Data Scientist / Pharma Manufacturing / Remote Work Duration: 12 months contract, extendable up to 24 Months Client Location: Titusville, NJ Note: The client has the right-to-hire you as a permanent ...
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Data Scientist / Pharma Manufacturing / Remote Work Duration: 12 months contract, extendable up to 24 Months Client Location: Titusville, NJ Note: The client has the right-to-hire you as a permanent ...
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Inventory Data Analyst (SAP, Power BI, Excel) Duration: 9 months contract, extendable up to 24 Months Location: Memphis, TN Note: The client has the right-to-hire you as a permanent employee at any ...
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RWE Scientist / Immunology Studies / Remote Work
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A typical Analytical Chemist ensures the accuracy and reliability of data through method development, validation, and adherence to regulatory standards. Job Responsibilities: Perform chemical ...
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Parsippany, NJ · On-site
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A typical Analytical Chemist ensures the accuracy and reliability of data through method development, validation, and adherence to regulatory standards. Job Responsibilities: Perform chemical ...
Quick apply
A typical Analytical Chemist ensures the accuracy and reliability of data through method development, validation, and adherence to regulatory standards. Job Responsibilities: Perform chemical ...
HR Coordinator / Pharma Industry / Hybrid Work
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Quick apply
HR Coordinator / Pharma Industry / Hybrid Work
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Biostatistician / Clinical Data Detailed Description: * Responsible for statistical aspects of clinical and pre-clinical research projects including study design, sample size estimation, patient ...
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Bench Scientist
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Strong data organization and analysis skills. Strong communication skills. Additional Information All your information will be kept confidential according to EEO guidelines.
Bench Scientist
$35.75 - $44.75/hr
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Bioanalytical Scientist / Molecular Assessment
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Document experiments, analyze data, and provide reporting using an electronic laboratory notebook in accordance with Client/GCLP requirements. With guidance, the individual will execute assay routine ...
You will collect and organize data, prepare reports, and ensure inspection readiness while addressing routine quality inquiries. Key Responsibilities Collaborate with cross-functional teams to ...
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You will collect and organize data, prepare reports, and ensure inspection readiness while addressing routine quality inquiries. Key Responsibilities Collaborate with cross-functional teams to ...
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The main function of a Pharmacology Associate is to support drug development and research by conducting laboratory experiments, analyzing pharmacological data, and assisting in the evaluation of drug ...
Maintain all related data and records in compliance with cGMPs and quality procedures. Track timelines and deliverables, and communicate effectively across teams to ensure alignment and timely ...
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Maintain all related data and records in compliance with cGMPs and quality procedures. Track timelines and deliverables, and communicate effectively across teams to ensure alignment and timely ...
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Contractor
Posted 4 days ago
Job description
Position Details:
Our client, a world-leading Pharmaceutical Company in Titusville, NJ is currently looking for a Data Scientist to join their expanding team.
Job Title: Data Scientist / Pharma Manufacturing / Remote Work
Duration: 12 months contract, extendable up to 24 Months
Client Location: Titusville, NJ
Duration: 12 months contract, extendable up to 24 Months
Client Location: Titusville, NJ
Note:
The client has the right-to-hire you as a permanent employee at any time during or after the end of the contract.
The client has the right-to-hire you as a permanent employee at any time during or after the end of the contract.
You may participate in the company group medical insurance plan
Job Description:
Position summary - Senior Scientist
Notes:
Role can be HYBRID or REMOTE, but must be in EST time zone, prefers the candidate lives in NJ or PA
Masters degree is required
Required experience with Python and SQL - REQUIRED
Must have MSAT or Manufacturing background
Will work on a major project, will help setup connections, and explore data analysis
Will research specific materials
Must be a critical thinker
Must be eager to learn
MUST HAVE PROGRAMMING AND CODING EXPERIENCE
Will help with coming up with unique ways to solve problems or obstacles
Must have hands on coding experience (versus using AI solutions)
Role can be HYBRID or REMOTE, but must be in EST time zone, prefers the candidate lives in NJ or PA
Masters degree is required
Required experience with Python and SQL - REQUIRED
Must have MSAT or Manufacturing background
Will work on a major project, will help setup connections, and explore data analysis
Will research specific materials
Must be a critical thinker
Must be eager to learn
MUST HAVE PROGRAMMING AND CODING EXPERIENCE
Will help with coming up with unique ways to solve problems or obstacles
Must have hands on coding experience (versus using AI solutions)
Description:
MSAT Material Science is seeking a scientist to drive raw material quality and traceability initiatives that support regulatory compliance and dependable manufacturing outputs.
This candidate will provide technical support to the MSAT Material Science team on a variety of deliverables critical to successful technical materials deliverables.
This role will support a range of activities including investigations, specification development, material qualification, change control and technology transfer support, analytical method evaluation and data driven traceability efforts.
The role will collaborate closely with Process, Planning, Manufacturing, Quality, Supply Chain/Procurement, Supplier Quality, and IT/data teams to improve raw material traceability, resolve material issues, and produce regulatory quality documentation.
This candidate will provide technical support to the MSAT Material Science team on a variety of deliverables critical to successful technical materials deliverables.
This role will support a range of activities including investigations, specification development, material qualification, change control and technology transfer support, analytical method evaluation and data driven traceability efforts.
The role will collaborate closely with Process, Planning, Manufacturing, Quality, Supply Chain/Procurement, Supplier Quality, and IT/data teams to improve raw material traceability, resolve material issues, and produce regulatory quality documentation.
Key responsibilities
Support the MSAT Material Science team on material related investigations and deviation analyses: gather and analyze manufacturing and analytical data, contribute to technical assessments, and help implement solutions as applicable.
Assist MSAT Material Science in developing and revising raw material specifications: draft language, define acceptance criteria, compile technical justification, compendial review and coordinate SME deliverables.
Support material qualification and requalification activities on behalf of the MSAT Material Science team: prepare qualification plans/protocols, coordinate testing with internal or external labs/vendors, analyze returned data, and draft qualification reports.
Provide technical input for change controls: prepare technical assessments, perform impact and risk evaluations, coordinate verification/validation activities, and compile evidence for closure.
Support technology transfer activities: prepare transfer documentation, align material requirements between development and manufacturing, and coordinate post transfer monitoring and follow up.
Contribute to material traceability and data mapping initiatives: work with Process, Planning, and IT/data teams to map raw material usage to manufacturing campaigns and produce actionable visualizations.
Interface with Supplier Quality and Procurement to support vendor qualification, incoming material review, sample evaluations, and supplier investigations.
Prepare and maintain regulatory grade documentation on behalf of MSAT Material Science: investigation summaries, specifications, test method rationales, SOPs, qualification packages, and technical reports.
Support audits and inspections by preparing evidence, supporting response to technical queries, and assisting in closure of material related findings under Quality oversight.
Communicate findings and recommendations to the MSAT Material Science team, cross functional partners, and leadership; present at technical meetings as required.
Mentor and guide junior staff, contractors, or interns on data review, documentation standards, and investigation best practices.
Support the MSAT Material Science team on material related investigations and deviation analyses: gather and analyze manufacturing and analytical data, contribute to technical assessments, and help implement solutions as applicable.
Assist MSAT Material Science in developing and revising raw material specifications: draft language, define acceptance criteria, compile technical justification, compendial review and coordinate SME deliverables.
Support material qualification and requalification activities on behalf of the MSAT Material Science team: prepare qualification plans/protocols, coordinate testing with internal or external labs/vendors, analyze returned data, and draft qualification reports.
Provide technical input for change controls: prepare technical assessments, perform impact and risk evaluations, coordinate verification/validation activities, and compile evidence for closure.
Support technology transfer activities: prepare transfer documentation, align material requirements between development and manufacturing, and coordinate post transfer monitoring and follow up.
Contribute to material traceability and data mapping initiatives: work with Process, Planning, and IT/data teams to map raw material usage to manufacturing campaigns and produce actionable visualizations.
Interface with Supplier Quality and Procurement to support vendor qualification, incoming material review, sample evaluations, and supplier investigations.
Prepare and maintain regulatory grade documentation on behalf of MSAT Material Science: investigation summaries, specifications, test method rationales, SOPs, qualification packages, and technical reports.
Support audits and inspections by preparing evidence, supporting response to technical queries, and assisting in closure of material related findings under Quality oversight.
Communicate findings and recommendations to the MSAT Material Science team, cross functional partners, and leadership; present at technical meetings as required.
Mentor and guide junior staff, contractors, or interns on data review, documentation standards, and investigation best practices.
Qualifications
Advanced degree in Materials Science, Chemical Engineering, Chemistry, Polymer Science, or closely related discipline preferred; Master's with 3-5+ years experience. PhD with 0-3+ years experience.
Experience coordinating testing with external/internal analytical labs and interpreting lab reports.
Knowledge of GMP principles, validation strategies, and risk assessment methodologies (e.g., FMEA).
Familiarity with supplier qualification practices and vendor communications.
Demonstrated experience supporting material investigations, specification setting, qualification oversight, change control, and tech transfer in a regulated manufacturing environment (pharma, biotech, medical device, or related) preferred.
Strong data analysis skills and ability to synthesize manufacturing and analytical datasets to support root cause and risk assessments.
Proven technical writing skills for regulatory grade reports, specifications, and protocols.
Experience collaborating with Process, Planning, Manufacturing, Quality, Supply Chain/Procurement, Supplier Quality, and IT/data teams.
Familiarity with electronic quality systems (eQMS, LIMS), manufacturing systems (MES), SAP and common data tools (Excel, Python/R, JMP, or similar).
Prior industry experience in MSAT or material science support roles within regulated manufacturing preferred.
Advanced degree in Materials Science, Chemical Engineering, Chemistry, Polymer Science, or closely related discipline preferred; Master's with 3-5+ years experience. PhD with 0-3+ years experience.
Experience coordinating testing with external/internal analytical labs and interpreting lab reports.
Knowledge of GMP principles, validation strategies, and risk assessment methodologies (e.g., FMEA).
Familiarity with supplier qualification practices and vendor communications.
Demonstrated experience supporting material investigations, specification setting, qualification oversight, change control, and tech transfer in a regulated manufacturing environment (pharma, biotech, medical device, or related) preferred.
Strong data analysis skills and ability to synthesize manufacturing and analytical datasets to support root cause and risk assessments.
Proven technical writing skills for regulatory grade reports, specifications, and protocols.
Experience collaborating with Process, Planning, Manufacturing, Quality, Supply Chain/Procurement, Supplier Quality, and IT/data teams.
Familiarity with electronic quality systems (eQMS, LIMS), manufacturing systems (MES), SAP and common data tools (Excel, Python/R, JMP, or similar).
Prior industry experience in MSAT or material science support roles within regulated manufacturing preferred.