Senior Scientist

Immediate need for a talented Senior Scientist . This is a 12 months contract opportunity with long-term potential and is located in Titusville, NJ (Remote) . Please review the job description below and contact me ASAP if you are interested. Job Diva ID: 26-19056 Pay Range: $45 - $68/hour. Employee benefits include, but are not limited to, health insurance (medical, dental, vision), 401(k) plan, and paid sick leave (depending on work location). 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. Key Requirements and Technology Experience Must have skills: MSAT or Manufacturing background Python and SQL Programming And Coding Experience Manufacturing environment (pharma, biotech, medical device, or related) 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) MUST SUBMIT CODING EXAMPLES WITH RESUMES or they will be rejected out 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. Pyramid Consulting, Inc. provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, colour, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws. #J-18808-Ljbffr Pyramid Consulting, Inc