Posts Tagged Assembly
Senior R&D Mechanical Engineer – N. San Jose, CA
This is a very exciting opportunity to work at grounds level on a stealth mode project, with a veteran entrepreneur, with several successful prior ventures. Requires 8+ years of medical device product development experience and strong expertise in Solidworks.
Director of Quality Engineering – Alameda, CA
There is an exciting #JOB opportunity for Director of Quality Engineering, in Alameda, CA in a global medtech company focused on design, development & manufacturing of novel products to address unmet medical needs.
Requirements include: Strong foundation in Quality, QE & Quality Management systems; Experience with growing & leading a high impact team; Proven record leading, mentoring, and developing Managers, Engineers; BS in engineering or related; 10+ years industry experience; 5+ years of people management experience. Also #medicaldevice experience, highly preferred.
Job Responsibilities: Provide leadership & drive quality results for company’s products; Ensure products are manufactured in a compliant manner; Risks are identified & mitigated during changes; New products are ushered into manufacturing in a timely manner, Work cross-functionally.
Assembler – San Jose, CA
There is an opening for an assembler with experience in assembling parts & components used in manufacturing medical devices.
Requires fine hand dexterity; Understand Good Documentation Practices, GMP & CAPA; Ability to comply w/ work schedules, comply with safety practices & government regulations and follow Quality System procedures; Experience in writing notes, writing & updating assembly procedures, protocols & checklists; work collaboratively with QA & production management.
Requires: High School Diploma or equivalent; 2+ years medical device or pharma experience; good math & English skills.
Business Development Manager – San Jose, CA
There is an exciting opportunity for a Business Development Manager to support all aspects of business development initiatives including BD research & scouting to assess market developments and identify partnering opportunities; support business development transactions including due diligence, onboarding for R&D collaborations & licensing. This role will report to the VP of BD.
Responsibilities: Lead research & analysis of pharma landscape to identify strategic partner opportunities; Present internally; Identify, analyze & prioritize external innovation opportunities; Conduct market research & competitive analysis; Create financial models to support BD decision-making; Cultivate relationships within biotech community, attend conferences & trade shows; Support due diligence efforts, coordination, data room management and maintenance.
Requirements: Excellent analytical, problem solving, organizational, communication & interpersonal skills; Min. BS degree PLUS 5+ years of BD experience preferably in pharma; Experience in financial modeling.
Senior Manufacturing Engineer – S. San Jose, CA
Bay Area start-up focusing on improving healthcare delivery through state-of-the-art catheter development has an immediate opening for senior manufacturing enginee, to support the development and production of innovative catheters ensuring high reliability, regulatory adherence, and cost-effective manufacturability.
Requirements: Minimum 10 years history of experience in medical device manufacturing environment; Proficiency in Solidworks; Experience writing protocols & test reports; Experience using inspection and test equipment (vision systems, tensile testing) are required.
Responsibilities: Support manufacturing activities; Spend time on the manufacturing line with the assemblers to improve processes & increase quality; Develop assembly & test fixturing; Create, validate & document new manufacturing processes; Write protocols & test reports; Prepare manufacturing lines for significant scale up; Conduct process verification & validation activities; Initiate failure analysis in manufacturing; Design, write & perform equipment qualifications & process validations; Facilitate transitioning development products to full scale production line; Collaborate with existing suppliers & bring up new ones with an eye towards partnership & efficiency.
Director of Clinical Operations – N. San Jose, CA
Unique vascular startup with state of the art catheter development, with platform technology has an immediate opportunity to staff clinical and regulatory positions at all levels. Stay tuned for full JD – coming soon.
Research Scientist- Formulation and Pharmaceutics – San Jose, CA
Research Scientist – Formulations & Pharmaceutics – San Jose, CA
There is an immediate opportunity for senior and junior research scientists in formulations to work in a multi-disciplinary environment to address chronic diseases.
Experience in scientific experiments in formulation & process development of parenteral dosage forms; Experience in immediate & sustained release parenteral formulations; Understand advanced drug delivery systems & pharmaceutical applications, such as emulsions, suspensions, polymer, nanoparticle, PLGA microspheres and colloidal systems; Exp. in chemical & physical stability of formulations, maintain documentation; Ability to identify stability, manufacturability & performance issues, interpret scientific data, communicate effectively & present data; Participate in tech transfer from R&D to Manufacturing. Required MS in Pharmaceutical Sciences or related PLUS 1+ yrs bio/pharma industry exp. Highly preferred pharma formulation experience & Exp working with drug-device combination.
Bioanalytical Scientist – N. San Jose, CA
There is an exciting immediate job opportunity for a bioanalytical scientist in San Jose, CA to work on novel drug device combinations for treating chronic diseases. There are three opportunities and position, salary and benefits will be commensurate with experience. This position will be involved in the development of in vitro/in vivo models by performing a variety of microplate assays; Configure, program and troubleshoot laboratory automated platforms; Optimize existing automated processes to improve efficiency, throughput, robustness and quality; Perform routine data management tasks; Support regulatory efforts; Perform other duties as assigned.
Requirements: BS with 2-5 years or MS with 0-3 years or Ph. D. with 2+ years of industry experience is required; Also required, Experience in preclinical & clinical research; experience in biochemical analysis such as spectrophotometric, fluorescence immuno assays, HPLC, CE, LC-MS; Experience with microplate assays; Hands-on experience in automation and liquid handling in a bioanalytical lab setting; Experience working with statistical software like Excel, GraphPad Prism and Softmax Pro; and Experience with writing reports/protocols and SOPs. Experience with Luminex MapX technology is an advantage.
R&D Scientist – N. San Jose
A drug delivery company with unique technology to deliver biologics has an exciting job opportunity in San Jose, CA for R&D Scientist.
Requirements: BS/MS in Pharmaceutical Sciences, Chemistry, Biochemistry, Chemical Engineering or related; 5+ years pharma or biotech experience in biologics analytical development, particularly, experience in biophysical techniques and analytical characterization of peptides and proteins is a must. Candidates must have experience of working in GLP/GMP regulated environment and working knowledge in product formulation (solid oral dosage, and/or parenteral sustained release) and process development from early to late phase development or at minimum hands on experience in providing analytical support to these activities. Also required, knowledge of state of the art analytical techniques such as various HPLC modes and detections, LC-MS, CE-SDS, peptide mapping, ELISA, cell based assays etc for product characterization, comparability testing and PK/PD analyses. Experience in working with drug-device combination products is a plus.
Responsibilities: Assessing chemical and physical stability of formulations and identifying appropriate stability, manufacturability, and performance critical quality attributes; Establishing and managing reference standard and stability programs; Participate in method and tech transfer from R&D to Manufacturing as appropriate; Writing, reviewing and approving CMC sections of regulatory filings; Assessing utilization of resources and identifying when, and where additional resources may be needed; Communicate effectively to the project team and present data at team meetings; Maintain high quality documentation of all activities in notebooks, Other duties as explained.
Molecular Biologist – South San Francisco, CA
An early stage biotechnology company located in S. San Francisco, CA has developed patented technology for engineering mammalian cells to vastly increase their productivity for therapeutic protein or virus production and has an exciting opportunity for senior molecular biologist.
Requirements: Must have PhD in a related field or equivalent amount of experience with recombinant mammalian cell line creation; mammalian cell culture expertise; experience with general molecular biology techniques for designing and constructing vectors and transfecting mammalian cells; experience with protein assay techniques for screening transfected cells. Also highly preferred, Experience with flow cytometry, virology, cell banking, transposase transfection methods; experience with protein analytical methods; knowledge of the regulatory environment related to creating and testing cells destined for GMP manufacturing; and photomicroscopy.
Responsibilities: This position is responsible for helping develop the technology toward full commercialization. Responsibilities include work with cell engineering, vector design and construction, transfection, mammalian cell culture, cloning and screening, flow cytometry, and other related molecular and cellular biology techniques.
Quality Assurance Engineer – North San Jose, CA
There is immediate opportunity for Quality Engineer in well funded startup by a veteran leader with a world class team to support compliance with applicable regulatory requirements by maintaining an effective quality management system and implementing continuous improvements. This position is responsible for activities ranging from product development through commercialization. This is a hands-on role where the Sr. Quality Engineer will apply diversified knowledge of engineering, quality principles and practices for class II and class III medical devices and combination products. This position also ensures that the company complies with all applicable federal, industry, and company procedures, guidelines, and regulations during the receipt, storage, manufacture, and distribution of products.
Responsibilities: Maintain and improve quality system in accordance with FDA Quality System Regulation and ISO 13485 requirements; Support quality assurance activities, including, but not limited to: Risk Management (FMEAs, HA), internal and external audits, NCMRs and CAPAs; Investigate product quality problems and determine root cause, gather and analyze data, and implement corrective actions to reduce or eliminate cause; Lead the resolution of quality issues related to non-conformance reports and CAPAs; Assist in development, review and approval of process and equipment validation/qualifications (IQ, OQ, PQ); Provide QE support to production, purchasing and engineering; Support/lead test method validation activities; Conduct and support the development and validation of appropriate test methods for product and process performance; Develop and initiate sampling procedures and statistical process control methods; Support product line manufacturing and design stages by ensuring validation of manufacturing equipment and processes are conducted in accordance with the Validation Master Plan; Address systemic quality issues with suppliers or internal groups; Oversee calibration and preventive maintenance program; Assist in the review of lot history records and disposition of product (subassembly and finished goods); Work with engineering to develop adequate inspection criteria; Perform statistical analysis such as capability, gage R&R, and statistical process control; Evaluate product changes for qualification and validation requirements and assist in change implementations.
Requirements: A minimum of 7 years quality assurance/engineering experience is required. Experience in a regulated industry (medical device), Experience with FDA Quality System Regulations, ISO Standards (ISO 13485 and ISO 14971), Experience with non-conformances, CAPA, and Risk Management, Experience in performing test method validation and Gage R&Rs, Extensive experience regarding root cause analysis and statistical techniques (such as Cause and Effect Analysis, Fishbone Diagram, 5 Whys, Six Sigma processes) and BS in Engineering is required. CQE, CQA preferred.