Note: The job is a remote job and is open to candidates in USA. DifGen Pharmaceuticals is a pharmaceutical manufacturer focused on innovative drug delivery technologies. They are seeking a Quality Assurance Engineer to become the subject matter expert for compliance related to production operations, assist with incident and deviation investigations, and provide quality assurance support across various departments.

Responsibilities

• Reviews and approves Investigations for product quality deviations
• Reviews validation and qualification documents
• Becomes Subject matter expert for company product line, production equipment, batch records and relevant SOP’s
• Reviews and analyzes documents and data such as batch records, lab testing, finished product material statuses so as to support completion of the investigation process
• Serves as an investigation team leader so as to assess impact on product quality and validation status
• Recommends and monitors improvements in manufacturing and control systems including corrective and preventative actions (CAPA)
• Works together with multiple departments to troubleshoot the production processes and identify process improvement opportunities
• Ensures compliance with GMP’s
• Provides training and mentoring to colleagues performing investigations
• Writes/revises SOPs relevant to the position’s responsibilities
• Working with the Production Quality team, assess events when they arise to determine ability to resume production
• Interpret specifications, standard operating procedures, and standard testing procedures
• Responsible for the review and approval of validation of analytical methodology (protocols and reports), specifications, master batch records, formulation spreadsheets and Standard Operating procedures (SOPs) in support of research projects involving pharmaceutical components and/or drug products components and/or drug products
• Performs assessments / approvals of change controls related to production activities
• Ensures compliance with all Company policies and procedures including safety rules and regulations
• Operates in accordance with our Code of Conduct and Business Ethics, and all established regulatory, compliance and safety requirements
• Performs all work in support of our Values: Innovate, Evolve, and Excel
• All other relevant duties as assigned

Skills

• A Bachelor's degree in Engineering or Life Sciences from an accredited college or university with a minimum of 5 - 8 years experience
• Master's degree and 3-5 years of experience in a cGMP regulated manufacturing environment or an equivalent combination of training and experience is required
• Knowledge of GMP's (21CFR Parts 210 and 211)
• Analyzing and troubleshooting problems, identifying root causes and recommending and implementing effective methods, procedures, systems and/or techniques
• Ability to prepare / edit all types of pharmaceutical documentation (batch records, SOPs, protocols, summary reports, etc.)
• Sound knowledge of the FDA, Health Canada, and other pharmaceutical regulations
• Thorough understanding of GMPs, specifically those relating to good documentation practices
• Ability to analyze and interpret analytical data
• Interpret specifications, standard operating procedures, and standard testing procedures
• Strong organizational skills
• Managing multiple projects, duties, and assignments
• Writing and interaction in English
• Preferred Bachelor's degree (B.S.) in chemistry or related field with at least 5-8 years of experience in pharmaceutical analytical laboratory with transdermal laboratory experience, or Master's degree (M.S.) with at least 3-5 years of experience
• Knowledgeable in multiple instrumentation techniques such as HPLC, GC, UV-VIS, dissolution equipment, pH measurement, titration, etc
• Knowledgeable in analytical testing of API, excipients and components following compendial and validated methods
• Analytical chemistry and common instrumentation

Company Overview