Raw Material Specification Specialist - Quality & Remediation - Hybrid

Are you ready to grow your career with a global pharmaceutical leader? A Top-Tier Global BioPharma Company is seeking a Material Sciences Specialist in Novato, CA for a hybrid role (onsite Tuesdays and Wednesdays). In this position, you will drive a global material specification remediation program supporting regulatory commitments and CAPA activities. Job Summary Are you ready to grow your career with a global pharmaceutical leader? A Top-Tier Global BioPharma Company is seeking a Material Sciences Specialist in Novato, CA for a hybrid role (onsite Tuesdays and Wednesdays). In this position, you will drive a global material specification remediation program supporting regulatory commitments and CAPA activities. location: Novato, California job type: Contract salary: $50 - 60 per hour work hours: 9 to 5 education: Bachelors Responsibilities Review and revise raw material specifications against current USP, Ph. Eur., JP, and ACS compendial standards. Initiate and execute change controls, compile technical justification packages, and track CAPA milestones. Maintain specification inventories, update implementation trackers, and generate status dashboards. Coordinate cross-functionally with Quality, Regulatory Affairs, Supply Chain, and Manufacturing teams to track impact assessments. Assemble supporting documentation to ensure continuous inspection readiness for regulatory audits. Qualifications Required: BS degree in Chemistry, Biochemistry, Pharmaceutical Sciences, Chemical Engineering, or a related scientific discipline. 3-4 years of experience in pharmaceutical manufacturing, quality, material sciences, or regulatory compliance. Hands-on experience with cGMP documentation, technical writing, change controls, and CAPA systems. Strong knowledge of pharmacopeial standards (USP, EP, JP). Preferred Direct experience with raw material specifications and supplier quality systems. Familiarity with Veeva or electronic quality management systems (eQMS). skills: Good Manufacturing Practices (GMP), Corrective and Preventive Actions (CAPA), Good Documentation Practices (GDP) Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact View email address on click.appcast.io. Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility). This posting is open for thirty (30) days. Qualified applicants in San Francisco with criminal histories will be considered for employment in accordance with the San Francisco Fair Chance Ordinance. Qualified applicants with arrest or conviction records will be considered for employment in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act. We will consider for employment all qualified Applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance. #J-18808-Ljbffr Randstad USA