Primary Talent Partners
Scientist, Analytical Sciences & Technology
Primary Talent Partners, Village Green, New York, United States
Scientist, Analytical Sciences & Technology
Scientist, Analytical Sciences & Technology
1 day ago Be among the first 25 applicants Get AI-powered advice on this job and more exclusive features. Primary Talent Partners provided pay range
This range is provided by Primary Talent Partners. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more. Base pay range
$35.00/hr - $40.00/hr Primary Talent Partners has a 12-month contract opening for a Scientist to join a large biologics company for an on-site position operating out of East Syracuse, NY.
Pay:
$35.00/hr - $40.00/hr, no benefits or PTO provided Contract:
12 months, extensions likely, conversion possible Type:
W-2, cannot support C2C or provide visa sponsorship
Summary: The Contractor Scientist within the Analytical Science and Technology team is responsible for supporting analytical method lifecycle activities including method development, qualification, validation, and technical transfer of methods for the testing of raw materials, excipients, biologics and other modalities in-process, drug substance, and drug product samples. The candidate will execute non-GMP testing, non-GMP stability testing, reference standard qualification, and comparability studies to support clinical and/or commercial GMP manufacturing.
Duties/Responsibilities: • Develop, author, and peer review standard operating procedures, analytical methods, protocols, reports, and other associated scientific technical documents. • Perform testing of study samples to support upstream and downstream manufacturing process development, characterization, and process improvements. • Document and evaluate experimental results and perform data verification and trending. • Provide technical expertise and guidance to support investigations and help troubleshoot analytical operational issues. • Identify new analytical technologies and opportunities for technical advancements. • Support the preparation and review of regulatory submissions related to analytical procedures, method development and validation, specifications, reference standards, extended characterization, and product stability/ shelf-life. • Support regulatory inspections, third-party audits, and customer audits through participating in inspection readiness and addressing inspectional findings. • Perform routine laboratory activities including sample management, instrument maintenance and calibration, inventory and ordering of supplies, general housekeeping, and other related activities. • Work in a diverse group environment while focusing on inclusivity and safety to produce high quality, compliant results.
Qualifications: Specific Knowledge, Skills, Abilities, etc: • Strong written, verbal, presentation, and interpersonal communication skills. • Detail oriented with good organization skills. • Ability to prioritize, independently manage and complete deliverables within given timelines. • Ability to problem solve and apply risk-based critical thinking in a technical environment. • Demonstrated history of continuous improvement is desired
Education/Experience/ Licenses/Certifications: • B.Sc./B.Eng. or M.Sc./M.Eng. in Biology, Chemistry, Biotechnology, or equivalent area of related study with 0-5 years industry experience in biologic/protein analytics. • Experience across the analytical method lifecycle in protein biotherapeutics for a variety of methodologies and instrumentation used in the testing and characterization of raw materials, excipients, in-process, drug substance, and drug product samples including HPLC/UPLC methods and various other analytical techniques (i.e., qPCR, ELISA, CE-SDS, iCIEF, SDS-PAGE, UV-VIS, western blotting, mass spectrometry, and cell-based assays) is preferred. • Working knowledge and experience in the biopharmaceutical development process, GMP, PAT, CMC and regulatory guidance, ICH guidelines, and compendial requirements is desired. • Experience authoring, validating, and coordinating timely transfer of test methods with and to Quality Control laboratories is desired.
Specific Knowledge, Skills, Abilities, etc: • Strong written, verbal, presentation, and interpersonal communication skills. • Detail oriented with good organization skills. • Ability to prioritize, independently manage and complete deliverables within given timelines. • Ability to problem solve and apply risk-based critical thinking in a technical environment. • Demonstrated history of continuous improvement is desired
Physical Demands: • The role is a combination of laboratory and office based work. • The laboratory work requires appropriate levels of personal protective equipment (PPE). The role may require contact with biohazardous materials such as live cell cultures and other hazardous chemicals including methotrexate, acids, and caustics. Powdered materials and high temperature liquids and solids may also be handled. Use of a respirator may be required. • Frequent repeated motions such as pipetting, lifting, bending, twisting, squatting, crouching, sitting, kneeling, climbing on stepstools, and reaching may be required. Repetitive use of arms/hands/wrists and grasping may be required. • The role may require unassisted lifting (not to exceed 50 lbs.).
Work Environment: • Position is primarily laboratory and office based with occasional work in a classified GMP manufacturing environment. • Dynamic, fast-paced, interactive, and entrepreneurial environment. • Position is a team and project-based position that may require occasional shift work, weekends, and holidays.
Travel: • This position may require up to 5% of domestic and/or international travel.
Primary Talent Partners is an Equal Opportunity / Affirmative Action employer committed to diversity in the workplace. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, age, national origin, disability, protected veteran status, gender identity, or any other factor protected by applicable federal, state, or local laws.
If you are a person with a disability needing assistance with the application or at any point in the hiring process, please contact us atinfo@primarytalentpartners.com
#PTPJobs
Seniority level
Seniority level Entry level Employment type
Employment type Contract Job function
Job function Research, Analyst, and Information Technology Industries Pharmaceutical Manufacturing Referrals increase your chances of interviewing at Primary Talent Partners by 2x Get notified about new Analytical Scientist jobs in
East Syracuse, NY . Scientist, Analytical Sciences and Technology
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#J-18808-Ljbffr
Scientist, Analytical Sciences & Technology
1 day ago Be among the first 25 applicants Get AI-powered advice on this job and more exclusive features. Primary Talent Partners provided pay range
This range is provided by Primary Talent Partners. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more. Base pay range
$35.00/hr - $40.00/hr Primary Talent Partners has a 12-month contract opening for a Scientist to join a large biologics company for an on-site position operating out of East Syracuse, NY.
Pay:
$35.00/hr - $40.00/hr, no benefits or PTO provided Contract:
12 months, extensions likely, conversion possible Type:
W-2, cannot support C2C or provide visa sponsorship
Summary: The Contractor Scientist within the Analytical Science and Technology team is responsible for supporting analytical method lifecycle activities including method development, qualification, validation, and technical transfer of methods for the testing of raw materials, excipients, biologics and other modalities in-process, drug substance, and drug product samples. The candidate will execute non-GMP testing, non-GMP stability testing, reference standard qualification, and comparability studies to support clinical and/or commercial GMP manufacturing.
Duties/Responsibilities: • Develop, author, and peer review standard operating procedures, analytical methods, protocols, reports, and other associated scientific technical documents. • Perform testing of study samples to support upstream and downstream manufacturing process development, characterization, and process improvements. • Document and evaluate experimental results and perform data verification and trending. • Provide technical expertise and guidance to support investigations and help troubleshoot analytical operational issues. • Identify new analytical technologies and opportunities for technical advancements. • Support the preparation and review of regulatory submissions related to analytical procedures, method development and validation, specifications, reference standards, extended characterization, and product stability/ shelf-life. • Support regulatory inspections, third-party audits, and customer audits through participating in inspection readiness and addressing inspectional findings. • Perform routine laboratory activities including sample management, instrument maintenance and calibration, inventory and ordering of supplies, general housekeeping, and other related activities. • Work in a diverse group environment while focusing on inclusivity and safety to produce high quality, compliant results.
Qualifications: Specific Knowledge, Skills, Abilities, etc: • Strong written, verbal, presentation, and interpersonal communication skills. • Detail oriented with good organization skills. • Ability to prioritize, independently manage and complete deliverables within given timelines. • Ability to problem solve and apply risk-based critical thinking in a technical environment. • Demonstrated history of continuous improvement is desired
Education/Experience/ Licenses/Certifications: • B.Sc./B.Eng. or M.Sc./M.Eng. in Biology, Chemistry, Biotechnology, or equivalent area of related study with 0-5 years industry experience in biologic/protein analytics. • Experience across the analytical method lifecycle in protein biotherapeutics for a variety of methodologies and instrumentation used in the testing and characterization of raw materials, excipients, in-process, drug substance, and drug product samples including HPLC/UPLC methods and various other analytical techniques (i.e., qPCR, ELISA, CE-SDS, iCIEF, SDS-PAGE, UV-VIS, western blotting, mass spectrometry, and cell-based assays) is preferred. • Working knowledge and experience in the biopharmaceutical development process, GMP, PAT, CMC and regulatory guidance, ICH guidelines, and compendial requirements is desired. • Experience authoring, validating, and coordinating timely transfer of test methods with and to Quality Control laboratories is desired.
Specific Knowledge, Skills, Abilities, etc: • Strong written, verbal, presentation, and interpersonal communication skills. • Detail oriented with good organization skills. • Ability to prioritize, independently manage and complete deliverables within given timelines. • Ability to problem solve and apply risk-based critical thinking in a technical environment. • Demonstrated history of continuous improvement is desired
Physical Demands: • The role is a combination of laboratory and office based work. • The laboratory work requires appropriate levels of personal protective equipment (PPE). The role may require contact with biohazardous materials such as live cell cultures and other hazardous chemicals including methotrexate, acids, and caustics. Powdered materials and high temperature liquids and solids may also be handled. Use of a respirator may be required. • Frequent repeated motions such as pipetting, lifting, bending, twisting, squatting, crouching, sitting, kneeling, climbing on stepstools, and reaching may be required. Repetitive use of arms/hands/wrists and grasping may be required. • The role may require unassisted lifting (not to exceed 50 lbs.).
Work Environment: • Position is primarily laboratory and office based with occasional work in a classified GMP manufacturing environment. • Dynamic, fast-paced, interactive, and entrepreneurial environment. • Position is a team and project-based position that may require occasional shift work, weekends, and holidays.
Travel: • This position may require up to 5% of domestic and/or international travel.
Primary Talent Partners is an Equal Opportunity / Affirmative Action employer committed to diversity in the workplace. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, age, national origin, disability, protected veteran status, gender identity, or any other factor protected by applicable federal, state, or local laws.
If you are a person with a disability needing assistance with the application or at any point in the hiring process, please contact us atinfo@primarytalentpartners.com
#PTPJobs
Seniority level
Seniority level Entry level Employment type
Employment type Contract Job function
Job function Research, Analyst, and Information Technology Industries Pharmaceutical Manufacturing Referrals increase your chances of interviewing at Primary Talent Partners by 2x Get notified about new Analytical Scientist jobs in
East Syracuse, NY . Scientist, Analytical Sciences and Technology
Scientist, Analytical Sciences & Technology
East Syracuse, NY $30.00-$40.00 20 hours ago Scientist, Analytical Sciences & Technology
New York, United States $110,000.00-$115,000.00 4 weeks ago Scientist, Analytical Sciences & Technology
Syracuse, NY $68,187.00-$120,947.00 1 day ago New York, United States $113,000.00-$195,200.00 1 week ago Assistant Scientist, In-Process Quality Control (Evening Shift)
New York, United States $85,000.00-$120,000.00 2 hours ago New York, United States $110,000.00-$160,000.00 1 day ago New York, United States $60,000.00-$120,000.00 1 week ago New York, United States $110,000.00-$160,000.00 1 day ago We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.
#J-18808-Ljbffr