Qc Scientist I Jobs
By ATR International At Carlsbad, CA, United States
• Identify and implement manufacturing procedures intended to optimize existing processes and ensure compliance with regulatory requirements.
• Experience in flow assays a MUST
• Experience in bioassays is a plus
Introductory Experience in the use of scientific laboratory techniques, equipment and materials:
• Excellent documentation and communication skills.
• Consistent, dependable, and accurate in carrying out responsibilities
Qc Associate Scientist, Em Data Analyst
By Pfizer At , Sanford
Exercise and build basic team effectiveness skills, such as commitment, feedback and consensus management, within the work group.
Experience within the biopharmaceutical industry, including knowledge and experience relevant to biopharmaceutical unity operations and/or laboratory operations.
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
Experience leading continuous improvement projects is a plus.
Principal Scientist Ii (Qc)
By Cambrex Corp. At , Durham
Learn new skills and enjoy new experiences in an engaging and safe environment
Communicates issues or challenges to senior staff and/or management
learn new skills and enjoy new experiences in an engaging and safe environment
Able to apply prior knowledge to accurately interpret structural data.
Participates in experimental design, including development of methods and testing requirements to demonstrate method suitability.
Assists with writings standard operating procedures (SOPs), methods, qualification protocols and other standard documents as directed
Data Review Auditor Jobs
By Catalent At , Greenville, 27834
Interpret data and make recommendations to management for improvement or potential concerns
Assist in complying with any other company and/or departmental objectives as directed by analytical management
Compare laboratory data against specifications and trend data where applicable to determine if results meet requirements
High school diploma or equivalent with at least 6 years of experience in a laboratory setting.
Associate degree in Biotechnology, Chemistry or equivalent science degree with 4 years of experience in a laboratory setting.
Bachelor’s degree in a science-related field (e.g. Biology, Chemistry, Pharmaceutical Sciences) with 3 years of experience in a laboratory setting.
Associate Scientist, Bio Qc
By Boehringer Ingelheim Animal Health USA At , Saint Joseph, 64506
Desired Skills, Experience and Abilities
Perform testing using a portion of the existing laboratory assays
Perform testing using a significant portion of the existing laboratory assays
Maintains laboratory reagents, supplies and calibrated equipment
Communicates schedule, test status and concerns
Write Laboratory Investigations, as needed.
Qc Senior Scientist, Analytical
By Evotec At , Redmond
Experience with the operation, deployment, and administration of laboratory information management systems (LIMS).
Collaborate with Quality Assurance, Manufacturing, Material Management, and other functions to ensure internal timelines, testing TAT and team milestones are achieved
Extensive knowledge of GdPs, GMPs and DS / DP multi-compendial assays (USP, EP, JP)
Excellent communication and collaboration skills
Experience with Waters HPLC, UPLC and Beckman PA800 CE systems
Experience with ELISA based impurity or potency methods
Data Review Clerk Jobs
By Harris County Toll Road Authority At Houston, TX, United States
Previous clerical or data entry experience.
Ability to work under instructions from supervisors and managers
Strong written, oral communication and interpersonal skills
Strong analytical skills. Ability to reason and solve problems independently
Verifies transaction data from external parties agrees to system transactions.
Receipts, reconciles, and posts cash/monies to appropriate accounts; may perform wire transfers as required.
Qc/Ad Scientist Iii, Ngs
By Thermo Fisher Scientific At , Carlsbad
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.
Associate Scientist Ii, Qc
By Catalent At , Saint Petersburg, 33716
Experience with IR and AA instrumentation
H.P.L.C. and G.C. instrumentation experience
Catalent offers rewarding opportunities to further your career!
Cultivate and identify bacteria or other microorganisms isolated on selective and non-selective media.
Maintains cultures according to ATCC and departmental Standard Operating Procedures.
Performs identification of microorganisms using techniques such as API, Gram Stain, etc. Prepares reagents, standards, Medias, etc. needed for analysis.
Sr. Qc Scientist - Instrumentation
By Catalent At , Harmans, 21077
Define project scope, goals and deliverables that support business goals in collaboration with senior management and stakeholders.
Manage onboarding and routine maintenance of laboratory instrumentation and systems.
Prepares and maintains SOP’s for the Laboratory directly related to assigned responsibilities.
A minimum of six (6) years of experience in the Pharmaceutical industry or relevant business experience.
A minimum of 4 years of experience with laboratory equipment onboarding and maintenance, is preferred
Opportunity to gain experience in the cutting-edge gene therapy space and help to develop critical lifesaving therapies for our clients
Qc Scientist I Jobs
By Thermo Fisher Scientific At , Plainville
1+ years of relevant experience within a laboratory setting.
Equivalent experience working in a cGMP environment preferred
Knowledge of GMP regulations in cGMP manufacturing environment preferred.
Excellent problem solving and critical thinking skills
Excellent organization and planning skills.
Medical, Dental, & Vision benefits-effective Day 1
Qc Scientist Method Transfer And Validation
By Pfizer At , Sanford
Ability to receive feedback from management and other colleagues, takes accountability for actions and personal development
Broad Knowledge and Hands-on experience in HPLC, compendial analytical and microbiological methods, capillary gel electrophoresis, ELISA and plate-based assays.
Experience in method verification, qualification, validation and transfer.
Excellent effective written and verbal communication and interpersonal skills; established relationships within business lines
Applies discipline’s principles, appropriate procedures, and leadership skills to action plan and contribute to executing toward team/project goals
Demonstrated experience in Quality Control
Senior Scientist, Qc Jobs
By Catalent At , Bloomington, 47403
Enters data into Laboratory Information Management System (LIMS) or laboratory reports.
Bachelor’s degree in science field with 5-7 years of experience, including 2 year GMP experience or regulated industry
Master’s degree in science field with 2-4 years of experience, including 2 year GMP experience regulated industry
PhD in science field with 3-5 years of experience, including 2 years GMP experience or other regulated industry
General laboratory equipment experience, including micropipettes
Must be able to read and understand English-written job instructions and safety requirements.
Qc Scientist Iii - 1St Shift
By Pfizer At , Andover
Interpret data and make recommendations and reach decisions based on data and management input.
Determine environmental monitoring locations and qualification requirements for aseptic facility modifications and new facilities.
Review and approval of environmental monitoring data and approval of data in Laboratory Information Management System for lot release.
Demonstrated experience in industrial and/or aseptic pharmaceutical production environment, technical knowledge of aseptic processing and sanitization
Basic computer skills, such as data entry, with a high level of attention to detail, are also required
Excellent effective written and verbal communication and interpersonal skills
Assistant Qc Scientist Jobs
By GSK At , Zebulon, 27597
Developing knowledge and application of the Quality Management System (QMS).
Associate degree or High School + 2 years pharmaceutical experience in Chemistry or Biology or a related physical science.
Experience of providing QC testing support to at least one value stream.
Full understanding of the requirements and application of GMP principles in a laboratory environment.
Continuously looking for opportunities to learn, build skills and share learning.
We are looking for professionals with these required skills to achieve our goals:
Qc Scientist I Jobs
By Thermo Fisher Scientific At , Plainville, 02762
1+ years of relevant experience within a laboratory setting.
Equivalent experience working in a cGMP environment preferred
Knowledge of GMP regulations in cGMP manufacturing environment preferred.
Excellent problem solving and critical thinking skills
Excellent organization and planning skills.
Medical, Dental, & Vision benefits-effective Day 1
Scientist, Clinical Qc Jobs
By Bristol Myers Squibb At , Township Of Warren
Advanced organizational and time management skills.
Communicate effectively with management regarding task completion, roadblocks, and needs.
Help manage reagent and control qualification
Help manage method co-qualification/transfer and analyst training.
Bachelor’s degree or equivalent experience, preferably in biology, Chemistry, Microbiology, or related science
Minimum of 3 years of working experience in a cGMP regulated environment
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
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

Are you looking for an exciting opportunity to use your scientific expertise to review data and ensure quality control? We are seeking a QC Data Review Scientist to join our team and help us ensure the accuracy and integrity of our data. You will be responsible for reviewing data, identifying discrepancies, and ensuring compliance with established standards. If you have a passion for science and a commitment to quality, this could be the perfect job for you!

What is QC Data Review Scientist Job Skills Required?

• Knowledge of laboratory techniques and processes
• Ability to interpret and analyze data
• Excellent problem-solving skills
• Ability to work independently and as part of a team
• Excellent communication and interpersonal skills
• Attention to detail
• Ability to work in a fast-paced environment
• Knowledge of laboratory safety protocols

What is QC Data Review Scientist Job Qualifications?

• Bachelor’s degree in a scientific field
• Previous experience in a laboratory setting
• Knowledge of Good Laboratory Practices (GLP)
• Knowledge of Quality Control (QC) principles
• Knowledge of laboratory instrumentation and software
• Ability to use Microsoft Office applications

What is QC Data Review Scientist Job Knowledge?

• Knowledge of laboratory techniques and processes
• Knowledge of Good Laboratory Practices (GLP)
• Knowledge of Quality Control (QC) principles
• Knowledge of laboratory instrumentation and software
• Knowledge of laboratory safety protocols

What is QC Data Review Scientist Job Experience?

• Previous experience in a laboratory setting
• Experience in data analysis and interpretation
• Experience in quality control and assurance

What is QC Data Review Scientist Job Responsibilities?

• Reviewing and analyzing laboratory data