Supervisor, Manufacturing Support
Supervisor, Manufacturing Support
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Job Description
MacroGenics is a leader in the discovery and development of innovative medicines that utilize our next generation antibody-based technologies. Our team of350 dedicated individuals is advancing a pipeline of product candidates to treat patients with products and platforms have attracted multiple partnerships with leading pharmaceuticaland biotechnologycompanies around the globe.
The Company considers its employees to be its most valuable asset and we are committed to providing opportunities for individuals to learn and grow as a means to further their professional development. MacroGenics corporate culture promotes an atmosphere of innovation open communication and teamwork where employees can see firsthand how they contribute to the success of the organization.
Summary of Position:
The Supervisor Manufacturing Support is a managerial position responsible for planning and executing activities in the Support area of a cGMP manufacturing facility which includes weigh and dispense buffer preparation media preparation facility cleaning equipment cleaning and material ordering. This individual will forecast monthly activities plan daily activities and ensure staff are focused on these activities. The individual will drive actions to ensure adherence to the overall production and lot release schedules while maintaining a high level of quality and compliance. This is a hands-on role where the supervisor will frequently work directly with the team to ensure that work is done accurately and on time.
Responsibilities and Job Duties
- Perform duties in accordance with Site SOPs EH&S standards and guidelines and relevant legal requirements and ensure that their team does the same.
- Ensure that activities meet all quality standards for cGMP and other applicable regulatory agencies.
- Perform and supervise others conducting weigh and dispense buffer preparation media preparation facility cleaning equipment cleaning and material ordering.
- Ensure successful implementation of new products and processes into the facility by creating new solution records SOPs change controls procuring new equipment and completing area changeover activities.
- Open and/or evaluate deviations for potential impact.
- Effectively troubleshoot production equipment and process problems of varying scope.
- Be accountable for Manufacturing Associate development and/or performance management through activities such as assignments and associated technical training programs.
- Ensure all staff are adequately trained on all cGMP manufacturing operations and documentation.
- Work on problems of advanced scope potentially cross-functional where analysis of situation or data requires a review of identifiable and unknown factors.
- Participate in and implement continuous improvement and operational excellence methods and tools to improve the overall efficiency of production operations.
- Schedule and coordinate activities with other departments such as Quality Assurance Quality Control Facilities and Engineering Supply Chain and Materials Management and Validation.
Qualifications
Education & Experience
- High school diploma or equivalent and a minimum of 9 years of related experience in a cGMP and/or bioprocessing environment
OR
- Associates degree in a related discipline and a minimum of 7 years of related experience in a cGMP and/or bioprocessing environment
OR
- Bachelors degree in a related discipline and a minimum of 5 years of related experience in a cGMP and/or bioprocessing environment
Knowledge Skills and Abilities
- Excellent interpersonal and people management skills with a demonstrated ability to engage influence and lead a team
- Ability to influence others without direct authority
- Excellent organizational skills and attention to detail
- Results driven with demonstrated successful outcomes
- Ability and desire to work well with diverse employees and customers in a cooperative and friendly manner
- Ability to handle multiple priorities in a fast-paced environment
- Excellent written and verbal communications skills
- Basic knowledge of chemistry
- High degree of comfort with basic arithmetic
- Proficient in the use of Microsoft software (word processing email spreadsheet database and Internet)
- Ability to lift at least 30 lbs
- Ability to work flexible hours including possible overtime and weekends
Supervisory Responsibilities
The individual will manage a group of Manufacturing Associates/Technicians
Preferred Qualifications
- Lean Six Sigma / Operational Excellence training
- Ability to lead and conduct formal documented risk assessments
- Experience writing documents for Regulatory submission (INDs BLAs etc.)
Additional Information
The annual rate of pay for this position ranges from $99200 - $151300. For non-exempt roles and according to applicable regulations there may be the possibility for overtime pay. This role is eligible for the Companys discretionary bonus and discretionary equity incentives. Eligible employees may participate in the Companys benefits programs including medical / dental / vision / prescription coverage employee wellness resources 401(k) plan with employer match access to an Employee Stock Purchase Plan (ESPP) paid time off & paid parental leave benefits and disability benefits.
The annual pay rate range is described in good faith and the Company believes is the range of possible compensation for this role at the time of this posting depending on the candidates experience qualifications geographic location and other factors permitted by law. The Company may ultimately pay more or less than the posted range and this range may be modified in the future. No amount is considered to be wages or compensation until such amount is earned vested and determinable under the terms and conditions of the applicable policies and plans. The amount and availability of any bonus commission benefits or any other form of compensation and benefits that are allocable to a particular employee remains in the Companys sole discretion unless and until paid and may be modified at the Companys sole discretion consistent with the law.
Statement
MacroGenics is proud to be an equal opportunity employer. Employment selection and related decisions are made without regard to race color national origin sex gender identity sexual orientation religion age disability protected veteran status or any other characteristic protected by federal state or local law. We are committed to working with and providing reasonable accommodation to individuals with disabilities. If because of a medical condition or disability you need a reasonable accommodation for any part of the employment process please email or call and/or 711 for TTD/TTY service.
Required Experience:
Manager
Employment Type
Full-Time
