Job Description
Within this role, you will manage the day-based support requirements of the manufacturing operations team while providing direction, troubleshooting, and guidance. You will maintain safety compliance and audit readiness, ensuring objectives are delivered to a high standard and on time.As an Associate Manager Biotech Production (Downstream Operations), a typical day may include, but is not limited to, the following:Ensuring that all documentation (SOPs, Manufacturing Records, Batch Sheets & Logbooks) is current, accurate, reviewed, and in accordance with regulatory requirements.Leading, motivating, and managing the operation manufacturing specialist teams.Preparing reports by collecting, analyzing, and summarizing information and trends.Tracking relevant metrics to ensure operations are performing effectively and efficiently.Implementing a contamination-free program to ensure the highest process success rates.Working to the highest safety standards and supporting safety initiatives and implementation of safety improvements.Interfacing with other departments, such as Facilities, Process Sciences, Regulatory, Quality Assurance, and Quality Control.Leading and implementing process improvements and robustness initiatives.Preparing and presenting manufacturing data for review.Performing cGMP audits of the production area and representing manufacturing during regulatory and client audits.Training, developing, and mentoring direct reports while effectively managing the performance of individuals.Working closely with staff to develop and manage individual goals and objectives.Conducting performance evaluations that are timely and constructive.This role might be for you if:You possess excellent verbal and written communication skills.You enjoy problem-solving.You demonstrate leadership skills.You are proficient in Microsoft Word, Excel, PowerPoint, and Outlook.To be considered for this opportunity, you should have a 3rd Level Qualification in Life Sciences with 7+ years of relevant experience in manufacturing within the Biopharma industry. This role requires 5+ years of supervisory experience.Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive and diverse culture that provides comprehensive benefits, which often include (depending on location) health and wellness programs, fitness centers, equity awards, annual bonuses, and paid time off for eligible employees at all levels!Regeneron is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. #J-18808-Ljbffr