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Qc Incoming Associate Scientist Jobs

Qa Incoming/Disposition Associate
By Lilly At , Concord, 28027
Experience in inventory management systems (EWM, SAP, etc.)
Excellent interpersonal and networking skills.
Previous facility or area start up experience.
Previous experience in GMP production and warehouse environments.
Practices safety behaviors with proper PPE and lifting techniques. Supports all HSE Corporate and Site Goals.
Documenting inspections in accordance with procedures and specifications.
Qc Associate Scientist Jobs
By Pfizer At , Sanford, Nc
Responsible for detailing requirements for Laboratory Information Management System builds, building, testing and managing its Master Data changes.
Experience within the biopharmaceutical industry, including knowledge and experience relevant to biopharmaceutical unity operations and/or laboratory operations.
Able to create, review, and approve compliant test method transfer and validation protocols and reports and equipment qualification/computer validation records.
Demonstrated experience in manufacturing, quality or engineering experience in the biotech or pharmaceutical industry.
Excellent effective written and verbal communication and interpersonal skills
Laboratory experience, including Cell Culture, Bioassay, Aseptic Technique, and ELISA
Incoming Materials Inspector Jobs
By Siemens At , Houston, Tx $49,200 - $84,400 a year
Ensure usage of the existing non-conformance reporting system for efficient non-conformance management.
Siemens offers a variety of health and wellness benefits to our employees. Details regarding our benefits can be found here: https://www.benefitsquickstart.com/siemens/index.html
5-7 years’ Experience in Quality-related position in a manufacturing environment.
Experience with multi meters, calipers, micrometers, thread gages, pin gages, and optical comparator.
Previous work experience in an ISO 9001 certified company.
Experience in Switchboard products in similar industries.
Qc Sr. Scientist Jobs
By Spark Therapeutics At , Philadelphia, 19104, Pa
Key Skills, Abilities, and Competencies
Documents\Reviews test data generated within and outside the department. Ensures testing conforms to current methods, GMP, and SOP requirements.
Perform laboratory equipment qualification, calibration and preventative maintenance program as needed. Maintain chemical and supply purchasing/inventory.
Working knowledge of protein, DNA or RNA, virus-based assays.
Experience in optimization and validation of bio-separation assays.
Prior experience working in either a clinical development or commercial cGMP environment is preferred.
Staff Scientist, Biopharma Qc And Oncology
By Bio-Rad Laboratories, Inc. At , Pleasanton, 94588, Ca $127,000 - $164,000 a year
Design effective experiments, perform data analysis, and document your research under a Quality Management System.
Education: PhD or a Master’s degree OR minimum of 8 years related experience and a Bachelor’s degree.
Aptitude for writing clear plans, reports, and SOPs and presenting your progress to colleagues and senior management.
Hire, nurture, and manage a team of research associates and scientists.
Work Experience: Minimum 6 years of related experience.
Experience with nucleic acid technology relating to PCR, qPCR, multiplex PCR, and digital PCR
Technical Development Senior/Principal Scientist Qc
By Genentech At , San Francisco, Ca
Strong work ethic, ability to work well with others, demonstrated trouble-shooting capabilities, and robust problem-solving skills
Previous industry experience in cell and gene therapy is preferred
Skilled in communication and presentation, and able to convey data clearly and effectively, both verbally and in writing
Minimum Requirements for Technical Development
Note that this is an on-site role; remote work is not an option for this position.
Relocation benefits are provided for this posting.
Qc Sr Associate Scientist - Qc Analytical Chemistry
By Pfizer At , Sanford, Nc
Experience with Laboratory Information Management System (LIMS)
Basic computer skills (data entry and attention to detail) in Microsoft
Demonstrated experience in manufacturing, quality or engineering experience in the biotech or pharmaceutical industry.
Excellent effective written and verbal communication and interpersonal skills
Experience in biotech or pharmaceutical industry
Experience leading continuous improvement projects.
Qc Scientist - Next Generation Sequencing
By Aldevron At , Fargo, 58102, Nd
Support other groups or as designated by Management team by providing insights and performing investigatory studies
Manage the lifecycle of each procedure by monitoring performance characteristics
Identify new techniques and instrumentation to expand internal capabilities. Prepare justification for new lab equipment.
M.S. in molecular biology, biochemistry, or microbiology or related field is required. Education in computational biology or bioinformatics is preferred.
Perform NGS testing, including library preparation, data analysis, result reporting
Provide training to Analysts for newly developed methods
Qc Scientist Iv Jobs
By Inclusively At , Andover, Ma
Performs all work in compliance with cGMPs and site requirements.
Perform microbiological assays and PCR-based assays for routine testing and qualification/validation of new methods.
Trains less experienced analysts in new and existing procedures, techniques and governmental regulations.
Mentors analysts by providing technical knowledge and support in resolving technical problems.
High technical knowledge and practical application of relevant techniques – classical microbiology techniques
Experience with novel rapid microbial technologies such as PCR or rapid bioburden
Qc/Ad Scientist Iii, Ngs
By Thermo Fisher Scientific At , Carlsbad, 92008, Ca
Bachelors in Life Sciences, Engineering, Biochemistry, Biology or related field with 6+ years of relevant industry experience.
Master’s or Ph.D. with 3+ years of relevant industry experience.
Excellent knowledge and understanding of NGS, preferably with Illumina MiSeq system.
Excellent understanding of quality and regulatory requirements in the pharmaceutical industry, including pharmaceutical GMPs and descriptive molecular biology.
Excellent problem-solving skills and logical approach to solving scientific problems utilizing QbD principles.
Skilled technical writer, able to convey complex topics through text and diagrams.
Qc Associate Scientist, Chemistry
By BioSpace At Redmond, WA, United States
Work cross-functionally ensuring successful method transfer, qualification, and method validation
Relevant experience with HPLC / UPLC chromatography and/or capillary electrophoresis techniques
Experience with Microsoft Office apps (Word, Excel, PowerPoint)
Experience in a cGMP environment
Perform QC chemistry release testing in support of the GMP manufacturing of drug substance and drug product
Assure timely completion of GMP documentation and adherence to good documentation practices.
Qc Scientist Jobs
By BioSpace At Redmond, WA, United States
Experience with a quality management system (QMS)
BS in Biochemistry, Chemistry or related field and 5 – 8 years of experience
5+ years of relevant experience in a cGMP QC laboratory or similar environment
Experience with Waters HPLC, UPLC and Beckman PA800 CE systems
Knowledge of GDPs, GMPs and DS / DP compendial assays (USP, EP, JP)
Experience with ELISA based impurity or potency methods
Qc Laboratory Associate Ii
By B. Braun Medical Inc. At , Allentown, 18109, Pa
Chemistry knowledge and skills as it pertains to a GxP laboratory;
LAL knowledge and skills as it pertains to a GxP Laboratory;
Stability knowledge and skills as it pertains to a GxP Laboratory;
Microbiology knowledge and skills as it pertains to a GxP Laboratory.
Training to current practices and be skills assessed on those practices,
Performs data entry in various formats, as required, to support departmental needs.
Qc Analytical Scientist Jobs
By Takeda Pharmaceutical At , Thousand Oaks, Ca $64,400 - $92,000 a year
Manage and perform assay control and important reagent qualifications, including monitoring and trending of method performance.
Excellent technical writing skills and able to write create technical documents and reports that meet company and regulatory requirements.
Knowledge about analytical method validation and important reagent qualification.
Basic knowledge about regulatory requirements concerning analytical instrumentation, test methods, and licenses.
Substantial knowledge regarding regulatory standards requirements e.g., CGMP, QSR, USP, 21CFR, ICH
Support the installation, operational qualification (IOQ), maintenance and troubleshooting of instrumentation in the AQC group.
Principal Scientist, Qc Technical Services
By Aimmune Therapeutics At , Remote
Develop working relationships with contract testing laboratories and manage assigned analytical activities.
Lead activities focused on the development and assessment of specifications attributes and acceptance criteria.
Develop protocols and prepare reports for method transfers and comparability studies
Lead method lifecycle projects and validate methods.
Support investigations, critical reagents, and stability studies by providing technical insight.
Author regulatory submissions and responses related to specification and analytical topics.
Qc Incoming Material Scientist
By Pfizer At , Rocky Mount, Nc
Document Change Management experience, SOP Revision Management
Serves as management designee and will have limited input into the OTE colleague performance assessment process.
Trains others in the theory and practice of both laboratory techniques and quality systems including investigations, instrument qualifications, etc.
Independently writes SOPs, technical reports, project plans, instrument qualifications, etc.
Applicant must have high school diploma (or equivalent) with six years of relevant experience.
OR an associate degree with four years of experience.
Bioassay Scientist I- Ad And Qc Bioassay
By Azzur Group At , Raleigh, Nc
Reagent qualification and raw material testing.
Method development incorporating quality-by-design concept into development, qualification, and validation of bioassays per the FDA and ICH guidelines.
Experience sterile culture technique, cell preservation studies, and subsequent analytical assessment platforms for both drug substance and drug products.
Experience with client-facing tech transfer process and internal and external analyst training.
Knowledge of GMP, GxP, ICH, and 21 CFR part 11 regulations relevant to a clinical QC lab operation.
A bonus to have experience in molecular detection techniques.
Scientist, Iii-Qc Analytical Devlopment
By PCI Pharma Services At , Bedford, 03110, Nh

Life changing therapies. Global impact. Bridge to thousands of biopharma companies and their patients.

PCI Pharma Services is an Equal

Qc Research Associate Jobs
By BRILTALENTA At El Segundo, CA, United States

Below Are The Details Our client, a leading pharmaceutical company, has a requirement for a QC Research Associate in El Segundo, CA. Title: Quality Control Research Associate Job id: ...

Qc Associate Jobs
By ASK Consulting At , , Ma
Technical lab skills using pipettes, analytical balances, pH meter, etc. is a must.
Expiry Date: 19 June 2023
Sialic acid, water testing (TOC, Conductivity, and Nitrates), and performing Sample Receipt functions.
Other analytical support as needed.
Must have a positive mindset, be a hard worker and a team player. Willing to learn.