What are the responsibilities and job description for the Inspection Supervisor (2nd Shift) position at Lead Candidate?
Inspection Supervisor (2nd Shift)
WHO?:
INCOG BioPharma is seeking an individual with subject matter expert (SME) capabilities in the inspection and/or packaging of sterile drug products. The primary purpose of this role is to provide strong compliance and Visual Inspection start-up process support as well as technical leadership in the creation and deployment of the visual inspection program within INCOG BioPharma Operations.
The primary function of this role is to facilitate the implementation and use of visual inspection processes and systems. This role will be responsible for developing and leading the inspection team and ensuring industry standards and regulatory requirements are met. This role will also provide direction related to automated visual inspection and packaging related technologies.
This is a 2nd shift role: 2pm – 10:30pm.
This role offers the opportunity to work at INCOG’s state-of-art sterile injectable CDMO during an exciting time of growth, contributing towards a better path to market for life-saving drugs.
WHAT?:
The role responsibilities are, but are not limited to:
- Provide technical support and project leadership in the implementation of visual inspection program.
- Train inspection operations and develop their capabilities to ensure Visual Inspection program sustainability.
- Coordinate the development of visual inspection specifications that maintain product quality and compliance.
- Develop processes to maintain and control the visual inspection requirements and coordinate the development of process procedures.
- Serve as Subject Matter Expert in visual inspection and packaging technologies and quality/compliance requirements.
- Assure compliance with cGMP requirements (current good manufacturing practices)
- Lead the team of qualified inspectors and manage manufacturing activities.
- 2nd shift role, following hours of 2pm-10:30pm.
YOU:
Ideally, candidates will have a BS or MS in Engineering/Science, or at least 8 years’ experience in the development or support of pharmaceutical inspection processes, quality systems or a closely related field. They also:
- Must pass health and visual checks and eye inspections annually.
- Must have previous leadership experience required.
- (Preferred) Strong understanding of Visual Inspection and Packaging requirements.
- (Preferred) Knowledge of Aseptic techniques and processing.
Curious? Send us your resume at apply@leadcandidate.com or you can find more information on our website.
Don’t meet all the requirements? Don’t sweat! We’re always looking for an excuse to discuss your next opportunity. You might just surprise yourself…
Lead Candidate wholeheartedly supports Equality and Diversity in employment and opposes all forms of unlawful or unfair discrimination on the grounds of age, disability, sex, gender reassignment, sexual orientation, pregnancy and maternity, race, religion or belief and marriage and civil partnerships.