RIM Recruitment Professionalshttps://www.rimrp.com/wp-content/uploads/2022/08/rim-200x200-1.pnghttps://www.rimrp.comhttps://www.rimrp.comUSD85000YEARtrue
Job Title: Validation Scientist Reports To: Department Leadership Direct Reports: None
Position Overview: The Validation Scientist is responsible for the execution and oversight of validation activities across equipment, processes, and cleaning procedures within a regulated manufacturing environment. This is a hands-on role focused on ensuring compliance with industry standards and internal quality requirements. The ideal candidate brings a strong scientific background, technical writing skills, and a collaborative, detail-oriented approach. Key Responsibilities:
Perform equipment qualification activities (IQ/OQ/PQ) for both new and existing manufacturing systems.
Author and execute validation and qualification protocols and reports.
Support cleaning and process validation initiatives in alignment with regulatory expectations.
Analyze and interpret data to prepare clear, accurate validation documentation.
Coordinate cross-functional validation activities across departments including Quality, Engineering, and Manufacturing.
Investigate and resolve validation deviations;propose and support corrective actions as needed.
Maintain current knowledge of validation requirements and evolving industry regulations.
Contribute to the development and revision of SOPs, policies, and risk assessments.
Represent the validation function during internal audits and regulatory inspections.
Participate in continuous improvement initiatives related to validation programs.
Qualifications:
Bachelor’s degree in a scientific discipline (e.G., Chemistry, Biology, Engineering, Pharmacy, or related field).
Minimum of 3 years of validation experience in the pharmaceutical or life sciences industry.
Strong working knowledge of cGMP guidelines and regulatory expectations.
Familiarity with a variety of pharmaceutical manufacturing equipment.
Proficient in Microsoft Office and related technical tools.
Exceptional attention to detail with strong organizational and technical writing skills.
Comfortable working in a hands-on, on-site environment.
Preferred Attributes:
Strong collaboration and interpersonal communication skills.
Ability to manage multiple priorities and deliver high-quality work under deadlines.
Demonstrated ability to drive change and lead without direct authority.
Previous exposure to operations, technical services, quality assurance, quality control, or regulatory affairs.
Experience preparing and presenting validation documentation during audits.
Familiarity with industry-standard validation practices including risk assessments and impact assessments.
Commitment to safety and compliance in all activities.
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