WHO?
INCOG BioPharma Services is seeking an experienced and detail-oriented Process Specialist. They will work directly with the operations team and work closely with Manufacturing and QA systems to investigate deviations related to MFG activities.
WHAT?- Support authoring, reviewing, and approving various SOPs & Work Instructions and if needed create news to improve efficiency.
- Maintain effective communication with other departments and employees
- Ability to develop and maintain collaborative relationships with peers and colleagues across the organization, as well as internal and external clients.
- Ability to work well autonomously managing multiple projects and within a team in a fast-paced and deadline-oriented environment.
YOU! Familiarity with relevant quality and regulatory requirements and trends and cGMP'sStrong communication skills and the ability to build relationships with colleagues across all levels of the organization,4 years minimum experience working in a GMP environment.2 years minimum Deviation and technical writing experience
Why INCOG?Paid time off, based on tenure11 paid holidays 401(k) plan with company match up, vested immediately
Choice of health & wellness plansFSA and HSA options
Onsite wellness facility
Employee engagement activities; food trucks, monthly luncheons, fundraising events, team building competitions, offsite celebrations
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.
