Supervisor, QC Micro

 

We go where others won’t, taking on some of the biggest public health challenges to protect and enhance millions of lives, and create a better, more secure world. Here, you will join passionate professionals who advance their scientific, technical and professional skills to develop products designed-to protect and enhance life.

The Supervisor position supports the Quality Control group at Emergent BioSolutions Canton Campus to maintain QC testing and Lab optimization activities. The Supervisor is responsible for maintaining a safe and professional work environment.  The position will ensure the lab provides completes testing per agreed upon timelines, including Potency testing and container closure integrity testing. The position is also responsible for submitting samples to contract testing labs as needed.  The position will provide direct supervision for up to 2 direct reports.

 

ESSENTIAL FUNCTIONS
Reasonable accommodations will be made to enable individuals with disabilities to perform the essential functions.

•    Supervise operational activities of laboratory personnel in an organized and efficient manner to prevent any delays in product release or stability timelines.
•    Perform testing as needed.
•    Perform trend analysis, CAPAs, CCRs, and investigate deviations, Invalid Assays and OOS investigations as needed.
•    Implement quality improvement initiatives and corrective actions.
•    Investigate, suggest, validate and implement new laboratory procedures/techniques.
•    Provides expertise and troubleshoots lab related issues.
•    Review record keeping and documentation of laboratory equipment maintenance.
•    Review and update existing techniques, specifications, testing standards and SOPs or write new documents.
•    Supervise and provide significant contribution to the development and implementation of CGMP.
•    Document all procedures and results.
•    Represent department in meetings with Production, QA/RA, Engineering and other related departments in the absence of the QC Director.
•    Advise, recommend, and implement resolutions for quality issues and non-compliance.
•    Maintain database of laboratory data tracking and trending.
•    Ensure that all equipment is fully calibrated and validated.
•    Assist Method Validation in validation report generation and review.
•    Identify and recommend equipment, supplies and vendors as needed.
•    Guide the professional development of supporting staff both as individual and as a group.
•    Participate in interviewing process for hiring supporting staff.
•    Participate and attend professional seminars, conferences and conventions. 
The above statements are intended to describe the nature of work performed by those in this job and are not an exhaustive list of all duties. Nothing in this job description restricts managements right to assign or reassign duties and responsibilities to this job at any time which reflects management’s assignment of essential functions. 

 

MINIMUM EDUCATION, EXPERIENCE, SKILLS
To perform the job successfully, an individual should demonstrate the following competencies to perform the essential functions of this position.
•    Technical/Professional Knowledge—having achieved a satisfactory level of technical and professional skill or knowledge in position-related areas, keeping up with current developments and trends in areas of expertise.
•    Delegation—the individual delegates work assignments, gives authority to work independently, sets expectations and monitors delegated activities. 
•    Leadership—the individual inspires and motivates others to perform well and accepts feedback from others.
•    Safety and Security—the individual observes safety and security procedures and uses equipment and materials properly. May be required to lift items that are approximately 25lbs.
•    Management Skills—the individual includes staff in planning, decision-making, facilitating and process improvement; makes self-available to staff; provides regular performance feedback; and develops subordinates’ skills and encourages growth. 
•    Quality Management—the individual looks for ways to improve and promote quality and demonstrates accuracy and thoroughness. 
•    Planning/Organizing—the individual prioritizes and plans work activities, uses time efficiently and develops realistic action plans.
•    Stress Tolerance— maintaining stable performance under pressure or opposition (such as time pressure or job ambiguity); handling stress in a manner that is acceptable to others and to the organization.
Desired Minimum Qualifications
Education and Experience:
•    B.S. in Microbiology/Biology/Chemistry or related field with a minimum of 5 years’ experience in the Pharmaceutical or Biotechnology industry and 2 ye