Manager Filling and Pkg Staff US - Vaccine

This is a 2nd shift position (3 PM – 11:30 PM) - Monday- Friday, covering Saturday's or Sunday's on a rotating schedule including rotating holidays.

Management experience**

POSITION OVERVIEW

This position will be an off-shift position. Applicants must be able to work 2nd shift hours, weekends, and holidays.

KEY RESPONSIBILITIES

Manages people process within a process/product team to meet goals and priorities.Assures those operations are conducted in compliance with regulatory authorities.Responsible for the packaging operations of syringes and vials vaccines to meet established requirements.Assures that operations are conducted in compliance with cGMPs, CBER, WHO, EP, and other regulatory bodies.Plans and initiates the overall production schedules, coordinating personnel activities with other Manufacturing staff.Reviews batch records for correctness and completeness.Overall responsibilities include employee selection, training, development, counseling recommendations for cost reductions, profit improvement opportunities, cost control, quality of product, incident investigations, managing departmental capital and operation's budgets.Chief duty involves providing managerial coverage for employees as required during third shift working hours.Additional responsibilities include determining and presenting technical process improvements and communicating issues to appropriate groups (e.g., IOC, Management Committee, staff meetings), and working for unit teams.When necessary, coordinates Maintenance, Metrology, and Validation activities with applicable leaders.Takes a role in implementing new equipment and procedures. Performs all other duties as required by department management.Deviation management, people development, and Quality Assurance of the Packaging Vaccines manufacturing area are required.

BASIC QUALIFICATIONS

HS/GED with 5 years' experience in a cGMP or similar environmentMust have previous experience in working with a production department of a pharmaceutical company. Working knowledge of cGMPs.Must have knowledge of continuous improvement techniques and problem-solving skills.Excellent verbal and written communication skills. Working knowledge of SAP is preferred.The candidate must be able to work overtime and flexible hours, including weekends.

PREFERRED QUALIFICATIONS

BS in Life Sciences or similar preferred

At Sanofi diversity and inclusion is foundational to how we operate and embedded in our Core Values. We recognize to truly tap into the richness diversity brings we must lead with inclusion and have a workplace where those differences can thrive and be leveraged to empower the lives of our colleagues, patients and customers. We respect and celebrate the diversity of our people, their backgrounds and experiences and provide equal opportunity for all.

Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.

Learn more about Sanofi M&S: https://www.youtube.com/watch?v=_xz_sSanXhc

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At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.

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