biotech industry. Salary Range: $160,000 - $230,000 About Angitia Established in June 2018, Angitia Biopharmaceuticals is a clinical-stage biotechnology company focused on the discovery and development of innovative therapeutics for serious musculoskeletal diseases. Angitia is currently studying 3 biologic product candidates in the clinic for the treatment of osteoporosis (Phase 2), osteogenesis imperfecta (OI) (Phase 1), and spinal fusion (Phase 3). Leveraging the team's extensive experience and scientific acumen in novel drug development, Angitia is committed to providing groundbreaking therapies to satisfy key unmet medical needs. The founder and the core team members of Angitia are seasoned scientific leaders in new drug discovery, development, and management from both overseas and domestic large multinational companies. The company has built an organization with offices in Westlake Village, CA and Guangzhou, China that is distinguished by world-class scientists with talents that are proficient in the pathophysiology of musculoskeletal diseases. We utilize cutting-edge technologies of genetics and molecular biology to uncover new mechanisms, signal transduction pathways and their interactions combined with computer aided drug design to identify new drug targets, and to discover and develop new biological and small molecule medicines. The company is committed to serving patients in need by carrying out innovative science including internal research and external collaborations with academics and global biopharmaceutical companies. We are seeking talented individuals who are innovative, ambitious, and great team players to join our vibrant group. Learn more at Benefits: • Medical, dental, and vision coverage for employees and their eligible dependents, • 401(K) Retirement Plan with Company match, • Company paid Long Term Disability Coverage, • Company-paid life Insurance & AD&D Coverage, • Voluntary Life Insurance & AD&D Coverage, • Employee Assistance Program (EAP), • Company-paid Holidays, • Vacation, • Paid Sick Leave, • Telecommunication Monthly Stipend, • Work-From-Home Equipment Reimbursement

Job Description Position: Senior/Executive Medical Director, Global Clinical Development Department: Translational Science Location: Remote with up to 20% global and domestic travel Reports To: Senior Vice President, Head of Translational Science Position Summary Angitia Biopharmaceuticals, a science-driven biotech company dedicated to developing breakthrough therapies for musculoskeletal diseases, is seeking an experienced Senior/Executive Medical Director of Global Clinical Development. This role provides strategic leadership and oversight of global clinical programs and is central to executing our late-stage clinical strategies, with a focus on Phase 2 and Phase 3 development for rare pediatric bone disorders. The ideal candidate will bring deep clinical and scientific expertise in rare pediatric bone disorders, with a strong foundation in endocrinology, and a proven ability to lead pivotal global trials in rare disease settings. Strong leadership experience is essential, including the ability to lead cross-functional teams in a fast-paced, collaborative environment, and effectively represent the company at key scientific engagements. Responsibilities • Provide strategic medical leadership across global clinical development programs in musculoskeletal and skeletal rare diseases, with particular focus on pediatric bone disorders., • Lead the design, execution, and oversight of late-stage clinical development programs (Phase 2 and Phase 3), ensuring scientific rigor, patient safety, and regulatory compliance., • Design and oversee innovative clinical trial protocols, ensuring alignment with regulatory standards and commercial objectives., • Lead cross-functional clinical teams, including medical monitors, clinical operations, biostatistics, and regulatory affairs, to ensure timely and high-quality trial execution., • Serve as medical lead for interactions with global regulatory agencies, including strategic planning for regulatory submissions, responses, and key milestone meetings (e.g., End-of-Phase 2, pre-NDA)., • Provide scientific and clinical input for the development of study protocols, investigator brochures, clinical study reports, scientific publications, and regulatory documents., • Maintain strong engagement with Key Opinion Leaders (KOLs) in pediatric bone disease and skeletal endocrinology to support study design and program direction., • Represent the company in global forums, including scientific conferences and advisory boards., • Actively contribute to the long-term clinical development roadmap and lifecycle management of investigational assets. Qualifications • MD or MD/PhD with board certification in endocrinology, pediatric endocrinology, or a related field, with a minimum of 10 years of clinical development experience in the biotech or pharmaceutical industry., • Prior success in global trial management and regulatory interactions in the U.S, EU, and other major markets preferred., • Proven track record in rare disease clinical development, especially in pediatric bone disorders (e.g., hypophosphatasia, osteogenesis imperfecta, X-linked hypophosphatemia)., • Successful track record of managing global studies and contributing to regulatory submissions (IND through BLA/NDA)., • Deep understanding of endocrine mechanisms impacting bone and mineral metabolism., • Experience interacting with regulatory authorities on a global scale., • Experience leading multidisciplinary clinical teams in a fast-paced, collaborative environment., • Proven leadership with strong communication and team-building skills. Salary Range: $250,000 to $310,000 About Angitia Established in June 2018, Angitia Biopharmaceuticals is a clinical-stage biotechnology company focused on the discovery and development of innovative therapeutics for serious musculoskeletal diseases. Angitia is currently studying 3 biologic product candidates in the clinic for the treatment of osteoporosis (Phase 2), osteogenesis imperfecta (OI) (Phase 1), and spinal fusion (Phase 3). Leveraging the team's extensive experience and scientific acumen in novel drug development, Angitia is committed to providing groundbreaking therapies to satisfy key unmet medical needs. The founder and the core team members of Angitia are seasoned scientific leaders in new drug discovery, development, and management from both overseas and domestic large multinational companies. The company has built an organization with offices in Westlake Village, CA and Guangzhou, China that is distinguished by world-class scientists with talents that are proficient in the pathophysiology of musculoskeletal diseases. We utilize cutting-edge technologies of genetics and molecular biology to uncover new mechanisms, signal transduction pathways and their interactions combined with computer aided drug design to identify new drug targets, and to discover and develop new biological and small molecule medicines. The company is committed to serving patients in need by carrying out innovative science including internal research and external collaborations with academics and global biopharmaceutical companies. We are seeking talented individuals who are innovative, ambitious, and great team players to join our vibrant group. Learn more at . Benefits: • Medical, dental, and vision coverage for employees and their eligible dependents, • 401(K) Retirement Plan with Company match, • Company paid Long Term Disability Coverage, • Company-paid life Insurance & AD&D Coverage, • Voluntary Life Insurance & AD&D Coverage, • Employee Assistance Program (EAP), • Company-paid Holidays, • Vacation, • Paid Sick Leave, • Telecommunication Monthly Stipend, • Work-From-Home Equipment Reimbursement

Job Description Position: Vice President, Head of Quality Department: CMC Location: Remote (PST Zone) with up to 20% global and domestic travel Reports To: Chief Technology Officer Position Summary Angitia is seeking a Head of Quality to lead all GxP Quality functions, including Quality Assurance, Quality Control, R&D Quality, Document Control, Supplier Quality, and Quality Systems. This position will define and drive the company's quality vision, ensuring compliance across global operations and supporting programs from early development through commercialization. The ideal candidate brings deep expertise in large molecule and aseptic manufacturing, regulatory requirements, and global vendor oversight, along with a proven ability to scale quality systems, lead inspections, and manage cross-functional teams in a dynamic, fast-paced environment. Responsibilities • Drive a culture of quality and set strategic goals in collaboration with cross-functional teams, ensuring compliance with regulations, guidelines, and corporate standards., • Shape and execute the path from pre-IND through commercialization by developing and implementing phase-appropriate Quality models aligned with ICH risk-based guidance., • Build and optimize scalable Quality Systems to support effective, compliant operations., • Oversee quality oversight of CDMOs, CROs, contract labs, and critical material suppliers; identify risks and lead remediation using a risk-based approach., • Partner with external Quality teams to ensure uninterrupted supply and support current and future production plans., • Lead and resolve major deviation investigations to safeguard product quality, safety, and efficacy., • Manage Quality metrics, monitor compliance trends, and implement mitigation plans as needed., • Support global regulatory submissions (IND, NDA, BLA) in partnership with Regulatory Affairs and lead company-wide readiness and execution for regulatory inspections., • Lead and host all FDA and Health Authority inspections and facilitate Quality related continuous improvement initiatives, • Oversee Quality Agreement negotiations and manage budget, capital planning, and cost optimization. Qualifications • Bachelor's or Master's degree in a scientific discipline, with at least 15+ years of Quality Assurance experience in the pharmaceutical industry, with at least 8 years in an executive leadership role., • Proven experience in large molecule and aseptic manufacturing; experience in tech transfer and GMP facility operations strongly desired., • Demonstrated success building Quality Systems in early-stage, science-driven organizations and supporting product commercialization., • Experience working with U.S. and international CDMOs, clinical sites, and leading audits of external labs and suppliers., • Deep understanding of CDE, FDA, and ICH GxP regulations, including GMP, GLP, GCP, and GDP., • Strong knowledge of regulatory requirements for sterile products, advanced therapies, and combination products., • Proven leadership in building and scaling high-performing teams in fast-paced environments., • Strong mentoring, problem-solving, and critical thinking skills. Salary Range: $300,000 to $340,000 About Angitia Established in June 2018, Angitia Biopharmaceuticals is a clinical-stage biotechnology company focused on the discovery and development of innovative therapeutics for serious musculoskeletal diseases. Angitia is currently studying 3 biologic product candidates in the clinic for the treatment of osteoporosis (Phase 2), osteogenesis imperfecta (OI) (Phase 1), and spinal fusion (Phase 3). Leveraging the team's extensive experience and scientific acumen in novel drug development, Angitia is committed to providing groundbreaking therapies to satisfy key unmet medical needs. The founder and the core team members of Angitia are seasoned scientific leaders in new drug discovery, development, and management from both overseas and domestic large multinational companies. The company has built an organization with offices in Westlake Village, CA and Guangzhou, China that is distinguished by world-class scientists with talents that are proficient in the pathophysiology of musculoskeletal diseases. We utilize cutting-edge technologies of genetics and molecular biology to uncover new mechanisms, signal transduction pathways and their interactions combined with computer aided drug design to identify new drug targets, and to discover and develop new biological and small molecule medicines. The company is committed to serving patients in need by carrying out innovative science including internal research and external collaborations with academics and global biopharmaceutical companies. We are seeking talented individuals who are innovative, ambitious, and great team players to join our vibrant group. Learn more at . Benefits: • Medical, dental, and vision coverage for employees and their eligible dependents, • 401(K) Retirement Plan with Company match, • Company paid Long Term Disability Coverage, • Company-paid life Insurance & AD&D Coverage, • Voluntary Life Insurance & AD&D Coverage, • Employee Assistance Program (EAP), • Company-paid Holidays, • Vacation, • Paid Sick Leave, • Telecommunication Monthly Stipend, • Work-From-Home Equipment Reimbursement

Job Description Position: Senior Manager to Associate Director, Bioanalytical and Biomarker Sciences Department: Translational Science Location: Remote with occasional onsite meetings, up to 20% travel Reports To: Director, Translational Science – Clinical Pharmacology Position Summary This Bioanalytical and Biomarker (BABM) position will lead and contribute to the BABM strategy to support assigned project progression from IND application to clinical development to BLA submission. This position will manage BABM CROs to ensure clinical BABM assay development and sample analysis meet project timelines. The ideal candidate will have in-depth BABM knowledge, strong strategic thinking, excellent verbal and written communication skills. Responsibilities • Serve as BABM expert on cross-functional drug development teams and lead BABM related program(s) and activities., • Lead internal process and procedure setup and develop corresponding SOPs., • Lead and manage BABM data interpretation, and reporting; present bioanalytical results and update BA status to study teams., • Interface with internal study and clinical teams to define and execute BABM strategies., • Write and review relevant sections of study protocols, analysis plans (assay development and validation plans, sample analysis plan), reports (validation report, sample analysis report), Investigator Brochures, documents for IND filings and NDA/BLA submissions, ensuring that designs and documents meet regulatory and compliance requirements and project timelines., • Select and manage BABM CROs conducting regulated (e.g. GLP, GCP) and non-regulated PK, immunogenicity (ADA and NAb), and Biomarker sample analysis., • Monitor BABM CROs process and procedures to ensure their work qualities. Qualifications • Doctor's or Master's degree in chemistry, biology, biochemistry, or related discipline with an emphasis on analytical techniques with 8+ years of industry work experience in BABM areas., • Expertise and knowledge of laboratory procedures, practices, and applicable SOPs., • Strong working knowledge of regulations, guidelines, standards that guide collection and utilization of non-clinical and clinical samples and data., • Familiarity with regulatory expectations (FDA and EMA) and industry's best practices in BABM method development and validation., • Ability to diagnose and solve complex technical and scientific problems., • Excellent communication skills and organization skills. Salary: $130,000 - $180,000 About Angitia Established in June 2018, Angitia Biopharmaceuticals is a clinical-stage biotechnology company focused on the discovery and development of innovative therapeutics for serious musculoskeletal diseases. Angitia is currently studying 3 biologic product candidates in the clinic for the treatment of osteoporosis (Phase 2), osteogenesis imperfecta (OI) (Phase 1), and spinal fusion (Phase 3). Leveraging the team's extensive experience and scientific acumen in novel drug development, Angitia is committed to providing groundbreaking therapies to satisfy key unmet medical needs. The founder and the core team members of Angitia are seasoned scientific leaders in new drug discovery, development, and management from both overseas and domestic large multinational companies. The company has built an organization with offices in Westlake Village, CA and Guangzhou, China that is distinguished by world-class scientists with talents that are proficient in the pathophysiology of musculoskeletal diseases. We utilize cutting-edge technologies of genetics and molecular biology to uncover new mechanisms, signal transduction pathways and their interactions combined with computer aided drug design to identify new drug targets, and to discover and develop new biological and small molecule medicines. The company is committed to serving patients in need by carrying out innovative science including internal research and external collaborations with academics and global biopharmaceutical companies. We are seeking talented individuals who are innovative, ambitious, and great team players to join our vibrant group. Learn more at Benefits: • Medical, dental, and vision coverage for employees and their eligible dependents, • 401(K) Retirement Plan with partial Company match, • Company paid Long Term Disability Coverage, • Company-paid life Insurance & AD&D Coverage, • Voluntary Life Insurance & AD&D Coverage, • Employee Assistance Program (EAP), • Company-paid Holidays, • Vacation, • Paid Sick Leave, • Telecommunication Monthly Stipend, • Work-From-Home Equipment Reimbursement

Sr. Associate, Biology (Contract) About the Company: We are seeking a highly motivated Sr. Associate, Biology to join a fast-paced, agile biotech team in Thousand Oaks. This contract role will support ongoing cell-based assay development and execution, contributing to cross-functional research efforts in Chemistry, DMPK, and Path/Tox. The ideal candidate will bring strong sterile technique, cell culture expertise, and a collaborative mindset to help drive innovation and maintain momentum during a team member’s leave of absence. About the Role: This is a contract role that will support ongoing cell-based assay development and execution. Responsibilities: • Cell-Based Assays:, • Design, troubleshoot, and execute cell-based assays using 96-well plates., • Plate and maintain both adherent and suspension cells with strong sterile technique., • Prepare media and identify issues in cell culture health and contamination., • Support development of novel assays and contribute to assay optimization., • Cell Culture & Sample Handling:, • Maintain cell line stocks and perform cell counts., • Avoid use of antibiotics in culture when possible., • Process biological fluids (e.g., blood to serum/plasma) and frozen tissues., • Lab Operations:, • Maintain lab inventory and restock kits, plastics, and chemicals., • Aliquot biological samples and manage freezer contents., • Ensure lab cleanliness and compliance with SOPs and safety protocols., • Cross-Functional Collaboration:, • Work closely with microscopy experts, chemistry teams, and DMPK scientists., • Communicate findings and contribute to team discussions., • Reporting & Documentation:, • Generate clear, timely reports and maintain accurate records in ELN., • Use lab software including Microsoft Office, GraphPad Prism, and SoftMax Pro. Qualifications: • Education: B.Sc. or M.Sc. in Life Sciences or related field., • Experience: Minimum 3 years of hands-on lab experience. Proficiency in cell culture, assay development, and sterile technique. Experience working in a GMP or biotech environment preferred. Work Environment: This is a high-paced, collaborative biotech setting where adaptability and teamwork are key. You’ll be part of a small, agile team focused on innovation and scientific rigor. Pay range and compensation package: $35–$42/hr DOE Equal Opportunity Statement: We are committed to diversity and inclusivity.

Innova Solutions has a client that is immediately hiring a Scientist. Position type: Full Time - Contract Duration: 12 Months Location: Thousand Oaks, CA As a Scientist, you will: Description Scientist – Oncology Research Join a cutting-edge team driving small-molecule cancer therapeutics. We're seeking scientist with hands-on experience in cell culture and molecular biology. What You’ll Do: • Lead lab-based experiments in cancer biology, • Analyze and present data with minimal meetings, • Collaborate to meet evolving project goalsMust-Have Skills:, • Mammalian cell culture, western blotting, qPCR, flow cytometry Qualified candidates should APPLY NOW for immediate consideration! Please hit APPLY to provide the required information, and we will be back in touch as soon as possible. We are currently interviewing to fill this and other similar positions. If this role is not a fit for you, we do offer a referral bonus program for referrals that we successfully place with our clients, subject to program guidelines. ASK ME HOW. Thank you! Pradip Joshi Phone: 213-401-2633 Email - PAY RANGE AND BENEFITS: Pay Range*: $37-$40/hr *Pay range offered to a successful candidate will be based on several factors, including the candidate's education, work experience, work location, specific job duties, certifications, etc. Benefits: Innova Solutions offers benefits( based on eligibility) that include the following: Medical & pharmacy coverage, Dental/vision insurance, 401(k), Health saving account (HSA) and Flexible spending account (FSA), Life Insurance, Pet Insurance, Short term and Long term Disability, Accident & Critical illness coverage, Pre-paid legal & ID theft protection, Sick time, and other types of paid leaves (as required by law), Employee Assistance Program (EAP). About Innova Solutions: Founded in 1998 and headquartered in Atlanta, Georgia, Innova Solutions employs approximately 50,000 professionals worldwide and reports an annual revenue approaching $3 Billion. Through our global delivery centers across North America, Asia, and Europe, we deliver strategic technology and business transformation solutions to our clients, enabling them to operate as leaders within their fields. Recent Recognitions: Named One of America’s Best Employers for New Grads by Forbes (2024 Named One of the Best Companies to Work for by U.S. News & World Report (Private Companies List, 2024-2025) One of the Largest IT Staffing Firms in the US – Ranked #3 by Staffing Industry Analysts (SIA, 2024) One of the Largest Staffing Firms in the US – Ranked #13 by Staffing Industry Analysts (SIA, 2024; includes Innova Solutions, Volt, & HireGenics) Named One of the Top Ten Private Companies in Atlanta by the Atlanta Business Chronicle (2023) One of the Largest Certified Minority Business Enterprises (MBEs) in the United States (NMSDC, 2024) AWS Advanced Tier Services Partner with 100+ certifications Website: Innova Solutions offers a referral bonus for qualified Ambassadors who refer eligible referrals. Submit referrals at and earn $250-$1,000 per referral. Innova Solutions is an Equal Opportunity Employer and prohibits any kind of unlawful discrimination and harassment. Innova Solutions is committed to the principle of equal employment opportunity for all employees and to providing employees with a work environment free of discrimination and harassment on the basis of race, color, religion or belief, national origin, citizenship, social or ethnic origin, sex, age, physical or mental disability, veteran status, marital status, domestic partner status, sexual orientation, or any other status protected by the statutes, rules, and regulations in the locations where it operates. If you are an individual with a disability and need a reasonable accommodation to assist with your job search or application for employment, please contact us at or (770) 493-5588. Please indicate the specifics of the assistance needed. Innova Solutions encourages all interested and qualified candidates to apply for employment opportunities. Innova Solutions (HireGenics/Volt) does not discriminate against applicants based on citizenship status, immigration status, or national origin, in accordance with 8 U.S.C. § 1324b. The company will consider for employment qualified applicants with arrest and conviction records in a manner that complies with the San Francisco Fair Chance Ordinance, the Los Angeles Fair Chance Initiative for Hiring Ordinance, and other applicable laws.

-2 year contract -$33/hr Must be flexible as it is possible worker will start on any shift and rotate every 6 months. DAY: 6 AM - 5 PM SWING: 1 PM to 12 AM NIGHT: 7 PM - 8 AM The ideal candidate f will have 1-2+ years of hands-on experience in a regulated GMP environment, preferably within the pharmaceutical, biotech, or food industries. While a bachelors degree in a relevant scientific field (e.g., biology, chemistry, biochemistry) is preferred, direct industry experience is more important. Candidates should be familiar with manufacturing or quality operations and understand the pace and expectations of a high-volume, highly cross-functional environment. This role requires individuals who are proactive, able to work independently with minimal oversight, and comfortable escalating issues appropriately. This position supports Quality Assurance program under the Plant QA organization providing daily oversight of the Drug Substance manufacturing areas. Under general supervision, the role provides support and compliance oversight to Manufacturing and Facilities & Engineering areas/staff in the execution of their processes, procedures, and use of quality systems. Duties include purposeful presence on the floor, electronic batch record review, SOP revision & approval, work order approval, and quality approval of minor deviations . Responsibilities will include evaluation of compliance issues, providing recommendations, and assuring progress of quality records to completion. The Sr. Associate will also represent functional area for the Drug Substance Quality Assurance department in the execution of projects necessary to achieve departmental operational goals and will work in a team matrix environment. Preferred Qualifications: • Bachelor's Degree in Biochemistry, Biology, Chemistry, or related science field., • Demonstrated ability to perform GMP operations including following detailed SOPS, maintaining training, and good documentation practices. Also, ability to make Quality based decisions in order to ensure compliance. • Experience managing projects through to completion & meeting timelines., • Evaluating documentation and operations according to company procedures., • Experience working with Quality Systems, Strong organizational skills and ability to manage multiple tasks at one time/ Effective communication skills (both written and verbal), • Demonstrated ability to work as both a team player and independently, • Display leadership attributes and drive improvement initiatives.

The Pre-Pivotal Drug Substance Technologies organization at develops, characterizes and supports clinical drug substance manufacturing processes for all early-stage programs in the portfolio. This lab-based position is located at our Thousand Oaks, CA site. The successful candidate will be responsible for support of the development, characterization, scale-up and support of upstream and downstream processes to enable clinical advancement of programs. This role is in an integrated bioprocess development group in which cell culture and purification scientists work together to advance rich, exciting and dynamic pipeline. With biology first approach, the position provides the unique opportunity to work on multiple modalities including antibodies, BiTEs, oncolytic viruses, bispecifics, and siRNAs. The successful candidate will design and execute experiments at the bench scale, spanning the end-to-end drug substance process, including both cell culture and purification operations. The candidate will apply established platform approaches and utilize problem-solving skills to rapidly solve day-to-day experimental challenges. Additionally, the candidate will utilize out-of-the-box thinking to contribute to technology development, including process automation. Finally, the candidate will also expand and develop skills in both cell culture and purification, thereby further contributing to the integrated group. Day to Day Responsibilities: • Work in a team environment to contribute to drug substance process development., • Complete mammalian cell culture experiments at different scales in shake flasks and bioreactors., • Implement purification experiments, mainly filtration and chromatography, at bench and pilot scale as needed., • Document experimental data in lab notebooks., • Analyze the data and present to the team., • Author technical reports and support regulatory filing as needed., • Contribute to technology development projects to seek continuous improvement in reliability and efficiency., • The candidate will have opportunities to work in cell culture development and purification development to become a well-rounded process development scientist with experience in upstream and downstream.

Fully onsite at ATO standard business hours but candidate should be flexible sometimes will need to work 4-5 hours on a weekend (1x/ month this is a rotation).The ideal candidate for this MCS Associate, Quality Control role will hold a bachelor's degree in Biology, Microbiology, or a related discipl

Duration: 12 Months Shift: Standard business hours Job Description: • The Pre-Pivotal Drug Substance Technologies organization at company develops, characterizes and supports clinical drug substance manufacturing processes for all early-stage programs in the company’s portfolio., • This lab-based position is located at our Thousand Oaks, CA site. The successful candidate will be responsible for support of the development, characterization, scale-up and support of upstream and downstream processes to enable clinical advancement of company programs., • This role is in an integrated bioprocess development group in which cell culture and purification scientists work together to advance company’s rich, exciting and dynamic pipeline. With company biology first approach, the position provides the unique opportunity to work on multiple modalities including antibodies, BiTEs, oncolytic viruses, bispecifics, and siRNAs., • Work in a team environment to contribute to drug substance process development., • Complete mammalian cell culture experiments at different scales in shake flasks and bioreactors., • Implement purification experiments, mainly filtration and chromatography, at bench and pilot scale as needed., • Document experimental data in lab notebooks., • Analyze the data and present to the team., • Author technical reports and support regulatory filing as needed., • Contribute to technology development projects to seek continuous improvement in reliability and efficiency., • Bachelors degree OR, • Associates degree and 2 years of experience OR, • Degree in Chemical Engineering, Biochemistry, Biotechnology, Bioengineering, Biomedical engineering, or Bioprocessing field or relevant experience in the pharmaceutical or related industry preferred., • 1+ years of relevant hands-on industry lab experience in cell culture or protein purification. (outside of education) US Tech Solutions is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.

Associate, Biology to join a fast-paced, agile biotech team in Thousand Oaks.

Associate, Biology to join a fast-paced, agile biotech team in Thousand Oaks.

We are seeking Biology tutors and teachers in Simi Valley.

Project Manager/ Sr Associate, Supplier Performance Analytics & Digital Enablement.Summary: The Project Manager/ Sr Associate, Supplier Performance Analytics & Digital Enablement plays a critical role in advancing R&D Supplier Management and Performance Analytics (SMPA).This role focuses on leveragi

Hold certifications for Agile, Scaled Agile, PMP, or PgMP.

Join Amgen's Mission of Serving Patients.At Amgen, if you feel like you're part of something bigger, it's because you are.Our shared missionto serve patients living with serious illnessesdrives all that we do.Since 1980, we've helped pioneer the world of biotech in our fight against the world's toug

At ALS, we encourage you to dream big.When you join ALS, you join a purpose and values-driven team that empowers you to innovate, create, and thrive.Our global team turns up each day with passion and commitment to do amazing things, always challenging our thinking to find ways to solve some of the w

PRIDE Health is seeking a travel Cath Lab Technologist for a travel job in Lodi, California.Job Description & Requirements Specialty: Cath Lab Technologist Discipline: Allied Health Professional Start Date: ASAP Duration: 13 weeks 40 hours per week Shift: 8 hours, days Employment Type: Travel A Cath

The City of Malibu is seeking a highly organized, detail-oriented, and Administrative Assistant to fill a vacancy in the City Clerk's Office.The Administrative Assistant will provide comprehensive administrative support within a dynamic and fast-paced City Clerk's Office.This position plays a key ro

The Project Manager is responsible for overseeing a contents restoration job (insurance claim) from start to finish.They schedule and manage field service work, track contents, oversee the billing and collection process, and communicate with estimators, adjusters, and customers (policy holders) on a

JLL Empowers You To Shape A Brighter Way.Our people at JLL and JLL Technologies are shaping the future of real estate for a better world by combining world class services, advisory and technology for our clients.We are committed to hiring the best, most talented people and empowering them to thrive,

Data Scientist Co-op - Summer/Fall 2026.Location: Newbury Park, CA, US.If you are looking for a challenging and exciting career in the world of technology, then look no further.Skyworks is an innovator of high-performance analog semiconductors whose solutions are powering the wireless networking rev

Conejo Valley Unified School District is offering a full-time position for a Construction Project Manager in Thousand Oaks, CA.This position is funded for up to 1 year and requires a cover letter, resume, and complete employment history within the application.Essential Duties/Responsibilities.Under

If you are looking for a challenging and exciting career in the world of technology, then look no further.Skyworks is an innovator of high-performance analog semiconductors whose solutions are powering the wireless networking revolution.Through our broad technology expertise and one of the most exte

Our associates celebrate lives.Consider the possibilities of joining a Great Place to Work!.Provides administrative support to a funeral home, cemetery, crematory or a combination of these facilities.Assists with special projects, research, and resolving problems.Schedules meetings, drafts memos, tr

As a Sr Project Manager you will be responsible for leading the successful delivery and execution of company commitments and large scale programs/projects.The position is part of the Digital Delivery Project Management Organization within the Digital Technology organization and will play a central r

Westlake Village, where your expertise will be crucial in steering the successful delivery and execution of our company's commitments and expansive programs/projects.As a key member of the Digital Delivery Project Management Organization within our Digital Technology division, you will be part of a

My client is seeking a Water/Wastewater Project Manager to join their team in the San Francisco Bay Area.They will manage a variety of water and wastewater projects, including water pipelines, sewer systems, tanks/reservoirs, pump stations, and treatment facilities.This position offers substantial c

Job Description: Locals Only | Required: Authorization/Referral Experience Shift: 40 D 0800-1630.

Are you ready for a culture that you deserve? We are ready for you.At Concuir, our team consciously executes a culture of Life/Work Integration.Leaders promote full psychological safety in the workplace to allow you to bring your full self to work every day.Our team members enjoy their work with inc

Cancer Biology/Molecular Biology or a related field with 3+ years of industry experience. Molecular Biology/Cancer Biology or related field. Molecular Biology, assay development, oncology, preclinical, spatial transcriptomics, pathology, immunofluorescence, histology biomarker assays.

We are looking for a Computational Scientist (Biology) who works at the intersection of high-dimensional biological data, cell biology, and ML. Deep mastery of your field—biologists who code, engineers who care about biology. Strong understanding of biology across systems (e.

Big Brand Tire & Service is looking for a sharp, organized Administrative Assistant to help manage our inventory and keep operations running like a well-oiled machine.If you love details and want to be part of a fast-paced, friendly team, we want you! Administrative Assistant with experience in:.Goo

BS or MS degree in cell biology, molecular biology, biochemistry, bioengineering or a related field is required. Research Associate, Cell Biology. Conduct molecular biology experiments, including cloning, PCR, qPCR, and sequencing.

Hybrid - San Francisco Bay Area.Senior Director, Program Management.A mid-sized life sciences company is seeking a dynamic and experienced.This role will be instrumental in driving strategic projects that support innovation and business growth.Lead cross-functional teams to execute complex projects

In 1984, three young architects embarked on a journey to design and build spaces that enhance and uplift the way communities live, learn, and serve.From the early days of working out of a spare bedroom and holding meetings by a furnace in the hallway, the purpose has always been to provide better se

Project Manager with either DSA or Healthcare.Inland Empire and surrounding Riverside- Moreno Valley areas.Comprehensive package including medical, dental, vision, PTO, and 401(k).A well-established $250M commercial General Contractor is seeking an experienced.DSA school projects across the Inland E

As one of the largest MEP design-build firms in the U.We focus on the entire building lifecycle—design, construction, operations, and energy performance—across diverse markets such as healthcare, data centers, commercial, transportation, and education.This individual will oversee multiple projec

Level Recruiting is searching for an Assistant Project Manager to support high-end residential projects in the Bay Area.We are dedicated to providing competitive pay and benefits, great company culture, opportunities for growth, and interesting and successful projects.As an Assistant Project Manager

Springpoint Group (formerly Whiteside Management) represents Owners in the building of high-end residential and commercial projects throughout the San Francisco Bay Area and across the United States.Our deep experience, client advocacy approach, and established process instill clarity and accountabi

Nibbi Brothers has been a member of the Bay Area’s construction community since 1950.The Company is known for its integrity, innovation, quality and contributions to the communities in which it works.Nibbi’s safety program often exceeds federal and state requirements, demonstrating that the safe

Morrow-Meadows Corporation is accepting applications for full-time Project Managers for its Electrical Division.Final accountability for all administrative duties on assigned projects.Follow up with customer on payment status and collections.Prepare project budgets and breakdown labor task codes for

SAN FRANCISCO BAY AREA (HYBRID).We’re seeking a Data Scientist II to drive next-generation personalization and discovery for a fast-growing social commerce marketplace.You’ll partner with Machine Learning Engineers and product teams to design, build, and deploy models that impact millions of dai

As a Senior Transportation Project Manager in San Luis Obispo, CA, you will have an opportunity to work with a multi-disciplinary team on meaningful, landmark projects in the San Luis Obispo region.As a team member, you will help clients and communities turn their dreams into reality.You will learn

Lead Data Scientist - Personalization & Recommendation Engines.SF Bay Area - Hybrid (3 days/week onsite).A leading commerce marketplace with 130M+ users and billions of daily events is hiring a Staff Machine Learning Scientist to drive innovation across personalization, feed ranking, computer vision

We are representing an established General Contractor in their search for a Drywall Project Manager to oversee construction projects in the Greater Bay Area.Direct and oversee all aspects of drywall construction projects including planning, scheduling, budgeting and quality control.Assess risks and