Quality Scientist I
2 weeks ago
Role DescriptionPosition Summary:This Quality Scientist I position is responsible for testing of blended vaccines and antigen stocks for potency, extraneous agents, inactivation, and identity using egg based and tissue culture-based methodology. Maintain testing schedules and prioritization of testing to ensure timely completion of assays to meet the established release dates. Following GMP documentation guidelines. Completion of test records and system data entry. Basic problem-solving skills and demonstrate trouble shooting ability and writing Laboratory Investigations when necessary, utilizing Method 1 and the DMAIC process. Contribute to the team’s productivity goals. Cleaning and maintaining lab equipment, instrumentation, and facility. The colleague should have the ability to follow detailed instructions.Position Responsibilities:Testing of samples from manufacturing to ensure Quality and compliance according to all applicable assays utilizing good aseptic practices.Maintaining testing schedules and reagent supplyCompletion of documentation following cGMP guidelinesCleaning and maintaining lab equipment, instrumentation, and facility.Following all Zoetis Quality Standards, Policies and ProceduresProviding minimum input for laboratory investigations (LIR), minimal project supportUnderstanding of the QC software packages used during routine work.Pipette work and analytical techniques.Preparation of media and reagentsEquipment monitoring.Properly utilize computer software used during routine work.Understand and execute excellent aseptic technique.Perform egg drilling, candling, and other egg manipulations.Perform culture of primary and continuous cell linesParticipate in Media Fill inspections.Participate in all required training activities.Work in a safe manner and follow safety policies and procedures.Demonstrate basic problem-solving skills and troubleshooting ability.Perform basic laboratory math accurately (dilutions, titrations, cell counts, etc.) Record procedures and results using proper cGMP documentation.Effectively work in a team environment and communicate with multiple departments.Education and Experience:2 to 4 Year Degree (science background preferred) and/or 0-3 years of relevant experience.Knowledge of cGMP/GLP requirements.Experience with Microsoft Office software (Word, Excel, and PowerPoint)Strong attention to detail, ability to work well independently and as a part of a team, and to work effectively with people at all levels within the organization.Ability to follow detailed instructions with coaching.Willingness to positively embrace change and flexibility in adjusting to changing priorities.Gain proficiency in 50% of the testing in a specified area.Preferred:Experience with cell culture and/or egg-based propagation of viruses.Experience using aseptic technique.Work experience in a cGMP/GLP environment.Physical Requirements:Must be able to walk, sit, or stand for long periods of time.Must be able to reach above shoulder level, bend/stoop, kneel, push/pull, and handle/grip frequently.Must be able to work scheduled 40 hours with the ability to work overtime as needed.Frequent lifting and carrying of 5 to 25 lbs.Regular reaching, bending, stooping, and twisting.Repetitive motion and substantial movement of the wrists, hands, and/or fingers.Ability to grasp and manipulate objects like pipettors, flasks, and bottles.Flexibility to cover rotating weekend duties.Full timeRegularColleagueAny unsolicited resumes sent to Zoetis from a third party, such as an Agency recruiter, including unsolicited resumes sent to a Zoetis mailing address, fax machine or email address, directly to Zoetis employees, or to Zoetis resume database will be considered Zoetis property. Zoetis will NOT pay a fee for any placement resulting from the receipt of an unsolicited resume.Zoetis will consider any candidate for whom an Agency has submitted an unsolicited resume to have been referred by the Agency free of any charges or fees. This includes any Agency that is an approved/engaged vendor but does not have the appropriate approvals to be engaged on a search.Zoetis is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status or any other protected classification. Disabled individuals are given an equal opportunity to use our online application system. We offer reasonable accommodations as an alternative if requested by an individual with a disability. Please contact Zoetis Colleague Services at to request an accommodation. Zoetis also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as employment eligibility verification requirements of the Immigration and Nationality Act. All applicants must possess or obtain authorization to work in the US for Zoetis. Zoetis retains sole and exclusive discretion to pursue sponsorship for the acquisition or maintenance of nonimmigrant status and employment eligibility, considering factors such as availability of qualified US workers. Individuals requiring sponsorship must disclose this fact. Please note that Zoetis seeks information related to job applications from candidates for jobs in the U.S. solely via the following: (1) our company website at www.Zoetis.com/careers site, or (2) via email to/from addresses using only the Zoetis domain of “@zoetis.com”. In addition, Zoetis does not use Google Hangout for any recruitment related activities. Any solicitation or request for information related to job applications with Zoetis via any other means and/or utilizing email addresses with any other domain should be disregarded. In addition, Zoetis will never ask candidates to make any type of personal financial investment related to gaining employment with Zoetis.
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Quality Scientist I
6 days ago
Charles City, United States Zoetis Full timeRole Description Position Summary: This Quality Scientist I position is responsible for testing of blended vaccines and antigen stocks for potency, extraneous agents, inactivation, and identity using egg based and tissue culture-based methodology. Maintain testing schedules and prioritization of testing to ensure timely completion of assays to meet the...
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Quality Scientist I
5 days ago
Charles City, IA, United States Zoetis Full timeRole DescriptionPosition Summary:This Quality Scientist I position is responsible for testing of blended vaccines and antigen stocks for potency, extraneous agents, inactivation, and identity using egg based and tissue culture-based methodology. Maintain testing schedules and prioritization of testing to ensure timely completion of assays to meet the...
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Quality Control Scientist
4 days ago
Charles City, United States Global Technical Talent Full timeQuality Control ScientistAlternate/Related Job Titles: QC Laboratory Scientist Quality Assurance Scientist QC Analytical Specialist Location:Charles City, IAOnsite Flexibility:OnsiteContract Details Position Type: Contract Contract Duration: 12 months Start: As Soon As Possible Job SummaryThe Quality Control Scientist supports manufacturing operations by...
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Quality Control Senior Associate Scientist I
2 weeks ago
Kansas City, Missouri, United States Catalent Full time $60,000 - $80,000 per yearQuality Control Senior Associate Scientist IPosition Summary:Work Schedule: Monday – Friday 12:00PM – 8:00PM 100% onsiteCatalent's Kansas City (KCM) facility is a premier site for integrated drug development, manufacturing, and clinical supply services, supporting a wide range of pharmaceutical and biotech products. With cutting-edge technologies and a...
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Quality Control Data Review Scientist
1 week ago
Charles City, United States Cambrex Full timeCompany InformationYou Matter to Cambrex.Cambrex is a leading global contract development and manufacturing organization (CDMO) that provides drug substance, drug product, and analytical services across the entire drug lifecycle. With more than 40 years of experience and a growing team of over 2,000 professionals servicing global clients, Cambrex is a...
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Quality Control Data Review Scientist
1 week ago
Charles City, United States Cambrex High Point Full timeCompany InformationYou Matter to Cambrex.Cambrex is a leading global contract development and manufacturing organization (CDMO) that provides drug substance, drug product, and analytical services across the entire drug lifecycle. With more than 40 years of experience and a growing team of over 2,000 professionals servicing global clients, Cambrex is a...
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Charles City, United States Cambrex Full timeCompany InformationYou Matter to Cambrex.Cambrex is a leading global contract development and manufacturing organization (CDMO) that provides drug substance development and manufacturing across the entire drug lifecycle, as well as comprehensive analytical and IND enabling services.With over 40 years of experience and a team of 2,000 experts servicing global...
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Charles City, United States Cambrex High Point Full timeCompany InformationYou Matter to Cambrex.Cambrex is a leading global contract development and manufacturing organization (CDMO) that provides drug substance development and manufacturing across the entire drug lifecycle, as well as comprehensive analytical and IND enabling services.With over 40 years of experience and a team of 2,000 experts servicing global...
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Clinical Laboratory Scientist I
4 weeks ago
Daly City, United States The Bowdoin Group Full timeTitle Clinical Laboratory Scientist (CLS) I Location Daly City, CA Reports to Sr. Director, Laboratory Operations Base pay range $50.00/hr - $60.00/hr About This Opportunity Our client, a leading diagnostics company, is focused on advancing women’s health through next-generation molecular diagnostic testing. They are building a state-of-the-art CLIA...
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Charles City, United States Cambrex Corporation Full timeJob Description Company InformationYou Matter to Cambrex. Cambrex is a leading global contract development and manufacturing organization (CDMO) that provides drug substance development and manufacturing across the entire drug lifecycle, as well as comprehensive analytical and IND enabling services. With over 40 years of experience and a team of 2,000...