Job Description
**Biotech Production Associate Manager** Manage day-to-day support requirements of manufacturing operations team, ensuring safety compliance and audit readiness while delivering objectives to a high standard and on time. **Key Responsibilities:** * Ensure all documentation (SOPs, Manufacturing Records, Batch Sheets & Logbooks) is current, accurate, reviewed and in accordance with regulatory requirements * Lead, motivate and manage manufacturing specialist teams * Prepare reports by collecting, analyzing and summarizing information and trends * Track relevant metrics to ensure operations are performing effectively and efficiently * Implement a contamination-free program to ensure highest process success rates * Work to the highest safety standards and support safety initiatives and implementation of safety improvements * Interface with other departments, such as Facilities, Process Sciences, Regulatory, Quality Assurance and Quality Control * Lead and implement process improvements and robustness initiatives * Prepare and present manufacturing data for review * Perform cGMP audits of production area * Represent manufacturing during regulatory and client audits * Train, develop and mentor direct reports and effectively manage the performance of individuals * Work closely with staff to develop and manage individual goals and objectives * Conduct performance evaluations that are timely and constructive **Requirements:** * 3rd Level Qualification in Life Sciences * 7+ years of relevant experience in manufacturing within the Biopharma industry * 5+ years supervisory experience * Excellent verbal and written communication skills * Problem-solving skills * Leadership skills * Proficient in Microsoft Word, Excel, PowerPoint, and Outlook